Turul T - Search Results

1

A DNA-PKcs mutation in a radiosensitive T-B- SCID patient inhibits Artemis activation and nonhomologous end-joining.

van der Burg M, Ijspeert H, Verkaik NS, Turul T, Wiegant WW, Morotomi-Yano K, Mari PO, Tezcan I, Chen DJ, Zdzienicka MZ, van Dongen JJ, van Gent DC. van der Burg M, et al. Among authors: turul t. J Clin Invest. 2009 Jan;119(1):91-8. doi: 10.1172/JCI37141. Epub 2008 Dec 15. J Clin Invest. 2009. PMID: 19075392 Free PMC article.

2

Clinical heterogeneity can hamper the diagnosis of patients with ZAP70 deficiency.

Turul T, Tezcan I, Artac H, de Bruin-Versteeg S, Barendregt BH, Reisli I, Sanal O, van Dongen JJ, van der Burg M. Turul T, et al. Eur J Pediatr. 2009 Jan;168(1):87-93. doi: 10.1007/s00431-008-0718-x. Epub 2008 May 29. Eur J Pediatr. 2009. PMID: 18509675

3

Presentation of interleukin-12/-23 receptor beta1 deficiency with various clinical symptoms of Salmonella infections.

Sanal O, Turul T, De Boer T, Van de Vosse E, Yalcin I, Tezcan I, Sun C, Memis L, Ottenhoff TH, Ersoy F. Sanal O, et al. Among authors: turul t. J Clin Immunol. 2006 Jan;26(1):1-6. doi: 10.1007/s10875-006-7830-3. J Clin Immunol. 2006. PMID: 16418797

4

A novel mutation leading to a deletion in the SH3 domain of Bruton's tyrosine kinase.

Mesci L, Ozdag H, Turul T, Ersoy F, Tezcan I, Sanal O. Mesci L, et al. Among authors: turul t. Turk J Pediatr. 2006 Oct-Dec;48(4):362-4. Turk J Pediatr. 2006. PMID: 17290574

5

Antibody response to a seven-valent pneumococcal conjugated vaccine in patients with ataxia-telangiectasia.

Sanal O, Ersoy F, Tezcan I, Metin A, Turul T, Gariboglu S, Yel L. Sanal O, et al. Among authors: turul t. J Clin Immunol. 2004 Jul;24(4):411-7. doi: 10.1023/B:JOCI.0000029109.15355.ba. J Clin Immunol. 2004. PMID: 15163897 Clinical Trial.

6

Long-term survival in severe combined immune deficiency: the role of persistent maternal engraftment.

Tezcan I, Ersoy F, Sanal O, Turul T, Uckan D, Balci S, Hicsonmez G, Prieur M, Caillat-Zucmann S, Le Deist F, De Saint Basile G. Tezcan I, et al. Among authors: turul t. J Pediatr. 2005 Jan;146(1):137-40. doi: 10.1016/j.jpeds.2004.09.010. J Pediatr. 2005. PMID: 15644840

7

Guillain-Barré syndrome in an immunocompromised patient with Wiskott-Aldrich syndrome.

Olmez A, Turul T, Tezcan I, Turanli G. Olmez A, et al. Among authors: turul t. Turk J Pediatr. 2008 Jul-Aug;50(4):412-3. Turk J Pediatr. 2008. PMID: 19014062 No abstract available.

8

Hematopoietic stem cell transplantation from a donor with Klinefelter syndrome for Wiskott-Aldrich syndrome.

Balci YI, Turul T, Daar G, Anak S, Devecioglu O, Tezcan I, Cetinkaya DU. Balci YI, et al. Among authors: turul t. Pediatr Transplant. 2008 Aug;12(5):597-9. doi: 10.1111/j.1399-3046.2008.00908.x. Epub 2008 Mar 10. Pediatr Transplant. 2008. PMID: 18331539

9

Parvovirus B19-induced persistent pure red cell aplasia in a child with T-cell immunodeficiency.

Tavil B, Sanal O, Turul T, Yel L, Gurgey A, Gumruk F. Tavil B, et al. Among authors: turul t. Pediatr Hematol Oncol. 2009 Mar;26(2):63-8. doi: 10.1080/08880010902754735. Pediatr Hematol Oncol. 2009. PMID: 19322736

10

Trimethoprim-sulfamethoxazole induced prolonged hypoglycemia in an infant with MHC class II deficiency: diazoxide as a treatment option.

Gonc EN, Turul T, Yordam N, Ersoy F. Gonc EN, et al. Among authors: turul t. J Pediatr Endocrinol Metab. 2003 Dec;16(9):1307-9. doi: 10.1515/jpem.2003.16.9.1307. J Pediatr Endocrinol Metab. 2003. PMID: 14714756

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