Pras E - Search Results

1

Hematologic biomarkers in childhood cataracts.

Wussuki-Lior O, Abu-Horowitz A, Netzer I, Almer Z, Morad Y, Goldich Y, Yahalom V, Pras E, Pras E. Wussuki-Lior O, et al. Among authors: pras e. Mol Vis. 2011 Apr 24;17:1011-5. Mol Vis. 2011. PMID: 21541272 Free PMC article.

2

A nonsense mutation (W9X) in CRYAA causes autosomal recessive cataract in an inbred Jewish Persian family.

Pras E, Frydman M, Levy-Nissenbaum E, Bakhan T, Raz J, Assia EI, Goldman B, Pras E. Pras E, et al. Invest Ophthalmol Vis Sci. 2000 Oct;41(11):3511-5. Invest Ophthalmol Vis Sci. 2000. PMID: 11006246

3

A gene causing autosomal recessive cataract maps to the short arm of chromosome 3.

Pras E, Pras E, Bakhan T, Levy-Nissenbaum E, Lahat H, Assia EI, Garzozi HJ, Kastner DL, Goldman B, Frydman M. Pras E, et al. Isr Med Assoc J. 2001 Aug;3(8):559-62. Isr Med Assoc J. 2001. PMID: 11519376

4

Autosomal recessive catecholamine- or exercise-induced polymorphic ventricular tachycardia: clinical features and assignment of the disease gene to chromosome 1p13-21.

Lahat H, Eldar M, Levy-Nissenbaum E, Bahan T, Friedman E, Khoury A, Lorber A, Kastner DL, Goldman B, Pras E. Lahat H, et al. Among authors: pras e. Circulation. 2001 Jun 12;103(23):2822-7. doi: 10.1161/01.cir.103.23.2822. Circulation. 2001. PMID: 11401939

5

A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel.

Lahat H, Pras E, Olender T, Avidan N, Ben-Asher E, Man O, Levy-Nissenbaum E, Khoury A, Lorber A, Goldman B, Lancet D, Eldar M. Lahat H, et al. Among authors: pras e. Am J Hum Genet. 2001 Dec;69(6):1378-84. doi: 10.1086/324565. Epub 2001 Oct 25. Am J Hum Genet. 2001. PMID: 11704930 Free PMC article.

6

A new locus for autosomal dominant posterior polar cataract in Moroccan Jews maps to chromosome 14q22-23.

Pras E, Mahler O, Kumar V, Frydman M, Gefen N, Pras E, Hejtmancik JF. Pras E, et al. J Med Genet. 2006 Oct;43(10):e50. doi: 10.1136/jmg.2005.034876. J Med Genet. 2006. PMID: 17047090 Free PMC article.

7

Genetic analysis of Brugada syndrome in Israel: two novel mutations and possible genetic heterogeneity.

Levy-Nissenbaum E, Eldar M, Wang Q, Lahat H, Belhassen B, Ries L, Friedman E, Pras E. Levy-Nissenbaum E, et al. Among authors: pras e. Genet Test. 2001 Winter;5(4):331-4. doi: 10.1089/109065701753617480. Genet Test. 2001. PMID: 11960580

8

Molecular analysis of cystinuria in Libyan Jews: exclusion of the SLC3A1 gene and mapping of a new locus on 19q.

Wartenfeld R, Golomb E, Katz G, Bale SJ, Goldman B, Pras M, Kastner DL, Pras E. Wartenfeld R, et al. Among authors: pras m, pras e. Am J Hum Genet. 1997 Mar;60(3):617-24. Am J Hum Genet. 1997. PMID: 9042922 Free PMC article.

9

Clinical differences between North African and Iraqi Jews with familial Mediterranean fever.

Pras E, Livneh A, Balow JE Jr, Pras E, Kastner DL, Pras M, Langevitz P. Pras E, et al. Among authors: pras m. Am J Med Genet. 1998 Jan 13;75(2):216-9. doi: 10.1002/(sici)1096-8628(19980113)75:2<216::aid-ajmg20>3.0.co;2-r. Am J Med Genet. 1998. PMID: 9450890

10

Refined mapping of the CSNU3 gene to a 1.8-Mb region on chromosome 19q13.1 using historical recombinants in Libyan Jewish cystinuria patients.

Pras E, Kreiss Y, Frishberg Y, Prosen L, Aksentijevich I, Kastner DL. Pras E, et al. Genomics. 1999 Sep 1;60(2):248-50. doi: 10.1006/geno.1999.5917. Genomics. 1999. PMID: 10486219

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