Suzanne Lesage

Suzanne Lesage

UNVERIFIED PROFILE

Are you Suzanne Lesage?   Register this Author

Register author
Suzanne Lesage

Suzanne Lesage

Publications by authors named "Suzanne Lesage"

Are you Suzanne Lesage?   Register this Author

100Publications

4579Reads

50Profile Views

Heritability and genetic variance of dementia with Lewy bodies.

Neurobiol Dis 2019 07 3;127:492-501. Epub 2019 Apr 3.

Department of Neurodegenerative Diseases, UCL Institute of Neurology, London, UK; UK Dementia Research Institute (UK DRI) at UCL, London, UK. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.nbd.2019.04.004DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6588425PMC
July 2019

A comprehensive screening of copy number variability in dementia with Lewy bodies.

Neurobiol Aging 2019 03 24;75:223.e1-223.e10. Epub 2018 Oct 24.

Department of Neurodegenerative Disease, UCL Institute of Neurology, London, UK; UK Dementia Research Institute (UK DRI) at UCL, London, UK; Department of Medical Sciences and Institute of Biomedicine, iBiMED, University of Aveiro, Aveiro, Portugal. Electronic address:

View Article

Download full-text PDF

Source
https://linkinghub.elsevier.com/retrieve/pii/S01974580183038
Publisher Site
http://dx.doi.org/10.1016/j.neurobiolaging.2018.10.019DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6541211PMC
March 2019

LRP10 in α-synucleinopathies.

Lancet Neurol 2018 12 13;17(12):1034. Epub 2018 Nov 13.

Inserm U1127, CNRS UMR 7225, UPMC Paris 06 University, UMR S1127, Sorbonne University, Brain and Spinal Cord Institute (ICM), Hôpital de la Salpêtrière, Paris, France; Department of Genetics, Pitié-Salpêtrière Hospital Group, GHPS, Public Hospitals of Paris, AP-HP, Paris, France. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/S1474-4422(18)30400-9DOI Listing
December 2018

LRRK2 G2019S Parkinson's disease with more benign phenotype than idiopathic.

Acta Neurol Scand 2018 Nov 10;138(5):425-431. Epub 2018 Jul 10.

Laboratory of Neurogenetics, Parkinson's Disease and Cerebrovascular Disease, University Hospital Habib Bourguiba, Sfax, Tunisia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/ane.12996DOI Listing
November 2018

Mutation analysis of Parkinson's disease genes in a Russian data set.

Neurobiol Aging 2018 11 9;71:267.e7-267.e10. Epub 2018 Jul 9.

Petersburg Nuclear Physics Institute named by B.P. Konstantinov of National Research Centre «Kurchatov Institute», Saint-Petersburg, Russia; First Pavlov State Medical University of St. Petersburg, St. Petersburg, Russia; Institute of Experimental Medicine, St. Petersburg, Russia. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.neurobiolaging.2018.06.027DOI Listing
November 2018

Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study.

Lancet Neurol 2018 01 16;17(1):64-74. Epub 2017 Dec 16.

UK Dementia Research Institute, University College London, London, UK; Department of Molecular Neuroscience, UCL Institute of Neurology, University College London, London, UK; Department of Medical Sciences and Institute of Biomedicine, iBiMED, University of Aveiro, Aveiro, Portugal. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/S1474-4422(17)30400-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5805394PMC
January 2018

Analysis of blood-based gene expression in idiopathic Parkinson disease.

Neurology 2017 Oct 15;89(16):1676-1683. Epub 2017 Sep 15.

From the School of Computer Science (R.S., D.A., H.S.), Tel Aviv University, Israel; Institute of Neurogenetics (C.K., E.-J.V., H.P., M.K.), University of Lübeck, Germany; Department of Psychiatry and Psychotherapy (E.-J.V., M.K.), University of Lübeck, Germany; Institute of Medical Genetics and Applied Genomics (M.B., S.P., O.R.), University of Tübingen, Germany; IMGM Laboratories GmbH (M.B.), Martinsried, Germany; Mediterranean Institute for Life Sciences (M.U.), Split, Croatia; Department of Neurology (Y.C.W., D.K.), Northwestern University Feinberg School of Medicine, Chicago, IL; Clinical Institute of Medical Genetics (A.M., B.P.), University Medical Center Ljubljana, Slovenia; Sorbonne Universités (J.C.-C., S.L., A.B.), UPMC Université Paris 6 UMR S 1127, Inserm U 1127, CNRS UMR 7225, Institut du Cerveau et de la Moelle épinière, ICM, Paris, France; Centre d'Investigation Clinique Pitié Neurosciences CIC-1422 (J.C.-C.), Paris, France; Machine Learning Technologies Group (O.L.), IBM Research-Haifa, Mount Carmel, Israel; Department of Neurology (G.D., G.K.), Kiel University, Germany; and Department of Biological Regulation (I.U.), Weizmann Institute of Science, Rehovot, Israel.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1212/WNL.0000000000004516DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5644465PMC
October 2017

Mutation Analysis of Consanguineous Moroccan Patients with Parkinson's Disease Combining Microarray and Gene Panel.

Front Neurol 2017 31;8:567. Epub 2017 Oct 31.

Sorbonne Universités, UPMC Université Paris 6 UMR_S 1127, INSERM U 1127, CNRS UMR 7225, Institut du Cerveau et de la Moelle épinière, ICM, Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.3389/fneur.2017.00567DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5674924PMC
October 2017

Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune Diseases.

JAMA Neurol 2017 07;74(7):780-792

Department of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany30Centre for Genetic Epidemiology, Institute for Clinical Epidemiology and Applied Biometry, University of Tübingen, Tübingen, Germany.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1001/jamaneurol.2017.0469DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5710535PMC
July 2017

Analysis of C9orf72 repeat expansions in a large international cohort of dementia with Lewy bodies.

Neurobiol Aging 2017 01 2;49:214.e13-214.e15. Epub 2016 Sep 2.

Department of Molecular Neuroscience, UCL Institute of Neurology, London, UK; Department of Medical Sciences and Institute of Biomedicine-iBiMED, University of Aveiro, Aveiro, Portugal. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.neurobiolaging.2016.08.023DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5154872PMC
January 2017

PINK1 and FLNA mutations association: A role for atypical parkinsonism?

Parkinsonism Relat Disord 2016 05 2;26:78-80. Epub 2016 Mar 2.

Département des Maladies du Système Nerveux, Centre Inter-Régional de Coordination de la Maladie de Parkinson, Hôpital Pitié-Salpêtrière, APHP, Paris, 75013, France; Université Pierre et Marie Curie-Paris 6, Laboratoire de Biologie du Développement, UMR 7622, Paris, 75005, France; Centre National de la Recherche Scientifique, Laboratoire de Biologie du Développement, UMR 7622 Paris, 75005, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.parkreldis.2016.02.023DOI Listing
May 2016

PARKIN Inactivation Links Parkinson's Disease to Melanoma.

J Natl Cancer Inst 2016 Mar 17;108(3). Epub 2015 Dec 17.

Affiliations of authors: INSERM, U976, Centre de Recherche sur la Peau, Hôpital Saint Louis , Paris , France (HHH, JA, SM, LM, VD, NBS, MB, AB, CL, ND, NS); AP-HP, Hôpital Bichat Claude Bernard, Département de Génétique , Paris , France (HHH, CK, AT, BG, NS); Université Paris Diderot, Sorbonne Paris Cité , UMRS976, Paris , France (HHH, CK, JA, LM, NBS, MB, AB, LD, AT, BG, ND, NS); Université Paris 6, INSERM UMRS975, Centre de Recherche de l'Institut du Cerveau et de la Moelle Epinière, Hôpital Pitié-Salpêtrière, AP-HP , Paris , France (SL, AB); INSERM, U940, Laboratoire de Pharmacologie, Hôpital Saint Louis Paris , France (SM); AP-HP, Hôpital Bichat Claude Bernard, Service de Dermatologie , Paris , France (VD); AP-HP, Hôpital Saint Louis, Service de Dermatologie , Paris , France (NBS, MB, CL, ND); INSERM, CRB3, Département de Pathologie, Hôpital Bichat, AP-HP , Paris , France (LD); AP-HP, Hôpital Ambroise Paré, Service de Dermatologie , Boulogne Billancourt , France (PS); CHU Grenoble, Service de Dermatologie , Grenoble , France (MTL); Gustave Roussy, Service de Génétique, Département de Biopathologie , Villejuif , France (BBdP); Division of Molecular Genetic Epidemiology, German Cancer Research Center, Im Neuenheimer Feld 580 , Heidelberg , Germany (RK); Department of Neurology, University Hospital of Würzburg , Würzburg , Germany (SK); Inserm UMR1037, Centre de Recherche en Cancérologie de Toulouse , Toulouse , France (NAA); Hôpital de l'Hôtel-Dieu, Service de Dermatologie , Lyon , France (LT); AP-HP, Groupe Pitié-Salpêtrière, Département de Génétique, Cytogénétique et Embryologie , Paris , France (AB).

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/jnci/djv340DOI Listing
March 2016

Familial Parkinson's disease/parkinsonism.

Biomed Res Int 2015 19;2015:736915. Epub 2015 Apr 19.

Department of Neurology, Seoul National University Hospital, Seoul, Republic of Korea.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1155/2015/736915DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4417557PMC
February 2016

Greater improvement in LRRK2 G2019S patients undergoing Subthalamic Nucleus Deep Brain Stimulation compared to non-mutation carriers.

BMC Neurosci 2016 Feb 1;17. Epub 2016 Feb 1.

Laboratory of Behavioral and Cognitive Neuroscience, FSB, University of Science and Technology Houari Boumediene, El Alia, Bab Ezzouar, BP 32, 16111, Algiers, Algeria.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1186/s12868-016-0240-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736184PMC
February 2016

EIF4G1 mutations do not cause Parkinson's disease.

Neurobiol Aging 2015 Aug 9;36(8):2444.e1-4. Epub 2015 May 9.

Laboratory of Neurogenetics, National Institute on Aging, Bethesda, MD, USA. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.neurobiolaging.2015.04.017DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4464946PMC
August 2015

A new F-box protein 7 gene mutation causing typical Parkinson's disease.

Mov Disord 2015 Jul 23;30(8):1130-3. Epub 2015 May 23.

Sorbonne Université, UPMC Univ Paris 06, UM 1127, ICM, Paris, France; Inserm, U 1127, ICM, Paris, France; Cnrs, UMR 7225, ICM, Paris, France; ICM, Paris, F-75013, Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/mds.26266DOI Listing
July 2015

CHCHD2 and Parkinson's disease.

Lancet Neurol 2015 Jul;14(7):678-9

Department of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany; Centre for Genetic Epidemiology, Institute for Clinical Epidemiology and Applied Biometry, University of Tübingen, Tübingen, Silcherstraße 5, 70276, Germany. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/S1474-4422(15)00094-0DOI Listing
July 2015

Synaptojanin 1 mutation in Parkinson's disease brings further insight into the neuropathological mechanisms.

Biomed Res Int 2014 16;2014:289728. Epub 2014 Sep 16.

Sorbonne Universités, UPMC (Paris 6), UMR S 1127, Inserm U 1127, CNRS UMR 7225, and ICM, 75013 Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1155/2014/289728DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4181773PMC
June 2015

Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease.

Neurol Genet 2015 Jun 18;1(1):e9. Epub 2015 Jun 18.

Institut du Cerveau et de la Moelle épinière, ICM, Inserm U 1127, CNRS, UMR 7225, Sorbonne Universités, UPMC University Paris 06 UMR S 1127 (S.L., F.C.-D., C.C., A.N., A.B.), Paris, France; Centre d'Investigation Clinique Pitié Neurosciences CIC-1422 (F.C.-D.); AP-HP, Hôpital de la Salpêtrière (A.B.), Department of Genetics and Cytogenetics, Paris, France; Department of Molecular Neuroscience (J.B., L.D., R.G., M.F., N.W., J.H.), UCL Institute of Neurology, London, United Kingdom; Laboratory of Neurogenetics (E.M., M.F., A.S.), National Institute on Aging, Bethesda, MD; Hertie Institute for Clinical Brain Research (P.H., T.G.), University of Tübingen and DZNE (P.H., T.G.), German Center for Neurodegenerative Diseases, Tübingen, Germany; and Institut des Maladies Neurodégénératives (F.T.), Université de Bordeaux et CHU de Bordeaux, Bordeaux, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1212/NXG.0000000000000009DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4821081PMC
June 2015

Electroencephalographic hypersynchrony in a child with night terrors.

Sleep Breath 2013 May 7;17(2):465-7. Epub 2012 Jul 7.

Department of Pulmonary, Critical Care and Sleep Medicine, Walter Reed National Military Medical Center, Bethesda, MD, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s11325-012-0730-2DOI Listing
May 2013

G51D α-synuclein mutation causes a novel parkinsonian-pyramidal syndrome.

Ann Neurol 2013 Apr;73(4):459-71

Pierre and Marie Curie University-Paris 6, Research Center of the Institute for Brain and Spinal Cord, National Institute of Health and Medical Research, Paris.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ana.23894DOI Listing
April 2013

C9orf72 repeat expansions are a rare genetic cause of parkinsonism.

Brain 2013 Feb;136(Pt 2):385-91

Université Pierre et Marie Curie-Paris 6, Centre de Recherche de l'Institut du Cerveau et de la Moelle épinière, UMR-S975; Inserm, U975, CNRS, UMR 7225, 75013 Paris, France

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/brain/aws357DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3984141PMC
February 2013

A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants.

J Med Genet 2012 Nov;49(11):721-6

Department. of Neurodegenerative diseases, Hertie-Institute for Clinical Brain Research and DZNE- German Center for Neurodegenerative Diseases, Tübingen, Hoppe-Seyler-Str. 3, Tübingen 72076, Germany.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1136/jmedgenet-2012-101155DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3488700PMC
November 2012

EIF4G1 in familial Parkinson's disease: pathogenic mutations or rare benign variants?

Neurobiol Aging 2012 Sep 1;33(9):2233.e1-2233.e5. Epub 2012 Jun 1.

Université Pierre et Marie Curie-Paris6, Centre de Recherche de l'Institut du Cerveau et de la Moelle épinière, UMR-S975, Inserm, U975, Cnrs, UMR 7225, Hôpital de la Pitié-Salpêtrière, Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.neurobiolaging.2012.05.006DOI Listing
September 2012

Role of mendelian genes in "sporadic" Parkinson's disease.

Parkinsonism Relat Disord 2012 Jan;18 Suppl 1:S66-70

Université Pierre et Marie Curie-Paris6, Centre de Recherche de l'Institut du Cerveau et de la Moelle épinière, UMR-S975, Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/S1353-8020(11)70022-0DOI Listing
January 2012

What genetics tells us about the causes and mechanisms of Parkinson's disease.

Physiol Rev 2011 Oct;91(4):1161-218

Université Pierre et Marie Curie-Paris 6, Centre de Recherche de l'Institut du Cerveau et de la Moelle épinière; Institut National de la Santé et de la Recherche Médicale U.975, Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1152/physrev.00022.2010DOI Listing
October 2011

Genetic characteristics of leucine-rich repeat kinase 2 (LRRK2) associated Parkinson's disease.

Parkinsonism Relat Disord 2011 Aug;17(7):501-8

Division of Molecular Biology and Human Genetics, Stellenbosch University, Cape Town, South Africa.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.parkreldis.2010.11.008DOI Listing
August 2011

Large-scale screening of the Gaucher's disease-related glucocerebrosidase gene in Europeans with Parkinson's disease.

Hum Mol Genet 2011 Jan 14;20(1):202-10. Epub 2010 Oct 14.

Université Pierre et Marie Curie-Paris 6, Centre de Recherche de l'Institut du Cerveau et de la Moelle épinière, UMR-S975, and Department of Genetics and Cytogenetics, Pitié-Salpêtrière Hospital, Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/hmg/ddq454DOI Listing
January 2011

LRRK2 G2019S mutation in Parkinson's disease: a neuropsychological and neuropsychiatric study in a large Algerian cohort.

Parkinsonism Relat Disord 2010 Dec 8;16(10):676-9. Epub 2010 Oct 8.

Laboratoire de Recherche en Neurosciences, Service de Neurologie, CHU Mustapha, Place du 1er Mai, Algiers 16000, Algeria.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.parkreldis.2010.09.003DOI Listing
December 2010

Polysomnogram changes in marijuana users who report sleep disturbances during prior abstinence.

Sleep Med 2010 Oct 3;11(9):882-9. Epub 2010 Aug 3.

Department of Neurology, Johns Hopkins Medical Institutions, Bayview Medical Center, Baltimore, MD 21224, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.sleep.2010.02.013DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2938870PMC
October 2010

Leucine-rich repeat kinase 2 is associated with the endoplasmic reticulum in dopaminergic neurons and accumulates in the core of Lewy bodies in Parkinson disease.

J Neuropathol Exp Neurol 2010 Sep;69(9):959-72

Laboratory of Molecular Basis, Physiopathology and Treatment of Neurodegenerative Diseases, Université Pierre et Marie Curie-Paris 6, Centre de Recherche de l'Institut du Cerveau et de la Moelle épinière, UMR-S975, Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/NEN.0b013e3181efc01cDOI Listing
September 2010

LRRK2 G2019S mutation: frequency and haplotype data in South African Parkinson's disease patients.

J Neural Transm (Vienna) 2010 Jul 11;117(7):847-53. Epub 2010 Jun 11.

Division of Molecular Biology and Human Genetics, University of Stellenbosch, 4th Floor Fisan Building, PO Box 19063, Tygerberg, Cape Town, 7505, South Africa.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00702-010-0423-6DOI Listing
July 2010

Assessing the prevalence of PINK1 genetic variants in South African patients diagnosed with early- and late-onset Parkinson's disease.

Biochem Biophys Res Commun 2010 Jul 15;398(1):125-9. Epub 2010 Jun 15.

Division of Molecular Biology and Human Genetics, Faculty of Health Sciences, University of Stellenbosch, Cape Town, South Africa.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.bbrc.2010.06.049DOI Listing
July 2010

Follow-up study of the GIGYF2 gene in French families with Parkinson's disease.

Neurobiol Aging 2010 Jun 8;31(6):1069-71; discussion 1072-4. Epub 2009 Dec 8.

INSERM, UMR_S975 (Formerly UMR_S679), Hôpital de la Salpêtrière, Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.neurobiolaging.2009.06.008DOI Listing
June 2010

Pearls: sleep disorders.

Authors:
Suzanne Lesage

Semin Neurol 2010 Feb 1;30(1):90-6. Epub 2010 Feb 1.

Sleep Disorders Center, Walter Reed Army Medical Center, Washington, District of Columbia, USA.

View Article

Download full-text PDF

Source
http://www.thieme-connect.de/DOI/DOI?10.1055/s-0029-1245003
Publisher Site
http://dx.doi.org/10.1055/s-0029-1245003DOI Listing
February 2010

From genes to proteins in mendelian Parkinson's disease: an overview.

Anat Rec (Hoboken) 2009 Dec;292(12):1893-901

Boğaziçi University, Molecular Biology and Genetics Department, Neurodegeneration Research Laboratory, Istanbul, Turkey.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ar.20968DOI Listing
December 2009

A clinical, neuropsychological and olfactory evaluation of a large family with LRRK2 mutations.

Parkinsonism Relat Disord 2009 May 21;15(4):273-6. Epub 2008 Aug 21.

INSERM, UMR_S679 Neurologie & Thérapeutique Expérimentale, F-75013 Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.parkreldis.2008.06.008DOI Listing
May 2009

Parkinson's disease: from monogenic forms to genetic susceptibility factors.

Hum Mol Genet 2009 Apr;18(R1):R48-59

INSERM, UMR_S679, Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/hmg/ddp012DOI Listing
April 2009

Alpha-synuclein gene rearrangements in dominantly inherited parkinsonism: frequency, phenotype, and mechanisms.

Arch Neurol 2009 Jan;66(1):102-8

Institut National de la Santé et de la Recherche Médicale (INSERM), Unité Mixte de Recherche en Santé (UMR)_S679 Neurologie & Thérapeutique Expérimentale, F-75013, Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1001/archneurol.2008.555DOI Listing
January 2009

Sleep disturbance in heavy marijuana users.

Sleep 2008 Jun;31(6):901-8

Department of Neurology, Johns Hopkins Medical Institutions, Bayview Medical Center, Baltimore, MD 21224, USA.

View Article

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2442418PMC
http://dx.doi.org/10.1093/sleep/31.6.901DOI Listing
June 2008

Validation of the Hopkins telephone diagnostic interview for restless legs syndrome.

Sleep Med 2008 Mar 17;9(3):283-9. Epub 2007 Jul 17.

RLS Center, Asthma & Allergy, SBTBLJH Bayview, 4940 Eastern Avenue, Baltimore, MD 21224, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.sleep.2007.04.021DOI Listing
March 2008

Gene symbol: PARK2. Disease: Parkinsonism, juvenile, autosomal recessive.

Hum Genet 2008 Feb;123(1):114

INSERM, U679, boulevard de l'Hôpital, 47, 75013 Paris,

View Article

Download full-text PDF

Source
February 2008

Frequency of the LRRK2 G2019S mutation in siblings with Parkinson's disease.

Neurodegener Dis 2007 ;4(2-3):195-8

INSERM, UMR 679, Neurology and Experimental Therapeutics, Hôpital de la Pitié-Salpêtrière, AP-HP, Faculté de Médecine, Université Pierre et Marie Curie-Paris 6, Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1159/000101844DOI Listing
October 2007

Bioremediation of tetrachloroethylene-contaminated groundwater in a model aquifer: effects on green frogs (Rana clamitans) and Xenopus laevis as potential wetland receptors.

Arch Environ Contam Toxicol 2007 Apr 25;52(3):410-7. Epub 2007 Jan 25.

Canadian Wildlife Service, Environment Canada, Burlington, Ontario, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00244-005-8218-8DOI Listing
April 2007

LRRK2 exon 41 mutations in sporadic Parkinson disease in Europeans.

Arch Neurol 2007 Mar;64(3):425-30

Institut National de la Santé et de la Recherche Médicale Unité 679, Neurology and Experimental Therapeutics, and Faculté de Médecine, Université Pierre et Marie Curie, 75651 Paris CEDEX 13, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1001/archneur.64.3.425DOI Listing
March 2007

Segregation analysis of restless legs syndrome: possible evidence for a major gene in a family study using blinded diagnoses.

Hum Hered 2006 24;62(3):157-64. Epub 2006 Oct 24.

Genometrics Section, Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, Baltimore, MD, USA.

View Article

Download full-text PDF

Source
https://www.karger.com/Article/FullText/96443
Publisher Site
http://dx.doi.org/10.1159/000096443DOI Listing
February 2007

Deletion of the parkin and PACRG gene promoter in early-onset parkinsonism.

Hum Mutat 2007 Jan;28(1):27-32

INSERM U679, Neurology and Experimental Therapeutics, Centre Hospitalier Universitaire (CHU) Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/humu.20436DOI Listing
January 2007

Beyond the usual suspects: approaching sleep in elderly people.

J Gerontol A Biol Sci Med Sci 2007 Jan;62(1):53-4

Sleep Disorders Center, Department of Neurology, University of Maryland, Baltimore, MD 21201, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/gerona/62.1.53DOI Listing
January 2007

Juvenile-onset Parkinsonism as a result of the first mutation in the adenosine triphosphate orientation domain of PINK1.

Arch Neurol 2006 Sep;63(9):1257-61

Institut National de la Santé et de la Recherche Médicale U679, Assistance Publique, Hôpitaux de Paris, Faculté de Médecine, Université Paris 6-Pierre et Marie Curie, Hôpital de la Pitié-Salpêtrière, 47 Blvd. de l'Hôpital, 75651 Paris CEDEX 13, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1001/archneur.63.9.1257DOI Listing
September 2006