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PUBMED FOR HANDHELDS

Journal Abstract Search

123 related items for PubMed ID: 7136488

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

  • 2. 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]

  • 3. Peroneal muscular atrophy. Electronmicroscopic studies.
    Gallai M.
    Neuropatol Pol; 1982 Oct; 20(1-2):129-35. PubMed ID: 7183920
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
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  • 5. [Formation of "onion bulbs" in Charcot-Marie-Tooth and Dejerine-Sottas hypertrophic neuropathies].
    Jedrzejowska H, Drac H, Sawicka E.
    Neuropatol Pol; 1975 Oct; 13(1):93-106. PubMed ID: 1118064
    [No Abstract] [Full Text] [Related]

  • 6. Benign familial spinal muscular atrophy with hypertrophy of the calves.
    D'Alessandro R, Montagna P, Govoni E, Pazzaglia P.
    Arch Neurol; 1982 Oct; 39(10):657-60. PubMed ID: 7125978
    [No Abstract] [Full Text] [Related]

  • 7. Peripheral neurofibromatosis and peroneal muscular atrophy.
    Bosch EP, Murphy MJ, Cancilla PA.
    Neurology; 1981 Nov; 31(11):1408-14. PubMed ID: 6796901
    [Abstract] [Full Text] [Related]

  • 8. [Four cases of hereditary motor and sensory neuropathy in childhood--light and electron microscopic studies of sural nerve biopsies].
    Sugie Y, Sugama M, Sugama S, Kosaka S, Shibuya T, Sugie H, Fukuyama Y.
    No To Hattatsu; 1985 Nov; 17(6):500-6. PubMed ID: 4084416
    [No Abstract] [Full Text] [Related]

  • 9. [Histological changes in peripheral nerves in spinal Werdnig-Hoffmann muscular atrophy].
    Drac H.
    Neuropatol Pol; 1977 Nov; 15(1):1-16. PubMed ID: 840382
    [No Abstract] [Full Text] [Related]

  • 10. An obscure inherited neuropathy characterized by pain and weakness.
    Isaacs H, Badenhorst M.
    S Afr Med J; 1977 Aug 06; 52(7):285-8. PubMed ID: 897927
    [Abstract] [Full Text] [Related]

  • 11. Spinal muscular atrophy and hypertrophy of the calves.
    Bouwsma G, Van Wijngaarden GK.
    J Neurol Sci; 1980 Jan 06; 44(2-3):275-9. PubMed ID: 7354373
    [Abstract] [Full Text] [Related]

  • 12. The peroneal muscular atrophy syndrome. Clinical, genetic, electrophysiological and nerve biopsy studies. Part 2. Observations on pathological changes in sural nerve biopsies.
    Madrid R, Bradley WG, Davis CJ.
    J Neurol Sci; 1977 May 06; 32(1):91-122. PubMed ID: 864493
    [Abstract] [Full Text] [Related]

  • 13. Distal amyotrophy of predominantly the upper limbs with pyramidal features in a large kinship.
    van Gent EM, Hoogland RA, Jennekens FG.
    J Neurol Neurosurg Psychiatry; 1985 Mar 06; 48(3):266-9. PubMed ID: 3981197
    [Abstract] [Full Text] [Related]

  • 14. Neurogenic muscular atrophy and low density of large myelinated fibres of sural nerve in chorea-acanthocytosis.
    Ohnishi A, Sato Y, Nagara H, Sakai T, Iwashita H, Kuroiwa Y, Nakamura T, Shida K.
    J Neurol Neurosurg Psychiatry; 1981 Jul 06; 44(7):645-8. PubMed ID: 7288454
    [Abstract] [Full Text] [Related]

  • 15. [Spinal muscle atrophy in the offspring of consanguineous parents].
    Borkowska J, Hausmanowa-Petrusewicz I.
    Neurol Neurochir Pol; 1977 Jul 06; 11(4):487-90. PubMed ID: 895985
    [Abstract] [Full Text] [Related]

  • 16. Hypertrophic form of peroneal muscular atrophy (PMA): unusual nerve conduction results.
    Streib EW, Sun SF, Kimberling W, Smith SA.
    Muscle Nerve; 1984 Jan 06; 7(1):32-4. PubMed ID: 6700627
    [Abstract] [Full Text] [Related]

  • 17. 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 06; 5(3):185-96. PubMed ID: 7088015
    [No Abstract] [Full Text] [Related]

  • 18. The differential diagnosis of scapuloperoneal amyotrophy.
    Spalke G, Hökendorf H, von Roques P.
    J Neurol; 1976 Jun 14; 212(3):253-69. PubMed ID: 58977
    [Abstract] [Full Text] [Related]

  • 19. Peroneal muscular atrophy with autosomal dominant inheritance.
    McLeod JG, Low PA.
    Clin Exp Neurol; 1977 Jun 14; 14():142-53. PubMed ID: 616594
    [Abstract] [Full Text] [Related]

  • 20. Peroneal muscular atrophy (PMA) and related disorders. I. Clinical manifestations as related to biopsy findings, nerve conduction and electromyography.
    Buchthal F, Behse F.
    Brain; 1977 Mar 14; 100 Pt 1():41-66. PubMed ID: 861715
    [No Abstract] [Full Text] [Related]

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