Zobrazeno 1 - 10
of 210
pro vyhledávání: '"Niall P. Quinn"'
Autor:
Niall P. Quinn, Lucía García-Gutiérrez, Carolanne Doherty, Alexander von Kriegsheim, Emma Fallahi, David B. Sacks, David Matallanas
Publikováno v:
Cells, Vol 10, Iss 2, p 478 (2021)
The Hippo pathway regulates a complex signalling network which mediates several biological functions including cell proliferation, organ size and apoptosis. Several scaffold proteins regulate the crosstalk of the members of the pathway with other sig
Externí odkaz:
https://doaj.org/article/065d6c56a6254d22acdb39ebe757a709
Autor:
Carlijn D.J.M. Borm, Florian Krismer, Gregor K. Wenning, Klaus Seppi, Werner Poewe, Maria Teresa Pellecchia, Paolo Barone, Erik L. Johnsen, Karen Østergaard, Tanya Gurevich, Ruth Djaldetti, Luisa Sambati, Pietro Cortelli, Igor Petrović, Vladimir S. Kostić, Hana Brožová, Evžen Růžička, Maria Jose Marti, Eduardo Tolosa, Margherita Canesi, Bart Post, Jorik Nonnekes, Bastiaan R. Bloem, Maria Stamelou, Vladimir S. Kostic, Thomas Klockgether, Richard Dodel, Michael Abele, Wassilios Meissner, Heinz Reichmann, Tim Lynch, Jaroslaw Slawek, Mag Klaus Seppi, Daniela Berg, Joaquim Ferreira, Henry Houlden, Niall P. Quinn, Håkan Widner, Alexander Gerhard, Karla Maria Eggert, Alberto Albanese, Francesca del Sorbo, Maria T. Pellecchia, Bas Bloem, Carlijn Borm, Alfredo Berardelli, Carlo Colosimo, Jose Berciano, Latchezar Traykov, Nir Giladi, Olivier Rascol, Monique Galitzky, Thomas Gasser
Publikováno v:
Parkinsonism & Related Disorders, 56, 33-40
Parkinsonism & Related Disorders, 56, pp. 33-40
Borm, C D J M, Krismer, F, Wenning, G K, Seppi, K, Poewe, W, Pellecchia, M T, Barone, P, Johnsen, E L, Østergaard, K, Gurevich, T, Djaldetti, R, Sambati, L, Cortelli, P, Petrović, I, Kostić, V S, Brožová, H, Růžička, E, Marti, M J, Tolosa, E, Canesi, M, Post, B, Nonnekes, J, Bloem, B R & European MSA Study Group (EMSA-SG) 2018, ' Axial motor clues to identify atypical parkinsonism : A multicentre European cohort study ', Parkinsonism and Related Disorders, vol. 56, pp. 33-40 . https://doi.org/10.1016/j.parkreldis.2018.06.015
Parkinsonism & Related Disorders, 56, pp. 33-40
Borm, C D J M, Krismer, F, Wenning, G K, Seppi, K, Poewe, W, Pellecchia, M T, Barone, P, Johnsen, E L, Østergaard, K, Gurevich, T, Djaldetti, R, Sambati, L, Cortelli, P, Petrović, I, Kostić, V S, Brožová, H, Růžička, E, Marti, M J, Tolosa, E, Canesi, M, Post, B, Nonnekes, J, Bloem, B R & European MSA Study Group (EMSA-SG) 2018, ' Axial motor clues to identify atypical parkinsonism : A multicentre European cohort study ', Parkinsonism and Related Disorders, vol. 56, pp. 33-40 . https://doi.org/10.1016/j.parkreldis.2018.06.015
Item does not contain fulltext OBJECTIVE: Differentiating Parkinson's disease (PD) from atypical parkinsonian disorders (APD) such as Multiple System Atrophy, parkinsonian type (MSA-p) or Progressive Supranuclear Palsy (PSP-RS) can be challenging. Ea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4220d0a02f401c3c9a914409fb38212d
https://doi.org/10.1016/j.parkreldis.2018.06.015
https://doi.org/10.1016/j.parkreldis.2018.06.015
Autor:
Roberto, Erro, Joshua, Hersheson, Christos, Ganos, Niccoló E, Mencacci, Maria, Stamelou, Amit, Batla, Stefanie Catherine, Thust, Jose M, Bras, Rita J, Guerreiro, John, Hardy, Niall P, Quinn, Henry, Houlden, Kailash P, Bhatia
Recently, mutations in the TUBB4A gene have been found to underlie hypomyelination with atrophy of the basal ganglia and cerebellum (H-ABC) syndrome, a rare neurodegenerative disorder of infancy and childhood. TUBB4A mutations also have been describe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::da8887fdf2c7043c4dd022a34919d06a
http://hdl.handle.net/11562/867374
http://hdl.handle.net/11562/867374
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
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 28(9)
Recently, a number of genetic parkinsonian conditions have been recognized that share some features with the clinical syndromes of progressive supranuclear palsy (PSP), corticobasal degeneration (CBD), and multiple system atrophy (MSA), the classic p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2c2301a7bff9933cdd4fada1dd423f54
https://pubmed.ncbi.nlm.nih.gov/23720239
https://pubmed.ncbi.nlm.nih.gov/23720239
Publikováno v:
British Journal of Psychiatry. 167:522-526
BackgroundThe growth hormone (GH) response to apomorphine, thought to reflect central dopaminergic receptor sensitivity, has been reported as enhanced in acute schizophrenia. We investigated this response in relation to the psychotic episodes associa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1869faaf4dd80a59f0a320f931d02338
https://doi.org/10.1192/bjp.167.4.522
https://doi.org/10.1192/bjp.167.4.522
Autor:
Florian, Krismer, Klaus, Seppi, François, Tison, Cristina, Sampaio, Anja, Zangerl, Cecilia, Peralta, Farid, Yekhlef, Imad, Ghorayeb, Fabienne, Ory-Magne, Monique, Galitzky, Maria, Bozi, Tommaso, Scaravilli, Carlo, Colosimo, Felix, Geser, Olivier, Rascol, Werner, Poewe, Niall P, Quinn, Gregor K, Wenning
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 27(13)
The Unified Multiple System Atrophy Rating Scale (UMSARS) was developed to provide a surrogate measure of disease progression in multiple system atrophy. In the present study, the intrarater agreement of the motor examination part of the UMSARS was d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b564e5077f013aafa9716a199d138543
https://pubmed.ncbi.nlm.nih.gov/23114993
https://pubmed.ncbi.nlm.nih.gov/23114993
Graft-induced dyskinesias in Parkinson's disease: High striatal serotonin/dopamine transporter ratio
Autor:
Marios, Politis, Wolfgang H, Oertel, Kit, Wu, Niall P, Quinn, Oliver, Pogarell, David J, Brooks, Anders, Bjorklund, Olle, Lindvall, Paola, Piccini
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 26(11)
Graft-induced dyskinesias are a serious complication after neural transplantation in Parkinson's disease. One patient with Parkinson's disease, treated with fetal grafts 14 years ago and deep brain stimulation 6 years ago, showed marked improvement o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::139c175b77bea1cf35ccabf21d63ab19
https://pubmed.ncbi.nlm.nih.gov/21611977
https://pubmed.ncbi.nlm.nih.gov/21611977
Autor:
Georg, Kägi, Christine, Klein, Nicholas W, Wood, Susanne A, Schneider, Peter P, Pramstaller, Vera, Tadic, Niall P, Quinn, Bart P C, van de Warrenburg, Kailash P, Bhatia
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 25(9)
The aim of the study was to explore the prevalence and differences of nonmotor symptoms (NMSs) in patients with young-onset Parkinson's disease (YOPD) with and without mutations in the Parkin gene and late-onset Parkinson's disease (LOPD). Twenty-sev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9a3127a7d17cb3eecbf31fd7338b7eec
https://pubmed.ncbi.nlm.nih.gov/20629119
https://pubmed.ncbi.nlm.nih.gov/20629119
Autor:
Susanne A, Schneider, Coro, Paisan-Ruiz, Niall P, Quinn, Andrew J, Lees, Henry, Houlden, John, Hardy, Kailash P, Bhatia
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 25(8)
Kufor Rakeb disease (KRD, PARK9) is an autosomal recessive extrapyramidal-pyramidal syndrome with generalized brain atrophy due to ATP13A2 gene mutations. We report clinical details and investigational results focusing on radiological findings of a g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::383b43090b2e84c42396fd0d3ce04161
https://pubmed.ncbi.nlm.nih.gov/21469196
https://pubmed.ncbi.nlm.nih.gov/21469196