Expanded-access use of elamipretide in a newborn with Barth syndrome: a case report. [PDF]
Ortmann L, Velasco D, Cole J.
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A novel <i>TAFAZZIN</i> gene variant c.525_533del causing Barth syndrome and leading to heart transplantation: a case report. [PDF]
Krawiec M +9 more
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Allogenic mitochondria transfer improves cardiac function in iPS-cell-differentiated cardiomyocytes of a patient with Barth syndrome. [PDF]
Kim YS +7 more
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What can ATP content tell us about Barth syndrome muscle phenotypes? [PDF]
Brault JJ, Conway SJ.
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Barth Syndrome: <i>TAFAZZIN</i> Gene, Cardiologic Aspects, and Mitochondrial Studies-A Comprehensive Narrative Review. [PDF]
Sergi CM.
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Cell-Penetrating Peptide Enhances Tafazzin Gene Therapy in Mouse Model of Barth Syndrome. [PDF]
Raghav R +5 more
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Case Report: A Chinese child with Barth syndrome caused by a novel TAFAZZIN mutation. [PDF]
Che M +6 more
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Health-related quality of life and family functioning in parents of children with Barth syndrome: an application of the Double ABCX model. [PDF]
Lim Y, Hong I, Han A.
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Rescue of mitochondrial dysfunction through alteration of extracellular matrix composition in barth syndrome cardiac fibroblasts. [PDF]
Piñeiro-Llanes J +8 more
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ECG Findings Are Poor Predictors for Adverse Events and Cardiac Death in Barth Syndrome. [PDF]
Hutchinson A +3 more
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