Wearable Platform for Automatic Recognition of Parkinson Disease by Muscular Implication Monitoring [PDF]
, 2017 The need for diagnostic tools for the characterization of progressive movement disorders - as the Parkinson Disease (PD) - aiming to early detect and monitor the pathology is getting more and more impelling.
Annese, V.F. +4 more
core +1 more source
Environmental Effects On Drosophila Brain Development And Learning [PDF]
, 2017 Brain development and behavior are sensitive to a variety of environmental influences including social interactions and physicochemical stressors. Sensory input in situ is a mosaic of both enrichment and stress, yet little is known about how multiple ...
Amei, Amei +3 more
core +5 more sources
Investigation of the Physiochemical Properties of the Phospholipid Cardiolipin: Implications for Oxphos Regulation and Barth Syndrome [PDF]
, 2016 Murugappan Sathappa +2 more
openalex +1 more source
Prenatal case report of Barth syndrome caused by novel TAFAZZIN mutation: Clinical characteristics of fetal dilated cardiomyopathy with ascites [PDF]
, 2022 Xuliang Zhao +5 more
openalex +1 more source
Human Inborn Errors of Immunity: 2019 Update of the IUIS Phenotypical Classification. [PDF]
, 2020 Since 2013, the International Union of Immunological Societies (IUIS) expert committee (EC) on Inborn Errors of Immunity (IEI) has published an updated phenotypic classification of IEI, which accompanies and complements their genotypic classification ...
Ailal, Fatima +18 more
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Role of Cardiolipin in Mitochondrial Signaling Pathways
Frontiers in Cell and Developmental Biology, 2017 The phospholipid cardiolipin (CL) is an essential constituent of mitochondrial membranes and plays a role in many mitochondrial processes, including respiration and energy conversion.
Jan Dudek
doaj +1 more source
Cardiomyopathy of Unknown Etiology: Barth Syndrome Unrecognized
Congenital Heart Disease, 2008 This is a report of a child who died at 20 months from what was clinically thought to be cardiomyopathy of unknown etiology. Barth syndrome, an X-linked mitochondrial cardioskeletal myopathy, was diagnosed by genetic testing at autopsy. Barth syndrome presents in infancy or childhood with cardiomyopathy, hypotonia, growth delays, and cyclic neutropenia.
Robert T, Sweeney +2 more
openaire +2 more sources
Effects of curative treatment emphasizing endurance training on the performance and blood pressure of hypertensive and normotensives [PDF]
The problem of normal values of blood pressure after exercise taking into account the blood pressure at the end of the exercise test is discussed. Hypertensives showed a lower working capacity than normotensives. In normotensives, however, systolic blood
Worms, F.
core +1 more source
Phospholipid abnormalities in children with Barth syndrome
Journal of the American College of Cardiology, 2003 We sought to identify characteristic lipid abnormalities in patients with Barth syndrome (BTHS) and to correlate the lipid profile to phenotype and genotype.Barth syndrome typically includes cardiomyopathy, skeletal myopathy, neutropenia, growth retardation, and 3-methylglutaconic aciduria, and it is commonly associated with mutations in the tafazzin ...
Schlame, Michael +8 more
openaire +3 more sources
Healthy Steps at 15: The Past and Future of an Innovative Preventive Care Model for Young Children [PDF]
, 2010 Evaluates a model for preventive pediatric care for children up to age 3 that relies on mid-level specialists, including the program's spread, operating costs, funding, challenges, and potential effects of healthcare reform.
Michael C. Barth
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