المؤلفون: Eva C Verbeek, Ingrid M C Bakker, Marianna R Bevova, Zoltán Bochdanovits, Patrizia Rizzu, David Sondervan, Gonneke Willemsen, Eco J de Geus, Johannes H Smit, Brenda W Penninx, Dorret I Boomsma, Witte J G Hoogendijk, Peter Heutink

المصدر: PLoS ONE, Vol 7, Iss 5, p e37384 (2012)

مصطلحات موضوعية: Medicine, Science

وصف الملف: electronic resource

العلاقة: http://europepmc.org/articles/PMC3359349?pdf=renderTest; https://doaj.org/toc/1932-6203Test

الوصول الحر: https://doaj.org/article/12e27116c15a470b9effc8a28fe5067fTest

المؤلفون: Verbeek, E.C., Bakker, I.M.C., Bevova, M.R., Bochdanovits, Z., Rizzu, P., Sondervan, D., Willemsen, G., de Geus, E.J.C., Smit, J.H., Penninx, B.W.J.H., Boomsma, D.I., Hoogendijk, W.J.G., Heutink, P.

المصدر: Verbeek , E C , Bakker , I M C , Bevova , M R , Bochdanovits , Z , Rizzu , P , Sondervan , D , Willemsen , G , de Geus , E J C , Smit , J H , Penninx , B W J H , Boomsma , D I , Hoogendijk , W J G & Heutink , P 2012 , ' A Fine-Mapping Study of 7 Top Scoring Genes from a GWAS for Major Depressive Disorder ' , PLoS ONE , vol. 7 , no. 5 , e37384 , pp. e37384 . ....

مصطلحات موضوعية: /dk/atira/pure/keywords/cohort_studies/netherlands_twin_register_ntr_, name=Netherlands Twin Register (NTR)

وصف الملف: application/pdf

العلاقة: https://research.vu.nl/en/publications/1279d778-3b5c-4385-9c8b-4a0cfc36b58aTest

الإتاحة: https://doi.org/10.1371/journal.pone.0037384Test
https://research.vu.nl/en/publications/1279d778-3b5c-4385-9c8b-4a0cfc36b58aTest
https://research.vu.nl/ws/files/636310/295544.pdfTest

المؤلفون: van Assema, D.M.E., Lubberink, J.M., Rizzu, P., van Swieten, J.C., Schuit, R.C., Eriksson, P.A.J., Scheltens, P., Koepp, M., Lammertsma, A.A., van Berckel, B.N.M.

المصدر: van Assema , D M E , Lubberink , J M , Rizzu , P , van Swieten , J C , Schuit , R C , Eriksson , P A J , Scheltens , P , Koepp , M , Lammertsma , A A & van Berckel , B N M 2012 , ' Blood-brain barrier P-glycoprotein function in healthy subjects and Alzheimer's disease patients: effect of polymorphisms in the ABCB1 gene ' , EJNMMI Research , vol. 2 , no. 1 , 57 , pp. 57 . https://doi.org/10.1186/2191-219X-2-57Test

وصف الملف: application/pdf

العلاقة: https://research.vumc.nl/en/publications/6c5f0506-2ed3-40a0-9b3f-45485b2e7e8bTest

الإتاحة: https://doi.org/10.1186/2191-219X-2-57Test
https://research.vumc.nl/en/publications/6c5f0506-2ed3-40a0-9b3f-45485b2e7e8bTest
https://research.vumc.nl/ws/files/271394/300419.pdfTest

المؤلفون: Assema, D.M.E. (Daniëlle) van, Lubberink, M. (Mark), Rizzu, P. (Patrizia), Swieten, J.C. (John) van, Schuit, R.C. (Robert), Eriksson, J. (Joel), Scheltens, P. (Philip), Koepp, M. (Matthias), Lammertsma, A.A. (Adriaan), Berckel, B.N.M. (Bart ) van

المصدر: EJNMMI Research vol. 2 no. 1, pp. 1-6

مصطلحات موضوعية: ABCB1, (R)-[11C]verapamil, Blood-brain barrier, MDR1, P-glycoprotein, PET, Polymorphisms

وصف الملف: application/pdf

العلاقة: info:eu-repo/grantAgreement/EC/FP7/201380; http://repub.eur.nl/pub/39741Test; urn:hdl:1765/39741

الإتاحة: https://doi.org/10.1186/2191-219X-2-57Test
http://repub.eur.nl/pub/39741Test

المؤلفون: van der Lee, Sven J, Conway, Olivia J, Zettergren, Anna, Christensen, Kaare, Ertekin-Taner, Nilüfer, Scholz, Sonja W, Ramirez, Alfredo, Ruiz, Agustín, Slagboom, Eline, van der Flier, Wiesje M, Holstege, Henne, Mead, S., Synofzik, M., Andlauer, Till F M, van Swieten, J. C., Leber, I., Ferrari, R., Hernandez, D. G., Nalls, M. A., Rohrer, J. D., Ramasamy, A., Kwok, J. B. J., Dobson-Stone, C., Schofield, P. R., Diez-Fairen, Monica, Halliday, G. M., Hodges, J. R., Piguet, O., Bartley, L., Thompson, E., Borroni, B., Padovani, A., Cruchaga, C., Cairns, N. J., Benussi, L., Simon-Sanchez, Javier, Binetti, G., Ghidoni, R., Forloni, G., Albani, D., Galimberti, D., Fenoglio, C., Serpente, M., Scarpini, E., Blesa, R., Landqvist Waldö, M., Lleó, Alberto, Nilsson, K., Nilsson, C., Mackenzie, I. R. A., Hsiung, G-Y R, Mann, D. M. A., Grafman, J., Morris, C. M., Attems, J., Griffiths, T. D., McKeith, I. G., Zetterberg, Henrik, Thomas, A. J., Pietrini, P., Huey, E. D., Wassermann, E. M., Baborie, A., Jaros, E., Tierney, M. C., Razquin, C., Ortega-Cubero, S., Alonso, E., Nygaard, Marianne, Perneczky, R., Diehl-Schmid, J., Alexopoulos, P., Kurz, A., Rainero, I., Rubino, E., Pinessi, L., Rogaeva, E., St George-Hyslop, P., Rossi, G., Blauwendraat, Cornelis, Tagliavini, F., Giaccone, G., Rowe, J. B., Schlachetzki, J. C. M., Uphill, J., Collinge, J., Danek, A., Van Deerlin, V. M., Grossman, M., Trojanowski, J. Q., Savage, Jeanne E, van der Zee, J., Van Broeckhoven, C., Cappa, S. F., Hannequin, D., Golfier, V., Vercelletto, M., Brice, A., Nacmias, B., Sorbi, S., Bagnoli, S., Mengel-From, Jonas, Piaceri, I., Nielsen, J. E., Hjermind, L. E., Riemenschneider, M., Mayhaus, M., Ibach, B., Gasparoni, G., Pichler, S., Gu, W., Rossor, M. N., Jansen, Iris, Moreno-Grau, Sonia, Fox, N. C., Warren, J. D., Spillantini, M. G., Morris, H. R., Rizzu, P., Snowden, J. S., Rollinson, S., Richardson, A., Gerhard, A., Bruni, A. C., Wagner, Michael, Maletta, R., Frangipane, F., Cupidi, C., Bernardi, L., Anfossi, M., Gallo, M., Conidi, M. E., Smirne, N., Baker, M., Josephs, K. A., Fortea, Juan, Parisi, J. E., Seeley, W. W., Miller, B. L., Karydas, A. M., Rosen, H., Dopper, E. G. P., Seelaar, H., Logroscino, G., Capozzo, R., Novelli, V., Keogh, Michael J, Puca, A. A., Franceschi, M., Postiglione, A., Milan, G., Sorrentino, P., Kristiansen, M., Chiang, H-H, Graff, C., Pasquier, F., Rollin, A., Blennow, Kaj, Deramecourt, V., Lebouvier, T., Kapogiannis, D., Ferrucci, L., Pickering-Brown, S., Singleton, A. B., Hardy, J., Momeni, P., Coppola, G., Skoog, Ingmar, Varpetian, A., Foroud, T. M., Levey, A. I., Kukull, W. A., Mendez, M. F., Ringman, J., Chui, H., Cotman, C., DeCarli, C., Friese, Manuel A, Geschwind, D. H., Pletnikova, Olga, Zulaica, Miren, Lage, Carmen, Carrasquillo, Minerva M, de Rojas, Itziar, Riedel-Heller, Steffi, Illán-Gala, Ignacio, Wei, Wei, Jeune, Bernard, Orellana, Adelina, Then Bergh, Florian, Wang, Xue, Hulsman, Marc, Beker, Nina, Kleineidam, Luca, Tesi, Niccolo, Morris, Christopher M, Indakoetxea, Begoña, Collij, Lyduine E, Scherer, Martin, Morenas-Rodríguez, Estrella, Ironside, James W, van Berckel, Bart N M, Alcolea, Daniel, Wiendl, Heinz, van den Akker, Erik, Strickland, Samantha L, Pastor, Pau, Rodríguez Rodríguez, Eloy, DESGESCO, EADB, IFGC, IPDGC, RiMod-FTD, Bank, Netherlands Brain, Boeve, Bradley F, Hernández, Isabel, Petersen, Ronald C, Ferman, Tanis J, van Gerpen, Jay A, Reinders, Marcel J T, Uitti, Ryan J, Tárraga, Lluís, Maier, Wolfgang, Dols-Icardo, Oriol, Kawalia, Amit, Dalmasso, Maria Carolina, van Eijk, Kristel R, Boada, Mercè, Zettl, Uwe K, van Schoor, Natasja M, Beekman, Marian, Allen, Mariet, Masliah, Eliezer, de Munain, Adolfo López, Pantelyat, Alexander, Wszolek, Zbigniew K, Ross, Owen A, Stringa, Najada, Dickson, Dennis W, Graff-Radford, Neill R, Knopman, David, Rademakers, Rosa, Lemstra, Afina W, Pijnenburg, Yolande A L, Scheltens, Philip, Gasser, Thomas, Chinnery, Patrick F, Hemmer, Bernhard, Chen, Jason A, Huisman, Martijn A, Troncoso, Juan, Moreno, Fermin, Nohr, Ellen A, Sørensen, Thorkild I A, Heutink, Peter, Sánchez-Juan, Pascual, Posthuma, Danielle, GIFT, Clarimón, Jordi

المصدر: van der Lee, S J, Conway, O J, Jansen, I, Carrasquillo, M M, Kleineidam, L, van den Akker, E, Hernández, I, van Eijk, K R, Stringa, N, Chen, J A, Zettergren, A, Andlauer, T F M, Diez-Fairen, M, Simon-Sanchez, J, Lleó, A, Zetterberg, H, Nygaard, M, Blauwendraat, C, Savage, J E, Mengel-From, J, Moreno-Grau, S, Wagner, M, Fortea, J, Keogh, M J, Blennow, K, Skoog, I, Friese, M A, Pletnikova, O, Zulaica, M, Lage, C, de Rojas, I, Riedel-Heller, S, Illán-Gala, I, Wei, W, Jeune, B, Orellana, A, Then Bergh, F, Wang, X, Hulsman, M, Beker, N, Tesi, N, Morris, C M, Indakoetxea, B, Collij, L E, Scherer, M, Morenas-Rodríguez, E, Ironside, J W, van Berckel, B N M, Nohr, E A, Sørensen, T I A, Christensen, K & DESGESCO (Dementia Genetics Spanish Consortium), EADB (Alzheimer Disease European DNA biobank) 2019, ' A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity ', Acta Neuropathologica, vol. 138, no. 2, pp. 237-250 . https://doi.org/10.1007/s00401-019-02026-8Test
van der Lee, S J, Conway, O J, Jansen, I, Carrasquillo, M M, Kleineidam, L, van den Akker, E, Hernández, I, van Eijk, K R, Stringa, N, Chen, J A, Zettergren, A, Andlauer, T F M, Diez-Fairen, M, Simon-Sanchez, J, Lleó, A, Zetterberg, H, Nygaard, M, Blauwendraat, C, Savage, J E, Mengel-From, J, Moreno-Grau, S, Wagner, M, Fortea, J, Keogh, M J, Blennow, K, Skoog, I, Friese, M A, Pletnikova, O, Zulaica, M, Lage, C, de Rojas, I, Riedel-Heller, S, Illán-Gala, I, Wei, W, Jeune, B, Orellana, A, Then Bergh, F, Wang, X, Hulsman, M, Beker, N, Tesi, N, Morris, C M, Indakoetxea, B, Collij, L E, Scherer, M, Morenas-Rodríguez, E, Ironside, J W, van Berckel, B N M, Alcolea, D & Wiendl, H 2019, ' Correction to : A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity ', Acta Neuropathologica . https://doi.org/10.1007/s00401-019-02107-8Test
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
EADB (Alzheimer Disease European DNA biobank), IFGC (International FTD-Genomics Consortium), IPDGC (The International Parkinson Disease Genomics Consortium), RiMod-FTD (Risk and Modifying factors in Fronto-Temporal Dementia), Netherlands Brain Bank (NBB), The GIFT (Genetic Investigation in Frontotemporal Dementia and Alzheimer’s Disease) Study Group & DESGESCO (Dementia Genetics Spanish Consortium) 2020, ' Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity ', Acta Neuropathologica, vol. 139, no. 5, pp. 959-962 . https://doi.org/10.1007/s00401-019-02107-8Test
Acta Neuropathologica
Acta neuropathologica 139(5), 959-962 (2020). doi:10.1007/s00401-019-02107-8

مصطلحات موضوعية: 0301 basic medicine, Dementia with Lewy bodies, Disease, Bioinformatics, Neurodegenerative disease, 0302 clinical medicine, Missense mutation, media_common, 2. Zero hunger, Longevity, Brain, Parkinson Disease, Phospholipase C Gamma 2, Biobank, 3. Good health, ddc, Frontotemporal Dementia, Microglia, Alzheimer's disease, Alzheimer’s disease, Amyotrophic lateral sclerosis, Frontotemporal dementia, Multiple sclerosis, PLCG2, Parkinson’s disease, Progressive supranuclear palsy, Lewy Body Disease, Risk, Multiple Sclerosis, media_common.quotation_subject, education, Neuroimaging, Genomics, Pathology and Forensic Medicine, 03 medical and health sciences, Cellular and Molecular Neuroscience, SDG 3 - Good Health and Well-being, Alzheimer Disease, medicine, Humans, Genetic Predisposition to Disease, ddc:610, Alleles, Phospholipase C gamma, business.industry, Amyotrophic Lateral Sclerosis, Correction, medicine.disease, 030104 developmental biology, Mutation, Dementia, Neurology (clinical), business, 030217 neurology & neurosurgery, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08e232742b5d2878a6e1cd88e83d667aTest
https://mediatum.ub.tum.de/1547001Test

المؤلفون: Vermeulen, R. J., Peeters-Scholte, C., Van Vugt, J. J.M.G., Barkhof, F., Rizzu, P., Van Der Schoor, S. R.D., Van Der Knaap, M. S.

المصدر: Vermeulen , R J , Peeters-Scholte , C , Van Vugt , J J M G , Barkhof , F , Rizzu , P , Van Der Schoor , S R D & Van Der Knaap , M S 2011 , ' Erratum : Fetal origin of brain damage in 2 infants with a COL4A1 mutation: Fetal and neonatal MRI (Neuropediatrics (2011) 42:1 (1-3) DOI:10.1055/s-0031-1275343) ' , Neuropediatrics , vol. 42 , no. 2 , pp. e1 . https://doi.org/10.1055/s-0031-1284388Test

العلاقة: https://research.vumc.nl/en/publications/105453f7-5277-4712-896a-9629e9f2d89cTest

الإتاحة: https://doi.org/10.1055/s-0031-1284388Test
https://doi.org/10.1055/s-0031-1275343Test
https://research.vumc.nl/en/publications/105453f7-5277-4712-896a-9629e9f2d89cTest
http://www.scopus.com/inward/record.url?scp=79960689891&partnerID=8YFLogxKTest

المؤلفون: Bettencourt, C., Santos, C., Coutinho, P., Rizzu, P., Vasconcelos, J., Kay, T., Cymbron, T., Raposo, M., Heutink, P., Lima, M.

المصدر: Bettencourt , C , Santos , C , Coutinho , P , Rizzu , P , Vasconcelos , J , Kay , T , Cymbron , T , Raposo , M , Heutink , P & Lima , M 2011 , ' Parkinsonian phenotype in Machado-Joseph disease (MJD/SCA3): a two-case report ' , BMC Neurology , vol. 11 , 131 . https://doi.org/10.1186/1471-2377-11-131Test

وصف الملف: application/pdf

العلاقة: https://research.vumc.nl/en/publications/8bfa038f-aa95-49f4-8910-cd4572b83508Test

الإتاحة: https://doi.org/10.1186/1471-2377-11-131Test
https://research.vumc.nl/en/publications/8bfa038f-aa95-49f4-8910-cd4572b83508Test
https://research.vumc.nl/ws/files/871708/282638.pdfTest

المؤلفون: Plagnol, V., Nalls, M.A., Bras, J.M., Hernandez, D.G., Sharma, M., Sheerin, U.M., Saad, M., Simon-Sanchez, J., Schulte, C., Lesage, S., Sveinbjornsdottir, S., Amouyel, P., Arepalli, S., Band, G., Barker, R.A., Bellinguez, C., Ben-Shlomo, Y., Berendse, H.W., Berg, D., Bhatia, K., de Bie, R.M.A., Biffi, A., Bloem, B., Bochdanovits, Z., Bonin, M., Brockmann, K., Brooks, J., Burn, D.J., Charlesworth, G., Chen, H.L., Chinnery, P.F., Chong, S., Clarke, C.E., Cookson, M.R., Cooper, J.M., Corvol, J.C., Counsell, C., Damier, P., Dartigues, J.F., Deloukas, P., Deuschl, G., Dexter, D.T., van Dijk, K.D., Dillman, A., Durif, F., Durr, A., Edkins, S., Evans, J.R., Foltynie, T., Freeman, C., Gao, J.J., Gardner, M., Gibbs, J.R., Goate, A., Gray, E., Guerreiro, R., Gustafsson, O., Harris, C, Hellenthal, G., van Hilten, J.J., Hofman, A., Hollenbeck, A., Holton, J., Hu, M., Huang, X.M., Huber, H., Hudson, G., Hunt, S.E., Huttenlocher, J., Illig, T., Jonsson, P.V., Langford, C., Lees, A., Lichtner, P., Limousin, P., Lopez, G., Lorenz, D., McNeill, A., Moorby, C., Moore, M., Morris, H., Morrison, K.E., Mudanohwo, E., O'Sullivan, S.S., Pearson, J., Pearson, R., Perlmutter, J.S., Petursson, H., Pirinen, M., Pollak, P., Post, B., Potter, S., Ravina, B., Revesz, T., Riess, O., Rivadeneira, F., Rizzu, P., Ryten, M., Sawcer, S., Heutink, P., Wood, N.W.

المصدر: Plagnol , V , Nalls , M A , Bras , J M , Hernandez , D G , Sharma , M , Sheerin , U M , Saad , M , Simon-Sanchez , J , Schulte , C , Lesage , S , Sveinbjornsdottir , S , Amouyel , P , Arepalli , S , Band , G , Barker , R A , Bellinguez , C , Ben-Shlomo , Y , Berendse , H W , Berg , D , Bhatia , K , de Bie , R M A , Biffi , A , Bloem , ....

وصف الملف: application/pdf

العلاقة: https://research.vumc.nl/en/publications/8e889490-45fd-4e6b-83e0-98824c3779a0Test

الإتاحة: https://doi.org/10.1371/journal.pgen.1002142Test
https://research.vumc.nl/en/publications/8e889490-45fd-4e6b-83e0-98824c3779a0Test
https://research.vumc.nl/ws/files/815595/281536.pdfTest

المؤلفون: Plagnol, V, Nalls, MA, Bras, JM, Hernandez, DG, Sharma, M, Sheerin, UM, Saad, M, Simon-Sanchez, J, Schulte, C, Lesage, S, Sveinbjornsdottir, S, Amouyel, P, Arepalli, S, Band, G, Barker, RA, Bellinguez, C, Ben-Shlomo, Y, Berendse, HW, Berg, D, Bhatia, K, de Bie, RMA, Biffi, A, Bloem, B, Bochdanovits, Z, Bonin, M, Brockmann, K, Brooks, J, Burn, DJ, Charlesworth, G, Chen, HL, Chinnery, PF, Chong, S, Clarke, CE, Cookson, MR, Cooper, JM, Corvol, JC, Counsell, C, Damier, P, Dartigues, JF, Deloukas, P, Deuschl, G, Dexter, DT, van Dijk, KD, Dillman, A, Durif, F, Durr, A, Edkins, S, Evans, JR, Foltynie, T, Freeman, C, Gao, JJ, Gardner, M, Gibbs, JR, Goate, A, Gray, E, Guerreiro, R, Gustafsson, O, Harris, C, Hellenthal, G, van Hilten, JJ, Hofman, A, Hollenbeck, A, Holton, J, Hu, M, Huang, XM, Huber, H, Hudson, G, Hunt, SE, Huttenlocher, J, Illig, T, Jonsson, PV, Langford, C, Lees, A, Lichtner, P, Limousin, P, Lopez, G, Lorenz, D, McNeill, A, Moorby, C, Moore, M, Morris, H, Morrison, KE, Mudanohwo, E, O'Sullivan, SS, Pearson, J, Pearson, R, Perlmutter, JS, Petursson, H, Pirinen, M, Pollak, P, Post, B, Potter, S, Ravina, B, Revesz, T, Riess, O, Rivadeneira, F, Rizzu, P, Ryten, M, Sawcer, S, Schapira, A, Scheffer, H, Shaw, K, Shoulson, I, Sidransky, E, de Silva, R, Smith, C, Spencer, CCA, Stefansson, H, Steinberg, S, Stockton, JD, Strange, A, Su, Z, Talbot, K, Tanner, CM, Tashakkori-Ghanbaria, A, Tison, F, Trabzuni, D, Traynor, BJ, Uitterlinden, AG, Vandrovcova, J, Velseboer, D, Vidailhet, M, Vukcevic, D, Walker, R, van de Warrenburg, B, Weale, ME, Wickremaratchi, M, Williams, N, Williams-Gray, CH, Winder-Rhodes, S, Stefansson, K, Martinez, M, Donnelly, P, Singleton, AB, Hardy, J, Heutink, P, Brice, A, Gasser, T, Wood, NW, WTCCC2

المصدر: PLoS Genetics , 7 (6) , Article e1002142. (2011)

مصطلحات موضوعية: genome-wide association, fibroblast-growth-factor, alpha-synuclein, gene, mutations, risk, population, haplotypes, variants, sequence

وصف الملف: application/pdf

العلاقة: https://discovery.ucl.ac.uk/id/eprint/1321806/1/journal.pgen.1002142.pdfTest; https://discovery.ucl.ac.uk/id/eprint/1321806Test/

الإتاحة: https://discovery.ucl.ac.uk/id/eprint/1321806/1/journal.pgen.1002142.pdfTest
https://discovery.ucl.ac.uk/id/eprint/1321806Test/

المؤلفون: Bettencourt, Conceição, Pereira dos Santos, Cristina Maria, Coutinho, Paula, Rizzu, P., Vasconcelos, João, Kay, Teresa, Cymbron, Teresa, Raposo, Mafalda, Heutink, Peter, Lima, Manuela

وصف الملف: application/pdf

العلاقة: BMC Neurology; Vol. 11, N. 131 (October 2011), p. 1-5; https://ddd.uab.cat/record/125681Test; urn:22023810; urn:10.1186/1471-2377-11-131; urn:pmid:22023810; urn:recercauab:ARE-64130; urn:articleid:14712377v24n11p131; urn:scopus_id:80054808790; urn:wos_id:000297057300001; urn:altmetric_id:426888; urn:oai:egreta.uab.cat:publications/bc20a066-43ba-437f-9b7c-3853629423df; urn:pmc-uid:3217914; urn:pmcid:PMC3217914; urn:oai:pubmedcentral.nih.gov:3217914

الإتاحة: https://ddd.uab.cat/record/125681Test