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Association of CAG Repeats With Long-term Progression in Huntington Disease

Autor: Langbehn, D.R., Stout, J.C., Gregory, S., Mills, J.A., Durr, A., Leavitt, B.R., Roos, R.A.C., Long, J.D., Owen, G., Johnson, H.J., Borowsky, B., Craufurd, D., Reilmann, R., Landwehrmeyer, G.B., Scahill, R.I., Tabrizi, S.J., Acharya, T., Andrews, S., Arran, N., Axelson, E., Bardinet, E., Bechtel, N., Berna, C., Bohlen, S., Callaghan, J., Cassidy, A., Coleman, A., Crawford, H., Santos, R.D., Decolongon, J., Dumas, E., Fan, M.N., Frost, C., Ghosh, R., Gibbard, C., Hensman-Moss, D., Hobbs, N., Jauffret, C., Johnson, E., Jones, R., Jurgens, C., Justo, D., Keogh, R., Koren, T., Labuschagne, I., Lahiri, N., Lehericy, S., Malone, I., Marelli, C., McColgan, P., Nigaud, K., O'Regan, A., Papoutsi, M., Pepple, T., Petkau, T., Queller, S., Read, J., Say, M., Schoonderbeek, A., Stopford, C., Sturrock, A., Hart, E. 't, Valabregue, R., Bogaard, S. van den, Grond, J. van der, Wang, C.C., Weber, N., Whitehead, D., Witjes-Ane, M.N., TRACK-HD Track-On HD Grps

Publikováno v: JAMA Neurology, 76(11), 1375-1385
JAMA Neurol

Importance In Huntington disease (HD), mutation severity is defined by the length of the CAG trinucleotide sequence, a well-known predictor of clinical onset age. The association with disease trajectory is less well characterized. Quantifiable summar

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::177da7de07750f9a3e1cdad1b83189d0
https://hdl.handle.net/1887/120789

Apathy associated with impaired recognition of happy facial expressions in Huntington's disease

Autor: Osborne-Crowley, K., Andrews, S.C., Labuschagne, I., Nair, A., Scahill, R., Craufurd, D., Tabrizi, S.J., Stout, J.C., Campbell, C., Campbell, M., Frajman, E., Milchman, C., O'Regan, A., Coleman, A., Santos, R.D., Decolongon, J., Sturrock, A., Bardinet, E., Jauffret, C., Justo, D., Lehericy, S., Marelli, C., Nigaud, K., Pourchot, P., Valabregue, R., Bechtel, N., Bohlen, S., Reilmann, R., Hoffman, A., Kraus, P., Landwehrmeyer, B., Bogaard, S.J.A. van den, Dumas, E.M., Grond, J. van der, t'Hart, E.P., Jurgens, C., Witjes-Ane, M.N., Arran, N., Callaghan, J., Stopford, C., Frost, C., Jones, R., Berna, C., Crawford, H., Fox, N., Gibbard, C., Hobbs, N., Lahiri, N., Malone, I., Ordidge, R., Owen, G., Patel, A., Pepple, T., Read, J., Say, M., Whitehead, D., Wild, E., Keenan, S., Cash, D.M., Hicks, S., Kennard, C., Acharya, T., Axelson, E., Johnson, H., Langbehn, D., Wang, C., Lee, S., Monaco, W., Rosas, H., Queller, S., Whitlock, K., Borowsky, B., Tobin, A., TRACK-HD Investigators

Publikováno v: Journal of the International Neuropsychological Society, 25(5), 453-461

Objectives: Previous research has demonstrated an association between emotion recognition and apathy in several neurological conditions involving fronto-striatal pathology, including Parkinson’s disease and brain injury. In line with these findings

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::936643670760a9137524f05d8bda6aac
https://acuresearchbank.acu.edu.au/item/8w21z/apathy-associated-with-impaired-recognition-of-happy-facial-expressions-in-huntington-s-disease

Testing a longitudinal compensation model in premanifest Huntington’s disease

Autor: Gregory, Sarah, Long, Jeffrey D, Klöppel, Stefan, Razi, Adeel, Scheller, Elisa, Minkova, Lora, Johnson, Eileanoir B, Durr, Alexandra, Roos, Raymund A C, Leavitt, Blair R, Mills, James A, Stout, Julie C, Scahill, Rachael I, Tabrizi, Sarah J, Rees, Geraint, Coleman, A, Decolongon, J, Fan, M, Koren, T, Leavitt, B, Durr, A, Jauffret, C, Justo, D, Lehericy, S, Nigaud, K, Valabrègue, R, Roos, R, Hart, E P ‘T, Schoonderbeek, A, Berna, C, Crawford, H, Ghosh, R, Hensman, D, Johnson, E, McColgan, P, Papoutsi, M, Read, J, Owen, G, Craufurd, D, Reilmann, R, Weber, N, Labuschagne, I, Landwehrmeyer, B, Orth, M

Publikováno v: Gregory, Sarah; Long, Jeffrey D; Klöppel, Stefan; Razi, Adeel; Scheller, Elisa; Minkova, Lora; Johnson, Eileanoir B; Durr, Alexandra; Roos, Raymund A C; Leavitt, Blair R; Mills, James A; Stout, Julie C; Scahill, Rachael I; Tabrizi, Sarah J; Rees, Geraint; Coleman, A; Decolongon, J; Fan, M; Koren, T; Leavitt, B; ... (2018). Testing a longitudinal compensation model in premanifest Huntington’s disease. Brain, 141(7), pp. 2156-2166. Oxford University Press 10.1093/brain/awy122

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7252054eabf5618ee8130576774da380
https://boris.unibe.ch/116919/1/awy122.pdf

Working memory-related effective connectivity in Huntington's disease patients

Autor: Lahr, Jacob, Minkova, Lora, Tabrizi, Sarah J., Stout, Julie C., Klöppel, Stefan, Scheller, Elisa, the TrackOn-HD Investigators, Labuschagne, I.

Huntington’s disease (HD) is a genetically caused neurodegenerative disorder characterized by heterogeneous motor, psychiatric, and cognitive symptoms. Although motor symptoms may be the most prominent presentation, cognitive symptoms such as memor

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3651::a70797b5992c1bddb41349485d732f12
https://acuresearchbank.acu.edu.au/item/8x3v8/working-memory-related-effective-connectivity-in-huntington-s-disease-patients