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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

161 related items for PubMed ID: 4340377

  • 21.
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  • 22. Diagnostic yield of testing for RFC1 repeat expansions in patients with unexplained adult-onset cerebellar ataxia.
    Van Daele SH, Vermeer S, Van Eesbeeck A, Lannoo L, Race V, van Damme P, Claeys K, Vandenberghe W.
    J Neurol Neurosurg Psychiatry; 2020 Nov; 91(11):1233-1234. PubMed ID: 32732387
    [No Abstract] [Full Text] [Related]

  • 23. Machado-Joseph disease in a Sicilian-American family.
    Suite ND, Sequeiros J, McKhann GM.
    J Neurogenet; 1986 May; 3(3):177-82. PubMed ID: 3734949
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  • 24. [Familial recurring polytopic neuropathy. A case report].
    Eckert P, Meyer-Wahl L.
    Nervenarzt; 1982 Oct; 53(10):598-602. PubMed ID: 6292756
    [No Abstract] [Full Text] [Related]

  • 25. [Electromyography in the peripheral neurogenic syndrome].
    Dumoulin J, de Bisschop G, Clauses I.
    Electrodiagn Ther; 1973 Oct; 10(3):97-110. PubMed ID: 4359525
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  • 29. [Friedreich's ataxia with peripheral nerve involvement resembling peroneal muscular atrophy].
    Hopf HC, Port FK.
    Dtsch Z Nervenheilkd; 1968 Oct; 194(1):1-16. PubMed ID: 4300543
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  • 32. Incidence of peripheral neuropathy and cerebellar ataxia in chronic alcoholics.
    Scholz E, Diener HC, Dichgans J, Langohr HD, Schied W, Schupmann A.
    J Neurol; 1986 Aug; 233(4):212-7. PubMed ID: 3018178
    [Abstract] [Full Text] [Related]

  • 33. Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies.
    Dyck PJ, Lambert EH.
    Arch Neurol; 1968 Jun; 18(6):603-18. PubMed ID: 4297451
    [No Abstract] [Full Text] [Related]

  • 34.
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  • 36. Disruptive SCYL1 Mutations Underlie a Syndrome Characterized by Recurrent Episodes of Liver Failure, Peripheral Neuropathy, Cerebellar Atrophy, and Ataxia.
    Schmidt WM, Rutledge SL, Schüle R, Mayerhofer B, Züchner S, Boltshauser E, Bittner RE.
    Am J Hum Genet; 2015 Dec 03; 97(6):855-61. PubMed ID: 26581903
    [Abstract] [Full Text] [Related]

  • 37. Neurogenic scapuloperoneal syndrome in childhood.
    Mercelis R, Demeester J, Martin JJ.
    J Neurol Neurosurg Psychiatry; 1980 Oct 03; 43(10):888-96. PubMed ID: 7441268
    [Abstract] [Full Text] [Related]

  • 38. Hereditary recurrent brachial plexus neuropathy with dysmorphic features.
    Airaksinen EM, Iivanainen M, Karli P, Sainio K, Haltia M.
    Acta Neurol Scand; 1985 Apr 03; 71(4):309-16. PubMed ID: 4003034
    [Abstract] [Full Text] [Related]

  • 39. Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22-q32.
    Brkanac Z, Fernandez M, Matsushita M, Lipe H, Wolff J, Bird TD, Raskind WH.
    Am J Med Genet; 2002 May 08; 114(4):450-7. PubMed ID: 11992570
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  • 40.
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