Zobrazeno 1 - 10
of 27
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
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
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
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
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
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
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
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 25(2)
There is an increasing awareness of impulsive-compulsive phenomena in patients treated for Parkinson's disease (PD). We describe another, potentially related phenomenon putatively associated with the use of dopamine agonists in 3 patients with PD, ch