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2. [The genetics of late forms of Erb's myopathy]. Dukhovnikova LM; Morozova EA Zh Nevropatol Psikhiatr Im S S Korsakova; 1970; 70(9):1297-303. PubMed ID: 5511107 [No Abstract] [Full Text] [Related]
3. An autosomal dominant type of congenital muscular dystrophy. Leyten QH; Gabreëls FJ; Joosten EM; Renier WO; Ter Laak HJ; Ter Haar BG; Stadhouders AM Brain Dev; 1986; 8(5):533-7. PubMed ID: 3799922 [TBL] [Abstract][Full Text] [Related]
4. Familial muscular dystrophy of late onset. Bacon PA; Smith B J Neurol Neurosurg Psychiatry; 1971 Feb; 34(1):93-7. PubMed ID: 5551698 [TBL] [Abstract][Full Text] [Related]
6. A late autosomal dominant form of limb-girdle muscular dystrophy. A clinical, genetic, and morphological study. De Coster W; De Reuck J; Thiery E Eur Neurol; 1974; 12(3):159-72. PubMed ID: 4426323 [No Abstract] [Full Text] [Related]
7. Facioscapulohumeral muscular dystrophy: the choice of a biopsy site. Bodensteiner JB; Schochet SS Muscle Nerve; 1986; 9(6):544-7. PubMed ID: 3736585 [TBL] [Abstract][Full Text] [Related]
8. [Clinicopathological study of a case of oculopharyngeal muscular dystrophy]. Moreno Martínez JM; Martín Araguz A; García de la Rocha ML; Masjuán Vallejo J; Barón Rubio M; Ginel Feito MD Arch Neurobiol (Madr); 1991; 54(5):229-32. PubMed ID: 1804038 [TBL] [Abstract][Full Text] [Related]
14. Skeletal muscle biopsy: indications and results in 200 patients. Ojeda VJ; Jacobsen PF; Spagnolo DV; Cole K Med J Aust; 1982 Feb; 1(3):127. PubMed ID: 6290860 [No Abstract] [Full Text] [Related]
15. [New data on the genetics and classification of muscular dystrophies]. Becker PE Humangenetik; 1972; 17(1):1-22. PubMed ID: 4567289 [No Abstract] [Full Text] [Related]
16. 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 [TBL] [Abstract][Full Text] [Related]
17. The natural history of Duchenne muscular dystrophy--an ultrastructural study. Papadimitriou JM; Mastaglia FL; Kakulas BA Proc Aust Assoc Neurol; 1969; 6():87-92. PubMed ID: 5349192 [No Abstract] [Full Text] [Related]
18. [Clinical and genetic aspects of progressive muscular dystrophy. Genetic and clinical forms of myopathy; clinical, anatomical, and EMG study]. Voiculescu V; Pruskauer-Apostol B; Mărcuţiu V; Alecu C; Stănescu A Neurol Psihiatr Neurochir; 1973; 18(4):347-58. PubMed ID: 4752178 [No Abstract] [Full Text] [Related]
19. [A pedigree of autosomal dominant limb-girdle myopathy with rimmed vacuole formation]. Kishibayashi J; Sunohara N; Saito Y Rinsho Shinkeigaku; 1997 Jul; 37(7):603-10. PubMed ID: 9396357 [TBL] [Abstract][Full Text] [Related]
20. Limb-girdle muscular dystrophy: clinical manifestations and detection of preclinical disease. Jackson CE; Strehler DA Pediatrics; 1968 Feb; 41(2):495-502. PubMed ID: 5637795 [No Abstract] [Full Text] [Related] [Next] [New Search]