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Journal Abstract Search

161 related items for PubMed ID: 4340377

  • 1. Late onset ataxia, rigidity, and peripheral neuropathy. A familial syndrome with variable therapeutic response to levodopa.
    Ziegler DK, Schimke RN, Kepes JJ, Rose DL, Klinkerfuss G.
    Arch Neurol; 1972 Jul; 27(1):52-66. PubMed ID: 4340377
    [No Abstract] [Full Text] [Related]

  • 2. [Hereditary cerebellar aataxia with spinal muscular atrophies].
    Hopf HC, Duensing F, Lowitzsch K, Krönke R.
    Z Neurol; 1971 Jul; 199(4):344-52. PubMed ID: 4104837
    [No Abstract] [Full Text] [Related]

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  • 4. Congenital non-progressive peripheral neuropathy with arthrogryposis multiplex.
    Yuill GM, Lynch PG.
    J Neurol Neurosurg Psychiatry; 1974 Mar; 37(3):316-23. PubMed ID: 4364274
    [Abstract] [Full Text] [Related]

  • 5. Proximal neurogenic muscular atrophy in adolescence and adulthood with X-linked recessive inheritance. Kugelberg-Welander disease and its variant of late onset in one pedigree.
    Tsukagoshi H, Shoji H, Furukawa T.
    Neurology; 1970 Dec; 20(12):1188-93. PubMed ID: 5529907
    [No Abstract] [Full Text] [Related]

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  • 7. Hereditary muscular atrophy with ataxia, retinitis pigmentosa, and diabetes mellitus. A clinical report of a family.
    Furukawa T, Takagi A, Nakao K, Sugita H, Tsukagoshi H.
    Neurology; 1968 Oct; 18(10):942-7. PubMed ID: 5748751
    [No Abstract] [Full Text] [Related]

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  • 10. [Cumulative familial incidence of Kugelberg-Welander disease].
    Nemes A, Károly E, Csenkér E, Pintér S.
    Orv Hetil; 1986 Nov 09; 127(45):2735-9. PubMed ID: 3796971
    [No Abstract] [Full Text] [Related]

  • 11. A familial neurological disease with symptomatic response to levodopa.
    Ziegler DK, Schimke RN, Kepes J, Rose D, Klinkerfuss G.
    Trans Am Neurol Assoc; 1971 Nov 09; 96():330-2. PubMed ID: 5159126
    [No Abstract] [Full Text] [Related]

  • 12. [Genetic aspects of some spino-cerebellar degenerations].
    Badiu G.
    Stud Cercet Neurol; 1969 Nov 09; 14(5):311-24. PubMed ID: 4906012
    [No Abstract] [Full Text] [Related]

  • 13. [Peripheral neurogenic amyotrophy in the Marinesco-Sjögren syndrome].
    Serratrice G, Gastaut JL, Dubois-Gambarelli D.
    Rev Neurol (Paris); 1973 Jun 09; 128(6):432-41. PubMed ID: 4368207
    [No Abstract] [Full Text] [Related]

  • 14. The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendants of the 'the Drew family of Walworth'.
    Harding AE.
    Brain; 1982 Mar 09; 105(Pt 1):1-28. PubMed ID: 7066668
    [Abstract] [Full Text] [Related]

  • 15. Hereditary cerebellar ataxia with peripheral neuropathy and mental retardation.
    Tachi N, Kozuka N, Ohya K, Chiba S, Sasaki K.
    Eur Neurol; 2000 Mar 09; 43(2):82-7. PubMed ID: 10686465
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  • 17. [Peripheral neuropathies associated with hereditary cerebellar ataxias].
    Anheim M, Tranchant C.
    Rev Neurol (Paris); 2011 Jan 09; 167(1):72-6. PubMed ID: 21195440
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  • 18. [Cerebellar imitation synkineses].
    Trouillas P.
    C R Acad Sci III; 1989 Jan 09; 309(19):715-21. PubMed ID: 2514971
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  • 20. Hereditary motor and sensory polyneuropathy (peroneal muscular atrophy).
    Thomas PK, Calne DB, Stewart G.
    Ann Hum Genet; 1974 Oct 09; 38(2):111-53. PubMed ID: 4467779
    [No Abstract] [Full Text] [Related]

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