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Journal Abstract Search

117 related items for PubMed ID: 5834704

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. A kinship of the Roussy-Levy syndrome: a clinical and electrophysiological study.
    Yudell A, Dyck PJ, Lambert EH.
    Trans Am Neurol Assoc; 1964; 89():45-50. PubMed ID: 5828526
    [No Abstract] [Full Text] [Related]

  • 3. Evidence that Charcot-Marie-tooth disease with tremor coincides with the Roussy-Levy syndrome.
    Barbieri F, Filla A, Ragno M, Crisci C, Santoro L, Corona M, Campanella G.
    Can J Neurol Sci; 1984 Nov; 11(4 Suppl):534-40. PubMed ID: 6509399
    [Abstract] [Full Text] [Related]

  • 4. [Family with Roussy-Lévy syndrome].
    Smolenski C, Ludin HP.
    Fortschr Neurol Psychiatr; 1984 Jun; 52(6):215-21. PubMed ID: 6745833
    [Abstract] [Full Text] [Related]

  • 5. [Hereditary areflexic dysstasia (Roussy-Lévy syndrome)].
    Badalian LO, Skvortsov IA, Dunaevskaia GN, Kamennykh LN, Aliev GK.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1981 Jun; 81(5):682-8. PubMed ID: 7269937
    [Abstract] [Full Text] [Related]

  • 6. Investigation of a family with hypertrophic neuropathy resembling Roussy-Levy syndrome. Clinical, electrophysiologic, histologic, and biochemical studies.
    Kriel RL, Cliffer KD, Berry J, Sung JH, Bland CS.
    Neurology; 1974 Sep; 24(9):801-9. PubMed ID: 4368842
    [No Abstract] [Full Text] [Related]

  • 7. Roussy-Lévy syndrome: report of a kindred and discussion of the nosology.
    Oelschlager R, White HH, Schimke RN.
    Acta Neurol Scand; 1971 Sep; 47(1):80-90. PubMed ID: 5576221
    [No Abstract] [Full Text] [Related]

  • 8. Hereditary polyneuropathy of Roussy-Lévy type with associated cardiomyopathy.
    Lascelles RG, Baker IA, Thomas PK.
    Guys Hosp Rep; 1970 Sep; 119(3):253-62. PubMed ID: 4321562
    [No Abstract] [Full Text] [Related]

  • 9. [Roussy-Lévy syndrome].
    Tsubaki T.
    Nihon Rinsho; 1977 Sep; 35 Suppl 1():578-9. PubMed ID: 612904
    [No Abstract] [Full Text] [Related]

  • 10. [Analysis of the neurological biotype of Roussy-Lévy disease drawn from the study of the Ver family. The false foot disease].
    Paolozzi C, Bravaccio F, Sanna G, Tata MR, Guazzi GC.
    Acta Neurol (Napoli); 1973 Sep; 28(5):501-31. PubMed ID: 4789491
    [No Abstract] [Full Text] [Related]

  • 11. [The Roussy-Lévy syndrome].
    Neundörfer B, Kuhn H.
    Nervenarzt; 1976 Mar; 47(3):153-6. PubMed ID: 1264299
    [No Abstract] [Full Text] [Related]

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

  • 13. [Contribution of morphological studies of the peripheral nerve to a better comprehension of Charcot-Marie-Tooth atrophy and Roussy-Levy hereditary areflexic dystaxia].
    Lapresle J.
    Acquis Med Recent; 1980 Feb; ():91-6. PubMed ID: 7395444
    [No Abstract] [Full Text] [Related]

  • 14. Roussy-Levy syndrome with functional impairment and anomalies of gastro-intestinal tract.
    Pruzanski W.
    Confin Neurol; 1965 Feb; 26(6):495-502. PubMed ID: 5868071
    [No Abstract] [Full Text] [Related]

  • 15. Motor nerve conduction velocity in peroneal muscular atrophy: evidence for genetic heterogeneity.
    Thomas PK, Calne DB.
    J Neurol Neurosurg Psychiatry; 1974 Jan; 37(1):68-75. PubMed ID: 4813428
    [Abstract] [Full Text] [Related]

  • 16. Brachial amyotrophic diplegia associated with a novel SOD1 mutation (L106P).
    Valentino P, Conforti FL, Pirritano D, Nisticò R, Mazzei R, Patitucci A, Sprovieri T, Gabriele AL, Muglia M, Clodomiro A, Gambardella A, Zappia M, Quattrone A.
    Neurology; 2005 Apr 26; 64(8):1477-8. PubMed ID: 15851752
    [No Abstract] [Full Text] [Related]

  • 17. [Conduction velocity in peripheral nerves in healthy and sick children].
    Ryniewicz B.
    Neurol Neurochir Pol; 1975 Apr 26; 9(6):701-4. PubMed ID: 1202397
    [Abstract] [Full Text] [Related]

  • 18. 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 26; 18(6):603-18. PubMed ID: 4297451
    [No Abstract] [Full Text] [Related]

  • 19. Use and misuse of the Roussy-Levy eponym.
    Salisachs P, Findley LJ, Codina M, La Torre P.
    J Neurol Neurosurg Psychiatry; 1982 Oct 26; 45(10):938-40. PubMed ID: 7143017
    [No Abstract] [Full Text] [Related]

  • 20. Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. II. Neurologic, genetic, and electrophysiologic findings in various neuronal degenerations.
    Dyck PJ, Lambert EH.
    Arch Neurol; 1968 Jun 26; 18(6):619-25. PubMed ID: 5652992
    [No Abstract] [Full Text] [Related]

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