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Results: 1-25 |

Table of contents of journal:

Results: 25
Application of molecular methodologies in muscular dystrophies
Authors: Bushby, KMD Anderson, LVB
Citation: Kmd. Bushby et Lvb. Anderson, Application of molecular methodologies in muscular dystrophies, METH MOL M, 43, 2000, pp. 3-8
Clinical examination as a tool for diagnosis - Historical perspective
Authors: Gardner-Medwin, D
Citation: D. Gardner-medwin, Clinical examination as a tool for diagnosis - Historical perspective, METH MOL M, 43, 2000, pp. 9-13
Histopathological diagnosis of muscular dystrophies
Authors: Johnson, MA
Citation: Ma. Johnson, Histopathological diagnosis of muscular dystrophies, METH MOL M, 43, 2000, pp. 15-30
Serum creatine kinase in progressive muscular dystrophies
Authors: Zatz, M Vainzof, M Passos-Bueno, MR
Citation: M. Zatz et al., Serum creatine kinase in progressive muscular dystrophies, METH MOL M, 43, 2000, pp. 31-49
Deletion and duplication analysis in males affected with Duchenne or Becker muscular dystrophy
Authors: Curtis, A Haggerty, D
Citation: A. Curtis et D. Haggerty, Deletion and duplication analysis in males affected with Duchenne or Becker muscular dystrophy, METH MOL M, 43, 2000, pp. 53-84
Point mutation detection in the dystrophin gene
Authors: den Dunnen, JT
Citation: Jt. Den Dunnen, Point mutation detection in the dystrophin gene, METH MOL M, 43, 2000, pp. 85-109
DNA-based techniques for detection of carriers of Duchenne and Becker muscular dystrophy
Authors: Bakker, E
Citation: E. Bakker, DNA-based techniques for detection of carriers of Duchenne and Becker muscular dystrophy, METH MOL M, 43, 2000, pp. 111-135
Fluorescence in situ hybridization analysis for carrier detection in Duchenne/Becker muscular dystrophy
Authors: Dore, JK Kingston, HM
Citation: Jk. Dore et Hm. Kingston, Fluorescence in situ hybridization analysis for carrier detection in Duchenne/Becker muscular dystrophy, METH MOL M, 43, 2000, pp. 137-146
DNA-based prenatal diagnosis for Duchenne and Becker muscular dystrophy
Authors: Curtis, A Haggerty, D
Citation: A. Curtis et D. Haggerty, DNA-based prenatal diagnosis for Duchenne and Becker muscular dystrophy, METH MOL M, 43, 2000, pp. 147-171
Molecular diagnosis and genetic counseling of the manifesting carrier of Duchenne muscular dystrophy
Authors: Hoffman, EP Giron, J
Citation: Ep. Hoffman et J. Giron, Molecular diagnosis and genetic counseling of the manifesting carrier of Duchenne muscular dystrophy, METH MOL M, 43, 2000, pp. 173-188
Mutation analysis of X-linked Emery-Dreifuss muscular dystrophy gene
Authors: Toniolo, D
Citation: D. Toniolo, Mutation analysis of X-linked Emery-Dreifuss muscular dystrophy gene, METH MOL M, 43, 2000, pp. 189-196
Analysis of LAMA2 gene in merosin-deficient congenital dystrophy
Authors: Helbling-Leclerc, A Guicheney, P
Citation: A. Helbling-leclerc et P. Guicheney, Analysis of LAMA2 gene in merosin-deficient congenital dystrophy, METH MOL M, 43, 2000, pp. 199-218
alpha-sarcoglycan mutations
Authors: Piccolo, F de Toma, C Jeanpierre, M
Citation: F. Piccolo et al., alpha-sarcoglycan mutations, METH MOL M, 43, 2000, pp. 219-226
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
Mutation analysis in delta-sarcoglycan (LGMD2F)
Authors: Nigro, V
Citation: V. Nigro, Mutation analysis in delta-sarcoglycan (LGMD2F), METH MOL M, 43, 2000, pp. 257-272
Molecular diagnosis of calpainopathies - Methods used for defection of mutations in CAPN3 gene implicated in limb-girdle muscular dystrophy type 2A
Authors: Richard, I Beckmann, J
Citation: I. Richard et J. Beckmann, Molecular diagnosis of calpainopathies - Methods used for defection of mutations in CAPN3 gene implicated in limb-girdle muscular dystrophy type 2A, METH MOL M, 43, 2000, pp. 273-287
Molecular investigation of LGMD2B-haplotype analysis and mutation screening
Authors: Bashir, R Harrison, R Brown, RH
Citation: R. Bashir et al., Molecular investigation of LGMD2B-haplotype analysis and mutation screening, METH MOL M, 43, 2000, pp. 289-303
Molecular analysis of facioscapulohumeral muscular dystrophy (FSHD1)
Authors: van der Maarel, SM Bakker, E Frants, RA
Citation: Sm. Van Der Maarel et al., Molecular analysis of facioscapulohumeral muscular dystrophy (FSHD1), METH MOL M, 43, 2000, pp. 305-316
Analysis of protein expression in muscular dystrophies
Authors: Anderson, LVB
Citation: Lvb. Anderson, Analysis of protein expression in muscular dystrophies, METH MOL M, 43, 2000, pp. 319-324
Immunological reagents and amplification systems
Authors: Sewry, CA Lu, Q
Citation: Ca. Sewry et Q. Lu, Immunological reagents and amplification systems, METH MOL M, 43, 2000, pp. 325-338
Immunocytochemical analysis
Authors: Johnson, MA
Citation: Ma. Johnson, Immunocytochemical analysis, METH MOL M, 43, 2000, pp. 339-367
Multiplex Western blot analysis of muscular dystrophy proteins
Authors: Anderson, LVB
Citation: Lvb. Anderson, Multiplex Western blot analysis of muscular dystrophy proteins, METH MOL M, 43, 2000, pp. 369-386
Fetal muscle biopsy
Authors: Hoffman, EP Evans, M
Citation: Ep. Hoffman et M. Evans, Fetal muscle biopsy, METH MOL M, 43, 2000, pp. 387-391
Use of animal models to understand human muscular dystrophy
Authors: Rich, MM Balice-Gordon, RJ Reddy, S
Citation: Mm. Rich et al., Use of animal models to understand human muscular dystrophy, METH MOL M, 43, 2000, pp. 395-408
Options for development of gene-based therapy for muscular dystrophy
Authors: Dunckley, MG Dickson, G
Citation: Mg. Dunckley et G. Dickson, Options for development of gene-based therapy for muscular dystrophy, METH MOL M, 43, 2000, pp. 409-434
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