Allogenic mitochondria transfer improves cardiac function in iPS-cell-differentiated cardiomyocytes of a patient with Barth syndrome. [PDF]
Exp Mol MedKim YS +7 more
europepmc +1 more source
What can ATP content tell us about Barth syndrome muscle phenotypes? [PDF]
J Transl Genet GenomBrault JJ, Conway SJ.
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Barth Syndrome: <i>TAFAZZIN</i> Gene, Cardiologic Aspects, and Mitochondrial Studies-A Comprehensive Narrative Review. [PDF]
Genes (Basel)Sergi CM.
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Memory, language and intellectual ability in low-functioning autism [PDF]
, 2008 Bigham, Sally, Boucher, J., Mayes, A.
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Functional exercise capacity, strength, balance and motion reaction time in Barth syndrome [PDF]
, 2019 Brittany Hornby +5 more
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Case Report: A Chinese child with Barth syndrome caused by a novel TAFAZZIN mutation. [PDF]
Front Cardiovasc MedChe M +6 more
europepmc +1 more source
Health-related quality of life and family functioning in parents of children with Barth syndrome: an application of the Double ABCX model. [PDF]
Orphanet J Rare DisLim Y, Hong I, Han A.
europepmc +1 more source
ECG Findings Are Poor Predictors for Adverse Events and Cardiac Death in Barth Syndrome. [PDF]
Prog Pediatr CardiolHutchinson A +3 more
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Stem cell models of TAFAZZIN deficiency reveal novel tissue-specific pathologies in Barth syndrome. [PDF]
Hum Mol GenetSniezek Carney O +8 more
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