| Document Type
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BL
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| Record Number
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700296
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| Doc. No
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b522485
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| Title & Author
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Neurogenetics : : scientific and clinical advances /\ edited by David R. Lynch ; associate editor Jennifer M. Farmer
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| Publication Statement
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New York :: Taylor & Francis,, 2006
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| Series Statement
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Neurological disease and therapy ;
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| Page. NO
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xxi, 755 p. :: ill. ;; 26 cm
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| ISBN
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0824729420 (hardcover : alk. paper)
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: 9780824729424 (hardcover : alk. paper)
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| Bibliographies/Indexes
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Includes bibliographical references and index
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| Contents
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Friedreich ataxia / Martin B. Delatycki ... [et al.] -- Autosomal dominant ataxias / Susan L. Perlman -- Huntington's disease: mechanisms of pathogenesis and development of new therapies / Blair R. Leavitt and Lynn A. Raymond -- Wilson's disease / George J. Brewer -- Neurogenetics of dystonia and paroxysmal dyskinesias / Jennifer Friedman and David G. Standaert -- Inherited epilepsies / Yr Sigurdardottir and Annapurna Poduri -- Leukodystrophies / James Y. Garbern -- Lysosomal storage disorders / David A. Wenger and Stephanie Coppola -- The tuberous sclerosis complex: clinical manifestations and molecular genetics / John R. Pollard and Peter B. Crino -- Neurofibromatosis / Amit Malhotra, James Dowling, and David H. Gutmann -- Genetics of Parkinson's disease / Sathya R. Sriram, Valina L. Dawson, and Ted M. Dawson -- Alzheimer's disease / R. Scott Turner -- Tauopathies / John C. van Swieten -- Amyotrophic lateral sclerosis / Teepu Siddique and Lisa Dellefave -- Prion diseases / William S. Baek and James A. Mastrianni
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Neurogenetics in the clinic / Thomas D. Bird -- Genetic testing for neurological disorders / Martha A. Nance -- Genetic counseling / Robin L. Bennett -- Gene therapy for inherited diseases of the central nervous system / Tyler Mark Pierson and John H. Wolfe -- Ethical dilemmas in neurogenetics / Wendy R. Uhlmann -- Autosominal dominant Charcot-Marie-Tooth disease and related disorders / Craig L. Bennett -- Duchenne and Becker muscular dystrophies / Leta S. Steffen and Louis M. Kunkel -- The congenital and limb-girdle muscular dystrophies / Janbernd Kirschner and Carsten G. Bönnemann -- Non-dystrophic myotonias and periodic paralyses / Arie Struyk and Stephen Cannon -- The myotonic dystrophies - effets of an RNA mutation / John W. Day and Laura P.W. Ranum -- Spinal muscular atrophy / Stephen J. Kolb and J. Paul Taylor -- Hereditary spastic paraplegia / Kleopas A. Kleopa -- Mitochondrial disorders / Clotilde Lagier-Tourenne and Michio Hirano --
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| Subject
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Nervous system-- Diseases-- Genetic aspects
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| Subject
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Neurogenetics
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| Subject
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Nervous System Diseases-- genetics
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| Subject
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Genetics, Medical
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| Dewey Classification
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616.8/0442
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| LC Classification
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RC346.4.N484 2005
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| NLM classification
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W1NE33LD v.75 2006
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WL 140N49147 2006
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| Added Entry
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Lynch, David R., (David Robinson)
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