Results 131 to 140 of about 4,442 (232)
Sleep and Rhythmic Profile After Pineal Gland Removal in Humans
ABSTRACT Melatonin, a hormone produced by the pineal gland, is classically described as a central circadian modulator. However, the impact of its absence on circadian rhythmicity in humans remains poorly understood. Pinealectomised patients, in whom melatonin secretion is chronically suppressed, represent a valuable clinical model to investigate the ...
Renata de Andrade Prado Gobetti +7 more
wiley +1 more source
ABSTRACT Background and Aims Extrahepatic portal vein obstruction (EHPVO) is among the main causes of childhood portal hypertension. We analysed nationwide long‐term outcomes of EHPVO in relation to various management options. Methods In total, 62 consecutive patients with EHPVO diagnosed between 1987 and 2023 were followed up through hospital records ...
Topi Luoto +2 more
wiley +1 more source
ABSTRACT Objectives To investigate the influence of non‐syndromic hypodontia on radiographic dental development and to estimate dental age in children with bilateral mandibular agenesis using a machine learning approach. Materials and Methods This retrospective cross‐sectional study included 626 children aged 6–15 years (311 with dental agenesis, 315 ...
Marine Crosnier +3 more
wiley +1 more source
Background Ivemark syndrome is a rare heterotaxy disorder characterized by right atrial isomerism, complex congenital heart defects, and thoraco-abdominal anomalies. Because of such defects, survival beyond infancy is rare.
Hind Hibatouallah +4 more
doaj +1 more source
The simultaneous occurrence of bilateral duplicated collecting systems and heterotaxy syndrome is extremely rare, with no previously reported cases from our setting to our knowledge.
Zubeir Zubeir +2 more
doaj +1 more source
Incidental abdominal heterotaxy syndrome [PDF]
Janaka Lovell +2 more
openaire +3 more sources
SHROOM3 is a novel candidate for heterotaxy identified by whole exome sequencing [PDF]
Muhammad Tariq +4 more
core +1 more source
A novel biallelic loss-of-function variant in DAND5 causes heterotaxy syndrome. [PDF]
Ganapathi M +9 more
europepmc +1 more source
ObjectiveTo analytically depict the associated malformations of polysplenia syndrome (PS) in adults via computed tomography (CT).Materials and methodsThe incidence of malformations associated with PS in twelve adult patients was retrospectively analyzed ...
Xinru Gu +8 more
doaj +1 more source
Splenic Torsion in Heterotaxy Syndrome with Left Isomerism: A Case Report and Literature Review. [PDF]
Cheang IN +4 more
europepmc +1 more source

