Handbook of Neurodevelopmental and Genetic Disorders in Children
Guilford Publications (Verlag)
978-1-60623-990-2 (ISBN)
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Sam Goldstein, PhD, is Assistant Clinical Instructor in the Department of Psychiatry at the University of Utah School of Medicine and Affiliate Research Professor of Psychology at George Mason University. As a neuropsychologist, he specializes in child development, school psychology, and traumatic brain injuries. Dr. Goldstein is also Clinical Director of the Neurology, Learning, and Behavior Center in Salt Lake City, where he provides assessment, case management, and treatment for individuals experiencing diverse neuropsychological impairments throughout the lifespan. He holds Fellow and Diplomate status in organizations spanning many disciplines. Dr. Goldstein is Editor-in-Chief of the Journal of Attention Disorders and serves on the editorial boards of six journals. He is an author or editor of over 30 books and an author of over 100 scholarly publications. Cecil R. Reynolds, PhD, is Emeritus Professor of Educational Psychology, Professor of Neuroscience, and Distinguished Research Scholar at Texas A&M University. He is an author of over 300 scholarly publications; an author or editor of over 50 books; and a creator of numerous widely used psychological tests of behavior, cognition, and personality. Dr. Reynolds maintained a clinical practice treating trauma victims and individuals with traumatic brain injury for 25 years before retiring from clinical work. He is past president of the National Academy of Neuropsychology (NAN) and the American Psychological Association (APA) Divisions of Evaluation, Measurement, and Statistics; Clinical Neuropsychology; and School Psychology. He serves on the editorial boards of 11 journals. Dr. Reynolds has been an editor or associate editor of several journals, and is currently editor-in-chief of Psychological Assessment. Dr. Reynolds has received numerous awards from NAN, APA, and other organizations.
I. Background _x000D_ 1. Introduction, Sam Goldstein and Cecil R. Reynolds _x000D_ 2. Neuropsychological Assessment in Genetically Linked Neurodevelopmental Disorders, Cecil R. Reynolds and Joan W. Mayfield _x000D_ 3. Neurodevelopmental Disorders and Medical Genetics: An Overview, Bonnie J. Baty, John C. Carey, and William M. McMahon _x000D_ 4. Neuroimaging and Genetic Disorders, Shelli R. Kesler, Elizabeth Wilde, Jennifer L. Bruno, and Erin D. Bigler _x000D_ 5. Integrative Developmental Neuropsychology: A General Systems and Social-Ecological Approach to the Neuropsychology of Children with Neurogenetic Disorders, Timothy B. Whelan and Melissa J. Mathews _x000D_ II. Disorders Primarily Affecting Learning and Behavior _x000D_ 6. Learning Disabilities, Sam Goldstein, Adam Schwebach, and Sean Cunningham _x000D_ 7. Attention-Deficit/Hyperactivity Disorder, Sam Goldstein _x000D_ 8. Oppositional, Conduct, and Aggressive Disorders, Lisa L. Weyandt, Genevieve Verdi, and Anthony Swentosky _x000D_ 9. Gilles de la Tourette Syndrome, Alicia Hughes, Brian P. Daly, and Ronald T. Brown _x000D_ 10. Anxiety Disorders, Steven R. Pliszka _x000D_ 11. Mood Disorders, Susan Swearer, Cixin Wang, Jami Givens, Brandi Berry, and Dawn Reinemann _x000D_ 12. Autism Spectrum Disorders, Blythe Corbett and Joan Gunther _x000D_ III. Disorders with Broader-Spectrum Effects _x000D_ 13. Turner Syndrome, M. Paige Powell and Timothy Schulte _x000D_ 14. Fragile X Syndrome and Fragile X-Associated Disorders, Randi J. Hagerman _x000D_ 15. The Mucopolysaccharidoses, Michael B. Brown _x000D_ 16. Noonan Syndrome, Phyllis Anne Teeter Ellison _x000D_ 17. Neurofibromatosis Type 1, Jonathan M. Payne and Kathryn N. North _x000D_ 18. Sickle Cell Disease, Julien T. Smith and David A. Baker _x000D_ 19. Down Syndrome, Heather C. Hazlett, Julie Hammer, Stephen R. Hooper, and Randy W. Kamphaus _x000D_ 20. Klinefelter Syndrome, Heather C. Hazlett, Mario Gaspar De Alba, and Stephen R. Hooper _x000D_ 21. Phenylketonuria, Susan E. Waisbren _x000D_ 22. Rett Syndrome: A Truly Pervasive Developmental Disorder, Robert T. Brown and Kathleen K. McMillan _x000D_ 23. Lesch–Nyhan Syndrome: A Sex-Linked Inborn Error of Metabolism, David L. Wodrich and Lori A. Long _x000D_ 24. Seizure Disorders, Thomas L. Bennett, Deana B. Davalos, Maile Ho-Turner, and Barbara C. Banz _x000D_ 25. Prader–Willi Syndrome, Elisabeth M. Dykens, Suzanne B. Cassidy, and Melissa L. DeVries _x000D_ 26. Disorders of Mitochrondrial Metabolism, Russell P. Saneto _x000D_ 27. Major Structural Anomalies of the Neocortex, Nancy L. Nussbaum, Gina B. Christopher, and Valerie Van Horn Kerne _x000D_
28. Spina Bifida Myelomeningocele, Angela Giacoletti Argento, Seth A. Warschausky, Laura Shank, and Joseph E. Hornyak 29. Inborn Errors of Metabolism: A Brief Overview, Robert T. Brown
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Erscheint lt. Verlag | 17.12.2010 |
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Verlagsort | New York |
Sprache | englisch |
Maße | 178 x 254 mm |
Gewicht | 1294 g |
Themenwelt | Schulbuch / Wörterbuch ► Lexikon / Chroniken |
Geisteswissenschaften ► Psychologie ► Biopsychologie / Neurowissenschaften | |
Geisteswissenschaften ► Psychologie ► Entwicklungspsychologie | |
Geisteswissenschaften ► Psychologie ► Test in der Psychologie | |
Medizin / Pharmazie ► Medizinische Fachgebiete ► Neurologie | |
Medizin / Pharmazie ► Medizinische Fachgebiete ► Pädiatrie | |
Studium ► 2. Studienabschnitt (Klinik) ► Humangenetik | |
ISBN-10 | 1-60623-990-2 / 1606239902 |
ISBN-13 | 978-1-60623-990-2 / 9781606239902 |
Zustand | Neuware |
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