Dogu F - Search Results

1

Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations.

Giardino G, Sharapova SO, Ciznar P, Dhalla F, Maragliano L, Radha Rama Devi A, Islamoglu C, Ikinciogullari A, Haskologlu S, Dogu F, Hanna-Wakim R, Dbaibo G, Chou J, Cirillo E, Borzacchiello C, Kreins AY, Worth A, Rota IA, Marques JG, Sayitoglu M, Firtina S, Mahdi M, Geha R, Neven B, Sousa AE, Benfenati F, Hollander GA, Davies EG, Pignata C. Giardino G, et al. Among authors: dogu f. J Clin Immunol. 2021 May;41(4):756-768. doi: 10.1007/s10875-021-00967-y. Epub 2021 Jan 19. J Clin Immunol. 2021. PMID: 33464451 Free PMC article.

2

Recurrent arterial thrombosis in a child: primary antiphospholipid antibody syndrome.

Uysal Z, Doğu F, Kürekçi AE, Culha VK, Deda G, Ekim M, Akar N, Erterm M, Ikincioğullari A, Babacan E, Gözdaşoğlu S. Uysal Z, et al. Among authors: dogu f. Pediatr Hematol Oncol. 2002 Jan-Feb;19(1):59-66. doi: 10.1080/088800102753356202. Pediatr Hematol Oncol. 2002. PMID: 11787868

3

657del5 mutation in the NBS1 gene is associated with Nijmegen breakage syndrome in a Turkish family.

Tekin M, Doğu F, Taçyíldiz N, Akar E, Ikincioğullari A, Oğur G, Yavuz G, Babacan E, Akar N. Tekin M, et al. Among authors: dogu f. Clin Genet. 2002 Jul;62(1):84-8. doi: 10.1034/j.1399-0004.2002.620112.x. Clin Genet. 2002. PMID: 12123493

4

Circulating adhesion molecule levels in childhood asthma.

Doğu F, Ikincioğullari A, Eğin Y, Babacan E. Doğu F, et al. Indian Pediatr. 2002 Nov;39(11):1017-21. Indian Pediatr. 2002. PMID: 12466571

5

Direct genetic correction as a new method for diagnosis and molecular characterization of MHC class II deficiency.

Matheux F, Ikinciogullari A, Zapata DA, Barras E, Zufferey M, Dogu F, Regueiro JR, Reith W, Villard J. Matheux F, et al. Among authors: dogu f. Mol Ther. 2002 Dec;6(6):824-9. doi: 10.1006/mthe.2002.0804. Mol Ther. 2002. PMID: 12498778 Free article.

6

Unusual cause of respiratory distress: Chilaiditi syndrome.

Dogu F, Reisli I, Ikinciogullari A, Fitöz S, Babacan E. Dogu F, et al. Pediatr Int. 2004 Apr;46(2):188-90. doi: 10.1046/j.1442-200x.2004.01856.x. Pediatr Int. 2004. PMID: 15056249 No abstract available.

7

Transient hypogammaglobulinemia of infancy and early childhood: outcome of 30 cases.

Doğu F, Ikincioğullari A, Babacan E. Doğu F, et al. Turk J Pediatr. 2004 Apr-Jun;46(2):120-4. Turk J Pediatr. 2004. PMID: 15214739

8

Peripheral blood lymphocyte subsets in healthy Turkish children.

Ikincioğullari A, Kendirli T, Doğu F, Eğin Y, Reisli I, Cin S, Babacan E. Ikincioğullari A, et al. Among authors: dogu f. Turk J Pediatr. 2004 Apr-Jun;46(2):125-30. Turk J Pediatr. 2004. PMID: 15214740

9

Granulocyte transfusions in children with chronic granulomatous disease and invasive aspergillosis.

Ikincioğullari A, Dogu F, Solaz N, Reisli I, Kemahli S, Cin S, Babacan E. Ikincioğullari A, et al. Among authors: dogu f. Ther Apher Dial. 2005 Apr;9(2):137-41. doi: 10.1111/j.1774-9987.2005.00227.x. Ther Apher Dial. 2005. PMID: 15828925

10

A case of Wiskott-Aldrich syndrome with de novo mutation at exon 4.

Doğu F, Ariga T, Ikincioğullari A, Bozdoğan G, Aytekin C, Metin A, Babacan E. Doğu F, et al. Turk J Pediatr. 2006 Jan-Mar;48(1):66-8. Turk J Pediatr. 2006. PMID: 16562789

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