Barth syndrome is associated with a cognitive phenotype (Q34577468)

3 August 2017

Barth syndrome is associated with a cognitive phenotype (English)

1 reference

3 August 2017

1 reference

1 reference

1

Michèle M M Mazzocco

1 reference

3 August 2017

Anne E Henry

2

1 reference

PubMed ID

17353728

3 August 2017

Richard I Kelly

series ordinal

3

1 reference

3 August 2017

1 February 2007

1 reference

Journal of Developmental and Behavioral Pediatrics

3 August 2017

1 reference

3 August 2017

28

1 reference

3 August 2017

22-30

1 reference

3 August 2017

1

1 reference

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

3 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813702

Characterization of lymphoblast mitochondria from patients with Barth syndrome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813702

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813702

Deficiency of tetralinoleoyl-cardiolipin in Barth syndrome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813702

Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndrome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813702

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813702

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813702

Neonatal, lethal noncompaction of the left ventricular myocardium is allelic with Barth syndrome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813702

The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813702

Mutation characterization and genotype-phenotype correlation in Barth syndrome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813702

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813702

Multiple syndromes of 3-methylglutaconic aciduria

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813702

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813702

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813702

Mapping of the locus for X-linked cardioskeletal myopathy with neutropenia and abnormal mitochondria (Barth syndrome) to Xq28

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813702

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813702

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813702

Visuospatial skills and their association with math performance in girls with fragile X or Turner syndrome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813702

Remodeling of cardiolipin by phospholipid transacylation.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813702

Preliminary evidence for a cognitive phenotype in Barth syndrome

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813702

Barth syndrome: clinical observations and genetic linkage studies.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2813702

Dilated cardiomyopathy with neutropenia, short stature, and abnormal carnitine metabolism

27 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17353728

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1097/01.DBP.0000257519.79803.90

1 reference

3 August 2017

1 reference

3 August 2017

1 reference

PubMed ID

17353728