Partial Right Atrial Inflow Occlusion for Transient Systemic Hypotension During Deployment of Thoracic Stentgrafts by Pietersen, L. C., van der Meer, R. W., Alders, D. J. C., van Schaik, J., Eefting, D., van Rijswijk, C. S. P.

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A 13C NMR double-labeling method to quantitate local myocardial O2 consumption using frozen tissue samples by VAN BEEK, J. H. G. M, VAN MIL, H. G. J, KING, R. B, DE KANTER, F. J. J, ALDERS, D. J. C, BUSSEMAKER, J

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Exploring brain connectivity changes in major depressive disorder using functional‐structural data fusion: A CAN‐BIND‐1 study by Ayyash, Sondos, Davis, Andrew D., Alders, Gésine L., MacQueen, Glenda, Strother, Stephen C., Hassel, Stefanie, Zamyadi, Mojdeh, Arnott, Stephen R., Harris, Jacqueline K., Lam, Raymond W., Milev, Roumen, Müller, Daniel J., Kennedy, Sidney H., Rotzinger, Susan, Frey, Benicio N., Minuzzi, Luciano, Hall, Geoffrey B.

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Experimental investigation and thermodynamic modelling assessment of the AECl2–NdCl3 (AE = Sr, Ba) systems by Alders, D C, Cette, D J, Konings, R J M, Smith, A L

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Experimental investigation and thermodynamic modelling assessment of the AECl 2 –NdCl 3 (AE = Sr, Ba) systems by Alders, D. C., Cette, D. J., Konings, R. J. M., Smith, A. L.

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Reduced accuracy accompanied by reduced neural activity during the performance of an emotional conflict task by unmedicated patients with major depression: A CAN-BIND fMRI study by Alders, Gésine L., Davis, Andrew D., MacQueen, Glenda, Strother, Stephen C., Hassel, Stefanie, Zamyadi, Mojdeh, Sharma, Gulshan B., Arnott, Stephen R., Downar, Jonathan, Harris, Jacqueline K., Lam, Raymond W., Milev, Roumen, Müller, Daniel J., Ravindran, Arun, Kennedy, Sidney H., Frey, Benicio N., Minuzzi, Luciano, Hall, Geoffrey B.

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Assessing remission in major depressive disorder using a functional-structural data fusion pipeline: A CAN-BIND-1 study by Ayyash, Sondos, Davis, Andrew D., Alders, Gésine L., MacQueen, Glenda, Strother, Stephen C., Hassel, Stefanie, Zamyadi, Mojdeh, Arnott, Stephen R., Harris, Jacqueline K., Lam, Raymond W., Milev, Roumen, Müller, Daniel J., Kennedy, Sidney H., Rotzinger, Susan, Frey, Benicio N., Minuzzi, Luciano, Hall, Geoffrey B.

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Experimental investigation and thermodynamic assessment of the BaCl2–CeCl3 system by Alders, D.C., Vlieland, J., Thijs, M., Konings, R.J.M., Smith, A.L.

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Reliability of a functional magnetic resonance imaging task of emotional conflict in healthy participants by Hassel, Stefanie, Sharma, Gulshan B., Alders, Gésine L., Davis, Andrew D., Arnott, Stephen R., Frey, Benicio N., Hall, Geoffrey B., Harris, Jacqueline K., Lam, Raymond W., Milev, Roumen, Müller, Daniel J., Rotzinger, Susan, Zamyadi, Mojdeh, Kennedy, Sidney H., Strother, Stephen C., MacQueen, Glenda M.

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Escitalopram ameliorates differences in neural activity between healthy comparison and major depressive disorder groups on an fMRI Emotional conflict task: A CAN-BIND-1 study by Alders, Gésine L., Davis, Andrew D., MacQueen, Glenda, Strother, Stephen C., Hassel, Stefanie, Zamyadi, Mojdeh, Sharma, Gulshan B., Arnott, Stephen R., Downar, Jonathan, Harris, Jacqueline K., Lam, Raymond W., Milev, Roumen, Müller, Daniel J., Ravindran, Arun, Kennedy, Sidney H., Frey, Benicio N., Minuzzi, Luciano, Hall, Geoffrey B.

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Mutations in TBL1X Are Associated With Central Hypothyroidism by Heinen, Charlotte A, Losekoot, Monique, Sun, Yu, Watson, Peter J, Fairall, Louise, Joustra, Sjoerd D, Zwaveling-Soonawala, Nitash, Oostdijk, Wilma, van den Akker, Erica L. T, Alders, Mariëlle, Santen, Gijs W. E, van Rijn, Rick R, Dreschler, Wouter A, Surovtseva, Olga V, Biermasz, Nienke R, Hennekam, Raoul C, Wit, Jan M, Schwabe, John W. R, Boelen, Anita, Fliers, Eric, van Trotsenburg, A. S. Paul

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Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations by Connaughton, Dervla M., Dai, Rufeng, Owen, Danielle J., Marquez, Jonathan, Mann, Nina, Graham-Paquin, Adda L., Nakayama, Makiko, Coyaud, Etienne, Laurent, Estelle M.N., St-Germain, Jonathan R., Blok, Lot Snijders, Vino, Arianna, Klämbt, Verena, Deutsch, Konstantin, Wu, Chen-Han Wilfred, Kolvenbach, Caroline M., Kause, Franziska, Ottlewski, Isabel, Schneider, Ronen, Kitzler, Thomas M., Majmundar, Amar J., Buerger, Florian, Onuchic-Whitford, Ana C., Youying, Mao, Kolb, Amy, Salmanullah, Daanya, Chen, Evan, van der Ven, Amelie T., Rao, Jia, Ityel, Hadas, Seltzsam, Steve, Rieke, Johanna M., Chen, Jing, Vivante, Asaf, Hwang, Daw-Yang, Kohl, Stefan, Dworschak, Gabriel C., Hermle, Tobias, Alders, Mariëlle, Bartolomaeus, Tobias, Bauer, Stuart B., Baum, Michelle A., Brilstra, Eva H., Challman, Thomas D., Zyskind, Jacob, Costin, Carrie E., Dipple, Katrina M., Duijkers, Floor A., Ferguson, Marcia, Fitzpatrick, David R., Fick, Roger, Glass, Ian A., Hulick, Peter J., Kline, Antonie D., Krey, Ilona, Kumar, Selvin, Lu, Weining, Marco, Elysa J., Wentzensen, Ingrid M., Mefford, Heather C., Platzer, Konrad, Povolotskaya, Inna S., Savatt, Juliann M., Shcherbakova, Natalia V., Senguttuvan, Prabha, Squire, Audrey E., Stein, Deborah R., Thiffault, Isabelle, Voinova, Victoria Y., Somers, Michael J.G., Ferguson, Michael A., Traum, Avram Z., Daouk, Ghaleb H., Daga, Ankana, Rodig, Nancy M., Terhal, Paulien A., van Binsbergen, Ellen, Eid, Loai A., Tasic, Velibor, Rasouly, Hila Milo, Lim, Tze Y., Ahram, Dina F., Gharavi, Ali G., Reutter, Heiko M., Rehm, Heidi L., MacArthur, Daniel G., Lek, Monkol, Laricchia, Kristen M., Lifton, Richard P., Xu, Hong, Mane, Shrikant M., Sanna-Cherchi, Simone, Sharrocks, Andrew D., Raught, Brian, Fisher, Simon E., Bouchard, Maxime, Khokha, Mustafa K., Shril, Shirlee, Hildebrandt, Friedhelm

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Evaluation of DNA Methylation Episignatures for Diagnosis and Phenotype Correlations in 42 Mendelian Neurodevelopmental Disorders by Aref-Eshghi, Erfan, Kerkhof, Jennifer, Pedro, Victor P., France, Groupe DI, Barat-Houari, Mouna, Ruiz-Pallares, Nathalie, Andrau, Jean-Christophe, Lacombe, Didier, Van-Gils, Julien, Fergelot, Patricia, Dubourg, Christéle, Cormier-Daire, Valerie, Rondeau, Sophie, Lecoquierre, François, Saugier-Veber, Pascale, Nicolas, Gaël, Lesca, Gaetan, Chatron, Nicolas, Sanlaville, Damien, Vitobello, Antonio, Faivre, Laurence, Thauvin-Robinet, Christel, Laumonnier, Frederic, Raynaud, Martine, Alders, Mariëlle, Mannens, Marcel, Henneman, Peter, Hennekam, Raoul C., Velasco, Guillaume, Francastel, Claire, Ulveling, Damien, Ciolfi, Andrea, Pizzi, Simone, Tartaglia, Marco, Heide, Solveig, Héron, Delphine, Mignot, Cyril, Keren, Boris, Whalen, Sandra, Afenjar, Alexandra, Bienvenu, Thierry, Campeau, Philippe M., Rousseau, Justine, Levy, Michael A., Brick, Lauren, Kozenko, Mariya, Balci, Tugce B., Siu, Victoria Mok, Stuart, Alan, Kadour, Mike, Masters, Jennifer, Takano, Kyoko, Kleefstra, Tjitske, de Leeuw, Nicole, Field, Michael, Shaw, Marie, Gecz, Jozef, Ainsworth, Peter J., Lin, Hanxin, Rodenhiser, David I., Friez, Michael J., Tedder, Matt, Lee, Jennifer A., DuPont, Barbara R., Stevenson, Roger E., Skinner, Steven A., Schwartz, Charles E., Genevieve, David, Sadikovic, Bekim

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Clinical relevance of Wilms tumor 1 gene mutations in childhood acute myeloid leukemia by Hollink, Iris H.I.M., van den Heuvel-Eibrink, Marry M., Zimmermann, Martin, Balgobind, Brian V., Arentsen-Peters, Susan T.C.J.M., Alders, Marielle, Willasch, Andre, Kaspers, Gertjan J.L., Trka, Jan, Baruchel, Andre, de Graaf, Siebold S.N., Creutzig, Ursula, Pieters, Rob, Reinhardt, Dirk, Zwaan, C. Michel

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Highly pathogenic avian influenza in Sekong province Lao PDR 2018 – Potential for improved surveillance and management by Annand, E., High, H., Wong, F., Phommachanh, P., Chanthavisouk, C., Happold, J., Dhingra, M., Eagles, D., Britton, P., Alders, R.

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Duration of second victim symptoms in the aftermath of a patient safety incident and association with the level of patient harm: a cross-sectional study in the Netherlands by Vanhaecht, Kris, Seys, Deborah, Schouten, Loes, Bruyneel, Luk, Coeckelberghs, Ellen, Panella, Massimiliano, Zeeman, Gerda

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International point prevalence study of Intensive Care Unit transfusion practices—Pilot study in the Netherlands by de Bruin, S., Alders, M.Y., van Bruggen, R., de Korte, D., Scheeren, T.W.L., Bakker, J., Aubron, C., Feldheiser, A., Meier, J., Cecconi, M., Vlaar, A.P.J., Antonelli, M., Dionne, J., Duranteau, J., Hunt, B., Lance, M., Müller, M., Murphy, G., Nielsen, N., Oczkowski, S., Perner, A., Schoechl, H., Walsh, T.

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SOX11 variants cause a neurodevelopmental disorder with infrequent ocular malformations and hypogonadotropic hypogonadism and with distinct DNA methylation profile by Al-Jawahiri, Reem, Foroutan, Aidin, McConkey, Haley, Levy, Michael, Haghshenas, Sadegheh, Rooney, Kathleen, Turner, Jasmin, Shears, Debbie, Holder, Muriel, Lefroy, Henrietta, Castle, Bruce, Reis, Linda M., Semina, Elena V., Nickerson, Deborah, Bamshad, Michael, Leal, Suzanne, Lachlan, Katherine, Chandler, Kate, Clayton-Smith, Jill, Hug, Franziska Phan, Pitteloud, Nelly, Bartoloni, Lucia, Hoffjan, Sabine, Park, Soo-Mi, Thankamony, Ajay, Lees, Melissa, Wakeling, Emma, Naik, Swati, Hanker, Britta, Girisha, Katta M., Agolini, Emanuele, Giuseppe, Zampino, Alban, Ziegler, Tessarech, Marine, Keren, Boris, Afenjar, Alexandra, Zweier, Christiane, Smol, Thomas, Nobuhiko, Okamoto, Sekiguchi, Futoshi, Tsuchida, Naomi, Matsumoto, Naomichi, Kou, Ikuyo, Yonezawa, Yoshiro, Ikegawa, Shiro, Callewaert, Bert, Ambrose, John C., Arumugam, Prabhu, Bleda, Marta, Boardman-Pretty, Freya, Boustred, Christopher R., Brittain, Helen, Caulfield, Mark J., Chan, Georgia C., Fowler, Tom, Giess, Adam, Hamblin, Angela, Henderson, Shirley, Hubbard, Tim J.P., Jones, Louise J., Kasperaviciute, Dalia, Kayikci, Melis, Kousathanas, Athanasios, Lahnstein, Lea, Leigh, Sarah E.A., Leong, Ivonne U.S., Lopez, Javier F., FionaMaleady-Crowe, McEntagart, Meriel, Minneci, Federico, Moutsianas, Loukas, Mueller, Michael, Murugaesu, Nirupa, Need, Anna C., Odhams, Chris A., Patch, Christine, Perez-Gil, Daniel, Pullinger, John, Rendon, Augusto, TimRogers, Savage, Kevin, Sawant, Kushmita, Scott, Richard H., Siddiq, Afshan, Sieghart, Alexander, Smith, Samuel C., Sosinsky, Alona, Stuckey, Alexander, Tanguy, Mélanie, Taylor Tavares, Ana Lisa, Thomas, Ellen R.A., Thompson, Simon R., Tucci, Arianna, Williams, Eleanor, Kleinendorst, Lotte, Donaldson, Alan, Alders, Marielle, De Paepe, Anne, Sadikovic, Bekim, McNeill, Alisdair

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Species-area relationships are modulated by trophic rank, habitat affinity, and dispersal ability by van Noordwijk, C. G. E. (Toos), Verberk, Wilco C. E. P., Turin, Hans, Heijerman, Theodoor, Alders, Kees, Dekoninck, Wouter, Hannig, Karsten, Regan, Eugenie, McCormack, Stephen, Brown, Mark J. F., Remke, Eva, Siepel, Henk, Berg, Matty P., Bonte, Dries

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Two cases of severe neonatal hypertrophic cardiomyopathy caused by compound heterozygous mutations in the MYBPC3 gene by Lekanne Deprez, R H, Muurling-Vlietman, J J, Hruda, J, Baars, M J H, Wijnaendts, L C D, Stolte-Dijkstra, I, Alders, M, van Hagen, J M

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