Anne Noreau

Anne Noreau

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Anne Noreau

Anne Noreau

Publications by authors named "Anne Noreau"

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SYNE1 mutations cause autosomal-recessive ataxia with retained reflexes in Brazilian patients.

Mov Disord 2016 11 27;31(11):1754-1756. Epub 2016 Sep 27.

Division of General Neurology and Ataxia Unit, Department of Neurology, Federal University of São Paulo (UNIFESP), São Paulo, Brazil.

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http://dx.doi.org/10.1002/mds.26810DOI Listing
November 2016

Novel SIL1 mutations cause cerebellar ataxia and atrophy in a French-Canadian family.

Neurogenetics 2015 Oct 11;16(4):315-8. Epub 2015 Aug 11.

Montreal Neurological Institute and Hospital, McGill University, 3801 University St., Room 636, Montreal, Quebec, Canada.

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https://www.rareconnect.org/uploads/documents/novel-sil1-mut
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http://link.springer.com/10.1007/s10048-015-0455-z
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http://dx.doi.org/10.1007/s10048-015-0455-zDOI Listing
October 2015

Exome sequencing revealed PMM2 gene mutations in a French-Canadian family with congenital atrophy of the cerebellum.

Cerebellum Ataxias 2014 4;1. Epub 2014 Jul 4.

Faculty of Medicine of Laval University and the Department of Neurological Sciences of the Centre Hopitalier, Universitaire de Québec, 1401, 18th Street, Quebec, QC G1J 1Z4 Canada.

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http://dx.doi.org/10.1186/2053-8871-1-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4552392PMC
September 2015

Dopamine transporter SLC6A3 genotype affects cortico-striatal activity of set-shifts in Parkinson's disease.

Brain 2014 Nov 10;137(Pt 11):3025-35. Epub 2014 Sep 10.

1 Research Centre, Institut universitaire de Gériatrie de Montréal, University of Montréal, Montréal, Québec, H3W 1W5, Canada 5 Département de Radiologie, Université de Montréal, Montréal, Québec, Canada

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http://dx.doi.org/10.1093/brain/awu251DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4208466PMC
November 2014

Molecular aspects of hereditary spastic paraplegia.

Exp Cell Res 2014 Jul 11;325(1):18-26. Epub 2014 Mar 11.

Montreal Neurological Institute and Hospital, Department of Neurology and Neurosurgery, McGill University, Montreal, Quebec, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.yexcr.2014.02.021DOI Listing
July 2014

Therapies for ataxias.

Curr Treat Options Neurol 2014 Jul;16(7):300

Department of Neurological Sciences of the Centre Hopitalier Universitaire de Québec and Faculty of Medicine, CHU de Québec, Laval University, 1401, 18th Street, Quebec City, Quebec, G1J 1Z4, Canada.

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http://dx.doi.org/10.1007/s11940-014-0300-yDOI Listing
July 2014

Loss of association of REEP2 with membranes leads to hereditary spastic paraplegia.

Am J Hum Genet 2014 Feb 2;94(2):268-77. Epub 2014 Jan 2.

Université Pierre and Marie Curie - Paris VI, Unité Mixte de Recherche S975, Centre de Recherche de l'Institut du Cerveau et de la Moelle épinière, Groupe Hospitalier Pitié-Salpêtrière, 75013 Paris, France; Institut National de la Santé et de la Recherche Médicale, Unité 975, 75013 Paris, France; Centre National de la Recherche Scientifique, Unité Mixte de Recherche 7225, 75013 Paris, France. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2013.12.005DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3928657PMC
February 2014

Investigation of C9orf72 repeat expansions in Parkinson's disease.

Neurobiol Aging 2013 Jun 27;34(6):1710.e7-9. Epub 2012 Dec 27.

Centre of Excellence in Neuroscience of Université de Montréal (CENUM), CHUM Research Center and the Department of Medicine, Montreal, Quebec, Canada.

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http://dx.doi.org/10.1016/j.neurobiolaging.2012.11.025DOI Listing
June 2013

Exome sequencing reveals SPG11 mutations causing juvenile ALS.

Neurobiol Aging 2012 Apr 10;33(4):839.e5-9. Epub 2011 Dec 10.

Centre of Excellence in Neuroscience of Université de Montréal, CHUM Research Center and the Department of Medicine, Montreal, Quebec, Canada.

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http://dx.doi.org/10.1016/j.neurobiolaging.2011.11.012DOI Listing
April 2012

CYP7B1 mutations in French-Canadian hereditary spastic paraplegia subjects.

Can J Neurol Sci 2012 Jan;39(1):91-4

Center of Excellence in Neuroscience of Université de Montréal, Centre de Recherche du Centre Hospitalier de l'Université de Montréal, Quebec, Canada.

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http://dx.doi.org/10.1017/s0317167100012774DOI Listing
January 2012

Glucocerebrosidase mutations in a French-Canadian Parkinson's disease cohort.

Can J Neurol Sci 2011 Sep;38(5):772-3

Center of Excellence in Neuroscience of Université de Montréal (CENUM), Centre de Recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM), Canada.

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http://dx.doi.org/10.1017/s0317167100012300DOI Listing
September 2011

Glucocerebrosidase mutations in a French-Canadian Parkinson's disease cohort.

Can J Neurol Sci 2011 Sep;38(5):772-3

Center of Excellence in Neuroscience of Université de Montréal (CENUM), Centre de Recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM), Canada.

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http://dx.doi.org/10.1017/s0317167100012300DOI Listing
September 2011

Restless legs syndrome-associated MEIS1 risk variant influences iron homeostasis.

Ann Neurol 2011 Jul 27;70(1):170-5. Epub 2011 Jun 27.

Centre of Excellence in Neuromics, CHUM Research Centre, University of Montreal, Montreal, Quebec, Canada.

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http://dx.doi.org/10.1002/ana.22435DOI Listing
July 2011

Increased exonic de novo mutation rate in individuals with schizophrenia.

Nat Genet 2011 Jul 10;43(9):860-3. Epub 2011 Jul 10.

Centre of Excellence in Neuromics of Université de Montréal, Centre Hospitalier de l'Université de Montréal Research Center, Montréal, Québec, Canada.

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http://www.nature.com/articles/ng.886
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http://dx.doi.org/10.1038/ng.886DOI Listing
July 2011

Early impact of 5-HTTLPR polymorphism on the neural correlates of sadness.

Neurosci Lett 2010 Nov 17;485(3):261-5. Epub 2010 Sep 17.

Centre de Recherche en Neuropsychologie et Cognition (CERNEC), Département de Psychologie, Université de Montréal, Montreal, Canada.

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http://dx.doi.org/10.1016/j.neulet.2010.09.026DOI Listing
November 2010

De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy.

Ann Neurol 2009 Jun;65(6):748-53

Centre of Excellence in Neuromics of Université de Montréal and Synapse to Disease Group, Centre Hospitalier Universitaire Sainte-Justine Research Center, Université de Montréal, Montreal, Quebec, Canada.

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http://dx.doi.org/10.1002/ana.21625DOI Listing
June 2009