Handbook of neurodevelopmental and genetic disorders in children [[electronic resource] /] / edited by Sam Goldstein, Cecil R. Reynolds |
Edizione | [2nd ed.] |
Pubbl/distr/stampa | New York, : Guilford Press, 2010 |
Descrizione fisica | 1 online resource (621 p.) |
Disciplina | 618.92/8588042 |
Altri autori (Persone) |
GoldsteinSam <1952->
ReynoldsCecil R. <1952-> |
Soggetto topico |
Developmental disabilities - Genetic aspects
Developmental neurobiology Genetic disorders in children Pediatric neuropsychology |
Soggetto genere / forma | Electronic books. |
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 | eng |
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 |
Record Nr. | UNINA-9910459477903321 |
New York, : Guilford Press, 2010 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|
Handbook of neurodevelopmental and genetic disorders in children [[electronic resource] /] / edited by Sam Goldstein, Cecil R. Reynolds |
Edizione | [2nd ed.] |
Pubbl/distr/stampa | New York, : Guilford Press, 2010 |
Descrizione fisica | 1 online resource (621 p.) |
Disciplina | 618.92/8588042 |
Altri autori (Persone) |
GoldsteinSam <1952->
ReynoldsCecil R. <1952-> |
Soggetto topico |
Developmental disabilities - Genetic aspects
Developmental neurobiology Genetic disorders in children Pediatric neuropsychology |
Soggetto genere / forma | Electronic books. |
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 | eng |
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 |
Record Nr. | UNINA-9910532682003321 |
New York, : Guilford Press, 2010 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
|