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8. Chronic ophthalmoparesis in limb girdle muscular dystrophy 1C. Filosto M; Tonin P; Vattemi G; Scarpelli M; Baronchelli C; Broglio L; Tentorio M; Cotelli M; Padovani A; Tomelleri G J Neurol Neurosurg Psychiatry; 2009 Apr; 80(4):448-9. PubMed ID: 19289483 [No Abstract] [Full Text] [Related]
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10. Endurance training: an effective and safe treatment for patients with LGMD2I. Sveen ML; Jeppesen TD; Hauerslev S; Krag TO; Vissing J Neurology; 2007 Jan; 68(1):59-61. PubMed ID: 17200494 [TBL] [Abstract][Full Text] [Related]
11. Mutation analysis in the FKRP gene provides an explanation for a rare cause of intrafamilial clinical variability in LGMD2I. Vieira NM; Schlesinger D; de Paula F; Vainzof M; Zatz M Neuromuscul Disord; 2006 Dec; 16(12):870-3. PubMed ID: 17113772 [TBL] [Abstract][Full Text] [Related]
12. Pathology of frontotemporal dementia with limb girdle muscular dystrophy caused by a DNAJB6 mutation. Yabe I; Tanino M; Yaguchi H; Takiyama A; Cai H; Kanno H; Takahashi I; Hayashi YK; Watanabe M; Takahashi H; Hatakeyama S; Tanaka S; Sasaki H Clin Neurol Neurosurg; 2014 Dec; 127():10-2. PubMed ID: 25306414 [No Abstract] [Full Text] [Related]
13. [Phenotypic aspects of FKRP-linked muscular dystrophy type 2I in a series of eleven patients]. Bourteel H; Stojkovic T; Cuisset JM; Maurage CA; Laforet P; Richard P; Vermersch P Rev Neurol (Paris); 2007 Feb; 163(2):189-96. PubMed ID: 17351538 [TBL] [Abstract][Full Text] [Related]
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18. Limb-girdle muscular dystrophy due to emerin gene mutations. Ura S; Hayashi YK; Goto K; Astejada MN; Murakami T; Nagato M; Ohta S; Daimon Y; Takekawa H; Hirata K; Nonaka I; Noguchi S; Nishino I Arch Neurol; 2007 Jul; 64(7):1038-41. PubMed ID: 17620497 [TBL] [Abstract][Full Text] [Related]
19. LGMD2I presenting with a characteristic Duchenne or Becker muscular dystrophy phenotype. Schwartz M; Hertz JM; Sveen ML; Vissing J Neurology; 2005 May; 64(9):1635-7. PubMed ID: 15883334 [TBL] [Abstract][Full Text] [Related]