UID:
almahu_9948025841402882
Format:
1 online resource (571 p.)
ISBN:
1-283-60897-9
,
9786613921413
,
9786613921420
,
0-444-53506-3
Series Statement:
Handbook of clinical neurology ; 3rd ser., v. 108
Content:
Epilepsy, Part II, Treatment, Volume 108, provides a full description of epilepsy pathology and etiology, antiepileptic drug treatment, the approach to surgical evaluation and alternative procedures to be considered, in both children and adults, as well as brain stimulation and diet treatment. Economic and psychosocial issues such as stigma are fully covered. The special problems of epilepsy treatment in the developing world are described. Chapters are authored by internationally respected neurologists with varied perspectives insuring depth to the content. Epilepsy, Part I, 〈
Note:
Description based upon print version of record.
,
Front Cover; Epilepsy; Copyright; Handbook of Clinical Neurology 3RD Series; Foreword; Preface; Contributors; Contents of Part II; Contents of Part I; Section 3: Etiologies of Epilepsy; Chapter 30: Metabolic and degenerative disorders; Introduction; Epilepsy Features in Metabolic and Degenerative Disorders; Neonatal Seizures; Early Epilepsy With Burst-suppression; West Syndrome; Epilepsy With Generalized Seizures; Epilepsy With Focal Seizures; Epilepsia Partialis Continua; Progressive MyocloniC epilepsies; Lafora Body Disease; Unverricht-Lundborg Disease
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Action Myoclonus-renal Failure SyndromeMyoclonic Epilepsy With Ragged-red Fibers; Sialidosis; Gaucher Disease Type Iii; Rarer Causes of Progressive Myoclonic epilepsies; Diagnostic Workup and Differential Diagnosis; Metabolic Diseases More Frequently Associated With Epilepsy; Mitochondrial Diseases; Mitochondrial Encephalopathies With Epilepsy Associated With Mtdna Mutations (maternal Inheritance); Mitochondrial Encephalomyopathy, Lactic acidosis, and Stroke-like Episodes Syndrome; Neurogenic Muscle Weakness-ataxia-retinitis pigmentosa Syndrome; Kearn-Sayre Syndrome
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Myoclonic Epilepsy With Ragged-red FibersMitochondrial Encephalopathies With Epilepsy Associated With Nuclear Dna Mutations (mendelian Inheritance); Alpers Syndrome (Alpers-Huttenlocher Syndrome, Alpers Hepatopathic Poliodystrophy); Leigh Syndrome (subacute Necrotizing encephalomyelopathy); Coenzyme Q10 Deficiency; Lysosomal Diseases; Neuronal Ceroid Lipofuscinosis; Ncl1 (early Infantile Neuronal Ceroid lipofuscinosis); Ncl2 (late Infantile Neuronal Ceroid lipofuscinosis); Ncl3 (juvenile Neuronal Ceroid Lipofuscinosis); Ncl4 (adult Form, Kufs Disease)
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Ncl10 (congenital Neuronal Ceroid lipofuscinosis)Sphingolipidoses; Gangliosidosis; Krabbe Disease; Metachromatic Leukodystrophy; Mucopolysaccharidosis; Peroxisomal Disorders; Organic Acidurias; Aminoacidurias; Urea Cycle Disorders; Miscellaneous Disorders; Menkes Disease; Canavan Disease; Congenital Disorders of Glycosylation; Molybdenum Cofactor Deficiency; Acute Porphyrias; Metabolic Disease Amenable to Specific Treatment; Glucose Transporter Type 1 Deficiency Syndrome; Disorders of Vitamin B6 Metabolism; Pyridoxine-dependent Epilepsy; Pyridoxal Phosphate-dependent Epilepsy
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Infantile HypophosphatasiaHyperprolinemia Type Ii; Folinic Acid Responsive Seizures; Disorders of the Biotin Cycle; Biotinidase Deficiency; Deficit of Holocarboxylase Synthetase; Deficit of Creatine Metabolism; Developmental Delay, Epilepsy, Neonatal diabetes; Deficiency of Serine Biosynthesis.; Conclusion; Acknowledgments; Chapter 31: Neurocutaneous syndromes; Introduction; Neurofibromatosis Type 1; Dermatological Manifestations of Nf1; Neurofibromatosis Type 2; Tuberous Sclerosis; Dermatological Symptoms Of tuberous sclerosis; Other Organs Affected By Tuberous Sclerosis
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Sturge-weber Syndrome
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English
Additional Edition:
ISBN 0-444-52899-7
Language:
English
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