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Sustained Alpha-Sarcoglycan Gene Expression after Gene Transfer in Limb- Girdle Muscular Dystrophy, Type 2DMENDELL, Jerry R; RODINO-KLAPAC, Louise R; CAMPBELL, Katherine J et al.Annals of neurology. 2010, Vol 68, Num 5, pp 629-638, issn 0364-5134, 10 p.Article

Mild POMGnTI Mutations Underlie a Novel Limb-Girdle Muscular Dystrophy VariantCLEMENT, Emma M; GODFREY, Caroline; MEIN, Rachael et al.Archives of neurology (Chicago). 2008, Vol 65, Num 1, pp 137-141, issn 0003-9942, 5 p.Article

Limb-girdle muscular dystrophy due to emerin gene mutationsURA, Shigehisa; HAYASHI, Yukiko K; NONAKA, Ikuya et al.Archives of neurology (Chicago). 2007, Vol 64, Num 7, pp 1038-1041, issn 0003-9942, 4 p.Article

The congenital and limb-girdle muscular dystrophies: Sharpening the focus, blurring the boundariesKIRSCHNER, Janbernd; BÖNNENANN, Carsten G.Archives of neurology (Chicago). 2004, Vol 61, Num 2, pp 189-199, issn 0003-9942, 11 p.Article

LIMB-GIRDLE MUSCULAR DYSTROPHY WITH α-DYSTROGLYCAN DEFICIENCY AND MUTATIONS IN THE ISPD GENETASCA, G; MORO, F; AIELLO, C et al.Neurology. 2013, Vol 80, Num 10, pp 963-965, issn 0028-3878, 3 p.Article

Lariat branch point mutation in the dysferlin gene with mild limb-girdle muscular dystrophySINNREICH, Michael; THERRIEN, Christian; KARPATI, George et al.Neurology. 2006, Vol 66, Num 7, pp 1114-1116, issn 0028-3878, 3 p.Article

Clinical and molecular characterization of patients with limb-girdle muscular dystrophy Type 2IBOITO, Chiara A; MELACINI, Paola; VIANELLO, Andrea et al.Archives of neurology (Chicago). 2005, Vol 62, Num 12, pp 1894-1899, issn 0003-9942, 6 p.Article

Childhood Onset of Limb-Girdle Muscular DystrophyROSALES, Xiomara Q; TSAO, Chang-Yong.Pediatric neurology. 2012, Vol 46, Num 1, pp 13-23, issn 0887-8994, 11 p.Article

The enigma of 7q36 linked autosomal dominant limb girdle muscular dystrophySANDELL, Satu; HUOVINEN, Sanna; SARPARANTA, Jaakko et al.Journal of neurology, neurosurgery and psychiatry. 2010, Vol 81, Num 8, pp 834-839, issn 0022-3050, 6 p.Article

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Diagnosis and management of the limb girdle muscular dystrophiesBUSHBY, Kate.Practical neurology (Print). 2009, Vol 9, Num 6, pp 314-323, issn 1474-7758, 10 p.Article

Clinical and mutational spectrum of limb-girdle muscular dystrophy type 21 in 11 French patientsBOURTEEL, H; VERMERSCH, P; CUISSET, J.-M et al.Journal of neurology, neurosurgery and psychiatry. 2009, Vol 80, Num 12, pp 1405-1408, issn 0022-3050, 4 p.Article

Limb-girdle muscular dystrophy in the Netherlands : Gene defect identified in half the familiesVAN DER KOOI, A. J; FRANKHUIZEN, W. S; BAKKER, E et al.Neurology. 2007, Vol 68, Num 24, pp 2125-2128, issn 0028-3878, 4 p.Article

A novel mutation in two families with limb-girdle muscular dystrophy type 2CDUNCAN, D. R; KANG, P. B; RABBAT, J. C et al.Neurology. 2006, Vol 67, Num 1, pp 167-169, issn 0028-3878, 3 p.Article

Fukutin gene mutations in steroid-responsive limb girdle muscular dystrophyGODFREY, Caroline; ESCOLAR, Diana; RUTHERFORD, Mary et al.Annals of neurology. 2006, Vol 60, Num 5, pp 603-610, issn 0364-5134, 8 p.Article

A new evidence for the maintenance of the sarcoglycan complex in muscle sarcolemma in spite of the primary absence of δ-SG proteinGOUVEIA, Telma L. F; KOSSUGUE, Patricia M; PAIM, Julia F et al.Journal of molecular medicine (Berlin. Print). 2007, Vol 85, Num 4, pp 415-420, issn 0946-2716, 6 p.Article

ε-Sarcoglycan compensates for lack of α-sarcoglycan in a mouse model of limb-girdle muscular dystrophyIMAMURA, Michihiro; MOCHIZUKI, Yasushi; ENGVALL, Eva et al.Human molecular genetics (Print). 2005, Vol 14, Num 6, pp 775-783, issn 0964-6906, 9 p.Article

The phenotype of limb-girdle muscular dystrophy type 21POPPE, M; CREE, L; WILLS, A et al.Neurology. 2003, Vol 60, Num 8, pp 1246-1251, issn 0028-3878, 6 p.Article

A novel, blood-based diagnostic assay for limb girdle muscular dystrophy 2B and Miyoshi myopathyHO, Mengfatt; GALLARDO, Eduard; MCKENNA-YASEK, Diane et al.Annals of neurology. 2002, Vol 51, Num 1, pp 129-133, issn 0364-5134Article

Etiology of Limb Girdle Muscular Dystrophy 1D/1E Determined by Laser Capture Microdissection ProteomicsGREENBERG, Steven A; SALAJEGHEH, Mohammad; JUDGE, Daniel P et al.Annals of neurology. 2012, Vol 71, Num 1, pp 141-145, issn 0364-5134, 5 p.Article

Reliability and accuracy of skeletal muscle imaging in limb-girdle muscular dystrophiesTEN DAM, Leroy; VAN DER KOOI, Anneke J; VAN WATTINGEN, Menno et al.Neurology. 2012, Vol 79, Num 16, pp 1716-1723, issn 0028-3878, 8 p.Article

Limb-girdle muscular dystrophy 1F is caused by a microdeletion in the transportin 3 geneMELIA, Maria J; KUBOTA, Akatsuki; GARCIA-ARUMI, Elena et al.Brain. 2013, Vol 136, pp 1508-1517, issn 0006-8950, 10 p., 5Article

A Dystroglycan Mutation Associated with Limb-Girdle Muscular DystrophyHARA, Yuji; BALCI-HAYTA, Burcu; KUNZ, Stefan et al.The New England journal of medicine. 2011, Vol 364, Num 10, pp 939-946, issn 0028-4793, 8 p.Article

A novel mutation in the myotilin gene (MYOT) causes a severe form of limb girdle muscular dystrophy 1A (LGMD1A)REILICH, Peter; KRAUSE, Sabine; SCHRAMM, Nicolai et al.Journal of neurology. 2011, Vol 258, Num 8, pp 1437-1444, issn 0340-5354, 8 p.Article