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Movement Disorders : Official Journal of the Movement Disorder Society|July 12, 2005
UCHL-1 gene in multiple system atrophy: a haplotype tagging approachDaniel G Healy, Patrick M Abou-Sleiman, Niall Quinn, et al.
Human Molecular Genetics|May 1, 2019
MRPS25 mutations impair mitochondrial translation and cause encephalomyopathyEnrico Bugiardini, Alice L Mitchell, Ilaria Dalla Rosa, et al.
Annals of Neurology|February 2, 2006
UCHL-1 is not a Parkinson's disease susceptibility geneDaniel G Healy, Patrick M Abou-Sleiman, Juan P Casas, et al.
Neuromuscular Disorders : NMD|September 29, 2019
Genetic and phenotypic characterisation of inherited myopathies in a tertiary neuromuscular centreEnrico Bugiardini, Alaa M Khan, Rahul Phadke, et al.
Nature|November 5, 2025
A probabilistic histological atlas of the human brain for MRI segmentationAdrià Casamitjana, Matteo Mancini, Eleanor Robinson, et al.
Brain : a Journal of Neurology|September 13, 2011
Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degenerationJonathan D Rohrer, Tammaryn Lashley, Jonathan M Schott, et al.
American Journal of Human Genetics|April 5, 2016
Cryptic Amyloidogenic Elements in the 3' UTRs of Neurofilament Genes Trigger Axonal NeuropathyAdriana P Rebelo, Alexander J Abrams, Ellen Cottenie, et al.
Biorxiv : the Preprint Server for Biology|September 16, 2024
A next-generation, histological atlas of the human brain and its application to automated brain MRI segmentationAdrià Casamitjana, Matteo Mancini, Eleanor Robinson, et al.
Arthritis and Rheumatism|October 2, 2007
International consensus on a proposed score system for muscle biopsy evaluation in patients with juvenile dermatomyositis: a tool for potential use in clinical trialsLucy R Wedderburn, Hemlata Varsani, Charles K C Li, et al.
Annals of the Rheumatic Diseases|September 26, 2013
Validation of a score tool for measurement of histological severity in juvenile dermatomyositis and association with clinical severity of diseaseHemlata Varsani, Susan C Charman, Charles K Li, et al.
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