المؤلفون: DeVries, Amber A, Dennis, Joe, Tyrer, Jonathan P, Peng, Pei-Chen, Coetzee, Simon G, Reyes, Alberto L, Plummer, Jasmine T, Davis, Brian D, Chen, Stephanie S, Dezem, Felipe Segato, Aben, Katja KH, Anton-Culver, Hoda, Antonenkova, Natalia N, Beckmann, Matthias W, Beeghly-Fadiel, Alicia, Berchuck, Andrew, Bogdanova, Natalia V, Bogdanova-Markov, Nadja, Brenton, James D, Butzow, Ralf, Campbell, Ian, Chang-Claude, Jenny, Chenevix-Trench, Georgia, Cook, Linda S, DeFazio, Anna, Doherty, Jennifer A, Dörk, Thilo, Eccles, Diana M, Eliassen, A Heather, Fasching, Peter A, Fortner, Renée T, Giles, Graham G, Goode, Ellen L, Goodman, Marc T, Gronwald, Jacek, Webb, P, DeFazio, A, Friedlander, M, Obermair, A, Grant, P, Nagle, C, Beesley, V, Chevenix-Trench, G, Bowtell, D, Blomfield, P, Brand, A, Davis, A, Leung, Y, Nicklin, J, Quinn, M, Livingstone, K, O'Neill, H, Williams, M, Black, A, Hadley, A, Glasgow, A, Garrett, A, Rao, A, Shannon, C, Steer, C, Allen, D, Neesham, D, Otton, G, Au-Yeung, G, Goss, G, Wain, G, Gard, G, Robertson, G, Lombard, J, Tan, J, McNeilage, J, Power, J, Coward, J, Miller, J, Carter, J, Lamont, J, Wong, KM, Reid, K, Perrin, L, Milishkin, L, Nascimento, M, Buck, M, Bunting, M, Harrison, M, Chetty, N, Hacker, N, McNally, O, Harnett, P, Beale, P, Awad, R, Mohan, R, Farrell, R, McIntosh, R, Rome, R, Sayer, R, Houghton, R, Hogg, R, Land, R, Baron-Hay, S, Paramasivum, S

المصدر: Journal of the National Cancer Institute. 114(11)

مصطلحات موضوعية: Biomedical and Clinical Sciences, Oncology and Carcinogenesis, Ovarian Cancer, Human Genome, Prevention, Genetic Testing, Genetics, Cancer, Clinical Research, Women's Health, Rare Diseases, 2.1 Biological and endogenous factors, Female, Humans, Carcinoma, Ovarian Epithelial, Genome-Wide Association Study, Alleles, DNA Copy Number Variations, Genetic Predisposition to Disease, Polymorphism, Single Nucleotide, Ovarian Neoplasms, OPAL Study Group, AOCS Group, Oncology & Carcinogenesis, Oncology and carcinogenesis

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/55j1b4gs
https://escholarship.org/content/qt55j1b4gs/qt55j1b4gs.pdf

المؤلفون: Stessman, HAF, Willemsen, MH, Fenckova, M, Penn, O, Hoischen, A, Xiong, B, Wang, TY, Hoekzema, K, Vives, L, Voge, I, Brunner, HG, van der Burgt, I, Ockeloen, CW, Schuurs-Hoeijmakers, JH, Wassink-Ruiter, JSK, Stumpel, C, Stevens, SJC, Vles, HS, Marcelis, CM, van Bokhoven, H, Cantagrel, V, Colleaux, L, Nicouleau, M, Lyonnet, S, Bernier, RA, Gerdts, J, Coe, BP, Romano, C, Alberti, A, Grillo, L, Scuderi, C, Nordenskjold, M, Kvarnung, M, Guo, H, Xia, K, Piton, A, Gerard, B, Genevieve, D, Delobel, B, Lehalle, D, Perrin, L, Prieur, F, Thevenon, J, Gecz, J, Shaw, M, Pfundt, R, Keren, B, Jacquette, A, Schenck, A, Eichler, EE, Kleefstra, Tz

المصدر: American journal of human genetics. 98(3):541-552

مصطلحات موضوعية: Medicin och hälsovetenskap

URL الوصول: http://kipublications.ki.se/Default.aspx?queryparsed=id:133190407

المؤلفون: Sarli, C, van der Laan, L, Reilly, J, Trajkova, S, Carli, D, Brusco, A, Levy, MA, Relator, R, Kerkhof, J, McConkey, H, Tedder, ML, Skinner, C, Alders, M, Henneman, P, Hennekam, RCM, Ciaccio, C, D'Arrigo, S, Vitobello, A, Faivre, L, Weber, S, Vincent‐Devulder, A, Perrin, L, Bourgois, A, Yamamoto, T, Kini, U

Relation: https://ora.ox.ac.uk/objects/uuid:378da813-396c-483e-a7c6-e92b24c7e0cc; https://doi.org/10.1002/ajmg.c.32089

الاتاحة: https://doi.org/10.1002/ajmg.c.32089
https://ora.ox.ac.uk/objects/uuid:378da813-396c-483e-a7c6-e92b24c7e0cc

المؤلفون: Seib, C, Harbeck, E, Anderson, D, Porter-Steele, J, Nehill, C, Sanmugarajah, J, Perrin, L, Shannon, C, Cabraal, N, Jennings, B, Otton, G, Adams, C, Mellon, A, Chambers, S

مصطلحات موضوعية: Oncology and carcinogenesis, Obstetrics and gynaecology, Biomedical and clinical sciences, Psychology

Relation: Psycho-Oncology; Seib, C; Harbeck, E; Anderson, D; Porter-Steele, J; Nehill, C; Sanmugarajah, J; Perrin, L; Shannon, C; Cabraal, N; Jennings, B; Otton, G; Adams, C; Mellon, A; Chambers, S, Establishing the sensitivity and specificity of the gynaecological cancer distress screen, Psycho-Oncology, 2024, 33 (3), pp. e6328-; https://hdl.handle.net/10072/430213

الاتاحة: https://hdl.handle.net/10072/430213
https://doi.org/10.1002/pon.6328

المؤلفون: Andersson, J, Kinloch, S, Sonnerborg, A, Nilsson, J, Fehniger, TE, Spetz, AL, Behbahani, H, Goh, LE, McDade, H, Gazzard, B, Stellbrink, H, Cooper, D, Perrin, L

المصدر: The Journal of infectious diseases. 185(9):1355-1358

مصطلحات موضوعية: Medicin och hälsovetenskap

URL الوصول: http://kipublications.ki.se/Default.aspx?queryparsed=id:1961561

المؤلفون: Van Vaerenbergh, K, Van Laethem, K, Albert, J, Boucher, CAB, Clotet, B, Floridia, M, Gerstoft, J, Hejdeman, B, Nielsen, C, Pannecouque, C, Perrin, L, Pirillo, MF, Ruiz, L, Schmit, JC, Schneider, F, Schoolmeester, A, Schuurman, R, Stellbrink, HJ, Stuyver, L, Van Lunzen, J, Van Remoortel, B, Van Wijngaerden, E, Vella, S, Witvrouw, M, Yerly, S, De Clercq, E, Desmyter, J, Vandamme, AM

المصدر: Antimicrobial agents and chemotherapy. 44(8):2109-2117

مصطلحات موضوعية: Medicin och hälsovetenskap

URL الوصول: http://kipublications.ki.se/Default.aspx?queryparsed=id:1933471

المؤلفون: Parenti, I., Leitão, E., Kuechler, A., Villard, L., Goizet, C., Courdier, C., Bayat, A., Rossi, A., Julia, S., Bruel, A. L., Tran Mau-Them, F., Nambot, S., Lehalle, D., Willems, M., Lespinasse, J., Ghoumid, Jamal, Caumes, Roselyne, Smol, Thomas, El Chehadeh, S., Schaefer, E., Abi-Warde, M. T., Keren, B., Afenjar, A., Tabet, A. C., Levy, J., Maruani, A., Aledo-Serrano, Á., Garming, W., Milleret-Pignot, C., Chassevent, A., Koopmans, M., Verbeek, N. E., Person, R., Belles, R., Bellus, G., Salbert, B. A., Kaiser, F. J., Mazzola, L., Convers, P., Perrin, L., Piton, A., Wiegand, G., Accogli, A., Brancati, F., Benfenati, F., Chatron, N., Lewis-Smith, D., Thomas, R. H., Zara, F., Striano, P., Lesca, G., Depienne, C.

المساهمون: Université de Lille, CHU Lille, Maladies Rares du Développement : Génétique, Régulation et Protéomique (RADEME) - ULR 7364, Maladies RAres du DEveloppement embryonnaire et du MEtabolisme : du Phénotype au Génotype et à la Fonction - ULR 7364 RADEME

مصطلحات موضوعية: SYN1, synapsins, reflex epilepsy, genotype-phenotype correlation, neurodevelopmental disorders, autism spectrum disorders

وصف الملف: application/rdf+xml; charset=utf-8; application/pdf

Relation: Frontiers in Cell and Developmental Biology; Front Cell Dev Biol; http://hdl.handle.net/20.500.12210/84132

الاتاحة: https://hdl.handle.net/20.500.12210/84132

المؤلفون: Goubeau, L., Guilbert, Z., Saadi, M., Picard, F., Perrin, L., Capdevila, L., Fontenay, M., Duchemin, J., Proulle, V., Brakta, C.

المصدر: Research and Practice in Thrombosis and Haemostasis ; volume 7, page 101257 ; ISSN 2475-0379

الاتاحة: http://dx.doi.org/10.1016/j.rpth.2023.101257
https://api.elsevier.com/content/article/PII:S247503792304534X?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S247503792304534X?httpAccept=text/plain

المؤلفون: Marcogliese P. C., Deal S. L., Andrews J., Harnish J. M., Bhavana V. H., Graves H. K., Jangam S., Luo X., Liu N., Bei D., Chao Y. -H., Hull B., Lee P. -T., Pan H., Bhadane P., Huang M. -C., Longley C. M., Chao H. -T., Chung H. -L., Haelterman N. A., Kanca O., Manivannan S. N., Rossetti L. Z., German R. J., Gerard A., Schwaibold E. M. C., Fehr S., Guerrini R., Vetro A., England E., Murali C. N., Barakat T. S., van Dooren M. F., Wilke M., van Slegtenhorst M., Lesca G., Sabatier I., Chatron N., Brownstein C. A., Madden J. A., Agrawal P. B., Keren B., Courtin T., Perrin L., Brugger M., Roser T., Leiz S., Mau-Them F. T., Delanne J., Sukarova-Angelovska E., Trajkova S., Rosenhahn E., Strehlow V., Platzer K., Keller R., Pavinato L., Brusco A., Rosenfeld J. A., Marom R., Wangler M. F., Yamamoto S.

المساهمون: Marcogliese P.C., Deal S.L., Andrews J., Harnish J.M., Bhavana V.H., Graves H.K., Jangam S., Luo X., Liu N., Bei D., Chao Y.-H., Hull B., Lee P.-T., Pan H., Bhadane P., Huang M.-C., Longley C.M., Chao H.-T., Chung H.-L., Haelterman N.A., Kanca O., Manivannan S.N., Rossetti L.Z., German R.J., Gerard A., Schwaibold E.M.C., Fehr S., Guerrini R., Vetro A., England E., Murali C.N., Barakat T.S., van Dooren M.F., Wilke M., van Slegtenhorst M., Lesca G., Sabatier I., Chatron N., Brownstein C.A., Madden J.A., Agrawal P.B., Keren B., Courtin T., Perrin L., Brugger M., Roser T., Leiz S., Mau-Them F.T., Delanne J., Sukarova-Angelovska E., Trajkova S., Rosenhahn E., Strehlow V., Platzer K., Keller R., Pavinato L., Brusco A., Rosenfeld J.A., Marom R., Wangler M.F., Yamamoto S.

مصطلحات موضوعية: autism spectrum disorder, Drosophila melanogaster, functional genomic, GLRA2, GluClalpha, humanization, missense variant, rare genetic disease, T2A-GAL4, TG4, undiagnosed disease, Animal, Genetic Predisposition to Disease, Human, Autistic Disorder, Drosophila, Neurodevelopmental Disorder, Receptors, Glycine

Relation: info:eu-repo/semantics/altIdentifier/pmid/35294868; info:eu-repo/semantics/altIdentifier/wos/WOS:000772210700003; volume:38; issue:11; firstpage:110517; lastpage:110532; numberofpages:16; journal:CELL REPORTS; http://hdl.handle.net/2318/1854165; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85126320885; https://www.cell.com/cell-reports/fulltext/S2211-1247(22)00253-4?_returnURL=https://linkinghub.elsevier.com/retrieve/pii/S2211124722002534?showall=true

الاتاحة: http://hdl.handle.net/2318/1854165
https://doi.org/10.1016/j.celrep.2022.110517
https://www.cell.com/cell-reports/fulltext/S2211-1247(22)00253-4?_returnURL=https://linkinghub.elsevier.com/retrieve/pii/S2211124722002534?showall=true

المؤلفون: Perrin, L. D.

مصطلحات موضوعية: 616.9

URL الوصول: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.736446

المؤلفون: Parenti I, Leitao E, Kuechler A, Villard L, Goizet C, Courdier C, Bayat A, Rossi A, Julia S, Bruel A-L, Tran Mau-Them F, Nambot S, Lehalle D, Willems M, Lespinasse J, Ghoumid J, Caumes R, Smol T, El Chehadeh S, Schaefer E, Abi-Warde M-T, Keren B, Afenjar A, Tabet A-C, Levy J, Maruani A, Aledo-Serrano A, Garming W, Milleret-Pignot C, Chassevent A, Koopmans M, Verbeek NE, Person R, Belles R, Bellus G, Salbert BA, Kaiser FJ, Mazzola L, Convers P, Perrin L, Piton A, Wiegand G, Accogli A, Brancati F, Benfenati F, Chatron N, Lewis-Smith D, Thomas RH, Zara F, Striano P, Lesca G, Depienne C

المصدر: Frontiers in Cell and Developmental Biology, 8 December 2022

وصف الملف: application/pdf

Relation: https://eprints.ncl.ac.uk/288746; https://eprints.ncl.ac.uk/fulltext.aspx?url=288746/A0DF378A-F879-4CC0-8E86-7F4425B9821A.pdf&pub_id=288746

الاتاحة: https://eprints.ncl.ac.uk/288746

المؤلفون: Bonazzi, VF, Kondrashova, O, Smith, D, Nones, K, Sengal, AT, Ju, R, Packer, LM, Koufariotis, LT, Kazakoff, SH, Davidson, AL, Ramarao-Milne, P, Lakis, V, Newell, F, Rogers, R, Davies, C, Nicklin, J, Garrett, A, Chetty, N, Perrin, L, Pearson, JV, Patch, A-M, Waddell, N, Pollock, PM

Relation: pii: 10.1186/s13073-021-00990-z; Bonazzi, V. F., Kondrashova, O., Smith, D., Nones, K., Sengal, A. T., Ju, R., Packer, L. M., Koufariotis, L. T., Kazakoff, S. H., Davidson, A. L., Ramarao-Milne, P., Lakis, V., Newell, F., Rogers, R., Davies, C., Nicklin, J., Garrett, A., Chetty, N., Perrin, L. ,. Pollock, P. M. (2022). Patient-derived xenograft models capture genomic heterogeneity in endometrial cancer. Genome Med, 14 (1), pp.3-. https://doi.org/10.1186/s13073-021-00990-z.; http://hdl.handle.net/11343/301692

الاتاحة: http://hdl.handle.net/11343/301692

المؤلفون: Mouillé, M., Rio, M., Breton, S., Piketty, M. L., Afenjar, A., Amiel, J., Capri, Y., Goldenberg, A., Francannet, C., Michot, C., Mignot, C., Perrin, L., Quelin, C., Van Gils, J., Barcia, G., Pingault, V., Maruani, G., Koumakis, E., Cormier-Daire, V.

المصدر: Orphanet Journal of Rare Diseases ; volume 17, issue 1 ; ISSN 1750-1172

الاتاحة: http://dx.doi.org/10.1186/s13023-022-02229-5
https://link.springer.com/content/pdf/10.1186/s13023-022-02229-5.pdf
https://link.springer.com/article/10.1186/s13023-022-02229-5/fulltext.html

المؤلفون: Monnier, R, Rey, L, Baschet, L, Kaboré, N, Perrin, L, Leproust, S

المصدر: Value in Health ; volume 25, issue 12, page S300 ; ISSN 1098-3015

الاتاحة: http://dx.doi.org/10.1016/j.jval.2022.09.1482
https://api.elsevier.com/content/article/PII:S1098301522036877?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S1098301522036877?httpAccept=text/plain

المؤلفون: Thompson, C, Van Driel, W, Perrin, L, Barry, S, Zivanovic, O, Moran, B, Brennan, D

المصدر: Ovarian cancer ; page A293.3-A294

الاتاحة: http://dx.doi.org/10.1136/ijgc-2021-esgo.510
https://syndication.highwire.org/content/doi/10.1136/ijgc-2021-ESGO.510

المؤلفون: Gerasimenko, A., Mignot, C., Naggara, O., Coulet, F., Ekram, S., Heide, S., Sorato, C., Mazowiecki, M., Perrin, L., Colas, C., Cusin, V., Caux, F., Dardenne, A., El Chehadeh, S., Verloes, A., Maurey, H., Afenjar, A., Petit, Florence, Barete, S., Boespflug-Tanguy, O., Bourrat, E., Capri, Y., Ciorna, V., Deb, W., Doummar, D., Perrier, A., Guédon, A., Houdart, E., Isidor, B., Jacquemont, M. L., Buffet, C., Mercier, S., Passemard, S., Riquet, A., Ruaud, L., Schaefer, E., Heron, D., Bisdorff, A., Benusiglio, P. R.

المساهمون: Université de Lille, CHU Lille, Institut du Cerveau et de la Moëlle Epinière = Brain and Spine Institute ICM, Institut du Cerveau = Paris Brain Institute ICM, Maladies Rares du Développement : Génétique, Régulation et Protéomique (RADEME) - ULR 7364, CHU Trousseau APHP

مصطلحات موضوعية: cancer genetics, cerebrovascular disorders, Cowden syndrome, DAVF, dural fistula, genetic predisposition to disease, MRI, PHTS, PTEN

وصف الملف: application/octet-stream

Relation: Clinical Genetics; Clin Genet; http://hdl.handle.net/20.500.12210/114220

الاتاحة: https://hdl.handle.net/20.500.12210/114220

المؤلفون: Husson, T., Lecoquierre, F., Nicolas, G., Richard, A. C., Afenjar, A., Audebert-Bellanger, S., Badens, C., Bilan, F., Bizaoui, V., Boland, A., Bonnet-Dupeyron, M. N., Brischoux-Boucher, E., Bonnet, C., Bournez, M., Boute, O., Brunelle, P., Caumes, R., Charles, P., Chassaing, N., Chatron, N., Cogné, B., Colin, E., Cormier-Daire, V., Dard, R., Dauriat, B., Delanne, J., Deleuze, J. F., Demurger, F., Denommé-Pichon, A. S., Depienne, C., Dieux, A., Dubourg, C., Edery, P., El Chehadeh, S., Faivre, L., Fergelot, P., Fradin, M., Garde, A., Geneviève, D., Gilbert-Dussardier, B., Goizet, C., Goldenberg, A., Gouy, E., Guerrot, A. M., Guimier, A., Harzalla, I., Héron, D., Isidor, B., Lacombe, D., Le Guillou Horn, X., Keren, B., Kuechler, A., Lacaze, E., Lavillaureix, A., Lehalle, D., Lesca, G., Lespinasse, J., Levy, J., Lyonnet, S., Morel, G., Jean-Marçais, N., Marlin, S., Marsili, L., Mignot, C., Nambot, S., Nizon, M., Olaso, R., Pasquier, L., Perrin, L., Petit, Florence, Pingault, V., Piton, A., Prieur, F., Putoux, A., Planes, M., Odent, S., Quélin, C., Quemener-Redon, S., Rama, M., Rio, M., Rossi, M., Schaefer, E., Rondeau, S., Saugier-Veber, P., Smol, T., Sigaudy, S., Touraine, R., Mau-Them, F. T., Trimouille, A., Van Gils, J., Vanlerberghe, C., Vantalon, V., Vera, G., Vincent, M., Ziegler, A., Guillin, O., Campion, D., Charbonnier, C.

المساهمون: Université de Lille, CHU Lille, Génomique et Médecine Personnalisée du Cancer et des Maladies Neuropsychiatriques GPMCND, Cancer and Brain Genomics CBG, Maladies Rares du Développement : Génétique, Régulation et Protéomique (RADEME) - ULR 7364, CHU Rouen

وصف الملف: application/octet-stream

Relation: European Journal of Human Genetics; Eur J Hum Genet; http://hdl.handle.net/20.500.12210/93287

الاتاحة: https://hdl.handle.net/20.500.12210/93287

المؤلفون: Bertacchi M., Romano A. L., Loubat A., Tran Mau-Them F., Willems M., Faivre L., Khau van Kien P., Perrin L., Devillard F., Sorlin A., Kuentz P., Philippe C., Garde A., Neri F., Di Giaimo R., Oliviero S., Cappello S., D'Incerti L., Frassoni C., Studer M.

المساهمون: Bertacchi M., Romano A.L., Loubat A., Tran Mau-Them F., Willems M., Faivre L., Khau van Kien P., Perrin L., Devillard F., Sorlin A., Kuentz P., Philippe C., Garde A., Neri F., Di Giaimo R., Oliviero S., Cappello S., D'Incerti L., Frassoni C., Studer M.

مصطلحات موضوعية: BBSOAS, cell cycle dynamic, cortical folding, neurodevelopmental disease, NR2F1/COUP-TFI

Relation: info:eu-repo/semantics/altIdentifier/pmid/32484994; info:eu-repo/semantics/altIdentifier/wos/WOS:000536997000001; volume:39; issue:13; firstpage:104163; lastpage:104188; numberofpages:25; journal:EMBO JOURNAL; http://hdl.handle.net/2318/1747523; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85085710289; https://pubmed.ncbi.nlm.nih.gov/32484994/

الاتاحة: http://hdl.handle.net/2318/1747523
https://doi.org/10.15252/embj.2019104163
https://pubmed.ncbi.nlm.nih.gov/32484994/

المؤلفون: Axfors, C, Schmitt, AM, Janiaud, P, Van't Hooft, J, Abd-Elsalam, S, Abdo, EF, Abella, BS, Akram, J, Amaravadi, RK, Angus, DC, Arabi, YM, Azhar, S, Baden, LR, Baker, AW, Belkhir, L, Benfield, T, Berrevoets, MAH, Chen, C-P, Chen, T-C, Cheng, S-H, Cheng, C-Y, Chung, W-S, Cohen, YZ, Cowan, LN, Dalgard, O, De Almeida e Val, FF, De Lacerda, MVG, De Melo, GC, Derde, L, Dubee, V, Elfakir, A, Gordon, AC, Hernandez-Cardenas, CM, Hills, T, Hoepelman, AIM, Huang, Y-W, Igau, B, Jin, R, Jurado-Camacho, F, Khan, KS, Kremsner, PG, Kreuels, B, Kuo, C-Y, Thuy, L, Lin, Y-C, Lin, W-P, Lin, T-H, Lyngbakken, MN, McArthur, C, McVerry, BJ, Meza-Meneses, P, Monteiro, WM, Morpeth, SC, Mourad, A, Mulligan, MJ, Murthy, S, Naggie, S, Narayanasamy, S, Nichol, A, Novack, LA, O'Brien, SM, Okeke, NL, Perez, L, Perez-Padilla, R, Perrin, L, Remigio-Luna, A, Rivera-Martinez, NE, Rockhold, FW, Rodriguez-Llamazares, S, Rolfe, R, Rosa, R, Rosjo, H, Sampaio, VS, Seto, TB, Shehzad, M, Soliman, S, Stout, JE, Thirion-Romero, I, Troxel, AB, Tseng, T-Y, Turner, NA, Ulrich, RJ, Walsh, SR, Webb, SA, Weehuizen, JM, Velinova, M, Wong, H-L, Wrenn, R, Zampieri, FG, Zhong, W, Moher, D, Goodman, SN, Ioannidis, JPA, Hemkens, LG

المساهمون: NIHR, National Institute for Health Research

المصدر: 13 ; 1

مصطلحات موضوعية: Science & Technology, Multidisciplinary Sciences, Science & Technology - Other Topics, Adult, COVID-19, Child, Chloroquine, Combined Modality Therapy, Comorbidity, Female, Humans, Hydroxychloroquine, International Cooperation, Odds Ratio, Patient Participation, Pregnancy, Pregnancy Complications, Infectious, Randomized Controlled Trials as Topic, SARS-CoV-2

Relation: Nature Communications; http://hdl.handle.net/10044/1/90447; COVID-19-REMAP-CAP

الاتاحة: http://hdl.handle.net/10044/1/90447
https://doi.org/10.1038/s41467-021-22446-z

المؤلفون: Axfors, C, Schmitt, AM, Janiaud, P, Van't Hooft, J, Abd-Elsalam, S, Abdo, EF, Abella, BS, Akram, J, Amaravadi, RK, Angus, DC, Arabi, YM, Azhar, S, Baden, LR, Baker, AW, Belkhir, L, Benfield, T, Berrevoets, MAH, Chen, C-P, Chen, T-C, Cheng, S-H, Cheng, C-Y, Chung, W-S, Cohen, YZ, Cowan, LN, Dalgard, O, De Almeida E Val, FF, De Lacerda, MVG, De Melo, GC, Derde, L, Dubee, V, Elfakir, A, Gordon, AC, Hernandez-Cardenas, CM, Hills, T, Hoepelman, AIM, Huang, Y-W, Igau, B, Jin, R, Jurado-Camacho, F, Khan, KS, Kremsner, PG, Kreuels, B, Kuo, C-Y, Le, T, Lin, Y-C, Lin, W-P, Lin, T-H, Lyngbakken, MN, McArthur, C, McVerry, BJ, Meza-Meneses, P, Monteiro, WM, Morpeth, SC, Mourad, A, Mulligan, MJ, Murthy, S, Naggie, S, Narayanasamy, S, Nichol, A, Novack, LA, O'Brien, SM, Okeke, NL, Perez, L, Perez-Padilla, R, Perrin, L, Remigio-Luna, A, Rivera-Martinez, NE, Rockhold, FW, Rodriguez-Llamazares, S, Rolfe, R, Rosa, R, Røsjø, H, Sampaio, VS, Seto, TB, Shahzad, M, Soliman, S, Stout, JE, Thirion-Romero, I, Troxel, AB, Tseng, T-Y, Turner, NA, Ulrich, RJ, Walsh, SR, Webb, SA, Weehuizen, JM, Velinova, M, Wong, H-L, Wrenn, R, Zampieri, FG, Zhong, W, Moher, D, Goodman, SN, Ioannidis, JPA, Hemkens, LG

المصدر: 2 ; 1

جغرافية الموضوع: England

Relation: Nature Communications; http://hdl.handle.net/10044/1/89425

الاتاحة: http://hdl.handle.net/10044/1/89425
https://doi.org/10.1038/s41467-021-23559-1