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International Journal of Colorectal Disease|May 13, 2005
The rare epidemiologic coincidence of diverticular disease and advanced colonic neoplasiaC J Krones, U Klinge, N Butz, et al.
Frontiers in Pediatrics|December 28, 2020
The BAL-Score Almost Perfectly Predicts Testicular Torsion in Children: A Two-Center Cohort StudyMichaela Klinke, Julia Elrod, Carolin Stiel, et al.
Communications Biology|November 25, 2023
ACO2 deficiency increases vulnerability to Parkinson's disease via dysregulating mitochondrial function and histone acetylation-mediated transcription of autophagy genesJunge Zhu, Fanxi Xu, Hong Lai, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|December 23, 2015
Copper-Based Photosensitisers in Water Reduction: A More Efficient In Situ Formed System and Improved Mechanistic UnderstandingAlastair J J Lennox, Steffen Fischer, Mark Jurrat, et al.
British Journal of Sports Medicine|November 5, 2024
Association of self-reported health problems and interpersonal violence in sport: a cross-sectional study in world-level performing athletesMargo Mountjoy, Karolien Adriaens, Astrid Junge, et al.
Frontiers in Physiology|November 22, 2019
Prolonged Heat Acclimation and Aerobic Performance in Endurance Trained AthletesC Jacob Mikkelsen, Nicklas Junge, Jacob F Piil, et al.
Der Chirurg; Zeitschrift Fur Alle Gebiete Der Operativen Medizen|February 10, 2017
[Video-assisted retroperitoneal debridement : Minimally invasive treatment and long-term results for necrotizing pancreatitis]R M Eickhoff, J Steinbusch, P Seppelt, et al.
BMC Medical Genomics|September 13, 2021
Sequencing of neurofilament genes identified NEFH Ser787Arg as a novel risk variant of sporadic amyotrophic lateral sclerosis in Chinese subjectsFeng Lin, Wanhui Lin, Chaofeng Zhu, et al.
Journal of Affective Disorders|November 13, 2022
Insomnia is a key risk factor for persistent anxiety and depressive symptoms: A 12-month longitudinal cohort study during the COVID-19 pandemicHailey Meaklim, William J Saunders, Michelle L Byrne, et al.
Cytogenetic and Genome Research|January 31, 2012
47,X,idic(Y),inv dup(Y): a non-mosaic case of a phenotypically normal boy with two different Y isochromosomes and neocentromere formationJ J Pasantes, R Wimmer, S Knebel, et al.
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