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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

122 related items for PubMed ID: 3981197

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  • 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
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  • 3. Peroneal muscular atrophy with pyramidal features.
    Harding AE, Thomas PK.
    J Neurol Neurosurg Psychiatry; 1984 Feb; 47(2):168-72. PubMed ID: 6707656
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  • 4. Peroneal muscular atrophy with autosomal dominant inheritance.
    McLeod JG, Low PA.
    Clin Exp Neurol; 1977 Feb; 14():142-53. PubMed ID: 616594
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  • 10. 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
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  • 14. Distal hereditary upper limb muscular atrophy.
    Gross DW, Rajput AH, Yeung M.
    J Neurol Neurosurg Psychiatry; 1998 Feb; 64(2):217-20. PubMed ID: 9489534
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  • 16. Spinal muscular atrophy with autosomal dominant inheritance. Report of a new kindred.
    Zellweger H, Simpson J, McCormick WF, Ionasescu V.
    Neurology; 1972 Sep; 22(9):957-63. PubMed ID: 4673381
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  • 19. An autopsy case of peroneal muscular atrophy with rigidity and tremor. Ultrastructural and systematic morphometrical studies on peripheral nerves.
    Itoh Y, Yagishita S, Amano N, Iwabuchi K.
    Acta Neuropathol; 1990 Sep; 80(6):671-9. PubMed ID: 2275341
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  • 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
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