99 related articles for article (PubMed ID: 7881446)
1. Adhalin gene polymorphism.
Allamand V; Leturcq F; Piccolo F; Jeanpierre M; Azibi K; Roberds SL; Lim LE; Campbell KP; Beckmann JS; Kaplan JC
Hum Mol Genet; 1994 Dec; 3(12):2269. PubMed ID: 7881446
[No Abstract] [Full Text] [Related]
2. Human adhalin is alternatively spliced and the gene is located on chromosome 17q21.
McNally EM; Yoshida M; Mizuno Y; Ozawa E; Kunkel LM
Proc Natl Acad Sci U S A; 1994 Oct; 91(21):9690-4. PubMed ID: 7937874
[TBL] [Abstract][Full Text] [Related]
3. Adhalin deficiency.
Hamida CB
Neurology; 1996 Jun; 46(6):1784-5. PubMed ID: 8649603
[No Abstract] [Full Text] [Related]
4. 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]
5. Deficiency of adhalin in a patient with muscular dystrophy and cardiomyopathy.
McNally EM; Bönnemann CG; Kunkel LM; Bhattacharya SK
N Engl J Med; 1996 Jun; 334(24):1610-1. PubMed ID: 8628353
[No Abstract] [Full Text] [Related]
6. 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]
7. 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]
8. Adhalin gene mutations and autosomal recessive limb-girdle muscular dystrophy.
Campbell KP
Ann Neurol; 1995 Sep; 38(3):353-4. PubMed ID: 7668818
[No Abstract] [Full Text] [Related]
9. 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]
10. Understanding the heterogeneity of the limb-girdle muscular dystrophies.
Bushby K
Biochem Soc Trans; 1996 May; 24(2):489-96. PubMed ID: 8736790
[No Abstract] [Full Text] [Related]
11. [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]
12. [Identification of adhalin gene mutation in limb-girdle muscular dystrophy in Chinese].
Sun G; Wu Y; Zhang K; Zhang X; Jin C; Sun K
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1998 Dec; 15(6):351-3. PubMed ID: 9845765
[TBL] [Abstract][Full Text] [Related]
13. [Muscular dystrophy due to a mutation in the gene of alpha-sarcoglycan subunit of dystrophin associated protein complex].
Urtasun M; Poza JJ; Gallano P; Lasa A; Sáenz A; Cobo AM; Leturcq F; López de Munain A; García-Bragado F
Med Clin (Barc); 1998 Apr; 110(14):538-42. PubMed ID: 9646269
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Muscular dystrophies: diseases of the dystrophin-glycoprotein complex.
Worton R
Science; 1995 Nov; 270(5237):755-6. PubMed ID: 7481760
[No Abstract] [Full Text] [Related]
16. [Adhalin(alpha-sarcoglycan) gene mutations in patients with malignant limb-girdle muscular dystrophy (MLGMD) (Miyoshi)].
Endo T; Kawai H
Nihon Rinsho; 1997 Dec; 55(12):3159-64. PubMed ID: 9436428
[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. Mouse adhalin: primary structure and expression during late stages of muscle differentiation in vitro.
Liu L; Vachon PH; Kuang W; Xu H; Wewer UM; Kylsten P; Engvall E
Biochem Biophys Res Commun; 1997 Jun; 235(1):227-35. PubMed ID: 9196068
[TBL] [Abstract][Full Text] [Related]
19. Genetic medicine and the muscular dystrophies: triumphs and tribulations.
Hoffman EP; Chen YW
Dev Med Child Neurol; 2002 Feb; 44(2):136-40. PubMed ID: 11848111
[No Abstract] [Full Text] [Related]
20. The muscular dystrophies--clarity or chaos?
Dubowitz V
N Engl J Med; 1997 Feb; 336(9):650-1. PubMed ID: 9032052
[No Abstract] [Full Text] [Related]
[Next] [New Search]