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Journal Abstract Search

186 related items for PubMed ID: 6357144

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

  • 2. [Clinical study of muscular atrophy].
    Shinoda M.
    Hokkaido Igaku Zasshi; 1974 Jan; 49(1):23-31. PubMed ID: 4376121
    [No Abstract] [Full Text] [Related]

  • 3. Characteristic clinical findings in some neurogenic myopathies and in some myogenic myopathies causing muscular weakness, hypotonia and atrophy in infancy and early childhood.
    Gamstorp I.
    Birth Defects Orig Artic Ser; 1971 Feb; 7(2):72-81. PubMed ID: 5173129
    [Abstract] [Full Text] [Related]

  • 4. Differential diagnosis of limb girdle syndromes.
    Ishpekova B, Milanov I.
    Electromyogr Clin Neurophysiol; 1996 Dec; 36(8):469-75. PubMed ID: 8985674
    [Abstract] [Full Text] [Related]

  • 5. [Calpain-3 gene defect causing limb gird muscular dystrophy in a Hungarian family].
    Horváth R, Walter MC, Lochmüller H, Hübner A, Karcagi V, Pikó H, Timár L, Komoly S.
    Ideggyogy Sz; 2005 Jan 20; 58(1-2):52-8. PubMed ID: 15884399
    [Abstract] [Full Text] [Related]

  • 6. Single fiber electromyography in the differential diagnosis of myopathic limb girdle syndromes and chronic spinal muscular atrophy.
    Shields RW.
    Muscle Nerve; 1984 May 20; 7(4):265-72. PubMed ID: 6727909
    [Abstract] [Full Text] [Related]

  • 7. Muscle MRI in inherited neuromuscular disorders: past, present, and future.
    Mercuri E, Pichiecchio A, Allsop J, Messina S, Pane M, Muntoni F.
    J Magn Reson Imaging; 2007 Feb 20; 25(2):433-40. PubMed ID: 17260395
    [Abstract] [Full Text] [Related]

  • 8. [Errors in the diagnosis of progressive muscular dystrophy and spinal muscular atrophy].
    Parnitzke C, Hagen EM.
    Z Arztl Fortbild (Jena); 1981 Jul 01; 75(13):577-81. PubMed ID: 7314671
    [No Abstract] [Full Text] [Related]

  • 9. The childhood limb-girdle muscular dystrophies.
    Straub V, Bushby K.
    Semin Pediatr Neurol; 2006 Jun 01; 13(2):104-14. PubMed ID: 17027860
    [Abstract] [Full Text] [Related]

  • 10. [Family studies in neuromuscular atrophy--electromyographic and clinical findings].
    Müller D.
    Psychiatr Neurol Med Psychol (Leipz); 1970 Jul 01; 22(7):256-9. PubMed ID: 5473387
    [No Abstract] [Full Text] [Related]

  • 11. Clinical and morphological phenotype of the filamin myopathy: a study of 31 German patients.
    Kley RA, Hellenbroich Y, van der Ven PF, Fürst DO, Huebner A, Bruchertseifer V, Peters SA, Heyer CM, Kirschner J, Schröder R, Fischer D, Müller K, Tolksdorf K, Eger K, Germing A, Brodherr T, Reum C, Walter MC, Lochmüller H, Ketelsen UP, Vorgerd M.
    Brain; 2007 Dec 01; 130(Pt 12):3250-64. PubMed ID: 18055494
    [Abstract] [Full Text] [Related]

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  • 15. [2 families with benign myopathy predominantly on the limb girdle with dominant autosomal heredity].
    Serratrice G, Pellissier JF.
    Rev Neurol (Paris); 1988 Dec 01; 144(1):43-6. PubMed ID: 3347807
    [Abstract] [Full Text] [Related]

  • 16. [Suspected muscular disease: what to do?].
    Strozzi S, Steinlin M.
    Ther Umsch; 2003 Jul 01; 60(7):399-406. PubMed ID: 12956033
    [Abstract] [Full Text] [Related]

  • 17. [Malate dehydrogenase activity in children with myopathy].
    Gil'manov VKh.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1973 Jul 01; 73(6):829-31. PubMed ID: 4753593
    [No Abstract] [Full Text] [Related]

  • 18. [Clinical polymorphism of X-linked myopathies].
    Grinio LP.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1974 Jul 01; 74(3):321-9. PubMed ID: 4466264
    [No Abstract] [Full Text] [Related]

  • 19. [Evoked potentials of the somatosensory system in patients with progressive muscular dystrophies].
    Avakian GN.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1983 Jul 01; 83(11):1628-32. PubMed ID: 6675359
    [Abstract] [Full Text] [Related]

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