PROF.DR. FATMA FATOŞ YALÇINKAYA    
Adı : FATMA FATOŞ
Soyadı : YALÇINKAYA
E-posta : fyalcin@medicine.ankara.edu.tr
Tel :
Ünvan : PROF.DR.
Birim : TIP FAKÜLTESİ
Bölüm : DAHİLİ TIP BİLİMLERİ BÖLÜMLERİ
Kişisel Akademik Bilgiler

 ÖZGEÇMİŞ

Adı Soyadı, Akademik Ünvanı: Fatma Fatoş Yalçınkaya, Profesör Dr.

 

A) KİŞİSEL BİLGİLER:

Doğum Tarihi: 12.03.1955

TC Kimlik No: 32278801034

İş Adresi: Ankara Üniversitesi Tıp Fakültesi

                  Çocuk Sağlığı ve Hastalıkları Anabilim Dalı

                  Çocuk Nefroloji - Çocuk Romatoloji Bilim Dalı, Dikimevi, 06100, Ankara

                  Tel: (312) 5956708

                  Faks: (312) 3191440

                  E-mail: fyalcin@medicine.ankara.edu.tr

Ev Adresi: Meksika cad. Çınar Sitesi 45/62 Ümitköy ANKARA

                   Tel: (312) 2350536

Yabancı dil: İngilizce

 

B) EĞİTİM GEÇMİŞİ:

          

Ortaöğretim ve Lise: TED Ankara Koleji-Ankara

Derece

Alan
Üniversite

Yıl

1)Lisans

Tıp Fakültesi

Hacettepe Üniversitesi

1973-1979

2)Uzmanlık

Çocuk Sağlığı ve Hastalıkları

Dr. Sami Ulus Çocuk Hastanesi

1980-1984

3)Yan dal    uzmanlık

Çocuk Nefroloji

Ankara Üniversitesi Tıp Fakültesi

Çocuk Sağlığı ve Hastalıkları Anabilim Dalı

Çocuk Nefroloji Bilim Dalı

1988-1991

 

C) GÖREVLER:

Görev Unvanı

Görev Yeri

Yıl

1)Araştırma Görevlisi

Dr. Sami Ulus Çocuk Hastanesi

1980-1988

2) Çocuk Nefroloji

Yan dal Araştırma Görevlisi

Ankara Üniversitesi Tıp Fakültesi;

 Çocuk Sağlığı ve Hastalıkları Anabilim Dalı

Çocuk Nefroloji Bilim Dalı

1988-1991

4)Çocuk Nefroloji Uzman Doktor

Ankara Üniversitesi Tıp Fakültesi;

 Çocuk Sağlığı ve Hastalıkları Anabilim Dalı

Çocuk Nefroloji Bilim Dalı

1991-1993

5)Doçent

Ankara Üniversitesi Tıp Fakültesi;

 Çocuk Sağlığı ve Hastalıkları Anabilim Dalı

Çocuk Nefroloji Bilim Dalı

1993-2000

6) Profesör

Ankara Üniversitesi Tıp Fakültesi;

 Çocuk Sağlığı ve Hastalıkları Anabilim Dalı

Çocuk Nefroloji & Romatoloji Bilim Dalı

2000-halen

 

D)  ULUSLARARASI YAYINLAR

 

1.        Yalçınkaya F, Tümer N, Ekim M, Şanlıdilek U. Fibromusculer dysplasia of the renal arteries treated with percutaneous transluminal angioplasty: A case report. Turk J Pediatr 32:265-271,1990.

 

2.        Yalçınkaya F, İnce E, Tümer N, Ekim M.  The correlation between the clinical, laboratory and histopathological features of chilhood membranoproliferative glomerulonephritis and response to treatment. Turk J Pediatr 34: 135-144, 1992.

 

3.        Ekim M, Tümer N, Öcal G, Yalçınkaya F, Ensari C.  Sexual maturation in children with chronic renal failure. Kidney Int 41: 1467, 1992.

 

4.        Ekim M, Tümer N, Öcal G, Yalçınkaya F, Ensari C, Çakar N.  Effect of corticosteroids on growth in children with steroid sensitive nephrotic syndrome. Child Nephrol Urol. 12: 10-14, 1992.

 

5.        Tümer N, Yalçınkaya F, Ekim M. Xanthogranulomatous pyelonephritis and amyloidosis. Pediatr Nephrol 7: 594, 1993.

 

6.        Yalçınkaya F, Tümer N, Çakar N, Ekim M.  Pediatric membranoproliferative glomerulonephritis is not decreasing in Turkey! Pediatr Nephrol 8: 131-132, 1994.

 

7.        Yalçınkaya F, Tümer N, Ekim M, Kuyucu S, Çakar N, Ensari C. Congenital microcephaly and infantile nephrotic syndrome - a case report. Pediatr Nephrol 8: 72-73, 1994.

 

8.        Yalçınkaya F, Tümer N, Salih M, Ekim M, Bedük Y, Akyar S, Çakar N, Kansu A. Vaginal ectopic ureter in a duplex system with renal dysplasia. Int Urol Nephrol 26: 7-12, 1994.

 

9.        Tümer N, Ekim M, Çakar N, Yalçınkaya F, Ensari C. Minimal change nephrotic syndrome and HLA system in Turkish children. Nephrol Dial Transp 9: 101 - 102, 1994.

 

10.    Yalçınkaya F, Tümer N, Akar N, Ekim M, Bildirici Y. Tuberculous osteomyelitis: An unsual case of tuberculous infection in a child undergoing continuous ambulatory peritoneal dialysis. Pediatr Nephrol 9:485-486,1995

 

11.    Yalçınkaya F, Tümer N, Gargani AN, Ekim M. Haemostatic Parameters in childhood nephrotic syndrome. Inter Urol & Nephrol 27 (6): 643-647, 1995.

 

12.    İnce E, Mumcu Y, Suskan E, Yalçınkaya F, Tümer N, Cin Ş. Infantile acute hemorrhagic edema: A variant of leukocytoklastic vasculitis. Pediatr Dermatol 12 (3): 224-227, 1995.

 

13.    Ekim M, Tümer N, Yalçınkaya F. Unilateral renal atrophy and hypertension. Int Urol & Nephrol 27 (4): 375-379, 1995.

 

14.    Tümer N, Ekim M, Yalçınkaya F, Çakar N, Ensari C. HLA system and the frequency of relapses in childhood MCNS in Turkish children. Acta Pediatr Japan (37) 419-421, 1995. 

 

15.    Yalçınkaya F, Tümer N, Çakar N, Özkaya N. Low dose erytropoietin is effective and safe in children on CAPD. Pediatr Nephrol 11:350-352,1997.

 

16.    Çakar N, Ekim M, Tümer N, Yalçınkaya F, Akar N, Onaran HO. Pharmocokinetics of recombinant erythropoietin in children with chronic renal failure. Int Urol Nephrol 29(3):377-383,1997. 

 

17.    İnce E, Mumcu Y, Suskan E, Yalçınkaya F, Tümer N, Cin Ş. Infantile acute      hemorrhagic edema: A variant of leukocytoklastic vasculitis. The Year Book of Dermatology 1997, 423-424.

 

18.    Yalçınkaya F, Tekin M, Tümer N, Özkaya N. Protracted arthritis of familial Mediterranean fever. An unusual complication. Br J Rheumatol 36:1-3,1997.

 

19.    Yalçınkaya F, Tümer N, Önder S, Kuzu I. Case of the month: an 8-year-old boy with renal failure, nephrolithiasis and bone pain. Eur J Pediatr 157: 255-256, 1997.

 

20.    Yalçınkaya F, Akar N, Mısırlıoğlu M. Familial Mediterranean fever - Amyloidosis and the Val726Ala mutation.  N. Eng J Med 338:993-994,1998.

 

21.    Tekin M, Yalçınkaya F, Tümer N, Çakar N, Koçak H, Özkaya N, Gençgönül H. Familial Mediterranean fever - renal involvement by disease other than amyloidosis. Nephrol Dial Transplant 14(2):475-479,1999.

 

22.     Tümer N, Yalçınkaya F, İnce E, Ekim M, Köse K, Çakar N, Kara N, Özkaya N, Ensari C, Önder S. Blood pressure nomograms for children and adolescents in Turkey. Pediatr Nephrol 13:438-443, 1999.     

 

23.    Yalçınkaya F, Tümer N. Glomerular lesions other than amyloidosis in patients with FMF. (Editorial)  Nephrol Dial Transplant 14(1):21-25,1999.  

 

24.     Tekin M, Yalçınkaya F, Tümer N, Çakar N, Koçak H. Familial Mediterranean fever and acute rheumatic fever: A pathogenetic relationship? Clinical Rheumatol 18: 446-449, 1999.

 

25.     Akar N, Mısırlıoğlu M, Yalçınkaya F, Akar E, Çakar N, Tümer N, Akçakuş M, Taştan H, Matzner Y. MEFV mutations in Turkish patients suffering from familial Mediterranean fever. Hum Mutation 1999.

 

26.    Akar N, Yalcınkaya F, Akar E, Çakar N. MEFV mutation analysis in Turkish familial Mediterranean fever patients with amyloidosis. Amyloid: Int J Exp Invest 6:301-302,1999. 

 

27.     Yalçınkaya F, İnce E, Tümer N, Ensari A, Özkaya N. Spectrum of renal osteodystrphy in children on continuous ambulatory peritoneal dialysis. Pediatr Int 42:53-57,2000

 

28.    Tekin M, Yalçınkaya F, Tümer N, Akar N, Mısırlıoğlu M, Çakar N. Clinical, laboratory and molecular characteristics of children with familial Mediterranean fever associated vasculitis. Acta Paediat 89:177-82,2000.

 

29.     Yalçınkaya F, Çakar N, Mısırlıoğlu M, Tümer N, Akar N, Tekin M, Taştan H, Koçak H, Özkaya N, Elhan A.H. Genotype-phenotype correlation in a large group of Turkish patients with familial Mediterranean fever: evidence for mutation-independent amyloidosis. Rheumatol 39:67-72,2000.

 

30.     Tekin M, Yalçınkaya F, Çakar N. Mısırlıoğlu M, Taştan H, Akar N, Tümer N. MEFV mutations in multiplex families with familial Mediterranean fever: is a particular genotype necessary for amyloidosis? Clin Genet 57:430-434,2000.

 

31.    Ensari C, Ensari A, Ayli D, Ekim M, Yalçınkaya F, Tümer N. Skin biopsy in Berger’s Disease: Is it really useful in the diagnosis? Nephron 84:276-277,2000.

 

32.    Yalçınkaya F, Tekin M, Çakar N, Akar E, Akar N, Tümer N. Familial Mediterranean fever and systemic amyloidosis in untreated Turkish patients. Q J Med 93:681-684, 2000.

 

33.    Akar E, Yalçınkaya F, Akar N. Is 138 GLY (G-A) alteration of MEFV gene important for amyloidosis? Human Mutation 382, 2000.

 

34.    Çetinkaya E, Öcal G, Berberoğlu M, Adıyaman P, Ekim M, Yalçınkaya F, Örün E. Association of partial gonadal dysgenesis, nephropathy and WT1 gene mutation without Wilms' tumor: Incomplete Denys-Drash Syndrome. J Pediatr Endocrinology & Metabolism 14(5):561-564, 2001.

 

35.    Akar N, Akar E, Yalçınkaya F. E148Q of the MEFV gene causes amyloidosis in FMF patients. Pediatrics 108(1):215, 2001.

 

36.    Çakar N, Yalçınkaya F, Özkaya N, Tekin M, Akar N, Koçak H, Mısırlıoğlu M, Akar E, Tümer N. Familial Mediterranean fever (FMF)-associated amyloidosis in childhood. Clinical features, course and outcome. Clin Exp Rheumatol 19:S63-S67, 2001.

 

37.    İnce E, Çakar N, Tekin M, Kendirli T, Özkaya N, Akar N, Yalçınkaya F. Arthritis in children with familial Mediterranean fever. Rheumatol Int 21: 213–217,2002.

 

38.    Tutar E, Akar N, Atalay S, Yılmaz E, Akar E, Yalçınkaya F. Familial Mediterranean fever gene (MEFV) mutations in patients with rheumatic heart disease. Heart 87:568-9,2002.

 

39.    Yalçınkaya F, İnce E, Uçar T, Özkaya N, Tekin M, Elhan A.H, Tutar E, Güriz H, Aysev D, Gökdemir R, Doğru Ü, Tümer N. Antistreptococcal response is exaggerrated in children with familial Mediterranean fever. Clin Rheumatol 21:378-381,2002.

 

40.    Tuğlular S, Yalçınkaya F, Paydaş S, Öner A, Utaş C, Bozfakioğlu S, Ataman R, Akpolat T, Ok E, Şen S, Düşünsel R, Evrenkaya R, Akoğlu E. A retrospective analysis for aetiology and clinical findings of 287 secondary amyloidosis cases in Turkey. Nephrol Dial Transplant 17:2003-2005,2002.

 

41.    Akar N, Akar E, Özel D, Tekin M, Ekim M, Yalçınkaya F. A note on mutation analysis in familial Mediterranean fever. Pediatr Nephrol 18:196-197,2003.

 

42.     Akar N, Hasipek M, Akar E, Ekim M, Yalçınkaya F, Çakar N. Serum amyloid A1 and tumor necrosis factor-alpha alleles in Turkish familial Mediterranean fever patients with and without amyloidosis. Amyloid: J. Protein Folding Disord 10:12-16,2003.

 

43.    Touitou I, Ben-Chetrit E, Gershoni-Boruh E, Grateau G, Kastner DL, Kone Paut I, Livneh A, Manna R, Mansour I, Ozdogan H, Ozen S, Sarkisyan T, Tunca M, Yalçınkaya F. Allogenic bone marrow transplantation: not a treatment yet for familial Mediterranean fever. Blood 1;102(1):409,2003.

 

44.    Tutar E, Yalçınkaya F, Özkaya N, Ekim M, Atalay S. Incidence of pericardial effusion during attacks of familial Mediterranean fever. Heart 89(10):1257-8,2003.

 

45.    Özkaya N, Yalçınkaya F. Colchicine treatment in children with familial Mediterranean fever. Clin Rheumatol 22:314-317,2003.

 

46.    Çiftçi E, Yalçınkaya F, İnce E, Ekim M, İleri M, Öngerin Z, Fitöz S, Güriz H, Aysev D, Doğru Ü. Pulmonary involvement in childhood-onset systemic lupus erythematosus: a report of five cases. Rheumatology (Oxford). 43:587-591,2004

 

47.    Özçakar ZB, Yalçınkaya F, Derelli E, Acar B, Yüksel S, Tulunay Ö, Ekim M. A favorable outcome of hemolytic uremic syndrome with factor H deficiency. Pediatr Nephrol 19: 815-816, 2004

 

48.    Ekim M, Özçakar B, Acar B, Yüksel S, Yalçınkaya F, Tulunay Ö, Ensari A, Erbay B. Three siblings with steroid-resistant nephrotic syndrome: New NPHS2 mutations in a Turkish family. Am J Kidney Dis 44(2):E22-E24,2004

 

49.    Özkaya N, Çakar N, Ekim M, Kara N, Akkök N, Yalçınkaya F. Primary nephrotic syndrome during childhood in Turkey. Pediatr Int 46:436-438,2004

 

50.    Özçakar ZB, Ekim M, Fitöz S, Teber S, Hızel S, Acar B, Yüksel S, Yalçınkaya F. Hypertension induced reversible posterior leukoencephalopathy syndrome: a report of two cases. Eur J Pediatr 163:728-730,2004

 

51.    Atasay B, Günlemez A, Arsan S, Bakkaloğlu S, Tulunay Ö, Yalçınkaya F. Renal tubular dysgenesis-a case presentation. Turk J Pediatr. 46(4):362-365, 2004.

 

52.    Tunca M, Akar S, Önen F, Özdoğan H, Kasapçapur Ö, Yalçınkaya F, Tutar E, Özen S, Topaloğlu R, Yılmaz E, Arıcı M, Bakkaloğlu A, Beşbaş N, Akpolat T, Dinç A, Erken E. Turkish FMF Study Group. Familial Mediterranean fever (FMF) in Turkey: results of a nationwide multicenter study. Medicine (Baltimore) 84:1-11,2005

 

 

53.    Yüksel S, Yalçınkaya F, Özçakar ZB, Acar B, Tulunay Ö, Ekim M. A girl with microskopic polyangiitis: an unexpected clinical course with long-term follow up. Pediatr Nephrol 20:694-695,2005

 

54.    Bakkaloğolu SA, Ekim M, Sever L, Noyan A, Aksu N, Akman S, Elhan AH, Yalçınkaya F, Öner A, Kara OD, Çalışkan S, Anarat A, Düşünsel R, Dönmez O, Güven AG, Bakkaloğlu A, Denizmen Y, Söylemezoğlu O, Özçelik G. Chronic peritoneal dialysis in Turkish children: a multicenter study. Pediatr Nephrol 20:644-651,2005

 

55.    Acar B, Özçakar ZB, Yüksel S, Pakacar T, Ekim M, Yalçınkaya F. A 12-month-old boy with high fever, erythematous lesions and haemorrhagic oedema.
Eur J Pediatr 164(7):453-454,2005

 

56.    Acar B, Yalçınkaya F, Öztürk B, Yüksel S, Özçakar ZB, Fitöz S, Büyükçelik M, Noyan A, Sanlıdilek U, Ekim M. Seronegative spondyloarthropathy associated with Takayasu's arteritis in a child. Clin Exp Rheumatol. 23(2):278-9, 2005.

 

57.    Ekim M, Fitöz S, Yağmurlu A, Ensari A, Yüksel S, Acar B, Özçakar ZB, Kendirli T, Bingöler B, Yalçınkaya F. Encapsulating peritoneal sclerosis in paediatric peritoneal dialysis patients. Nephrology (Carlton) 10(4):341-3, 2006

 

58.    Özçakar ZB, Yalçınkaya F, Yüksel S, Acar B, Gökmen D, Ekim M. Possible effect of subclinical inflammation on daily life in familial Mediterranean fever. Clin Rheumatol 25(2):149-152, 2006

 

59.    Özçakar ZB, Yalçınkaya F, Yüksel S, Acar B, Fitöz S, Uçar Y, Ekim M. An unusual complication of peritoneal dialysis. Pediatr Nephrol 21(1):129-30 2006

 

60.    Özçakar ZB, Yalçınkaya F, Fitöz S, Yüksel S, Acar B, Çaltık A, Ekim M. Polyarteritis nodosa: succesful diagnostic imaging utilasing pulsed and color Doppler ultrasonograpy and computed tomograpy angiography. Eur J Pediatr 165(2):120-123,2006

 

 

61.    Ekim M, Özçakar ZB, Fitöz S, Soygür T, Yüksel S, Acar B, Yalçınkaya F, Arıkan N. The “nutcracker phenomenon” with orthostatic proteinuria: case reports. Clin Nephrol 65(4):280-283,2006.

 

62.    Tekin M, Hişmi BO, Fitoz S, Yalçınkaya F, Ekim M, Kansu A, Ertem M, Deda G, Tutar E, Arsan S, Zhou XP, Pilarski R, Eng C, Akar N. A germline PTEN mutation with  manifestations  of prenatal onset and verrucous epidermal nevus. Am J Med Genet  140(13):1472-5, 2006

 

63.    Yüksel S, Ekim M, Fitoz S, Soygür T, Sertçelik A, Perçinel S, Acar B, Özçakar ZB, Comba A,  Yalçınkaya F. The association of cystic nephroma with pulmonary sequestration: is it a coincidence or not? Pediatr Nephrol. 21(7):1041-1044, 2006

 

64.    Acar B, Yalçınkaya F, Fitoz S, Özçakar ZB, Yüksel S, Soygür T, Ekim M. Multicystic kidney and calicial diverticulum in a child a coincidence or an association? Int Urol Nephrol,2006

 

65.    Özçakar ZB, Yalçınkaya F, Tutar E, Çakar N, Uçar T, Elhan A, Acar B, Yüksel S, Uncu N, Kara N, Atalay S, Ekim M. Hypertension and Left Ventricular Hypertrophy in Pediatric Peritoneal Dialysis Patients: Ambulatory Blood Pressure Monitoring and Echocardiographic Evaluation. Nephron Clin Pract. 104(2):c101-106, 2006

 

66.    Özçakar ZB, Cengiz FB, Çakar N, Uncu N, Kara N, Acar B, Yüksel S, Ekim M, Tekin M, Yalçınkaya F. Analysis of NPHS2 mutations in Turkish steroid-resistant nephrotic syndrome patients. Pediatr Nephrol.21(8):1093-1096,2006

 

67.    Ekim M, Yüksel S, Fitoz S, Özmert A, Acar B, Özçakar ZB, Güvence N, Atalay S, Yalçınkaya F. Systemic vascular calcification with retinal calcification in an adolescent treated with long-term peritoneal dialysis. Pediatr Nephrol.21(12):1915-1916,2006

 

68.    Özçakar ZB, Ekim M, Ensari A, Kuloğlu Z, Yüksel S, Acar B, Kirsaçlıoğlu C, Kansu A, Yalçınkaya F, Girgin N. Membranoproliferative glomerulonephritis in a patient with Wilson's disease. J Nephrol 19(6):831-833,2006

 

69.    Yalçınkaya F, Çakar N, Acar B, Tutar E, Güriz H, Elhan AH, Öztürk S, Kansu A, İnce E, Atalay S, Girgin N, Doğru Ü, Aysev D, Ekim M. The value of the levels of acute phase reactants for the prediction of familial Mediterranean fever associated amyloidosis: a case control study. Rheumatol Int 27(6):517-522,2006

 

70.    Kalyoncu M, Acar B, Çakar N, Bakkaloğlu A, Öztürk S, Dereli E, Tunca M, Kasapçapur Ö, Yalçınkaya F, Özen S. Are carriers for MEFV mutations "healthy" ? Clin Exp Rheumatol.24(5 Suppl 42):S120-122,2006.

 

71.    Özçakar ZB, Yalçınkaya F, Yüksel S, Ekim M. The expanded clinical spectrum of familial Mediterranean fever. Clin Rheumatol. 26(9):1557-1560,2006

 

72.    Özen S, Berdeli A, Türel B, Kutlay S, Yalçınkaya F, Arıcı M, Beşbaş N, Bakkaloğlu A, Yılmaz E. Arg753Gln TLR-2 Polymorphism in Familial Mediterranean Fever: Linking the Environment to the Phenotype in a Monogenic Inflammatory Disease. J Rheumatol 33(12):2498-2500,2006

 

73.    Yüksel S, Yalçınkaya F, Acar B, Özçakar ZB, Öztürk B, Ekim M. Clinical improvement with infliximab in a child with amyloidosis secondary to familial Mediterranean fever. Rheumatology 45:1307-1321,2006

 

74.    Yüksel S, Öztürk B, Kavaz A, Özçakar ZB, Acar B, Güriz H, Aysev D, Ekim M, Yalçınkaya F. Antibiotic resistance of urinary tract pathogens and evaluation of empirical treatment in Turkish children with urinary tract infections. Int J Antimicrob Agents 28(5):413-6,2006

 

75.    Özçakar ZB, Yüksel S, Ensari A, Ekim M, Yalçınkaya F. Acute renal failure in a patient with familial Mediterranean fever. Rheumatol Int. 27:309-310,2006

 

76.    Kendirli T, Yüksel S, Oral M, Ünal N, Tulunay M, Şanlıdilek U, Yalçınkaya F. Fatal polyarteritis nodosa with gastrointestinal involvement in a child. Pediatric Emergency Care 22(12):810-812,2006

 

77.    Karabay Bayazıt A, Yalçınkaya F, Çakar N, Düzova A, Bircan Z, Bakkaloğlu A, Canpolat N, Kara N, Şirin A, Ekim M, Öner A, Akman S, Mir S, Baskın E, Poyrazoğlu HM; Noyan A, Akil İ, Bakkaloğlu S, Soylu A. Renovascular hypertension in childhood: a nationwide survey. Pediatr Nephrol 22(9):1327-1333,2007

 

78.    Touitou I, Sarkisian T, Madlej-Hashim M, Tunca M, Livneh A, Cattan D, Yalçınkaya F, Özen S, Majeed H, Özdoğan H, Kastner D, Booth D, Ben-Chetrit E, Pugnere D, Michelon C, Sequret F, Gershoni-Baruch R; International Study Group for Phenotype-Genotype Correlation in Familial Mediterranean Fever. Country as the primary risk factor for renal amyloidosis in familial Mediterranean fever. Arthritis Rheum 56(5):1706-1712,2007

 

79.    Fitoz S, Ekim M, Özçakar ZB, Elhan AH, Yalçınkaya F. Nutcracker syndrome in children: the role of upright position examination and superior mesenteric artery angle measurement in diagnosis. J Ultrasaund Med. 26(5):573-580,2007

 

80.    Acar B, Yalçınkaya F, Fitoz S, Özçakar ZB, Yüksel S, Soygür T, Ekim M. Multicystic dysplastic Kidney and caliceal diverticulum in a child. A coincidance or an association? Int Urol Nephrol 39(1):27-29,2007

 

81.    Yalçınkaya F, Özçakar ZB, Kasapçapur Ö, Öztürk A, Akar N, Bakkaloğlu A, Arısoy N, Ekim M, Özen S. Prevalence of the MEFV gene mutations in childhood polyarteritis nodosa. J Pediatr 151(6):675-678,2007

 

82.    Kendirli T, Ekim M, Özçakar B, Yüksel S, Acar B, Öztürk B, Dereli E, Kavaz A, Yalaki Z, Yalçınkaya F. Renal replacement therapies in pediatric intensive care patients. Experiences of one center in Turkey. Pediatr Int 49:345-348, 2007

 

83.    Fitoz S, Yalçınkaya F. Compression of left inferior vena cava: A form of nutcracker syndrome. J Clin Ultrasound 36(2):101-104, 2008

 

84.    Uçar T,  Tutar E, Yalçınkaya F, Çakar N, Özçakar ZB, Atalay S, Uncu N, Kara N, Ekim M. Global left-ventricular function by tissue Doppler imaging in pediatric dialysis patients. Pediatr Nephrol. 23(5):779-785,2008

 

85.    Çakar N, Özçakar ZB, Soy D, Uçar Y, Fitoz S, Kara N, Uncu N, Atakan C, Ekim M, Yalçınkaya F. Renal Involvement in childhood vasculitis. Nephron Clin Pract. 108(3):c202-c206,2008

 

86.    Kuloğlu Z, Özçakar ZB, Kırsaçlıoğlu C, Yüksel S, Kansu A, Girgin N, Ekim M, Yalçınkaya F. Is there an association between FMF and celiac disease? Clin Rheum 27(9):1135-1139,2008

 

87.    Çakar N, Yalçınkaya F, Düzova A, Çalışkan S, Şirin A, Öner A, Baskın E, Bek K, Soylu A, Fitoz S, Bayazıt AK, Bircan Z, Özen S, Uncu N, Ekim M. Takayasu arteritis in children J Rheum 35(5):913-919, 2008

 

88.    Özçakar ZB, Yalçınkaya F, Ödek C, Ekim M. Oxcarbazepin and valproic acid-inducef lupus in a 7-year-old boy. Acta Paediatr 97(8):1000-1001,2008

 

89.    Acar B, Yalçınkaya F, Çakar N, Yüksel S, Özçakar ZB, Uncu N, Kara N, Elhan AH, Ekim M. The outcome for pediatric patients on peritoneal dialysis. J Nephrol 21(3):394-399,2008

 

90.    Özçakar ZB, Yalçınkaya F, Çakar N, Acar B, Kasapçapur O, Ugüten D, Kara N, Uncu N, Arısoy N, Ekim M. MEFV Mutations Modify the Clinical Presentation of Henoch-Schönlein Purpura. 35(12):2427-2429, 2008

 

91.    Kuloğlu Z, Kansu A, Tutar E, Yalçınkaya F, Ensari A, Girgin N. Association of familial Mediterranean fever and celiac disease in a 14-year-old girl with recurrent arthritis. Clin Exp Rheumatol 26(4Suppl 50):8131,2008

 

92.    Özçakar ZB, Yalçınkaya F, Ödek Ç, Ekim M. Oxcarbazepin and valproic acid-induced lupus in a 7-year-old boy. Acta Paediatrica, 97(8):1000-1, 2008 

 

93.    Özçakar ZB, Yalçınkaya F, Ensari A, Kendirli T, Ekim M, Fitoz S. Thrombotic microangiopathy in a pediatric patient: Pediatr Nephrol 24(6):1137-1142, answer 1137-42, 2009

 

94.    Yalçınkaya F, Özen S, Özçakar ZB, Aktay N, Çakar N, Düzova A, Kasapçapur Ö, Elhan AH, Doğanay B, Ekim M, Uncu N, Bakkaloğlu A. A new set of criteria for the diagnosis of familial Mediterranean fever in childhood. Rheumatology (Oxford) 48(4):395-398,2009

 

95.    Özçakar ZB, Yalçınkaya F, Altaş B, Ergün H, Kendirli T, Ateş C, Elhan AH, Ekim M. Application of the new classification criteria of the Acute Kidney Injury Network: a pilot study in a pediatric population. Pediatr Nephrol 24(7):1379-1384,2009

 

96.    İleri T, Ertem M, Özçakar ZB, İnce EU, Bıyıklı Z, Uysal Z, Ekim M, Yalçınkaya F. Prospective evaluation of acute and chronic renal function in children following matched related donor hematopoetic stem cell transplantation. Pediatr Transplant 2009

 

97.    Özçakar ZB, Burgu B, Altugan FŞ, Fitoz S, Ekim M, Soygür T, Yalçınkaya F. Neurogenic bladder in twins: Pediatr Nephrol 2010 ;25(6):1057; answer 1059-61.

 

98. Bircan Z, Duzova A, Cakar N, Bayazıt AK, Elhan A, Tutar E, Ozcakar ZB, Ucar T, Kargin E, Erdem S, Karagöz T, Babaoglu A, Sancak B, Noyan A, Soylemezoglu O, Bakkaloglu A, Yalçınkaya F. Predictors of left ventricular hypertrophy in children on chronic peritoneal dialysis. Pediatr Nephrol 25(7):1311-8

 

 

99.    Aydoğdu O, Burgu B, Demirel F, Soygür T, Özçakar ZB, Yalçınkaya F, Tekgül S. Ochoa syndrome: a spectrum of urofascial syndrome. Eur J Pediatr 169(4):431-5, 2010

 

100.                        Altugan FŞ, Özçakar ZB, Fitoz S, Ensari A, Konrad M, Yalçınkaya F. Medullary nephrocalcinosis in a pediatric patient: question & answer. Pediatr Nephrol 25(8):1429-30, 1431-3,2010

 

101.                        Özçakar ZB, Kadıoğlu G, Şıklar Z, Kavaz A, Nur Aksanal F, Berberoğlu M, Ekim M, Öcal G, Yalçınkaya F. The effect of colchicines on physical growth in children with familial Mediterranean fever. Eur J Pediatr 169(7):825-8, 2010

 

102.                        Altugan FS, Ekim M, Fitöz S, Özçakar ZB, Burgu B, Yalçınkaya F, Soygür T. Nutcracker syndrome with urolithiasis. J Pediatr Urol. 6(5):519-21, 2010

 

103.                        Özçakar ZB, Fitöz S, Kavaz A, Burgu B, Soygür T, Akpınar E, Ekim M, Sertçelik A, Yalçınkaya F. Hypertension and hypokalemia in a 15-year-old boy: question. Pediatr Nephrol. 25:2443-7, 2010.

 

104.                        Özçakar ZB, Yalçınkaya F, Cakar N, Acar B, Bilgiç AE, Uncu N, Kara N, Ekim M, Kasapçopur O. Application of the new pediatric criteria and Tel Hashomer criteria in heterozygous patients with clinical features of FMF. Eur J Pediatr 170(8):1055-7, 2011.

 

105.                        Özçakar ZB, Yalçınkaya F, Kavaz A, Kadıoğlu G, Elhan AH, Aysev D, Güriz H, Ekim M. Urinary tract infections owing to ESBL-producing bacteria: microorganisms change - clinical pattern does not. Acta Paediatr 100(8):e61-4,2011

 

106.                        Özçakar ZB, Yalçınkaya F. Vascular comorbidities in familial Mediterranean fever. Rheumatol Int 31(10):1275-81, 2011

 

107.                        Yalçınkaya F, Özçakar ZB,, Tanyıldız M, Elhan AH. Familial Mediterranean fever in small children in Turkey.Clin Exp Rheumatol. 29(4 Suppl 67):S87-90,2011.

 

108.                        Kuloğlu Z, Özçakar ZB, Kansu A, Ustündağ G, Ekim M, Altugan FŞ, Kendirli T, Cınar K, Yalçınkaya F, Angiodysplasia as a cause of severe hematochezia in a child with end-stage renal failure. Ren Fail. 33(2):252-4,2011.

 

109.                        Kavaz A, Özçakar ZB,, Karadeniz C, Tutar E, Yalçınkaya F. Pericardial tamponade in a child with nephrotic syndrome. Pediatr Nephrol 26(6):993-4,2011

 

110.                        Özçakar ZB, Yalçınkaya F, Fitöz S, Cipe G, Soygür T, Ozdemir H, KöksoyC. Nutcracker syndrome manifesting with severe proteinuria: a challenging scenario in a single-kidney patient. Pediatr Nephrol 26:987-90, 2011

 

111.                        Ekim M, Fitoz S, Özçakar ZB, Yalçınkaya F. Vascular calcification in an adolescent treated with long-term peritoneal dialysis. Int J Nephrol. 2011:702406,2011

 

 

112.  Kavaz A, Ozçakar ZB, Kendirli T, Oztürk BB, Ekim M, Yalçınkaya F. Acute kidney injury in a paediatric intensive care unit: comparison of the pRIFLE and AKIN criteria. Acta Paediatr.101(3):e126-9,2012

 

113. Gökaslan F, Yalçınkaya F, Fitöz S, Özçakar ZB. Evaluation and outcome of antenatal hydronephrosis: a prospective study. Ren Fail.34(6):718-21, 2012

 

114.   Özçakar ZB, Yüksel S, Ekim M, Yalçınkaya F. Infliximab therapy for familial Mediterranean fever-related amyloidosis: case series with long term follow-up. Clin Rheumatol. 31(8):1267-71,2012

115.                        Özçakar ZB, Erdogan BD, Elhan AH, Yalçınkaya F. Familial Mediterranean fever in siblings. J Rheumatol. 39(11):2170-4,2012

116.                        Yüksel S, Ekim M, Özçakar ZB, Yalçınkaya F, Acar B, Oztuna D, Akar N. The value of procalcitonin measurements in children with familial Mediterranean fever. Rheumatol Int. 2012;32:3443-7

117.                        Söylemezoğlu O, Düzova A, Yalçınkaya F, Arınsoy T, Süleymanlar G. Chronic renal disease in children aged 5-18 years: a population-based survey in Turkey, the CREDIT-C study. Nephrol Dial Transplant.27 Suppl 3:iii146-51, 2012

 

118.                        Bulum B, Özçakar ZB, Ustüner E, Düşünceli E, Kavaz A, Duman D, Walz K, Fitoz S, Tekin M, Yalçınkaya F. High frequency of kidney and urinary tract anomalies in asymptomatic first-degree relatives of patients with CAKUT. Pediatr Nephrol. 2013;28(11):2143-7

 

 

119.                        Subaşıoğlu Uzak A, Çakar N, Comak E, Yalçınkaya F, Tekin M. ATP6V1B1 mutations in distal renal tubular acidosis and sensorineural hearing loss: clinical and genetic spectrum of five families. Ren Fail. 2013;35(9):1281-4

 

120.                        Düzova A, Yalçınkaya F, Baskın E, Bakkaloğlu A, Söylemezoglu O. Prevalence of hypertension and decreased glomerular filtration rate in obese children: results of a population-based field study. Nephrol Dial Transplant. 2013;28 Suppl 4:iv166-iv171

 

121.                          Kavaz A, Özçakar ZB, Bulum B, Tüzüner A, Keven K, Şengül Ş, Ekim M, Yalçınkaya F. Pediatric renal transplantation: a single center experience. Transplant Proc 2013;45(3):917-8

 

122.                        Stuart HM, Roberts NA, Burgu B, Daly SB, Urquhart JE, Bhaskar S, Dickerson JE, Mermerkaya M, Silay MS, Lewis MA, Olondriz MB, Gener B, Beetz C, Varga RE, Gülpınar O, Süer E, Soygür T, Ozçakar ZB, Yalçınkaya F, Kavaz A, Bulum B, Gücük A, Yue WW, Erdogan F, Berry A, Hanley NA, McKenzie EA, Hilton EN, Woolf AS, Newman WG. LRIG2 Mutations Cause Urofacial Syndrome. Am J Hum Genet. 2013;7;92(2):259-64

 

123.                        Özçakar ZB, Yalçınkaya F, Altugan FS, Kavaz A, Ensari A, Ekim M. Hypocomplementemic urticarial vasculitis syndrome in three siblings. Rheumatol Int 2013;33(3):763-6

 

124.                        Çakır U, Alan S, Zeybek C, Erdeve O, Atasay B, Yalçınkaya F, Arsan S. Acquired bartter-like syndrome associated with colistin use in a preterm infant. Ren Fail. 2013;35(3):411-3

 

125.                        Özçakar ZB, Bolkent MG, Kavaz A, Öztürk BB, Deda G, Ekim M, Yalçınkaya F. An adolescent girl with hypertension and neuropsychiatric symptoms: questions & answer. Pediatr Nephrol. 2013;28(3):427, 429-31

 

126.                        Mermerkaya M, Burgu B, Hamidi N, Yüksel S, Özçakar ZB, Sertçelik A, Yalçınkaya F, Soygür T. Mayer-Rokitansky-Küster-Hauser Syndrome Accompanied by Renal Cell Carcinoma: A Case Report. J Pediatr Hematol Oncol 2013;35:e 309-10.

 

127.                        Özçakar ZB, Foster J 2nd, Diaz-Horta O, Kasapçopur Ö, Fan YS, Yalçınkaya F, Tekin M. DNASE1L3 mutations in hypocomplementemic urticarial vasculitis syndrome. Arthritis Rheum. 2013;65(8):2183-9

 

 

128.   Subaşıoğlu Uzak A, Çakar N, Çomak E, Yalçınkaya F, Tekin M. ATP6V1B1 mutations in distal renal tubular acidosis and sensorineural hearing loss: clinical and genetic spectrum of five families. Ren Fail. 2013 35(9):1281-4.

 

129.                        Çaycı FS, Ekim M, Eğin Y, Gökçe H, Yalçınkaya F, Özçakar B, Akar N. An Analysis of the Levels of the Soluble Form of the Endothelial Protein C Receptor in Children with Henoch-Schönlein Purpura. Pediatr Hematol Oncol. 2013

 

130.   Düzova A, Yalçınkaya F, Baskın E, Bakkaloğlu A, Söylemezoğlu O. Prevalence of hypertension and decreased glomerular filtration rate in obese children: results of a population-based field study. Nephrol Dial Transplant. 2013 Suppl 4:iv166-71.

 

131.                        Navon Elkan P, Pierce SB, Segel R, Walsh T, Barash J, Padeh S, Zlotogorski A, Berkun Y, Press JJ, Mukamel M, Voth I, Hashkes PJ, Harel L, Hoffer V, Ling E, Yalçınkaya F, Kasapçopur Ö, Lee MK, Klevit RE, Renbaum P, Weinberg-Shukron A, Sener EF, Schormair B, Zeligson S, Marek-Yagel D, Strom TM, Shohat M, Singer A, Rubinow A, Pras E, Winkelmann J, Tekin M, Anikster Y, King MC, Levy-Lahad E. Mutant adenosine deaminase 2 in a polyarteritis nodosa vasculopathy. N Engl J Med. 2014 6;370(10):921-31.

 

 

132.                         Özçakar ZB, Elhan AH, Yalçınkaya F. Can colchicine response be predicted in familial Mediterranean fever patients? Rheumatology (Oxford) 2014;53:1767-72

 

133.                        Bulum B, Özçakar ZB, Kavaz A, Hüseynova M, Ekim M, Yalçınkaya F. Lower urinary tract dysfunction is frequently seen in urinary tract infections in children and is often associated with reduced quality of life. Acta Paediatr 2014;103:e454-8

 

134.                        Yılmaz S, Özçakar ZB, Bulum B, Kiremitçi S, Ensari A, Ekim M, Keven K, Yalçınkaya F. De novo amyloidosis in a renal transplant patient. Pediatr Transplant 2014;18:E259-61

 

135.                        Navon Elkan P, Pierce SB, Segel R, Walsh T, Barash J, Padeh S, Zlotogorski A, Berkun Y, Press JJ, Mukamel M, Voth I, Hashkes PJ, Harel L, Hoffer V, Ling E, Yalçınkaya F, Kasapcopur O, Lee MK, Klevit RE, Renbaum P, Weinberg-Shukron A, Sener EF, Schormair B, Zeligson S, Marek-Yagel D, Strom TM, Shohat M, Singer A, Rubinow A, Pras E, Winkelmann J, Tekin M, Anikster Y, King MC, Levy-Lahad E. Mutant adenosine deaminase 2 in a polyarteritis nodosa vasculopathy. N Engl J Med. 2014 Mar 6;370(10):921-31.

 

136.                        Kurt-Sukur ED, Özçakar ZB, Yılmaz S, Özdel S, Kuloğlu Z, Ekim M, Kansu A, Yalçınkaya F. Proteinuria in a Crohn's disease patient: Questions and Answers. Pediatr Nephrol 2015;30:1433, 1435-6

 

137.                        Bulum B, Özçakar ZB, Duman D, Cengiz FB, Kavaz A, Burgu B, Baskın E, Çakar N, Soygür T, Ekim M, Tekin M, Yalçınkaya F. HPSE2 mutations in urofacial syndrome, non-neurogenic neurogenic bladder and lower urinary tract dysfunction. Nephron 2015;130:54-8

 

138.                        Kurt-Sukur ED, Özçakar ZB, Fitöz S, Yilmaz S, Hoppe B, Yalçınkaya F. Primary Hyperoxaluria Type 1: A Cause for Infantile Renal Failure and Massive Nephrocalcinosis.  Klin Padiatr. 2015 Sep;227:293-5

 

139.                        Kurt-Şükür ED, Özçakar ZB, Fitöz S, Yilmaz S, Teber S, Ünal İnce E, Ekim M, Yalçınkaya F. Two children with steroid-responsive nephrotic syndrome complicated by cerebral venous sinus thrombosis. Nefrologia. 2015;35:497-500

 

140.                        Çaycı FS, Ekim M, Egin Y, Gökce H, Yalçınkaya F, Ozcakar B, Akar N. An analysis of the levels of the soluble form of the endothelial protein C receptor in children with Henoch-Schönlein Purpura..Pediatr Hematol Oncol. 2015;32:115-22.

 

141.                        İlarslan NE, Fitöz ÖS, Öztuna DG, Küçük NÖ, Yalçınkaya F. The role of tissue harmonic imaging ultrasound combined with power Doppler ultrasound in the diagnosis of childhood febrile urinary tract infections. Turk Pediatri Ars. 2015 Jun 1;50(2):90-5

 

142.                        Aksu K, Dokuyucu O, Ertenli AI, Gul A, Karaaslan Y, Kasapcopur O, Kiraz S, Onat AM, Ozdogan AH, Ozbalas T, Ozen S, Saylan M, Senturk A, Tatar M, Tuna E, Turanli M, Yalçınkaya F. Cost of Familial Mediterranean Fever (Fmf) Disease In Turkey. Value Health. 2015 Nov;18(7):A666.

 

 

143.                        Söylemezoğlu O, Kandur Y, Duzova A, Ozkaya O, Kasapcopur O, Baskin E, Fidan K, Yalçınkaya F. Familial Mediterranean fever with a single MEFV mutation: comparison of rare and common mutations in a Turkish paediatric cohort. Clin Exp Rheumatol. 2015 Nov-Dec;33(6 Suppl 94):152-5