Results 261 to 270 of about 258,050 (341)

Comparative analysis of the relationship of sarcopenia or sarcopenic obesity with functional impairment: A cross‐sectional study

open access: yesNutrition in Clinical Practice, EarlyView.
Abstract Growing evidence suggests that sarcopenic obesity (SO) may have a more pronounced effect on functionality compared with isolated sarcopenia, but research in this crucial area remains scarce. Therefore, this study aimed to evaluate whether the combination of sarcopenia and obesity is associated with increased functional impairment in ...
Flavia Alves Gomes   +6 more
wiley   +1 more source

Unseen crisis: the unexpected face of acute haemorrhagic pancreatitis. [PDF]

open access: yesJ Surg Case Rep
Nathaniel A   +6 more
europepmc   +1 more source

Efficacy of Preoperative Chemotherapy in Patients With Nephroblastoma and Imaging Findings Suggestive of Preoperative Tumor Rupture

open access: yesPediatric Blood &Cancer, EarlyView.
ABSTRACT Background and aims If Wilms tumor (WT) rupture is suspected preoperatively, it is unclear whether preoperative chemotherapy (preop‐CT) can be safely given and whether such patients need to be treated according to local stage III postoperatively.
Marvin Mergen   +9 more
wiley   +1 more source

Assessment of central blood volume in cirrhosis by radionuclide angiography [PDF]

open access: yes, 1994
Bendtsen, Flemming   +10 more
core  

Diagnosis and Management of Prenatal Hereditary Pyropoikilocytosis

open access: yesPrenatal Diagnosis, EarlyView.
ABSTRACT Hereditary pyropoikilocytosis (HPP) is a severe hemolytic anemia caused by variants in SPTA1, SPTB, and EPB41. These weaken horizontal interactions in the erythrocyte cytoskeleton, causing membrane fragmentation and splenic sequestration. It will readily cause fetal anemia and often hydrops fetalis. Prenatal diagnosis requires first ruling out
Connor Hartzell   +6 more
wiley   +1 more source

Yield of Whole Genome Sequencing for Pathogenic Single Nucleotide Variants in Congenital Heart Disease: A Systematic Review and Meta‐Analysis

open access: yesPrenatal Diagnosis, EarlyView.
ABSTRACT Objective This systematic review and meta‐analysis aimed to assess the diagnostic yield of pathogenic or likely pathogenic (P/LP) single nucleotide variants (SNVs) using whole genome sequencing (WGS) in congenital heart disease (CHD). Methods A systematic search of three databases (2000–2024) was conducted, and two reviewers independently ...
Hiba J. Mustafa   +7 more
wiley   +1 more source

Hemolytic Disease of the Fetus and Newborn: Fetal RHD Genotyping, Targeted Prophylaxis, and Prenatal Therapies

open access: yesPrenatal Diagnosis, EarlyView.
ABSTRACT Hemolytic disease of the fetus and newborn (HDFN) remains a significant concern in prenatal care primarily caused by maternal alloimmunization against fetal red blood cell antigens, most commonly the D antigen. Noninvasive fetal RHD genotyping, used as a screening tool, enables targeted antenatal prophylaxis and has been implemented in several
Emilie Thorup   +4 more
wiley   +1 more source

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