Barth Syndrome: <i>TAFAZZIN</i> Gene, Cardiologic Aspects, and Mitochondrial Studies-A Comprehensive Narrative Review. [PDF]
Sergi CM.
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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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Adaptive mechanisms in pancreatic islets counteract mitochondrial dysfunction in Barth syndrome. [PDF]
Carlein C +21 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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Tafazzin-deficient zebrafish display mitochondrial dysfunction, neutropenia, and metabolic defects without myopathy. [PDF]
Oyarbide U +10 more
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Emerging roles of pyruvate dehydrogenase phosphatase 1: a key player in metabolic health. [PDF]
Kumar V, Greenberg ML.
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Cranial, Renal, and Skeletal Anomalies in a Fetus With a Pathogenic Variant in the TAFAZZIN Gene. [PDF]
Muir CR, Gilmore KL, Singh S, Vora NL.
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Contemporary insights into elamipretide's mitochondrial mechanism of action and therapeutic effects. [PDF]
Sabbah HN +8 more
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Rescue of mitochondrial dysfunction through alteration of extracellular matrix composition in barth syndrome cardiac fibroblasts. [PDF]
PiƱeiro-Llanes J +8 more
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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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