Results 141 to 150 of about 59,848 (234)

Clinical Presentation of the Longest Reported Living Individual With Bent Bone Dysplasia—FGFR2‐Related

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 3, Page 728-732, March 2026.
ABSTRACT The FGFR2 gene, encoding the FGFR2 protein, plays a crucial role in embryonic cell development, particularly in bone tissue. Bent Bone Dysplasia (BBD), FGFR2‐related (MIM# 614592), is a rare severe skeletal dysplasia characterized by craniofacial differences, reduced bone mineral density, and bowed long bones.
Cheyenne Bates   +6 more
wiley   +1 more source

Prevention and Management of Percutaneous Coronary Intervention‐Related Complications: Assessing the Impact of Simulation‐Based Learning and Human Factors Training

open access: yesCatheterization and Cardiovascular Interventions, Volume 107, Issue 4, Page 960-968, March 1, 2026.
ABSTRACT Background Complications of percutaneous coronary intervention (PCI) remain infrequent but are associated with a risk of serious injury or death. The techniques and devices required to manage them may be unfamiliar or unavailable to operators.
Junichi Fukamizu   +25 more
wiley   +1 more source

The Role of Open Cell Foams Supports on the Kinetics of PdO/Co3O4 for the Wet and Dry Lean Methane Combustion

open access: yesChemCatChem, Volume 18, Issue 5, 13 March 2026.
Kinetic analysis performed on FeCrAl, SiC and alumina open‐cell foams, washcoated with PdO/Co3O4 for the lean CH4 combustion in wet & dry environments. All structures demonstrated comparable catalytic activity and excellent H2O stability over time. The activation energies were 117 and 129 kJ mol−1 in dry & wet conditions.
Hernan G. Mazzei   +5 more
wiley   +1 more source

Quantitative Measurement of Hexoses by Betaine Aldehyde Derivatisation. [PDF]

open access: yesInt J Mol Sci
Kret-Bułat P   +5 more
europepmc   +1 more source

An International Delphi Study on Barriers to On‐Demand Treatment of Hereditary Angioedema Attacks

open access: yesClinical and Translational Allergy, Volume 16, Issue 3, March 2026.
ABSTRACT Background Hereditary angioedema (HAE) is a rare inherited disorder characterized by unpredictable and potentially life‐threatening attacks of swelling. This international Delphi panel aimed to address questions related to on‐demand treatment of HAE attacks. Methods A modified Delphi method was conducted with three rounds of surveys.
Aleena Banerji   +20 more
wiley   +1 more source

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