Results 131 to 140 of about 4,442 (232)

Sleep and Rhythmic Profile After Pineal Gland Removal in Humans

open access: yesJournal of Sleep Research, Volume 35, Issue 2, April 2026.
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

Long‐Term Outcomes of Extrahepatic Portal Vein Obstruction—A Nationwide Registry‐Based Follow‐Up Study From 1987 to 2023

open access: yesLiver International, Volume 46, Issue 4, April 2026.
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

Delayed Dental Development in Children With Non‐Syndromic Hypodontia: A Cross‐Sectional Study Using a Machine Learning Approach to Dental Age Estimation

open access: yesOrthodontics &Craniofacial Research, Volume 29, Issue 2, Page 347-356, April 2026.
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

Ivemark syndrome in an adult with complete atrioventricular septal defect and a single ventricle with L-transposition of the great arteries: a case report

open access: yesJournal of Medical Case Reports
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

A Rare Syndromic Coexistence: Bilateral Duplicated Collecting Systems with Bilateral Ureterovesical Junction Obstruction in a Child with Heterotaxy Syndrome and Polysplenia: A Case Report

open access: yesDr. Sulaiman Al Habib Medical Journal
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]

open access: yesANZ Journal of Surgery, 2019
Janaka Lovell   +2 more
openaire   +3 more sources

SHROOM3 is a novel candidate for heterotaxy identified by whole exome sequencing [PDF]

open access: yes, 2011
Muhammad Tariq   +4 more
core   +1 more source

A novel biallelic loss-of-function variant in DAND5 causes heterotaxy syndrome. [PDF]

open access: yesCold Spring Harb Mol Case Stud, 2022
Ganapathi M   +9 more
europepmc   +1 more source

Analysis of associated malformations by computed tomography in adults with polysplenia syndrome: A pilot study.

open access: yesPLoS ONE
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

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