المؤلفون: Grover S., Sreelatha A. A. K., Pihlstrom L., Domenighetti C., Schulte C., Sugier P. -E., Radivojkov-Blagojevic M., Lichtner P., Mohamed O., Portugal B., Landoulsi Z., May P., Bobbili D., Edsall C., Bartusch F., Hanussek M., Kruger J., Hernandez D. G., Blauwendraat C., Mellick G. D., Zimprich A., Pirker W., Tan M., Rogaeva E., Lang A., Koks S., Taba P., Lesage S., Brice A., Corvol J. -C., Chartier-Harlin M. -C., Mutez E., Brockmann K., Deutschlander A. B., Hadjigeorgiou G. M., Dardiotis E., Stefanis L., Simitsi A. M., Valente E. M., Petrucci S., Straniero L., Zecchinelli A., Pezzoli G., Brighina L., Ferrarese C., Annesi G., Quattrone A., Gagliardi M., Burbulla L. F., Matsuo H., Kawamura Y., Hattori N., Nishioka K., Chung S. J., Kim Y. J., Pavelka L., Van De Warrenburg B. P. C., Bloem B. R., Singleton A. B., Aasly J., Toft M., Guedes L. C., Ferreira J. J., Bardien S., Carr J., Tolosa E., Ezquerra M., Pastor P., Diez-Fairen M., Wirdefeldt K., Pedersen N. L., Ran C., Belin A. C., Puschmann A., Hellberg C., Clarke C. E., Morrison K. E., Krainc D., Farrer M. J., Kruger R., Elbaz A., Gasser T., Sharma M.

المساهمون: Grover, S., Sreelatha, A. A. K., Pihlstrom, L., Domenighetti, C., Schulte, C., Sugier, P. -E., Radivojkov-Blagojevic, M., Lichtner, P., Mohamed, O., Portugal, B., Landoulsi, Z., May, P., Bobbili, D., Edsall, C., Bartusch, F., Hanussek, M., Kruger, J., Hernandez, D. G., Blauwendraat, C., Mellick, G. D., Zimprich, A., Pirker, W., Tan, M., Rogaeva, E., Lang, A., Koks, S., Taba, P., Lesage, S., Brice, A., Corvol, J. -C., Chartier-Harlin, M. -C., Mutez, E., Brockmann, K., Deutschlander, A. B., Hadjigeorgiou, G. M., Dardiotis, E., Stefanis, L., Simitsi, A. M., Valente, E. M., Petrucci, S., Straniero, L., Zecchinelli, A., Pezzoli, G., Brighina, L., Ferrarese, C., Annesi, G., Quattrone, A., Gagliardi, M., Burbulla, L. F., Matsuo, H., Kawamura, Y., Hattori, N., Nishioka, K., Chung, S. J., Kim, Y. J., Pavelka, L., Van De Warrenburg, B. P. C., Bloem, B. R., Singleton, A. B., Aasly, J., Toft, M., Guedes, L. C., Ferreira, J. J., Bardien, S., Carr, J., Tolosa, E., Ezquerra, M., Pastor, P., Diez-Fairen, M., Wirdefeldt, K., Pedersen, N. L., Ran, C., Belin, A. C., Puschmann, A., Hellberg, C., Clarke, C. E., Morrison, K. E., Krainc, D., Farrer, M. J., Kruger, R., Elbaz, A., Gasser, T., Sharma, M.

مصطلحات موضوعية: Age at onset, Burden of disease, Duration of disease, Genetic heritability, Parkinson’s disease, Age of Onset, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Human, Polymorphism, Single Nucleotide, Courage, Parkinson Disease

وصف الملف: STAMPA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/35618440; volume:99; issue:7; firstpage:698; lastpage:710; numberofpages:13; journal:NEUROLOGY; https://hdl.handle.net/11571/1465424Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85136019610

الإتاحة: https://doi.org/10.1212/WNL.0000000000200699Test
https://hdl.handle.net/11571/1465424Test

المؤلفون: Brockmann, K., Schulte, C., Knorpp, T., Joos, T. O., Bernard, A., Gasser, T., Marras, C., Schüle, B., Aasly, J. O., Foroud, T., Marti-Masso, J. F., Brice, A., Schneiderhan-Marra, N., Tolosa, E., Berg, D., Maetzler, W., Apel, A., Pont-Sunyer, C., Vilas, D., Ruiz-Martinez, J., Langkamp, M., Corvol, J-C, Cormier, F.

المصدر: European journal of neurology 24(2), 427-e6 (2017). doi:10.1111/ene.13223

مصطلحات موضوعية: info:eu-repo/classification/ddc/610, Adult, Age of Onset, Aged, 80 and over, Biomarkers: blood, Brain-Derived Neurotrophic Factor: blood, Chemokine CCL2: blood, Chemokine CCL4: blood, Cohort Studies, Cytokines: blood, Disease Progression, Female, Humans, Inflammation: etiology, Inflammation: genetics, Inflammation: pathology, Leucine-Rich Repeat Serine-Threonine Protein Kinase-2: genetics, Male, Middle Aged, Mutation, Parkinson Disease: genetics, Parkinson Disease: pathology, Biomarkers, Brain-Derived Neurotrophic Factor, CCL2 protein, human, CCL4 protein, Chemokine CCL2, Chemokine CCL4

جغرافية الموضوع: DE

العلاقة: info:eu-repo/semantics/altIdentifier/issn/1471-0552; info:eu-repo/semantics/altIdentifier/issn/1468-1331; info:eu-repo/semantics/altIdentifier/issn/1351-5101; info:eu-repo/semantics/altIdentifier/pmid/pmid:28102045; https://pub.dzne.de/record/139002Test; https://pub.dzne.de/search?p=id:%22DZNE-2020-05324%22Test

الإتاحة: https://doi.org/10.1111/ene.13223Test
https://pub.dzne.de/record/139002Test
https://pub.dzne.de/search?p=id:%22DZNE-2020-05324%22Test

المؤلفون: Elbaz, A, Ross, O, Ioannidis, J, Soto Ortolaza, A, Moisan, F, Aasly, J, Annesi, G, Bozi, M, Brighina, L, Chartier Harlin, M, Destée, A, Ferraris, A, Gibson, J, Gispert, S, Hadjigeorgiou, G, Jasinska Myga, B, Klein, C, Krüger, R, Lambert, J, Lohmann, K, van de Loo, S, Loriot, M, Lynch, T, Mellick, G, Mutez, E, Nilsson, C, Opala, G, Puschmann, A, Quattrone, A, Sharma, M, Silburn, P, Stefanis, L, Uitti, R, Valente, E, Vilariño Güell, C, Wirdefeldt, K, Wszolek, Z, Xiromerisiou, G, Maraganore, D, Farrer, M., FERRARESE, CARLO

المساهمون: Elbaz, A, Ross, O, Ioannidis, J, Soto Ortolaza, A, Moisan, F, Aasly, J, Annesi, G, Bozi, M, Brighina, L, Chartier Harlin, M, Destée, A, Ferrarese, C, Ferraris, A, Gibson, J, Gispert, S, Hadjigeorgiou, G, Jasinska Myga, B, Klein, C, Krüger, R, Lambert, J, Lohmann, K, van de Loo, S, Loriot, M, Lynch, T, Mellick, G, Mutez, E, Nilsson, C, Opala, G, Puschmann, A, Quattrone, A, Sharma, M, Silburn, P, Stefanis, L, Uitti, R, Valente, E, Vilariño Güell, C, Wirdefeldt, K, Wszolek, Z, Xiromerisiou, G, Maraganore, D, Farrer, M

مصطلحات موضوعية: Polymorphism, Single Nucleotide, Odds Ratio, Age of Onset, Human, Retrospective Studie, Aged, tau Protein, 80 and over, Logistic Model, Parkinson Disease, alpha-Synuclein, Adult, Case-Control Studie, Middle Aged, Genetic Predisposition to Disease, Female, Male

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/21391235; info:eu-repo/semantics/altIdentifier/wos/WOS:000290156300005; volume:69; issue:5; firstpage:778; lastpage:792; numberofpages:15; journal:ANNALS OF NEUROLOGY; http://hdl.handle.net/10281/33168Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-79955389000

الإتاحة: https://doi.org/10.1002/ana.22321Test
http://hdl.handle.net/10281/33168Test

المؤلفون: Engelsen B. A., Tzoulis C., Karlsen B., Lillebo A., Laegreid L. M., Aasly J., Zeviani M., Bindoff L. A.

المساهمون: Engelsen, B. A., Tzoulis, C., Karlsen, B., Lillebo, A., Laegreid, L. M., Aasly, J., Zeviani, M., Bindoff, L. A.

مصطلحات موضوعية: Epilepsy, Mitochondrial disease, Occipital lobe, POLG, Status epilepticu, Adolescent, Adult, Age of Onset, Anticonvulsant, Brain, Child, DNA Polymerase gamma, DNA-Directed DNA Polymerase, Disease Progression, Electroencephalography, Epilepsies, Partial, Female, Human, Magnetic Resonance Imaging, Male, Middle Aged, Prognosi, Syndrome, Mutation

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/18238797; info:eu-repo/semantics/altIdentifier/wos/WOS:000253489800022; volume:131; issue:3; firstpage:818; lastpage:828; numberofpages:11; journal:BRAIN; http://hdl.handle.net/11577/3354319Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-39749121457

الإتاحة: https://doi.org/10.1093/brain/awn007Test
http://hdl.handle.net/11577/3354319Test

المؤلفون: Tzoulis C., Engelsen B. A., Telstad W., Aasly J., Zeviani M., Winterthun S., Ferrari G., Aarseth J. H., Bindoff L. A.

المساهمون: Tzoulis, C., Engelsen, B. A., Telstad, W., Aasly, J., Zeviani, M., Winterthun, S., Ferrari, G., Aarseth, J. H., Bindoff, L. A.

مصطلحات موضوعية: Alper, Ataxia, Hepatic, Mitochondrial, POLG, Adolescent, Adult, Age of Onset, Aged, Child, DNA Polymerase gamma, DNA, DNA-Directed DNA Polymerase, Developmental Disabilitie, Diffuse Cerebral Sclerosis of Schilder, Disease Progression, Epidemiologic Method, Epilepsy, Tonic-Clonic, Female, Genotype, Heredodegenerative Disorders, Nervous System, Human, Liver Failure, Magnetic Resonance Imaging, Male, Middle Aged, Mitochondrial Disease, Mutation

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/16638794; info:eu-repo/semantics/altIdentifier/wos/WOS:000238761200012; volume:129; issue:7; firstpage:1685; lastpage:1692; numberofpages:8; journal:BRAIN; http://hdl.handle.net/11577/3354339Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-33745685519

الإتاحة: https://doi.org/10.1093/brain/awl097Test
http://hdl.handle.net/11577/3354339Test

المؤلفون: Elbaz, A., Ross, O. A., Ioannidis, J. P., Soto-Ortolaza, A. I., Moisan, F., Aasly, J. O., Annesi, G., Bozi, M., Brighina, L., Chartier-Harlin, M. C., Destee, A., Ferrarese, C., Ferraris, A., Gibson, J. M., Gispert, S., Hadjigeorgiou, G. M., Jasinska-Myga, B., Klein, C., Kruger, R., Lambert, J. C., Lohmann, K., van de Loo, S., Loriot, M. A., Lynch, T., Mellick, G. D., Mutez, E., Nilsson, C., Opala, G., Puschmann, A., Quattrone, A., Sharma, M., Silburn, P. A., Stefanis, L., Uitti, R. J., Valente, E. M., Vilarino-Guell, C., Wirdefeldt, K., Wszolek, Z. K., Xiromerisiou, G., Maraganore, D. M., Farrer, M. J.

مصطلحات موضوعية: Adult, Age of Onset, Aged, 80 and over, Case-Control Studies, Female, Genetic Predisposition to Disease, Humans, Logistic Models, Male, Middle Aged, Odds Ratio, Parkinson Disease/*genetics, Polymorphism, Single Nucleotide/*genetics, Retrospective Studies, alpha-Synuclein/*genetics, tau Proteins/*genetics

العلاقة: http://olympias.lib.uoi.gr/jspui/handle/123456789/20844Test

الإتاحة: http://olympias.lib.uoi.gr/jspui/handle/123456789/20844Test

المؤلفون: Maraganore, D. M., de Andrade, M., Elbaz, A., Farrer, M. J., Ioannidis, J. P., Kruger, R., Rocca, W. A., Schneider, N. K., Lesnick, T. G., Lincoln, S. J., Hulihan, M. M., Aasly, J. O., Ashizawa, T., Chartier-Harlin, M. C., Checkoway, H., Ferrarese, C., Hadjigeorgiou, G., Hattori, N., Kawakami, H., Lambert, J. C., Lynch, T., Mellick, G. D., Papapetropoulos, S., Parsian, A., Quattrone, A., Riess, O., Tan, E. K., Van Broeckhoven, C.

مصطلحات موضوعية: Adult, Age of Onset, Aged, 80 and over, Alleles, Dinucleotide Repeats, Female, Genetic Predisposition to Disease, Genetic Variation, Genotype, Haplotypes, Humans, Male, Middle Aged, Parkinson Disease/epidemiology/*genetics, Promoter Regions, Genetic, alpha-Synuclein/*genetics

العلاقة: http://olympias.lib.uoi.gr/jspui/handle/123456789/23007Test

الإتاحة: http://olympias.lib.uoi.gr/jspui/handle/123456789/23007Test

المؤلفون: Elbaz, Alexis, Ross, Owen A, Destée, Alain, Ferrarese, Carlo, Ferraris, Alessandro, Gibson, J Mark, Gispert, Suzana, Hadjigeorgiou, Georgios M, Jasinska-Myga, Barbara, Klein, Christine, Krüger, Rejko, Lambert, Jean-Charles, Ioannidis, John P A, Lohmann, Katja, van de Loo, Simone, Loriot, Marie-Anne, Lynch, Timothy, Mellick, George D, Mutez, Eugénie, Nilsson, Christer, Opala, Grzegorz, Puschmann, Andreas, Quattrone, Aldo, Soto-Ortolaza, Alexandra I, Sharma, Manu, Silburn, Peter A, Stefanis, Leonidas, Uitti, Ryan J, Valente, Enza Maria, Vilariño-Güell, Carles, Wirdefeldt, Karin, Wszolek, Zbigniew K, Xiromerisiou, Georgia, Maraganore, Demetrius M, Moisan, Frédéric, Farrer, Matthew J, Disease, Genetic Epidemiology of Parkinson's, Amouyel, Philippe, Tzourio, Christophe, Mulot, Claire, Bacon, Justin A, Cobb, Stephanie A, Sutherland, Greg T, Siebert, Gerhard A, Dissanayaka, Nadeeka, Aasly, Jan, O'Sullivan, John D, Boyle, Richard S, Pasquier, Florence, Bordet, Régis, Legendre, Jean-Philippe, Auburger, Georg, Hilker, Rüdiger, Abahuni, Nadine, Geisen, Christof, Winkler, Susen, Annesi, Grazia, Gasser, Thomas, Riess, Olaf, Berg, Daniela, Schulte, Claudia, Vassilatis, Demitris, Stamboulis, Eleftherios, Dardiotis, Efthimios, Patramani, Ioanna, Kountra, Persa-Maria, Vogiatzi, Christina, Bozi, Maria, Markou, Katerina, Tarantino, Patrizia, Annesi, Ferdinanda, Bentivoglio, Anna Rita, Guidubaldi, Arianna, Caccialupi, Matilde, De Nigris, Francesca, Riva, Chiara, Pedersen, Nancy L, Nilsson, Karin, Brighina, Laura, Reimer, Jan, Van Gerpen, Jay, Lash, Jennifer, Searcy, Jill, Strongosky, Audrey, Chartier-Harlin, Marie-Christine

المساهمون: Elbaz, A, Ross, O, Ioannidis, J, Soto Ortolaza, A, Moisan, F, Aasly, J, Annesi, G, Bozi, M, Brighina, L, Chartier Harlin, M, Destée, A, Ferrarese, C, Ferraris, A, Gibson, J, Gispert, S, Hadjigeorgiou, G, Jasinska Myga, B, Klein, C, Krüger, R, Lambert, J, Lohmann, K, van de Loo, S, Loriot, M, Lynch, T, Mellick, G, Mutez, E, Nilsson, C, Opala, G, Puschmann, A, Quattrone, A, Sharma, M, Silburn, P, Stefanis, L, Uitti, R, Valente, E, Vilariño Güell, C, Wirdefeldt, K, Wszolek, Z, Xiromerisiou, G, Maraganore, D, Farrer, M

المصدر: Annals of neurology 69(5), 778-792 (2011). doi:10.1002/ana.22321

مصطلحات موضوعية: Adult, Male, Parkinson Disease/*genetics, Logistic Model, Polymorphism, Single Nucleotide/*genetics, Single-nucleotide polymorphism, Genome-wide association study, MAPT protein, human, tau Proteins, Biology, alpha-Synuclein/*genetics, Polymorphism, Single Nucleotide, Article, Gene interaction, genetics [Parkinson Disease], Retrospective Studie, Genotype, Odds Ratio, SNP, Humans, genetics, Genetic Predisposition to Disease, ddc:610, SNCA protein, human, Age of Onset, Retrospective Studies, Aged, Genetics, Aged, 80 and over, Haplotype, tau Protein, Parkinson Disease, Middle Aged, genetics [tau Proteins], Settore MED/26 - NEUROLOGIA, Logistic Models, Neurology, Genetic epidemiology, Case-Control Studies, Multiple comparisons problem, genetics [Polymorphism, Single Nucleotide], genetics [alpha-Synuclein], alpha-Synuclein, Female, Neurology (clinical), tau Proteins/*genetics, Case-Control Studie, Human

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4af5ae0523d662a62ec7cc0d3c73608Test
http://hdl.handle.net/11386/3949653Test

المؤلفون: Rejko Krüger, Spiridon Papapetropoulos, Jan O. Aasly, Sarah Lincoln, Georgios M. Hadjigeorgiou, Jean-Charles Lambert, Olaf Riess, Timothy G. Lesnick, Harvey Checkoway, Alexis Elbaz, Hideshi Kawakami, Mariza de Andrade, Timothy Lynch, John P. A. Ioannidis, Matthew J. Farrer, Nicole K. Schneider, Demetrius M. Maraganore, Carlo Ferrarese, Nobutaka Hattori, George D. Mellick, Eng-King Tan, Abbas Parsian, Marie-Christine Chartier-Harlin, Tetsuo Ashizawa, Mary M. Hulihan, Aldo Quattrone, Christine Van Broeckhoven, Walter A. Rocca

المساهمون: Department of Neurology, Mayo Clinic College of Medicine, Department of Health Sciences Research [Mayo Clinic] (HSR), Mayo Clinic, Neuroépidémiologie, Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM), Centre d'étude du sommeil, Hôpital du Sacré-Coeur de Montréal, Biomedical Research Institute, Foundation for Research and Technology-Hellas and Department of Hygiene and Epidemiology, University of Ioannina, Center of Neurology and Hertie-Institute for Clinical Brain Research, Eberhard Karls Universität Tübingen = Eberhard Karls University of Tuebingen, University Hospital, Trondheim, Texas A&M University [College Station], Institut de Recherche sur le Cancer, Institut de Recherche sur le Cancer de Lille, Department of Environmental and Occupational Health Sciences, University of Washington [Seattle], Università degli Studi di Milano-Bicocca = University of Milano-Bicocca (UNIMIB), School of Medicine, University of Thessaly [Volos] (UTH), Juntendo University School of Medicine, Department of Epidemiology, Research Institute for Radiation Biology and Medicine-Hiroshima University, Epidémiologie des maladies chroniques : impact des interactions gène environnement sur la santé des populations, Institut Pasteur de Lille, Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lille, Droit et Santé, University College Dublin [Dublin] (UCD)-Mater Misericordiae University Hospital (The Mater Hospital), University of Queensland [Brisbane], University of Miami [Coral Gables], Department of Pediatrics, University of Arkansas for Medical Sciences (UAMS), Institute of Neurology, Università degli Studi 'Magna Graecia' di Catanzaro = University of Catanzaro (UMG), Department of Medical Genetics, Singapore General Hospital, Neurodegenerative Brain Diseases Group, University of Antwerp (UA)-Flanders Interuniversity Institute of Biotechnology, University of Ioannina School of Medicine, Università degli Studi di Milano-Bicocca [Milano] (UNIMIB), University College Dublin [Dublin] (UCD)-Mater Misericordiae University Hospital and Conway Institute, Università degli Studi 'Magna Graecia' di Catanzaro [Catanzaro, Italie] (UMG), Tzourio, Christophe, Maraganore, D, de Andrade, M, Elbaz, A, Farrer, M, Ioannidis, J, Kruger, R, Rocca, W, Schneider, N, Lesnick, T, Lincoln, S, Hulihan, M, Aasly, J, Ashizawa, T, Chartier Harlin, M, Checkoway, H, Ferrarese, C, Hadjigeorgiou, G, Hattori, N, Kawakami, H, Lambert, J, Lynch, T, Mellick, G, Papapetropoulos, S, Parsian, A, Quattrone, A, Riess, O, Tan, E, Van Broeckhoven, C, Genetic Epidemiology of Parkinson's Disease (GEO-PD) Consortium

المصدر: Journal of the American Medical Association
Journal of the American Medical Association, 2006, 296 (6), pp.661-70. ⟨10.1001/jama.296.6.661⟩
Journal of the American Medical Association, American Medical Association (AMA), 2006, 296 (6), pp.661-70. ⟨10.1001/jama.296.6.661⟩
JAMA : the journal of the American Medical Association

مصطلحات موضوعية: Male, Pathology, alpha-Synuclein/*genetics, MESH: Variation (Genetics), MESH: Genotype, 0302 clinical medicine, MESH: Aged, 80 and over, Genotype, MESH: Dinucleotide Repeats, Age of Onset, Dinucleotide Repeats, Promoter Regions, Genetic, Aged, 80 and over, Genetics, MESH: Aged, 0303 health sciences, MESH: Middle Aged, MESH: Genetic Predisposition to Disease, Parkinson Disease, General Medicine, Middle Aged, Hardy–Weinberg principle, 3. Good health, MESH: Promoter Regions (Genetics), alpha-Synuclein, Female, [SDV.NEU]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC], Adult, medicine.medical_specialty, MESH: Age of Onset, Parkinson Disease/epidemiology/*genetics, 03 medical and health sciences, Genetic variation, MESH: alpha-Synuclein, medicine, Humans, Genetic Predisposition to Disease, [SDV.NEU] Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC], Allele, Genotyping, Alleles, Aged, 030304 developmental biology, MED/26 - NEUROLOGIA, MESH: Humans, business.industry, MESH: Alleles, Haplotype, Genetic Variation, MESH: Adult, Odds ratio, MESH: Haplotypes, MESH: Male, Haplotypes, [SDV.SPEE] Life Sciences [q-bio]/Santé publique et épidémiologie, [SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie, Human medicine, Age of onset, business, Parkinson, genetic variability, SNP, REP1, MESH: Female, 030217 neurology & neurosurgery, MESH: Parkinson Disease

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e442095f7201df9d5074dc6ae679bf57Test
https://www.hal.inserm.fr/inserm-00180153Test