Download PDF BookSyndrome of Nonverbal Learning Disabilities Neurodevelopmental Manifestations

Download Syndrome of Nonverbal Learning Disabilities Neurodevelopmental Manifestations



Download Syndrome of Nonverbal Learning Disabilities Neurodevelopmental Manifestations

Download Syndrome of Nonverbal Learning Disabilities Neurodevelopmental Manifestations

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Published on: 1995-06-23
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Original language: English
Download Syndrome of Nonverbal Learning Disabilities Neurodevelopmental Manifestations

The syndrome of nonverbal learning disabilities (NLD) is a subtype of learning disabilities whose neuropsychological assets and deficits have predictable academic and psychosocial outcomes. Developed by Byron P. Rourke and elucidated in his previous work, the "white matter model" was designed to encompass the complex manifestations and neurophysiological underpinnings of the NLD syndrome. Now, for the first time, evidence that bears upon the white matter model has been gathered into a single volume. Building upon Rourke's previous work on NLD, Syndrome of Nonverbal Learning Disabilities: Neurodevelopmental Manifestations, further explores the ramifications of NLD in the neuropsychology of learning disabilities and in pediatric neurological disease, disorder, and dysfunction.Following an overview of the white matter model, chapters cover a wide range of pediatric neurological diseases and disorders through which the model is examined with particular attention to its neurophysiological aspects. The diseases and disorders discussed include callosal agenesis, Asperger syndrome, velocardiofacial syndrome, Williams syndrome, de Lange syndrome, early hydrocephalus, Sotos syndrome, congenital hypothyroidism, acute lymphocytic leukemia, metachromatic leukodystrophy, Turner syndrome, fetal alcohol syndrome, multiple sclerosis, traumatic brain injury, and toxicant-induced encephalopathy. Dimensions relevant to both assessment and treatment are raised throughout the work, as are suggestions for future research.Recommended for neuropsychologists, neurologists, psychologists, psychiatrists, and pediatricians treating children with learning disabilities or with pediatric neurological disease, disorder, and dysfunction, Syndrome of Nonverbal Learning Disabilities serves both as an authoritative update on recent advances and as a text for advanced courses in child/developmental neuropsychology, pediatric neurology, and learning disabilities. Autism Spectrum Disorder: References - ASHA Abrahams B. S. & Geschwind D. H. (2010). Connecting genes to brain in the autism spectrum disorders. Archives of Neurology 67(4) 395399. OMIM Entry - 608636 - CHROMOSOME 15q11-q13 DUPLICATION ... 608636 - chromosome 15q11-q13 duplication syndrome - duplication 15q11-q13 syndrome - autism susceptibility to 4 ... Autism - Wikipedia Autism is a highly variable neurodevelopmental disorder that first appears during infancy or childhood and generally follows a steady course without remission ... Identifying Infants and Young Children With Developmental ... Identifying Infants and Young Children With Developmental Disorders in the Medical Home: An Algorithm for Developmental Surveillance and Screening OMIM Entry - 192430 - VELOCARDIOFACIAL SYNDROME VCFS is the most common syndrome that has palatal anomalies as a major feature. A possible strategy for early detection of VCFS is the routine screening for 22q11 ... Health Care Guidelines for People with Down Syndrome with Down Syndrome: Reprinted from Down Syndrome Quarterly Volume 4 Number 3 September 1999: Edited by William I. Cohen M.D. for the Down Syndrome Medical ... Syndrome d'Asperger Wikipdia Le syndrome d'Asperger (prononc / a s p g /) est un trouble du spectre autistique ou trouble envahissant du dveloppement qui se caractrise comme ... Identification and Evaluation of Children With Autism ... INTRODUCTION. Public and physician awareness of autism has increased markedly in the new millennium because of increased media coverage and a rapidly expanding body ... Microdeletions and molecular genetics : from clinical ... ABSTRACT. Microdeletions are often characterised by a complex clinical and behavioural phenotype resulting from the imbalance of normal dosage of genes located in ... Guidelines for Assessment of and Intervention with Persons ... These guidelines were developed by the APA Task Force on Guidelines for Assessment and Treatment of Persons with Disabilities 1. The task force members included Kurt ...
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