Learning disabilities in neuromuscular disorders: a springboard for adult life

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Duchenne and Becker muscular dystrophy in adolescents: current perspectives.Cognitive impairment in neuromuscular diseases: A systematic review

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Learning disabilities in neuromuscular disorders: a springboard for adult life

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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2016年论文

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2016年论文

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name

Learning disabilities in neuromuscular disorders: a springboard for adult life

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Learning disabilities in neuromuscular disorders: a springboard for adult life

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Learning disabilities in neuromuscular disorders: a springboard for adult life

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Learning disabilities in neuromuscular disorders: a springboard for adult life

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Learning disabilities in neuromuscular disorders: a springboard for adult life

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Learning disabilities in neuromuscular disorders: a springboard for adult life

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P1476

Learning disabilities in neuromuscular disorders: a springboard for adult life

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Chiara Pecini

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Filippo M Santorelli

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Guja Astrea

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Roberta Battini

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Sara Lenzi

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Silvia Bonetti

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Silvia Frosini

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Silvia Perazza

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Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported

P2860

Exome sequencing identifies a DYNC1H1 mutation in a large pedigree with dominant axonal Charcot-Marie-Tooth disease

Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome

A gradient of childhood self-control predicts health, wealth, and public safety

The expanding phenotype of laminin alpha2 chain (merosin) abnormalities: case series and review

Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of alpha-dystroglycan

Cognitive functions in Duchenne muscular dystrophy: a reappraisal and comparison with spinal muscular atrophy

Intelligence and cognitive function in children and adolescents with spinal muscular atrophy

Nemaline myopathy: a clinical study of 143 cases

Scapuloperoneal spinal muscular atrophy and CMT2C are allelic disorders caused by alterations in TRPV4.

Congenital muscular dystrophies.

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scholarly article

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Elena Moretti

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2016-10-01T00:00:00Z

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muscular dystrophy

disability

intellectual disability

learning disability

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Learning disabilities in neuromuscular disorders: a springboard for adult life

about

P2860

P2860

Learning disabilities in neuromuscular disorders: a springboard for adult life

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P1476

P2093

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P921

P932