Results 141 to 150 of about 817 (152)

A Zebrafish Model of Human Barth Syndrome Reveals the Essential Role of Tafazzin in Cardiac Development and Function

Circulation Research, 2006
Zaza Khuchua
exaly  

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

Nature Genetics, 1996
Silvia Bione, Patrizia D'Adamo, Elena Maestrini   +2 more
exaly  

Endocardial Fibroelastosis (Barth syndrome, cardioskeletal myopathy with neutropenia and abnormal mitochondria, BTHS)

2008
openaire   +1 more source

Cardiac‐specific succinate dehydrogenase deficiency in Barth syndrome

EMBO Molecular Medicine, 2016
Sylvie Callegari, Karl Toischer, Britta Brügger   +2 more
exaly  

Cardiomyopathy, mitochondria and Barth syndrome: iPSCs reveal a connection

Nature Medicine, 2014
Timothy J Kamp
exaly  

<p>Barth syndrome: mechanisms and management</p>

The Application of Clinical Genetics, 2019
Josef Finsterer
exaly  

Cardiolipin metabolism and Barth Syndrome

Progress in Lipid Research, 2006
Kristin D Hauff, Grant M Hatch
exaly  

Barth syndrome: Cellular compensation of mitochondrial dysfunction and apoptosis inhibition due to changes in cardiolipin remodeling linked to tafazzin (TAZ) gene mutation

Biochimica Et Biophysica Acta - Molecular Basis of Disease, 2013
Guillaume Vial, Riekelt H Houtkooper, Eyal Gottlieb   +2 more
exaly  

Barth Syndrome (BTHS)

openaire   +1 more source

Mutation Characterization and Genotype-Phenotype Correlation in Barth Syndrome

American Journal of Human Genetics, 1997
exaly