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Understanding Rett Syndrome

Understanding Rett Syndrome offers a concise, evidence-based introduction to Rett Syndrome (RTT), covering a range of topics from diagnosis;

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Rett Syndrome (RTT)

Rett syndrome, a rare genetic disease caused by mutations of the MECP2 gene, includes severe to profound developmental impairments;

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Rett Syndrome

Rett Syndrome is a severe neuro-developmental disorder characterised by losses in the areas of intellectual functioning, fine and gross;

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Rett Syndrome

Among the vast body of literature that has grown around Rett syndrome, this volume is the first to be aimed at both clinicians and;

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Pathways to Learning in Rett Syndrome

First Published in 1998. Parents and teachers of girls with Rett Syndrome will welcome this book which offers accessible advice on the;

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Rett Syndrome and Other Communication Disorders

Rett syndrome is a X-linked neurodevelopmental disorder that affects 1 in 10,000 females. It presents itself clinically with developmental;

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Creating Conditions

Based on original ethnographic research with scientists, clinicians and families, this book examines Rett syndrome to illuminate more;

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Creating Conditions: The making and remaking of a genetic syndrome

Based on original ethnographic research with scientists, clinicians and families, this book examines Rett syndrome to illuminate more;

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Pathways to Learning in Rett Sydrome

First Published in 1998. Parents and teachers of girls with Rett Syndrome will welcome this book which offers accessible advice on the;

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Medical Care

neurophysiotherapy, five girls with Rett syndrome were included in an experimental study to assess gross motor function before and after habilitation. Rett;

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Advances in Genetics Research

health. The authors go on to discuss Rett Syndrome, a rare, neurodevelopmental genetic disorder that develops in early childhood and influences;

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iPSCs for Modeling Central Nervous System Disorders, Volume 6

Sclerosis, Schizophrenia, Fragile X Syndrome, Spinal Muscular Atrophy, Rett Syndrome, Angelman syndrome, Parkinson`s Disease, Leber Hereditary Optic;

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Advances in Genetics Research

mediate particularly high TNBC risk by defective estrogen signaling; genotype-phenotype relationships in language processes in Rett syndrome;

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Het Rett handboek

Naslagwerk voor ouders en verzorgers van mensen met het Rett Syndroom. Auteur: Kathy Hunter. 319 pagina's over gezin, zorg, zintuigen;

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Induced Stem Cells

and Rett syndrome. In this book, the authors present current research in the study of induced stem cells, including the cryopreservation;

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Start Your Own Sole Proprietorship

, a portion of all sales go to research a cure for Rett Syndrome. Rett Syndrome affects a girl born every fifteen minutes. Boys born with the;

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Autism, Asperger Syndrome And Pervasive Developmental Disord

procedures involve. Associated disorders such as Rett Syndrome, Childhood Disintegrative Disorder and OCD are reviewed, and the authors describe the;

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Genetics and Genomics of Neurobehavioral Disorders

disorders (ATRX, Rett, and fragile X) and nonsyndromal disorders (FRAXE and MRX) are also discussed. An insightful introduction surveys the history;

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Advances in Medicine & Biology

; hydrogenases and nitrogenases as key enzymes in the production of H2 in the biological process; L-acetylcarnitine and Rett Syndrome; somatostatins and;

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Examination Paediatrics

> 5 new long cases, including hypopituitarism, neurofibromatosis type 1 and Rett syndrome 8 new short cases,

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Music Interventions for Neurodevelopmental Disorders

hyperactivity disorder), autism, and Rett syndrome. Rehabilitation interventions based on the use of music, termed music therapy , are relatively;

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Lipodystrophy Syndrome in HIV

The evolution ofdata about the HIV-Associated Lipodystrophy Syndrome has been rapid. The syndrome it;...

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