(Q37938707)

25 August 2017

1 reference

title

Eponym: Barth syndrome (English)

1 reference

25 August 2017

6

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25 August 2017

Atsuhito Takeda

1

1 reference

25 August 2017

Akira Sudo

2

1 reference

25 August 2017

Masafumi Yamada

3

1 reference

25 August 2017

Hirokuni Yamazawa

4

1 reference

25 August 2017

Gaku Izumi

5

1 reference

25 August 2017

Tadashi Ariga

7

1 reference

25 August 2017

publication date

23 September 2011

1 reference

European Journal of Pediatrics

25 August 2017

published in

1 reference

25 August 2017

volume

170

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25 August 2017

issue

11

1 reference

25 August 2017

page(s)

1365-1367

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

25 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1575-6

Heart transplantation for Barth syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1575-6

An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1575-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1575-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1575-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1575-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1575-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1575-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1575-6

Cardiolipin metabolism and Barth Syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1575-6

Cardiolipin and monolysocardiolipin analysis in fibroblasts, lymphocytes, and tissues using high-performance liquid chromatography-mass spectrometry as a diagnostic test for Barth syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1575-6

Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1575-6

Mutation characterization and genotype-phenotype correlation in Barth syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1575-6

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1575-6

Bloodspot assay using HPLC-tandem mass spectrometry for detection of Barth syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1575-6

21 January 2018

Lipid storage myopathy

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1575-6

Barth syndrome may be due to an acyltransferase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1575-6

Phospholipid abnormalities in children with Barth syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1575-6

Deficiency of tetralinoleoyl-cardiolipin in Barth syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1575-6

Cardiac and clinical phenotype in Barth syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1575-6

Ventricular arrhythmia in the X-linked cardiomyopathy Barth syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1575-6

Molecular basis and therapy of disorders associated with chronic neutropenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1575-6

Barth syndrome: an X-linked cause of fetal cardiomyopathy and stillbirth

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1575-6

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

21 January 2018

2 references

https://api.crossref.org/works/10.1007%2FS00431-011-1575-6

21 January 2018

https://pubmed.ncbi.nlm.nih.gov/21947198

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S00431-011-1575-6

1 reference

25 August 2017

1 reference