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School liaison program supporting children with neurofibromatosis type 1: a model of care for children with chronic disease.

08:00 EDT 26th October 2017 | BioPortfolio

Summary of "School liaison program supporting children with neurofibromatosis type 1: a model of care for children with chronic disease."

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Name: Genetics in medicine : official journal of the American College of Medical Genetics
ISSN: 1530-0366
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PubMed Articles [17874 Associated PubMed Articles listed on BioPortfolio]

First report of the efficacy of vestibular rehabilitation in improving function in patients with Neurofibromatosis type 2: an observational cohort study in a clinical setting.

Patients with Neurofibromatosis type 2 often experience debilitating neuro-otological problems which affect their mobility and balance. This study examined the efficacy of a personalised program of ve...

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Germline mutation of CHEK2 in neurofibromatosis 1 and 2: Two case reports.

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Amusia and its electrophysiological correlates in neurofibromatosis type 1.

Auditory processing deficits are common in people with neurofibromatosis type 1 (NF1) and they often report difficulties in musical performance.

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KEYS to Succeed: Cognitive and Academic Intervention Program for Children and Adolescents Surviving Cancer

The study will examine whether school liaison services and home-based parental tutoring can help with academic difficulties of paediatric brain tumour survivors who received cranial spinal...

Neurobiology and Treatment of Reading Disability in NF-1

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A Single Center Pilot Study to Assess the Intra-observer Reliability of Measuring Muscle Strength Using a Hand Held Dynamometer in Children and Adults With Neurofibromatosis Type 1 (NF1) and Type 2 (NF2)

Patients with clinically confirmed neurofibromatosis type 1 (NF1) or neurofibromatosis type 2 (NF2) or a known neurofibromatosis (NF) mutation aged 5 years and above will be eligible to pa...

Effects of Physical Training on Bone and Muscle Quality, Muscle Strength, and Motor Coordination in Children With NF1

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NF1-Attention: Study of Children With Neurofibromatosis Type 1 Treated by Methylphenidate

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Medical and Biotech [MESH] Definitions

Federal program, enacted in 1997, for the funding of children's health insurance coverage at the state level for low-income families, affording them effective protection against erosions in employer sponsored coverage.

A group of disorders characterized by an autosomal dominant pattern of inheritance with high rates of spontaneous mutation and multiple neurofibromas or neurilemmomas. NEUROFIBROMATOSIS 1 (generalized neurofibromatosis) accounts for approximately 95% of cases, although multiple additional subtypes (e.g., NEUROFIBROMATOSIS 2, neurofibromatosis 3, etc.) have been described. (From Neurochirurgie 1998 Nov;44(4):267-72)

The type species of ERYTHROVIRUS and the etiological agent of ERYTHEMA INFECTIOSUM, a disease most commonly seen in school-age children.

Facilities which provide care for pre-school and school-age children.

An individual intelligence test designed primarily for school children to predict school performance and the ability to adjust to everyday demands.

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Pediatrics
Pediatrics is the general medicine of childhood. Because of the developmental processes (psychological and physical) of childhood, the involvement of parents, and the social management of conditions at home and at school, pediatrics is a specialty. With ...


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