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Chest|December 22, 2025
Challenges and Recommendations for Integrating Circadian Medicine in Critical Care: A RoadmapFloor W Hiemstra, Liliana Bustos González, Lilian J Engelhardt, et al.
Nature Reviews. Neurology|September 8, 2020
International consensus recommendations on the diagnostic work-up for malformations of cortical developmentRenske Oegema, Tahsin Stefan Barakat, Martina Wilke, et al.
Emerging Microbes & Infections|October 31, 2023
First evidence of tick-borne encephalitis (TBE) outside of Hokkaido Island in JapanMasayuki Ohira, Kentaro Yoshii, Yasuhiro Aso, et al.
Journal of the American College of Surgeons|April 16, 2026
Validation of the Southampton Difficulty Scoring System in Robotic Liver Surgery and Development of the International RoboLiver Difficulty Scoring SystemSoufyan El Adel, Gabriela Pilz da Cunha, Rong Liu, et al.
American Journal of Medical Genetics. Part A|October 13, 2006
Polymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common cortical malformationNathaniel H Robin, Clare J Taylor, Donna M McDonald-McGinn, et al.
Nutrients|August 30, 2020
Interleukin-6 Gene Expression Changes after a 4-Week Intake of a Multispecies Probiotic in Major Depressive Disorder-Preliminary Results of the PROVIT StudyAlexandra Reiter, Susanne A Bengesser, Anne-Christin Hauschild, et al.
Journal of Medical Genetics|September 29, 2011
Phenotypic spectrum associated with CASK loss-of-function mutationsUte Moog, Kerstin Kutsche, Fanny Kortüm, et al.
Brain : a Journal of Neurology|July 15, 2019
Incidence and phenotypes of childhood-onset genetic epilepsies: a prospective population-based national cohortJoseph D Symonds, Sameer M Zuberi, Kirsty Stewart, et al.
The Lancet. Respiratory Medicine|September 10, 2022
Anti-C5a antibody (vilobelimab) therapy for critically ill, invasively mechanically ventilated patients with COVID-19 (PANAMO): a multicentre, double-blind, randomised, placebo-controlled, phase 3 trialAlexander P J Vlaar, Martin Witzenrath, Pieter van Paassen, et al.
American Journal of Human Genetics|October 23, 2018
Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal FeaturesPeter D Turnpenny, Michael J Wright, Melissa Sloman, et al.
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