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Clinical, immunologic and genetic analysis of 29 patients with autosomal recessive hyper-IgM syndrome due to Activation-Induced Cytidine Deaminase deficiency.
Quartier P, Bustamante J, Sanal O, Plebani A, Debré M, Deville A, Litzman J, Levy J, Fermand JP, Lane P, Horneff G, Aksu G, Yalçin I, Davies G, Tezcan I, Ersoy F, Catalan N, Imai K, Fischer A, Durandy A. Quartier P, et al. Among authors: yalcin i. Clin Immunol. 2004 Jan;110(1):22-9. doi: 10.1016/j.clim.2003.10.007. Clin Immunol. 2004. PMID: 14962793
In vitro chromosomal radiosensitivity in common variable immune deficiency.
Palanduz S, Palanduz A, Yalcin I, Somer A, Ones U, Ustek D, Ozturk S, Salman N, Guler N, Bilge H. Palanduz S, et al. Among authors: yalcin i. Clin Immunol Immunopathol. 1998 Feb;86(2):180-2. doi: 10.1006/clin.1997.4478. Clin Immunol Immunopathol. 1998. PMID: 9473380
Low immunoglobulin G3 levels in wheezy children.
Ones U, Güler N, Somer A, Salman N, Yalçin I. Ones U, et al. Among authors: yalcin i. Acta Paediatr. 1998 Apr;87(4):368-70. Acta Paediatr. 1998. PMID: 9628287
A review of 43 cases of tetanus neonatorum.
Yalçin I, Güler N, Kebudi R, Oneş U, Salman N. Yalçin I, et al. Turk J Pediatr. 1992 Jul-Sep;34(3):121-5. Turk J Pediatr. 1992. PMID: 1485378
234 results