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.
133 related articles for article (PubMed ID: 11770249)
1. Adhalin deficiency: an unusual cause of muscular dystrophy. Dua T; Kalra V; Sharma MC; Kabra M Indian J Pediatr; 2001 Nov; 68(11):1083-5. PubMed ID: 11770249 [TBL] [Abstract][Full Text] [Related]
2. A common missense mutation in the adhalin gene in three unrelated Brazilian families with a relatively mild form of autosomal recessive limb-girdle muscular dystrophy. Bueno MR; Moreira ES; Vainzof M; Chamberlain J; Marie SK; Pereira L; Akiyama J; Roberds SL; Campbell KP; Zatz M Hum Mol Genet; 1995 Jul; 4(7):1163-7. PubMed ID: 8528203 [TBL] [Abstract][Full Text] [Related]
3. Genetic heterogeneity of severe childhood autosomal recessive muscular dystrophy with adhalin (50 kDa dystrophin-associated glycoprotein) deficiency. Romero NB; Tomé FM; Leturcq F; el Kerch FE; Azibi K; Bachner L; Anderson RD; Roberds SL; Campbell KP; Fardeau M C R Acad Sci III; 1994 Jan; 317(1):70-6. PubMed ID: 7987694 [TBL] [Abstract][Full Text] [Related]
4. Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity. Piccolo F; Roberds SL; Jeanpierre M; Leturcq F; Azibi K; Beldjord C; Carrié A; Récan D; Chaouch M; Reghis A Nat Genet; 1995 Jun; 10(2):243-5. PubMed ID: 7663524 [TBL] [Abstract][Full Text] [Related]
5. [Adhalin gene mutations in malignant limb-girdle muscular dystrophy and clinical features in adhalin-deficient muscular dystrophy]. Endo T; Akaike M; Kawai H; Matsumura K; Saito S Rinsho Shinkeigaku; 1996 Mar; 36(3):415-22. PubMed ID: 8741343 [TBL] [Abstract][Full Text] [Related]
6. [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]
7. alpha-Sarcoglycan (adhalin) deficiency: complete deficiency patients are 5% of childhood-onset dystrophin-normal muscular dystrophy and most partial deficiency patients do not have gene mutations. Duggan DJ; Fanin M; Pegoraro E; Angelini C; Hoffman EP J Neurol Sci; 1996 Sep; 140(1-2):30-9. PubMed ID: 8866424 [TBL] [Abstract][Full Text] [Related]
8. Adhalin gene mutations in patients with autosomal recessive childhood onset muscular dystrophy with adhalin deficiency. Kawai H; Akaike M; Endo T; Adachi K; Inui T; Mitsui T; Kashiwagi S; Fujiwara T; Okuno S; Shin S J Clin Invest; 1995 Sep; 96(3):1202-7. PubMed ID: 7657792 [TBL] [Abstract][Full Text] [Related]
9. Selective defect of sarcoglycan complex in severe childhood autosomal recessive muscular dystrophy muscle. Mizuno Y; Noguchi S; Yamamoto H; Yoshida M; Suzuki A; Hagiwara Y; Hayashi YK; Arahata K; Nonaka I; Hirai S Biochem Biophys Res Commun; 1994 Sep; 203(2):979-83. PubMed ID: 8093083 [TBL] [Abstract][Full Text] [Related]
10. Primary adhalinopathy (alpha-sarcoglycanopathy): clinical, pathologic, and genetic correlation in 20 patients with autosomal recessive muscular dystrophy. Eymard B; Romero NB; Leturcq F; Piccolo F; Carrié A; Jeanpierre M; Collin H; Deburgrave N; Azibi K; Chaouch M; Merlini L; Thémar-Noël C; Penisson I; Mayer M; Tanguy O; Campbell KP; Kaplan JC; Tomé FM; Fardeau M Neurology; 1997 May; 48(5):1227-34. PubMed ID: 9153448 [TBL] [Abstract][Full Text] [Related]
11. [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]
12. gamma-sarcoglycan deficiency muscular dystrophy in two adults. Lin KL; Wang HS; Chen ST; Ro LS J Formos Med Assoc; 2000 Oct; 99(10):789-91. PubMed ID: 11061077 [TBL] [Abstract][Full Text] [Related]
14. Primary adhalin deficiency as a cause of muscular dystrophy in patients with normal dystrophin. Ljunggren A; Duggan D; McNally E; Boylan KB; Gama CH; Kunkel LM; Hoffman EP Ann Neurol; 1995 Sep; 38(3):367-72. PubMed ID: 7668821 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy. Roberds SL; Leturcq F; Allamand V; Piccolo F; Jeanpierre M; Anderson RD; Lim LE; Lee JC; Tomé FM; Romero NB Cell; 1994 Aug; 78(4):625-33. PubMed ID: 8069911 [TBL] [Abstract][Full Text] [Related]
18. New missense mutation in the alpha-sarcoglycan gene in a Japanese patient with severe childhood autosomal recessive muscular dystrophy with incomplete alpha-sarcoglycan deficiency. Higuchi I; Iwaki H; Kawai H; Endo T; Kunishige M; Fukunaga H; Nakagawa M; Arimura K; Osame M J Neurol Sci; 1997 Dec; 153(1):100-5. PubMed ID: 9455986 [TBL] [Abstract][Full Text] [Related]