Neurodegenerative Disease Risk in Carriers of Autosomal Recessive Disease

by Sophia R. L. Vieira, Huw R. Morris
Published 2021-06-01

Early Onset Parkinson’s Disease in a family of Moroccan origin caused by a p.A217D mutation in PINK1: a case report

by Brendan P. Norman, Steven J. Lubbe, Manuela Tan, Naomi Warren, Huw R. Morris
Published 2017-08-01

Neural correlates of early cognitive dysfunction in Parkinson's disease

by Rimona S. Weil, Joel S. Winston, Louise‐Ann Leyland, Katerina Pappa, Ribeya B. Mahmood, Huw R. Morris, Geraint Rees
Published 2019-05-01

Comparison between four published definitions of hyposmia in Parkinson's disease

by Sofia Kanavou, Vanessa Pitz, Michael A. Lawton, Naveed Malek, Katherine A. Grosset, Huw R. Morris, Yoav Ben‐Shlomo, Donald G. Grosset
Published 2021-08-01

A Case of Treatment Resistance and Complications in a Patient with Stiff Person Syndrome and Cerebellar Ataxia

by Lliwen A. Jones, Waqaar Baber, Mark Wardle, Neil P. Robertson, Huw R Morris, Alistair Church, John G. Llewelyn, Kathryn J. Peall
Published 2019-10-01

Sensitivity and Specificity of the ECAS in Parkinson’s Disease and Progressive Supranuclear Palsy

by Jennifer A. Foley, Elaine H. Niven, Andrew Paget, Kailash P. Bhatia, Simon F. Farmer, Paul R. Jarman, Patricia Limousin, Thomas T. Warner, Huw R. Morris, Thomas H. Bak, Sharon Abrahams, Lisa Cipolotti
Published 2018-01-01

Automated Brainstem Segmentation Detects Differential Involvement in Atypical Parkinsonian Syndromes

by Martina Bocchetta, Juan Eugenio Iglesias, Viorica Chelban, Edwin Jabbari, Ruth Lamb, Lucy L. Russell, Caroline V. Greaves, Mollie Neason, David M. Cash, David L. Thomas, Jason D. Warren, John Woodside, Henry Houlden, Huw R. Morris, Jonathan D. Rohrer
Published 2020-01-01

Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease.

by Javier Simón-Sánchez, Laura L Kilarski, Michael A Nalls, Maria Martinez, Claudia Schulte, Peter Holmans, International Parkinson's Disease Genomics Consortium, Wellcome Trust Case Control Consortium, Thomas Gasser, John Hardy, Andrew B Singleton, Nicholas W Wood, Alexis Brice, Peter Heutink, Nigel Williams, Huw R Morris
Published 2012-01-01

Creation of an open-access, mutation-defined fibroblast resource for neurological disease research.

by Selina Wray, Matthew Self, NINDS Parkinson's Disease iPSC Consortium, NINDS Huntington's Disease iPSC Consortium, NINDS ALS iPSC Consortium, Patrick A Lewis, Jan-Willem Taanman, Natalie S Ryan, Colin J Mahoney, Yuying Liang, Michael J Devine, Una-Marie Sheerin, Henry Houlden, Huw R Morris, Daniel Healy, Jose-Felix Marti-Masso, Elisavet Preza, Suzanne Barker, Margaret Sutherland, Roderick A Corriveau, Michael D'Andrea, Anthony H V Schapira, Ryan J Uitti, Mark Guttman, Grzegorz Opala, Barbara Jasinska-Myga, Andreas Puschmann, Christer Nilsson, Alberto J Espay, Jaroslaw Slawek, Ludwig Gutmann, Bradley F Boeve, Kevin Boylan, A Jon Stoessl, Owen A Ross, Nicholas J Maragakis, Jay Van Gerpen, Melissa Gerstenhaber, Katrina Gwinn, Ted M Dawson, Ole Isacson, Karen S Marder, Lorraine N Clark, Serge E Przedborski, Steven Finkbeiner, Jeffrey D Rothstein, Zbigniew K Wszolek, Martin N Rossor, John Hardy
Published 2012-01-01