Shohat T - Search Results

1

Further mapping of the properdin deficiency gene in a Tunisian Jewish family--evidence for genetic homogeneity.

Ash S, Johnson C, Shohat M, Shohat T, Schlesinger M. Ash S, et al. Among authors: shohat t, shohat m. Isr J Med Sci. 1994 Aug;30(8):626-8. Isr J Med Sci. 1994. PMID: 8045746

2

The gene for familial Mediterranean fever in both Armenians and non-Ashkenazi Jews is linked to the alpha-globin complex on 16p: evidence for locus homogeneity.

Shohat M, Bu X, Shohat T, Fischel-Ghodsian N, Magal N, Nakamura Y, Schwabe AD, Schlezinger M, Danon Y, Rotter JI. Shohat M, et al. Among authors: shohat t. Am J Hum Genet. 1992 Dec;51(6):1349-54. Am J Hum Genet. 1992. PMID: 1463015 Free PMC article.

3

Familial Mediterranean fever: high gene frequency among the non-Ashkenazic and Ashkenazic Jewish populations in Israel.

Daniels M, Shohat T, Brenner-Ullman A, Shohat M. Daniels M, et al. Among authors: shohat t, shohat m. Am J Med Genet. 1995 Jan 30;55(3):311-4. doi: 10.1002/ajmg.1320550313. Am J Med Genet. 1995. PMID: 7726228

4

The lower incidence of myotonic dystrophy in Ashkenazic Jews compared to North African Jews is associated with a significantly lower number of CTG trinucleotide repeats.

Mor-Cohen R, Magal N, Gadoth N, Achiron A, Shohat T, Shohat M. Mor-Cohen R, et al. Among authors: shohat t, shohat m. Isr J Med Sci. 1997 Mar;33(3):190-3. Isr J Med Sci. 1997. PMID: 9313789

5

A gene for arthrogryposis multiplex congenita neuropathic type is linked to D5S394 on chromosome 5qter.

Shohat M, Lotan R, Magal N, Shohat T, Fischel-Ghodsian N, Rotter JI, Jaber L. Shohat M, et al. Among authors: shohat t. Am J Hum Genet. 1997 Nov;61(5):1139-43. doi: 10.1086/301598. Am J Hum Genet. 1997. PMID: 9345093 Free PMC article.

6

Higher than expected carrier rates for familial Mediterranean fever in various Jewish ethnic groups.

Stoffman N, Magal N, Shohat T, Lotan R, Koman S, Oron A, Danon Y, Halpern GJ, Lifshitz Y, Shohat M. Stoffman N, et al. Among authors: shohat t, shohat m. Eur J Hum Genet. 2000 Apr;8(4):307-10. doi: 10.1038/sj.ejhg.5200446. Eur J Hum Genet. 2000. PMID: 10854115

7

A locus for an autosomal dominant form of progressive renal failure and hypertension at chromosome 1q21.

Cohn DH, Shohat T, Yahav M, Ilan T, Rechavi G, King L, Shohat M. Cohn DH, et al. Among authors: shohat t, shohat m. Am J Hum Genet. 2000 Sep;67(3):647-51. doi: 10.1086/303051. Epub 2000 Aug 4. Am J Hum Genet. 2000. PMID: 10930359 Free PMC article.

8

Correlation between the incidence of myotonic dystrophy in different groups in Israel and the number of CTG trinucleotide repeats in the myotonin gene.

Mor-Cohen R, Magal N, Gadoth N, Shohat T, Shohat M. Mor-Cohen R, et al. Among authors: shohat t, shohat m. Am J Med Genet. 1997 Aug 8;71(2):156-9. doi: 10.1002/(sici)1096-8628(19970808)71:2<156::aid-ajmg7>3.0.co;2-w. Am J Med Genet. 1997. PMID: 9217214

9

Autosomal dominant nephritis with renal failure of non-Alport type: clinical and molecular studies.

Ilan T, Shohat T, Tobar A, Magal N, Yahav M, Halpern GJ, Rechavi G, Shohat M. Ilan T, et al. Among authors: shohat t, shohat m. Isr Med Assoc J. 2001 Jul;3(7):488-91. Isr Med Assoc J. 2001. PMID: 11791413 Free article.

10

Serum amyloid A and P protein genes in familial Mediterranean fever.

Shohat M, Shohat T, Rotter JI, Schlesinger M, Petersen GM, Pribyl T, Sack G, Schwabe AD, Korenberg JR. Shohat M, et al. Among authors: shohat t. Genomics. 1990 Sep;8(1):83-9. doi: 10.1016/0888-7543(90)90228-m. Genomics. 1990. PMID: 1981994

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