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Orphanet Journal of Rare Diseases|November 6, 2019
Peripheral neuropathy in metachromatic leukodystrophy: current status and future perspectiveShanice Beerepoot, Stefan Nierkens, Jaap Jan Boelens, et al.Handbook of Clinical Neurology|March 27, 2025
Neuroglia in leukodystrophiesElly M Hol, Werner Dykstra, Juliette Chevalier, et al.Glia|December 30, 2017
Affected astrocytes in the spinal cord of the leukodystrophy vanishing white matterPrisca S Leferink, Nicole Breeuwsma, Marianna Bugiani, et al.Brain Pathology (Zurich, Switzerland)|April 22, 2026
Human brain matters: Navigating the neuropathology of COVID-19Juliana M Nieuwland, Angelica Scaramuzza, Marianna Bugiani, et al.Journal of Neuropathology and Experimental Neurology|September 15, 2010
Leukoencephalopathy with vanishing white matter: a reviewMarianna Bugiani, Ilja Boor, James M Powers, et al.Journal of Neuropathology and Experimental Neurology|April 2, 2004
Neuropathological and clinical phenotype of an Italian Alzheimer family with M239V mutation of presenilin 2 geneGabriella Marcon, Giorgio Giaccone, Chiara Cupidi, et al.Acta Neuropathologica|December 8, 2021
Heterogeneity of white matter astrocytes in the human brainMarianna Bugiani, Bonnie C Plug, Jodie H K Man, et al.Plos One|December 7, 2013
Amniotic fluid deficiency and congenital abnormalities both influence fluctuating asymmetry in developing limbs of human deceased fetusesClara Mariquita Antoinette ten Broek, Jessica Bots, Irma Varela-Lasheras, et al.BMJ Case Reports|June 21, 2011
A novel phenotype of sporadic Creutzfeldt-Jakob diseaseG Giaccone, Giuseppe Di Fede, Michela Mangieri, et al.Acta Neuropathologica Communications|June 4, 2021
Pathology of the neurovascular unit in leukodystrophiesParand Zarekiani, Marjolein Breur, Nicole I Wolf, et al.Pageof 18