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Brain Pathology (Zurich, Switzerland)|August 15, 2023
Myelin protein zero mutation-related hereditary neuropathies: Neuropathological insight from a new nerve biopsy cohortJuliane Bremer, Axel Meinhardt, Istvan Katona, et al.
Plos Medicine|July 19, 2019
Correction: Discovery and validation of a prognostic proteomic signature for tuberculosis progression: A prospective cohort studyAdam Penn-Nicholson, Thomas Hraha, Ethan G Thompson, et al.
The Lancet. Respiratory Medicine|January 12, 2019
Efficacy and safety of delamanid in combination with an optimised background regimen for treatment of multidrug-resistant tuberculosis: a multicentre, randomised, double-blind, placebo-controlled, parallel group phase 3 trialFlorian von Groote-Bidlingmaier, Ramonde Patientia, Epifanio Sanchez, et al.
Nutrients|January 21, 2022
Prescription, Compliance, and Burden Associated with Salt-Restricted Diets in Heart Failure Patients: Results from the French National OFICSel ObservatoryThibaud Damy, Véronique Benedyga, Théo Pezel, et al.
Tuberculosis (Edinburgh, Scotland)|December 5, 2022
Microbiological profile, preclinical pharmacokinetics and efficacy of CRS0393, a novel antimycobacterial agent targeting MmpL3Urs A Ochsner, Mary A De Groote, Thale C Jarvis, et al.
European Urology Oncology|November 30, 2023
Positive Surgical Margins After Anterior Robot-assisted Radical Prostatectomy: Assessing the Learning Curve in a Multi-institutional CollaborationCarlo A Bravi, Paolo Dell'Oglio, Pietro Piazza, et al.
Eclinicalmedicine|July 21, 2025
Development of a World Health Organization indicator and corresponding questions to measure effective coverage of rehabilitationWouter De Groote, Pierre Côté, Jessica J Wong, et al.
Orphanet Journal of Rare Diseases|June 10, 2025
Comparison of two genetic strategies for diagnostic work-up of hypertrophic cardiomyopathy: impact on the diagnosis of Fabry disease or transthyretin amyloidosisAurélien Palmyre, Fairouz Koraichi, Flavie Ader, et al.
Clinical Neurology and Neurosurgery|December 11, 2012
Phenotypical characterization of α-galactosidase A gene mutations identified in a large Fabry disease screening program in stroke in the youngIsabel De Brabander, Laetitia Yperzeele, Chantal Ceuterick-De Groote, et al.
Cell Death and Differentiation|May 9, 2025
Development and validation of a high-throughput screening pipeline of compound libraries to target EMTSven Jonckheere, Joachim Taminau, Jamie Adams, et al.
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