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Frontiers in Medicine|January 5, 2024
Bronchial obstruction in osteogenesis imperfecta can be detected by forced oscillation techniqueSilvia Storoni, Sara J E Verdonk, Dimitra Micha, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|August 27, 2024
Case Series of 6 Fetuses With Osteogenesis Imperfecta Type II: A Retrospective Study of Heart PathologySara J E Verdonk, Silvia Storoni, Lidiia Zhytnik, et al.
Neurobiology of Disease|February 7, 2026
Astrocyte-specific deletion of LRRC8A causes neurological dysfunction but not chronic white matter edemaSven Kerst, Leoni Hoogterp, Marjolein Breur, et al.
Acta Neuropathologica Communications|June 22, 2023
Regional vulnerability of brain white matter in vanishing white matterJodie H K Man, Charlotte A G H van Gelder, Marjolein Breur, et al.
American Journal of Medical Genetics. Part A|May 5, 2021
Childhood onset nexilin dilated cardiomyopathy: A heterozygous and a homozygous caseLuc Bruyndonckx, Judith L Vogelzang, Marianna Bugiani, et al.
Annals of Neurology|October 27, 2025
Endogenous Repair in Vanishing White MatterBonnie C Plug, Jodie H K Man, Marjolein Breur, et al.
Cellular and Molecular Life Sciences : CMLS|May 24, 2024
Proteomic dissection of vanishing white matter pathogenesisJodie H K Man, Parand Zarekiani, Peter Mosen, et al.
Advanced Healthcare Materials|December 20, 2019
Modulating Macrophage Phenotype by Sustained MicroRNA Delivery Improves Host-Implant IntegrationJunquan Lin, Ibrahim Mohamed, Po Hen Lin, et al.
Journal of Neuropathology and Experimental Neurology|October 11, 2005
Sporadic Creutzfeldt-Jakob disease: the extent of microglia activation is dependent on the biochemical type of PrPScGianfranco Puoti, Giorgio Giaccone, Michela Mangieri, et al.
Neuropediatrics|January 13, 2022
Early-Onset Vascular Leukoencephalopathy Caused by Bi-Allelic NOTCH3 VariantsMenno D Stellingwerff, Corinne Nulton, Guy Helman, et al.
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