Tezcan I - Search Results

1

Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the Hyper-IgM syndrome (HIGM2).

Revy P, Muto T, Levy Y, Geissmann F, Plebani A, Sanal O, Catalan N, Forveille M, Dufourcq-Labelouse R, Gennery A, Tezcan I, Ersoy F, Kayserili H, Ugazio AG, Brousse N, Muramatsu M, Notarangelo LD, Kinoshita K, Honjo T, Fischer A, Durandy A. Revy P, et al. Among authors: tezcan i. Cell. 2000 Sep 1;102(5):565-75. doi: 10.1016/s0092-8674(00)00079-9. Cell. 2000. PMID: 11007475 Free article.

2

Artemis, a novel DNA double-strand break repair/V(D)J recombination protein, is mutated in human severe combined immune deficiency.

Moshous D, Callebaut I, de Chasseval R, Corneo B, Cavazzana-Calvo M, Le Deist F, Tezcan I, Sanal O, Bertrand Y, Philippe N, Fischer A, de Villartay JP. Moshous D, et al. Among authors: tezcan i. Cell. 2001 Apr 20;105(2):177-86. doi: 10.1016/s0092-8674(01)00309-9. Cell. 2001. PMID: 11336668 Free article.

3

Clinical and immunological aspects of hyper-IgM syndrome.

Ersoy F, Sanal O, Tezcan I. Ersoy F, et al. Among authors: tezcan i. Turk J Pediatr. 1990 Jan-Mar;32(1):13-20. Turk J Pediatr. 1990. PMID: 2288014

4

Two genes are responsible for Griscelli syndrome at the same 15q21 locus.

Pastural E, Ersoy F, Yalman N, Wulffraat N, Grillo E, Ozkinay F, Tezcan I, Gediköglu G, Philippe N, Fischer A, de Saint Basile G. Pastural E, et al. Among authors: tezcan i. Genomics. 2000 Feb 1;63(3):299-306. doi: 10.1006/geno.1999.6081. Genomics. 2000. PMID: 10704277

5

IgG subclasses in symptomatic IgA deficiency.

Tezcan I, Ersoy F, Sanal O. Tezcan I, et al. Turk J Pediatr. 1992 Jan-Mar;34(1):1-4. Turk J Pediatr. 1992. PMID: 1509524

6

Serum IgD concentrations in patients with ataxia telangiectasia and with selective IgA deficiency.

Sanal O, Ozaltin F, Tezcan I, Ersoy F. Sanal O, et al. Among authors: tezcan i. Int Arch Allergy Immunol. 1998 Jul;116(3):246. doi: 10.1159/000023951. Int Arch Allergy Immunol. 1998. PMID: 9696048 Free article. No abstract available.

7

Mutations of chronic granulomatous disease in Turkish families.

Köker MY, Sanal O, De Boer M, Tezcan I, Metin A, Ersoy F, Roos D. Köker MY, et al. Among authors: tezcan i. Eur J Clin Invest. 2007 Jul;37(7):589-95. doi: 10.1111/j.1365-2362.2007.01828.x. Eur J Clin Invest. 2007. PMID: 17576211

8

Hyper-IgE syndrome: a case report.

Sanal O, Göçmen A, Tezcan I, Ersoy F, Adalioğlu G. Sanal O, et al. Among authors: tezcan i. Turk J Pediatr. 1990 Oct-Dec;32(4):273-8. Turk J Pediatr. 1990. PMID: 2135680

9

Effects of intravenous immunoglobulin on clinical and immunological findings of patients with humoral immunodeficiency diseases.

Ersoy F, Tezcan I, Sanal O. Ersoy F, et al. Among authors: tezcan i. Turk J Pediatr. 1992 Oct-Dec;34(4):203-9. Turk J Pediatr. 1992. PMID: 1306339

10

Serum IgD concentrations in immunodeficiency diseases.

Sanal O, Ersoy F, Tezcan I, Yeniay I. Sanal O, et al. Among authors: tezcan i. Turk J Pediatr. 1990 Jul-Sep;32(3):175-82. Turk J Pediatr. 1990. PMID: 2093253

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

236 results

Search Page