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Journal Abstract Search

106 related items for PubMed ID: 3347807

  • 81. "Wetherbee Ail"; the inheritance of progressive muscular atrophy as a dominant trait in two New England families.
    BROWN MR.
    N Engl J Med; 1951 Oct 25; 245(17):645-7. PubMed ID: 14875225
    [No Abstract] [Full Text] [Related]

  • 82. Benign focal amyotrophy or monomelic amyotrophy.
    Gouri-Devi M, Suresh TG, Shankar SK.
    Arch Neurol; 1986 Dec 25; 43(12):1223. PubMed ID: 3778256
    [No Abstract] [Full Text] [Related]

  • 83. [Problem of so-called "moist extremities" and certain causes of neural dystrophies].
    SHALAEV MI.
    Khirurgiia (Mosk); 1951 Mar 25; 3():41-6. PubMed ID: 14825570
    [No Abstract] [Full Text] [Related]

  • 84. A Certain Form of Muscular Atrophy Peculiar to the Lower Extremities.
    Chic Med J Exam; 1882 Oct 25; 45(4):424-425. PubMed ID: 37617858
    [No Abstract] [Full Text] [Related]

  • 85. [2 families with benign myopathy predominantly on the limb girdle with dominant autosomal heredity].
    Serratrice G, Pellissier JF.
    Rev Neurol (Paris); 1988 Oct 25; 144(1):43-6. PubMed ID: 3347807
    [Abstract] [Full Text] [Related]

  • 86. Adult-onset autosomal dominant limb-girdle muscular dystrophy.
    Chutkow JG, Heffner RR, Kramer AA, Edwards JA.
    Ann Neurol; 1986 Aug 25; 20(2):240-8. PubMed ID: 3752967
    [Abstract] [Full Text] [Related]

  • 87. [A pedigree of autosomal dominant limb-girdle myopathy with rimmed vacuole formation].
    Kishibayashi J, Sunohara N, Saito Y.
    Rinsho Shinkeigaku; 1997 Jul 25; 37(7):603-10. PubMed ID: 9396357
    [Abstract] [Full Text] [Related]

  • 88. Scapuloperoneal myopathy.
    Todman DH, Cooke RA.
    Clin Exp Neurol; 1984 Jul 25; 20():169-74. PubMed ID: 6568938
    [Abstract] [Full Text] [Related]

  • 89. [A family of autosomal dominant facio-limb-girdle muscular dystrophy].
    Takao S, Kira J, Kohtake N, Yoshimura T, Goto I.
    Fukuoka Igaku Zasshi; 1996 Dec 25; 87(12):278-82. PubMed ID: 9011111
    [Abstract] [Full Text] [Related]

  • 90. [2 families with benign myopathy predominantly on the limb girdle with dominant autosomal heredity].
    Serratrice G, Pellissier JF.
    Rev Neurol (Paris); 1988 Dec 25; 144(1):43-6. PubMed ID: 3347807
    [Abstract] [Full Text] [Related]

  • 91. Adult-onset autosomal dominant limb-girdle muscular dystrophy.
    Chutkow JG, Heffner RR, Kramer AA, Edwards JA.
    Ann Neurol; 1986 Aug 25; 20(2):240-8. PubMed ID: 3752967
    [Abstract] [Full Text] [Related]

  • 92. [A pedigree of autosomal dominant limb-girdle myopathy with rimmed vacuole formation].
    Kishibayashi J, Sunohara N, Saito Y.
    Rinsho Shinkeigaku; 1997 Jul 25; 37(7):603-10. PubMed ID: 9396357
    [Abstract] [Full Text] [Related]

  • 93. Scapuloperoneal myopathy.
    Todman DH, Cooke RA.
    Clin Exp Neurol; 1984 Jul 25; 20():169-74. PubMed ID: 6568938
    [Abstract] [Full Text] [Related]

  • 94. [A family of autosomal dominant facio-limb-girdle muscular dystrophy].
    Takao S, Kira J, Kohtake N, Yoshimura T, Goto I.
    Fukuoka Igaku Zasshi; 1996 Dec 25; 87(12):278-82. PubMed ID: 9011111
    [Abstract] [Full Text] [Related]

  • 95. [2 families with benign myopathy predominantly on the limb girdle with dominant autosomal heredity].
    Serratrice G, Pellissier JF.
    Rev Neurol (Paris); 1988 Dec 25; 144(1):43-6. PubMed ID: 3347807
    [Abstract] [Full Text] [Related]

  • 96. [A family of autosomal dominant facio-limb-girdle muscular dystrophy].
    Takao S, Kira J, Kohtake N, Yoshimura T, Goto I.
    Fukuoka Igaku Zasshi; 1996 Dec 25; 87(12):278-82. PubMed ID: 9011111
    [Abstract] [Full Text] [Related]

  • 97. [Clinical and genetic heterogeneity of limb-girdle muscular dystrophy].
    Kozłowska M.
    Neurol Neurochir Pol; 1995 Dec 25; 29(4):569-75. PubMed ID: 8544936
    [Abstract] [Full Text] [Related]

  • 98. [Autosomal dominant centronuclear myopathy].
    Ferrer X, Vital C, Coquet M, Deleplanque B, Ellie E, Lagueny A, Julien J.
    Rev Neurol (Paris); 1992 Dec 25; 148(10):622-30. PubMed ID: 1295057
    [Abstract] [Full Text] [Related]

  • 99. Slowly progressive proximal weakness: limb-girdle syndromes.
    Fowler WM, Nayak NN.
    Arch Phys Med Rehabil; 1983 Nov 25; 64(11):527-38. PubMed ID: 6357144
    [Abstract] [Full Text] [Related]

  • 100. Diagnosing and managing muscular dystrophy.
    Orrell RW.
    Practitioner; 2012 Sep 25; 256(1754):21-4, 2-3. PubMed ID: 23252132
    [Abstract] [Full Text] [Related]

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