Results 191 to 200 of about 41,331 (231)

Correction: Stimulating the sir2-spargel axis rescues exercise capacity and mitochondrial respiration in a Drosophila model of Barth syndrome.

Dis Model Mech
Damschroder D, Zapata-Pérez R, Richardson K, Vaz FM, Houtkooper RH, Wessells R.   +5 more
europepmc   +1 more source

Defective cardiomyocyte mitophagy in TAFAZZIN deficiency: New implications for cellular pathogenesis in Barth syndrome

Olivia Sniezek Carney, Kyuna Lee, Kodi Williams Harris, Grant Butschek, Arianna Anzmann, Anne Hammacher-Brady, Hilary J. Vernon   +6 more
openalex   +1 more source

The Legal Ethics of the Two Kingdoms [PDF]

, 2011
Shaffer, Thomas L.
core   +1 more source

Hypocholesterolemia in Barth Syndrome

, 2009
openaire   +1 more source

Cardiolipin metabolism in Barth syndrome

, 2009
openaire   +2 more sources

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Cardiolipin metabolism and Barth Syndrome

Progress in Lipid Research, 2006
Many advances have occurred in the field of Barth Syndrome biology in the 26 years since it was first described as an X-linked cardiomyopathy. Barth Syndrome is the first human disease recognized in which the primary causative factor is an alteration in cardiolipin remodeling. Cardiolipin is required for the optimal function of many proteins within the
Kristin D Hauff, Grant M Hatch
exaly   +3 more sources

Dysmorphology of Barth syndrome

Clinical Dysmorphology, 2009
Barth syndrome is an X-linked recessive condition caused by defective remodelling of cardiolipins in mitochondrial membranes because of mutations in the tafazzin (TAZ1/G4.5) gene located at Xq28. The cardinal features of Barth syndrome are cardiac and skeletal myopathy and neutropaenia, reported in the initial description of this condition by Barth et ...
Rob, Hastings, Colin, Steward, Beverly, Tsai-Goodman, Ruth, Newbury-Ecob   +3 more
openaire   +3 more sources

CLINICOPATHOLOGIC CONFERENCE: BARTH SYNDROME

Fetal and Pediatric Pathology, 2005
A case of Barth Syndrome is presented and discussed by both clinician and pathologist, in this traditional clinico-pathologic conference. The current understanding of etiology is included, including elevation of 3-methylglutaconic acid (3MGC).
James C, Huhta, Herbert H, Pomerance, Enid Gilbert, Barness   +2 more
openaire   +2 more sources

Heart Transplantation for Barth Syndrome

Pediatric Cardiology, 1997
Barth syndrome is an X-linked recessive disorder comprising dilated cardiomyopathy, muscular hypotonia, and cyclical neutropenia. Affected children usually die during infancy as a consequence of septicemia, cardiac failure, or both. We report a patient with Barth syndrome who underwent successful heart transplantation.
S S, Adwani, B F, Whitehead, P G, Rees, A, Morris, D M, Turnball, M J, Elliott, M R, de Leval   +6 more
openaire   +2 more sources

Stroke Associated With Barth Syndrome

Journal of Child Neurology, 2006
Barth syndrome is an inherited disorder characterized by dilated cardiomyopathy, neutropenia, growth retardation, and skeletal myopathy. We describe a case of acute stroke owing to Barth syndrome that required intra-arterial thrombolysis. This case suggests that cardiovascular complications can be observed in patients with Barth syndrome.
Beau M, Ances, Joseph, Sullivan, John B, Weigele, Vivian, Hwang, Steven R, Messé, Scott E, Kasner, David S, Liebeskind   +6 more
openaire   +2 more sources