Inherited Prion Disease (PrP Lysine 200) In Britain: Two Case Reports

Autor: Collinge, John, Palmer, Mark S., Campbell, Tracy, Sidle, Katie C. L., Carroll, Desmond, Harding, Anita

Publikováno v: BMJ: British Medical Journal, 1993 Jan . 306(6873), 301-302.

Externí odkaz: https://www.jstor.org/stable/29718386

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Molecular classification of sporadic Creutzfeldt-Jakob disease.

Autor: Hill, Andrew F, Joiner, Susan, Wadsworth, Jonathan D F, Sidle, Katie C L, Bell, Jeanne E, Budka, Herbert, Ironside, James W, Collinge, John

Publikováno v: Brain: A Journal of Neurology; June 2003, Vol. 126 Issue: 6 p1333-1346, 14p

Impact of disease, cognitive and behavioural factors on caregiver outcome in amyotrophic lateral sclerosis

Autor: Tamlyn J. Watermeyer, Brown, Richard G., Sidle, Katie C. L., Oliver, David J., Allen, Christopher, Karlsson, Joanna, Ellis, Cathy, Shaw, Christopher E., Al-Chalabi, Ammar, Goldstein, Laura H.

Up to 50% of patients with amyotrophic lateral sclerosis (ALS) show mild to moderate cognitive-behavioural change alongside their progressive functional impairment. This study examines the relative impact of patients’ disease symptoms, behavioural

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5f33afa5b9b3f4d29e2c7030b4bfc9ca

Molecular classification of sporadic Creutzfeldt-Jakob disease.

Autor: Hill AF; MRC Prion Unit, Department of Neurodegenerative Disease, Institute of Neurology, National Hospital for Neurology and Neurosurgery, London, UK., Joiner S, Wadsworth JD, Sidle KC, Bell JE, Budka H, Ironside JW, Collinge J

Publikováno v: Brain : a journal of neurology [Brain] 2003 Jun; Vol. 126 (Pt 6), pp. 1333-46.