Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Vasiliki Koukouni"'
Autor:
Christoph Kamm, Gregor K. Wenning, Eduardo Tolosa, Felix Geser, Olivier Rascol, Klaus Seppi, Nir Giladi, Christer Nilsson, Håkan Widner, Carlo Colosimo, Wassilios G. Meissner, Eldad Melamed, François Tison, Francesca Del Sorbo, Ruth Djaldetti, Sylvia Boesch, Erik Dupont, Florian Krismer, Günther Deuschl, Adriana Cardozo, Giuseppe Meco, Maria Teresa Pellecchia, Martin Köllensperger, Thomas Gasser, Christopher J. Mathias, Miguel Coelho, Niall Quinn, Karen Østergaard, Susanne Duerr, Tanya Gurevich, Richard Dodel, Alberto Albanese, Karl P. Pfeiffer, Karla Eggert, Anette Schrag, Georg Goebel, Thomas Klockgether, Werner Poewe, Wolfgang H. Oertel, Paolo Barone, Clare J. Fowler, Vasiliki Koukouni, Cristina Sampaio, Helge Hellriegel
Publikováno v:
Wenning, G K, Geser, F, Krismer, F, Seppi, K, Duerr, S, Boesch, S, Köllensperger, M, Goebel, G, Pfeiffer, K P, Barone, P, Pellecchia, M T, Quinn, N P, Koukouni, V, Fowler, C J, Schrag, A, Mathias, C J, Giladi, N, Gurevich, T, Dupont, E, Ostergaard, K, Nilsson, C F, Widner, H, Oertel, W, Eggert, K M, Albanese, A, Del Sorbo, F, Tolosa, E, Cardozo, A, Deuschl, G, Hellriegel, H, Klockgether, T, Dodel, R, Sampaio, C, Coelho, M, Djaldetti, R, Melamed, E, Gasser, T, Kamm, C, Meco, G, Colosimo, C, Rascol, O, Meissner, W G, Tison, F, Poewe, W & European Multiple System Atrophy Study Group 2013, ' The natural history of multiple system atrophy: a prospective European cohort study ', Lancet Neurology, vol. 12, no. 3, pp. 264-74 . https://doi.org/10.1016/S1474-4422(12)70327-7
Lancet Neurology
The lancet / Neurology 12(3), 264-274 (2013). doi:10.1016/S1474-4422(12)70327-7
Lancet Neurology
The lancet
Summary Background Multiple system atrophy (MSA) is a fatal and still poorly understood degenerative movement disorder that is characterised by autonomic failure, cerebellar ataxia, and parkinsonism in various combinations. Here we present the final
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1e1a99f9355747235020deb11457670
https://pure.au.dk/portal/da/publications/the-natural-history-of-multiple-system-atrophy-a-prospective-european-cohort-study(888596a0-c0a4-4450-ae05-7d423cd3aa51).html
https://pure.au.dk/portal/da/publications/the-natural-history-of-multiple-system-atrophy-a-prospective-european-cohort-study(888596a0-c0a4-4450-ae05-7d423cd3aa51).html
Autor:
Vasiliki, Koukouni, Kailash P, Bhatia
Publikováno v:
Handbook of clinical neurology. 84
Inherited myoclonus dystonia (M-D, DYTH) is an autosomal dominant dystonia-plus syndrome, which in many families is caused by mutations in the SGCE/tepsilon-sarcoglycan gene. We present a family with M-D, with an unusual presentaion characterized by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fc4b1ab44d66dd098d312ed3b2d2be0
http://hdl.handle.net/11386/3949690
http://hdl.handle.net/11386/3949690
Autor:
Martin, Kollensperger, Felix, Geser, Klaus, Seppi, Michaela Stampfer Kountchev, Martin, Sawires, Christoph, Scherfler, Sylvia, Boesch, Joerg, Mueller, Vasiliki, Koukouni, Niall, Quinn, Maria Teresa Pellecchia, Paolo, Barone, Nicole, Schimke, Richard, Dodel, Wolfgang, Oertel, Erik, Dupont, Ostergaard, K., Christine, Daniels, Günther, Deuschl, Tanya, Gurevich, Nir, Giladi, Miguel, Coelho, Cristina, Sampaio, Christer, Nilsson, Hakan, Widner, Francesca Del Sorbo, Alberto, Albanese, Adriana, Cardozo, Eduardo, Tolosa, Michael, Abele, Thomas, Klockgether, Christoph, Kamm, Thomas, Gasser, Ruth, Djaldetti, Colosimo, Carlo, Meco, Giuseppe, Anette, Schrag, Werner, Poewe, Wenning, Gregor K., Study Group Emsa Behalf Of The European Msa, O. N.
Publikováno v:
Köllensperger, M, Geser, F, Seppi, K, Stampfer-Kountchev, M, Sawires, M, Scherfler, C, Boesch, S, Mueller, J, Koukouni, V, Quinn, N, Pellecchia, M T, Barone, P, Schimke, N, Dodel, R, Oertel, W, Dupont, E, Østergaard, K, Daniels, C, Deuschl, G, Gurevich, T, Giladi, N, Coelho, M, Sampaio, C, Nilsson, C, Widner, H, Sorbo, F D, Albanese, A, Cardozo, A, Tolosa, E, Abele, M, Klockgether, T, Kamm, C, Gasser, T, Djaldetti, R, Colosimo, C, Meco, G, Schrag, A, Poewe, W, Wenning, G K & European MSA Study Group 2008, ' Red flags for multiple system atrophy ', Movement Disorders, vol. 23, no. 8, pp. 1093-9 . https://doi.org/10.1002/mds.21992
The clinical diagnosis Of Multiple system atrophy (MSA) is fraught with difficulty and there are no pathognomonic features to discriminate the parkinsonian variant (MSA-P) from Parkinson's disease (PD). Besides the poor response to levodopa, and the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5956cd1b5ada1454d4069c1faf22f3f6
http://hdl.handle.net/11386/3099441
http://hdl.handle.net/11386/3099441
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 22(6)
Primary cervical dystonia is typically an adult onset condition with symptom onset usually in the fifth and sixth decade. Young onset (
Autor:
Vasiliki Koukouni, MD 1, Davide Martino, MD 1 2, Gennarina Arabia, MD 1 3, Niall P. Quinn, Kailash P. Bhatia
Publikováno v:
Movement disorders 22(6) (2007): 843–847.
info:cnr-pdr/source/autori:Vasiliki Koukouni, MD 1, Davide Martino, MD 1 2, Gennarina Arabia, MD 1 3, Niall P. Quinn, MD 1, Kailash P. Bhatia, MD 1/titolo:The entity of young onset primary cervical dystonia/doi:/rivista:Movement disorders/anno:2007/pagina_da:843/pagina_a:847/intervallo_pagine:843–847/volume:22(6)
info:cnr-pdr/source/autori:Vasiliki Koukouni, MD 1, Davide Martino, MD 1 2, Gennarina Arabia, MD 1 3, Niall P. Quinn, MD 1, Kailash P. Bhatia, MD 1/titolo:The entity of young onset primary cervical dystonia/doi:/rivista:Movement disorders/anno:2007/pagina_da:843/pagina_a:847/intervallo_pagine:843–847/volume:22(6)
Primary cervical dystonia is typically an adult onset condition with symptom onset usually in the fifth and sixth decade. Young onset (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=cnr_________::6fd767ac55c4a3e10efb7331beed9121
https://publications.cnr.it/doc/50068
https://publications.cnr.it/doc/50068
Autor:
Eschlboeck, Sabine1 (AUTHOR), Goebel, Georg2 (AUTHOR), Eckhardt, Christine1,3 (AUTHOR), Fanciulli, Alessandra1 (AUTHOR), Raccagni, Cecilia1,4 (AUTHOR), Boesch, Sylvia1 (AUTHOR), Djamshidian, Atbin1 (AUTHOR), Heim, Beatrice1 (AUTHOR), Mahlknecht, Philipp1 (AUTHOR), Mair, Katherina1 (AUTHOR), Nachbauer, Wolfgang1 (AUTHOR), Scherfler, Christoph1 (AUTHOR), Stockner, Heike1 (AUTHOR), Poewe, Werner1 (AUTHOR), Seppi, Klaus1,5 (AUTHOR), Kiechl, Stefan1 (AUTHOR), Wenning, Gregor1 (AUTHOR) gregor.wenning@i-med.ac.at, Krismer, Florian1 (AUTHOR) florian.krismer@i-med.ac.at, Barone, Paolo (AUTHOR), Pellecchia, Maria Teresa (AUTHOR)
Publikováno v:
Movement Disorders Clinical Practice. Sep2023, Vol. 10 Issue 9, p1368-1376. 9p.
Autor:
Sako, Wataru, Goto, Satoshi, Shimazu, Hideki, Murase, Nagako, Matsuzaki, Kazuhito, Tamura, Tetsuya, Mure, Hideo, Tomogane, Yusuke, Arita, Norio, Yoshikawa, Hiroo, Nagahiro, Shinji, Kaji, Ryuji
Publikováno v:
Movement Disorders; Oct2008, Vol. 23 Issue 13, p1929-1931, 4p
Autor:
Boesch, Sylvia, Sturm, Brigitte, Hering, Sascha, Scheiber-Mojdehkar, Barbara, Steinkellner, Hannes, Goldenberg, Hans, Poewe, Werner
Publikováno v:
Movement Disorders; Oct2008, Vol. 23 Issue 13, p1940-1944, 9p
Autor:
Fasano, Alfonso, Piano, Carla, De Simone, Celestino, Cioni, Beatrice, Di Giuda, Daniela, Zinno, Massimiliano, Daniele, Antonio, Meglio, Mario, Giordano, Alessandro, Bentivoglio, Anna Rita
Publikováno v:
Movement Disorders; Oct2008, Vol. 23 Issue 13, p1916-1919, 7p