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6. Autosomal recessive distal muscular dystrophy: a comparative study with distal myopathy with rimmed vacuole formation. Nonaka I; Sunohara N; Satoyoshi E; Terasawa K; Yonemoto K Ann Neurol; 1985 Jan; 17(1):51-9. PubMed ID: 3985587 [TBL] [Abstract][Full Text] [Related]
7. [Autosomal dominant distal myopathy with rimmed vacuoles and cytoplasmic inclusions: report of a family]. Uesaka Y; Nakamichi K; Kojima S; Ida M; Takagi A Rinsho Shinkeigaku; 1997 Jan; 37(1):1-6. PubMed ID: 9146065 [TBL] [Abstract][Full Text] [Related]
8. A newly recognized autosomal dominant limb girdle muscular dystrophy with cardiac involvement. van der Kooi AJ; Ledderhof TM; de Voogt WG; Res CJ; Bouwsma G; Troost D; Busch HF; Becker AE; de Visser M Ann Neurol; 1996 May; 39(5):636-42. PubMed ID: 8619549 [TBL] [Abstract][Full Text] [Related]
9. [A family with oculopharyngeal muscular dystrophy with (GCG)9 expansion in which a sister had neck as well as proximal and her brother proximal lower limb muscle weakness]. Takahashi T; Tateyama M; Aoki M; Shiga Y; Uyama E; Itoyama Y Rinsho Shinkeigaku; 2000 Sep; 40(9):911-4. PubMed ID: 11257788 [TBL] [Abstract][Full Text] [Related]
10. 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; 49(4):443-52. PubMed ID: 11310621 [TBL] [Abstract][Full Text] [Related]
11. 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; 128(Pt 7):1716-27. PubMed ID: 15857933 [TBL] [Abstract][Full Text] [Related]
12. [2 families with benign myopathy predominantly on the limb girdle with dominant autosomal heredity]. Serratrice G; Pellissier JF Rev Neurol (Paris); 1988; 144(1):43-6. PubMed ID: 3347807 [TBL] [Abstract][Full Text] [Related]
13. 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 [TBL] [Abstract][Full Text] [Related]
14. Childhood-onset autosomal-dominant limb-girdle muscular dystrophy with cardiac conduction block. Fang W; Huang CC; Chu NS; Chen CJ; Lu CS; Wang CC Muscle Nerve; 1997 Mar; 20(3):286-92. PubMed ID: 9052806 [TBL] [Abstract][Full Text] [Related]
15. Late-onset autosomal dominant limb girdle muscular dystrophy and Paget's disease of bone unlinked to the VCP gene locus. Kottlors M; Moske-Eick O; Huebner A; Krause S; Mueller K; Kress W; Schwarzwald R; Bornemann A; Haug V; Heitzer M; Kirschner J J Neurol Sci; 2010 Apr; 291(1-2):79-85. PubMed ID: 20116073 [TBL] [Abstract][Full Text] [Related]
16. A new form of autosomal dominant limb-girdle muscular dystrophy (LGMD1G) with progressive fingers and toes flexion limitation maps to chromosome 4p21. Starling A; Kok F; Passos-Bueno MR; Vainzof M; Zatz M Eur J Hum Genet; 2004 Dec; 12(12):1033-40. PubMed ID: 15367920 [TBL] [Abstract][Full Text] [Related]
17. [A case of distal myopathy with rimmed vacuole formation, progresses into proximal-dominant muscle involvement]. Ishikawa K; Ohkoshi N; Arasaki K; Mizusawa H; Kanazawa I Rinsho Shinkeigaku; 1992 Sep; 32(9):1044-7. PubMed ID: 1338627 [TBL] [Abstract][Full Text] [Related]
18. [A case of senile onset rimmed vacuole myopathy with proximally dominant involvement]. Yamamoto K; Takase Y; Fukusako T; Nogaki H; Morimatsu M Rinsho Shinkeigaku; 1990 Oct; 30(10):1128-32. PubMed ID: 2279364 [TBL] [Abstract][Full Text] [Related]