Temporal Effects of Safflower Oil Diet-Based Linoleic Acid Supplementation on Barth Syndrome Cardiomyopathy. [PDF]
Zhu S +10 more
europepmc +1 more source
A Barth Syndrome Patient-Derived D75H Point Mutation in TAFAZZIN Drives Progressive Cardiomyopathy in Mice. [PDF]
Snider PL +14 more
europepmc +1 more source
Tafazzin deficiency causes substantial remodeling in the lipidome of a mouse model of Barth Syndrome cardiomyopathy. [PDF]
Hachmann M +10 more
europepmc +1 more source
Editorial: Mitochondrial dysfunction affects mechano-energetic coupling in heart failure. [PDF]
Dudek J, Ritterhoff J.
europepmc +1 more source
Mitochondrial cardiolipin remodeling facilitates efficient myoblast differentiation. [PDF]
Ohba Y, Fujiwara CA, Arita M.
europepmc +1 more source
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Neutrophils in Barth syndrome (BTHS) avidly bind annexin-V in the absence of apoptosis
Blood, 2004Barth syndrome (BTHS) is a rare X-linked disease characterized by a triad of dilated cardiomyopathy, skeletal myopathy, and neutropenia. The disease is associated with mutations of the TAZ gene, resulting in defective cardiolipin (CL), an important inner mitochondrial membrane component.
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PP03.3 – 2376: A non-classical clinical course of Barth syndrome (BTHS)
European Journal of Paediatric Neurology, 2015A non-classical clinical course of Barth Syndrome (BTHS) A six year-old boy, born to non-consanguineous, healthy parents was primarily referred because of growth retardation. Auxological parameters were below the 3rd percentile after having been normal at birth.
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