Hujirat Y - Search Results

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A novel missense mutation in CIAS1 encoding the pyrin-like protein, cryopyrin, causes familial cold autoinflammatory syndrome in a family of Ethiopian origin.

Shalev SA, Sprecher E, Indelman M, Hujirat Y, Bergman R, Rottem M. Shalev SA, et al. Among authors: hujirat y. Int Arch Allergy Immunol. 2007;143(3):190-3. doi: 10.1159/000099311. Epub 2007 Feb 6. Int Arch Allergy Immunol. 2007. PMID: 17284928

Thrombophilia in infancy: factor V Leiden and MTHFR or factor II double heterozygocity as a risk factor.

Koren A, Levin C, Hujirat Y, El-Hasid R, Kutai M, Lanir N, Shalev S, Brenner B. Koren A, et al. Among authors: hujirat y. Pediatr Hematol Oncol. 2003 Apr-May;20(3):219-27. Pediatr Hematol Oncol. 2003. PMID: 12637218

Thrombophilia and stillbirth: possible connection by intrauterine growth restriction.

Weiner Z, Beck-Fruchter R, Weiss A, Hujirat Y, Shalev E, Shalev SA. Weiner Z, et al. Among authors: hujirat y. BJOG. 2004 Aug;111(8):780-3. doi: 10.1111/j.1471-0528.2004.00182.x. BJOG. 2004. PMID: 15270924

Maternal origin of a de novo mutation of the connexin 26 gene resulting in recessive nonsyndromic deafness.

Shalev SA, Hujirat Y. Shalev SA, et al. Among authors: hujirat y. Am J Med Genet A. 2004 Feb 1;124A(4):411-2. doi: 10.1002/ajmg.a.20406. Am J Med Genet A. 2004. PMID: 14735592 No abstract available.

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