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The limb-girdle muscular dystrophies -proposal for a new nomenclature (30th and 31st ENMC workshops report)
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Optimised protein diagnosis in the autosomal recessive limb-girdle muscular dystrophies
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Anderson LVB: Optimised protein diagnosis in the autosomal recessive limb-girdle muscular dystrophies. Neuromuscul Disord 1996, 6:443-446
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Late onset muscular dystrophy with cerebral white matter changes due to partial merosin deficiency
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Tan E, Topaloglu H, Sewry C, Zorlu Y, Naom I, Erdem S, D'Alessandro M, Muntoni F, Dubowitz V: Late onset muscular dystrophy with cerebral white matter changes due to partial merosin deficiency. Neuromuscul Disord 1997, 7:85-89
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Early presentation of X-linked Emery-Dreifuss muscular dystrophy resembling limb-girdle muscular dystrophy
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Muntoni F, Lichtarowicz-Krynska EJ, Sewry CA, Manilal S, Recan D, Llense S, Taylor J, Morris GE, Dubowitz V: Early presentation of X-linked Emery-Dreifuss muscular dystrophy resembling limb-girdle muscular dystrophy. Neuromuscul Disord 1998, 8:72-76
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Early onset autosomal dominant myopathy with rigidity of the spine: A possible role for laminin β1?
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Taylor J, Muntoni F, Robb S, Dubowitz V, Sewry C: Early onset autosomal dominant myopathy with rigidity of the spine: a possible role for laminin β1? Neuromuscul Disord 1997, 7:211-216
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Abnormal merosin in adults - A new form of late onset muscular dystrophy not linked to chromosome 6q2
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Bushby KMD, Anderson LVB, Pollitt C, Naom I, Muntoni F, Bindoff L: Abnormal merosin in adults - a new form of late onset muscular dystrophy not linked to chromosome 6q2. Brain 1998, 121:581-588
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Characterization of monoclonal antibodies to calpain 3 and protein expression in muscle from patients with limb-girdle muscular dystrophy type 2A
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Anderson LVB, Davison K, Moss JA, Richard I, Fardeau M, Tomé FMS, Hübner C, Lasa A, Colomer J, Beckmann JS: Characterization of monoclonal antibodies to calpain 3 and protein expression in muscle from patients with limb-girdle muscular dystrophy type 2A. Am J Pathol 1998, 153:1169-1179
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Multiplex western blot analysis of the muscular dystrophy proteins
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Edited by KMD Bushby, LVB Anderson. From The Methods in Molecular Medicine Series edited by JM Walker. Totowa, NJ, Humana Press, In press
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Dystrophin in skeletal muscle: I. Western blot analysis using a monoclonal antibody
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Heterogeneity of dystrophin expression in patients with Duchenne and Becker muscular dystrophy
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Abnormalities in α-, β-, and γ-sarcoglycan in patients with limb-girdle muscular dystrophy
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Sewry C, Taylor J, Anderson LVB, Ozawa E, Pogue R, Piccolo F, Bushby KMD, Dubowitz V, Muntoni F: Abnormalities in α-, β-, and γ-sarcoglycan in patients with limb-girdle muscular dystrophy. Neuromuscul Disord 1996, 6:467-474
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