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Journal Abstract Search

142 related items for PubMed ID: 4467779

  • 1. Hereditary motor and sensory polyneuropathy (peroneal muscular atrophy).
    Thomas PK, Calne DB, Stewart G.
    Ann Hum Genet; 1974 Oct; 38(2):111-53. PubMed ID: 4467779
    [No Abstract] [Full Text] [Related]

  • 2. Autosomal recessive forms of hereditary motor and sensory neuropathy.
    Harding AE, Thomas PK.
    J Neurol Neurosurg Psychiatry; 1980 Aug; 43(8):669-78. PubMed ID: 7431027
    [Abstract] [Full Text] [Related]

  • 3. Hereditary distal spinal muscular atrophy. A report on 34 cases and a review of the literature.
    Harding AE, Thomas PK.
    J Neurol Sci; 1980 Mar; 45(2-3):337-48. PubMed ID: 7365507
    [Abstract] [Full Text] [Related]

  • 4. Peroneal muscular atrophy with pyramidal tract features (hereditary motor and sensory neuropathy type V): a clinical, neurophysiological, and pathological study of a large kindred.
    Frith JA, McLeod JG, Nicholson GA, Yang F.
    J Neurol Neurosurg Psychiatry; 1994 Nov; 57(11):1343-6. PubMed ID: 7964809
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  • 7. Hereditary motor sensory neuropathies in childhood.
    Rossi LN, Lütschg J, Meier C, Vassella F.
    Dev Med Child Neurol; 1983 Feb; 25(1):19-31. PubMed ID: 6832495
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  • 8. 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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  • 10. Linkage of autosomal dominant type I hereditary motor and sensory neuropathy to the Duffy locus on chromosome 1.
    Guiloff RJ, Thomas PK, Contreras M, Armitage S, Schwarz G, Sedgwick EM.
    J Neurol Neurosurg Psychiatry; 1982 Aug; 45(8):669-74. PubMed ID: 7130990
    [Abstract] [Full Text] [Related]

  • 11. Hypertrophic form of peroneal muscular atrophy (PMA): unusual nerve conduction results.
    Streib EW, Sun SF, Kimberling W, Smith SA.
    Muscle Nerve; 1984 Jan; 7(1):32-4. PubMed ID: 6700627
    [Abstract] [Full Text] [Related]

  • 12. Nemaline rod myopathy and Charcot-Marie-Tooth disease. Report of a case in a 10-year-old girl.
    Danon MJ, Sarpel G, Manaligod JR.
    Arch Neurol; 1980 Feb; 37(2):123-7. PubMed ID: 7356407
    [Abstract] [Full Text] [Related]

  • 13. Centronuclear myopathy with special consideration of the adult form.
    Goebel HH, Meinck HM, Reinecke M, Schimrigk K, Mielke U.
    Eur Neurol; 1984 Feb; 23(6):425-34. PubMed ID: 6542524
    [Abstract] [Full Text] [Related]

  • 14. Some features of the neuromuscular complications of pulmonary carcinoma.
    Teräväinen H, Larsen A.
    Ann Neurol; 1977 Dec; 2(6):495-502. PubMed ID: 215075
    [No Abstract] [Full Text] [Related]

  • 15. Variability in nerve biopsy findings in a kinship with dominantly inherited Charcot-Marie-Tooth disease.
    Van Weerden TW, Houthoff HJ, Sie O, Minderhoud JM.
    Muscle Nerve; 1982 Mar; 5(3):185-96. PubMed ID: 7088015
    [No Abstract] [Full Text] [Related]

  • 16. Chronic inflammatory demyelinating polyneuropathy in two siblings.
    Gabreëls-Festen AA, Hageman AT, Gabreëls FJ, Joosten EM, Renier WO, Weemaes CM, ter Laak HJ.
    J Neurol Neurosurg Psychiatry; 1986 Feb; 49(2):152-6. PubMed ID: 3456424
    [Abstract] [Full Text] [Related]

  • 17. Response to immunosuppressive therapy in patients with hereditary motor and sensory neuropathy and associated dysimmune neuromuscular disorders.
    Mitchell GW, Bosch EP, Hart MN.
    Eur Neurol; 1987 Feb; 27(3):188-96. PubMed ID: 3476306
    [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; 18(6):603-18. PubMed ID: 4297451
    [No Abstract] [Full Text] [Related]

  • 19. The nosology of genetic peripheral neuropathies in Swedish children.
    Hagberg B, Westerberg B.
    Dev Med Child Neurol; 1983 Feb; 25(1):3-18. PubMed ID: 6299869
    [Abstract] [Full Text] [Related]

  • 20. Hypertrophic type of peroneal muscular atrophy and spinal muscular atrophy in siblings.
    Lope ES, del Campo F, Cabello A.
    Acta Neurol Scand; 1982 Aug; 66(2):237-47. PubMed ID: 7136488
    [No Abstract] [Full Text] [Related]

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