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The molecular and genetic basis of neurological disease / edited by Roger N. Rosenberg ... [et al.].

Contributor(s): Publication details: Boston : Butterworth-Heinemann, c1997.Edition: 2nd editionDescription: xix, 1430 p. : ill. ; 29 cmISBN:
  • 0750696680
Subject(s): NLM classification:
  • WL 140 M718 1997
Contents:
Contents Part I : General topics 1. Molecular Genetics and Neurologic Disease: An Introduction; 2. A Neurologic Gene Map; 3. Finding and Excluding Gene Locations by Linkage Analysis; 4. Gene Targeting Part II : Chromosomes 5. Down Syndrome; 6. Fragile X Syndrome; Part III : Prions Part IV : Mitochondrial disorders Part V : Peroxisomes Part VI : Lysosomal disorders Part VII : Degenerative disorders Part VIII : Demyelinating disease of the central nervous system Part IX :Neuro-oncology Part X : Ion channel disorders Part XI : Epilepsy Part XII : Neuropathies and Neuronopathies Part XIII : Muscle Disorders Part XIV : The Phakomatoses: Disorders of skin and brain Part XV : lipoprotein disorders Part XVI: Carbohydrate disorders Part XVII: Amino acids Part XVIII: Purines Part XIX: Porphyrins Part XX: Metal Metabolism Part XXI: Vitamins Part XXII : psychiatric disease Part XXIII : Gene therapy and human genome
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Holdings
Item type Current library Call number Copy number Status Date due Barcode
Book Open Access Book Open Access Health Sciences Library WL 140 M718 1997 (Browse shelf(Opens below)) 1 Available MBAL22010760

Contents

Part I : General topics
1. Molecular Genetics and Neurologic Disease: An Introduction;
2. A Neurologic Gene Map;
3. Finding and Excluding Gene Locations by Linkage Analysis;
4. Gene Targeting

Part II : Chromosomes
5. Down Syndrome;
6. Fragile X Syndrome;

Part III : Prions
Part IV : Mitochondrial disorders
Part V : Peroxisomes
Part VI : Lysosomal disorders
Part VII : Degenerative disorders
Part VIII : Demyelinating disease of the central nervous system
Part IX :Neuro-oncology
Part X : Ion channel disorders
Part XI : Epilepsy
Part XII : Neuropathies and Neuronopathies
Part XIII : Muscle Disorders
Part XIV : The Phakomatoses: Disorders of skin and brain
Part XV : lipoprotein disorders
Part XVI: Carbohydrate disorders
Part XVII: Amino acids
Part XVIII: Purines
Part XIX: Porphyrins
Part XX: Metal Metabolism
Part XXI: Vitamins
Part XXII : psychiatric disease
Part XXIII : Gene therapy and human genome

Includes bibliographical references (p. 1386-1388) and index.

Contents

Part I : General topics
1. Molecular Genetics and Neurologic Disease: An Introduction;
2. A Neurologic Gene Map;
3. Finding and Excluding Gene Locations by Linkage Analysis;
4. Gene Targeting

Part II : Chromosomes
5. Down Syndrome;
6. Fragile X Syndrome;

Part III : Prions
Part IV : Mitochondrial disorders
Part V : Peroxisomes
Part VI : Lysosomal disorders
Part VII : Degenerative disorders
Part VIII : Demyelinating disease of the central nervous system
Part IX :Neuro-oncology
Part X : Ion channel disorders
Part XI : Epilepsy
Part XII : Neuropathies and Neuronopathies
Part XIII : Muscle Disorders
Part XIV : The Phakomatoses: Disorders of skin and brain
Part XV : lipoprotein disorders
Part XVI: Carbohydrate disorders
Part XVII: Amino acids
Part XVIII: Purines
Part XIX: Porphyrins
Part XX: Metal Metabolism
Part XXI: Vitamins
Part XXII : psychiatric disease
Part XXIII : Gene therapy and human genome

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