Results 101 to 110 of about 505 (112)

Loss of Mitochondrial Ca 2+ Uniporter Limits Inotropic Reserve and Provides Trigger and Substrate for Arrhythmias in Barth Syndrome Cardiomyopathy

Circulation, 2021
Peter Rehling, Mathias Hohl, Markus Hoth   +2 more
exaly  

Barth Syndrome Cardiomyopathy: An Update

Genes, 2022
Xi Fang, Yutong Bao, Jennifer Veevers
exaly  

Cardiolipin Remodeling Defects Impair Mitochondrial Architecture and Function in a Murine Model of Barth Syndrome Cardiomyopathy

Circulation: Heart Failure, 2021
Sylvia Evans, Asa Gustafsson, Ying Shen   +2 more
exaly  

Increased Reactive Oxygen Species–Mediated Ca 2+ /Calmodulin-Dependent Protein Kinase II Activation Contributes to Calcium Handling Abnormalities and Impaired Contraction in Barth Syndrome

Circulation, 2021
Donghui Zhang, Yifei Li, William T Pu
exaly  

Endocardial Fibroelastosis (Barth syndrome, cardioskeletal myopathy with neutropenia and abnormal mitochondria, BTHS)

2008
openaire   +1 more source

Cardiac‐specific succinate dehydrogenase deficiency in Barth syndrome

EMBO Molecular Medicine, 2016
Peter Rehling, Kaomei Guan, Britta Brugger   +2 more
exaly  

The Barth Syndrome Registry: Distinguishing disease characteristics and growth data from a longitudinal study

American Journal of Medical Genetics, Part A, 2012
Barry J Byrne
exaly  

X Chromosome Inactivation in Carriers of Barth Syndrome

American Journal of Human Genetics, 1998
Anna K Naumova, Daniela Toniolo, Patrizia D'Adamo   +2 more
exaly  

X‐linked cardioskeletal myopathy and neutropenia (Barth syndrome): An update

American Journal of Medical Genetics, Part A, 2004
Ronald Wanders, Frédéric Vaz, Frédéric M Vaz   +2 more
exaly  

Real-world disease burden and health care resource utilization for patients with Barth syndrome

Journal of Medical Economics
Mary Kay Koenig, Lindsay Marjoram, Bruce Cohen   +2 more
exaly