Tezcan I - Search Results

1

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.

2

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.

3

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

4

Cernunnos deficiency: a case report.

Turul T, Tezcan I, Sanal O. Turul T, et al. Among authors: tezcan i. J Investig Allergol Clin Immunol. 2011;21(4):313-6. J Investig Allergol Clin Immunol. 2011. PMID: 21721379 Free article.

5

Transplantation in patients with SCID: mismatched related stem cells or unrelated cord blood?

Fernandes JF, Rocha V, Labopin M, Neven B, Moshous D, Gennery AR, Friedrich W, Porta F, Diaz de Heredia C, Wall D, Bertrand Y, Veys P, Slatter M, Schulz A, Chan KW, Grimley M, Ayas M, Gungor T, Ebell W, Bonfim C, Kalwak K, Taupin P, Blanche S, Gaspar HB, Landais P, Fischer A, Gluckman E, Cavazzana-Calvo M; Eurocord and Inborn Errors Working Party of European Group for Blood and Marrow Transplantation. Fernandes JF, et al. Blood. 2012 Mar 22;119(12):2949-55. doi: 10.1182/blood-2011-06-363572. Epub 2012 Feb 3. Blood. 2012. PMID: 22308292 Free article.

6

Kidney pathology in a patient with severe combined immunodeficiency disease.

Sanal O, Cağlar M, Ersoy F, Coşkun Y, Tezcan I. Sanal O, et al. Among authors: tezcan i. Turk J Pediatr. 1994 Oct-Dec;36(4):319-23. Turk J Pediatr. 1994. PMID: 7825238

7

Low expression of T-cell receptor-CD3 complex: a case with a clinical presentation resembling humoral immunodeficiency.

Sanal O, Yel L, Ersoy F, Tezcan I, Berkel AI. Sanal O, et al. Among authors: tezcan i. Turk J Pediatr. 1996 Jan-Mar;38(1):81-4. Turk J Pediatr. 1996. PMID: 8819625

8

Bare lymphocyte syndrome with lack of HLA class I and II antigens. Presentation of two cases.

Ersoy F, Sanal O, Tezcan I, Yel L, Metin A. Ersoy F, et al. Among authors: tezcan i. Turk J Pediatr. 1995 Apr-Jun;37(2):141-6. Turk J Pediatr. 1995. PMID: 7597764

9

A case of adenosine deaminase-negative severe combined immunodeficiency with neurological abnormalities.

Tezcan I, Ersoy F, Cağlar M, Sanal O, Kotiloğlu E, Aysun S. Tezcan I, et al. Turk J Pediatr. 1995 Oct-Dec;37(4):383-9. Turk J Pediatr. 1995. PMID: 8560606

10

Investigation of Genetic Defects in Severe Combined Immunodeficiency Patients from Turkey by Targeted Sequencing.

Erman B, Bilic I, Hirschmugl T, Salzer E, Boztug H, Sanal Ö, Çağdaş Ayvaz D, Tezcan I, Boztug K. Erman B, et al. Among authors: tezcan i. Scand J Immunol. 2017 Mar;85(3):227-234. doi: 10.1111/sji.12523. Scand J Immunol. 2017. PMID: 28109013 Free article.

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