THE INCIDENCE OF LOBULATED FIBRES IN THE FACIOSCAPULOHUMERAL TYPE OF MUSCULAR DYSTROPHY AND THE LIMBGIRDLE SYNDROME = L'INCIDENCE DES FIBRES LOBULEES DANS LA DYSTROPHIE MUSCULAIRE DE TYPE FACIOSCAPULOHUMERALE ET DANS LE SYNDROME DES CEINTURESBETHLEM J; VAN WIJNGAARDEN GK; DE JONG J et al.1973; J. NEUROL. SCI.; NETHERL.; DA. 1973; VOL. 18; NO 3; PP. 351-358; BIBL. 3 REF.Serial Issue

MIOPATIE E RIABILITAZIONE = MYOPATHIES ET REEDUCATIONMORONI BULGHERONI E; PURICELLI R.1972; MINERVA MED.; ITAL.; DA. 1972; VOL. 63; NO 64; PP. 3497-3500; BIBL. 7 REF.Serial Issue

NOUVELLES CONCEPTIONS DE LA MALADIE NEUROMUSCULAIREWALTON JN.1973; CONCOURS MED.; FR.; DA. 1973; VOL. 95; NO 3; PP. 357-370 (10P.); ABS. ANGL.; BIBL. 1P.Serial Issue

NEUES ZUR GENETIK UND KLASSIFIKATION DER MUSKELDYSTROPHIEN = ACTUALITES SUR LA GENETIQUE ET LA CLASSIFICATION DES DYSTROPHIES MUSCULAIRESBECKER PE.1972; HUMANGENETIK; DTSCH.; DA. 1972; VOL. 17; NO 1; PP. 1-22; ABS. ANGL.; BIBL. 2P.1/2Serial Issue

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

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

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

Why is the reproductive performance lower in Becker (BMD) as compared to limb girdle (LGMD) muscular dystrophy male patients ?EGGERS, S; LAURIANO, V; MELO, M et al.American journal of medical genetics. 1995, Vol 60, Num 1, pp 27-32, issn 0148-7299Article

Becker and Limb-Girdle muscular dystrophies : a psychiatric and intellectual level comparative studyMELO, M; LAURIANO, V; ZATZ, M et al.American journal of medical genetics. 1995, Vol 60, Num 1, pp 33-38, issn 0148-7299Article

Limb girdle muscular dystrophy : description of a phenotypeSTÜBGEN, J.-P.Muscle & nerve. 1994, Vol 17, Num 12, pp 1449-1455, issn 0148-639XArticle

DIPHENOLOXIDASES IN VARIOUS FORMS OF MYOPATHY WHICH ARE TRANSMITTED BY DIFFERENT GENETIC MECHANISMSDEMOS JJ; TUIL DG; KATZ PC et al.1982; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1982; VOL. 61; NO 3; PP. 185-189; BIBL. 15 REF.Article

Correlations between clinical severity, genotype and muscle pathology in limb girdle muscular dystrophy type 2AFANIN, M; NARDETTO, L; NASCIMBENI, A. C et al.Journal of medical genetics. 2007, Vol 44, Num 10, pp 609-614, issn 0022-2593, 6 p.Article

Limb-girdle muscular dystrophies: from genetics to molecular pathologyLAVAL, S. H; BUSHBY, K. M. D.Neuropathology and applied neurobiology (Print). 2004, Vol 30, Num 2, pp 91-105, issn 0305-1846, 15 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

Distrofia muscular de cinturas 2C: valoración y tratamiento rehabilitador en 11 casos = Limb-girdle muscular dystrophy 2C: Assessment and rehabilitation treatment in ii casesFLORES CALVETE, J; RODRIGUEZ MACIA, A; MUNOZ MATEO, J et al.Rehabilitación (Madrid). 2000, Vol 34, Num 2, pp 184-188, issn 0048-7120Article

The limb-girdle muscular dystrophies-multiple genes, multiple mechanismsBUSHBY, K. M. D.Human molecular genetics (Print). 1999, Vol 8, Num 10, pp 1875-1882, issn 0964-6906Article

High prevalence and phenotype-genotype correlations of limb girdle muscular dystrophy type 21 in DenmarkSVEEN, Marie-Louise; SCHWARTZ, Marianne; VISSING, John et al.Annals of neurology. 2006, Vol 59, Num 5, pp 808-815, issn 0364-5134, 8 p.Article

Hutterite brothers both affected with two forms of limb girdle muscular dystrophy : LGMD2H and LGMD21FROSK, Patrick; DEL BIGIO, Marc R; WROGEMANN, Klaus et al.European journal of human genetics. 2005, Vol 13, Num 8, pp 978-982, issn 1018-4813, 5 p.Article