Handbook of Neurodevelopmental and Genetic Disorders in Children, 2/e
Guilford Publications (Verlag)
978-1-57230-448-2 (ISBN)
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This important Handbook presents the latest research and practical knowledge about a broad range of disorders with a genetic component that affect children's learning, behavior, and development. The book demonstrates the difference that well-planned interventions and accommodations can make in the health and functioning of children with mild to severe neurodevelopmental impairment. Chapters offer in-depth discussions of specific disorders, including learning disabilities, ADHD, Tourerette syndrome, anxiety disorders, pervasive developmental disorders, and numerous less frequently encountered conditions. Current research on etiologies is reviewed, neurodevelopmental, psychosocial, and medical implications are considered, and practical suggestions are provided for assessment and clinical management.
Sam Goldstein, PhD, Neurology, Learning and Behavior Center, University of Utah Cecil R. Reynolds, PhD, Department of Educational Psychology, Texas A&M University
Part I: Basic Principles and Applications. Goldstein, Reynolds, Neurodevelopmental and Genetic Disorders in Children: An Introduction. Reynolds, Mayfield, Neuropsychological Assessment in Genetically Linked Neurodevelopmental Disorders. Carey, McMahon, Neurobehavioral Disorders and Medical Genetics: An Overview. Bigler, Nielsen, Wilde, Bartholomew, Brooks, Bradford, Neuroimaging and Genetic Disorders. Whelan, 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.Ingalls, Goldstein, Learning Disabilities. Goldstein, Attention-deficit/Hyperactivity Disorder. Brown, Ivers, Gilles de la Tourette Syndrome. Pliszka, Olvera, Anxiety Disorders. Klin, Volkmar, Autism and Other Pervasive Developmental Disorders. Part III: Disorders with Broader-Spectrum Effects.Powell, Schulte, Turner Syndrome. Hagerman, Lampe, Fragile X Syndrome. M.B. Brown, The Mucopolysaccharidoses. Teeter, Noonan Syndrome. Nilsson, Bradford, Neurofibromatosis. Smith, Sickle Cell Disease. Cody, Kamphaus, Down Syndrome. Cody, Hynd, Klinefelter Syndrome. Waisbren, Phenylketonuria. Brown, Hoadley, Rett Syndrome. Morales, Lesch-Nyhan Syndrome. Bennett, Ho-Turner, Seizure Disorders. Dykens, Cassidy, Prader-Willi Syndrome. Morris, Mervis, Williams Syndrome.
| Erscheint lt. Verlag | 5.8.1999 |
|---|---|
| Verlagsort | New York |
| Sprache | englisch |
| Gewicht | 1238 g |
| Themenwelt | Schulbuch / Wörterbuch ► Lexikon / Chroniken |
| Geisteswissenschaften ► Psychologie ► Biopsychologie / Neurowissenschaften | |
| Geisteswissenschaften ► Psychologie ► Entwicklungspsychologie | |
| Medizin / Pharmazie ► Medizinische Fachgebiete ► Pädiatrie | |
| Studium ► 2. Studienabschnitt (Klinik) ► Humangenetik | |
| ISBN-10 | 1-57230-448-0 / 1572304480 |
| ISBN-13 | 978-1-57230-448-2 / 9781572304482 |
| Zustand | Neuware |
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