The movement disorder associated with NMDAR antibody-encephalitis is complex and characteristic: an expert video-rating study

Autor: Varley, J, Webb, A, Balint, B, Fung, V, Sethi, K, Tijssen, MAJ, Lynch, T, Mohammad, SS, Britton, F, Evans, M, Hacohen, Y, Lin, JP, Nardocci, N, Granata, T, Dale, RC, Lim, RM, Bhatia, K, Lang, A, Irani, SR

Publikováno v: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 90(6), 724-726. BMJ PUBLISHING GROUP

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::c7e9fbdb29f98bda63f94a6810f75952
https://doi.org/10.1136/jnnp-2018-318584

The eye of the beholder: Inter-rater agreement among experts on psychogenic jerky movement disorders

Autor: Van Der Salm SMA, De Haan RJ, Cath DC, Van Rootselaar A-F, Tijssen MAJ, Bhatia KP, Brown P, Carson A, Cavanna A, Caviness JN, Davenport R, Edwards MJ, Espay A, Ferlazzo E, Franceschetti S, Fung V, Gilbert DL, Goetz CG, Guerrini R, Hallett M, Hounie AG, Jankovic J, Klein C, Lang A, Limousin P, Martino D, Muller-Vahl KR, Münchau A, Nahab F, Orth M, Reuber M, Roze E, Rubboli G, Sandor P, Schrader C, Schrag A, Shibasaki H, Stone J, Striano P, Striano S, Tolosa E, Ugawa Y, Vidailhet M, Weiner W

Publikováno v: JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 84(7), 742-747. BMJ PUBLISHING GROUP
Journal of neurology, neurosurgery, and psychiatry, 84(7), 742-747. BMJ Publishing Group

Objective The current criteria for conversion disorder in the Diagnostic and Statistical Manual of Mental Disorders rely on the assumption that neurological disorders can be distinguished from conversion disorders through clinical assessment. This st

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b03b577cb221cccb216f79029ec85b89
https://hdl.handle.net/11567/1023879

Mutations in the Na+/K+-ATPase alpha 3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism

Autor: Aguiar, PD, Sweadner, KJ, Penniston, JT, Zaremba, J, Liu, L, Caton, M, Linazasoro, G, Borg, M, Tijssen, MAJ, Bressman, SB, Dobyns, WB, Brashear, A, Ozelius, LJ

Publikováno v: Neuron, 43(2), 169-175. CELL PRESS

Rapid-onset dystonia-parkinsonism (RDP, DYT12) is a distinctive autosomal-dominant movement disorder with variable expressivity and reduced penetrance characterized by abrupt onset of dystonia, usually accompanied by signs of parkinsonism. The sudden

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=narcis______::65cd3abb591529aa5d46e8841cc8d304
https://research.rug.nl/en/publications/089cf45a-122b-427b-9e87-19e8476224e6

A Dutch family with 'familial cortical tremor with epilepsy' - Clinical characteristics and exclusion of linkage to chromosome 8q23.3-q24.1

Autor: van Rootselaar, F, Callenbach, PMC, Hottenga, JJ, Vermeulen, FLMG, Speelman, HD, Brouwer, OF, Tijssen, MAJ

Publikováno v: Journal of Neurology, 249(7), 829-834. SPRINGER HEIDELBERG

Objectives To describe the clinical characteristics of a large Dutch family with cortical tremor with epilepsy (FCTE) and to test for genetic linkage of FCTE to chromosome 8q23.3-q24.1. Background FCTE is an idiopathic generalised epilepsy of adult o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=narcis______::07ada88070f23b7027111e8096917deb
https://research.rug.nl/en/publications/37e7fab9-4f1e-49b1-bb65-22c726267509

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.