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Results: 1-25/29
Authors:
HASSINBAER S
STEINER I
ACHIRON A
SADEH M
VONSOVER A
HASSIN D
Citation: S. Hassinbaer et al., UNUSUAL NEUROLOGICAL MANIFESTATIONS OF PRIMARY HUMAN-IMMUNODEFICIENCY-VIRUS INFECTION, European journal of neurology, 5(4), 1998, pp. 369-373
Authors:
BASHIR R
BRITTON S
STRACHAN T
KEERS S
VAFIADAKI E
LAKO M
RICHARD I
MARCHAND S
BOURG N
ARGOV Z
SADEH M
MAHJNEH I
MARCONI G
PASSOSBUENO MR
MOREIRA ED
ZATZ M
BECKMANN JS
BUSHBY K
Citation: R. Bashir et al., A GENE-RELATED TO CAENORHABDITIS-ELEGANS SPERMATOGENESIS FACTOR FER-1IS MUTATED IN LIMB-GIRDLE MUSCULAR-DYSTROPHY TYPE 2B, Nature genetics, 20(1), 1998, pp. 37-42
Authors:
LEV D
LERMANSAGIE T
TANNER MS
LIECHETIGALLATI S
SADEH M
Citation: D. Lev et al., X-LINKED MYOTUBULAR MYOPATHY IN A WOMAN SUFFERING FROM PROGRESSIVE MUSCLE WEAKNESS, European journal of human genetics, 6, 1998, pp. 1068-1068
Authors:
NISSENKORN A
WEINTRAUB S
SADEH M
LERMANSAGIE T
Citation: A. Nissenkorn et al., LISSENCEPHALY ASSOCIATED WITH CONGENITAL HYPOMYELINATING AND AXONAL NEUROPATHY, Pediatric neurology, 19(4), 1998, pp. 313-316
Authors:
MAOZ CR
LANGEVITZ P
LIVNEH A
BLUMSTEIN Z
SADEH M
BANK I
GUR H
EHRENFELD M
Citation: Cr. Maoz et al., HIGH-INCIDENCE OF MALIGNANCIES IN PATIENTS WITH DERMATOMYOSITIS AND POLYMYOSITIS - AN 11-YEAR ANALYSIS, Seminars in arthritis and rheumatism, 27(5), 1998, pp. 319-324
Authors:
ARGOV Z
SADEH M
EISENBERG I
KARPATI G
MITRANIROSENBAUM S
Citation: Z. Argov et al., FACIAL WEAKNESS IN HEREDITARY INCLUSION-BODY MYOPATHIES, Neurology, 50(6), 1998, pp. 1925-1926
Authors:
FURUKAWA Y
LANG AE
TRUGMAN JM
BIRD TD
HUNTER A
SADEH M
TAGAWA T
STGEORGEHYSLOP PH
GUTTMAN M
MORRIS LW
HORNYKIEWICZ O
SHIMADZU M
KISH SJ
Citation: Y. Furukawa et al., GENDER-RELATED PENETRANCE AND DE-NOVO GTP-CYCLOHYDROLASE-I GENE-MUTATIONS IN DOPA-RESPONSIVE DYSTONIA, Neurology, 50(4), 1998, pp. 1015-1020
Authors:
MENOLD MM
SADEH M
LENNON F
BLATT I
GOLDHAMMER Y
YAMAOKA LH
VANCE JM
PERICAKVANCE MA
Citation: Mm. Menold et al., EVIDENCE FOR GENETIC-HETEROGENEITY SUPPORTS CLINICAL DIFFERENCES IN CONGENITAL MYASTHENIC SYNDROMES, Human heredity, 48(6), 1998, pp. 325-332
Authors:
BLUMEN SC
NISIPEANU P
SADEH M
ASHEROV A
BLUMEN N
WIRGUIN Y
KHILKEVICH O
CARASSO RL
KORCZYN AD
Citation: Sc. Blumen et al., EPIDEMIOLOGY AND INHERITANCE OF OCULOPHARYNGEAL MUSCULAR-DYSTROPHY INISRAEL, Neuromuscular disorders, 7, 1997, pp. 38-40
Authors:
KUSHNIR T
KNUBOVETS T
ITZCHAK Y
ELIAV U
SADEH M
RAPOPORT L
KOTT E
NAVON G
Citation: T. Kushnir et al., IN-VIVO NA-23 NMR-STUDIES OF MYOTONIC-DYSTROPHY, Magnetic resonance in medicine, 37(2), 1997, pp. 192-196
Authors:
ARGOV Z
TIRAM E
EISENBERG I
SADEH M
SEIDMAN CE
SEIDMAN JG
KARPATI G
MITRANIROSENBAUM S
Citation: Z. Argov et al., VARIOUS TYPES OF HEREDITARY INCLUSION-BODY MYOPATHIES MAP TO CHROMOSOME 9P1-Q1, Annals of neurology, 41(4), 1997, pp. 548-551
Authors:
INBAR D
HALPERN GJ
WEITZ R
SADEH M
SHOHAT M
Citation: D. Inbar et al., AGENESIS OF THE CORPUS-CALLOSUM IN A MOTHER AND SON, American journal of medical genetics, 69(2), 1997, pp. 152-154
Authors:
SADEH M
RIVER Y
ARGOV Z
Citation: M. Sadeh et al., STIMULATED SINGLE-FIBER ELECTROMYOGRAPHY IN LAMBERT-EATON-MYASTHENIC-SYNDROME BEFORE AND AFTER 3,4-DIAMINOPYRIDINE, Muscle & nerve, 20(6), 1997, pp. 735-739
Authors:
ARGOV Z
SADEH M
KARPATI G
EISENBERG I
TIRAM E
MITRANIROSENBAUM S
Citation: Z. Argov et al., NEW FORMS OF HEREDITARY INCLUSION-BODY MYOPATHY (HIBM) AND THEIR GENETIC SPECTRUM, Neurology, 48(3), 1997, pp. 41001-41001
Authors:
IYENGAR S
KALINSKY H
WEISS S
KOROSTISHEVSKY M
SADEH M
ZHAO Y
KIDD KK
BONNETAMIR B
Citation: S. Iyengar et al., HOMOZYGOSITY BY DESCENT FOR A RARE MUTATION IN THE MYOPHOSPHORYLASE GENE IS ASSOCIATED WITH VARIABLE PHENOTYPES IN A DRUZE FAMILY WITH MCARDLE DISEASE, Journal of Medical Genetics, 34(5), 1997, pp. 391-394
Authors:
MENOLD MM
LENNON F
SADEH M
GOLDHAMMER Y
BLATT I
YAMAOKA LH
VANCE JM
PERICAKVANCE MA
Citation: Mm. Menold et al., EVIDENCE FOR GENETIC-HETEROGENEITY SUPPORTS CLINICAL DIFFERENCES IN CONGENITAL MYASTHENIC SYNDROMES (CMS), American journal of human genetics, 61(4), 1997, pp. 1667-1667
Authors:
NAVON R
SEIFRIED B
GALON NS
SADEH M
Citation: R. Navon et al., A NEW POINT MUTATION AFFECTING THE 4TH TRANSMEMBRANE DOMAIN OF PMP22 RESULTS IN SEVERE, DE-NOVO CHARCOT-MARIE-TOOTH DISEASE, Human genetics, 97(5), 1996, pp. 685-687
Authors:
NEUMANN Y
TOREN A
RECHAVI G
SEIFRIED B
SHOHAM NG
MANDEL M
KENET G
SHARON N
SADEH M
NAVON R
Citation: Y. Neumann et al., VINCRISTINE TREATMENT TRIGGERING THE EXPRESSION OF ASYMPTOMATIC CHARCOT-MARIE-TOOTH DISEASE, Medical and pediatric oncology, 26(4), 1996, pp. 280-283
Authors:
BLUMEN SC
SADEH M
KORCZYN AD
ROUCHE A
NISIPEANU P
ASHEROV A
TOME FMS
Citation: Sc. Blumen et al., INTRANUCLEAR INCLUSIONS IN OCULOPHARYNGEAL MUSCULAR-DYSTROPHY AMONG BUKHARA JEWS, Neurology, 46(5), 1996, pp. 1324-1328
Authors:
ARIEL R
SADEH M
Citation: R. Ariel et M. Sadeh, CONGENITAL VISUAL AGNOSIA AND PROSOPAGNOSIA IN A CHILD - A CASE-REPORT, Cortex, 32(2), 1996, pp. 221-240
Authors:
SHUPER A
ZEHARIA A
KORENREICH L
SADEH M
MIMOUNI M
Citation: A. Shuper et al., CEREBRAL CALCINOSIS AND LEARNING-DISABILITIES IN HYPOPARATHYROIDISM -A CAUSE AND EFFECT OR A COINCIDENCE, Pediatric neurology, 13(3), 1995, pp. 252-254
Authors:
NEUFELD MY
SADEH M
ASSA B
KUSHNIR M
KORCZYN AD
Citation: My. Neufeld et al., PHENOTYPIC HETEROGENEITY IN FAMILIAL INCLUSION-BODY MYOPATHY, Muscle & nerve, 18(5), 1995, pp. 546-548
Authors:
GOLDBERGSTERN H
NAVON R
SEIFRIED B
SADEH M
MEER J
GABAY U
MELAMED E
GADOTH N
Citation: H. Goldbergstern et al., CHARCOT-MARIE-TOOTH (CMT) DISEASE IN ISRAEL - CLINICAL, EPIDEMIOLOGIC, AND GENETIC-ASPECTS, Neurology, 45(4), 1995, pp. 243-244
Authors:
NAVON R
SEIFRIED B
GADOT N
KORCYN A
SADEH M
MERR J
GOLDBERGSTERN H
Citation: R. Navon et al., CHAREOT-MARIE-TOOTH DISEASE TYPE 1A AND HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES - AN ISARALI STUDY, American journal of human genetics, 57(4), 1995, pp. 1430-1430
Authors:
KALINSKY H
IYENGAR S
WEISS S
SADEH M
BONNETAMIR B
KIDD KK
Citation: H. Kalinsky et al., MUTATION AND HAPLOTYPE ANALYSIS OF A DRUZE PEDIGREE WITH MCARDLES-DISEASE, American journal of human genetics, 57(4), 1995, pp. 1923-1923