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Malformations of the nervous system /

'Malformations of the Nervous System' describes the advances which have occurred in clinical neurology and the neurosciences, their impact on the understanding of neurological disorders and on patient care.

Detalles Bibliográficos
Clasificación:Libro Electrónico
Otros Autores: Sarnat, Harvey B., Curatolo, Paolo
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Edinburgh ; New York : Elsevier, 2008.
Colección:Handbook of clinical neurology ; 3rd ser., v. 87.
Temas:
Acceso en línea:Texto completo
Texto completo
Texto completo

MARC

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245 0 0 |a Malformations of the nervous system /  |c volume editors, Harvey B. Sarnat and Paolo Curatolo. 
260 |a Edinburgh ;  |a New York :  |b Elsevier,  |c 2008. 
300 |a 1 online resource (xv, 644 pages, 28 unnumbered pages of plates) :  |b illustrations (some color) 
336 |a text  |b txt  |2 rdacontent 
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490 1 |a Handbook of clinical neurology ;  |v 3rd ser., v. 87 
504 |a Includes bibliographical references and index. 
588 0 |a Print version record. 
520 |a 'Malformations of the Nervous System' describes the advances which have occurred in clinical neurology and the neurosciences, their impact on the understanding of neurological disorders and on patient care. 
505 0 |a Front Cover; Malformations of the Nervous System; Copyright Page; Handbook of Clinical Neurology 3rd Series; Foreword; Preface; List of contributors; Contents; Section I: Specific malformations using the new integrative classification; Revised classification; Chapter 1: Axes and gradients of the neural tube for a morphological/molecular genetic classification of nervous system malformations; 1.1.1. Axes of the neural tube and gradients of genetic expression; 1.2. Upregulation/downregulation versus overexpression/underexpression; 1.3.1. Longitudinal axis 
505 8 |a 1.6. Scheme of classification of central nervous system malformations1.7. Conclusions; Midline hypoplasias; Chapter 2: Holoprosencephaly; 2.3.5. Newer classification schema; 2.4.2. Genetic causes; 2.4.4. Nodal/TGFbeta pathway; 2.4.5. Other gene mutations; 2.4.6. Genotype-phenotype correlation; 2.4.7. Environmental causes; 2.5.2. Midline dorsal cyst; 2.5.3. Cortical gyral abnormalities; 2.5.4. White matter abnormalities; 2.5.5. Other cerebral anomalies; 2.5.7. Middle interhemispheric variant; 2.5.8. Neuroimaging technical approaches; 2.5.9. Fetal neuroimaging; 2.7. Clinical manifestations 
505 8 |a 2.7.1. Craniofacial anomalies2.7.2. Developmental dysfunction and behavior; 2.7.3. Seizures and epilepsy; 2.7.4. Endocrinopathies; 2.7.5. Temperature dysregulation; 2.7.6. Microcephaly; 2.7.7. Dorsal cyst and hydrocephalus; 2.7.8. Motor dysfunction; 2.8. Conclusion; Chapter 3: Septo-optic-pituitary dysplasia; 3.4.2. The identification of relevant cerebral anomalies; Chapter 4: Rhombencephalosynapsis; 4.3. The confines of rhombencephalosynapsis defined by neuroimaging; 4.4.6. Holoprosencephaly; 4.4.8. Neocortical dysplasia; 4.7. Inherited disorders 
505 8 |a Chapter 5: Embryology and malformations of the forebrain commissures5.7. Genetics of callosal agenesis; 5.9.4. Hemimegalencephaly; 5.9.8. Association of callosal agenesis with metabolic diseases; Disorders of segmentation of the neural tube; Chapter 6: Disorders of segmentation of the neural tube: Chiari malformations; 6.3.3. Hydromyelia and aqueductal atresia in Chiari malformations; 6.7. Historical note; Chapter 7: Disorders of segmentation of the neural tube: agenesis of selective neuromeres; 7.3. Agenesis of isolated neuromeres; Chapter 8: Cerebellar hypoplasias 
505 8 |a 8.1.6. Classification of cerebellar malformations8.4.2. Cerebello-oculo-renal and related syndromes; Hamartomatous disorders of cellular lineage; Chapter 9: Tuberous sclerosis; 9.3. Molecular genetics; 9.4.3. Genotype/phenotype correlations; 9.6.4. Lungs; 9.7. Treatment; Chapter 10: Hemimegalencephaly syndrome; 10.3. Pathogenesis of neurocutaneous syndromes; 10.3.1. Classification; 10.7. Associated hemimegalencephaly; 10.7.1. With neurocutaneous syndromes; 10.8.1. Imaging features; References; Disorders of radial neuroblast migration and cerebral cortical architecture 
546 |a English. 
650 0 |a Nervous system  |x Abnormalities. 
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650 2 2 |a Nervous System  |x embryology  |0 (DNLM)D009420Q000196 
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650 7 |a Nervensystem  |2 gnd  |0 (DE-588)4041643-4 
650 1 7 |a Centraal zenuwstelsel.  |2 gtt 
650 1 7 |a Afwijkingen.  |2 gtt 
700 1 |a Sarnat, Harvey B. 
700 1 |a Curatolo, Paolo. 
776 0 8 |i Print version:  |t Malformations of the nervous system.  |d Edinburgh ; New York : Elsevier, 2008  |z 9780444518965  |z 0444518967  |w (OCoLC)176806306 
830 0 |a Handbook of clinical neurology ;  |v 3rd ser., v. 87.  |x 0072-9752 
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856 4 0 |u https://sciencedirect.uam.elogim.com/science/handbooks/00729752/87  |z Texto completo 
856 4 0 |u https://sciencedirect.uam.elogim.com/science/publication?issn=00729752&volume=87  |z Texto completo