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Journal Abstract Search

295 related items for PubMed ID: 6568938

  • 21. An autopsy study of a familial oculopharyngeal muscular dystrophy (OPMD) with distal spread and neurogenic involvement.
    Schmitt HP, Krause KH.
    Muscle Nerve; 1981; 4(4):296-305. PubMed ID: 7254232
    [Abstract] [Full Text] [Related]

  • 22. Muscular dystrophy with separate clinical phenotypes in a large family.
    Udd B, Kääriänen H, Somer H.
    Muscle Nerve; 1991 Nov; 14(11):1050-8. PubMed ID: 1745277
    [Abstract] [Full Text] [Related]

  • 23. Emery-Dreifuss muscular dystrophy with unusual features.
    Deymeer F, Oge AE, Bayindir C, Kaymaz C, Nişanci Y, Adalet K, Yates JR, Ozdemir C.
    Muscle Nerve; 1993 Dec; 16(12):1359-65. PubMed ID: 8232393
    [Abstract] [Full Text] [Related]

  • 24. [Scapuloperoneal syndrome].
    Uyama E.
    Ryoikibetsu Shokogun Shirizu; 2001 Dec; (36):462-6. PubMed ID: 11596438
    [No Abstract] [Full Text] [Related]

  • 25. [Diagnosis of a myopathic disease in adult].
    Eymard B.
    Rev Prat; 2008 Dec 31; 58(20):2229-43. PubMed ID: 19209654
    [Abstract] [Full Text] [Related]

  • 26. Familial scapuloperoneal myopathy and mitochondrial DNA defect.
    Pál E, Bedekovics T, Gáti I.
    Eur Neurol; 1999 Dec 31; 42(4):211-6. PubMed ID: 10567817
    [Abstract] [Full Text] [Related]

  • 27. A novel autosomal dominant distal myopathy with early respiratory failure: clinico-pathologic characteristics and exclusion of linkage to candidate genetic loci.
    Chinnery PF, Johnson MA, Walls TJ, Gibson GJ, Fawcett PR, Jamieson S, Fulthorpe JJ, Cullen M, Hudgson P, Bushby KM.
    Ann Neurol; 2001 Apr 31; 49(4):443-52. PubMed ID: 11310621
    [Abstract] [Full Text] [Related]

  • 28. Autosomal dominant congenital fibre type disproportion: a clinicopathological and imaging study of a large family.
    Sobrido MJ, Fernández JM, Fontoira E, Pérez-Sousa C, Cabello A, Castro M, Teijeira S, Alvarez S, Mederer S, Rivas E, Seijo-Martínez M, Navarro C.
    Brain; 2005 Jul 31; 128(Pt 7):1716-27. PubMed ID: 15857933
    [Abstract] [Full Text] [Related]

  • 29. [Articulation disorder as the initial manifestation of facioscapulohumeral muscular dystrophy in childhood].
    Lischka A, Grisold W, Weninger M, Toifl K, Tatzer E.
    Klin Padiatr; 1986 Jul 31; 198(2):119-21. PubMed ID: 3702273
    [Abstract] [Full Text] [Related]

  • 30. [Abnormal head drooping in facioscapulohumeral muscular dystrophy].
    Ichikawa Y, Yamada H, Motoyoshi Y, Shimizu T, Kawai M.
    Rinsho Shinkeigaku; 1996 Mar 31; 36(3):503-6. PubMed ID: 8741360
    [Abstract] [Full Text] [Related]

  • 31. Sporadic distal myopathy with early adult onset.
    Miller RG, Blank NK, Layzer RB.
    Ann Neurol; 1979 Mar 31; 5(3):220-7. PubMed ID: 443754
    [Abstract] [Full Text] [Related]

  • 32. [The first Japanese case of autosomal dominant Emery-Dreifuss muscular dystrophy with a novel mutation in the lamin A/C gene].
    Onishi Y, Higuchi J, Ogawa T, Namekawa A, Hayashi H, Odakura H, Goto K, Hayashi YK.
    Rinsho Shinkeigaku; 2002 Feb 31; 42(2):140-4. PubMed ID: 12424964
    [Abstract] [Full Text] [Related]

  • 33. Facioscapulohumeral muscular dystrophy: the choice of a biopsy site.
    Bodensteiner JB, Schochet SS.
    Muscle Nerve; 1986 Feb 31; 9(6):544-7. PubMed ID: 3736585
    [Abstract] [Full Text] [Related]

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  • 38. Congenital muscular dystrophy with rigid spine syndrome: a clinical, pathological, radiological, and genetic study.
    Flanigan KM, Kerr L, Bromberg MB, Leonard C, Tsuruda J, Zhang P, Gonzalez-Gomez I, Cohn R, Campbell KP, Leppert M.
    Ann Neurol; 2000 Feb 31; 47(2):152-61. PubMed ID: 10665485
    [Abstract] [Full Text] [Related]

  • 39. [Familial scapuloperoneal-type myopathy associated with a marked elevation of serum creatine kinase and hepatomegaly].
    Maruoka A, Ideguchi H, Nawata H, Goto I, Ibayashi H.
    Rinsho Shinkeigaku; 1989 Mar 31; 29(3):325-31. PubMed ID: 2752661
    [Abstract] [Full Text] [Related]

  • 40. [Late scapuloperoneal form of progressive muscular dystrophy].
    Stamatoiu I, Florea G, Vasilescu C.
    Neurol Psihiatr Neurochir; 1965 Mar 31; 10(1):21-7. PubMed ID: 5827299
    [No Abstract] [Full Text] [Related]

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