Myotonic dystrophy is the most common of the inherited muscular dystrophies and has a profound and troubling effect on individuals who are diagnosed with it. This book explains in simple terms exactly what the condition is, what the symptoms are, how they can develop, and new approaches to therapy and management of the condition.
Myotonic dystrophy is the most common of the inherited muscular dystrophies and has a profound and troubling effect on individuals who are diagnosed with it. This book explains in simple terms exactly what the condition is, what the symptoms are, how they can develop, and new approaches to therapy and management of the condition.Hinweis: Dieser Artikel kann nur an eine deutsche Lieferadresse ausgeliefert werden.
Peter Harper is a University Research Professor in Human Genetics at Cardiff University, Wales. He is a member of the UK's Advisory Committee on Genetic Testing, and has a long-standing research interest in inherited neurological disorders, especially Huntington disease and Myotonic dystrophy.
Inhaltsangabe
1: What is Myotonic dystrophy? 2: Muscle symptoms and Myotonic dystrophy 3: Looking ahead 4: Not just a muscle disease 5: Children with Myotonic dystrophy 6: 'Type 2' Myotonic dystrophy 7: Family aspects and genetic risks 8: Advances in research 9: Support and information 10: Management and treatment now 11: The future-towards effective prevention and cure for Myotonic dystrophy 12: Conclusion Appendices Bibliography Index
1: What is Myotonic dystrophy? 2: Muscle symptoms and Myotonic dystrophy 3: Looking ahead 4: Not just a muscle disease 5: Children with Myotonic dystrophy 6: 'Type 2' Myotonic dystrophy 7: Family aspects and genetic risks 8: Advances in research 9: Support and information 10: Management and treatment now 11: The future-towards effective prevention and cure for Myotonic dystrophy 12: Conclusion Appendices Bibliography Index
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