Results 171 to 180 of about 710,185 (341)

Bloodstream Infections in Patients With Pulmonary Arterial Hypertension Treated With Intravenous Prostanoids: Insights From the REVEAL REGISTRY® [PDF]

, 2012
Natalie Kitterman, Abby Poms, Dave P. Miller, Sandra Lombardi, Harrison W. Farber, Robyn J. Barst   +5 more
openalex   +1 more source

Accelerating Primary Screening of USP8 Inhibitors from Drug Repurposing Databases with Tree‐Based Machine Learning

Advanced Intelligent Discovery, EarlyView.
This study introduces a tree‐based machine learning approach to accelerate USP8 inhibitor discovery. The best‐performing model identified 100 high‐confidence repurposable compounds, half already approved or in clinical trials, and uncovered novel scaffolds not previously studied. These findings offer a solid foundation for rapid experimental follow‐up,
Yik Kwong Ng, Sharon Ai Er Lam, Wei Chun Lim, Hannah Hui Min Toh, Shi Jun Ang   +4 more
wiley   +1 more source

Progress in the understanding and management of pulmonary arterial hypertension

, 2015
Anob M. Chakrabarti, Jane A. Mitchell, Stephen J. Wort   +2 more
openalex   +1 more source

Arterial hypertension in childhood [PDF]

, 2003
Cláudia Salgado, João Thomaz de Abreu Carvalhaes   +1 more
openalex   +1 more source

Mortality Patterns and Phenotypic Clusters in Trisomy 13: A Population‐Based Study From Japan

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Trisomy 13, the third most common autosomal trisomy after trisomy 21 and trisomy 18, is associated with a significantly high infant mortality rate. However, large‐scale studies examining causes of death in trisomy 13 remain scarce. Therefore, we aimed to better understand the mortality patterns.
Narumi Kato, Naho Morisaki, Akinori Moriichi   +2 more
wiley   +1 more source

The carotid body as a putative therapeutic target for the treatment of neurogenic hypertension [PDF]

, 2013
Abdala, Ana P, Hendy, Emma B, Marvar, Paul, McBryde, Fiona D, Moraes, Davi J A, Paton, Julian F R, Pijacka, Wioletta, Sobotka, Paul A   +7 more
core   +1 more source

Descriptive Epidemiology From the Myhre Syndrome Foundation Registry: The Value of Self‐Reported Data

American Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Myhre syndrome is an ultrarare genetic disease characterized by short stature, distinct craniofacial features, cardiovascular and respiratory fibrosis and stenosis, neurodevelopmental delays, autism, intellectual disability, and hearing loss. The natural history of Myhre syndrome is still not fully understood due to a small patient population ...
Mary K. Young, Armelle Pindon, Maggie R. Brand, Kate Wears, Katherine H. Young, Alyssa Mendel, Michael J. Lyons   +6 more
wiley   +1 more source

Meta-Analysis of the Association Between the rs228570 Vitamin D Receptor Gene Polymorphism and Arterial Hypertension Risk

, 2020
Ivone F O C Nunes, Ana Amélia de Carvalho Melo Cavalcante, Marcus Vinícius Oliveira Barros de Alencar, Marcos David Figueiredo de Carvalho, José Lindenberg Rocha Sarmento, Nayra S C C A Teixeira, Adriana A. Paiva, Lídia Ribeiro de Carvalho, Leopoldo Fabrício Marçal do Nascimento, Maria do Socorro Pires e Cruz, Marcelo Macedo Rogero, Andréia C B Lima, Cecilia M R G Carvalho   +12 more
openalex   +2 more sources

N‐terminal pro brain natriuretic peptide in arterial hypertension—a marker for left ventricular dimensions and prognosis [PDF]

, 2004
Per Hildebrandt, Mikael Boesen, Michael Hecht Olsen, Kristian Wachtell, Bjoern A. Groenning   +4 more
openalex   +1 more source

The Circulation in Arterial Hypertension--I [PDF]

BMJ, 1943
openaire   +4 more sources