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ÖZGEÇMİŞ 1. Adı Soyadı : Fatih ÖZALTIN 2. Doğum Tarihi : 11 Şubat 1971 3. Unvanı : Doçent Dr. 4. Öğrenim Durumu : Derece Lisans Y. Lisans Doktora Alan Tıp Fakültesi Çocuk Sağ.ve Hast. Çocuk Nefroloji Üniversite Ege Üniversitesi Hacettepe Universitesi Hacettepe Üniversitesi Yıl 1994 2000 2002 5. Akademik Unvanlar Yardımcı Doçent Çocuk Sağ. Ve Hastalıkları Hacettepe Üniv. 2005-2006 Doçent Çocuk Sağ. Ve Hastalıkları Hacettepe Üniv 2006- Doçent unvanını aldığı tarih: 2006 6. Yönetilen Yüksek Lisans ve Doktora Tezleri 6.1 Yüksek Lisans Tezleri Gür, P..”2000-2010 yılları arasında Pediatrik Nefroloji ve Pediatrik Patoloji Ünitelerinde Üriner Sistemin Konjenital Anomalilerinin Değerlendirilmesi”, Hacettepe Üniversitesi, Devam ediyor 7. Yayınlar 7.1 Uluslararası hakemli dergilerde yayınlanan makaleler 7.1.1 Uluslararası hakemli dergilerde yayınlanan orijinal araştırma makaleleri 1 Ozaltin F., N. Besbas, D. Uckan, M. Tuncer, R. Topaloglu, S. Ozen, U. Saatci ve A.Bakkaloglu. “The role of apoptosis in childhood Henoch Schonlein purpura”. Clin. Rheumatol. 22, 265-267 (2003) Duzova A., A. Bakkaloglu, N. Besbas, R. Topaloglu, S. Ozen, F. Ozaltin, Y. Bassoy, ve E. Yilmaz. “Role of A-SAA in monitoring subclinical inflammation and in colchicine dosage in familial Mediterranean fever”. Clin. Exp. Rheumatol. 21, 509-514 (2003) Besbas N., F. Ozaltin, T. Coskun, S. Ozalp, U. Saatci, A. Bakkaloglu ve A.M.El Nahas. “Relationship of leptin and insulin-like growth factor I to nutritional status in hemodialyzed children”. Pediatr. Nephrol. 18, 1255-1259 (2003) Sackesen C., A. Bakkaloglu, B. E. Sekerel, F. Ozaltin, N. Besbas, E. Yilmaz, G. Adalioglu ve S. Ozen. “Decreased frequency of atopy in pediatric patients with Familial Mediterranean Fever”. Ann. Rheum. Dis. 63, 187-190 (2004) Bakkaloglu A., A.Duzova, S. Ozen, B. Balci, N. Besbas, R. Topaloglu, F. Ozaltin ve E. Yilmaz. “The influence of SAA1, SAA2 gene polymorphisms on renal amyloidosis, and on SAA/CRP value in patients with familial Mediterranean fever in the Turkish population”. J. Rheumatol. 31, 1139-42 (2004) Ozaltin F., A.Bakkaloglu, S. Ozen, R. Topaloglu, U. Kavak, M. Kalyoncu ve N. Besbas. “The significance of IgA class of antineutrophil cytoplasmic antibodies (ANCA) in childhood Henoch-Schonlein purpura”. Clin. Rheumatol. 23, 426-429 (2004) Duzova A., F. Ozaltin, A.Ozon, N. Besbas, R. Topaloglu, S. Ozen ve A.Bakkaloglu. “Bone mineral density in children with familial Mediterranean fever”. Clin. Rheumatol. 23, 230-234 (2004) Besbas N., F. Ozaltin, F. Catal, S. Ozen, R.Topaloglu ve A.Bakkaloglu. “Macrophage chemoattractant protein-1 and interleukin-8 in acute poststreptococcal glomerulonephritis”. Pediatr. Nephrol. 9, 864-868 (2004) Ruf R.G., M. Schultheiss, A. Lichtenberger, S.M. Karle, I. Zalewski, B. Mucha, A.S. Everding, T. Neuhaus, L. Patzer, C. Plank, J.P. Haas, F. Ozaltin , A. Imm, A. Fuchshuber, A. Bakkaloglu, F. Hildebrandt ve APN Study Group. “Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroidsensitive nephrotic syndrome”. Kidney. Int. 66, 564-570 (2004) Topaloglu R., F. Ozaltin, E. Yilmaz, S. Ozen, B. Balci, N. Besbas ve A. Bakkaloglu. “E148Q is a disease causing MEFV mutation: a phenotypic evaluation in patients with familial Mediterranean fever”. Ann. Rheum. Dis. 64, 750-752 (2005) Turkish FMF Study Group. “Familial Mediterranean Fever (FMF) in Turkey: Results of a Nationwide Multicenter Study”. Medicine (Baltimore), 84, 1-11 (2005) 2 Ozaltin F., N.Besbas, A.Bakkaloglu, S. Gucer, S. Ozen, R. Topaloglu, G. Kale ve M. Caglar. “Apoptosis and proliferation in childhood proliferative glomerulonephritis”. Pediatr. Nephrol. 20, 1572-1577 (2005) Mucha B., F. Ozaltin, B.G. Hinkes, K. Hasselbacher, R.G. Ruf, M. Schultheiss, D. Hangan, B. Hoskins, A.S. Everding, R. Bogdanovic, T. Seeman, B. Hoppe, F. Hildebrandt ve Members of the APN Study Group. “Mutations in the Wilms’ Tumor 1 Gene Cause Isolated Steroid Resistant Nephrotic Syndrome and Occur in Exons 8 and 9”. Pediatr. Res. 59, 325-331 (2006) Kalyoncu M., R. Topaloglu, U. Bayrakci, A. Bakkaloglu, N. Besbas, F. Ozaltin, M. Bakkaloglu. “Cyclosporine drug monitoring with C0 and C2 concentrations in children with stable renal allograft function.” Pediatr. Transplant 10, 168-171 (2006) Hasselbacher K., R.C. Wiggins, V. Matejas, B.G. Hinkes, B. Mucha, B.E. Hoskins, F. Ozaltin, G. Nurnberg, C. Becker, D. Hangan, M. Pohl, E. KuwertzBroking, M. Griebel, V. Schumacher, B. Royer-Pokora, A. Bakkaloglu, P. Nurnberg, M. Zenker, F. Hildebrandt. “Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders.” Kidney Int. 70(6), 1008-1012 (2006) Hinkes B., R.C. Wiggins, R. Gbadegesin, C.N. Vlangos, D. Seelow, G. Nürnberg, P. Garg, R. Verma, H. Chaib, B.E. Hoskins, S. Ashraf, C. Becker, H.C. Hennies, M. Goyal, B.L. Wharram, A.D. Schachter, S. Mudumana, I. Drummond, D. Kerjaschki, R. Waldherr, A. Dietrich, F. Ozaltin, A. Bakkaloglu, R. Cleper, L. Basel-Vanagaite, M. Pohl, M. Griebel, A.N. Tsygin, A. Soylu, D. Müller, C.S. Sorli, T.D. Bunney, M. Katan, J. Liu, M. Attanasio, J.F. O'Toole, K. Hasselbacher, B. Mucha, E.A. Otto, R. Airik, A. Kispert, G.G. Kelley, A.V. Smrcka, T. Gudermann, L.B. Holzman, P. Nürnberg, F. Hildebrandt. “Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible.” Nat. Genet. 38(12), 1397-1405 (2006) Utsch B., A. Bokenkamp, M.R. Benz, N. Besbas, J. Dotsch, I. Franke, S. Frund, F. Gok, B. Hoppe, S. Karle, E. Kuwertz-Broking, G. Laube, M. Neb, M. Nuutinen, F. Ozaltin, W. Rascher, T. Ring, V. Tasic, J.A. van Wijk, M. Ludwig. “Novel OCRL1 Mutations in Patients With the Phenotype of Dent Disease.” Am. J. Kidney Dis. 48(6), 942-954 (2006) Ozen S., A. Bakkaloglu, R. Dusunsel, O. Soylemezoglu, F. Ozaltin, H. Poyrazoglu, O. Kasapcopur, O. Ozkaya, F. Yalcinkaya, A. Balat, N. Kural, O. Donmez, H. Alpay, A. Anarat, S. Mir, A. Gur-Guven, F. Sonmez, F. Gok. “On behalf of Turkish Pediatric Vasculitis Study Group. Childhood vasculitides in Turkey: a nationwide survey.” Clin. Rheumatol. 26(2),196-200 (2007) Hinkes B.G., B.Mucha, C.N. Vlangos, R. Gbadegesin, J.Liu, K. Hasselbacher, D. Hangan, F. Ozaltin, M. Zenker, F. Hildebrandt and Members of the APN Study Group. “Nephrotic syndrome in the first year of life: Two thirds of cases are caused by mutations in four genes (NPHS1, NPHS2, WT1, or LAMB2).” Pediatrics. 119(4), e907-19 (2007) 3 Bilginer Y., F. Ozaltin, C. Basaran, T.F. Aki, E. Karabulut, A. Duzova, N. Besbas, R. Topaloglu, S. Ozen, M. Bakkaloglu, A. Bakkaloglu. “Carotid intimamedia thickness in children and young adults with renal transplant: internal carotid artery vs. common carotid artery.” Pediatr. Transplant. 11(8), 888-894 (2007) Ozaltin F., S. Heeringa, C.E. Poyraz, Y. Bilginer, S. Kadayifcilar, N. Besbas, R. Topaloglu, S. Ozen, F. Hildebrandt, A. Bakkaloglu. “Eye involvement in children with primary focal segmental glomerulosclerosis.” Pediatr. Nephrol. 23(3), 421427 (2008) Gbadegesin R., B.G. Hinkes, B.E. Hoskins, C.N. Vlangos, S.F. Heeringa, J. Liu, C. Loirat, F. Ozaltin, S. Hashmi, F. Ulmer, R. Cleper, R.Ettenger, C. Antignac, R.C.Wiggins, M. Zenker, F. Hildebrandt. “Mutations in PLCE1 are a Major Cause of Isolated Diffuse Mesangial Sclerosis (IDMS).” Nephrol. Dial. Transplant. 23(4), 1291-1297 (2007) Hinkes B., C. Vlangos, S. Heeringa, B. Mucha, R. Gbadegesin, J. Liu, K. Hasselbacher, F. Ozaltin, F. Hildebrandt; and Members of the APN Study Group. “Specific podocin mutations correlate with age of onset in steroidresistant nephrotic syndrome.” J. Am. Soc. Nephrol. 19(2),365-371 (2008) Duzova A., T. Aki, A. Bakkaloglu, N. Besbas, R. Topaloglu, S. Ozen, F. Ozaltin, Y. Bilginer, E. Demirkaya, M. Bakkaloglu. “Triple immunosuppression with tacrolimus in pediatric renal transplantation: single-center experience.” Transplant. Proc. 40(1),132-134 (2008) Bilginer Y., R. Topaloglu, F.T. Aki, E.Demirkaya, F. Ozaltin, N. Besbas, S. Ozen, A. Bakkaloglu, I. Erkan, M. Bakkaloglu. “Outcome of primary glomerular disease in pediatric renal transplantation: a single-center experience.” Transplant. Proc. 40(1),129-131 (2008) Bilginer Y., F. Ozaltin, C. Basaran, A. Duzova, N. Besbas, R. Topaloglu, S. Ozen, A. Bakkaloglu. “Evaluation of intima media thickness of the common and internal carotid arteries with inflammatory markers in familial Mediterranean fever as possible predictors for atherosclerosis.” Rheumatol. Int. 28, 1211-1216 (2008) Heeringa S.F., C.N.Vlangos, G. Chernin, B. Hinkes, R. Gbadegesin, J. Liu, B.E. Hoskins, F. Ozaltin, F. Hildebrandt; Members of the APN Study Group. “Thirteen novel NPHS1 mutations in a large cohort of children with congenital nephrotic syndrome.” Nephrol. Dial. Transplant. 23(11),3527-3533 (2008) Besbas N., M. Draaken, M. Ludwig, O. Deren, D. Orhan, Y. Bilginer, F. Ozaltin. “A novel CLCN7 mutation resulting in a most severe form of autosomal recessive osteopetrosis.” Eur. J. Pediatr. 168, 1449-1454 (2009) 4 Altugan F.S., S. Ozen, N. Aktay-Ayaz, Ş. Güçer, R. Topaloğlu, A. Düzova, F. Ozaltin, N. Beşbaş.”Treatment of severe Henoch-Schönlein nephritis: justifying more immunosuppression.” Turk. J. Pediatr. 51(6), 551-555 (2009) Canpınar H., F. Özaltın, Y. Bilginer, A. Bakkaloğlu, S. Özen. “Toll-like receptors 2 and 4 cell surface expression reflects endotoxin tolerance in Henoch-Schönlein purpura.” Turk. J. Pediatr. 52, 22-27 (2010) Topaloglu R., I. Er, B.G. Dogan, Y. Bilginer, F. Ozaltin, N. Besbas, S. Ozen, A. Bakkaloglu, D. Gur. “Risk factors in community-acquired urinary tract infections caused by ESBL-producing bacteria in children.” Pediatr. Nephrol. 25(5),919-925 (2010) Beşbaş N., F. Ozaltin, S. Emre, A. Anarat, H. Alpay, A. Bakkaloğlu, E. Baskin, N. Buyan, O. Dönmez, R. Düşünsel, M. Ekim, F. Gök, A. Gür-Güven, S. Kavukçu, S. Mir, F. Sönmez. “Clinical course of primary focal segmental glomerulosclerosis (FSGS) in Turkish children: a report from the Turkish Pediatric Nephrology FSGS Study Group.” Turk. J. Pediatr. 52(3), 255-261 (2010) Chernin G., V. Vega-Warner, D.S. Schoeb, S.F. Heeringa, B. Ovunc, P. Saisawat, R. Cleper, F. Ozaltin, F. Hildebrandt; Group Members of the GPN Study. “Genotype/Phenotype Correlation in Nephrotic Syndrome Caused by WT1 Mutations.” Clin. J. Am. Soc. Nephrol. 5(9), 1655-1662 (2010) Borzych D., L. Rees, I.S. Ha, A. Chua, P.G. Valles, M. Lipka, P. Zambrano, T. Ahlenstiel, S.A. Bakkaloglu, A.P. Spizzirri, L. Lopez, F. Ozaltin, N. Printza, P. Hari, H. Klaus, M. Bak, A. Vogel, G. Ariceta, H.K. Yap, B.A. Warady, F. Schaefer. “The bone and mineral disorder of children undergoing chronic peritoneal dialysis.” Kidney. Int. 78(12), 1295-304 (2010) Demirkaya E., S. Ozen, Y. Bilginer, N.A. Ayaz, B.B. Makay, E. Unsal, M. Erguven, H. Poyrazoglu, O. Kasapcopur, F. Gok, S. Akman, A. Balat, O. Cavkaytar, B. Kaya, A. Duzova, F. Ozaltin, R. Topaloglu, N. Besbas, A. Bakkaloglu, N. Arisoy, H. Ozdogan, S. Bakkaloglu, T. Turker. “The distribution of juvenile idiopathic arthritis in the eastern Mediterranean: results from the registry of the Turkish Paediatric Rheumatology Association.” Clin. Exp. Rheumatol. 29(1), 111-116 (2011) Topaloğlu R., Y. Bilginer, A. Alikaşifoğlu, F. Ozaltin, N. Beşbaş, S. Ozen, A.Bakkaloğlu. “Neuroendocrine immune system in familial Mediterranean fever.” Turk. J. Pediatr. 52(6):588-593 (2010) Tayfur A.C., N. Besbas, Y. Bilginer, F. Ozaltin, A. Duzova, M. Bakkaloglu, F.T. Aki, S. Ozen, R. Topaloglu, A. Bakkaloglu. “Follow-up of patients with juvenile nephronophthisis after renal transplantation: a single center experience.” Transplant. Proc. 43(3):847-849 (2011) Heeringa S.F., G. Chernin, M. Chaki, W. Zhou, A.J. Sloan, Z. Ji, L.X. Xie, L. Salviati, T.W. Hurd, V. Vega-Warner, P.D. Killen, Y. Raphael, S. Ashraf, B. 5 Ovunc, D.S Schoeb, H.M. McLaughlin, R. Airik, C.N. Vlangos, R. Gbadegesin, B. Hinkes, P. Saisawat, E. Trevisson, M. Doimo, A. Casarin, V. Pertegato, G. Giorgi, H. Prokisch, A. Rötig, G. Nürnberg, C. Becker, S. Wang, F. Ozaltin, R. Topaloglu, A. Bakkaloglu, S.A. Bakkaloglu, D. Müller, A. Beissert, S. Mir, A. Berdeli, S. Varpizen, M. Zenker, V. Matejas, C. Santos-Ocaña, P. Navas, T. Kusakabe, A. Kispert, S. Akman, N.A. Soliman, S. Krick, P. Mundel, J. Reiser, P. Nürnberg, C.F. Clarke, R.C. Wiggins, C. Faul, F. Hildebrandt. “COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness.” J. Clin. Invest. 121(5):2013-24 (2011) Ozaltin F., T. Ibsirlioglu, E.Z. Taskiran, D.E. Baydar, F. Kaymaz, M. Buyukcelik, B.D. Kilic, A. Balat, P. Iatropoulos, E. Asan, N.A. Akarsu, F. Schaefer, E. Yilmaz, A. Bakkaloglu; the PodoNet Consortium. “Disruption of PTPRO Causes Childhood-Onset Nephrotic Syndrome.” Am. J. Hum. Genet. 89, 139-147 (2011) Mele C., P. Iatropoulos, R. Donadelli, A. Calabria, R. Maranta, P. Cassis, S. Buelli, Tomasoni, R. Piras, M. Krendel, S. Bettoni, M. Morigi, M. Delledonne, C. Pecoraro, I. Abbate, M.R. Capobianchi, F. Hildebrandt, E. Otto, F. Schaefer, F. Macciardi, F. Ozaltin, S. Emre, T. Ibsirlioglu, A. Benigni, G. Remuzzi, M. Noris, PodoNet Consortium. “MYO1E Mutations and Childhood Familial Focal Segmental Glomerulosclerosis.” N. Engl. J. Med. 365, 295-306 (2011) Gürakan F., G. Bassoy, S. Wedenoja, N. Uslu, H. Ozen, F. Ozaltin, P. Höglund. “Three cases of a rare disease, congenital chloride diarrhea, summons up the variation in the clinical course and significance of early diagnosis and adequate treatment in the prevention of intellectual disability.” Turk. J. Pediatr. 53(2),1948 (2011) Topaloglu R., T. Vilboux, T. Coskun, F. Ozaltin, B. Tinloy, M. Gunay-Aygun, A. Bakkaloglu, N. Besbas, L. van den Heuvel, R. Kleta, W.A. Gahl. “Genetic basis of cystinosis in Turkish patients: a single-center experience.” Pediatr. Nephrol. 27(1):115-121 (2012) Cil O., M. Ertunc, K.S. Gucer, F. Ozaltin, A.B. Iskit, R. Onur. “Endothelial Dysfunction and Increased Responses to Renal Nerve Stimulation in Rat Kidneys during Rhabdomyolysis-Induced Acute Renal Failure: Role of Hydroxyl Radical.” Ren. Fail. 34(2):211-220 (2012) Gokce M., Y. Bilginer, N. Besbas, F. Ozaltin, M. Cetin, F. Gumruk, S. Ozen. “Hematological features of pediatric systemic lupus erythematosus: suggesting management strategies in children.” Lupus. 21(8), 878-884 (2012) Wei C., H. Trachtman, J. Li, C. Dong, A.L. Friedman, J.J. Gassman, J.L. McMahan, M. Radeva, K.M. Heil, A. Trautmann, A. Anarat, S. Emre, G.M. Ghiggeri, F. Ozaltin, D. Haffner, D.S. Gipson, F. Kaskel, D.C.Fischer, F. Schaefer, J. Reiser; for the PodoNet and FSGS CT Study Consortia. “Circulating suPAR in Two Cohorts of Primary FSGS.” J. Am. Soc. Nephrol. (2012) 7.1.2. Uluslararası hakemli dergilerde yayınlanan vaka sunumları 6 Balci S., S. Bostanoglu, G. Altınok, F.Özaltın, “Sibs diagnosed prenatally with situs inversus totalis, renal and pancreatic dysplasia, and cysts: a new syndrome?” Am. J. Med. Genet. 82(2),166-169 (1999) Balcı, S., G. Altınok, F. Ozaltin, D. Aktas, E. A. Niron, B. Önol, “Laryngeal atresia presenting as fetal ascites, olygohydramnios and lung appearance mimicking cystic adenomatoid malformation in a 25-week-old fetus with Fraser syndrome”, Prenat. Diagn. 19(9), 856-858 (1999) Balci, S., S. Bostanoğlu, G.Altınok, F. Özaltin, “New syndrome?: Three sibs diagnosed prenatally with situs inversus totalis, renal and pancreatic dysplasia, and cysts”, Am. J. Med. Genet. 90(3),185-187 (2000) Yetgin, S., M. Çetin , I. Yenicesu, F. Özaltın, D.Uckan, “Acute parvovirus B19 infection mimicking juvenile myelomonocytic leukemia”, Eur. J. Haematol. 65(4), 276-278 (2000) Besbas, N., A. Duzova, R. Topaloglu, F. Gok, F. Ozaltin, S. Ozen, A. Bakkaloglu, “Pulmonary haemorrhage in a 6-year-old boy with Henoch-Schonlein purpura”, Clin. Rheumatol. 20(4), 293-296 (2001) Semerci, C.N.,, I. Bebitoglu, A. Kacar, S. Yurttagül, S. Erçakmak, D. Ertoy, F. Özaltin, S. Balci, “An unusual fetus with complete absence of thoracic, lumbar and sacral vertebrae, bilateral renal agenesis, VSD, meningomyelocele, imperforate anus, and teratoma” Clin. Dysmorphol. 10(1), 57-60 (2001) Balcı, S., S.M. Nabaei, F. Ozaltin, B. Onol, “Bilateral subpleural ectopic brain tissue in a 23-week-old fetus”, Turk. J. Pediatr. 43(3), 273-275 (2001) Beşbas, N., E. Özyürek, F. Balkancı, S. Ozen, I. Saatçi, F. Özaltın, A.Bakkaloğlu, “Behçet’s disease with severe arterial involvement in a child”, Clin. Rheumatol. 21(2), 176-179 (2002) Besbas N., F. Ozaltin, K. Tinaztepe, S. Gucer , S. Ozen, M. Bakkaloglu, A. Bakkaloglu, “Successful renal transplantation in a child with ANCA associated microscopic polyangiitis”, Pediatr. Nephrol., 18: 696-699, 2003 Ozaltin F., B. Yalcin, D. Orhan, N. Sari, M. Caglar, N. Besbas, A. Bakkaloglu, “An unusual cause of acute renal failure: renal lymphoma”, Pediatr. Nephrol.,19(8): 912-4, 2004 Ozaltin, F., E. Aypar, N. Besbas, N. Kiper, G. Kale, D. Orhan, A. Bakkaloglu ve S. Ozen, “Sino-Pulmonary-Renal disease in a child”, Pediatric Rheumatology Online Journal 2(1), 51-62 (2004) Besbas, N., F. Ozaltin, N. Jeck, H. Seyberth, M. Ludwig, “CLCN5 mutation (R347X) associated with hypokalemic metabolic alkalosis in a Turkish child: an unusual presentation of Dent’s disease”, Nephrol. Dial. Transplant. 20, 1476-1479 (2005) 7 Balcı, S., A.B. Akcan, M.E. Şenocak, A.Ö. Çiftçi, F. Özaltın, “A 13-year-old female with Turner syndrome and achalasia”, Turk. J. Pediatr. 48, 272-274 (2006) Bilginer, Y., F. Ozaltin, A. Duzova, I. Erdogan, T.F. Aki, M. Demircin, M. Bakkaloglu, A. Bakkaloglu, “Right atrial thrombosis complicating renal transplantation in a child”, Pediatr. Transplant. 12, 251-255 (2008) Yildirim, I., M. Ceyhan, N. Bayrakci, M. Uysal, B. Kuskonmaz, F. Ozaltin, “A case report of thrombocytopenia-associated multiple organ failure secondary to salmonella enterica serotype typhi infection in a pediatric patient: successful treatment with plasma Exchange”, Ther. Apher. Dial. 14(2), 226-229 (2010) Hakan, N., M. Aydin, O. Erdogan, Y.H. Cavusoglu, Z. Aycan, F. Ozaltin, A. Zenciroglu, S. Apaydin, R. Gunes, G. Sahin, G. Cinar, N. Okumus, “A novel WT1 gene mutation in a newborn infant diagnosed with Denys-Drash syndrome”, Genet. Counsel. 23(2), 255-261 (2012) Baskin E, S. Bayrakci, F. Alehan, H. Ozdemir, A. Oner, R. Horvath, V. VegaWarner, F. Hildebrandt, F. Ozaltin, “Respiratory-chain deficiency presenting as diffuse mesangial sclerosis with NPHS3 mutation”, Pediatr. Nephrol. 26:1157-61, 2011 Ameli, S., M. Mazaheri, A. Zare-Shahabadi, F. Ozaltin, F. Asgarian, M. Monajemzadeh, B. Bazargani, N. Ataei, N. Hajezadeh, A. Madani, T. Esfahani, A. Isaian, M. Zenker, N. Rezaei, “NPHS2 gene mutation in an Iranian family with familial steroid-resistant nephrotic syndrome”, Nefrologia. 32(5), 674-676 (2012) Topaloglu, R., E.Z. Taskiran, C. Tan, B. Erman, F. Ozaltin, O. Sanal, “C1q deficiency: identification of a novel missense mutation and treatment with fresh frozen plasma”, Clin. Rheumatol. 31(7), 1123-1126 (2012) Besbas N, B. Gulhan, D. Karpman, R. Topaloglu, A. Duzova, E. Korkmaz, F. Ozaltin, “Neonatal onset atypical hemolytic uremic syndrome successfully treated with eculizumab”, Pediatr. Nephrol. 2012 8 7.1.3. Uluslararası hakemli dergilerde yayınlanan editöre mektuplar Sanal, Ö., F. Özaltin, İ.Tezcan, F. Ersoy, “Serum IgD concentrations in patients with ataxia telangiectasia and with selective IgA deficiency”, Int. Arch. Allergy. Immunol. 116(3), 246 (1998) Ozaltın, F., A. Bakkaloglu, M. Orhon, A. Duzova, M. Irkec, “Bilateral uveitis in a 7-year-old patient with familial Mediterranean fever. An extremely rare complication”, Clin. Exp. Rheumatol. 19 (5 Suppl 24), S80-81 (2001) Ozaltin, F. A. Bakkaloglu, I.N. Saltik, H.Demir, A.Duzova, A. Bulun, N.Besbas, R. Topaloglu, S. Ozen, “Helicobacter pylori infection in Turkish children with familial Mediterranean fever: is it a cause of persistent inflammation?” Clin. Rheum. 23, 186-187 (2004) Balci, Y.I., B. Tavil, G. Fidan, F. Ozaltin, “Cerebral sinovenous thrombosis in a child with steroid sensitive nephrotic syndrome”, Eur. J. Pediatr. 166,757-758 (2007) Balci, S., F. Ozaltin, S. Bostanoğlu, “New syndrome--situs inversus totalis with cystic dysplasia of kidneys, pancreas and bowing”, Clin. Dysmorphol. 19(3),173174 (2004) 7.2 Uluslararası bilimsel toplantılarda sunulan ve bildiri kitabında (Proceeedins) basılan bildiriler. 7.2.1. Sözlü sunumlar Ozaltın, F., N. Besbas, D. Uçkan, M.Tuncer, R.Topaloğlu, S.Özen ve A.Bakkaloğlu, “The role of apoptosis in childhood Henoch Schonlein purpura,” XXXVIII Congress of the ERA-EDTA, Vieanna, Nephrol. Dial. Transplant. 16, A59 (2001) 9 Ozaltin, F., N. Besbas, T. Coskun, A. Duzova, S. Ozen, R.Topaloglu ve A. Bakkaloglu, “The value of leptin and IGF-I in the malnutrition of children under CAPD,” 36th Annual Meeting of European Society of Paediatric Nephrology, Bilbao, Pediatr. Nephrol. (Abstracts) 17, C54,O35 (2002) Besbas, N., F. Catal, F.Ozaltin, R. Topaloglu, A. Duzova, S. Ozen, Y.Bassoy ve A. Bakkaloglu, “The role of MCP-1 and IL-8 in acute poststreptococcal glomerulonephritis,” 36th Annual Meeting of European Society of Paediatric Nephrology, Bilbao, Pediatr Nephrol (Abstracts) 17, C51, O25 (2002) Ozaltin, F., A. Bakkaloglu, S. Ozen, U. Kavak, M. Kalyoncu, R.Topaloglu ve N. Besbas, “The significance of IgA class of antineutrophil cytoplasmic antibodies (ANCA) in childhood Henoch Schonlein purpura,” Xth European Pediatric Rheumatology Congress Annual Scientific Meeting of PRES, Stresa, (2003) Hasselbacher, K., R. Wiggins, B. Mucha, B. Hinkes, M. Pohl, M. Zenker, F. Ozaltin, A. Bakkaloglu, D. Hangan ve F. Hildebrandt, “Recessive Mutations in LAMB2 as cause of congenital nephrotic syndrome (CNS),” The American Society of Nephrology Renal Week, Philadelphia, J. Am. Soc. Nephrol. (Abstracts issue),16, 92A, SA-FC048 (2005) Bilginer, Y., C. Basaran, F. Ozaltin, N. Besbas, R. Topaloglu, S. Ozen, M. Ozmen ve A. Bakkaloglu, “Long term implications of inflammation in familial Mediterranean fever assessed by intima media thickness: a predictor for atherosclerosis?” Annual European Congress of Rheumatology (EULAR 2006), Amsterdam, Ann. Rheum.Dis., 65(Suppl II), p100, OP0152 (2006) Bilginer, Y., R.Topaloglu, A. Alikasifoglu, F. Ozaltin, N. Besbas, S. Ozen ve A.Bakkaloglu, “Is there a defect in the neuroendocrine immune system in familial Mediterranean fever?” 14th European Paediatric Rheumatology Congress, İstanbul, Abstract YIM OP-9, p 31, (2007) Schaefer, F., D. Borzych, S.Testa, M.Cantwell, M.Lipka, F. Ozaltin, A.R. Watson, G. Klaus, E. Verrina, S. Bakkaloglu, N. Aksu, B.A. Warrady ve International Pediatric PD Network (IPPN), “Are the pediatric K/DOQI bone guidelines appropriate for children on chronic peritoneal dialysis?” 42nd Annual Meeting ESPN, Lyon, Pediatr. Nephrol., 23, 1585, O11 (2008) Ozaltin, F., T. Ibsirlioglu, Z.E.Taskiran, D.Ertoy Baydar, F. Kaymaz, M. Buyukcelik, P.Iatropoulos, N.A. Akarsu, F. Schaefer ve A. Bakkaloglu, “Disruption of the ptpro gene causes childhood onset nephrotic syndrome,” 44th Annual Scientific Meeting of the European Society for Paediatric Nephrology, Dubrovnik-Cavtat, Pediatr. Nephrol. 26, 1573-1590, OS3-FRI-139 (2011) Trautmann, A., K. Heil, F. Ozaltin, M. Azocar, S. Emre, S. Caliskan, F. Emma, G.M. Ghiggeri ve F. Schaefer, for the PodoNet consortium, “Multidrug resistance and genetic diagnosis define poor long-term prognosis in Steroid Resistant Nephrotic Syndrome (SRNS),” 44th Annual Scientific Meeting of the European Society for Paediatric Nephrology, Dubrovnik-Cavtat, Pediatr. Nephrol. 26, 1573-1590, OS3-FRI-456 (2011) 10 Besbas, N., B. Gulhan, S. Ozen, R. Topaloglu, A. Duzova, C. Yildiz ve F. Ozaltin, “Atypical HUS and Eculizumab Treatment: Experience of a Tertiary Center,” 45th Annual Scientific Meeting of the European Society for Paediatric Nephrology, Krakow, Pediatr. Nephrol. 27, 1630, #OP47 (2012) 7.2.2. Poster sunumları Ozaltin, F., S. Balci, G. Tekinalp, Z. Akçören, M. Eryılmaz, S. Göğüs ve C.A. Öztürk, “A severe case of Walker-Warburg syndrome with hydrencephalus, cataract, glaucoma, microphtalmia and anorchia in a one day old male infant,” 29th Annual Meeting of The European Society of Human Genetics, Genova, P2.023, (1997) Ozaltin, F., N. Beşbaş, A. Tuncer, A. Gürgey, G. Tuncer ve Ü. Saatçi, “Evidence of disseminated intravascular coagulation associated with rheumatoid vasculitis: could it be related to macrophage activation syndrome?” Fifth European Conference On Pediatric Rheumatology, Garmisch-Partenkirchen, F18,(1997) Yılmaz, E., S. Ozen , A.Bakkaloglu, A.Duzova , F.Ozaltin , R.Topaloglu , N.Besbas, Ü. Saatci ve M. Ozguc, “Mutation analysis and amyloidosis and evidence for a high carrier rate in the Turkish population,” XXXVIII Congress of the ERA-EDTA, Vienna, pp25, (2001) Duzova, A. , S. Ozen, N. Besbas , F. Ozaltin , F. Catal , R. Topaloglu , A. Bakkaloglu, “Acute renal failure in children: Experience of a tertiary health center in Turkey”, XXXVIII Congress of the ERA-EDTA, Vieanna, pp83, (2001) Ozaltin F., N. Besbas , A. Bakkaloglu, T. Coskun , A. Duzova , S. Ozen , R. Emre, R. Topaloglu , S. Tekgül, M. Bakkaloglu, “Nutritional assessment of children on continuous ambulatory peritonela diaysis: value of leptin snd IGF-1”, XXXVIII Congress of the ERA-EDTA, Vieanna, pp224, (2001) Ozaltin F., A. Bakkaloglu, N. Besbas , D. Us, M. Bakkaloglu, A. Duzova , R. Topaloglu, S. Ozen, ”Serum bone turnover parameters in uremic children under continuous ambulatory peritoneal dialysis”, XXXVIII Congress of the ERAEDTA, Vieanna, pp307, (2001) Ozaltin F., N. Besbas, T. Coskun, A. Duzova, S. Ozen, R. Topaloglu, A. Bakkaloglu, “The value of leptin and IGF-I in the malnutrition of children under continuous ambulatory peritoneal dialysis (CAPD)”, XXXIX ERA-EDTA Congress, Cophenhagen, P422, (2002) Besbas N., F. Ozaltin, F. Catal, R. Topaloglu, A. Duzova, S. Ozen, Y. Bassoy, A. Bakkaloglu, “The role of MCP-1 and IL-8 in acute poststreptococcal glomerulonephritis”, XXXIX ERA-EDTA Congress, Cophenhagen, P422, (2002) Bakkaloğlu A, E. Yilmaz, B. Balcı, S. Kutlay, S. Ozen, R. Topaloglu, A. Duzova, F. Ozaltin, S. Erturk, A. Oner, N. Besbas, “SAA1 polymorphism is a predictor for amyloid development in familial Mediterranean fever”, 36th Annual Meeting 11 of European Society of Paediatric Nephrology, Bilbao, Pediatr. Nephrol. (Abstracts) 17; C84:P090, (2002) Duzova A, F. Ozaltin, N. Besbas, R. Topaloglu, S. Ozen, A. Bakkaloglu, “Bone mineral content, serum and urinary bone turnover parameters in familial Mediterranean fever”, III International Conference on Familial Mediterranean Fever and Hereditary Inflammatory Disorders, Montpellier, Clin. Exp. Rheumatol., 20(4) (Suppl 26): S-81: B20, (2002) Topaloglu R, F. Ozaltin, B. Balci, A. Bakkaloglu, S. Ozen, N. Besbas, “The phenotypic features of the E148Q mutation in the Turkish patients with FMF”, III International Conference on Familial Mediterranean Fever and Hereditary Inflammatory Disorders, Montpellier. Clin. Exp. Rheumatol., 20(4) (Suppl 26): S-82: B23, (2002) Sackesen C, S. Ozen, F. Ozaltin, N. Besbas, B. Sekerel, A. Bakkaloglu, “Decreased atopic sensitization in children with familial Mediterranean fever”, III International Conference on Familial Mediterranean Fever and Hereditary Inflammatory Disorders”, Montpellier, Clin. Exp. Rheumatol., 20(4) (Suppl 26): S-86: C6, (2002) Ozaltin F, A. Bakkaloglu, I.N. Saltik, A. Duzova, S. Ozen, N. Besbas, “Helicobacter pylori infection in Turkish children with familial Mediterranean fever: is it a causative agent inducing inflammation?”, III International Conference on Familial Mediterranean Fever and Hereditary Inflammatory Disorders, Montpellier. Clin Exp Rheumatol, 20(4) (Suppl 26): S-87: C9, (2002) Duzova A, F. Gumruk, F. Ozaltin, R. Topaloglu, C. Altay, A. Bakkaloglu, “The prevalence of beta-thalassemia trait in patients with familial Mediterranean fever”, III International Conference on Familial Mediterranean Fever and Hereditary Inflammatory Disorders, Montpellier, Clin. Exp. Rheumatol., 20(4) (Suppl 26): S-89: C17, (2002) Ozaltin F, N. Besbas, A. Bakkaloglu, S. Gucer, S. Ozen, R. Topaloglu, M. Caglar, “The role of apoptosis in the course of crescentic glomerulonephritis in childhood”, World Congress of Nephrology, Berlin, Nephrol. Dial. Transplant., 18 (Suppl 4): S-526: T761, (2003) Besbas N., M. Alikasifoglu, S. Ozen, F. Ozaltin, R. Topaloglu, E. Tuncbilek, A. Bakkaloglu, “Do RAS gene (ACE and AT1) polymorphisms affect the risk and outcome of focal segmental glomerulosclerosis?”, World Congress of Nephrology, Berlin, Nephrol. Dial. Transplant., 18 (Suppl 4): S-257: M802, (2003) Besbas N., F. Ozaltin, M. Alikasifoglu, R. Topaloglu, S. Ozen, A. Bakkaloglu, “The efficacy of ınfliximab in the treatment of juvenile idiopathic arthritis”, Xth European Pediatric Rheumatology Congress Annual Scientific Meeting of PRES, Stresa, Italy, (2003) Kavak U., R. Topaloglu, N. Besbas, S. Ozen, A. Duzova, F. Ozaltın, M. Kalyoncu, A. Bakkaloglu, “Effect of early corticosteroid therapy on developing 12 delayed nephritis in Henoch-Schonlein purpura”, Xth European Pediatric Rheumatology Congress Annual Scientific Meeting of PRES, Stresa, Italy, (2003) Ozaltin F., A. Duzova, A. Ozon, N. Besbas, R. Topaloglu, S. Ozen, A. Bakkaloglu, “Bone mineral density in children with familial mediterranean fever”, Xth European Pediatric Rheumatology Congress Annual Scientific Meeting of PRES, Stresa, Italy, (2003) Sackesen C., A. Bakkaloglu, F. Ozaltin, R. Topaloglu, N. Besbas, S. Ozen, “Atopy is decreased in pediatric patients wıth familial mediterranean fever”, Xth European Pediatric Rheumatology Congress Annual Scientific Meeting of PRES, Stresa, Italy, (2003) Guc D., A.L. Dogan, A. Bakkaloglu, F. Ozaltin, N. Besbas, B. Prakken, S. Albani, S. Ozen, “Cellular response against streptococci in paediatric Henoch Schonlein purpura and polyarteritis nodosa”, Annual European Congress of Rheumatology, Berlin, FRI0461, (2004) Yigitbas E, A. Uner, M.T. Dorak, W.Z. Ding, G. Tatayoglu, B. Balci, A. Duzova, F. Ozaltin, S. Ozen, N. Besbas, R. Topaloglu, E. Yilmaz, A. Bakkaloglu, M. Ozguc, E. Kansu, P.A. Fraser, “MICA exon 5 microsatellite alleles in Turkish patients with FMF”, Hum. Immunol., 65 (Suppl 1): S105-S105, (2004) Bilginer Y, D. Guc, L. Dogan, A. Bakkaloglu, N. Besbas, F. Ozaltin, B. Prakken, S. Albani, S. Ozen S, “T-Cell response against heat shock peptides and streptococci in pediatric Henoch Schonlein purpura and polyarteritis nodosa”, Arthritis Rheum., 50 (12): 4093-4093, (2004) Duzova A. , M. Kalyoncu, T. Aki, U. Bayrakci, F. Ozaltin, M. Bakkaloglu, “Calcineurin inhibitors combined with mycophenolate mofetil and prednisolone in pediatric renal recipients: single center experience”, 39th Annual Meeting of the European Society for Paediatric Nephrology, Istanbul, Pediatr. Nephrol., 20: C44; PP-061, (2005) Ozaltin F., N. Besbas, A. Bakkaloglu, S. Gucer, G. Kale, A. Duzova, S. Ozen, R. Topaloglu, M. Caglar, “Prognosis of acute poststreptococcal crescentic glomerulonephritis (APSCG) in children”, 39th Annual Meeting of the European Society for Paediatric Nephrology, Istanbul, Pediatr. Nephrol., 20: C68; PP-200, (2005) Kalyoncu M., N. Besbas, K. Ozgul, A. Duzova, F. Ozaltin, R. Topaloglu, S. Ozen, M. Ozguc, A. Bakkaloglu, “G/A polymorhism and levels of monocyte chemoattractant protein-1 in children with focal segmental glomerulosclerosis”, 39th Annual Meeting of the European Society for Paediatric Nephrology , Istanbul, Pediatr. Nephrol., 20: C73; PP-230, (2005) Mucha BE, F. Ozaltin, B. Hinkes, K. Hasselbacher, R.G. Ruf, M. Schultheiss, A. Bakkaloglu, F. Hildebrandt, “ Mutations in the WT1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 9”, The American Society 13 of Nephrology Renal Week, Philadelphia, J. Am. Soc. Nephrol., 16: 365A; FPO126, (2005) Mucha BE, B. Hinkes, F. Ozaltin, M. Schultheis , R.G. Ruf, K. Hasselbacher, A. Bakkaloglu, F. Hildebrandt, “Congenital nephrotic syndrome is primarily caused by mutations in nephrin, podocin and WT1”, The American Society of Nephrology Renal Week, Philadelphia, USA, J. Am. Soc. Nephrol., 16: 365A; FPO127, (2005) Besbas N, F. Ozaltin, A. Duzova, M. Kalyoncu, O. Sakalli, U. Bayrakci, R. Emre, A. Bakkaloglu, “Peritoneal function test as a basis of assessment od adequate therapy in children on continuous ambulatory peritoneal dialysis (CAPD)”, 26th Annual Conference on Peritoneal Dialysis, San Francisco, Perit. Dial. Int., 26 (Suppl 1); pp s48, (2006) Bilginer Y., B. Salancı, S. Ozen, M. A. Kasifoglu, O. Kasapcopur, F. Ozaltin, R. Topaloglu, A. Bakkaloglu, “Methylenetetrahydrofolate reductase gene A1298C polymorphism does not reflect the efficiacy of methotrexate in juvenile idiopathic arthritis”, Annual European Congress of Rheumatology (EULAR 2006), Amsterdam, Ann. Rheum. Dis., 65(Suppl II): p245, THU0430, (2006) Bilginer Y., C.E. Poyraz, F. Ozaltin, S. Kadayifcilar, N. Besbas, R. Topaloglu, S. Ozen, F. Hildebrandt, A. Bakkaloglu, “Eye involvement in children with primary FSGS”, XLIV ERA-EDTA Congress, Barcelona, Abstract ERA07L_1494: SaP178, (2007) Duzova A., O. Bircan, S. Ozen, F. Ozaltin, R. Topaloglu, N. Besbas, A. Bakkaloglu, “Final diagnosis of patients referred to a tertiary referral center with rheumatic complaints”, 14th European Paediatric Rheumatology Congress, İstanbul, Abstract PP-186, p 307, (2007) Bilginer Y., N. Besbas, F. Ozaltin, A. Duzova, S. Ozen, R. Topaloglu, A. Bakkaloglu, “Cerebral and pulmonary involvement: rare manifestations in Henoch-Schonlein purpura with familial Mediterrranean fever”, 14th European Paediatric Rheumatology Congress, İstanbul, Abstract PP-255, p383, (2007) Ozaltin F., H. Canpinar, Y. Bilginer, U. Kalyoncu, R. Topaloglu, A. Bakkaloglu, S. Ozen, “TLR expression in peripheral blood samples of patients with HenochSchonlein purpura and Behcet’s disease”, 14th European Paediatric Rheumatology Congress, İstanbul, Abstract PP,256, p 384, (2007) Bilginer Y., N. Gonc, A. Duzova, F. Ozaltin, S. Ozen, R. Topaloglu, N. Besbas, A. Bakkaloglu, “Adrenocortical functions in children with chronic renal failure”, 14th Congress of the International Pediatric Nephrology Association, Budapest, Pediatr. Nephrol., 22(9): 1560, 600(P), (2007) Bilginer Y., R. Topaloglu, F. Aki, I. Erkan, F. Ozaltin, N. Besbas, S. Ozen, A. Bakkaloglu, “Outcome of primary glomerular disease in pediatric 14 transplantation: a single center experience”, 14th Congress of the International Pediatric Nephrology Association, Budapest, Pediatr. Nephrol., 22(9): 1577, 669(P), (2007) Bilginer Y., S. Heeringa, C. Poyraz, F. Ozaltin, S. Kadayifcilar, N. Besbas, R. Topaloglu, S. Ozen, F. Hildebrandt, A. Bakkaloglu, “Eye involvement in children with primary FSGS”, 14th Congress of the International Pediatric Nephrology Association, Budapest, Pediatr. Nephrol., 22(9): 1612, 811(P), (2007) Berdeli A., A. N. Ayaz, S. Ozen, E. Demirkaya, F. Ozaltin, R. Topaloglu, N. Besbas, A. Bakkaloglu, “Can Toll-like receptor 2 polymorphism affect the phenotype of heterozygous?”, 5th International Congress on FMF and Systemic Autoinflammatory Diseases, Rome, Clin. Exp. Rheumatol., 26(2): 188, N1, (2008) Bilginer Y., A. Duzova, N. Gonc, F. Ozaltin, E. Baskin, E. Demirkaya, S. Ozen, R. Topaloglu, N. Besbas, A. Bakkaloglu, “Is there a defect in neuroendocrine immune system contributing the inflammation in chronic renal failure?”, 42nd Annual Meeting ESPN, Lyon, Pediatr. Nephrol., 23: 1612, P063, (2008) Besbas N., M. Draaken, M. Ludwig, O. Deren, D. Orhan, Y. Bilginer, F. Ozaltin, “A family with a novel VLCN7 mutation presented with autosomal recessive osteopetrosis and tubulopathy”, 42nd Annual Meeting ESPN, Lyon, Pediatr. Nephrol., 23: 1650, P216, (2008) Bilginer Y., I. Erdogan, A. Duzova, N. Besbas, M. Sahin, F. Ozaltin, E. Demirkaya, A. Celiker, S. Ozen, R. Topaloglu, A. Bakkaloglu, “42nd Annual Meeting ESPN, Lyon, Pediatr. Nephrol., 23: 1688, P365, (2008) Topaloglu R., I. Er, B. Dogan-Guciz, D. Gur, Y. Bilginer, F. Ozaltin, N. Besbas, A. Bakkaloglu, “Treatment and outcome in community acquired UTI caused by extended-spectrum beta lactamase producing enteric bacteria in children”, 42nd Annual Meeting ESPN, Lyon, Pediatr. Nephrol., 23: 1703, P428, (2008) Duzova A., Y. Bilginer, F. Ozaltin, R. Topaloglu, N. Besbas, E. Demirkaya, M. Bakkaloglu, A. Bakkaloglu, “Comparison between serum creatinine and serum csytatin C level in monitoring renal transplantation”, 5th Congress of the International Pediatric Transplant Association, İstanbul, Pediatr Transplant, 13 (Suppl 1): 73; Abstract #115, (2009) Duzova A., Y. Bilginer, F.T. Aki, F. Ozaltin, R. Topaloglu, A. Bakkaloglu, “Preemptive renal transplantation in a mediterranean country”, 5th Congress of the International Pediatric Transplant Association, İstanbul, Pediatr. Transplant., 13 (Suppl 1): 82, Abstract #155, (2009) Bilginer Y., I. Erdogan, A. Duzova, N. Besbas, F. Ozaltin, S. Ozen, R. Topaloglu, A. Bakkaloglu, M. Bakkaloglu, “Sinus tachycardia related to tacrolimus after kidney transplantation in children and young adults”, 5th Congress of the International Pediatric Transplant Association, İstanbul, Pediatr. Transplant., 13 (Suppl 1): 133, Abstract #363, (2009) 15 Ozaltin F., N. Besbas, A.B. Iskit, O. Cil, Z. Akcoren, G. Kale, A. Bakkaloglu, “CKR-1 may play a role in inflammation in experimental mesangioproliferative glomerulonephritis”, 44th Annual Scientific Meeting of the European Society for Paediatric Nephrology, Dubrovnik-Cavtat, Pediatr. Nephrol., 26: 1573-1590, PS1-FRI-140, (2011) Gulhan B., D. Ö. Hacıhamdioğlu, Y. Bilginer, F. Özaltın, T. Aki, A. Düzova, S. Özan, N. Beşbaş, R. Topaloğlu, “Hypertension after renal transplantation in children”, 44th Annual Scientific Meeting of the European Society for Paediatric Nephrology, Dubrovnik-Cavtat, Pediatr. Nephrol., 26: 1573-1590, PS1-THU-411, (2011) Hacihamdioglu D.O., F. Ozaltin, C. Zeybek, S. Kalman, E. Demirkaya, F. Gok, “The benefits of cyclosporine treatment of the patient with NPHS2 mutation”, 45th Annual Scientific Meeting of the European Society for Paediatric Nephrology, Auditorium Maximum of the Jagiellonian University, Krakow, Pediatr. Nephrol., 27: 1703, #P131, (2012) Topaloglu R., B. Gulhan, F. Ozaltin, A. Duzova, N. Besbas, “Rituximab in steroid dependent and resistant nephrotic syndrome patients”, 45th Annual Scientific Meeting of the European Society for Paediatric Nephrology, Auditorium Maximum of the Jagiellonian University, Krakow, Pediatr. Nephrol., 27: 1710, #P146, (2012) Gulhan B., A. Duzova, F. Ozaltin, R. Topaloglu, S. Ozen, Y. Bilginer, A.C. Tayfur, C. Yildiz, N. Besbas, “Peritoneal dialysis in children under two years of age”, 45th Annual Scientific Meeting of the European Society for Paediatric Nephrology, Auditorium Maximum of the Jagiellonian University, Krakow, Pediatr. Nephrol., 27: 1799, #P341, (2012) Gulhan B., R. Topaloglu, Y. Bilginer, A.C. Tayfur, C. Yildiz, F. Ozaltin, A. Duzova, S. Ozen, F.T. Aki, N. Besbas, “Conversion to sirolimus in pediatric renal transplant recipients”, 45th Annual Scientific Meeting of the European Society for Paediatric Nephrology, Auditorium Maximum of the Jagiellonian University, Krakow, Pediatr. Nephrol., 27: 1818, #P381, (2012) 7.3 Yazılan uluslararası kitaplar veya kitaplarda bölümler Ozaltin, F. ve S. Ozen, “Childhood Polyarteritis Nodosa”, Textbook of Clinical Pediatrics, 2nd Edition, ed A.Y. Elzouki, F.B. Stapleton, R.J. Whitley, W. Oh, H.A. Harfi, H. Nazer, 2nd edition, 1685-1687. Springer-Verlag, Berlin Heidelberg. 2011. Ozaltin, F. ve S. Ozen, “Vasculitis: Takayasu Arteritis”, Textbook of Clinical Pediatrics, 2nd Edition, ed A.Y. Elzouki, F.B. Stapleton, R.J. Whitley, W. Oh, 16 H.A. Harfi, H. Nazer, 2nd edition, 1695-1696. Springer-Verlag, Berlin Heidelberg. 2011. Ozaltin, F. ve S. Ozen, “Vasculitis: Other Forms of Vasculitis”, Textbook of Clinical Pediatrics, 2nd Edition, ed A.Y. Elzouki, F.B. Stapleton, R.J. Whitley, W. Oh, H.A. Harfi, H. Nazer, 2nd edition, 1697-1699. Springer-Verlag, Berlin Heidelberg. 2011. Ozaltin, F. ve S. Ozen, “Antineutrophil Cytoplasmic Antibody (ANCA)Associated Small-Vessel Vasculitides”, Textbook of Clinical Pediatrics, 2nd Edition, ed A.Y. Elzouki, F.B. Stapleton, R.J. Whitley, W. Oh, H.A. Harfi, H. Nazer, 2nd edition, 1689-1693. Springer-Verlag, Berlin Heidelberg. 2011. 7.4 Ulusal hakemli dergilerde yayımlanan makaleler Beşbaş, N. ve F. Özaltın, “Renal osteodistrofi: patogenez ve tedavi ilkeleri”, Çocuk Sağlığı ve Hastalıkları Dergisi, 41, 565-580 (1998). Beşbaş, N. ve F. Özaltın, “Sistemik Vaskülitler”, Katkı Pediatri Dergisi, 20(6), 703-25 (1999). Özaltın, F. ve A. Bakkaloğlu, “Hipertansiyon taraması”, Katkı Pediatri Dergisi, 21(3), 353-61 (2000). Özaltın, F. ve N. Beşbaş, “Nefrolojide Otoimmunite”, Katkı Pediatri Dergisi, 23(4), 414-25 (2002). Özaltın, F. ve S. Özen, “Ailevi Akdeniz Ateşi”, Türkiye Tıp Dergisi, 10(2), 93-97 (2003). Özaltin,F. ve S. Özen, “Jüvenil spondiloartritler”, Türkiye Klinikleri İmmunoloji Romatoloji, 4(1), 58-67 (2004). Özaltın, F. ve A. Bakkaloğlu, “Sodyum ve su dengesi”, Katkı Pediatri Dergisi, 29(1), 41-60 (2007). Özaltın, F. ve A. Bakkaloğlu, “Sodyum dengesi bozuklukları ve tedavisi”, Katkı Pediatri Dergisi, 29(1), 61-92 (2007). Özaltın, F., “Nefroloji ve Genetik”, Türkiye Klinikleri J. Pediatr. Sci., 4(1), 164178 (2008). 7.5 Ulusal bilimsel toplantılarda sunulan ve bildiri kitabında basılan bildiriler 17 Balcı S., B. Onol, M. Nabei, F. Özaltın, F. Söylemezoğlu, “Akciğerde ektopik beyin dokusunun görüldüğü 23 haftalık bir fetusun sunumu”, XIII. Ulusal Patoloji Kongresi, S18. İstanbul 1997. Balcı S., S. Bostanoğlu, G. Altınok, F. Özaltın, “Prenatal fetal US ile tanı alan iki kardeşte renal, pankreatik displazi ve kist, timik hipoplazi, situs inversus totalis, alt ektremite kemiklerinde yaylanma ila karakterize yeni otozomal resesif bir sendrom”, 3.Tıbbi Görüntüleme ve Girişimsel Radyoloji Kongresi, S802. Antalya 1997. Özaltın F., N. Beşbaş, A. Tuncer, A. Gürgey, S. Özdemir, G. Tuncer, “Sistemik Juvenil Romatoid Artrit’e (JRA) Bağlı Vaskülit ve DİK”, I.Ulusal Pediatrik Romatoloji Kongresi, Ankara 1997. Özaltın F., N. Besbas, D. Uçkan, M. Tuncer, R. Topaloğlu, S. Özen, A. Bakkaloğlu, “Çocuklarda Henoch-Schönlein purpurasında apoptosisin rolü”, 18. Ulusal Nefroloji, Hipertansiyon, Diyaliz ve Transplantasyon Kongresi, Sayfa 8, SS/021. Kapadokya 2001. Çatal F., N. Besbas , F. Özaltın , R. Topaloglu, A. Düzova , S. Özen, A. Bakkaloğlu, “Akut poststreptokoksik glomerulonefritte MCP-1 ve IL-8'in patogenezdeki yeri”, 18. Ulusal Nefroloji, Hipertansiyon, Diyaliz ve Transplantasyon Kongresi, Sayfa 8, SS/023. Kapadokya 2001. Özaltın F. , S. Tekgül, M. Bakkaloğlu , S. Eskiçorapçı, S. Özen , R. Topaloğlu , N. Besbas , A. Bakkaloğlu, “Pediatrik SAPD: Hacettepe Üniversitesi Deneyimi”, 6. Ulusal Çocuk Ürolojisi Kongresi, Samsun 2001. Düzova A., F. Özaltın, N. Beşbaş, R. Topaloğlu, S. Özen, A. Bakkaloğlu, “Ailevi Akdeniz ateşinde kemik mineral kontenti, serum ve idrar kemik döngüsü belirleyicileri”, 1.Ulusal Osteoporoz Kongresi, Antalya 2002. Bakkaloğlu A., A. Düzova, B. Balcı, N. Beşbaş, R. Topaloğlu, F. Özaltın, S. Özen, E. Yılmaz, “Ailevi Akdeniz ateşinde SAA1, SAA2 gen polimorfizmlerinin renal amiloidoz ve SAA düzeyleri üzerine etkisi”, 3.Ulusal Pediatrik Nefroloji Kongresi, Antalya 2002. Özaltın F, N. Beşbaş, T. Coşkun, A. Düzova, S. Özen, R. Topaloğlu, A. Bakkaloğlu, “Sürekli ayaktan periton diaylizi uygulanan son dönem böbrek yetmezliğindeki çocuklarda beslenme durumunun değerlendirilmesinde leptin ve IGF-1'in yeri”, 3.Ulusal Pediatrik Nefroloji Kongresi, Antalya 2002. Balcı S., B. Akcan, A. Ö. Çiftçi, M. E. Şenocak, F. Özaltın, “Turner sendromlu ve akalazyalı bir vaka. Çocukluktan Erişkinliğe Turner Sendromu”, Pediatrik Endokrinoloji ve Oksoloji Derneği Sempozyumu-II, İstanbul 2003. Özaltın F. , N. Besbas , D. Uçkan , M. Tuncer , R. Topaloğlu , S. Özen , A. Bakkaloğlu, “The role of apoptosis in childhood Henoch Schonlein purpura”, 1st 18 Meeting of Southeastern European Pediatric Nephrology Working Group, pp49 , P6 . İstanbul 2001. Duzova A., A. Bakkaoglu , N. Besbas , Ş. Gücer , K. Tinaztepe , R. Topalglu , S. Ozen, F. Ozaltin, Ü. Saatci , “Cyclophosphamide and cyclosporin A in the treatment of primary MPGN in children”, 1st Meeting of Southeastern European Pediatric Nephrology Working Group, pp49 , P7. İstanbul 2001. Duzova A. , S. Ozen , N. Besbas , F. Ozaltin , F. Catal , R. Topaloglu, A. Bakkaloglu, “Acute renal failure in children: Experience of a tertiary health center in Turkey”, 1st Meeting of Southeastern European Pediatric Nephrology Working Group, pp 52, P20. İstanbul 2001. Ozaltin F. , A. Bakkaloglu , N. Besbas , D. Us , M. Bakkaloglu , A. Duzova, R. Topaloglu , S. Ozen, “Serum bone turnover parameters in uremic children under continuous ambulatory peritoneal dialysis”, 1st Meeting of Southeastern European Pediatric Nephrology Working Group, pp 53, P21. İstanbul 2001. Ozaltin F. , N. Besbas, A. Bakkaloglu, T. Coskun, A. Duzova, S. Ozen, R. Emre, R. Topaloglu, S. Tekgül, M. Bakkaloglu, “Nutritional assessment of children on continuous ambulatory peritoneal diaysis: value of leptin snd IGF-1”, 1st Meeting of Southeastern European Pediatric Nephrology Working Group, pp 53, P22. İstanbul 2001. Ozen S. , E. Yılmaz, A. Bakkaloglu, A. Duzova, F. Ozaltin , R. Topaloglu , N. Besbas , Ü. Saatci, “Mutation analysis in Familial Mediterranean fever and amyloidosis and evidence for a high carrier rate in the Turkish population”, 1st Meeting of Southeastern European Pediatric Nephrology Working Group, pp 57, P40. İstanbul 2001. Ozen S , D. Ertoy, I. Heidet, L. Cohen-Solal, N. Besbas, R. Topaloglu, A. Duzova, F. Ozaltin, H. Ozen, A. Bakkaloglu, C. Antignac, “Benign Familial hematuria associated with a novel COL4A4 mutation”, 1st Meeting of Southeastern European Pediatric Nephrology Working Group, pp 58, P44. İstanbul 2001. Düzova A., A. Bakkaloğlu , N. Besbas , Ş. Güçer , K. Tınaztepe , R. Topaloğlu , S. Özen , F. Özaltın , Ü. Saatçi, “Çocukluk çağı MPGN tedavisinde silofosfamid ve siklosporin A tedavisi”, 18. Ulusal Nefroloji, Hipertansiyon, Diyaliz ve Transplantasyon Kongresi, Sayfa 14, P-GN/007. Kapadokya 2001. Özaltın F. , A. Bakkaloglu, N. Besbas, D. Us, A. Düzova, R. Emre, S. Özen, R. Topaloglu, S. Tekgül, M. Bakkaloglu, “Sürekli ayaktan periton diyalizi uygulanan çocuk hastalarda serum kemik turnover parametreleri”, 18. Ulusal Nefroloji, Hipertansiyon, Diyaliz ve Transplantasyon Kongresi, Sayfa 50, PP/116. Kapadokya 2001. Özaltın F. , N. Besbas, A. Bakkaloglu, T. Coskun, A. Düzova, S. Özen, R. Emre, R. Topaloglu, S. Tekgül, M. Bakkaloglu, “Sürekli ayaktan periton diyalizi 19 uygulanan çocukların nutrisyonel değerlendirmesi: Leptin ve IGF-1'in değeri”, 18. Ulusal Nefroloji, Hipertansiyon, Diyaliz ve Transplantasyon Kongresi, Sayfa 50, P-PD/117. Kapadokya 2001. Kavak U, F. Özaltın, D. Orhan, N. Beşbaş, G. Kale, A. Bakkaloğlu, “Nefrokalsinozisin eşlik ettiği konjenital mezoblastik nefroma”, 3.Ulusal Pediatrik Nefroloji Kongresi, Antalya 2002.. 8. Projeler “Ailevi Akdeniz Ateşinde SAA1, SAA2 ve ApoE Polimorfizmleri ve Bu Polimorfizmlerin Amiloidoz ile Hastalardaki Kolşisin Farmakogenetiği ile İlişkisi”, Hacettepe Üniversitesi Tıp Fakültesi Güdümlü altyapı projesi, 01 G 003, Yardımcı Araştırıcı, 2003 “Deneysel Proliferatif Glomerulonefrit Modelinde MCP-1 ve Reseptörlerinin Rolü ile Siklosporin A’nın Yeri”, Hacettepe Üniversitesi Araştırma Projesi, 01 02 101023, Yardımcı Araştırıcı, 2004 Moleküler Nefroloji laboratuarının Kurulması, Hacettepe Üniversitesi Alt Yapı Projesi, 06A 101 008. Proje Yürütücüsü, 2007. “PodoNet: Consortium for Clinical, Genetic and Experimental Research into Hereditary Diseases of the Podocyte”, E-RARE (ERA-Net for research programs on rare diseases) Projesi, Yardımcı Araştırıcı, 2008. A multicenter, randomized, double-blind, paralel-group, evaluation of 12 weeks of valsartan compared to enalapril on sitting systolic blood pressure in children 6 to 17 years of age with hypertension (CVAL489K2302), Faz 3 çalışma, Yardımcı Araştırıcı (08/05/2008) A randomized, multicenter, double-blind, 6 week study to evaluate the dose response of valsartan on blood pressure reduction in children 1-5 years old with hypertension, followed by a 2 week placebo withdrawal period (CVAL489K2303). Faz 3 çalışma, Yardımcı Araştırıcı, 2008 European Consortium for High-Throughput Research in Rare Kidney Diseases, EURenOmics, AB 7.Çerçeve Projesi, Partner, Devam ediyor 9. İdari Görevler Başasistanlık Hacettepe Üniversitesi Tıp Fakültesi Çocuk Sağ.ve Hast. 1998-1999 10. Bilimsel Kuruluşlara Üyelikler Çocuk Nefroloji Derneği Çocuk Romatoloji Derneği European Society For Paediatric Nephrology 20 Türk Nefroloji Derneği ERA-EDTA 11. Ödüller a. The role of apoptosis in childhood Henoch Schonlein purpura. European Renal Association-European Dialysis and Transplant Association Annual Congress, Vienna, Austria 24-27 June, 2001. “Best abstracts presented by young authors” ödülü b. The value of leptin and IGF-I in the malnutrition of children under CAPD (sözlü sunum). 36th Annual Meeting of European Society of Paediatric Nephrology, 20-23 September 2002, Bilbao. Kongre "grant" i (kayıt ve konaklama ücreti kongre sekreteryası tarafından karşılandı). c. Ailevi Akdeniz ateşinde kemik mineral kontenti, serum ve idrar kemik döngüsü belirleyicileri (sözlü sunum). 1.Ulusal Osteoporoz Kongresi, 7-11 Ekim 2002, Antalya (birincilik) d. Sürekli ayaktan periton diaylizi uygulanan son dönem böbrek yetmezliğindeki çocuklarda beslenme durumunun değerlendirilmesinde leptin ve IGF-1'in yeri (sözlü sunum). 3.Ulusal Pediatrik Nefroloji Kongresi, 10-13 Kasım 2002, Antalya, (Anadolu Böbrek Vakfı Eğitim Teşvik Ödülü) e. The role of apoptosis in the course of crescentic glomerulonephritis in childhood. World Congress of Nephrology. 8-12 June2003, Berlin (ESPN ödülü) f. Hacettepe Üniversitesi 2004-2005 Akademik Yılı Bilimde Teşvik Ödülü (26.09.2006) 21 12. Son beş yılda verdiğiniz lisans ve lisansüstü düzeydeki dersler için aşağıdaki tabloyu doldurunuz. Dönem ve Dersler 2006-2007: Sürekli ayaktan periton diyalizi (Asistan) 2006-2007: Sıvı-elektrolit tedavisi (Asistan) 2006-2007: Sıvı-elektrolit (Dönem IV, PDÖ), 2 yarıyıl 2006-2007: Dehidratasyon ve tedavisi (Dönem IV, Türkçe Tıp), 2 yarıyıl 2006-2007: Dehidratasyon ve tedavisi (Dönem IV, İngilizce Tıp), 2 yarıyıl 2006-2007: Kanıta dayalı tıp (Dönem IV) 2007-2008: Sürekli ayaktan periton diyalizi (Asistan) 2007-2008: Sıvı-elektrolit tedavisi (Asistan) 2007-2008: Dehidratasyon ve tedavisi (Dönem IV, Türkçe Tıp), 2 yarıyıl 2007-2008: Dehidratasyon ve tedavisi (Dönem IV, İngilizce Tıp), 2 yarıyıl 2007-2007: Dehidratasyon (Dönem IV, PDÖ), 2 yarıyıl 2007-2008: Preterm eylem (Dönem III, PDÖ) 2007-2008: Sodyum ve su dengesi bozuklukları (Dönem III, Türkçe Tıp) 2007-2008: Sodyum ve su dengesi bozuklukları (Dönem III, İngilizce Tıp) 2007-2008: Akut böbrek yetmezliği (Dönem III, Türkçe Tıp) 2008-2009: Sıvı-elektrolit tedavisi (Asistan) 2008-2009: Sürekli ayaktan periton diyalizi (Asistan) 2008-2009: Dehidratasyon ve tedavisi (Dönem IV, Türkçe Tıp), 2 yarıyıl 2008-2009: Dehidratasyon ve tedavisi (Dönem IV, İngilizce Tıp), 2 yarıyıl 2008-2009: Dehidratasyon (Dönem IV, PDÖ), 2 yarıyıl 2008-2009: İyi hekimlik uygulamaları (Dönem III), 2 yarıyıl 2008-2009: Sodyum ve su dengesi bozuklukları (Dönem III, Türkçe Tıp) 22 2008-2009: Sodyum ve su dengesi bozuklukları (Dönem III, İngilizce Tıp) 2008-2009: Akut böbrek yetmezliği (Dönem III, Türkçe Tıp) 2008-2009: Başağrısı (Dönem III, PDÖ) 2009-2010: Sıvı-elektrolit tedavisi (Asistan) 2009-2010: Dehidratasyon ve tedavisi (Dönem IV, Türkçe Tıp), 2 yarıyıl 2009-2010: Dehidratasyon ve tedavisi (Dönem IV, İngilizce Tıp), 2 yarıyıl 2009-2010: Poliüri-polidipsi (Dönem IV PDÖ), 2 yarıyıl 2009-2010: Kanıta dayalı tıp (Dönem IV) 2008-2009: Sodyum ve su dengesi bozuklukları (Dönem III, Türkçe Tıp) 2008-2009: Sodyum ve su dengesi bozuklukları (Dönem III, İngilizce Tıp) 2008-2009: Akut böbrek yetmezliği (Dönem III, Türkçe Tıp) 2009-2010: İyi hekimlik uygulamaları (Dönem I), 2 yarıyıl 2010-2011: Sıvı-elektrolit tedavisi (Asistan) 2010-2011: Dehidratasyon ve tedavisi (Dönem IV, Türkçe Tıp), 2 yarıyıl 2010-2011: Dehidratasyon ve tedavisi (Dönem IV, İngilizce Tıp), 2 yarıyıl 2010-2011: Poliüri-polidipsi (Dönem IV PDÖ) 2010-2011: Sodyum ve su dengesi bozuklukları (Dönem III, İngilizce Tıp) 2010-2011: Potasyum dengesi ve bozuklukları (Dönem III, İngilizce Tıp) 2010-2011: Akut böbrek yetmezliği (Dönem III, Türkçe Tıp) Not: Açılmışsa yaz döneminde verilen dersler de tabloya ilave edilecektir. 23