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Patient Education and Counseling|April 28, 2015
Learning from marketing: Rapid development of medication messages that engage patientsVeronica Yank, Erika Tribett, Lydia Green, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|May 6, 2004
Risk of bone loss in men with multiple sclerosisBianca Weinstock-Guttman, Eileen Gallagher, Monika Baier, et al.
Developmental Medicine and Child Neurology|August 28, 2018
Is chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids (CLIPPERS) in children the same condition as in adults?Mario Sa, Lydia Green, Omar Abdel-Mannan, et al.
European Journal of Human Genetics : EJHG|February 26, 2022
Missense mutation of MAL causes a rare leukodystrophy similar to Pelizaeus-Merzbacher diseaseMarilena Elpidorou, James A Poulter, Katarzyna Szymanska, et al.
F1000Research|December 20, 2016
Evaluation of recombinant monoclonal antibody SVmab1 binding to Na V1.7 target sequences and block of human Na V1.7 currentsDong Liu, Mandy Tseng, Linda F Epstein, et al.
Neuropediatrics|December 19, 2017
Whole Exon Deletion in the GFAP Gene Is a Novel Molecular Mechanism Causing Alexander DiseaseLydia Green, Ian R Berry, Anne-Marie Childs, et al.
European Journal of Human Genetics : EJHG|July 8, 2026
Whole-exome sequencing reveals novel and previously reported variants in genes linked to white matter pathology in neurodevelopmental disordersNaeem Ahmad, Tooba Aleem, Chunyu Liu, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 15, 2021
Prior activation state shapes the microglia response to antihuman TREM2 in a mouse model of Alzheimer's diseaseDaniel C Ellwanger, Shoutang Wang, Simone Brioschi, et al.
Human Mutation|February 12, 2019
Cerebral hypomyelination associated with biallelic variants of FIG4Guy M Lenk, Ian R Berry, Chloe A Stutterd, et al.
Research Square|July 17, 2026
Biallelic variants in SUPV3L1 cause a variable leukodystrophy due to impaired mitochondrial degradosome functionLydia Green, Noémie Hamilton, Marilena Elpidorou, et al.
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