Results 191 to 200 of about 506,036 (266)
Artificial Intelligence-Augmented Clinical Decision Support Systems for Pregnancy Care: Systematic Review. [PDF]
Lin X +5 more
europepmc +1 more source
ABSTRACT Since 2015, Ann and Robert H. Lurie Children's Hospital has performed diagnostic testing for infants who screen positive for mucopolysaccharidosis type II (MPS II) on the Illinois newborn screen. Preliminary diagnostic testing includes measurement of plasma iduronate‐2‐sulfatase enzyme activity and urinary glycosaminoglycan analysis, followed ...
Carly A. Rasmussen +5 more
wiley +1 more source
Experiences of Obstetrician-Gynecologists Providing Pregnancy Care After Dobbs.
Cutler AS +4 more
europepmc +1 more source
Pregnancy in women with mitochondrial disease-A literature review and suggested guidance for preconception and pregnancy care. [PDF]
Hui L +9 more
europepmc +1 more source
ABSTRACT The transformation/transcription domain‐associated protein (TRRAP) gene encodes a large multidomain protein, a member of the phosphatidylinositol 3‐kinase‐related kinase (PIKK) family. TRRAP is a component of the histone acetyltransferase (HAT) complex, and it plays an important role in gene transcription, DNA repair, and cell‐cycle regulation.
Roseli Maria Zechi‐Ceide +10 more
wiley +1 more source
Not all Medicaid for pregnancy care is delivered equally. [PDF]
Swartz JJ, Kaufman M, Rodriguez MI.
europepmc +1 more source
ABSTRACT Autosomal recessive loss‐of‐function variants in PPP1R13L cause an ultra‐rare cardiocutaneous syndrome characterized by rapidly progressive arrhythmogenic cardiomyopathy (ACM). PPP1R13L encodes iASPP, which has two potentially overlapping mechanisms driving ACM as both a regulator of NFκB‐mediated inflammation and a binding partner within the ...
Aaron Renberg +9 more
wiley +1 more source
Pre-pregnancy care in general practice in England: cross-sectional observational study using administrative routine health data. [PDF]
Li Y +10 more
europepmc +1 more source
ABSTRACT Long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency (LCHADD) is an autosomal recessive mitochondrial defect of long‐chain fatty acid β‐oxidation, caused by biallelic pathogenic variants in HADHA or HADHB. We report a 22‐year‐old male with an atypically mild presentation of LCHADD who was referred to the Undiagnosed Diseases Network (UDN ...
Yutaka Furuta +9 more
wiley +1 more source
Midwives' and registered nurses' role and scope of practice in acute early pregnancy care services: a scoping review. [PDF]
Freeman N +4 more
europepmc +1 more source

