These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
371 related articles for article (PubMed ID: 9505924)
1. The heart in limb girdle muscular dystrophy. van der Kooi AJ; de Voogt WG; Barth PG; Busch HF; Jennekens FG; Jongen PJ; de Visser M Heart; 1998 Jan; 79(1):73-7. PubMed ID: 9505924 [TBL] [Abstract][Full Text] [Related]
2. Mutations in the delta-sarcoglycan gene are a rare cause of autosomal recessive limb-girdle muscular dystrophy (LGMD2). Duggan DJ; Manchester D; Stears KP; Mathews DJ; Hart C; Hoffman EP Neurogenetics; 1997 May; 1(1):49-58. PubMed ID: 10735275 [TBL] [Abstract][Full Text] [Related]
3. Deficiency of the 50 kDa dystrophin-associated-glycoprotein (adhalin) in an Indian autosomal recessive limb girdle muscular dystrophy patient : immunochemical analysis and clinical aspects. Handa V; Mital A; Gupta M; Goyle S Neurol India; 2001 Mar; 49(1):19-24. PubMed ID: 11303236 [TBL] [Abstract][Full Text] [Related]
4. Abnormalities in alpha-, beta- and gamma-sarcoglycan in patients with limb-girdle muscular dystrophy. Sewry CA; Taylor J; Anderson LV; Ozawa E; Pogue R; Piccolo F; Bushby K; Dubowitz V; Muntoni F Neuromuscul Disord; 1996 Dec; 6(6):467-74. PubMed ID: 9027857 [TBL] [Abstract][Full Text] [Related]
5. Autosomal recessive muscular dystrophy and mutations of the sarcoglycan complex. Duggan DJ; Hoffman EP Neuromuscul Disord; 1996 Dec; 6(6):475-82. PubMed ID: 9027858 [TBL] [Abstract][Full Text] [Related]
6. A novel gamma-sarcoglycan mutation causing childhood onset, slowly progressive limb girdle muscular dystrophy. van der Kooi AJ; de Visser M; van Meegen M; Ginjaar HB; van Essen AJ; Jennekens FG; Jongen PJ; Leschot NJ; Bolhuis PA Neuromuscul Disord; 1998 Jun; 8(5):305-8. PubMed ID: 9673983 [TBL] [Abstract][Full Text] [Related]
7. Limb girdle muscular dystrophy: a pathological and immunohistochemical reevaluation. van der Kooi AJ; Ginjaar HB; Busch HF; Wokke JH; Barth PG; de Visser M Muscle Nerve; 1998 May; 21(5):584-90. PubMed ID: 9572237 [TBL] [Abstract][Full Text] [Related]
8. [Muscular dystrophy due to a deficit of gamma-sarcoglycan. A report of three patients with the Delta-521t mutation]. Eirís-Puñal J; Pintos-Martínez E; Lasa A; Gallano P; Castro-Gago M Rev Neurol; 2002 Mar 1-15; 34(5):486-9. PubMed ID: 12040521 [TBL] [Abstract][Full Text] [Related]
9. Mutations in the sarcoglycan genes in patients with myopathy. Duggan DJ; Gorospe JR; Fanin M; Hoffman EP; Angelini C N Engl J Med; 1997 Feb; 336(9):618-24. PubMed ID: 9032047 [TBL] [Abstract][Full Text] [Related]
10. Gene transfer establishes primacy of striated vs. smooth muscle sarcoglycan complex in limb-girdle muscular dystrophy. Durbeej M; Sawatzki SM; Barresi R; Schmainda KM; Allamand V; Michele DE; Campbell KP Proc Natl Acad Sci U S A; 2003 Jul; 100(15):8910-5. PubMed ID: 12851463 [TBL] [Abstract][Full Text] [Related]
11. A novel form of recessive limb girdle muscular dystrophy with mental retardation and abnormal expression of alpha-dystroglycan. Dinçer P; Balci B; Yuva Y; Talim B; Brockington M; Dinçel D; Torelli S; Brown S; Kale G; Haliloglu G; Gerçeker FO; Atalay RC; Yakicier C; Longman C; Muntoni F; Topaloglu H Neuromuscul Disord; 2003 Dec; 13(10):771-8. PubMed ID: 14678799 [TBL] [Abstract][Full Text] [Related]
12. Advances in the molecular genetics of the limb-girdle type of autosomal recessive progressive muscular dystrophy. Beckmann JS; Bushby KM Curr Opin Neurol; 1996 Oct; 9(5):389-93. PubMed ID: 8894416 [TBL] [Abstract][Full Text] [Related]
13. [The frequency of patients with adhalin deficiency in a muscular dystrophy patient population]. Hayashi YK; Arahata K Nihon Rinsho; 1997 Dec; 55(12):3165-8. PubMed ID: 9436429 [TBL] [Abstract][Full Text] [Related]
14. [Gamma-sarcoglycanopathy: clinico-pathological and genetic study of 11 cases]. García-García D; Teijeira-Bautista S; Fernández-Rodríguez JM; Flores-Calvete J; Sánchez-Espíldora P; Fernández-Couto D; Cimas-Hernando I; Teijeiro-Ferreira A; Fernández-Hojas R; Brasa-Fernández Fierros J; Martínez de Alegría A; Escribano-Arias JL; Núñez-Delgado M; Navarro-Fernández Balbuena C Rev Neurol; 1998 Jun; 26(154):905-11. PubMed ID: 9658457 [TBL] [Abstract][Full Text] [Related]
15. A cross section of autosomal recessive limb-girdle muscular dystrophies in 38 families. Dinçer P; Akçören Z; Demir E; Richard I; Sancak O; Kale G; Ozme S; Karaduman A; Tan E; Urtizberea JA; Beckmann JS; Topaloğlu H J Med Genet; 2000 May; 37(5):361-7. PubMed ID: 10807695 [TBL] [Abstract][Full Text] [Related]
16. [Clinicopathological characteristics and molecular genetics of adhalin deficiency (severe childhood autosomal recessive muscular dystrophy/SCARMD)]. Matsumura K Nihon Rinsho; 1997 Dec; 55(12):3154-8. PubMed ID: 9436427 [TBL] [Abstract][Full Text] [Related]
17. Beta-sarcoglycan: characterization and role in limb-girdle muscular dystrophy linked to 4q12. Lim LE; Duclos F; Broux O; Bourg N; Sunada Y; Allamand V; Meyer J; Richard I; Moomaw C; Slaughter C Nat Genet; 1995 Nov; 11(3):257-65. PubMed ID: 7581448 [TBL] [Abstract][Full Text] [Related]
18. [Gene analysis in patients with muscular dystrophy: alpha-sarcoglycan (adhalin) gene mutations in patients with malignant limb-girdle muscular dystrophy]. Akaike M; Kawai H Rinsho Byori; 1997 Feb; 45(2):136-40. PubMed ID: 9120997 [TBL] [Abstract][Full Text] [Related]
19. Mutations that disrupt the carboxyl-terminus of gamma-sarcoglycan cause muscular dystrophy. McNally EM; Duggan D; Gorospe JR; Bönnemann CG; Fanin M; Pegoraro E; Lidov HG; Noguchi S; Ozawa E; Finkel RS; Cruse RP; Angelini C; Kunkel LM; Hoffman EP Hum Mol Genet; 1996 Nov; 5(11):1841-7. PubMed ID: 8923014 [TBL] [Abstract][Full Text] [Related]
20. Molecular and genetic characterization of sarcospan: insights into sarcoglycan-sarcospan interactions. Crosbie RH; Lim LE; Moore SA; Hirano M; Hays AP; Maybaum SW; Collin H; Dovico SA; Stolle CA; Fardeau M; Tomé FM; Campbell KP Hum Mol Genet; 2000 Aug; 9(13):2019-27. PubMed ID: 10942431 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]