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Home > Muscular Dystrophy: Methods and Protocols > Use of Animal Models to Understand Human Muscular Dystrophy
Muscular Dystrophy: Methods and Protocols |
Katharine M.D. Bushby; Louise V.B. Anderson
Humana Press
Muscular Dystrophy: Methods and Protocols
Use of Animal Models to Understand Human Muscular Dystrophy
Authors

Mark M. Rich; Rita J. Balice-Gordon; Sita Reddy

ARI Id

1674219685169_2311214

Access

Open/Free Access

Pages

395-408

DOI

10.1385/1-59259-138-8:395

Chapter URL

https://rd.springer.com/protocol/10.1385/1-59259-138-8:395

Table of Contents of Book
Showing 1 to 20 of 30 entries
Chapters/HeadingsAuthor(s)PagesInfo
Front Matter
i-xii
Front Matter
1-1
Application of Molecular Methodologies in Muscular Dystrophies
Katharine M. D. Bushby; Louise V. B. Anderson
3-8
Clinical Examination as a Tool for Diagnosis
David Gardner-Medwin
9-13
Histopathological Diagnosis of Muscular Dystrophies
Margaret A. Johnson
15-30
Serum Creatine Kinase in Progressive Muscular Dystrophies
Mayana Zatz; Mariz Vainzof; Maria Rita Passos-Bueno
31-49
Front Matter
51-51
Deletion and Duplication Analysis in Males Affected with Duchenne or Becker Muscular Dystrophy
Ann Curtis; Daisy Haggerty
53-84
Point Mutation Detection in the Dystrophin Gene
Johan T. den Dunnen
85-109
DNA-Based Techniques for Detection of Carriers of Duchenne and Becker Muscular Dystrophy
Egbert Bakker
111-135
Fluorescence In Situ Hybridization Analysis for Carrier Detection in Duchenne/Becker Muscular Dystrophy
Jonathan K. Dore; Helen M. Kingston
137-146
DNA- Based Prenatal Diagnosis for Duchenne and Becker Muscular Dystrophy
Ann Curtis; Daisy Haggerty
147-171
Molecular Diagnosis and Genetic Counseling of the Manifesting Carrier of Duchenne Muscular Dystrophy
Eric P. Hoffman; James Giron
173-188
Mutation Analysis of X-Linked Emery-Dreifuss Muscular Dystrophy Gene
Daniela Toniolo
189-196
Analysis of LAMA2 Gene in Merosin- Deficient Congenital Dystrophy
Anne Helbling-Leclerc; Pascale Guicheney
199-218
α-Sarcoglycan Mutations
Frederica Piccolo; C. de Toma; Marc Jeanpierre
219-226
Mutation Detection in β- and γ-Sarcoglycan (LGMD2E and LGMD2C)
Carsten G. Bönnemann; Louis M. Kunkel
227-255
Mutation Analysis in δ-Sarcoglycan (LGMD2F)
Vincenzo Nigro
257-272
Molecular Diagnosis of Calpainopathies
Isabelle Richard; Jacques Beckmann
273-287
Molecular Investigation of LGMD2B-Haplotype Analysis and Mutation Screening
Rumaisa Bashir; Ruth Harrison; Robert H. Brown Jr.
289-303
Chapters/HeadingsAuthor(s)PagesInfo
Showing 1 to 20 of 30 entries
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