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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

136 related items for PubMed ID: 754009

  • 1.
    ; . PubMed ID:
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  • 2. [Problem of phenotypic polymorphism in hereditary neuromuscular diseases].
    Badalian LO.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1979; 79(3):257-61. PubMed ID: 571656
    [No Abstract] [Full Text] [Related]

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  • 5. The value of electromyography in the aetiological diagnosis of hypotonia in infants and toddlers.
    Cetin E, Cuisset JM, Tiffreau V, Vallée L, Hurtevent JF, Thevenon A.
    Ann Phys Rehabil Med; 2009; 52(7-8):546-55. PubMed ID: 19713169
    [Abstract] [Full Text] [Related]

  • 6. [Cardiomyopathy in Heredofamilial Neuromyopathies (author's transl)].
    Sekiguchi M, Numao Y, Hiroe M.
    Kokyu To Junkan; 1975 Mar; 23(3):209-24. PubMed ID: 1093249
    [No Abstract] [Full Text] [Related]

  • 7. Friedreich's ataxia mimicking hereditary motor and sensory neuropathy.
    Panas M, Kalfakis N, Karadima G, Davaki P, Vassilopoulos D.
    J Neurol; 2002 Nov; 249(11):1583-6. PubMed ID: 12420100
    [Abstract] [Full Text] [Related]

  • 8. [Automatic analysis of needle EMG in the differential diagnosis of neuromuscular diseases].
    Babkin PS, Gekht BM, Polukazakov SN, Fedotov VP.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1986 Nov; 86(11):1623-8. PubMed ID: 3811721
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  • 9. 2nd Workshop of the European CMT Consortium: 53rd ENMC International Workshop on Classification and Diagnostic Guidelines for Charcot-Marie-Tooth Type 2 (CMT2-HMSN II) and Distal Hereditary Motor Neuropathy (distal HMN-Spinal CMT) 26-28 September 1997, Naarden, The Netherlands.
    Neuromuscul Disord; 1998 Aug; 8(6):426-31. PubMed ID: 9713862
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  • 10.
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  • 11. [Charcot-Marie neural amyotrophy (review)].
    Savchenko IuN.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1984 Aug; 84(11):1718-22. PubMed ID: 6098115
    [No Abstract] [Full Text] [Related]

  • 12.
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  • 13. Molecular basis of neuromuscular diseases.
    Chance PF, Ashizawa T, Hoffman EP, Crawford TO.
    Phys Med Rehabil Clin N Am; 1998 Feb; 9(1):49-81, vi. PubMed ID: 9894134
    [Abstract] [Full Text] [Related]

  • 14. A practical approach to molecular diagnostic testing in neuromuscular diseases.
    Arnold WD, Flanigan KM.
    Phys Med Rehabil Clin N Am; 2012 Aug; 23(3):589-608. PubMed ID: 22938877
    [Abstract] [Full Text] [Related]

  • 15. Paediatric electromyography in the modern world: a personal view.
    Pitt M.
    Dev Med Child Neurol; 2011 Feb; 53(2):120-4. PubMed ID: 21087239
    [Abstract] [Full Text] [Related]

  • 16. Diagnosis and management of adult hereditary cardio-neuromuscular disorders: A model for the multidisciplinary care of complex genetic disorders.
    Sommerville RB, Vincenti MG, Winborn K, Casey A, Stitziel NO, Connolly AM, Mann DL.
    Trends Cardiovasc Med; 2017 Jan; 27(1):51-58. PubMed ID: 27452966
    [Abstract] [Full Text] [Related]

  • 17. [Charcot-Marie-Tooth disease: electromyography is still useful in diagnosis and classification].
    Birouk N, Maisonobe T, Le Forestier N, Gouider R, Léger JM, Bouche P.
    Rev Neurol (Paris); 1997 Dec; 153(12):727-36. PubMed ID: 9686263
    [Abstract] [Full Text] [Related]

  • 18. [Hereditary areflexic dysstasia (Roussy-Lévy syndrome)].
    Badalian LO, Skvortsov IA, Dunaevskaia GN, Kamennykh LN, Aliev GK.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1981 Dec; 81(5):682-8. PubMed ID: 7269937
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  • 19. [Clinicoelectrophysiological aspects of hereditary amyotrophies].
    Avakian GN, Podobedova NS, Bystrova ES.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1981 Dec; 81(11):1639-42. PubMed ID: 6275641
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  • 20. [Various features of muscle tissue metabolism in various muscular and neuromuscular diseases of a hereditary nature (clinico-histochemical study)].
    Anosov NN, Saĭkova LA.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1982 Dec; 82(3):22-5. PubMed ID: 6952668
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