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pro vyhledávání: '"Bhatia, Kp."'
Attention plays a crucial role in functional neurological disorders. Attention to the symptoms leads to their exacerbation and distraction to their improvement or even transitory disappearance. Objective: The aim was to test if the alerting, orientin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::c3b7a918ac2b71cc53d712a2e6593efe
https://openaccess.sgul.ac.uk/id/eprint/112565/1/fneur-11-00969.pdf
https://openaccess.sgul.ac.uk/id/eprint/112565/1/fneur-11-00969.pdf
Autor:
Mencacci, NE, Kamsteeg, E-J, Nakashima, K, R'Bibo, L, Lynch, DS, Balint, B, Willemsen, MAAP, Adams, ME, Wiethoff, S, Suzuki, K, Davies, CH, Ng, J, Meyer, E, Veneziano, L, Giunti, P, Hughes, D, Raymond, FL, Carecchio, M, Zorzi, G, Nardocci, N, Barzaghi, C, Garavaglia, B, Salpietro, V, Hardy, J, Pittman, AM, Houlden, H, Kurian, MA, Kimura, H, Vissers, LELM, Wood, NW, Bhatia, KP
Publikováno v:
European Human Genetics Conference 2016, pp. 32–33, Barcellona, Spain, 21-24/5/2016
info:cnr-pdr/source/autori:Mencacci, N. E.; Kamsteeg, E. J.; Nakashima, K; R'Bibo, L.; Lynch, D.; Balint, B.; Willemsen, M.; Adams, M.; Wiethoff, S.; Suzuki K; Davies, J; Ng, J.; Meyer, E.; Veneziano, L.; Giunti, P.; Hughes, D.; Raymond, L; Carecchio, M.; Zorzi, G.; Nardocci, N.; Barzaghi, C.; Garavaglia, B.; Salpietro, V.; Hardy, J.; Pittman, A.; Houlden, H.; Kurian, M.; Kimura H; Wood, N.; Bhatia, K; Vissers L./congresso_nome:European Human Genetics Conference 2016/congresso_luogo:Barcellona, Spain/congresso_data:21-24%2F5%2F2016/anno:2016/pagina_da:32/pagina_a:33/intervallo_pagine:32–33
American Journal of Human Genetics, 98, 4, pp. 763-71
American Journal of Human Genetics, 98, 763-71
info:cnr-pdr/source/autori:Mencacci, N. E.; Kamsteeg, E. J.; Nakashima, K; R'Bibo, L.; Lynch, D.; Balint, B.; Willemsen, M.; Adams, M.; Wiethoff, S.; Suzuki K; Davies, J; Ng, J.; Meyer, E.; Veneziano, L.; Giunti, P.; Hughes, D.; Raymond, L; Carecchio, M.; Zorzi, G.; Nardocci, N.; Barzaghi, C.; Garavaglia, B.; Salpietro, V.; Hardy, J.; Pittman, A.; Houlden, H.; Kurian, M.; Kimura H; Wood, N.; Bhatia, K; Vissers L./congresso_nome:European Human Genetics Conference 2016/congresso_luogo:Barcellona, Spain/congresso_data:21-24%2F5%2F2016/anno:2016/pagina_da:32/pagina_a:33/intervallo_pagine:32–33
American Journal of Human Genetics, 98, 4, pp. 763-71
American Journal of Human Genetics, 98, 763-71
Contains fulltext : 167700.pdf (Publisher’s version ) (Open Access) Chorea is a hyperkinetic movement disorder resulting from dysfunction of striatal medium spiny neurons (MSNs), which form the main output projections from the basal ganglia. Here,
Autor:
Balint, B, Mencacci, Ne, Valente, Em, Pisani, A, Rothwell, J, Jankovic, J, Vidailhet, M, Bhatia, Kp
Publikováno v:
Nature Reviews Disease Primers. 4
Autor:
Kassavetis, P, Sadnicka, A, Saifee, TA, Pareés, I, Kojovic, M, Bhatia, KP, Rothwell, JC, Edwards, MJ
BACKGROUND: Surround inhibition (SI) in the motor system has been described to be decreased in patients with focal hand dystonia (FHD) but no evidence currently exists for patients with cervical dystonia (CD). OBJECTIVE: To characterise the SI profil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::533bb816bf15c95b91ebdf7075939a76
Autor:
Balint, B, Killaspy, H, Marston, L, Barnes, T, Latorre, A, Joyce, E, Clarke, CS, De Micco, R, Edwards, MJ, Erro, R, Foltynie, T, Hunter, RM, Nolan, F, Schrag, A, Freemantle, N, Foreshaw, Y, Green, N, Bhatia, KP, Martino, D
Publikováno v:
BJPsych Open
Background: Movement disorders associated with exposure to antipsychotic drugs are common and stigmatising but underdiagnosed. Aims: To develop and evaluate a new clinical procedure, the ScanMove instrument, for the screening of antipsychotic-associa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::7cbdd014c308d0ab09f637692313b562
http://hdl.handle.net/11386/4717372
http://hdl.handle.net/11386/4717372
Autor:
Batla, A, De Pablo-Fernandez, E, Erro, R, Reich, M, Calandra-Buonaura, G, Barbosa, P, Balint, B, Ling, H, Islam, S, Cortelli, P, Volkmann, J, Quinn, N, Holton, Jl, Warner, Tt, Bhatia, Kp.
Background: The onset of multiple system atrophy (MSA) before age 40 years is referred to as “young-onset MSA.” We identified clinical and pathological characteristics that might help with its early diagnosis and distinction from young-onset Park
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::a78690779c3833d956a5127c1220e0cd
http://hdl.handle.net/11585/642763
http://hdl.handle.net/11585/642763
Publikováno v:
Brain
Movement disorders are a common feature of autoantibody-associated diseases. Balint et al. provide a novel phenotype-oriented algorithmic approach to guide diagnosis. They review the underlying pathophysiology and point out parallels between immune-m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::6892c93a001873f481895cd070b55bf9
https://doi.org/10.1093/brain/awx189
https://doi.org/10.1093/brain/awx189
Autor:
Bhatia, KP, Bain, P, Bajaj, N, Elble, RJ, Hallett, M, Louis, ED, Raethjen, J, Stamelou, M, Testa, CM, Deuschl, G, Tremor Task Force of the International Parkinson and Movement Disorder Society
BACKGROUND: Consensus criteria for classifying tremor disorders were published by the International Parkinson and Movement Disorder Society in 1998. Subsequent advances with regard to essential tremor, tremor associated with dystonia, and other monos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1032::056b57a72e0fdc1b2762a8e7b741d405
http://hdl.handle.net/10044/1/58115
http://hdl.handle.net/10044/1/58115
Autor:
Meyer E, Carss KJ, Rankin J, Nichols JM, Grozeva D, Joseph AP, Mencacci NE, Papandreou A, Ng J, Barral S, Ngoh A, Ben-Pazi H, Willemsen MA, Arkadir D, Barnicoat A, Bergman H, Bhate S, Boys A, Darin N, Foulds N, Gutowski N, Hills A, Houlden H, Hurst JA, Israel Z, Kaminska M, Limousin P, Lumsden D, McKee S, Misra S, Mohammed SS, Nakou V, Nicolai J, Nilsson M, Pall H, Peall KJ, Peters GB, Prabhakar P, Reuter MS, Rump P, Segel R, Sinnema M, Smith M, Turnpenny P, White SM, Wieczorek D, Wiethoff S, Wilson BT, Winter G, Wragg C, Pope S, Heales SJ, Morrogh D, UK10K Consortium, Deciphering Developmental Disorders Study, NIHR BioResource Rare Diseases Consortium, Pittman A, Carr LJ, Pérez-Dueñas B, Lin JP, Reis A, Gahl WA, Toro C, Bhatia KP, Wood NW, Kamsteeg EJ, Chong WK, Gissen P, Topf M, Dale RC, Chubb JR, Raymond FL, Kurian MA
Publikováno v:
NATURE GENETICS
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
Histone lysine methylation, mediated by mixed-lineage leukemia (MLL) proteins, is now known to be critical in the regulation of gene expression, genomic stability, cell cycle and nuclear architecture. Despite MLL proteins being postulated as essentia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::2704902d0305fbe3d8dc66d2b7cbf736
https://www.repository.cam.ac.uk/handle/1810/296243
https://www.repository.cam.ac.uk/handle/1810/296243