المؤلفون: Yuri L. Sosero, Eric Yu, Mehrdad A. Estiar, Lynne Krohn, Kheireddin Mufti, Uladzislau Rudakou, Jennifer A. Ruskey, Farnaz Asayesh, Sandra B. Laurent, Dan Spiegelman, Jean-Fran(c(c))ois Trempe, Timothy G. Quinnell, Nicholas Oscroft, Isabelle Arnulf, Jacques Y. Montplaisir, Jean-Fran(c(c))ois Gagnon, Alex Desautels, Yves Dauvilliers, Gian Luigi Gigli, Mariarosaria Valente, Francesco Janes, Andrea Bernardini, Karel Sonka, David Kemlink, Wolfgang Oertel, Annette Janzen, Giuseppe Plazzi, Elena Antelmi, Francesco Biscarini, Michela Figorilli, Monica Puligheddu, Brit Mollenhauer, Claudia Trenkwalder, Friederike Sixel-Döring, Val('(e))rie Cochen De Cock, Christelle Charley Monaca, Anna Heidbreder, Luigi Ferini-Strambi, Femke Dijkstra, Mineke Viaene, Beatriz Abril, Bradley F. Boeve, Ronald B. Postuma, Guy A. Rouleau, Abubaker Ibrahim, Ambra Stefani, Birgit Högl, Michele T. M. Hu, Ziv Gan-Or

المساهمون: Yuri L. Sosero, Eric Yu, Mehrdad A. Estiar, Lynne Krohn, Kheireddin Mufti, Uladzislau Rudakou, Jennifer A. Ruskey, Farnaz Asayesh, Sandra B. Laurent, Dan Spiegelman, Jean-Fran{\c{c}}ois Trempe, Timothy G. Quinnell, Nicholas Oscroft, Isabelle Arnulf, Jacques Y. Montplaisir, Jean-Fran{\c{c}}ois Gagnon, Alex Desautel, Yves Dauvillier, Gian Luigi Gigli, Mariarosaria Valente, Francesco Jane, Andrea Bernardini, Karel Sonka, David Kemlink, Wolfgang Oertel, Annette Janzen, Giuseppe Plazzi, Elena Antelmi, Francesco Biscarini, Michela Figorilli, Monica Puligheddu, Brit Mollenhauer, Claudia Trenkwalder, Friederike Sixel-Döring, Val{\'{e}}rie Cochen De Cock, Christelle Charley Monaca, Anna Heidbreder, Luigi Ferini-Strambi, Femke Dijkstra, Mineke Viaene, Beatriz Abril, Bradley F. Boeve, Ronald B. Postuma, Guy A. Rouleau, Abubaker Ibrahim, Ambra Stefani, Birgit Högl, Michele T.M. Hu, Ziv Gan-Or

مصطلحات موضوعية: GBA, PSAP, Parkinson’s disease, REM sleep behavior disorder, genetic, glucocerebrosidase, saposin C

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/34690151; info:eu-repo/semantics/altIdentifier/wos/WOS:000747072700024; volume:12; issue:1; firstpage:333; lastpage:340; numberofpages:8; journal:JOURNAL OF PARKINSON'S DISEASE; https://hdl.handle.net/11585/918291Test

الإتاحة: https://doi.org/10.3233/jpd-212867Test
https://hdl.handle.net/11585/918291Test

المؤلفون: Christelle Charley Monaca, Gian Luigi Gigli, Wolfgang H. Oertel, Francesco Biscarini, Monica Puligheddu, Michela Figorilli, Uladzislau Rudakou, Yuri L. Sosero, Farnaz Asayesh, Guy A. Rouleau, Jean-François Gagnon, Anna Heidbreder, Jennifer A. Ruskey, Femke Dijkstra, Sandra B. Laurent, Birgit Högl, Claudia Trenkwalder, Michele T.M. Hu, Kheireddin Mufti, Mariarosaria Valente, Abubaker Ibrahim, Jacques Montplaisir, Alex Desautels, Nicholas Oscroft, Lynne Krohn, Friederike Sixel-Döring, Karel Sonka, Timothy Quinnell, Luigi Ferini-Strambi, Francesco Janes, Eric Yu, Ziv Gan-Or, Valérie Cochen De Cock, David Kemlink, Ambra Stefani, Isabelle Arnulf, Andrea Bernardini, Elena Antelmi, Mineke Viaene, Annette Janzen, Beatriz Abril, Giuseppe Plazzi, Dan Spiegelman, Bradley F. Boeve, Brit Mollenhauer, Y. Dauvilliers, Mehrdad Asghari Estiar, Ronald B. Postuma, Jean-François Trempe

المصدر: Journal of Parkinson's Disease

مصطلحات موضوعية: Association test, Parkinson's disease, Motor dysfunction, Synucleinopathies, REM sleep behavior disorder, saposin C, PSAP, Saposins, 03 medical and health sciences, Cellular and Molecular Neuroscience, 0302 clinical medicine, medicine, Humans, genetics, Cognitive impairment, 030304 developmental biology, Genetics, 0303 health sciences, Genetic interaction, business.industry, glucocerebrosidase, Prodromal Stage, Parkinson Disease, GBA, medicine.disease, Parkinson’s disease, Glucosylceramidase, Human medicine, Neurology (clinical), business, Glucocerebrosidase, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15596f0cbeb5e0e24f828b6eb262cb40Test
http://hdl.handle.net/11390/1220691Test

المؤلفون: Edward A. Fon, Armaghan Alam, Richard Y.J. Wu, Cornelis Blauwendraat, Jennifer A. Ruskey, Luigi Ferini-Strambi, Paul Cannon, Mathias Toft, Mariarosaria Valente, Alex Desautels, Andrew B. Singleton, Valérie Cochen De Cock, Yves Dauvilliers, Elena Antelmi, C. Trenkwalder, Kari Anne Bjørnarå, Abril Beatriz, Christelle Charley Monaca, Jacques Montplaisir, Nicolas Dupré, Mineke Viaene, Peter Young, Birgit Högl, Giuseppe Plazzi, Monica Puligheddu, W. H. Oertel, Marco Toffoli, Bradley F. Boeve, Owen A. Ross, Friederike Sixel-Döring, Lasse Pihlstrøm, Michele T.M. Hu, Isabelle Arnulf, Sandra B. Laurent, Karl Heilbron, Michela Figorilli, Anna Heidbreder, Lynne Krohn, Guy A. Rouleau, Karel Sonka, Ziv Gan-Or, Mike A. Nalls, Jean-François Gagnon, David Kemlink, Evi Holzknecht, Femke Dijkstra, Ambra Stefani, Gian Luigi Gigli, Brit Mollenhauer, Ronald B. Postuma

المساهمون: Krohn L., Wu R.Y.J., Heilbron K., Ruskey J.A., Laurent S.B., Blauwendraat C., Alam A., Arnulf I., Hu M.T.M., Dauvilliers Y., Hogl B., Toft M., Bjornara K.A., Stefani A., Holzknecht E., Monaca C.C., Abril B., Plazzi G., Antelmi E., Ferini-Strambi L., Young P., Heidbreder A., Cochen De Cock V., Mollenhauer B., Sixel-Doring F., Trenkwalder C., Sonka K., Kemlink D., Figorilli M., Puligheddu M., Dijkstra F., Viaene M., Oertel W., Toffoli M., Gigli G.L., Valente M., Gagnon J.-F., Nalls M.A., Singleton A.B., Desautels A., Montplaisir J.Y., Cannon P., Ross O.A., Boeve B.F., Dupre N., Fon E.A., Postuma R.B., Pihlstrom L., Rouleau G.A., Gan-Or Z., Krohn, L., R. Y. J., Wu, Heilbron, K., Ruskey, J. A., Laurent, S. B., Blauwendraat, C., Alam, A., Arnulf, I., M. T. M., Hu, Dauvilliers, Y., Hogl, B., Toft, M., Bjornara, K. A., Stefani, A., Holzknecht, E., Monaca, C. C., Abril, B., Plazzi, G., Antelmi, E., Ferini-Strambi, L., Young, P., Heidbreder, A., Cochen De Cock, V., Mollenhauer, B., Sixel-Doring, F., Trenkwalder, C., Sonka, K., Kemlink, D., Figorilli, M., Puligheddu, M., Dijkstra, F., Viaene, M., Oertel, W., Toffoli, M., Gigli, G. L., Valente, M., Gagnon, J. -F., Nalls, M. A., Singleton, A. B., Desautels, A., Montplaisir, J. Y., Cannon, P., Ross, O. A., Boeve, B. F., Dupre, N., Fon, E. A., Postuma, R. B., Pihlstrom, L., Rouleau, G. A., Gan-Or, Z., McGill University Health Center [Montreal] (MUHC), Montreal Neurological Institute and Hospital, McGill University = Université McGill [Montréal, Canada], Imperial College London, 23andMe Inc., National Institute on Aging [Bethesda, USA] (NIA), National Institutes of Health [Bethesda] (NIH), Centre d'investigation clinique Neurosciences [CHU Pitié Salpêtrière] (CIC Neurosciences), CHU Pitié-Salpêtrière [AP-HP], Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), University of Oxford [Oxford], Nuffield Department of Clinical Neurosciences [Oxford], Département de neurologie [Montpellier], Hôpital Gui de Chauliac [Montpellier]-Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier)-Université Montpellier 1 (UM1)-Université de Montpellier (UM), Innsbruck Medical University [Austria] (IMU), Oslo University Hospital [Oslo], Service de neurophysiologie clinique (CHRU Lille), Centre Hospitalier Régional Universitaire [Lille] (CHRU Lille), Hôpital Universitaire Carémeau [Nîmes] (CHU Nîmes), Centre Hospitalier Universitaire de Nîmes (CHU Nîmes), Alma Mater Studiorum University of Bologna (UNIBO), University of Bologna, Department of Biomedical and Neuromotor Sciences [Bologna, Italy], Universita Vita Salute San Raffaele = Vita-Salute San Raffaele University [Milan, Italie] (UniSR), University of Münster, Clinique Beau Soleil [Montpellier], EuroMov - Digital Health in Motion (Euromov DHM), IMT - MINES ALES (IMT - MINES ALES), Institut Mines-Télécom [Paris] (IMT)-Institut Mines-Télécom [Paris] (IMT)-Université de Montpellier (UM), Paracelsus-Elena-Klinik, Kassel, Germany., University Medical Center Göttingen (UMG), First Faculty of Medicine Charles University [Prague], Universita degli Studi di Cagliari [Cagliari], Algemeen Ziekenhuis Sint-Dimpna, Philipps University of Marburg, Università degli Studi di Udine - University of Udine [Italie], University College of London [London] (UCL), Department of Mathematics and Computer Science [Udine], Hôpital du Sacré-Coeur de Montréal, Université du Québec à Montréal = University of Québec in Montréal (UQAM), Data Tecnica International, Centre d'études avancées en Médecine du Sommeil (CEAMS), Université de Montréal (UdeM)-Hôpital du Sacré-Coeur de Montréal, Mayo Clinic [Jacksonville], Mayo Clinic [Rochester], Laval University Medical center, Université Laval [Québec] (ULaval)

المصدر: Ann Neurol
Annals of Neurology
Annals of Neurology, Wiley, 2020, 87 (4), pp.584-598. ⟨10.1002/ana.25687⟩

مصطلحات موضوعية: Male, 0301 basic medicine, Oncology, Linkage disequilibrium, Synucleinopathies, REM sleep behavior disorder, MESH: Logistic Models, REM Sleep Behavior Disorder, 0302 clinical medicine, synucleinopathy, SNCA, Odds Ratio, RBD-specific risk variants, MESH: Aged, MESH: Middle Aged, Rapid eye movement sleep behavior disorder (RBD), MESH: Polymorphism, Single Nucleotide, MESH: Genetic Predisposition to Disease, Parkinson Disease, Middle Aged, MESH: Case-Control Studies, 3. Good health, Neurology, MESH: Synucleinopathies, alpha-Synuclein, Female, Adult, Lewy Body Disease, medicine.medical_specialty, Prodromal Symptoms, Single-nucleotide polymorphism, Locus (genetics), Polymorphism, Single Nucleotide, Article, 03 medical and health sciences, Internal medicine, MESH: alpha-Synuclein, medicine, Humans, Genetic Predisposition to Disease, MESH: Prodromal Symptoms, Allele frequency, MESH: Lewy Body Disease, Aged, MESH: Humans, business.industry, Dementia with Lewy bodies, [SCCO.NEUR]Cognitive science/Neuroscience, MESH: Adult, Odds ratio, medicine.disease, MESH: Odds Ratio, MESH: Male, synucleinopathies, Logistic Models, 030104 developmental biology, MESH: REM Sleep Behavior Disorder, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, Case-Control Studies, Synuclein, Neurology (clinical), business, MESH: Female, MESH: Parkinson Disease, 030217 neurology & neurosurgery

وصف الملف: STAMPA

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3823fcd180b0bab90c34617e51467610Test
https://doi.org/10.1002/ana.25687Test

المؤلفون: Luigi Ferini-Strambi, Andrea Bernardini, Michele T.M. Hu, Nicholas Oscroft, Lynne Krohn, Giuseppe Plazzi, Mehrdad Asghari Estiar, Farnaz Asayesh, Guy A. Rouleau, Birgit Högl, Mineke Viaene, Friederike Sixel-Döring, Jacques Montplaisir, Ronald B. Postuma, Ambra Stefani, Jean-François Gagnon, David Kemlink, Brit Mollenhauer, Jean-François Trempe, Claudia Trenkwalder, Bradley F. Boeve, Francesco Janes, Isabelle Arnulf, Anna Heidbreder, Y. Dauvilliers, Karel Sonka, Christelle Charley Monaca, Dan Spiegelman, Ziv Gan-Or, Michela Figorilli, Monica Puligheddu, Wolfgang H. Oertel, Kheireddin Mufti, Uladzislau Rudakou, Francesco Biscarini, Sandra B. Laurent, Annette Janzen, Timothy Quinnell, Abubaker Ibrahim, Mariarosaria Valente, Alex Desautels, Valérie Cochen De Cock, Elena Antelmi, Beatriz Abril, Eric Yu, Jennifer A. Ruskey, Femke Dijkstra, Yuri L. Sosero, Gian Luigi Gigli

مصطلحات موضوعية: Genetics, 0303 health sciences, Association test, Motor dysfunction, Genetic interaction, business.industry, Prodromal Stage, Population based, medicine.disease, REM sleep behavior disorder, 03 medical and health sciences, 0302 clinical medicine, Medicine, business, Cognitive impairment, Glucocerebrosidase, 030217 neurology & neurosurgery, 030304 developmental biology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::b70075eae34fb78a75d8e4f96086ac7cTest
https://doi.org/10.1101/2021.07.13.21258405Test

المؤلفون: Prabhjyot Saini, Guy A. Rouleau, Sandra B. Laurent, Ziv Gan-Or, Stanley Fahn, Sharon Hassin-Baer, Jennifer A. Ruskey, Eric Yu, Yves Dauvilliers, Uladzislau Rudakou, Nicolas Dupré, Edward A. Fon, Roy N. Alcalay, Alberto J. Espay, Dan Spiegelman, Ronald B. Postuma, Cheryl Waters, Oury Monchi, Farnaz Asayesh, Lior Greenbaum

المساهمون: Montreal Neurological Institute and Hospital, McGill University = Université McGill [Montréal, Canada], Department of Human Genetics [Montréal], Department of Neurology and Neurosurgery [Montreal], McGill University = Université McGill [Montréal, Canada]-McGill University = Université McGill [Montréal, Canada], Columbia University College of Physicians and Surgeons, Columbia University Medical Center (CUMC), Columbia University [New York], University of Calgary, Hotchkiss Brain Institute, Département de neurologie [Montpellier], Université Montpellier 1 (UM1)-Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier)-Hôpital Gui de Chauliac [Montpellier]-Université de Montpellier (UM), Neuropsychiatrie : recherche épidémiologique et clinique (PSNREC), Université Montpellier 1 (UM1)-Université de Montpellier (UM)-Institut National de la Santé et de la Recherche Médicale (INSERM), CHU de Québec–Université Laval, Université Laval [Québec] (ULaval), Sackler Faculty of Medicine, Tel Aviv University [Tel Aviv], Chaim Sheba Medical Center, University of Cincinnati (UC), Hôpital Gui de Chauliac [Montpellier]-Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier)-Université Montpellier 1 (UM1)-Université de Montpellier (UM), Université Montpellier 1 (UM1)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM), Tel Aviv University (TAU), Herrada, Anthony

المصدر: Neurobiology of Aging
Neurobiology of Aging, Elsevier, 2021, 100, pp.119.e7-119.e13. ⟨10.1016/j.neurobiolaging.2020.10.019⟩
Neurobiol Aging
Neurobiology of Aging, 2021, 100, pp.119.e7-119.e13. ⟨10.1016/j.neurobiolaging.2020.10.019⟩

مصطلحات موضوعية: 0301 basic medicine, Male, Aging, Association test, Parkinson's disease, French-Canadian, Disease, Biology, UCHL1, White People, Article, Cohort Studies, 03 medical and health sciences, 0302 clinical medicine, Rare mutations, medicine, Humans, [SDV.NEU] Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC], Association (psychology), Gene, Ashkenazi-Jewish, Genetic Association Studies, EIF4G1, Genetics, HTRA2, [SDV.MHEP.GEG] Life Sciences [q-bio]/Human health and pathology/Geriatry and gerontology, DNAJC13, General Neuroscience, [SDV.MHEP.GEG]Life Sciences [q-bio]/Human health and pathology/Geriatry and gerontology, Parkinson Disease, High-Temperature Requirement A Serine Peptidase 2, medicine.disease, GIGYF2, SKAT-O, 030104 developmental biology, Increased risk, Multiple comparisons problem, Female, [SDV.NEU]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC], Neurology (clinical), Geriatrics and Gerontology, Carrier Proteins, Eukaryotic Initiation Factor-4G, Negative Results, Ubiquitin Thiolesterase, 030217 neurology & neurosurgery, Developmental Biology, Molecular Chaperones

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::975c3abee915f6605caa9ab023db45e9Test
https://hal.umontpellier.fr/hal-03226126Test

المؤلفون: Jean-François Trempe, Omid Tavassoly, Karen Marder, Patrick A. Dion, Edward A. Fon, Roy N. Alcalay, Petra Oliva, Un Jung Kang, Xiaokui Kate Zhang, Mélanie Langlois, Richard Y.J. Wu, Cheryl Waters, Sandra B. Laurent, Claire S. Leblond, Nicolas Dupré, Christopher Liong, Jennifer A. Ruskey, Wendy K. Chung, Sheng-Han Kuo, Blair Ford, Oren A. Levy, Lorraine N. Clark, Alexandre Dionne-Laporte, Pavlina Wolf, Amirthagowri Ambalavanan, Ziv Gan-Or, Benoît Vanderperre, Yves Dauvilliers, Victoria Mallett, Guy A. Rouleau, Dan Spiegelman, Sharon Hassin-Baer, Stanley Fahn, Lior Greenbaum

المصدر: Movement Disorders. 34:526-535

مصطلحات موضوعية: 0301 basic medicine, medicine.medical_specialty, Parkinson's disease, Disease, medicine.disease_cause, 03 medical and health sciences, 0302 clinical medicine, Lysosome, Internal medicine, medicine, Mutation, Gene knockdown, business.industry, medicine.disease, In vitro, 3. Good health, 030104 developmental biology, medicine.anatomical_structure, Endocrinology, Neurology, Cohort, Neurology (clinical), Acid sphingomyelinase, business, 030217 neurology & neurosurgery, medicine.drug

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::d2163eb8eaeea99d54fa5d1862d6af3cTest
https://doi.org/10.1002/mds.27642Test

المؤلفون: Alex Rajput, Sandra B. Laurent, Claire S. Leblond, Gabrielle Houle, Carles Vilariño-Güell, Cynthia V. Bourassa, Guy A. Rouleau, Jean-François Schmouth, Amirthagowri Ambalavanan, Sylvain Chouinard, Dan Spiegelman, Patrick A. Dion, Michel Panisset, Nicolas Dupré

المصدر: Molecular Neurobiology. 56:4317-4321

مصطلحات موضوعية: 0301 basic medicine, Canada, Candidate gene, Cerebellum, medicine.medical_specialty, Neurology, Essential Tremor, Mutation, Missense, Neuroscience (miscellaneous), Neurological disorder, Biology, medicine.disease_cause, 03 medical and health sciences, Cellular and Molecular Neuroscience, 0302 clinical medicine, medicine, Humans, Gene, Conserved Sequence, Genetic Association Studies, Phylogeny, Aged, Genetics, Mutation, Essential tremor, Motor Cortex, Middle Aged, medicine.disease, 030104 developmental biology, medicine.anatomical_structure, Cohort, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83a961e1f3b0a0b4f48dbc29b814ffd5Test
https://doi.org/10.1007/s12035-018-1369-1Test

المؤلفون: Christelle Charley Monaca, Alex Desautels, Yves Dauvilliers, Beatriz Abril, Elena Antelmi, Ambra Stefani, Giuseppe Plazzi, Karel Sonka, Monica Puligheddu, Brit Mollenhauer, Birgit Högl, Sandra B. Laurent, Eric Yu, Farnaz Asayesh, Luigi Ferini-Strambi, Mariarosaria Valente, Jennifer A. Ruskey, Michela Figorilli, Uladzislau Rudakou, Annette Janzen, Ziv Gan-Or, Francesco Janes, Mineke Viaene, Ronald B. Postuma, Valérie Cochen De Cock, Bradley F. Boeve, David Kemlink, Evi Holzknecht, Dan Spiegelman, Jacques Montplaisir, Anna Heidbreder, Gian Luigi Gigli, Michele T.M. Hu, Friederike Sixel-Döring, Lynne Krohn, Kheireddin Mufti, Guy A. Rouleau, Isabelle Arnulf, Claudia Trenkwalder, Wolfgang H. Oertel, Femke Dijkstra, Jean-François Gagnon

المساهمون: Centre de Recherche de l'Institut du Cerveau et de la Moelle épinière (CRICM), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Hôpital Gui de Chauliac [CHU Montpellier], Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier), Clinique Beau Soleil [Montpellier], EuroMov - Digital Health in Motion (Euromov DHM), IMT - MINES ALES (IMT - MINES ALES), Institut Mines-Télécom [Paris] (IMT)-Institut Mines-Télécom [Paris] (IMT)-Université de Montpellier (UM), CHU Lille, Université de Lille, Hôpital Universitaire Carémeau [Nîmes] (CHU Nîmes), Centre Hospitalier Universitaire de Nîmes (CHU Nîmes), Mufti, K., Rudakou, U., Yu, E., Krohn, L., Ruskey, J. A., Asayesh, F., Laurent, S. B., Spiegelman, D., Arnulf, I., M. T. M., Hu, Montplaisir, J. Y., Gagnon, J. -F., Desautels, A., Dauvilliers, Y., Gigli, G. L., Valente, M., Janes, F., Hogl, B., Stefani, A., Holzknecht, E., Sonka, K., Kemlink, D., Oertel, W., Janzen, A., Plazzi, G., Antelmi, E., Figorilli, M., Puligheddu, M., Mollenhauer, B., Trenkwalder, C., Sixel-Doring, F., Cochen De Cock, V., Monaca, C. C., Heidbreder, A., Ferini-Strambi, L., Dijkstra, F., Viaene, M., Abril, B., Boeve, B. F., Postuma, R. B., Rouleau, G. A., Gan-Or, Z.

المصدر: Movement Disorders
Movement Disorders, 2021, 36 (1), pp.235-240. ⟨10.1002/mds.28318⟩
Movement disorders: video, videotape supplements

مصطلحات موضوعية: 0301 basic medicine, Heterozygote, Parkinson's disease, MESH: Sleep, [SDV]Life Sciences [q-bio], REM sleep behavior disorder, Rapid eye movement sleep, Disease, genetic analysis, Compound heterozygosity, Genetic analysis, 03 medical and health sciences, 0302 clinical medicine, Parkinsonian Disorders, Medicine, Humans, MESH: Heterozygote, Genetics, MESH: Humans, business.industry, MESH: Parkinsonian Disorders, PARK7, Parkinson Disease, medicine.disease, LRRK2, 3. Good health, 030104 developmental biology, Neurology, MESH: REM Sleep Behavior Disorder, Human medicine, Neurology (clinical), business, Sleep, 030217 neurology & neurosurgery, MESH: Parkinson Disease

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::477997d598700bcb6755c87370c28a67Test
https://hal.science/hal-03653760Test

المؤلفون: Kheireddin, Mufti, Eric, Yu, Uladzislau, Rudakou, Lynne, Krohn, Jennifer A, Ruskey, Farnaz, Asayesh, Sandra B, Laurent, Dan, Spiegelman, Isabelle, Arnulf, Michele T M, Hu, Jacques Y, Montplaisir, Jean-François, Gagnon, Alex, Desautels, Yves, Dauvilliers, Gian Luigi, Gigli, Mariarosaria, Valente, Francesco, Janes, Andrea, Bernardini, Birgit, Högl, Ambra, Stefani, Evi, Holzknecht, Karel, Sonka, David, Kemlink, Wolfgang, Oertel, Annette, Janzen, Giuseppe, Plazzi, Elena, Antelmi, Michela, Figorilli, Monica, Puligheddu, Brit, Mollenhauer, Claudia, Trenkwalder, Friederike, Sixel-Döring, Valérie, Cochen De Cock, Christelle Charley, Monaca, Anna, Heidbreder, Luigi, Ferini-Strambi, Femke, Dijkstra, Mineke, Viaene, Beatriz, Abril, Bradley F, Boeve, Jean-François, Trempe, Guy A, Rouleau, Ronald B, Postuma, Ziv, Gan-Or

المصدر: Neurology
article-version (Version of Record) 3

مصطلحات موضوعية: Male, Heterozygote, Polysomnography, Genetic Variation, Lysosome-Associated Membrane Glycoproteins, REM Sleep Behavior Disorder, Middle Aged, GPI-Linked Proteins, Protein Structure, Secondary, Article, Neoplasm Proteins, Antigens, CD, Databases, Genetic, Humans, Computer Simulation, Female, ADP-ribosyl Cyclase, Aged, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::2d9ecaacdf00a60935a51c391a15f73aTest
https://pubmed.ncbi.nlm.nih.gov/33397775Test

المؤلفون: Patrick A. Dion, William Camu, Claire S. Leblond, Guy A. Rouleau, Nicolas Dupré, Alexandre Dionne-Laporte, Dan Spiegelman, Sandra B. Laurent, Jay P. Ross

المساهمون: McGill University = Université McGill [Montréal, Canada], Génétique humaine et fonctions cognitives - Human Genetics and Cognitive Functions (GHFC (UMR_3571 / U-Pasteur_1)), Institut Pasteur [Paris] (IP)-Université Paris Diderot - Paris 7 (UPD7)-Centre National de la Recherche Scientifique (CNRS), Hôpital Gui de Chauliac [CHU Montpellier], Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier), Université de Montpellier (UM), CHU de Québec–Université Laval, Université Laval [Québec] (ULaval), Faculté de médecine de l'Université Laval [Québec] (ULaval), Department of Neurology and Neurosurgery [Montreal], Montreal Neurological Institute and Hospital, McGill University = Université McGill [Montréal, Canada]-McGill University = Université McGill [Montréal, Canada], Jay Ross has received a doctoral student fellowship from the ALS Society of Canada and a Canadian Institutes of Health Research Frederick Banting & Charles Best Canada Graduate Scholarship (FRN 159279). We thank the ALS Society of Canada, the Canadian Institutes of Health Research, and Brain Canada for research funding.

المصدر: neurogenetics
neurogenetics, 2020, 21 (3), pp.227-242. ⟨10.1007/s10048-020-00612-7⟩

مصطلحات موضوعية: 0301 basic medicine, Male, Multifactorial Inheritance, MESH: Sequence Analysis, DNA, MESH: DNA Repeat Expansion, Pathogenesis, Cohort Studies, C9orf72 expansion, 0302 clinical medicine, C9orf72, MESH: Genetic Variation, Amyotrophic lateral sclerosis, MESH: Cohort Studies, Genetics (clinical), MESH: Amyotrophic Lateral Sclerosis, Genetics, MESH: Aged, DNA Repeat Expansion, MESH: Middle Aged, Variant severity, Oligogenic Inheritance, Middle Aged, Frontotemporal Dementia, Female, [SDV.NEU]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC], France, MESH: C9orf72 Protein, Adult, Canada, MESH: Frontotemporal Dementia, Biology, 03 medical and health sciences, Cellular and Molecular Neuroscience, MESH: Canada, medicine, Humans, Gene, Aged, MESH: Humans, C9orf72 Protein, Amyotrophic Lateral Sclerosis, Genetic Variation, MESH: Adult, Sequence Analysis, DNA, medicine.disease, Molecular medicine, Human genetics, MESH: Male, Oligogenicity, MESH: France, 030104 developmental biology, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, Disease Presentation, ALS, MESH: Multifactorial Inheritance, MESH: Female, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::718283b11f85b322bab4041e3dc3c512Test
https://hal.umontpellier.fr/hal-03564841Test