Zobrazeno 1 - 10
of 28
pro vyhledávání: '"J. G. de Yebenes"'
Autor:
J G, de Yebenes
Publikováno v:
Revista de neurologia. 65(9)
Cervantes y la enfermedad de Parkinson.
Autor:
J. R. Davila, M-J Sobrido, Conceição Bettencourt, Orr Shomroni, Marianna R. Bevova, Jose Lopez-Sendon, Beatriz Quintáns, I. Bakker, Peter Heutink, Juan García-Caldentey, J. G. de Yebenes, Patrizia Rizzu
Publikováno v:
Clinical Genetics. 85:154-158
Hereditary spastic paraplegias constitute a heterogeneous group of neurodegenerative diseases encompassing pure and complicated forms, for which at least 52 loci and 31 causative genes have been identified. Although mutations in the SPAST gene explai
Autor:
Peter Heutink, David J. Burn, Bernhard Landwehrmeyer, J. C. van Swieten, S. Wagner, K. A. Frey, Zygmunt Jamrozik, T. Gasser, Günter U. Höglinger, Hans A. Kretzschmar, D. Caparros-Lefebvre, A. Saint-Raymond, Zbigniew K. Wszolek, Jan Kassubek, T. Reum, Markus Otto, Markus Tolnay, A. Kazantsev, Wolfgang H. Oertel, J. J. Lucas, John C. Steele, Stacey Melquist, M. T. Vanier, Dominic C. Paviour, Anthony E. Lang, Eva Maria Mandelkow, Jean Paul G. Vonsattel, Irene Litvan, Hayrettin Tumani, Albert C. Ludolph, Patrick L. McGeer, Kurt A. Jellinger, J. G. de Yebenes, E. M. Mandelkow
Publikováno v:
Ludolph, A C, Kassubek, J, Landwehrmeyer, B G, Mandelkow, E, Mandelkow, E M, Burn, D J, Caparros-Lefebvre, D, Frey, K A, Yebenes, J G, Gasser, T, Heutink, P, Hoglinger, G, Jamrozik, Z, Jellinger, K A, Kazantsev, A, Kretzschmar, H, Lang, A E, Litvan, I, Lucas, J J, McGeer, P L, Melquist, S, Oertel, W, Otto, M, Paviour, D, Reum, T, Saint-Raymond, A, Steele, J C, Tolnay, M, Tumani, H, van Swieten, J C, Vanier, M T, Vonsattel, J P, Wagner, S & Wszolek, Z K 2009, ' Tauopathies with parkinsonism: clinical spectrum, neuropathologic basis, biological markers, and treatment options ', European Journal of Neurology, vol. 16, no. 3, pp. 297-309 . https://doi.org/10.1111/j.1468-1331.2008.02513.x
European Journal of Neurology, 16(3), 297-309. Wiley-Blackwell
European Journal of Neurology, 16(3), 297-309. Wiley-Blackwell
Tauopathies with parkinsonism represent a spectrum of disease entities unified by the pathologic accumulation of hyperphosphorylated tau protein fragments within the central nervous system. These pathologic characteristics suggest shared pathogenetic
Publikováno v:
Clinical Neuropharmacology. 15:375-380
In this study, the effects of a diet rich in insoluble fiber (DRIF) on motor disability and the peripheral pharmacokinetics of orally administered L-dopa in Parkinsonian patients with marked constipation are analyzed. We found a useful effect of a DR
Autor:
Stanley Fahn, Oscar S. Gershanik, Christopher G. Goetz, Matthias C. Kurth, Fabrizio Stocchi, W. H. Oertel, J. G. de Yebenes, Pierre Pollak, T. N. Chase, Jose A. Obeso, Rita Raisman-Vozari, A. J. Lees, S. Przedzorski, Y. Mizuno, Alberto Albanese, W. C. Koller, Stewart A. Factor, W. Poewe, D. Marsden, A. H. Rajput, Anthony E. Lang, Warren Olanow, E. Ahlskog, Eva Tolosa, Yves Agid, Patrick P. Michel, D. B. Calne, Peter A LeWitt, Eldad Melamed, Niall Quinn
Publikováno v:
Movement Disorders. 14:911-913
Levodopa (in combination with a peripheral dopadecarboxylase inhibitor) substantially improves the quality of life of patients. However, physicians are not always comfortable prescribing it, and its administration is often delayed to retard the devel
Publikováno v:
Journal of neural transmission (Vienna, Austria : 1996). 114(3)
We analyzed (18)F-dopa PET data from 11 members of kindreds with familial progressive supranuclear palsy (PSP) to characterize their cerebral dopaminergic dysfunction. Three clinically-affected PSP patients showed reduced (18)F-dopa uptake in the str
Autor:
J, Carmona, J A, Burguera, B, Mollà, F, Mulas, P, Smeyers, F, Carratalà, J G, De Yebenes, J, Hoenicka, F, Palau
Publikováno v:
Clinical genetics. 64(2)
Mutations in the DYT1 gene cause idiopathic torsion dystonia (ITD) transmitted in families as an autosomal dominant trait with incomplete penetrance. The most common mutation, 946delGAG, has been observed in populations with different ethnic and geog
Autor:
J G, de Yebenes
Publikováno v:
European journal of neurology. 7
Publikováno v:
Brain : a journal of neurology. 118
Summary We describe a family with autosomal dominant progressive supranuclear palsy (PSP) involving five generations which was confirmed in one patient. The proband presented with progressive slowness at age 53 years, followed by ocular palsy, loss o
Publikováno v:
Polish journal of pharmacology. 46(5)
Intrastriatal infusion of amiloride and 12-0-tetradeconoyl phorbol-13-acetate (TPA) in 6-OHDA lesioned rats increased the apomorphine (APO)-induced rotation. This behavioral effect occurred in the presence of a decrease in the density and an increase