المؤلفون: Fridlich, R, Delalande, F, Jaillard, C, Lu, J, Poidevin, L, Cronin, T, Perrocheau, L, Millet-Puel, G, Niepon, ML, Poch, O, Holmgren, A, Van Dorsselaer, A, Sahel, JA, Leveillard, T

المصدر: Molecular & cellular proteomics : MCP. 8(6):1206-1218

مصطلحات موضوعية: Medicin och hälsovetenskap

URL الوصول: http://kipublications.ki.se/Default.aspx?queryparsed=id:118912340

المؤلفون: Chalmel, F, Leveillard, T, Jaillard, C, Lardenois, A, Berdugo, N, Morel, E, Koehl, P, Lambrou, G, Holmgren, A, Sahel, JA, Poch, O

المصدر: BMC molecular biology. 8:74

مصطلحات موضوعية: Medicin och hälsovetenskap

URL الوصول: http://kipublications.ki.se/Default.aspx?queryparsed=id:116170078

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المؤلفون: Muqit, Mahi M.K., Hubschman, J. P., Picard, S., McCreery, D. B., van Meurs, J. C., Nouvel-Jaillard, C., Fovet, C-M., Hantraye, P., Sahel, J., Martel, J. N., Le Mer, Y.

المصدر: Artificial Vision 2019; 20191213-20191214; Aachen; DOC19artvis30 /20191210/

مصطلحات موضوعية: genetic structures, ddc: 610, sense organs, 610 Medical sciences, Medicine, eye diseases

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a6081ea47ebe9d52005e28d325e59cd
http://www.egms.de/en/meetings/artvis2019/19artvis30.shtml

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المؤلفون: Prévot, Paul-Henri, Dalouz, S., Blaize, K., Dubus, E., Porceddu, J., Nouvel-Jaillard, C., Goetz, G., Deterre, M., Buc, G., Sahel, J.A., Picaud, S.

المصدر: Artificial Vision 2015; 20151127-20151128; Aachen; DOC15artvis17 /20160307/

مصطلحات موضوعية: genetic structures, ddc: 610, sense organs, 610 Medical sciences, Medicine, eye diseases

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d256ce61475be0613133f6b4b76c3c9a
http://www.egms.de/en/meetings/artvis2015/15artvis17.shtml

المؤلفون: Lambert JC, Heath S, Even G, Campion D, Sleegers K, Hiltunen M, Combarros O, Zelenika D, Bullido MJ, Tavernier B, Letenneur L, Bettens K, Berr C, Pasquier F, Fiévet N, Barberger-Gateau P, Engelborghs S, De Deyn P, Mateo I, Franck A, Helisalmi S, Porcellini E, Hanon O, European Alzheimer's Disease Initiative Investigators, de Pancorbo MM, Lendon C, Dufouil C, Jaillard C, Leveillard T, Alvarez V, Bosco P, Mancuso M, Panza F, Nacmias B, Bossù P, Piccardi P, Annoni G, Seripa D, Galimberti D, Hannequin D, Licastro F, Soininen H, Ritchie K, Blanché H, Dartigues JF, Tzourio C, Gut I, Van Broeckhoven C, Alpérovitch A, Lathrop M, Amouyel P, FORTI, PAOLA

المساهمون: Lambert, J, Heath, S, Even, G, Campion, D, Sleegers, K, Hiltunen, M, Cambarros, O, Zelenika, D, Bullido, M, Tavernier, B, Letenneur, L, Bettens, K, Berr, C, Pasquier, F, Fiévet, N, Barbager Gateau, P, Engelborghs, S, De Deyn, P, Mateo, I, Franck, A, Helisalmi, S, Porcellini, E, Hanon, O, the European Alzheimer’s disease Initiative, I, de Pancorbo, M, Lendon, C, Dufouil, C, Jaillard, C, Leveillard, T, Alvarez, V, Bosco, P, Mancuso, M, Panza, F, Nacmias, B, Bossù, P, Piccardi, P, Annoni, G, Seripa, D, Galimberti, D, Hannequin, D, Licastro, F, Soininen, H, Ritchie, K, Blanché, H, Dartigues, J, Tzourio, C, Gut, I, Broeckhoven, C, Alpérovitch, A, Lathrop, M, Amouyel, P, Lambert JC, Heath S, Even G, Campion D, Sleegers K, Hiltunen M, Combarros O, Zelenika D, Bullido MJ, Tavernier B, Letenneur L, Bettens K, Berr C, Pasquier F, Fiévet N, Barberger-Gateau P, Engelborghs S, De Deyn P, Mateo I, Franck A, Helisalmi S, Porcellini E, Hanon O, European Alzheimer's Disease Initiative Investigator, de Pancorbo MM, Lendon C, Dufouil C, Jaillard C, Leveillard T, Alvarez V, Bosco P, Mancuso M, Panza F, Nacmias B, Bossù P, Piccardi P, Annoni G, Seripa D, Galimberti D, Hannequin D, Licastro F, Soininen H, Ritchie K, Blanché H, Dartigues JF, Tzourio C, Gut I, Van Broeckhoven C, Alpérovitch A, Lathrop M, Amouyel P, Electronics and Informatics, Clinical sciences, Neurology, Pathologic Biochemistry and Physiology

المصدر: Nature genetics

مصطلحات موضوعية: Apolipoprotein E, SORL1, Genome-wide association study, Disease, Polymorphism, Single Nucleotide, White People, ABCA7, PICALM, Alzheimer Disease, Genetics, Humans, Genetic Predisposition to Disease, European Continental Ancestry Group/genetics, Alzheimer's disease, genome-wide association, APOE, APOJ, Medicine(all), Alzheimer Disease/genetics, biology, Phosphatidylinositol binding, Clusterin, Haplotypes, Receptors, Complement 3b, biology.protein, Human medicine, Clusterin/genetics, Receptors, Complement 3b/genetics, Genome-Wide Association Study

وصف الملف: ELETTRONICO

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e16990d3e5991d9bc0ff2e91a3e3ebd
http://hdl.handle.net/10281/9031

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