Vai al contenuto principale della pagina
Titolo: | Handbook of neurodevelopmental and genetic disorders in children [[electronic resource] /] / edited by Sam Goldstein, Cecil R. Reynolds |
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 |
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 |