Results 111 to 120 of about 32,855 (128)

Validation of the Leuven Postprandial Distress Scale, a questionnaire for symptom assessment in the functional dyspepsia/postprandial distress syndrome

Alimentary Pharmacology and Therapeutics, 2016
F. Carbone, A. Vandenberghe, L. Holvoet, T. Vanuytsel, L. Oudenhove, Michael P. Jones, Jan Tack   +6 more
semanticscholar   +1 more source

A Bayesian Analysis to Determine the Prevalence of Barth Syndrome in the Pediatric Population

Journal of Pediatrics, 2020
Michael Schlame, Colin Phoon, Mindong Ren   +2 more
exaly  

Metabolic switch from fatty acid oxidation to glycolysis in knock‐in mouse model of Barth syndrome

EMBO Molecular Medicine, 2023
Peter Rehling, Ivan Silbern, Henning Urlaub   +2 more
exaly  

Quantitative assessment of autonomic symptom burden in Postural tachycardia syndrome (POTS).

Journal of Neurological Sciences, 2017
Natalie A. Rea, C. Campbell, Melissa M. Cortez   +2 more
semanticscholar   +1 more source

Functional dyspepsia: outcome of focus groups for the development of a questionnaire for symptom assessment in patients suffering from postprandial distress syndrome (PDS)

Neurogastroenterology and Motility, 2014
F. Carbone, L. Holvoet, A. Vandenberghe, Jan Tack   +3 more
semanticscholar   +1 more source

AAV Gene Therapy Prevents and Reverses Heart Failure in a Murine Knockout Model of Barth Syndrome

Circulation Research, 2020
Yang Xu, Zhiqiang Lin, Yifei Li
exaly  

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  

Neurological & psychological aspects of Barth syndrome: Clinical manifestations and potential pathogenic mechanisms

Mitochondrion, 2021
Colin Phoon, Mindong Ren
exaly  

<p>Barth syndrome: mechanisms and management</p>

The Application of Clinical Genetics, 2019
Josef Finsterer
exaly  

Mutation Characterization and Genotype-Phenotype Correlation in Barth Syndrome

American Journal of Human Genetics, 1997
Annette Feigenbaum, Vicky L Funanage, Gerald F Cox   +2 more
exaly