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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

96 related items for PubMed ID: 4633637

  • 41.
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    [No Abstract] [Full Text] [Related]

  • 42. [Early diagnosis and differentiation of Charcot-Marie neural atrophy].
    Lobzin VS, Saĭkova LA, Poliakova LA, Kosachev VD.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1984; 84(11):1601-5. PubMed ID: 6524176
    [Abstract] [Full Text] [Related]

  • 43.
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  • 44. Genetic linkage evidence for heterogeneity in Charcot-Marie-Tooth neuropathy (HMSN type I).
    Bird TD, Ott J, Giblett ER, Chance PF, Sumi SM, Kraft GH.
    Ann Neurol; 1983 Dec; 14(6):679-84. PubMed ID: 6651251
    [Abstract] [Full Text] [Related]

  • 45. Spinal muscular atrophy type II. A separate genetic and clinical entity from type I (Werdnig-Hoffmann disease) and type 3 (Kugelberg-Welander disease).
    Fried K, Emery AE.
    Clin Genet; 1971 Dec; 2(4):203-9. PubMed ID: 5146579
    [No Abstract] [Full Text] [Related]

  • 46. High incidence of sudden cardiac death with conduction disturbances and atrial cardiomyopathy caused by a nonsense mutation in the STA gene.
    Sakata K, Shimizu M, Ino H, Yamaguchi M, Terai H, Fujino N, Hayashi K, Kaneda T, Inoue M, Oda Y, Fujita T, Kaku B, Kanaya H, Mabuchi H.
    Circulation; 2005 Jun 28; 111(25):3352-8. PubMed ID: 15967842
    [Abstract] [Full Text] [Related]

  • 47. [Charcot-Marie-Tooth disease and hyperthrophic myocardiopathy].
    Rodríguez Cuartero A, López Luque A, Pomares Mora J, Cano Pérez M, Guijarro Morales A.
    Rev Clin Esp; 1980 Feb 15; 156(3):197-201. PubMed ID: 6445074
    [No Abstract] [Full Text] [Related]

  • 48. Roussy-Levy hereditary areflexic dystasis presenting as Charcot-Marie-Tooth syndrome.
    Murdoch JL, Beighton PH.
    Birth Defects Orig Artic Ser; 1971 Feb 15; 7(2):106-7. PubMed ID: 5173115
    [No Abstract] [Full Text] [Related]

  • 49.
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  • 50.
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  • 51. [Genealogic study of a family with Carcot-Marie-Tooth disease].
    Gencík A, Jágr J, Matulová B.
    Cesk Neurol Neurochir; 1974 Sep 15; 37(5):316-20. PubMed ID: 4409642
    [No Abstract] [Full Text] [Related]

  • 52.
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  • 53.
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  • 54. [Click syndrome and mesotelesystolic murmur (apropos of familial forms)].
    Froment R, Silie M, Boissel JP, Normand J.
    Arch Mal Coeur Vaiss; 1972 Nov 15; 65(11):1357-64. PubMed ID: 4632806
    [No Abstract] [Full Text] [Related]

  • 55. [A sporadic case of Charcot-Marie-Tooth syndrome, with oligophrenia and epilepsy].
    Peña Yáñez A, Raya Muñóz J, Rico Irles J, Gómez valverde E.
    Rev Clin Esp; 1974 Oct 15; 135(1):65-72. PubMed ID: 4457982
    [No Abstract] [Full Text] [Related]

  • 56.
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  • 57. Familial deficiency of growth hormone and spinal muscular atrophy.
    Leroy JG, Craen MM.
    Prog Clin Biol Res; 1985 Oct 15; 200():113-21. PubMed ID: 2867557
    [No Abstract] [Full Text] [Related]

  • 58. Scapuloperoneal muscular atrophy with cardiopathy. An X-linked recessive trait.
    Mawatari S, Katayama K.
    Arch Neurol; 1973 Jan 15; 28(1):55-9. PubMed ID: 4682070
    [No Abstract] [Full Text] [Related]

  • 59. [Kinetocardiography and phonocardiography for the diagnosis of idiopathic cardiomyopathies].
    Hirose K, Kadoya M.
    Nihon Rinsho; 1980 Jan 15; 38(5):2133-43. PubMed ID: 6997558
    [No Abstract] [Full Text] [Related]

  • 60.
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