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Results: 1-25/37
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
Authors:
Bykhovskaya, Y
Yang, HY
Taylor, K
Hang, T
Tun, RYM
Estivill, X
Casano, RAMS
Majamaa, K
Shohat, M
Fischel-Ghodsian, N
Citation: Y. Bykhovskaya et al., Modifier locus for mitochondrial DNA disease: Linkage and linkage disequilibrium mapping of a nuclear modifier gene for maternally inherited deafness, GENET MED, 3(3), 2001, pp. 177-180
Authors:
Bar-Hava, I
Yitzhak, M
Krissi, H
Shohat, M
Shalev, J
Czitron, B
Ben-Rafael, Z
Orvieto, R
Citation: I. Bar-hava et al., Triple-test screening in in vitro fertilization pregnancies, J AS REPROD, 18(4), 2001, pp. 226-229
Authors:
Toudjarska, I
Kilpatrick, MW
Lembessis, P
Carra, S
Harton, GL
Sisson, ME
Black, SH
Stern, HJ
Gelman-Kohan, Z
Shohat, M
Tsipouras, P
Citation: I. Toudjarska et al., Novel approach to the molecular diagnosis of Marfan syndrome: Application to sporadic cases and in prenatal diagnosis, AM J MED G, 99(4), 2001, pp. 294-302
Authors:
Tanamy, MG
Magal, N
Halpern, GJ
Jaber, L
Shohat, M
Citation: Mg. Tanamy et al., Fine mapping places the gene for arthrogryposis multiplex congenita neuropathic type between D5S394 and D5S2069 on chromosome 5qter, AM J MED G, 104(2), 2001, pp. 152-156
Authors:
Udler, Y
Kauschansky, A
Yeshaya, J
Freedman, J
Barkai, U
Tobar, A
Okon, E
Halpern, GJ
Shohat, M
Legum, C
Citation: Y. Udler et al., Phenotypic expression of tissue mosaicism in a 45,X/46,X,dicY(q11.2) female, AM J MED G, 102(4), 2001, pp. 318-323
Authors:
Senecky, Y
Halpern, GJ
Inbar, D
Attias, J
Shohat, M
Citation: Y. Senecky et al., Ectodermal dysplasia, ectrodactyly and macular dystrophy (EEM syndrome) insiblings, AM J MED G, 101(3), 2001, pp. 195-197
Authors:
Halpern, GJ
Mimouni, A
Shohat, M
Citation: Gj. Halpern et al., E148Q of the MEFV gene causes amyloidosis in familial Mediterranean fever patients - Reply, PEDIATRICS, 108(1), 2001, pp. 215-215
Authors:
Toledano-Alhadef, H
Basel-Vanagaite, L
Magal, N
Davidov, B
Ehrlich, S
Drasinover, V
Taub, E
Halpern, GJ
Ginott, N
Shohat, M
Citation: H. Toledano-alhadef et al., Fragile-X carrier screening and the prevalence of premutation and full-mutation carriers in Israel, AM J HU GEN, 69(2), 2001, pp. 351-360
Authors:
Shohat, M
Hodak, E
Sredni, B
Shohat, B
Sredni, D
David, M
Citation: M. Shohat et al., Cytokine profile of patients with mycosis fungoides and the immunomodulatory effect of AS101, ACT DER-VEN, 81(4), 2001, pp. 255-257
Authors:
Shohat, M
Citation: M. Shohat, The future of genetics: Where are we going in the next forty years?, ISR MED ASS, 2(9), 2000, pp. 690-691
Authors:
Falik-Zaccai, TC
Shachak, E
Abeliovitch, D
Lerer, I
Shefer, R
Carmi, R
Ries, L
Friedman, M
Shohat, M
Borochowitz, Z
Citation: Tc. Falik-zaccai et al., Achondroplasia in diverse Jewish and Arab populations in Israel: Clinical and molecular characterization, ISR MED ASS, 2(8), 2000, pp. 601-604
Authors:
Shohat, T
Green, MS
Nakar, O
Ballin, A
Duvdevani, P
Cohen, A
Shohat, M
Citation: T. Shohat et al., Gender differences in the reactogenicity of measles-mumps-rubella vaccine, ISR MED ASS, 2(3), 2000, pp. 192-195
Authors:
Lotem, Y
Barak, A
Mussaffi, H
Shohat, M
Wilschanski, M
Sivan, Y
Blau, H
Citation: Y. Lotem et al., Reaching the diagnosis of cystic fibrosis - the limits of the spectrum, ISR MED ASS, 2(2), 2000, pp. 94-98
Authors:
Jaber, L
Eisenstein, B
Shohat, M
Citation: L. Jaber et al., Blood pressure measurements in Israeli Arab children and adolescents, ISR MED ASS, 2(2), 2000, pp. 118-121
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:
Sobe, T
Vreugde, S
Shahin, H
Berlin, M
Davis, N
Kanaan, M
Yaron, Y
Orr-Urtreger, A
Frydman, M
Shohat, M
Avraham, KB
Citation: T. Sobe et al., The prevalence and expression of inherited connexin 26 mutations associated with nonsyndromic hearing loss in the Israeli population, HUM GENET, 106(1), 2000, pp. 50-57
Authors:
Udler, Y
Halpern, GJ
Lachman, RS
Rimoin, DL
Shohat, M
Citation: Y. Udler et al., Pathological fractures in spondyloenchondrodysplasia: case report, PEDIAT RAD, 30(2), 2000, pp. 119-120
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:
Molad, Y
Gal, E
Magal, N
Sulkes, J
Mukamel, M
Weinberger, A
Lalazari, S
Shohat, M
Citation: Y. Molad et al., Renal outcome and vascular morbidity in systemic lupus erythematosus (SLE): Lack of association with the angiotensin-converting enzyme gene polymorphism, SEM ARTH RH, 30(2), 2000, pp. 132-137
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:
Bykhovskaya, Y
Estivill, X
Taylor, K
Hang, T
Hamon, M
Casano, RAMS
Yang, HY
Rotter, JI
Shohat, M
Fischel-Ghodsian, N
Citation: Y. Bykhovskaya et al., Candidate locus for a nuclear modifier gene for maternally inherited deafness, AM J HU GEN, 66(6), 2000, pp. 1905-1910
Authors:
Michaelovsky, E
Frisch, A
Rockah, R
Peleg, L
Magal, N
Shohat, M
Weizman, R
Citation: E. Michaelovsky et al., A novel allele in the promoter region of the human serotonin transporter gene, MOL PSYCHI, 4(1), 1999, pp. 97-99
Authors:
Horowitz, M
Pasmanik-Chor, M
Borochowitz, Z
Falik-Zaccai, T
Heldmann, K
Carmi, R
Parvari, R
Beit-Or, H
Goldman, B
Peleg, L
Levy-Lahad, E
Renbaum, P
Legum, S
Shomrat, R
Yeger, H
Benbenisti, D
Navon, R
Dror, V
Shohat, M
Magal, N
Navot, N
Eyal, N
Citation: M. Horowitz et al., Prevalence of glucocerebrosidase mutations in the Israeli Ashkenazi Jewishpopulation (vol 12, pg 240, 1998), HUM MUTAT, 13(3), 1999, pp. 255-255