Results 191 to 200 of about 39,836 (205)

Barth syndrome associated with triple mutation

Pediatrics International, 2018
Nobuyuki Tsujii, Takeharu Hayashi, Tamaki Hayashi, Akinori Kimura, Toshiya Nishikubo   +4 more
openaire   +2 more sources

Cardiac‐specific succinate dehydrogenase deficiency in Barth syndrome

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

Barth Syndrome

2008
openaire   +1 more source

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  

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  

Modeling Barth Syndrome in Zebrafish

Journal of Investigative Medicine, 2005
A.W. Strauss, Z. Khuchua, J. Miller, Z. Yue, B. Appel   +4 more
openaire   +1 more source

[Barth syndrome].

Ryoikibetsu shokogun shirizu, 2001
openaire   +1 more source

Mutation Characterization and Genotype-Phenotype Correlation in Barth Syndrome

American Journal of Human Genetics, 1997
exaly  

What is Barth syndrome?

Midwives, 2014
Vanessa, Garratt, Debbie, Riddiford, Colin, Steward, Beverly, Tsai-Goodman, Ruth, Newbury-Ecob   +4 more
openaire   +1 more source