Tezcan I - Search Results

1

Clinical features of chronic granulomatous disease: a series of 26 patients from a single center.

Turul-Ozgür T, Türkkani-Asal G, Tezcan I, Köker MY, Metin A, Yel L, Ersoy F, Sanal O. Turul-Ozgür T, et al. Among authors: tezcan i. Turk J Pediatr. 2010 Nov-Dec;52(6):576-81. Turk J Pediatr. 2010. PMID: 21428188

2

Genetic analysis of patients with leukocyte adhesion deficiency: genomic sequencing reveals otherwise undetectable mutations.

Roos D, Meischl C, de Boer M, Simsek S, Weening RS, Sanal O, Tezcan I, Güngör T, Law SK. Roos D, et al. Among authors: tezcan i. Exp Hematol. 2002 Mar;30(3):252-61. doi: 10.1016/s0301-472x(01)00782-2. Exp Hematol. 2002. PMID: 11882363 Free article.

3

Novel Igalpha (CD79a) gene mutation in a Turkish patient with B cell-deficient agammaglobulinemia.

Wang Y, Kanegane H, Sanal O, Tezcan I, Ersoy F, Futatani T, Miyawaki T. Wang Y, et al. Among authors: tezcan i. Am J Med Genet. 2002 Apr 1;108(4):333-6. doi: 10.1002/ajmg.10296. Am J Med Genet. 2002. PMID: 11920841

4

Griscelli disease: genotype-phenotype correlation in an array of clinical heterogeneity.

Sanal O, Ersoy F, Tezcan I, Metin A, Yel L, Ménasché G, Gürgey A, Berkel I, de Saint Basile G. Sanal O, et al. Among authors: tezcan i. J Clin Immunol. 2002 Jul;22(4):237-43. doi: 10.1023/a:1016045026204. J Clin Immunol. 2002. PMID: 12148598

5

Osteochondritis dissecans in a patient with hyperimmunoglobulin E syndrome.

Kiliç SS, Sanal O, Tezcan I, Ersoy F. Kiliç SS, et al. Among authors: tezcan i. Turk J Pediatr. 2002 Oct-Dec;44(4):357-9. Turk J Pediatr. 2002. PMID: 12458817

6

Severe Mycobacterium bovis BCG infections in a large series of novel IL-12 receptor beta1 deficient patients and evidence for the existence of partial IL-12 receptor beta1 deficiency.

Lichtenauer-Kaligis EG, de Boer T, Verreck FA, van Voorden S, Hoeve MA, van de Vosse E, Ersoy F, Tezcan I, van Dissel JT, Sanal O, Ottenhoff TH. Lichtenauer-Kaligis EG, et al. Among authors: tezcan i. Eur J Immunol. 2003 Jan;33(1):59-69. doi: 10.1002/immu.200390008. Eur J Immunol. 2003. PMID: 12594833 Free article.

7

Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1).

Ménasché G, Ho CH, Sanal O, Feldmann J, Tezcan I, Ersoy F, Houdusse A, Fischer A, de Saint Basile G. Ménasché G, et al. Among authors: tezcan i. J Clin Invest. 2003 Aug;112(3):450-6. doi: 10.1172/JCI18264. J Clin Invest. 2003. PMID: 12897212 Free PMC article.

8

The effect of mannose-binding protein gene polymorphisms in recurrent respiratory system infections in children and lung tuberculosis.

Ozbaş-Gerçeker F, Tezcan I, Berkel AI, Ozkara S, Ozcan A, Ersoy F, Sanal O, Ozgüç M. Ozbaş-Gerçeker F, et al. Among authors: tezcan i. Turk J Pediatr. 2003 Apr-Jun;45(2):95-8. Turk J Pediatr. 2003. PMID: 12921293

9

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: tezcan i. 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.

10

Antioxidant enzymes in red blood cells and lymphocytes of ataxia-telangiectasia patients.

Aksoy Y, Sanal O, Metin A, Tezcan I, Ersoy F, Oğüş H, Ozer N. Aksoy Y, et al. Among authors: tezcan i. Turk J Pediatr. 2004 Jul-Sep;46(3):204-7. Turk J Pediatr. 2004. PMID: 15503471

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