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Practical guide to neurogenetics
~
Warner, Thomas T., (1963-)
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Practical guide to neurogenetics
Record Type:
Electronic resources : Monograph/item
Title/Author:
Practical guide to neurogenetics/ [edited by] Thomas T. Warner, Simon R. Hammans.{me_controlnum}
other author:
Warner, Thomas T.,
Published:
Philadelphia :Saunders/Elsevier, : c2009.,
Description:
1 online resource (xiii, 330 p.) :ill.
[NT 15003449]:
DNA, genes, and mutations / Thomas T. Warner -- Genetic advice and testing : basics of inheritance, counseling, and rationale for testing / Diana M. Eccles -- Dementia / Thomas T. Warner -- Epilepsy / Simon R. Hammans -- Disorders of vision / Andrea H. Nemeth and Susan M. Downes -- Cerebellar and spinocerebellar disorders / Simon R. Hammans -- Disorders of myelin : multiple sclerosis and leukodystrophies / Simon R. Hammans -- Movement disorders / Thomas T. Warner -- Cerebrovascular disease / Thomas T. Warner -- Motor neuron diseases / Thomas T. Warner -- Neuropathies / Simon R. Hammans -- Muscle disease / Simon R. Hammans -- Muscle channelopathies and metabolic myopathies / Simon R. Hammans -- Mitochondrial disease / Simon R. Hammans -- Tumor predisposition syndromes : VHL, NF1 and NF2, tuberous sclerosis, and malignant CNS tumors / Diana M. Eccles -- Metabolic and degenerative disorders of childhood / Lucinda Carr -- Neurological aspects of chromosomal disorders / Andrea H. Nemeth.
Subject:
Nervous system - Diseases -
Online resource:
http://www.sciencedirect.com/science/book/9780750654104An electronic book accessible through the World Wide Web; click for information
ISBN:
9780702038457 (electronic bk.)
Practical guide to neurogenetics
Practical guide to neurogenetics
[electronic resource] /[edited by] Thomas T. Warner, Simon R. Hammans.{me_controlnum} - Philadelphia :Saunders/Elsevier,c2009. - 1 online resource (xiii, 330 p.) :ill.
Includes bibliographical references and index.
DNA, genes, and mutations / Thomas T. Warner -- Genetic advice and testing : basics of inheritance, counseling, and rationale for testing / Diana M. Eccles -- Dementia / Thomas T. Warner -- Epilepsy / Simon R. Hammans -- Disorders of vision / Andrea H. Nemeth and Susan M. Downes -- Cerebellar and spinocerebellar disorders / Simon R. Hammans -- Disorders of myelin : multiple sclerosis and leukodystrophies / Simon R. Hammans -- Movement disorders / Thomas T. Warner -- Cerebrovascular disease / Thomas T. Warner -- Motor neuron diseases / Thomas T. Warner -- Neuropathies / Simon R. Hammans -- Muscle disease / Simon R. Hammans -- Muscle channelopathies and metabolic myopathies / Simon R. Hammans -- Mitochondrial disease / Simon R. Hammans -- Tumor predisposition syndromes : VHL, NF1 and NF2, tuberous sclerosis, and malignant CNS tumors / Diana M. Eccles -- Metabolic and degenerative disorders of childhood / Lucinda Carr -- Neurological aspects of chromosomal disorders / Andrea H. Nemeth.
This simple guide to neurogenetics demystifies the overwhelming amount of information on the subject so you can identify key clinical features and understand your management options. Reach relevant differential diagnoses and provide appropriate counseling to your patients using the symptom-based approach. By integrating genetic and neurological approaches to diagnoses, this book ensures that the neurological consequences of a genetic diagnosis and the genetic consequences of a neurological diagnosis are clear and explicit. Concise and portable, this book is ideal for easy reference in clinical use. Details the underlying basic science and clinical features of genetic disorders by taking a symptom-based approach to provide you with a comprehensive understanding of the field. Focuses on the clinical application of neurogenetics to be of practical use to you in the clinic. Clarifies the neurological consequences of a genetic diagnosis and the genetic consequences of a neurological diagnosis by integrating genetic and neurological approaches to diagnoses. Discusses and evaluates necessary investigations so you know when to use them and when to refer. Highlights diagnostic and therapeutic tips so you can learn new concepts or refine your skills in practice. Refers to online sources, such as Online Mendelian Inheritance in Man (OMIM) and others, to help you supplement your knowledge.
ISBN: 9780702038457 (electronic bk.)
Source: 30124:30126Elsevier Science & Technologyhttp://www.sciencedirect.comSubjects--Topical Terms:
682330
Nervous system
--DiseasesIndex Terms--Genre/Form:
542853
Electronic books.
LC Class. No.: RC346.4 / .W37 2009
Dewey Class. No.: 616.8/0442
National Library of Medicine Call No.: 2008 M-287
Practical guide to neurogenetics
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DNA, genes, and mutations / Thomas T. Warner -- Genetic advice and testing : basics of inheritance, counseling, and rationale for testing / Diana M. Eccles -- Dementia / Thomas T. Warner -- Epilepsy / Simon R. Hammans -- Disorders of vision / Andrea H. Nemeth and Susan M. Downes -- Cerebellar and spinocerebellar disorders / Simon R. Hammans -- Disorders of myelin : multiple sclerosis and leukodystrophies / Simon R. Hammans -- Movement disorders / Thomas T. Warner -- Cerebrovascular disease / Thomas T. Warner -- Motor neuron diseases / Thomas T. Warner -- Neuropathies / Simon R. Hammans -- Muscle disease / Simon R. Hammans -- Muscle channelopathies and metabolic myopathies / Simon R. Hammans -- Mitochondrial disease / Simon R. Hammans -- Tumor predisposition syndromes : VHL, NF1 and NF2, tuberous sclerosis, and malignant CNS tumors / Diana M. Eccles -- Metabolic and degenerative disorders of childhood / Lucinda Carr -- Neurological aspects of chromosomal disorders / Andrea H. Nemeth.
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This simple guide to neurogenetics demystifies the overwhelming amount of information on the subject so you can identify key clinical features and understand your management options. Reach relevant differential diagnoses and provide appropriate counseling to your patients using the symptom-based approach. By integrating genetic and neurological approaches to diagnoses, this book ensures that the neurological consequences of a genetic diagnosis and the genetic consequences of a neurological diagnosis are clear and explicit. Concise and portable, this book is ideal for easy reference in clinical use. Details the underlying basic science and clinical features of genetic disorders by taking a symptom-based approach to provide you with a comprehensive understanding of the field. Focuses on the clinical application of neurogenetics to be of practical use to you in the clinic. Clarifies the neurological consequences of a genetic diagnosis and the genetic consequences of a neurological diagnosis by integrating genetic and neurological approaches to diagnoses. Discusses and evaluates necessary investigations so you know when to use them and when to refer. Highlights diagnostic and therapeutic tips so you can learn new concepts or refine your skills in practice. Refers to online sources, such as Online Mendelian Inheritance in Man (OMIM) and others, to help you supplement your knowledge.
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An electronic book accessible through the World Wide Web; click for information
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TEF
based on 0 review(s)
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W9134776
電子資源
11.線上閱覽_V
電子書
EB RC346.4 .W37 2009
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