Ozgür TT - Search Results

1

Four different NCF2 mutations in six families from Turkey and an overview of NCF2 gene mutations.

Köker MY, Sanal O, van Leeuwen K, de Boer M, Metin A, Patiroğlu T, Ozgür TT, Tezcan I, Roos D. Köker MY, et al. Among authors: ozgur tt. Eur J Clin Invest. 2009 Oct;39(10):942-51. doi: 10.1111/j.1365-2362.2009.02195.x. Epub 2009 Jul 17. Eur J Clin Invest. 2009. PMID: 19624736

2

Acquired factor VIII deficiency associated with a novel primary immunodeficiency suggestive of autosomal recessive hyper IgE syndrome.

Ozgur TT, Asal GT, Gurgey A, Tezcan I, Ersoy F, Sanal O. Ozgur TT, et al. J Pediatr Hematol Oncol. 2007 May;29(5):327-9. doi: 10.1097/MPH.0b013e318059c236. J Pediatr Hematol Oncol. 2007. PMID: 17483712

3

Hematopoietic stem cell transplantation in a CD3 gamma-deficient infant with inflammatory bowel disease.

Ozgür TT, Asal GT, Cetinkaya D, Orhan D, Kiliç SS, Usta Y, Ozen H, Tezcan I. Ozgür TT, et al. Pediatr Transplant. 2008 Dec;12(8):910-3. doi: 10.1111/j.1399-3046.2008.00957.x. Epub 2008 May 11. Pediatr Transplant. 2008. PMID: 18482219

4

Prenatal diagnosis of chronic granulomatous disease in a male fetus.

Yavuz Köker M, Metin A, Ozgür TT, de Boer M, Roos D. Yavuz Köker M, et al. Among authors: ozgur tt. Iran J Allergy Asthma Immunol. 2009 Mar;8(1):57-61. Iran J Allergy Asthma Immunol. 2009. PMID: 19279361 Free article.

5

Six different CYBA mutations including three novel mutations in ten families from Turkey, resulting in autosomal recessive chronic granulomatous disease.

Köker MY, van Leeuwen K, de Boer M, Celmeli F, Metin A, Ozgür TT, Tezcan I, Sanal O, Roos D. Köker MY, et al. Among authors: ozgur tt. Eur J Clin Invest. 2009 Apr;39(4):311-9. doi: 10.1111/j.1365-2362.2009.02093.x. Eur J Clin Invest. 2009. PMID: 19292887

6

Hereditary C1q deficiency: a new family with C1qA deficiency.

Sun-Tan C, Ozgür TT, Kilinç G, Topaloğlu R, Gököz O, Ersoy-Evans S, Sanal O. Sun-Tan C, et al. Among authors: ozgur tt. Turk J Pediatr. 2010 Mar-Apr;52(2):184-6. Turk J Pediatr. 2010. PMID: 20560256

7

Increased availability of family donors for hematopoietic stem cell transplantation in a population with increased incidence of consanguinity.

Balcı YI, Tavil B, Tan CS, Ozgur TT, Bulum B, Cetin M, Balcı M, Yalcın S, Tezcan I, Uckan D. Balcı YI, et al. Among authors: ozgur tt. Clin Transplant. 2011 May-Jun;25(3):475-80. doi: 10.1111/j.1399-0012.2010.01310.x. Epub 2010 Jul 14. Clin Transplant. 2011. PMID: 20636407

8

H2AX gene does not have a modifier effect on ataxia-telangiectasia phenotype.

Mesci L, Ozdag H, Yel L, Ozgur TT, Tan C, Sanal O. Mesci L, et al. Among authors: ozgur tt. Int J Immunogenet. 2011 Jun;38(3):209-13. doi: 10.1111/j.1744-313X.2010.00989.x. Epub 2011 Jan 4. Int J Immunogenet. 2011. PMID: 21199394

9

Two SCID cases with Cernunnos-XLF deficiency successfully treated by hematopoietic stem cell transplantation.

Çağdaş D, Özgür TT, Asal GT, Revy P, De Villartay JP, van der Burg M, Sanal Ö, Tezcan I. Çağdaş D, et al. Among authors: ozgur tt. Pediatr Transplant. 2012 Aug;16(5):E167-71. doi: 10.1111/j.1399-3046.2011.01491.x. Epub 2011 Apr 27. Pediatr Transplant. 2012. PMID: 21535335

10

Chronic granulomatous disease presenting with hypogammaglobulinemia.

Hanoglu D, Ozgür TT, Ayvaz D, Köker MY, Sanal O. Hanoglu D, et al. Among authors: ozgur tt. J Investig Allergol Clin Immunol. 2011;21(4):310-2. J Investig Allergol Clin Immunol. 2011. PMID: 21721378 Free article.

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