MARC 主機 00000cam  2200469Ia 4500 
001    ocn460883315 
003    OCoLC 
005    20110615082906.0 
006    m        d         
007    cr cn||||||||| 
008    091029s2009    paua    ob    001 0 eng d 
020    9780702038457 (electronic bk.) 
020    0702038458 (electronic bk.) 
020    |z9780750654104 
020    |z0750654104 
035    (OCoLC)460883315|z(OCoLC)489070993 
037    30124:30126|bElsevier Science & Technology|nhttp:// 
049    TEFA 
050 14 RC346.4|b.W37 2009 
060 14 2008 M-287 
060 14 WL 140|bW284p 2009 
082 04 616.8/0442|222 
245 00 Practical guide to neurogenetics|h[electronic resource] /
       |c[edited by] Thomas T. Warner, Simon R. Hammans 
260    Philadelphia :|bSaunders/Elsevier,|cc2009 
300    1 online resource (xiii, 330 p.) :|bill 
504    Includes bibliographical references and index 
505 0  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 
520    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 
590    Elsevier 
650  0 Nervous system|xDiseases|xGenetic aspects 
650  0 Neurogenetics 
650 12 Nervous System Diseases|xgenetics 
650 22 Genetics, Medical 
655  4 Electronic books 
700 1  Warner, Thomas T.,|d1963- 
700 1  Hammans, Simon R 
776 08 |iPrint version:|aWarner, Thomas T., 1963-|tPractical 
       guide to neurogenetics.|dPhiladelphia : Saunders/Elsevier,
       2009.|z9780750654104|z0750654104|w(DLC)  2008030067
856 40 |3ScienceDirect|u