Barth syndrome (Q59615706)

22 March 2019

24 March 2019

22 April 2019

17 June 2019

22 December 2019

6 July 2020

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22 December 2020

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cites work

Defective remodeling of cardiolipin and phosphatidylglycerol in Barth syndrome

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12 December 2020

Mitochondria as a therapeutic target in heart failure

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12 December 2020

Cardiolipin prevents rate-dependent uncoupling and provides osmotic stability in yeast mitochondria.

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12 December 2020

Deficiency of tetralinoleoyl-cardiolipin in Barth syndrome

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12 December 2020

The Epidemiology of Childhood Cardiomyopathy in Australia

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12 December 2020

Clinical characterization of left ventricular noncompaction in children: a relatively common form of cardiomyopathy

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12 December 2020

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

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12 December 2020

Neutrophils in Barth syndrome (BTHS) avidly bind annexin-V in the absence of apoptosis

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12 December 2020

An X-linked recessive cardiomyopathy with abnormal mitochondria

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Barth syndrome: clinical observations and genetic linkage studies.

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12 December 2020

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

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12 December 2020

Barth syndrome may be due to an acyltransferase deficiency

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12 December 2020

Mutation characterization and genotype-phenotype correlation in Barth syndrome

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12 December 2020

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

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12 December 2020

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

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12 December 2020

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

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12 December 2020

Successful mechanical circulatory support for 251 days in a child with intermittent severe neutropenia due to Barth syndrome

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12 December 2020

Natural history of Barth syndrome: a national cohort study of 22 patients

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12 December 2020

Mortality and sudden death in pediatric left ventricular noncompaction in a tertiary referral center

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12 December 2020

Barth syndrome: TAZ gene mutations, mRNAs, and evolution

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12 December 2020

Monolysocardiolipins accumulate in Barth syndrome but do not lead to enhanced apoptosis

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12 December 2020

Ventricular arrhythmia in the X-linked cardiomyopathy Barth syndrome.

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12 December 2020

Cardiac and clinical phenotype in Barth syndrome

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12 December 2020

Comparison of lymphoblast mitochondria from normal subjects and patients with Barth syndrome using electron microscopic tomography

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12 December 2020

Successful cardiac transplantation in Barth syndrome--single-centre experience of four patients

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12 December 2020

Cardiolipin: setting the beat of apoptosis

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12 December 2020

Guidelines for the management of heart failure: differences in guideline perspectives

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12 December 2020

Mutations in sarcomere protein genes in left ventricular noncompaction

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12 December 2020

Acute metabolic decompensation and sudden death in Barth syndrome: report of a family and a literature review.

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12 December 2020

New indications and controversies in arginine therapy

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12 December 2020

Cardiolipin and electron transport chain abnormalities in mouse brain tumor mitochondria: lipidomic evidence supporting the Warburg theory of cancer

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12 December 2020

Mitochondrial defects lie at the basis of neutropenia in Barth syndrome

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12 December 2020

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

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12 December 2020

Cardiolipin and mitochondrial carriers

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12 December 2020

Executive Summary: Heart Disease and Stroke Statistics—2010 Update

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12 December 2020

Dilated cardiomyopathy

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12 December 2020

Gonadal mosaicism of a TAZ (G4.5) mutation in a Japanese family with Barth syndrome and left ventricular noncompaction

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12 December 2020

Left ventricular noncompaction: a new form of heart failure

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12 December 2020

Cardiac and skeletal muscle defects in a mouse model of human Barth syndrome

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12 December 2020

2011 ACCF/AHA guideline for the diagnosis and treatment of hypertrophic cardiomyopathy: executive summary: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines

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12 December 2020

Barth syndrome in a female patient

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12 December 2020

Mechanical circulatory support in children: bridge to transplant versus recovery

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12 December 2020

Prospective trial of a pediatric ventricular assist device.

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12 December 2020

The Barth Syndrome Registry: Distinguishing disease characteristics and growth data from a longitudinal study

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12 December 2020

Intrafamilial variability for novel TAZ gene mutation: Barth syndrome with dilated cardiomyopathy and heart failure in an infant and left ventricular noncompaction in his great-uncle

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12 December 2020

Left ventricular noncompaction cardiomyopathy in Barth syndrome: an example of an undulating cardiac phenotype necessitating mechanical circulatory support as a bridge to transplantation

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12 December 2020

Haematological features in Barth syndrome

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12 December 2020

NGS identifies TAZ mutation in a family with X-linked dilated cardiomyopathy

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12 December 2020

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12 December 2020