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Results: 1-11 |
Results: 11
Evaluation of the dystrophin-glycoprotein complex, alpha-actinin, dysferlin and calpain 3 in an autosomal recessive muscular dystrophy in Labrador retrievers
Authors: Olby, NJ Sharp, NJH Anderson, LVB Kunkel, LM Bonnemann, CG
Citation: Nj. Olby et al., Evaluation of the dystrophin-glycoprotein complex, alpha-actinin, dysferlin and calpain 3 in an autosomal recessive muscular dystrophy in Labrador retrievers, NEUROMUSC D, 11(1), 2001, pp. 41-49
Early and selective disappearance of telethonin protein from the sarcomerein neurogenic atrophy
Authors: Schroder, R Reimann, J Iakovenko, A Mues, A Bonnemann, CG Matten, J Gautel, M
Citation: R. Schroder et al., Early and selective disappearance of telethonin protein from the sarcomerein neurogenic atrophy, J MUSCLE R, 22(3), 2001, pp. 259-264
Disorders of the sarcoglycan complex (sarcoglycanopathies)
Authors: Bonnemann, CG
Citation: Cg. Bonnemann, Disorders of the sarcoglycan complex (sarcoglycanopathies), MG CLIN NEU, 18, 2000, pp. 26-43
A homozygous nonsense mutation in delta-sarcoglycan exon 3 in a case of LGMD2F
Authors: Dincer, P Bonnemann, CG Aker, OE Akcoren, Z Nigro, V Kunkel, LM Topaloglu, H
Citation: P. Dincer et al., A homozygous nonsense mutation in delta-sarcoglycan exon 3 in a case of LGMD2F, NEUROMUSC D, 10(4-5), 2000, pp. 247-250
Sarcoglycanopathies in Dutch patients with autosomal recessive limb girdlemuscular dystrophy
Authors: Ginjaar, HB van der Kooi, AJ Ceelie, H Kneppers, ALJ van Meegen, M Barth, PG Busch, HFM Wokke, JHJ Anderson, LVB Bonnemann, CG Jeanpierre, M Bolhuis, PA Moorman, AFM de Visser, M Bakker, E Von Ommen, GJB
Citation: Hb. Ginjaar et al., Sarcoglycanopathies in Dutch patients with autosomal recessive limb girdlemuscular dystrophy, J NEUROL, 247(7), 2000, pp. 524-529
Intrafamilial phenotypic variation in limb-girdle muscular dystrophy type 2C with compound heterozygous mutations
Authors: Takano, A Bonnemann, CG Honda, H Sakai, M Feener, CA Kunkel, LM Sobue, G
Citation: A. Takano et al., Intrafamilial phenotypic variation in limb-girdle muscular dystrophy type 2C with compound heterozygous mutations, MUSCLE NERV, 23(5), 2000, pp. 807-810
A mutation in the alpha 3 chain of type IX collagen causes autosomal dominant multiple epiphyseal dysplasia with mild myopathy
Authors: Bonnemann, CG Cox, GF Shapiro, F Wu, JJ Feener, CA Thompson, TG Anthony, DC Eyre, DR Darras, BT Kunkel, LM
Citation: Cg. Bonnemann et al., A mutation in the alpha 3 chain of type IX collagen causes autosomal dominant multiple epiphyseal dysplasia with mild myopathy, P NAS US, 97(3), 2000, pp. 1212-1217
Mutation detection in beta- and gamma-sarcoglycan (LGMD2E and LGMD2C)
Authors: Bonnemann, CG Kunkel, LM
Citation: Cg. Bonnemann et Lm. Kunkel, Mutation detection in beta- and gamma-sarcoglycan (LGMD2E and LGMD2C), METH MOL M, 43, 2000, pp. 227-255
Identification of FLRT1, FLRT2, and FLRT3: A novel family of transmembraneleucine-rich repeat proteins
Authors: Lacy, SE Bonnemann, CG Buzney, EA Kunkel, LM
Citation: Se. Lacy et al., Identification of FLRT1, FLRT2, and FLRT3: A novel family of transmembraneleucine-rich repeat proteins, GENOMICS, 62(3), 1999, pp. 417-426
Limb-girdle muscular dystrophies: An overview
Authors: Bonnemann, CG
Citation: Cg. Bonnemann, Limb-girdle muscular dystrophies: An overview, J CHILD NEU, 14(1), 1999, pp. 31-33
Molecular organization of sarcoglycan complex in mouse myotubes in culture
Authors: Chan, YM Bonnemann, CG Lidov, HGW Kunkel, LM
Citation: Ym. Chan et al., Molecular organization of sarcoglycan complex in mouse myotubes in culture, J CELL BIOL, 143(7), 1998, pp. 2033-2044
Risultati: 1-11 |