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.
2. Making sense of the limb-girdle muscular dystrophies. Bushby KM Brain; 1999 Aug; 122 ( Pt 8)():1403-20. PubMed ID: 10430828 [TBL] [Abstract][Full Text] [Related]
3. Strategy for mutation analysis in the autosomal recessive limb-girdle muscular dystrophies. Pogue R; Anderson LV; Pyle A; Sewry C; Pollitt C; Johnson MA; Davison K; Moss JA; Mercuri E; Muntoni F; Bushby KM Neuromuscul Disord; 2001 Jan; 11(1):80-7. PubMed ID: 11166169 [TBL] [Abstract][Full Text] [Related]
4. Dysferlin protein analysis in limb-girdle muscular dystrophies. Vainzof M; Anderson LV; McNally EM; Davis DB; Faulkner G; Valle G; Moreira ES; Pavanello RC; Passos-Bueno MR; Zatz M J Mol Neurosci; 2001 Aug; 17(1):71-80. PubMed ID: 11665864 [TBL] [Abstract][Full Text] [Related]
5. Sarcolemmal proteins and the spectrum of limb-girdle muscular dystrophies. Bönnemann CG; Finkel RS Semin Pediatr Neurol; 2002 Jun; 9(2):81-99. PubMed ID: 12139001 [TBL] [Abstract][Full Text] [Related]
6. The 10 autosomal recessive limb-girdle muscular dystrophies. Zatz M; de Paula F; Starling A; Vainzof M Neuromuscul Disord; 2003 Sep; 13(7-8):532-44. PubMed ID: 12921790 [TBL] [Abstract][Full Text] [Related]
7. Phenotypic behavior of caveolin-3 mutations that cause autosomal dominant limb girdle muscular dystrophy (LGMD-1C). Retention of LGMD-1C caveolin-3 mutants within the golgi complex. Galbiati F; Volonte D; Minetti C; Chu JB; Lisanti MP J Biol Chem; 1999 Sep; 274(36):25632-41. PubMed ID: 10464299 [TBL] [Abstract][Full Text] [Related]
8. Disruption of muscle membrane and phenotype divergence in two novel mouse models of dysferlin deficiency. Ho M; Post CM; Donahue LR; Lidov HG; Bronson RT; Goolsby H; Watkins SC; Cox GA; Brown RH Hum Mol Genet; 2004 Sep; 13(18):1999-2010. PubMed ID: 15254015 [TBL] [Abstract][Full Text] [Related]
9. Evaluation of the dystrophin-glycoprotein complex, alpha-actinin, dysferlin and calpain 3 in an autosomal recessive muscular dystrophy in Labrador retrievers. Olby NJ; Sharp NJ; Anderson LV; Kunkel LM; Bönnemann CG Neuromuscul Disord; 2001 Jan; 11(1):41-9. PubMed ID: 11166165 [TBL] [Abstract][Full Text] [Related]
10. Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies). Anderson LV; Harrison RM; Pogue R; Vafiadaki E; Pollitt C; Davison K; Moss JA; Keers S; Pyle A; Shaw PJ; Mahjneh I; Argov Z; Greenberg CR; Wrogemann K; Bertorini T; Goebel HH; Beckmann JS; Bashir R; Bushby KM Neuromuscul Disord; 2000 Dec; 10(8):553-9. PubMed ID: 11053681 [TBL] [Abstract][Full Text] [Related]
11. Dissociation of the dystroglycan complex in caveolin-3-deficient limb girdle muscular dystrophy. Herrmann R; Straub V; Blank M; Kutzick C; Franke N; Jacob EN; Lenard HG; Kröger S; Voit T Hum Mol Genet; 2000 Sep; 9(15):2335-40. PubMed ID: 11001938 [TBL] [Abstract][Full Text] [Related]
12. Dysferlin and muscular dystrophy. Bushby KM Acta Neurol Belg; 2000 Sep; 100(3):142-5. PubMed ID: 11098285 [TBL] [Abstract][Full Text] [Related]
13. Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy. Minetti C; Sotgia F; Bruno C; Scartezzini P; Broda P; Bado M; Masetti E; Mazzocco M; Egeo A; Donati MA; Volonte D; Galbiati F; Cordone G; Bricarelli FD; Lisanti MP; Zara F Nat Genet; 1998 Apr; 18(4):365-8. PubMed ID: 9537420 [TBL] [Abstract][Full Text] [Related]
15. Frequency of LGMD gene mutations in Italian patients with distinct clinical phenotypes. Fanin M; Nascimbeni AC; Aurino S; Tasca E; Pegoraro E; Nigro V; Angelini C Neurology; 2009 Apr; 72(16):1432-5. PubMed ID: 19380703 [TBL] [Abstract][Full Text] [Related]
16. Limb-girdle muscular dystrophy in a 71-year-old woman with an R27Q mutation in the CAV3 gene. Figarella-Branger D; Pouget J; Bernard R; Krahn M; Fernandez C; Lévy N; Pellissier JF Neurology; 2003 Aug; 61(4):562-4. PubMed ID: 12939441 [TBL] [Abstract][Full Text] [Related]
17. Phenotypic study in 40 patients with dysferlin gene mutations: high frequency of atypical phenotypes. Nguyen K; Bassez G; Krahn M; Bernard R; Laforêt P; Labelle V; Urtizberea JA; Figarella-Branger D; Romero N; Attarian S; Leturcq F; Pouget J; Lévy N; Eymard B Arch Neurol; 2007 Aug; 64(8):1176-82. PubMed ID: 17698709 [TBL] [Abstract][Full Text] [Related]
18. Protein and gene analyses of dysferlinopathy in a large group of Japanese muscular dystrophy patients. Tagawa K; Ogawa M; Kawabe K; Yamanaka G; Matsumura T; Goto K; Nonaka I; Nishino I; Hayashi YK J Neurol Sci; 2003 Jul; 211(1-2):23-8. PubMed ID: 12767493 [TBL] [Abstract][Full Text] [Related]
20. Limb girdle muscular dystrophy type 2A in India: a study based on semi-quantitative protein analysis, with clinical and histopathological correlation. Pathak P; Sharma MC; Sarkar C; Jha P; Suri V; Mohd H; Singh S; Bhatia R; Gulati S Neurol India; 2010; 58(4):549-54. PubMed ID: 20739790 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]