Authors:
Ilan, T
Shohat, T
Tobar, A
Magal, N
Yahav, M
Halpern, GJ
Rechavi, G
Shohat, M
Citation: T. Ilan et al., Autosomal dominant nephritis with renal failure of non-alport type: Clinical and molecular studies, ISR MED ASS, 3(7), 2001, pp. 488-491
Citation: T. Shohat et O. Romano-zelekha, Ultrasonographic measurements of fetal femur length and biparietal diameter in an Israeli population, ISR MED ASS, 3(3), 2001, pp. 166-168
Authors:
Weinberger, M
Pitlik, SD
Gandacu, D
Lang, R
Nassar, F
Ben David, D
Rubinstein, E
Izthaki, A
Mishal, J
Kitzes, R
Siegman-Igra, Y
Giladi, M
Pick, N
Mendelson, E
Bin, H
Shohat, T
Chowers, MY
Citation: M. Weinberger et al., West Nile fever outbreak, Israel, 2000: Epidemiologic aspects, EM INFECT D, 7(4), 2001, pp. 686-691
Authors:
Romano-Zelekha, O
Hirsh, R
Blieden, L
Green, MS
Shohat, T
Citation: O. Romano-zelekha et al., The risk for congenital heart defects in offspring of individuals with congenital heart defects, CLIN GENET, 59(5), 2001, pp. 325-329
Authors:
Jaber, L
Dolfin, T
Shohat, T
Halpern, GJ
Reish, O
Fejgin, M
Citation: L. Jaber et al., Prenatal diagnosis for detecting congenital malformations: Acceptance among Israeli Arab women, ISR MED ASS, 2(5), 2000, pp. 346-350
Authors:
Stoffman, N
Magal, N
Shohat, T
Lotan, R
Koman, S
Oron, A
Danon, Y
Halpern, GJ
Lifshitz, Y
Shohat, M
Citation: N. Stoffman et al., Higher than expected carrier rates for familial Mediterranean fever in various Jewish ethnic groups, EUR J HUM G, 8(4), 2000, pp. 307-310
Authors:
Drasinover, V
Ehrlich, S
Magal, N
Taub, E
Libman, V
Shohat, T
Halpern, GJ
Shohat, M
Citation: V. Drasinover et al., Increased transmission of intermediate alleles of the FMR1 gene compared with normal alleles among female heterozygotes, AM J MED G, 93(2), 2000, pp. 155-157
Authors:
Mimouni, A
Magal, N
Stoffman, N
Shohat, T
Minasian, A
Krasnov, M
Halpern, GJ
Rotter, JI
Fischel-Ghodsian, N
Danon, YL
Shohat, M
Citation: A. Mimouni et al., Familial Mediterranean fever: Effects of genotype and ethnicity on inflammatory attacks and amyloidosis, PEDIATRICS, 105(5), 2000, pp. E701-E707
Authors:
Cohn, DH
Shohat, T
Yahav, M
Ilan, T
Rechavi, G
King, L
Shohat, M
Citation: Dh. Cohn et al., A locus for an autosomal dominant form of progressive renal failure and hypertension at chromosome 1q21, AM J HU GEN, 67(3), 2000, pp. 647-651
Authors:
Shohat, M
Magal, N
Shohat, T
Chen, X
Dagan, T
Mimouni, A
Danon, Y
Lotan, R
Ogur, G
Sirin, A
Schlezinger, M
Halpern, GJ
Schwabe, A
Kastner, D
Rotter, JI
Fischel-Ghodsian, N
Citation: M. Shohat et al., Phenotype-genotype correlation in familial Mediterranean fever: evidence for an association between Met694Val and amyloidosis, EUR J HUM G, 7(3), 1999, pp. 287-292
Citation: T. Shohat et al., Mortality from infectious diseases in Israel, 1979-1992, based on revised ICD-9 codes: Implications for international comparisons, AM J PUB HE, 89(12), 1999, pp. 1855-1857
Authors:
Mager, A
Lalezari, S
Shohat, T
Birnbaum, Y
Adler, Y
Magal, N
Shohat, M
Citation: A. Mager et al., Methylenetetrahydrofolate reductase genotypes and early-onset coronary artery disease, CIRCULATION, 100(24), 1999, pp. 2406-2410
Authors:
Shohat, M
Lotan, R
Magal, N
Danon, Y
Ogur, G
Tokguz, G
Schlezinger, M
Schwabe, A
Halpern, G
Fischel-Ghodsian, N
Kastner, D
Shohat, T
Rotter, JI
Citation: M. Shohat et al., Amyloidosis in familial Mediterranean fever is associated with a specific ancestral haplotype in the MEFV locus, MOL GEN MET, 65(3), 1998, pp. 197-202