Barth syndrome is associated with a cognitive phenotype. - Wikidata - wikimedia - TriplyDB

Barth syndrome is associated with a cognitive phenotype.

Barth syndrome is associated with a cognitive phenotype.

http://www.wikidata.org/entity/Q34577468

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Successful management of Barth syndrome: a systematic review highlighting the importance of a flexible and multidisciplinary approach Barth syndrome.Cellular functions of cardiolipin in yeast Psychosocial Functioning in Youth with Barth Syndrome.The 3-methylglutaconic acidurias: what's new?Genetic ablation of calcium-independent phospholipase A2{gamma} leads to alterations in hippocampal cardiolipin content and molecular species distribution, mitochondrial degeneration, autophagy, and cognitive dysfunction.Disruption of mitochondrial homeostasis in organic acidurias: insights from human and animal studies.Reduction in cholesterol synthesis in response to serum starvation in lymphoblasts of a patient with Barth syndrome.Influence of tissue, diet, and enzymatic remodeling on cardiolipin fatty acyl profile.Loss of tafazzin results in decreased myoblast differentiation in C2C12 cells: A myoblast model of Barth syndrome and cardiolipin deficiency.

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Barth syndrome is associated with a cognitive phenotype.

http://www.wikidata.org/entity/Q34577468

description

2007 nî lūn-bûn

@nan

2007 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2007 թվականի փետրվարին հրատարակված գիտական հոդված

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2007年の論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年論文

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2007年论文

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name

Barth syndrome is associated with a cognitive phenotype.

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Barth syndrome is associated with a cognitive phenotype.

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Barth syndrome is associated with a cognitive phenotype.

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type

label

Barth syndrome is associated with a cognitive phenotype.

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Barth syndrome is associated with a cognitive phenotype.

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Barth syndrome is associated with a cognitive phenotype.

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Barth syndrome is associated with a cognitive phenotype.

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Barth syndrome is associated with a cognitive phenotype.

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Barth syndrome is associated with a cognitive phenotype.

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Journal of Developmental and Behavioral Pediatrics

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Barth syndrome is associated with a cognitive phenotype.

@en

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Anne E Henry

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Richard I Kelly

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P2860

Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndrome

X-linked cardioskeletal myopathy and neutropenia (Barth syndrome) (MIM 302060)

X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): an update

A novel X-linked gene, G4.5. is responsible for Barth syndrome

X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome.

Genetic analysis of the G4.5 gene in families with suspected Barth syndrome.

Rapid "automatized" naming (R.A.N): dyslexia differentiated from other learning disabilities.

X-linked dilated cardiomyopathy with neutropenia, growth retardation, and 3-methylglutaconic aciduria.

Barth syndrome: clinical features and confirmation of gene localisation to distal Xq28.

Complexities in Identifying and Defining Mathematics Learning Disability in the Primary School-Age Years

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22-30

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scholarly article

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10.1097/01.DBP.0000257519.79803.90

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Michèle M M Mazzocco

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6452874

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