Small Fibre Neuropathy in Parkinson’s Disease: Comparison of Skin Biopsies from the More Affected and Less Affected Sides

Autor Jeziorska, Maria, Atkinson, Andrew, Kass-Iliyya, Lewis, Kobylecki, Christopher, Gosal, David, Marshall, Andrew, Malik, Rayaz A., Silverdale, Monty
Vydáno v J Parkinsons Dis (2019)

Spinal cord compression from hypertrophic nerve roots in chronic inflammatory demyelinating polyradiculoneuropathy – A case report

Autor Hasan, Md Tanvir, Patil, Subodh, Chauhan, Vanisha, Gosal, David, Ealing, John, Du Plessis, Daniel, Soh, Calvin, George, K. Joshi
Vydáno v Surg Neurol Int (2021)

Increased Intraepidermal Nerve Fiber Degeneration and Impaired Regeneration Relate to Symptoms and Deficits in Parkinson's Disease

Autor Jeziorska, Maria, Atkinson, Andrew, Kass-Iliyya, Lewis, Javed, Saad, Kobylecki, Christopher, Gosal, David, Marshall, Andrew, Silverdale, Monty, Malik, Rayaz A.
Vydáno v Front Neurol (2019)

Familial genes in sporadic disease: Common variants of α-Synuclein gene associate with Parkinson’s disease

Autor Ross, Owen A., Gosal, David, Stone, Jeremy T., Lincoln, Sarah J., Heckman, Michael G., Irvine, Brent G., Johnston, Janet A., Gibson, J. Mark, Farrer, Matthew J., Lynch, Timothy
Vydáno 2007

Small fiber neuropathy in Parkinson's disease: A clinical, pathological and corneal confocal microscopy study

Autor Kass-Iliyya, Lewis, Javed, Saad, Gosal, David, Kobylecki, Christopher, Marshall, Andrew, Petropoulos, Ioannis N., Ponirakis, Georgios, Tavakoli, Mitra, Ferdousi, Maryam, Chaudhuri, Kallol Ray, Jeziorska, Maria, Malik, Rayaz A., Silverdale, Monty A.
Vydáno v Parkinsonism Relat Disord (2015)

Genomewide Association, Parkinson Disease, and PARK10

Autor Farrer, Matthew J., Haugarvoll, Kristoffer, Ross, Owen A., Stone, Jeremy T., Milkovic, Nicole M., Cobb, Stephanie A., Whittle, Andrew J., Lincoln, Sarah J., Hulihan, Mary M., Heckman, Michael G., White, Linda R., Aasly, Jan O., Gibson, J. Mark, Gosal, David, Lynch, Timothy, Wszolek, Zbigniew K., Uitti, Ryan J., Toft, Mathias
Vydáno 2006

Translation Initiator EIF4G1 Mutations in Familial Parkinson Disease

Autor Chartier-Harlin, Marie-Christine, Dachsel, Justus C., Vilariño-Güell, Carles, Lincoln, Sarah J., Leprêtre, Frédéric, Hulihan, Mary M., Kachergus, Jennifer, Milnerwood, Austen J., Tapia, Lucia, Song, Mee-Sook, Le Rhun, Emilie, Mutez, Eugénie, Larvor, Lydie, Duflot, Aurélie, Vanbesien-Mailliot, Christel, Kreisler, Alexandre, Ross, Owen A., Nishioka, Kenya, Soto-Ortolaza, Alexandra I., Cobb, Stephanie A., Melrose, Heather L., Behrouz, Bahareh, Keeling, Brett H., Bacon, Justin A., Hentati, Emna, Williams, Lindsey, Yanagiya, Akiko, Sonenberg, Nahum, Lockhart, Paul J., Zubair, Abba C., Uitti, Ryan J., Aasly, Jan O., Krygowska-Wajs, Anna, Opala, Grzegorz, Wszolek, Zbigniew K., Frigerio, Roberta, Maraganore, Demetrius M., Gosal, David, Lynch, Tim, Hutchinson, Michael, Bentivoglio, Anna Rita, Valente, Enza Maria, Nichols, William C., Pankratz, Nathan, Foroud, Tatiana, Gibson, Rachel A., Hentati, Faycal, Dickson, Dennis W., Destée, Alain, Farrer, Matthew J.
Vydáno 2011