Results 31 to 40 of about 251,261 (303)
Case Report: Two Chinese Infants of Sengers Syndrome Caused by Mutations in AGK Gene
Frontiers in Pediatrics, 2021 Sengers syndrome (OMIM #212350) is a rare autosomal recessive disorder due to mutations in acylglycerol kinase (AGK) gene. We report two cases that were diagnosed clinically and confirmed genetically.
Benzhen Wang +6 more
doaj +1 more source
The role of reactive astrocitose in the chronological evolution of traumatic brain injury [PDF]
, 2018 Introduction and objectives. This study aims to investigate whether the cerebral modifications of posttraumatic reactive astrocitose can be considered an objective criterion for determining the age of traumatic cranio-cerebral lesions.
Belis, Vladimir +5 more
core +4 more sources
Availability and Utilization of Automated External Defibrillators in New York State Schools
Frontiers in Pediatrics, 2021 Background: Use of automated external defibrillators (AEDs) in out-of-hospital cardiac arrests (OHCAs) improve survival. Professional health organizations recommend that AEDs be available in crowded places, including schools but currently only 18 US ...
Milla Arabadjian +3 more
doaj +1 more source
Prediction of sarcomere mutations in subclinical hypertrophic cardiomyopathy. [PDF]
, 2014 BACKGROUND: Sarcomere protein mutations in hypertrophic cardiomyopathy induce subtle cardiac structural changes before the development of left ventricular hypertrophy (LVH).
Bassett, P +18 more
core +1 more source
Strength Training Prior to Endurance Exercise: Impact on the Neuromuscular System, Endurance Performance and Cardiorespiratory Responses [PDF]
, 2014 This study aimed to investigate the acute effects of two strength-training protocols on the neuromuscular and cardiorespiratory responses during endurance exercise. Thirteen young males (23.2 ± 1.6 years old) participated in this study.
Bottaro, Martim +11 more
core +2 more sources
Journal of the American Heart Association: Cardiovascular and Cerebrovascular DiseaseBackground Our objective was to assess real‐world outcomes and health care use associated with commercial mavacamten use in patients with obstructive hypertrophic cardiomyopathy.
Ingy Mahana +7 more
doaj +1 more source
Journal of Nanobiotechnology, 2018 Background Theranostic perfluorocarbon nanoprobes have recently attracted attention due to their fascinating versatility in integrating diagnostics and therapeutics into a single system.
Xueli Zhao +11 more
doaj +1 more source
Hypertrophic cardiomyopathy: Totally a ST-elevation myocardial infarction mimic
Journal of the Practice of Cardiovascular Sciences, 2021 Hypertrophic cardiomyopathy (HCM) commonly presents with nonspecific ST-T changes in an electrocardiogram (EKG), and a paucity of literature description exists about index presentation of HCM totally as ST-elevation myocardial infarction (STEMI) in a ...
Debasish Das +5 more
doaj +1 more source
Smad4 regulates growth plate matrix production and chondrocyte polarity. [PDF]
, 2017 Smad4 is an intracellular effector of the TGFβ family that has been implicated in Myhre syndrome, a skeletal dysplasia characterized by short stature, brachydactyly and stiff joints.
Alliston, Tamara +4 more
core +3 more sources
Journal of the American Heart Association: Cardiovascular and Cerebrovascular DiseaseBackground In obstructive hypertrophic cardiomyopathy, myectomy improves symptoms, quality of life, and left ventricular (LV) outflow tract gradients. We prospectively evaluated the temporal changes in various echo parameters after myectomy.
Milind Y. Desai +10 more
doaj +1 more source