Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Anne, Noreau"'
Autor:
Simon L Girard, Cynthia V Bourassa, Louis-Philippe Lemieux Perreault, Marc-André Legault, Amina Barhdadi, Amirthagowri Ambalavanan, Mara Brendgen, Frank Vitaro, Anne Noreau, Ginette Dionne, Richard E Tremblay, Patrick A Dion, Michel Boivin, Marie-Pierre Dubé, Guy A Rouleau
Publikováno v:
PLoS ONE, Vol 11, Iss 10, p e0164212 (2016)
De novo mutations (DNM) are an important source of rare variants and are increasingly being linked to the development of many diseases. Recently, the paternal age effect has been the focus of a number of studies that attempt to explain the observatio
Externí odkaz:
https://doaj.org/article/05ab7a88bf8c483d8065d32bee30e9de
Autor:
Marc Parisien, Guy A. Rouleau, Samar Khoury, Luda Diatchenko, Julia Segal, Anne Noreau, Rodrigo Benavides, Inna Belfer, Patrick A. Dion, Ronald Denis, Gilles Lavigne, Jean-François Giguère
Publikováno v:
Canadian Journal of Pain
article-version (VoR) Version of Record
article-version (VoR) Version of Record
Background: Mild traumatic brain injury (mTBI) often results in post-concussion symptoms, chronic pain, and sleepiness. Genetic factors are thought to play an important role in poor prognosis. Aims: The aims of this study are to (1) document the prev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1037b6cd69f117d0361f0a5dcf2ea0a8
https://pubmed.ncbi.nlm.nih.gov/35005347
https://pubmed.ncbi.nlm.nih.gov/35005347
Autor:
Ikhlass Haj Salem, Anne Noreau, Jean-Pierre Bouchard, Patrick A. Dion, Guy A. Rouleau, Nicolas Dupré
Publikováno v:
Handbook of the Cerebellum and Cerebellar Disorders ISBN: 9783319979113
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c9749b5b33d5d1bded6f3c99b1492ee
https://doi.org/10.1007/978-3-319-97911-3_100-2
https://doi.org/10.1007/978-3-319-97911-3_100-2
Autor:
Simon Girard, Christelle Charley Monaca, Jean-François Gagnon, Guy A. Rouleau, Thomas Mitterling, Alex Desautels, V. Cochen De Cock, C. Mirarchi, Patrick A. Dion, Anne Noreau, Isabelle Arnulf, Birgit Högl, Claire S. Leblond, Ziv Gan-Or, Birgit Frauscher, Jacques Montplaisir, Yves Dauvilliers, Ronald B. Postuma
Publikováno v:
Journal of Molecular Neuroscience
Journal of Molecular Neuroscience, Humana Press, 2015, 56 (3), pp.617-622. ⟨10.1007/s12031-015-0569-7⟩
Journal of Molecular Neuroscience, Humana Press, 2015, 56 (3), pp.617-622. ⟨10.1007/s12031-015-0569-7⟩
International audience; Rapid eye movement (REM) sleep behavior disorder (RBD) is a prodromal condition for Parkinson's disease (PD) and other synucleinopathies, which often occurs many years before the onset of PD. We analyzed 261 RBD patients and 3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7e33391700756f0ad67b6566423fe0a
https://doi.org/10.1007/s12031-015-0569-7
https://doi.org/10.1007/s12031-015-0569-7
Autor:
José Luiz Pedroso, Orlando Graziani Povoas Barsottini, Patrick A. Dion, Alexandre Dionne-Laporte, Anne Noreau, Maria Thereza Drumond Gama, Guy A. Rouleau, Gabrielle Houle
Publikováno v:
Movement Disorders. 31:1754-1756
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ada32a35d0c01fe318b28106d9158d6
https://doi.org/10.1002/mds.26810
https://doi.org/10.1002/mds.26810
Autor:
Oury Monchi, Sylvain Chouinard, Guy A. Rouleau, Anne-Louise Lafontaine, Atsuko Nagano-Saito, Claudine Habak, Clotilde Degroot, Antonio P. Strafella, Anne Noreau, Béatriz Mejia-Constain
Publikováno v:
Brain. 137:3025-3035
Parkinson’s disease is a neurodegenerative condition that affects motor function along with a wide range of cognitive domains, including executive function. The hallmark of the pathology is its significant loss of nigrostriatal dopamine, which is n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f214f2ac944abac3bd81eb59431d3a01
https://doi.org/10.1093/brain/awu251
https://doi.org/10.1093/brain/awu251
Publikováno v:
Experimental Cell Research. 325:18-26
Hereditary spastic paraplegia (HSP) is a clinically and genetically heterogeneous group of neurodegenerative disorders characterized by progressive lower limbs spasticity and weakness. What was first thought to be a small group of rare Mendelian diso
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::442da3b44c4f253e20a830fbc58555c3
https://doi.org/10.1016/j.yexcr.2014.02.021
https://doi.org/10.1016/j.yexcr.2014.02.021
Autor:
Typhaine Esteves, Khalid H. El-Hachimi, Emeline Mundwiller, Maxime Boutry, Rafael F. Acosta Lebrigio, José Leal Loureiro, Alexandre Dionne-Laporte, Patrick A. Dion, Michael A. Gonzalez, Christel Depienne, Alexis Brice, Anne Noreau, Guy A. Rouleau, Julie Gauthier, Fiorella Speziani, Stephan Züchner, Marion Gaussen, Paula Coutinho, Marie Paule Muriel, Alexandra Durr, Frédéric Darios, Jean-François Deleuze, Giovanni Stevanin
Publikováno v:
The American Journal of Human Genetics
Hereditary spastic paraplegias (HSPs) are clinically and genetically heterogeneous neurological conditions. Their main pathogenic mechanisms are thought to involve alterations in endomembrane trafficking, mitochondrial function, and lipid metabolism.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fed3a2dc52b2a8cd857dc60f37f3b14
Autor:
Marc-André Legault, Louis-Philippe Lemieux Perreault, Frank Vitaro, Amina Barhdadi, Marie-Pierre Dubé, Cynthia V. Bourassa, Patrick A. Dion, Ginette Dionne, Michel Boivin, Amirthagowri Ambalavanan, Richard E. Tremblay, Mara Brendgen, Guy A. Rouleau, Anne Noreau, Simon Girard
Publikováno v:
PLoS ONE, Vol 11, Iss 10, p e0164212 (2016)
PLoS ONE
PLoS ONE
De novo mutations (DNM) are an important source of rare variants and are increasingly being linked to the development of many diseases. Recently, the paternal age effect has been the focus of a number of studies that attempt to explain the observatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de714987caca64386d9d19400b5cf675
http://europepmc.org/articles/PMC5056704?pdf=render
http://europepmc.org/articles/PMC5056704?pdf=render
Autor:
Anne Noreau, Franco Lepore, Mario Beauregard, Émilie Fortier, Michel Boivin, Guy A. Rouleau, Daniel Pérusse
Publikováno v:
Journal of Affective Disorders. 135:336-340
Background CREB1 has previously been implicated in mood disorders, suicide, and antidepressant response. There is some evidence that the T allele in rs4675690, a single-nucleotide polymorphism near the CREB1 gene, is involved in the modulation of neu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13ba74325f082ece9b735ed6dd9c87c8
https://doi.org/10.1016/j.jad.2011.06.039
https://doi.org/10.1016/j.jad.2011.06.039