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Journal Abstract Search

111 related items for PubMed ID: 5308546

  • 1. [Detection of healthy carriers of the myopathic trait in human myopathy].
    Demos J.
    Ann Genet; 1969 Sep; 12(3):191-201. PubMed ID: 5308546
    [No Abstract] [Full Text] [Related]

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  • 3. Familial "myotubular" myopathy.
    van Wijngaarden GK, Fleury P, Bethlem J, Meijer AE.
    Neurology; 1969 Sep; 19(9):901-8. PubMed ID: 5816884
    [No Abstract] [Full Text] [Related]

  • 4. Symptomatic dysferlin gene mutation carriers: characterization of two cases.
    Illa I, De Luna N, Domínguez-Perles R, Rojas-García R, Paradas C, Palmer J, Márquez C, Gallano P, Gallardo E.
    Neurology; 2007 Apr 17; 68(16):1284-9. PubMed ID: 17287450
    [Abstract] [Full Text] [Related]

  • 5. Carrier detection in X-linked muscular dystrophy.
    Walton JN.
    J Genet Hum; 1969 Oct 17; 17(3):497-510. PubMed ID: 5387424
    [No Abstract] [Full Text] [Related]

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  • 7. A malignant form of neurogenic muscular atrophy in adults, with dominant inheritance.
    Zatz M, Penha-Serrano C, Frota-Pessoa O, Klein D.
    J Genet Hum; 1971 Dec 17; 19(4):337-54. PubMed ID: 5152133
    [No Abstract] [Full Text] [Related]

  • 8. DNAJB6 myopathy: a vacuolar myopathy with childhood onset.
    Suarez-Cedeno G, Winder T, Milone M.
    Muscle Nerve; 2014 Apr 17; 49(4):607-10. PubMed ID: 24170373
    [Abstract] [Full Text] [Related]

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  • 11. [Relationships between genotype and phenotype in Charcot-Marie-Tooth disease].
    Câmpeanu E, Morariu M.
    Rev Roum Neurol; 1970 Apr 17; 7(1):47-56. PubMed ID: 5527990
    [No Abstract] [Full Text] [Related]

  • 12. [Rigid spine syndrome].
    Aver'ianov IuN, Il'ina NA, Vinogradova NV, Potomskaia LZ, Sokolina NA.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1981 Apr 17; 81(10):1457-61. PubMed ID: 7315025
    [Abstract] [Full Text] [Related]

  • 13. [Estimation of the probability of heterozygosity in Duchenne-type progressive muscular dystrophy].
    Guízar Vázquez J, Navarrete Cadena C, Rico R, Mora G, Zavala C.
    Bol Med Hosp Infant Mex; 1981 Apr 17; 38(1):23-33. PubMed ID: 7284070
    [Abstract] [Full Text] [Related]

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  • 15. [Serum creatine phosphokinase in various muscular diseases seen in the field of orthopedic surgery].
    Iwamoto A.
    Igaku Kenkyu; 1969 May 17; 39(2):108-21. PubMed ID: 5389323
    [No Abstract] [Full Text] [Related]

  • 16. The clinical and myopathological features of oculopharyngodistal myopathy in a Chinese family.
    Lu H, Luan X, Yuan Y, Dong M, Sun W, Yan C.
    Neuropathology; 2008 Dec 17; 28(6):599-603. PubMed ID: 18503509
    [Abstract] [Full Text] [Related]

  • 17. How to approach the patient with muscular symptoms in the general neurological practice?
    De Bleecker JL.
    Acta Neurol Belg; 2005 Mar 17; 105(1):18-22. PubMed ID: 15861991
    [Abstract] [Full Text] [Related]

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  • 19. [[Myotubular myopathy or centronuclear myopathy. Two case reports and review of literature (author's transl)]?].
    Pascual Castroviejo I, Ricoy JR.
    An Esp Pediatr; 1974 Mar 17; 7(6):537-50. PubMed ID: 4458579
    [No Abstract] [Full Text] [Related]

  • 20. Distal myopathy.
    Satoyoshi E.
    Tohoku J Exp Med; 1990 Aug 17; 161 Suppl():1-19. PubMed ID: 2082493
    [Abstract] [Full Text] [Related]

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