Results 331 to 340 of about 796,036 (401)
Mass spectrometry imaging of N‐linked glycans: Fundamentals and recent advances
Abstract With implications in several medical conditions, N‐linked glycosylation is one of the most important posttranslation modifications present in all living organisms. Due to their nontemplate synthesis, glycan structures are extraordinarily complex and require multiple analytical techniques for complete structural elucidation.
Tana V. Palomino, David C. Muddiman
wiley +1 more source
Longitudinal Outcomes of Patients with Aortic Stenosis Stratified by Sex: An Asian Perspective. [PDF]
Ong JYS+8 more
europepmc +1 more source
Gastric Antral Vascular Ectasia Syndrome With Aortic Stenosis: A Twist on Heyde Syndrome? [PDF]
Bathobakae L+8 more
europepmc +1 more source
Abstract Background The 2019 Enhanced Recovery After Cardiac Surgery (ERACS) guidelines presented perioperative recommendations to optimize treatment for patients undergoing cardiac surgery (CS). However, the guidelines have not established postoperative nutrition recommendations.
Bianca Beaulieu+3 more
wiley +1 more source
Surgical treatment of supravalvular aortic stenosis
G.C. Rastelli+4 more
openalex +1 more source
Multiorgan Dysfunction and its Association With Congestion and Outcome in Aortic Stenosis Treated With TAVI. [PDF]
Halavina K+19 more
europepmc +1 more source
ABSTRACT This manuscript summarises the debate held at the 2024 annual meeting of The International Society for Prenatal Diagnosis (ISPD). Experts discussed whether all fetuses undergoing fetal therapy should undergo exome sequencing. Arguments in favor included that, with increasing experience and better clinical availability, exome sequencing can ...
Teresa N. Sparks+2 more
wiley +1 more source
Genetics of Calcific Aortic Stenosis: A Systematic Review. [PDF]
Vassiliou VS+3 more
europepmc +1 more source
Brain Abnormalities in Prenatally Diagnosed Rubinstein‐Taybi Syndrome
ABSTRACT Rubinstein‐Taybi syndrome (RSTS; OMIM 180849) is a rare autosomal dominant disorder characterized by craniofacial dysmorphism, broad halluces and thumbs, variable structural abnormalities and intellectual disability. It is caused by a pathogenic variant in the CREBBP or EP300 genes.
Laurence S. Carmant+6 more
wiley +1 more source