Vai al contenuto principale della pagina

Handbook of neurodevelopmental and genetic disorders in children [[electronic resource] /] / edited by Sam Goldstein, Cecil R. Reynolds



(Visualizza in formato marc)    (Visualizza in BIBFRAME)

Titolo: Handbook of neurodevelopmental and genetic disorders in children [[electronic resource] /] / edited by Sam Goldstein, Cecil R. Reynolds Visualizza cluster
Pubblicazione: New York, : Guilford Press, 2010
Edizione: 2nd ed.
Descrizione fisica: 1 online resource (621 p.)
Disciplina: 618.92/8588042
Soggetto topico: Developmental disabilities - Genetic aspects
Developmental neurobiology
Genetic disorders in children
Pediatric neuropsychology
Soggetto genere / forma: Electronic books.
Altri autori: GoldsteinSam <1952->  
ReynoldsCecil R. <1952->  
Note generali: Description based upon print version of record.
Nota di bibliografia: Includes bibliographical references and index.
Nota di contenuto: Cover; Copyright Page; Dedication; About the Editors; Contributors; Preface; Acknowledgments; Contents; PART I. BACKGROUND; 1. Introduction; 2. Neuropsychological Assessment in Genetically Linked Neurodevelopmental Disorders; 3. Neurodevelopmental Disorders and Medical Genetics: An Overview; 4. Neuroimaging and Genetic Disorders; 5. Integrative Developmental Neuropsychology: A General Systems and Social- Ecological Approach to the Neuropsychology of Children with Neurogenetic Disorders; PART II. DISORDERS PRIMARILY AFFECTING LEARNING AND BEHAVIOR; 6. Learning Disabilities
7. Attention-Deficit/Hyperactivity Disorder8. Oppositional, Conduct, and Aggressive Disorders; 9. Gilles de la Tourette Syndrome; 10. Anxiety Disorders; 11. Mood Disorders; 12. Autism Spectrum Disorders; PART III. DISORDERS WITH BROADER-SPECTRUM EFFECTS; 13. Turner Syndrome; 14. Fragile X Syndrome and Fragile X-Associated Disorders; 15. The Mucopolysaccharidoses; 16. Noonan Syndrome; 17. Neurofibromatosis Type 1; 18. Sickle Cell Disease; 19. Down Syndrome; 20. Klinefelter Syndrome; 21. Phenylketonuria; 22. Rett Syndrome: A Truly Pervasive Developmental Disorder
23. Lesch-Nyhan Syndrome: A Sex-Linked Inborn Error of Metabolism24. Seizure Disorders; 25. Prader-Willi Syndrome; 26. Disorders of Mitochondrial Metabolism; 27. Major Structural Anomalies of the Neocortex; 28. Spina Bifida Myelomeningocele; 29. Inborn Errors of Metabolism: A Brief Overview; Index; Color Plate; About Guilford Publications; From the Publisher; Back Cover
Sommario/riassunto: Recognized as the definitive reference in the field, this book addresses a broad range of biologically based disorders that affect children's learning and development. Leading authorities review the genetics of each disorder; its course and outcome; associated developmental, cognitive, and psychosocial challenges; and what clinicians and educators need to know about effective approaches to assessment and intervention. Coverage encompasses more frequently diagnosed learning and behavior problems with a genetic component as well as numerous lower-incidence neurodevelopmental disabilities. Ill
Titolo autorizzato: Handbook of neurodevelopmental and genetic disorders in children  Visualizza cluster
ISBN: 1-4625-0161-3
1-283-10895-X
9786613108951
1-60918-000-3
1-60918-001-1
Formato: Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione: Inglese
Record Nr.: 9910459477903321
Lo trovi qui: Univ. Federico II
Opac: Controlla la disponibilità qui