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La ricerca find articoli where authors phrase all words ' SADEH M' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 48 riferimenti
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    1. Rapoport, A; Sadeh, M
      Posterior semicircular canal type benign paroxysmal positioning vertigo with ageotropic paroxysmal positioning nystagmus

      AUDIOLOGY AND NEURO-OTOLOGY
    2. Eisenberg, I; Avidan, N; Potikha, T; Hochner, H; Chen, M; Olender, T; Barash, M; Shemesh, M; Sadeh, M; Grabov-Nardini, G; Shmilevich, I; Friedmann, A; Karpati, G; Bradley, WG; Baumbach, L; Lancet, D; Ben Asher, E; Beckmann, JS; Argov, Z; Mitrani-Rosenbaum, S
      The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene ismutated in recessive hereditary inclusion body myopathy

      NATURE GENETICS
    3. Eisenberg, I; Hochner, H; Shemesh, M; Levi, T; Potikha, T; Sadeh, M; Argov, Z; Jackson, CL; Mitrani-Rosenbaum, S
      Physical and transcriptional map of the hereditary inclusion body myopathylocus on chromosome 9p12-p13

      EUROPEAN JOURNAL OF HUMAN GENETICS
    4. Gilad, R; Lampl, Y; Eschel, Y; Sadeh, M
      Antiepileptic treatment in patients with early postischemic stroke seizures: A retrospective study

      CEREBROVASCULAR DISEASES
    5. Sadeh, M; Cohen, I
      Transient loss of speech after removal of posterior fossa tumors - One aspect of a larger neuropsychological entity: The cerebellar cognitive affective syndrome

      PEDIATRIC HEMATOLOGY AND ONCOLOGY
    6. Lampl, Y; Gilad, R; Geva, D; Eshel, Y; Sadeh, M
      Intravenous administration of magnesium sulfate in acute stroke: A randomized double-blind study

      CLINICAL NEUROPHARMACOLOGY
    7. Lorberboym, M; Lampl, Y; Kesler, A; Sadeh, M; Gadot, N
      Benign intracranial hypertension: correlation of cerebral blood flow with disease severity

      CLINICAL NEUROLOGY AND NEUROSURGERY
    8. Gilad, R; Giladi, N; Korczyn, AD; Gurevich, T; Sadeh, M
      Quantitative anal sphincter EMG in multisystem atrophy and 100 controls

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    9. Palta, M; Sadeh-Badawi, M; Evans, M; Weinstein, MR; McGuinness, G
      Functional assessment of a multicenter very low-birth-weight cohort at age5 years

      ARCHIVES OF PEDIATRICS & ADOLESCENT MEDICINE
    10. Toren, P; Sadeh, M; Wolmer, L; Eldar, S; Koren, S; Weizman, R; Laor, N
      Neurocognitive correlates of anxiety disorders in children: A preliminary report

      JOURNAL OF ANXIETY DISORDERS
    11. Rapaport, A; Sadeh, M; Stein, D; Levine, J; Sirota, P; Mosheva, T; Stir, S; Elitzur, A; Reznik, I; Geva, D; Rabey, JM
      Botulinum toxin for the treatment of oro-facial-lingual-masticatory tardive dyskinesia

      MOVEMENT DISORDERS
    12. Watemberg, N; Amsel, S; Sadeh, M; Lerman-Sagie, T
      Common peroneal neuropathy due to surfing

      JOURNAL OF CHILD NEUROLOGY
    13. Shuper, A; Stark, B; Yaniv, Y; Zaizov, R; Carel, C; Sadeh, M; Steinmetz, A
      Cerebellar involvement in Langerhans' cell histiocytosis: A progressive neuropsychiatric disease

      JOURNAL OF CHILD NEUROLOGY
    14. Argov, Z; Sadeh, M; Mazor, K; Soffer, D; Kahana, E; Eisenberg, I; Mitrani-Rosenbaum, S; Richard, I; Beckmann, J; Keers, S; Bashir, R; Bushby, K; Rosenmann, H
      Muscular dystrophy due to dysferlin deficiency in Libyan Jews - Clinical and genetic features

      BRAIN
    15. Eisenberg, I; Thiel, C; Levi, T; Tiram, E; Argov, Z; Sadeh, M; Jackson, CL; Thierfelder, L; Mitrani-Rosenbaum, S
      Fine-structure mapping of the hereditary inclusion body myopathy locus

      GENOMICS
    16. Nass, D; Goldberg, I; Sadeh, M
      Laminin alpha 2 deficient congenital muscular dystrophy: prenatal diagnosis

      EARLY HUMAN DEVELOPMENT
    17. Tanner, SM; Orstavik, KH; Kristiansen, M; Lev, D; Lerman-Sagie, T; Sadeh, M; Liechti-Gallati, S
      Skewed X-inactivation in a manifesting carrier of X-linked myotubular myopathy and in her non-manifesting carrier mother

      HUMAN GENETICS
    18. Steiner, I; Cohen, O; Leker, RR; Rubinovitch, B; Handsher, R; Hassin-Baer, S; Gilden, DH; Sadeh, M
      Subacute painful lumbosacral polyradiculoneuropathy in immunocompromised patients

      JOURNAL OF THE NEUROLOGICAL SCIENCES
    19. Gilad, R; Lampl, Y; Lev, D; Sadeh, M
      Cerebrotendinous xanthomatosis without xanthomas

      CLINICAL GENETICS
    20. HASSINBAER S; STEINER I; ACHIRON A; SADEH M; VONSOVER A; HASSIN D
      UNUSUAL NEUROLOGICAL MANIFESTATIONS OF PRIMARY HUMAN-IMMUNODEFICIENCY-VIRUS INFECTION

      European journal of neurology
    21. 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
      A GENE-RELATED TO CAENORHABDITIS-ELEGANS SPERMATOGENESIS FACTOR FER-1IS MUTATED IN LIMB-GIRDLE MUSCULAR-DYSTROPHY TYPE 2B

      Nature genetics
    22. LEV D; LERMANSAGIE T; TANNER MS; LIECHETIGALLATI S; SADEH M
      X-LINKED MYOTUBULAR MYOPATHY IN A WOMAN SUFFERING FROM PROGRESSIVE MUSCLE WEAKNESS

      European journal of human genetics
    23. NISSENKORN A; WEINTRAUB S; SADEH M; LERMANSAGIE T
      LISSENCEPHALY ASSOCIATED WITH CONGENITAL HYPOMYELINATING AND AXONAL NEUROPATHY

      Pediatric neurology
    24. MAOZ CR; LANGEVITZ P; LIVNEH A; BLUMSTEIN Z; SADEH M; BANK I; GUR H; EHRENFELD M
      HIGH-INCIDENCE OF MALIGNANCIES IN PATIENTS WITH DERMATOMYOSITIS AND POLYMYOSITIS - AN 11-YEAR ANALYSIS

      Seminars in arthritis and rheumatism
    25. ARGOV Z; SADEH M; EISENBERG I; KARPATI G; MITRANIROSENBAUM S
      FACIAL WEAKNESS IN HEREDITARY INCLUSION-BODY MYOPATHIES

      Neurology
    26. 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
      GENDER-RELATED PENETRANCE AND DE-NOVO GTP-CYCLOHYDROLASE-I GENE-MUTATIONS IN DOPA-RESPONSIVE DYSTONIA

      Neurology
    27. MENOLD MM; SADEH M; LENNON F; BLATT I; GOLDHAMMER Y; YAMAOKA LH; VANCE JM; PERICAKVANCE MA
      EVIDENCE FOR GENETIC-HETEROGENEITY SUPPORTS CLINICAL DIFFERENCES IN CONGENITAL MYASTHENIC SYNDROMES

      Human heredity
    28. BLUMEN SC; NISIPEANU P; SADEH M; ASHEROV A; BLUMEN N; WIRGUIN Y; KHILKEVICH O; CARASSO RL; KORCZYN AD
      EPIDEMIOLOGY AND INHERITANCE OF OCULOPHARYNGEAL MUSCULAR-DYSTROPHY INISRAEL

      Neuromuscular disorders
    29. KUSHNIR T; KNUBOVETS T; ITZCHAK Y; ELIAV U; SADEH M; RAPOPORT L; KOTT E; NAVON G
      IN-VIVO NA-23 NMR-STUDIES OF MYOTONIC-DYSTROPHY

      Magnetic resonance in medicine
    30. ARGOV Z; TIRAM E; EISENBERG I; SADEH M; SEIDMAN CE; SEIDMAN JG; KARPATI G; MITRANIROSENBAUM S
      VARIOUS TYPES OF HEREDITARY INCLUSION-BODY MYOPATHIES MAP TO CHROMOSOME 9P1-Q1

      Annals of neurology
    31. INBAR D; HALPERN GJ; WEITZ R; SADEH M; SHOHAT M
      AGENESIS OF THE CORPUS-CALLOSUM IN A MOTHER AND SON

      American journal of medical genetics
    32. SADEH M; RIVER Y; ARGOV Z
      STIMULATED SINGLE-FIBER ELECTROMYOGRAPHY IN LAMBERT-EATON-MYASTHENIC-SYNDROME BEFORE AND AFTER 3,4-DIAMINOPYRIDINE

      Muscle & nerve
    33. ARGOV Z; SADEH M; KARPATI G; EISENBERG I; TIRAM E; MITRANIROSENBAUM S
      NEW FORMS OF HEREDITARY INCLUSION-BODY MYOPATHY (HIBM) AND THEIR GENETIC SPECTRUM

      Neurology
    34. IYENGAR S; KALINSKY H; WEISS S; KOROSTISHEVSKY M; SADEH M; ZHAO Y; KIDD KK; BONNETAMIR B
      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
    35. MENOLD MM; LENNON F; SADEH M; GOLDHAMMER Y; BLATT I; YAMAOKA LH; VANCE JM; PERICAKVANCE MA
      EVIDENCE FOR GENETIC-HETEROGENEITY SUPPORTS CLINICAL DIFFERENCES IN CONGENITAL MYASTHENIC SYNDROMES (CMS)

      American journal of human genetics
    36. NAVON R; SEIFRIED B; GALON NS; SADEH M
      A NEW POINT MUTATION AFFECTING THE 4TH TRANSMEMBRANE DOMAIN OF PMP22 RESULTS IN SEVERE, DE-NOVO CHARCOT-MARIE-TOOTH DISEASE

      Human genetics
    37. NEUMANN Y; TOREN A; RECHAVI G; SEIFRIED B; SHOHAM NG; MANDEL M; KENET G; SHARON N; SADEH M; NAVON R
      VINCRISTINE TREATMENT TRIGGERING THE EXPRESSION OF ASYMPTOMATIC CHARCOT-MARIE-TOOTH DISEASE

      Medical and pediatric oncology
    38. BLUMEN SC; SADEH M; KORCZYN AD; ROUCHE A; NISIPEANU P; ASHEROV A; TOME FMS
      INTRANUCLEAR INCLUSIONS IN OCULOPHARYNGEAL MUSCULAR-DYSTROPHY AMONG BUKHARA JEWS

      Neurology
    39. ARIEL R; SADEH M
      CONGENITAL VISUAL AGNOSIA AND PROSOPAGNOSIA IN A CHILD - A CASE-REPORT

      Cortex
    40. SHUPER A; ZEHARIA A; KORENREICH L; SADEH M; MIMOUNI M
      CEREBRAL CALCINOSIS AND LEARNING-DISABILITIES IN HYPOPARATHYROIDISM -A CAUSE AND EFFECT OR A COINCIDENCE

      Pediatric neurology
    41. NEUFELD MY; SADEH M; ASSA B; KUSHNIR M; KORCZYN AD
      PHENOTYPIC HETEROGENEITY IN FAMILIAL INCLUSION-BODY MYOPATHY

      Muscle & nerve
    42. GOLDBERGSTERN H; NAVON R; SEIFRIED B; SADEH M; MEER J; GABAY U; MELAMED E; GADOTH N
      CHARCOT-MARIE-TOOTH (CMT) DISEASE IN ISRAEL - CLINICAL, EPIDEMIOLOGIC, AND GENETIC-ASPECTS

      Neurology
    43. NAVON R; SEIFRIED B; GADOT N; KORCYN A; SADEH M; MERR J; GOLDBERGSTERN H
      CHAREOT-MARIE-TOOTH DISEASE TYPE 1A AND HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES - AN ISARALI STUDY

      American journal of human genetics
    44. KALINSKY H; IYENGAR S; WEISS S; SADEH M; BONNETAMIR B; KIDD KK
      MUTATION AND HAPLOTYPE ANALYSIS OF A DRUZE PEDIGREE WITH MCARDLES-DISEASE

      American journal of human genetics
    45. SADEH M
      ACH RECEPTOR IN OCULAR MG

      Neurology
    46. NEUMANN Y; TOREN A; RECHAVI G; SEFRIED B; MANDEL M; KENET G; GALONSHOAM N; BENBASSAT I; SADEH M; NAVON R
      VINCRISTINE TREATMENT TRIGGERING THE EXPRESSION OF A PREVIOUSLY ASYMPTOMATIC CHARCOT-MARIE-TOOTH DISEASE

      Blood
    47. SADEH M; PAUZNER R; BLATT I; MOUALLEM M; FARFEL Z
      MITOCHONDRIAL ABNORMALITIES IN OCULOPHARYNGEAL MUSCULAR-DYSTROPHY

      Muscle & nerve
    48. GOLDHAMMER Y; GABIZON R; MEINER Z; SADEH M
      AN ISRAELI FAMILY WITH GERSTMANN-STRAUSSLER-SCHEINKER DISEASE MANIFESTING THE CODON-102 MUTATION IN THE PRION PROTEIN GENE

      Neurology


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 20/10/20 alle ore 14:53:31