المؤلفون: Pitcher, Alex, Spata, Enti, Emberson, Jonathan, Davies, Kelly, Halls, Heather, Holland, Lisa, Wilson, Kate, Reith, Christina, Child, Anne H, Clayton, Tim, Dodd, Matthew, Flather, Marcus, Jin, Xu Yu, Sandor, George, Groenink, Maarten, Mulder, Barbara, De Backer, Julie, Evangelista, Arturo, Forteza, Alberto, Teixido-Turà, Gisela, Boileau, Catherine, Jondeau, Guillaume, Milleron, Olivier, Lacro, Ronald V, Sleeper, Lynn A, Chiu, Hsin-Hui, Wu, Mei-Hwan, Neubauer, Stefan, Watkins, Hugh, Dietz, Hal, Baigent, Colin

المصدر: LANCET ; ISSN: 0140-6736 ; ISSN: 1474-547X

مصطلحات موضوعية: Medicine and Health Sciences, General Medicine

وصف الملف: application/pdf

Relation: https://biblio.ugent.be/publication/8765008; http://hdl.handle.net/1854/LU-8765008; http://dx.doi.org/10.1016/s0140-6736(22)01534-3; https://biblio.ugent.be/publication/8765008/file/8765009

الاتاحة: https://biblio.ugent.be/publication/8765008
http://hdl.handle.net/1854/LU-8765008
https://doi.org/10.1016/s0140-6736(22)01534-3
https://biblio.ugent.be/publication/8765008/file/8765009

المؤلفون: Pitcher, Alex, Spata, Enti, Emberson, Jonathan, Davies, Kelly, Halls, Heather, Holland, Lisa, Wilson, Kate, Reith, Christina, Child, Anne H, Clayton, Tim, Dodd, Matthew, Flather, Marcus, Jin, Xu Yu, Sandor, George, Groenink, Maarten, Mulder, Barbara, Backer, Julie De, Evangelista Masip, Arturo, Forteza, Alberto, Teixido-Tura, Gisela, Boileau, Catherine, Jondeau, Guillaume, Milleron, Olivier, Lacro, Ronald V., Sleeper, Lynn A, Chiu, Hsin-Hui, Wu, Mei-Hwan, Neubauer, Stefan, Watkins, Hugh, Dietz, Hal, Baigent, Colin, Universitat Autònoma de Barcelona

وصف الملف: application/pdf

Relation: The Lancet (British); Vol. 400 (august 2022), p. 822-831; https://ddd.uab.cat/record/272834; urn:10.1016/S0140-6736(22)01534-3; urn:oai:ddd.uab.cat:272834; urn:pmcid:PMC7613630; urn:pmc-uid:7613630; urn:pmid:36049495; urn:oai:pubmedcentral.nih.gov:7613630; urn:articleid:1474547Xv400p822

الاتاحة: https://ddd.uab.cat/record/272834

المؤلفون: Gati, Sabiha, Malhotra, Aneil, Sedgwick, Catherine, Papamichael, Nikolaos, Dhutia, Harshil, Sharma, Rajan, Child, Anne H, Papadakis, Michael, Sharma, Sanjay

مصطلحات موضوعية: Special populations

وصف الملف: text/html

Relation: http://heart.bmj.com/cgi/content/short/105/12/920; http://dx.doi.org/10.1136/heartjnl-2018-314288

الاتاحة: http://heart.bmj.com/cgi/content/short/105/12/920
https://doi.org/10.1136/heartjnl-2018-314288

المؤلفون: Child, Anne H., Aragon-Martin, Jose, Wan, Y. B. Alexander

المصدر: Oxford Textbook of Vascular Surgery ; page 571-577

الاتاحة: https://doi.org/10.1093/med/9780199658220.003.0054

المؤلفون: Bown, Matthew J., Jones, Gregory T., Harrison, Seamus C., Wright, Benjamin J., Bumpstead, Suzannah, Baas, Annette F., Gretarsdottir, Solveig, Badger, Stephen A., Bradley, Declan T., Burnand, Kevin, Child, Anne H., Clough, Rachel E., Cockerill, Gillian, Hafez, Hany, Scott, D Julian A., Futers, Simon, Johnson, Anne, Sohrabi, Soroush, Smith, Alberto, Thompson, Matthew M., van Bockxmeer, Frank M., Waltham, Matthew, Matthiasson, Stefan E., Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Blankensteijn, Jan D., Teijink, Joep A. W., Wijmenga, Cisca, de Graaf, Jacqueline, Kiemeney, Lambertus A., Assimes, Themistocles L., McPherson, Ruth, Folkersen, Lasse, Franco-Cereceda, Anders, Palmen, Jutta, Smith, Andrew J., Sylvius, Nicolas, Wild, John B., Refstrup, Mette, Edkins, Sarah, Gwilliam, Rhian, Hunt, Sarah E., Potter, Simon, Lindholt, Jes S., Frikke-Schmidt, Ruth, Tybjærg-Hansen, Anne, Hughes, Anne E., Golledge, Jonathan, Norman, Paul E., van Rij, Andre, Powell, Janet T., Eriksson, Per, Stefansson, Kari, Thompson, John R., Humphries, Steve E., Sayers, Robert D., Deloukas, Panos, Samani, Nilesh J., Schunkert, Heribert, König, Inke R., Kathiresan, Sekar, Reilly, Muredach P., Holm, Hilma, Preuss, Michael, Stewart, Alexandre F. R., Barbalic, Maja, Gieger, Christian, Absher, Devin, Aherrahrou, Zouhair, Allayee, Hooman, Altshuler, David, Anand, Sonia S., Andersen, Karl, Anderson, Jeffrey L., Ardissino, Diego, Ball, Stephen G., Balmforth, Anthony J., Barnes, Timothy A., Becker, Diane M., Becker, Lewis C., Berger, Klaus, Bis, Joshua C., Matthijs Boekholdt, S., Boerwinkle, Eric, Braund, Peter S., Susan Burnett, Mary, Buysschaert, Ian, Carlquist, John F., Chen, Li, Cichon, Sven, Codd, Veryan, Davies, Robert W., Dedoussis, George, Dehghan, Abbas, Demissie, Serkalem, Devaney, Joseph M., Diemert, Patrick, Do, Ron, Doering, Angela, Eifert, Sandra, El Mokhtari, Nour Eddine, Ellis, Stephen G., Elosua, Roberto, Engert, James C., Epstein, Stephen E., de Faire, Ulf, Fischer, Marcus, Folsom, Aaron R., Freyer, Jennifer, Gigante, Bruna, Girelli, Domenico, Gudnason, Vilmundur, Gulcher, Jeffrey R., Halperin, Eran, Hammond, Naomi, Hazen, Stanley L., Hofman, Albert, Horne, Benjamin D., Illig, Thomas, Iribarren, Carlos, Wouter Jukema, J., Kaiser, Michael A., Kaplan, Lee M., Kastelein, John J. P., Khaw, Kay-Tee, Knowles, Joshua W., Kolovou, Genovefa, Kong, Augustine, Laaksonen, Reijo, Lambrechts, Diether, Leander, Karin, Lettre, Guillaume, Li, Mingyao, Lieb, Wolfgang, Loley, Christina, Lotery, Andrew J., Mannucci, Pier M., Maouche, Seraya, Martinelli, Nicola, McKeown, Pascal P., Meisinger, Christa, Meitinger, Thomas, Melander, Olle, Angelica Merlini, Pier, Mooser, Vincent, Morgan, Thomas, Mühleisen, Thomas W., Muhlestein, Joseph B., Münzel, Thomas, Musunuru, Kiran, Nahrstaedt, Janja, Nelson, Christopher P., Nöthen, Markus M., Olivieri, Oliviero, Patel, Riyaz S., Patterson, Chris C., Peters, Annette, Peyvandi, Flora, Qu, Liming, Quyyumi, Arshed A., Rader, Daniel J., Rallidis, Loukianos S., Rice, Catherine, Rosendaal, Frits R., Rubin, Diana, Salomaa, Veikko, Lourdes Sampietro, M., Sandhu, Manjinder S., Schadt, Eric, Schäfer, Arne, Schillert, Arne, Schreiber, Stefan, Schrezenmeir, Jürgen, Schwartz, Stephen M., Siscovick, David S., Sivananthan, Mohan, Sivapalaratnam, Suthesh, Smith, Tamara B., Snoep, Jaapjan D., Soranzo, Nicole, Spertus, John A., Stark, Klaus, Stirrups, Kathy, Stoll, Monika, Wilson Tang, W. H., Tennstedt, Stephanie, Thorgeirsson, Gudmundur, Tomaszewski, Maciej, Uitterlinden, Andre G., van Rij, Andre M., Voight, Benjamin F., Wareham, Nicholas J., Wells, George A., Wichmann, H-Erich, Wild, Philipp S., Willenborg, Christina, Witteman, Jaqueline C. M., Ye, Shu, Zeller, Tanja, Ziegler, Andreas, Cambien, Francois, Goodall, Alison H., Adrienne Cupples, L., Quertermous, Thomas, März, Winfried, Hengstenberg, Christian, Blankenberg, Stefan, Ouwehand, Willem H., Hall, Alistair S., Roberts, Robert, O'Donnell, Christopher J., Erdmann, Jeanette, Newton-Cheh, Christopher, Johnson, Toby, Gateva, Vesela, Tobin, Martin D., Bochud, Murielle, Coin, Lachlan, Najjar, Samer S., Hua Zhao, Jing, Heath, Simon C., Eyheramendy, Susana, Papadakis, Konstantinos, Scott, Laura J., Zhang, Feng, Farrall, Martin, Tanaka, Toshiko, Wallace, Chris, Chambers, John C., Nilsson, Peter, van der Harst, Pim, Polidoro, Silvia, Grobbee, Diederick E., Onland-Moret, N. Charlotte, Bots, Michiel L., Wain, Louise V., Elliott, Katherine S., Teumer, Alexander, Luan, Jian'an, Lucas, Gavin, Kuusisto, Johanna, Burton, Paul R., Hadley, David, McArdle, Wendy L., Brown, Morris, Dominiczak, Anna, Newhouse, Stephen J., Webster, John, Zeggini, Eleftheria, Beckmann, Jacques S., Lim, Noha, Song, Kijoung, Vollenweider, Peter, Waeber, Gerard, Waterworth, Dawn M., Yuan, Xin, Groop, Leif, Orho-Melander, Marju, Allione, Alessandra, Di Gregorio, Alessandra, Guarrera, Simonetta, Panico, Salvatore, Ricceri, Fulvio, Romanazzi, Valeria, Sacerdote, Carlotta, Vineis, Paolo, Barroso, Inês, Luben, Robert N., Crawford, Gabriel J., Jousilahti, Pekka, Perola, Markus, Boehnke, Michael, Bonnycastle, Lori L., Jackson, Anne U., Mohlke, Karen L., Stringham, Heather M., Valle, Timo T., Willer, Cristen J., Bergman, Richard N., Morken, Mario A., Döring, Angela, Org, Elin, Pfeufer, Arne, Marrugat, Jaume, Subirana, Isaac, Freimer, Nelson B., Hartikainen, Anna-Liisa, McCarthy, Mark I., O'Reilly, Paul F., Peltonen, Leena, Pouta, Anneli, de Jong, Paul E., Snieder, Harold, van Gilst, Wiek H., Clarke, Robert, Goel, Anuj, Hamsten, Anders, Peden, John F., Seedorf, Udo, Syvänen, Ann-Christine, Tognoni, Giovanni, Lakatta, Edward G., Sanna, Serena, Scheet, Paul, Schlessinger, David, Scuteri, Angelo, Dörr, Marcus, Ernst, Florian, Felix, Stephan B., Homuth, Georg, Lorbeer, Roberto, Reffelmann, Thorsten, Rettig, Rainer, Völker, Uwe, Galan, Pilar, Gut, Ivo G., Hercberg, Serge, Mark Lathrop, G., Zelenika, Diana, Williams, Frances M., Zhai, Guangju, Laakso, Markku, Forouhi, Nita G., Völzke, Henry, Uiterwaal, Cuno S., van der Schouw, Yvonne T., Numans, Mattijs E., Matullo, Giuseppe, Navis, Gerjan, Berglund, Göran, Bingham, Sheila A., Kooner, Jaspal S., Connell, John M., Bandinelli, Stefania, Ferrucci, Luigi, Watkins, Hugh, Spector, Tim D., Tuomilehto, Jaakko, Strachan, David P., Laan, Maris, Meneton, Pierre, Uda, Manuela, Jarvelin, Marjo-Riitta, Loos, Ruth J. F., Elliott, Paul, Abecasis, Gonçalo R., Caulfield, Mark, Munroe, Patricia B., Steinthorsdottir, Valgerdur, Morris, Andrew P., Dina, Christian, Welch, Ryan P., Huth, Cornelia, Aulchenko, Yurii S., McCulloch, Laura J., Ferreira, Teresa, Grallert, Harald, Amin, Najaf, Wu, Guanming, Raychaudhuri, Soumya, McCarroll, Steve A., Langenberg, Claudia, Hofmann, Oliver M., Dupuis, Josée, Qi, Lu, Segrè, Ayellet V., van Hoek, Mandy, Navarro, Pau, Ardlie, Kristin, Balkau, Beverley, Benediktsson, Rafn, Bennett, Amanda J., Blagieva, Roza, Bengtsson Boström, Kristina, Bravenboer, Bert, Burtt, Noël P., Charpentier, Guillaume, Chines, Peter S., Cornelis, Marilyn, Couper, David J., Crawford, Gabe, Doney, Alex S. F., Elliott, Amanda L., Erdos, Michael R., Fox, Caroline S., Franklin, Christopher S., Ganser, Martha, Grarup, Niels, Green, Todd, Griffin, Simon, Groves, Christopher J., Guiducci, Candace, Hadjadj, Samy, Hassanali, Neelam, Herder, Christian, Isomaa, Bo, Johnson, Paul R. V., Jørgensen, Torben, Kao, Wen H. L., Klopp, Norman, Kraft, Peter, Lauritzen, Torsten, Lieverse, Aloysius, Lindgren, Cecilia M., Lyssenko, Valeriya, Marre, Michel, Midthjell, Kristian, Narisu, Narisu, Owen, Katharine R., Payne, Felicity, Perry, John R. B., Petersen, Ann-Kristin, Platou, Carl, Proença, Christine, Prokopenko, Inga, Rathmann, Wolfgang, William Rayner, N., Robertson, Neil R., Rocheleau, Ghislain, Roden, Michael, Sampson, Michael J., Saxena, Richa, Shields, Beverley M., Shrader, Peter, Sigurdsson, Gunnar, Sparsø, Thomas, Strassburger, Klaus, Sun, Qi, Swift, Amy J., Thorand, Barbara, Tichet, Jean, Tuomi, Tiinamaija, van Dam, Rob M., van Haeften, Timon W., van Herpt, Thijs, van Vliet-Ostaptchouk, Jana V., Bragi Walters, G., Weedon, Michael N., Cauchi, Stephane, Gloyn, Anna L., Gyllensten, Ulf, Hansen, Torben, Hide, Winston A., Hitman, Graham A., Hunter, David J., Hveem, Kristian, Morris, Andrew D., Palmer, Colin N. A., Pramstaller, Peter P., Rudan, Igor, Sijbrands, Eric, Stein, Lincoln D., Uitterlinden, Andre, Walker, Mark, Watanabe, Richard M., Boehm, Bernhard O., Campbell, Harry, Daly, Mark J., Hattersley, Andrew T., Hu, Frank B., Meigs, James B., Pankow, James S., Pedersen, Oluf, Florez, Jose C., Frayling, Timothy M., Sladek, Rob, Wilson, James F., Froguel, Philippe, van Duijn, Cornelia M., Blair, Ross D., Hill, Andrew A., Gerry Hill, B., Lewis, David R., McNoe, Les A., Merriman, Tony R., Naik, Dilip K., Vicky Phillips, L., Thomson, Ian A., Topless, Ruth, Vasudevan, Thodur M., Yu, Grace

المساهمون: Bown, Matthew J., Jones, Gregory T., Harrison, Seamus C., Wright, Benjamin J., Bumpstead, Suzannah, Baas, Annette F., Gretarsdottir, Solveig, Badger, Stephen A., Bradley, Declan T., Burnand, Kevin, Child, Anne H., Clough, Rachel E., Cockerill, Gillian, Hafez, Hany, Scott, D Julian A., Futers, Simon, Johnson, Anne, Sohrabi, Soroush, Smith, Alberto, Thompson, Matthew M., van Bockxmeer, Frank M., Waltham, Matthew, Matthiasson, Stefan E., Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Blankensteijn, Jan D., Teijink, Joep A. W., Wijmenga, Cisca, de Graaf, Jacqueline, Kiemeney, Lambertus A., Assimes, Themistocles L., Mcpherson, Ruth, Folkersen, Lasse, Franco-Cereceda, Ander, Palmen, Jutta, Smith, Andrew J., Sylvius, Nicola, Wild, John B., Refstrup, Mette, Edkins, Sarah, Gwilliam, Rhian, Hunt, Sarah E., Potter, Simon, Lindholt, Jes S., Frikke-Schmidt, Ruth, Tybjærg-Hansen, Anne, Hughes, Anne E., Golledge, Jonathan, Norman, Paul E., van Rij, Andre, Powell, Janet T., Eriksson, Per, Stefansson, Kari, Thompson, John R., Humphries, Steve E., Sayers, Robert D., Deloukas, Pano, Samani, Nilesh J., Schunkert, Heribert, König, Inke R., Kathiresan, Sekar, Reilly, Muredach P., Holm, Hilma, Preuss, Michael, Stewart, Alexandre F. R., Barbalic, Maja, Gieger, Christian, Absher, Devin, Aherrahrou, Zouhair, Allayee, Hooman, Altshuler, David, Anand, Sonia S., Andersen, Karl, Anderson, Jeffrey L., Ardissino, Diego, Ball, Stephen G., Balmforth, Anthony J., Barnes, Timothy A., Becker, Diane M., Becker, Lewis C., Berger, Klau, Bis, Joshua C., Matthijs Boekholdt, S., Boerwinkle, Eric, Braund, Peter S., Susan Burnett, Mary, Buysschaert, Ian, Carlquist, John F., Chen, Li, Cichon, Sven, Codd, Veryan, Davies, Robert W., Dedoussis, George, Dehghan, Abba, Demissie, Serkalem, Devaney, Joseph M., Diemert, Patrick, Do, Ron, Doering, Angela, Eifert, Sandra

مصطلحات موضوعية: Aged, Aorta, Aortic Aneurysm, Abdominal, Case-Control Studies, Cell Line, Tumor, Data Interpretation, Statistical, Female, Follow-Up Studies, Genetic Loci, Genetic Predisposition to Disease, Genome-Wide Association Study, Homozygote, Humans, Low Density Lipoprotein Receptor-Related Protein-1, Male, Odds Ratio, Organ Specificity, Risk Factors, Sterol Regulatory Element Binding Protein 1, Polymorphism, Single Nucleotide, Genetics, Genetics (clinical)

Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000297090100003; volume:89; issue:5; firstpage:619; lastpage:627; numberofpages:9; journal:AMERICAN JOURNAL OF HUMAN GENETICS; http://hdl.handle.net/11584/306546; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84945173643; http://www.elsevier.com/wps/find/journaldescription.cws_home/713561/description#description

الاتاحة: http://hdl.handle.net/11584/306546
https://doi.org/10.1016/j.ajhg.2011.10.002
http://www.elsevier.com/wps/find/journaldescription.cws_home/713561/description#description

المؤلفون: Pitcher, Alex, Emberson, Jonathan, Lacro, Ronald V, Sleeper, Lynn A, Stylianou, Mario, Mahony, Lynn, Pearson, Gail D, Groenink, Maarten, Mulder, Barbara J, Zwinderman, Aeilko H, De Backer, Julie, De Paepe, Anne, Arbustini, Eloisa, Erdem, Guliz, Jin, Xu Yu, Flather, Marcus D, Mullen, Michael J, Child, Anne H, Forteza, Alberto, Evangelista, Arturo, Chiu, Hsin-Hui, Wu, Mei-Hwan, Sandor, George, Bhatt, Ami B, Creager, Mark A, Devereux, Richard B, Loeys, Bart, Forfar, J Colin, Neubauer, Stefan, Watkins, Hugh, Boileau, Catherine, Jondeau, Guillaume, Dietz, Harry C, Baigent, Colin

المصدر: AMERICAN HEART JOURNAL ; ISSN: 0002-8703

مصطلحات موضوعية: Medicine and Health Sciences, THERAPY, ATENOLOL, PROGRESSION, ANEURYSM, CHILDREN, AORTIC-ROOT DILATION, CLINICAL-TRIAL, YOUNG-ADULTS, BETA-BLOCKER, LOSARTAN

وصف الملف: application/pdf

Relation: https://biblio.ugent.be/publication/6835858; http://hdl.handle.net/1854/LU-6835858; http://dx.doi.org/10.1016/j.ahj.2015.01.011; https://biblio.ugent.be/publication/6835858/file/6835898

الاتاحة: https://biblio.ugent.be/publication/6835858
http://hdl.handle.net/1854/LU-6835858
https://doi.org/10.1016/j.ahj.2015.01.011
https://biblio.ugent.be/publication/6835858/file/6835898

المؤلفون: Arslan-Kirchner, Mine, Arbustini, Eloisa, Boileau, Catherine, Charron, Philippe, Child, Anne H, Collod-Beroud, Gwenaelle, De Backer, Julie, De Paepe, Anne, Dierking, Anna, Faivre, Laurence, Hoffjan, Sabine, Jondeau, Guillaume, Keyser, Britta, Loeys, Bart, Mayer, Karin, Robinson, Peter N, Schmidtke, Jörg

المصدر: European Journal of Human Genetics ; volume 24, issue 1, page 146-150 ; ISSN 1018-4813 1476-5438

الاتاحة: http://dx.doi.org/10.1038/ejhg.2015.225
http://www.nature.com/articles/ejhg2015225.pdf
http://www.nature.com/articles/ejhg2015225

المؤلفون: Bradley, Declan T., Hughes, Anne E., Badger, Stephen A., Jones, Gregory T, Harrison, Seamus C., Wright, Benjamin J., Bumpstead, Suzannah J., Baas, Annette F., Gretarsdottir, Solveig, Burnand, Kevin, Child, Anne H., Clough, Rachel E., Cockerill, Gillian, Hafez, Hany, Scott, D. Julian A., Ariens, Robert A. S., Johnson, Anne, Sohrabi, Soroush, Smith, Alberto, Thompson, Matthew, van Bockxmeer, Frank M., Waltham, Matthew, Matthiasson, Stefan E, Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Blankensteijn, Jan D., Teijink, Joep A. W., Wijmenga, Cisca, de Graaf, Jacqueline, Kiemeney, Lambertus A., Wild, John B., Edkins, Sarah, Gwilliam, Rhian, Hunt, Sarah E., Potter, Simon C., Lindholt, Jes S, Golledge, Jonathan, Norman, Paul E., van Rij, Andre M, Powell, Janet T., Eriksson, Per, Stefansson, Kari, Thompson, John R, Humphries, Steve E., Sayers, Robert D., Deloukas, Panos, Samani, Nilesh J., Bown, Matthew J.

المصدر: Bradley , D T , Hughes , A E , Badger , S A , Jones , G T , Harrison , S C , Wright , B J , Bumpstead , S J , Baas , A F , Gretarsdottir , S , Burnand , K , Child , A H , Clough , R E , Cockerill , G , Hafez , H , Scott , D J A , Ariens , R A S , Johnson , A , Sohrabi , S , Smith , A , Thompson , M , van Bockxmeer , F M ....

مصطلحات موضوعية: aneurysm, cholesterol, LDL, genome-wide association study, lipids

الاتاحة: https://cris.maastrichtuniversity.nl/en/publications/cc36b47a-4888-40c5-b201-ff701d6685c6
https://doi.org/10.1161/CIRCGENETICS.113.000165

المؤلفون: Bown, Matthew J., Jones, Gregory T., Harrison, Seamus C., Wright, Benjamin J., Bumpstead, Suzannah, Baas, Annette F., Gretarsdottir, Solveig, Badger, Stephen A., Bradley, Declan T., Burnand, Kevin, Child, Anne H., Clough, Rachel E., Cockerill, Gillian, Hafez, Hany, Scott, D. Julian A., Futers, Simon, Johnson, Anne, Sohrabi, Soroush, Smith, Alberto, Thompson, Matthew M., van Bockxmeer, Frank M., Waltham, Matthew, Matthiasson, Stefan E., Thorleifsson, Gudmar, Thorsteinsdottir, Unnar, Blankensteijn, Jan D., Teijink, Joep A. W., Wijmenga, Cisca, de Graaf, Jacqueline, Kiemeney, Lambertus A., Assimes, Themistocles L., McPherson, Ruth, CARDIoGRAM Consortium, Global BPgen Consortium, DIAGRAM Consortium, VRCNZ Consortium, Folkersen, Lasse, Franco-Cereceda, Anders, Palmen, Jutta, Smith, Andrew J., Sylvius, Nicolas, Wild, John B., Refstrup, Mette, Edkins, Sarah, Gwilliam, Rhian, Hunt, Sarah E., Potter, Simon, Lindholt, Jes S., Frikke-Schmidt, Ruth, Tybjaerg-Hansen, Anne, Hughes, Anne E., Golledge, Jonathan, Norman, Paul E., Van Rij, Andre, Powell, Janet T., Eriksson, Per, Stefansson, Kari, Thompson, John R., Humphries, Steve E., Sayers, Robert D., Deloukas, Panos, Samani, Nilesh J.

وصف الملف: application/pdf

Relation: http://dx.doi.org/10.1016/j.ajhg.2011.10.002; https://researchonline.jcu.edu.au/19303/; https://researchonline.jcu.edu.au/19303/2/19303_Bown_et_al_2011_.pdf; Bown, Matthew J., Jones, Gregory T., Harrison, Seamus C., Wright, Benjamin J., Bumpstead, Suzannah, Baas, Annette F., Gretarsdottir, Solveig, Badger, Stephen A., Bradley, Declan T., Burnand, Kevin, Child, Anne H., Clough, Rachel E., Cockerill, Gillian, Hafez, Hany, Scott, D. Julian A., Futers, Simon, Johnson, Anne, Sohrabi, Soroush, Smith, Alberto, Thompson, Matthew M., van Bockxmeer, Frank M., Waltham, Matthew, Matthiasson, Stefan E., Thorleifsson, Gudmar, Thorsteinsdottir, Unnar, Blankensteijn, Jan D., Teijink, Joep A. W., Wijmenga, Cisca, de Graaf, Jacqueline, Kiemeney, Lambertus A., Assimes, Themistocles L., McPherson, Ruth, CARDIoGRAM Consortium, , Global BPgen Consortium, , DIAGRAM Consortium, , VRCNZ Consortium, , Folkersen, Lasse, Franco-Cereceda, Anders, Palmen, Jutta, Smith, Andrew J., Sylvius, Nicolas, Wild, John B., Refstrup, Mette, Edkins, Sarah, Gwilliam, Rhian, Hunt, Sarah E., Potter, Simon, Lindholt, Jes S., Frikke-Schmidt, Ruth, Tybjaerg-Hansen, Anne, Hughes, Anne E., Golledge, Jonathan, Norman, Paul E., Van Rij, Andre, Powell, Janet T., Eriksson, Per, Stefansson, Kari, Thompson, John R., Humphries, Steve E., Sayers, Robert D., Deloukas, Panos, and Samani, Nilesh J. (2011) Abdominal aortic aneurysm is associated with a variant in the low density lipoprotein receptor related protein 1(LRP1) gene. American Journal of Human Genetics, 89 (5). pp. 619-627.

الاتاحة: https://researchonline.jcu.edu.au/19303/2/19303_Bown_et_al_2011_.pdf

المؤلفون: Vasu, Vimal, Child, Anne H, Modi, Neena, Rutherford, Mary, Cowan, Frances

مصطلحات موضوعية: case-report

وصف الملف: text/html

Relation: http://casereports.bmj.com/cgi/content/short/2011/jul28_1/bcr0620114328; http://dx.doi.org/10.1136/bcr.06.2011.4328

الاتاحة: http://casereports.bmj.com/cgi/content/short/2011/jul28_1/bcr0620114328
https://doi.org/10.1136/bcr.06.2011.4328

المؤلفون: Ostergaard, Pia, Simpson, Michael A, Brice, Glen, Mansour, Sahar, Connell, Fiona C, Onoufriadis, Alexandros, Child, Anne H, Hwang, Jae, Kalidas, Kamini, Mortimer, Peter S, Trembath, Richard, Jeffery, Steve

مصطلحات موضوعية: Original article

وصف الملف: text/html

Relation: http://jmg.bmj.com/cgi/content/short/48/4/251; http://dx.doi.org/10.1136/jmg.2010.085563

الاتاحة: http://jmg.bmj.com/cgi/content/short/48/4/251
https://doi.org/10.1136/jmg.2010.085563

المؤلفون: Stheneur, Chantal, Faivre, Laurence, Collod-Béroud, Gwenaëlle, Gautier, Elodie, Binquet, Christine, Bonithon-Kopp, Claire, Claustres, Mireille, Child, Anne H, Arbustini, Eloisa, Adès, Lesley C, Francke, Uta, Mayer, Karin, Arslan-Kirchner, Mine, De Paepe, Anne, Chevallier, Bertrand, Bonnet, Damien, Jondeau, Guillaume, Boileau, Catherine

المصدر: Pediatric Research ; volume 69, issue 3, page 265-270 ; ISSN 0031-3998 1530-0447

الاتاحة: http://dx.doi.org/10.1203/pdr.0b013e3182097219

المؤلفون: Détaint, Delphine, Faivre, Laurence, Collod-Beroud, Gwenaelle, Child, Anne H., Loeys, Bart L., Binquet, Christine, Gautier, Elodie, Arbustini, Eloisa, Mayer, Karin, Arslan-Kirchner, Mine, Stheneur, Chantal, Halliday, Dorothy, Beroud, Christophe, Bonithon-Kopp, Claire, Claustres, Mireille, Plauchu, Henri, Robinson, Peter N., Kiotsekoglou, Anatoli, De Backer, Julie, Adès, Lesley, Francke, Uta, De Paepe, Anne, Boileau, Catherine, Jondeau, Guillaume

المصدر: European Heart Journal ; volume 31, issue 18, page 2223-2229 ; ISSN 0195-668X 1522-9645

الاتاحة: https://doi.org/10.1093/eurheartj/ehq258
http://academic.oup.com/eurheartj/article-pdf/31/18/2223/17049007/ehq258.pdf

المؤلفون: Faivre, Laurence, Collod-Beroud, Gwenaëlle, Callewaert, Bert, L., Child, Anne, H., Binquet, Christine, Gautier, Elodie, Loeys, Bart, L., Arbustini, Eloisa, Mayer, Karin, Arslan-Kirchner, Mine, Stheneur, Chantal, Kiotsekoglou, Anatoli, Comeglio, Paolo, Marziliano, Nicola, Wolf, Jean-Eric, Bouchot, Olivier, Khau-Van-Kien, Philippe, Béroud, Christophe, Claustres, Mireille, Bonithon-Kopp, Claire, Robinson, Peter, N., Adès, Lesley, C., de Backer, Julie, Coucke, Paul, Francke, Uta, de Paepe, Anne, Jondeau, Guillaume, Boileau, Catherine

المساهمون: Centre d'Investigation Clinique 1432 (Dijon) - Epidemiologie Clinique/Essais Cliniques (CIC-EC), Université de Bourgogne (UB)-Centre Hospitalier Universitaire de Dijon - Hôpital François Mitterrand (CHU Dijon)-Institut National de la Santé et de la Recherche Médicale (INSERM), Centre de génétique - Centre de référence des maladies rares, anomalies du développement et syndromes malformatifs (CHU de Dijon), Centre Hospitalier Universitaire de Dijon - Hôpital François Mitterrand (CHU Dijon), Laboratoire de génétique des maladies rares. Pathologie moleculaire, etudes fonctionnelles et banque de données génétiques (LGMR), Université Montpellier 1 (UM1)-IFR3, Université Montpellier 1 (UM1)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM), Center for Medical Genetics Ghent, Ghent University Hospital, Department of Cardiological Sciences, St George's Hospital, Institute of Genetic Medicine and the Howard Hughes Medical Institute, Johns Hopkins University (JHU), Centre for Inherited Cardiovacular Diseases, Foundation IRCCS Policlinico San Matteo, Center for Human Genetics and Laboratory Medicine, Center of Human Genetics and Laboratory Medicine, Institut für Humagenetik, Institut für Humagenetik-Medizinische Hochschule Hannover = Hannover Medical School (MHH), Service de pédiatrie, urgences enfants CHU Ambroise-Paré, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Ambroise Paré AP-HP, Laboratoire Electronique, Informatique et Image UMR6306 (Le2i), Université de Bourgogne (UB)-École Nationale Supérieure d'Arts et Métiers (ENSAM), Arts et Métiers Sciences et Technologies-Arts et Métiers Sciences et Technologies-AgroSup Dijon - Institut National Supérieur des Sciences Agronomiques, de l'Alimentation et de l'Environnement-Centre National de la Recherche Scientifique (CNRS), Service de Cardiologie CHU de Dijon, Service de chirurgie cardio-vasculaire et thoracique (CHU Dijon), Institut für Medizinische Genetik, Charité - UniversitätsMedizin = Berlin University Medicine, Discipline of Paediatrics and Child Health, The University of Sydney, Marfan Research Group, Westmead Hospital Sydney, Department of Clinical Genetics, Department of Genetics Stanford, Stanford Medicine, Stanford University-Stanford University, Centre de Référence Maladies Rares Syndrome de Marfan et Maladies Apparentées AP-HP (CRMR Marfan), AP-HP - Hôpital Bichat - Claude Bernard Paris, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Service de biochimie, d'hormonologie et de génétique moléculaire CHU Amrboise Paré, Génétique et épigénétique des maladies métaboliques, neurosensorielles et du développement (Inserm U781), Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM), This study was supported by a grant from the French ministry of health (PHRC 2004), GIS maladies rares 2004, Bourse de la Société Francaise de Cardiologie, Fédération Franc¸aise de Cardiologie 2005 and ANR-05-PCOD-014. BC and BL are respectively a research fellow and a senior clinical investigator of the Fund for Scientific Research – Flanders. AC and PC thank the Marfan Trust and the Bluff Field Charitable Fund for support.

المصدر: ISSN: 1018-4813.

مصطلحات موضوعية: Marfan syndrome, Neonatal Marfan syndrome, FBN1 mutations, exons 24–32, clinical and mutation-type analysis, [SDV.GEN]Life Sciences [q-bio]/Genetics

Relation: info:eu-repo/semantics/altIdentifier/pmid/19002209; PUBMED: 19002209

الاتاحة: https://inserm.hal.science/inserm-00343925
https://inserm.hal.science/inserm-00343925v2/document
https://inserm.hal.science/inserm-00343925v2/file/2009-EJHG%20%20%20%20%20%20%20%20%20%20%20%20%20%20%20%20%20%20%20%20%20%20%20%20%20HAL%20%20%20%20%20%20%20%20%20%20%20%20%20FBN1%20mutations%2024-32.pdf
https://doi.org/10.1038/ejhg.2008.207

المؤلفون: Faivre, Laurence, Masurel-Paulet, Alice, Collod-Béroud, Gwenaëlle, Callewaert, Bert, L., Child, Anne, H., Stheneur, Chantal, Binquet, Christine, Gautier, Elodie, Chevallier, Bertrand, Huet, Frédéric, Loeys, Bart, L., Arbustini, Eloisa, Mayer, Karin, Arslan-Kirchner, Mine, Kiotsekoglou, Anatoli, Comeglio, Paolo, Grasso, Maurizia, Halliday, Dorothy, J., Béroud, Christophe, Bonithon-Kopp, Claire, Claustres, Mireille, Robinson, Peter, N., Adès, Lesley, C., de Backer, Julie, Coucke, Paul, Francke, Uta, de Paepe, Anne, Boileau, Catherine, Jondeau, Guillaume

المساهمون: Centre de génétique - Centre de référence des maladies rares, anomalies du développement et syndromes malformatifs (CHU de Dijon), Centre Hospitalier Universitaire de Dijon - Hôpital François Mitterrand (CHU Dijon), Centre d'Investigation Clinique 1432 (Dijon) - Epidemiologie Clinique/Essais Cliniques (CIC-EC), Université de Bourgogne (UB)-Centre Hospitalier Universitaire de Dijon - Hôpital François Mitterrand (CHU Dijon)-Institut National de la Santé et de la Recherche Médicale (INSERM), Laboratoire de génétique des maladies rares. Pathologie moleculaire, etudes fonctionnelles et banque de données génétiques (LGMR), Université Montpellier 1 (UM1)-IFR3, Université Montpellier 1 (UM1)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM), Center for Medical Genetics Ghent, Ghent University Hospital, Department of Cardiological Sciences, St George's Hospital, Service de pédiatrie, urgences enfants CHU Ambroise-Paré, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Ambroise Paré AP-HP, Howard Hughes Medical Institute (HHMI), Centre for Inherited Cardiovacular Diseases, Foundation IRCCS Policlinico San Matteo, Center for Human Genetics and Laboratory Medicine, Center of Human Genetics and Laboratory Medicine, Institut für Humagenetik, Institut für Humagenetik-Medizinische Hochschule Hannover = Hannover Medical School (MHH), Department of Biochemistry Oxford, University of Oxford, Institut für Medizinische Genetik, Charité - UniversitätsMedizin = Berlin University Medicine, Discipline of Paediatrics and Child Health, The University of Sydney, Marfan Research Group, Westmead Hospital Sydney, Department of Clinical Genetics, Department of Genetics Stanford, Stanford Medicine, Stanford University-Stanford University, Service de biochimie, d'hormonologie et de génétique moléculaire CHU Amrboise Paré, Consultation Marfan, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Bichat, Service de cardiologie, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-AP-HP - Hôpital Bichat - Claude Bernard Paris, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Université Paris Diderot - Paris 7 (UPD7), This work was supported by a grant from the French Ministry of Health (grant Programme Hospitalier de Recherche Clinique 2004), Groupement d’Intérêt Scientifique Maladies Rares 2004, Bourse de la Société Francaise de Cardiologie, Fédération Franc¸aise de Cardiologie 2005, and ANR-05-PCOD-014. Drs Callewaert and Loeys are a research fellow and a senior clinical investigator, respectively, of the Fund for Scientific ResearchFlanders. Drs Child and Comeglio thank the Marfan Trust and the Bluff Field Charitable Fund for support.

المصدر: ISSN: 0031-4005.

مصطلحات موضوعية: Marfan syndrome, FBN1, childhood, international criteria, Abbreviations, AAD—ascending aortic dilation, CI— confidence interval, EL— ectopia lentis, MFS—Marfan syndrome, PTC—premature termination codon, MESH: Adolescent, MESH: Child, MESH: Marfan Syndrome, MESH: Microfilament Proteins, MESH: Mutation, Preschool, MESH: Female, MESH: Follow-Up Studies, MESH: Genetic Screening, MESH: Humans, MESH: Male, [SDV.GEN]Life Sciences [q-bio]/Genetics

Relation: info:eu-repo/semantics/altIdentifier/pmid/19117906; PUBMED: 19117906

الاتاحة: https://inserm.hal.science/inserm-00396263
https://inserm.hal.science/inserm-00396263v1/document
https://inserm.hal.science/inserm-00396263v1/file/2009-Pediatrics%20%20%20%20%20%20%20%20%20%20%20%20%20%20%20%20%20HAL%20%20%20%20%20%20%20%20%20%20%20%20%20%20%20Clinical%20and%20molecular%20FBN1.pdf
https://doi.org/10.1542/peds.2008-0703

المؤلفون: Kiotsekoglou, Anatoli, Sutherland, George R., Moggridge, James C., Kapetanakis, Venedictos, Bajpai, Abhay, Bunce, Nicholas, Mullen, Michael J., Louridas, George, Nassiri, Dariush K., Camm, John, Child, Anne H.

مصطلحات موضوعية: CLINICAL/ORIGINAL PAPERS

وصف الملف: text/html

Relation: http://ehjcimaging.oxfordjournals.org/cgi/content/short/10/2/295; http://dx.doi.org/10.1093/ejechocard/jen239

الاتاحة: http://ehjcimaging.oxfordjournals.org/cgi/content/short/10/2/295
https://doi.org/10.1093/ejechocard/jen239

المؤلفون: Kiotsekoglou, Anatoli, Moggridge, James C., Bijnens, Bart H., Kapetanakis, Venediktos, Alpendurada, Francisco, Mullen, Michael J., Saha, Samir, Nassiri, Dariush K., Camm, John, Sutherland, George R., Child, Anne H.

مصطلحات موضوعية: CLINICAL/ORIGINAL PAPERS

وصف الملف: text/html

Relation: http://ehjcimaging.oxfordjournals.org/cgi/content/short/10/8/947; http://dx.doi.org/10.1093/ejechocard/jep110

الاتاحة: http://ehjcimaging.oxfordjournals.org/cgi/content/short/10/8/947
https://doi.org/10.1093/ejechocard/jep110

المؤلفون: Kiotsekoglou, Anatoli, Sutherland, George R, Moggridge, James C, Nassiri, Dariush K, Camm, John, Child, Anne H

مصطلحات موضوعية: Reviews

وصف الملف: text/html

Relation: http://heart.bmj.com/cgi/content/short/hrt.2008.152934v1; http://dx.doi.org/10.1136/hrt.2008.152934

الاتاحة: http://heart.bmj.com/cgi/content/short/hrt.2008.152934v1
https://doi.org/10.1136/hrt.2008.152934

المؤلفون: Faivre, Laurence, Collod-Beroud, Gwenaëlle, Child, Anne, H., Callewaert, Bert, L., Loeys, Bart, L., Binquet, Christine, Gautier, Elodie, Arbustini, Eloisa, Mayer, Karin, Arslan-Kirchner, Mine, Stheneur, Chantal, Kiotsekoglou, Anatoli, Comeglio, Paolo, Marziliano, Nicola, Halliday, Dorothy, J., Béroud, Christophe, Bonithon-Kopp, Claire, Claustres, Mireille, Plauchu, Henri, Robinson, Peter, N., Adès, Lesley, C., de Backer, Julie, Coucke, Paul, Francke, Uta, de Paepe, Anne, Boileau, Catherine, Jondeau, Guillaume

المساهمون: Centre de génétique - Centre de référence des maladies rares, anomalies du développement et syndromes malformatifs (CHU de Dijon), Centre Hospitalier Universitaire de Dijon - Hôpital François Mitterrand (CHU Dijon), Centre d'Investigation Clinique 1432 (Dijon) - Epidemiologie Clinique/Essais Cliniques (CIC-EC), Université de Bourgogne (UB)-Centre Hospitalier Universitaire de Dijon - Hôpital François Mitterrand (CHU Dijon)-Institut National de la Santé et de la Recherche Médicale (INSERM), Laboratoire de génétique des maladies rares. Pathologie moleculaire, etudes fonctionnelles et banque de données génétiques (LGMR), Université Montpellier 1 (UM1)-IFR3, Université Montpellier 1 (UM1)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM), Department of Cardiological Sciences, St George's Hospital, Center for Medical Genetics Ghent, Ghent University Hospital, Institute of Genetic Medicine and the Howard Hughes Medical Institute, Johns Hopkins University (JHU), Centre for Inherited Cardiovacular Diseases, Foundation IRCCS Policlinico San Matteo, Center for Human Genetics and Laboratory Medicine, Center of Human Genetics and Laboratory Medicine, Institut für Humagenetik, Institut für Humagenetik-Medizinische Hochschule Hannover = Hannover Medical School (MHH), Service de pédiatrie, urgences enfants CHU Ambroise-Paré, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Ambroise Paré AP-HP, Consultation Marfan, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Bichat, Department of Biochemistry Oxford, University of Oxford, Service de Génétique, Hôtel Dieu, Institut für Medizinische Genetik, Charité - UniversitätsMedizin = Berlin University Medicine, Marfan Research Group, Westmead Hospital Sydney, Department of Clinical Genetics, Discipline of Paediatrics and Child Health, The University of Sydney, Department of Genetics Stanford, Stanford Medicine, Stanford University-Stanford University, Service de biochimie, d'hormonologie et de génétique moléculaire CHU Amrboise Paré, This work was supported by a grant from the French ministry of health (PHRC 2004), GIS maladies rares 2004, Bourse de la Socie´te´ Francaise de Cardiologie, Fédération Franc¸aise de Cardiologie 2005, and ANR-05-PCOD-014. BC and BL are respectively a research fellow and a senior clinical investigator of the Fund for Scientific Research – Flanders. AC and PC thank the Marfan Trust, and the Bluff Field Charitable Fund for support.

المصدر: ISSN: 0022-2593.

مصطلحات موضوعية: MESH: Adolescent, MESH: Adult, MESH: Humans, MESH: International Cooperation, MESH: Male, MESH: Marfan Syndrome, MESH: Microfilament Proteins, MESH: Mutation, MESH: Aged, MESH: Aorta, MESH: Child, MESH: Female, [SDV.GEN]Life Sciences [q-bio]/Genetics

Relation: info:eu-repo/semantics/altIdentifier/pmid/18310266; PUBMED: 18310266

الاتاحة: https://inserm.hal.science/inserm-00343946
https://inserm.hal.science/inserm-00343946v1/document
https://inserm.hal.science/inserm-00343946v1/file/2008-JMedGenet%20%20%20%20%20%20%20%20%20%20%20%20%20%20%20HAL%20%20%20%20%20%20%20%20%20%20%20%20%20Contribution%20of%20molecular%20FBN1.pdf.pdf
https://doi.org/10.1136/jmg.2007.056382

المؤلفون: Kiotsekoglou, Anatoli, Bajpai, Abhay, Bijnens, Bart H., Kapetanakis, Venedictos, Athanassopoulos, George, Moggridge, James C., Mullen, Mike J., Nassiri, Dariush K., Camm, John, Sutherland, George R., Child, Anne H.

مصطلحات موضوعية: Original Paper

وصف الملف: text/html

Relation: http://ehjcimaging.oxfordjournals.org/cgi/content/short/jen003v1; http://dx.doi.org/10.1093/ejechocard/jen003

الاتاحة: http://ehjcimaging.oxfordjournals.org/cgi/content/short/jen003v1
https://doi.org/10.1093/ejechocard/jen003