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Movement Disorders Clinical Practice|July 18, 2022
Longitudinal Follow-Up of Mood in Cervical Dystonia and Influence on Age at OnsetAndrew Moriarty, Shameer Rafee, Ihedinachi Ndukwe, et al.Movement Disorders Clinical Practice|April 27, 2026
Age at Onset Predicts Motor and Non-motor Severity in Cervical DystoniaShameer Rafee, Laura Williams, Sean O'Riordan, et al.Clinical Neuropathology|December 22, 2018
Blood-brain barrier dysfunction in a boxer with chronic traumatic encephalopathy and schizophreniaMichael Farrell, Susan Aherne, Sean O'Riordan, et al.The Neuroradiology Journal|April 21, 2017
Semi-quantitative analysis of cerebral FDG-PET reveals striatal hypermetabolism and normal cortical metabolism in a case of VGKCC limbic encephalitisPatrick Moloney, Ruth Boylan, Marwa Elamin, et al.Cardiovascular and Interventional Radiology|February 16, 2017
Non-surgical Management of a Mycotic Internal Iliac Artery Aneurysm in a Neonate: Case Report and Review of the LiteraturePhilippa Jackson, Helen Bryant, Jeanette Kraft, et al.CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|November 21, 2009
Risk factors and outcomes among children admitted to hospital with pandemic H1N1 influenzaSean O'Riordan, Michelle Barton, Yvonne Yau, et al.Journal of Neurology, Neurosurgery, and Psychiatry|August 21, 2007
Sporadic adult onset dystonia: sensory abnormalities as an endophenotype in unaffected relativesRichard Walsh, John P O'Dwyer, Ifthikar H Sheikh, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 25, 2004
Inherited myoclonus-dystonia and epilepsy: further evidence of an association?Sean O'Riordan, Laurie J Ozelius, Patricia de Carvalho Aguiar, et al.Disability and Rehabilitation|December 24, 2024
"A young person in an old person's body": a reflexive thematic analysis of the experience of living with young onset Parkinson's diseaseEmma Cullen, Fiona J R Eccles, Gary Byrne, et al.Genes and Immunity|March 10, 2022
Identification of a novel MAGT1 mutation supports a diagnosis of XMEN diseaseChristopher M Watson, Fatima Nadat, Sammiya Ahmed, et al.Pageof 6