Smoking-induced coronary vasoconstriction in patients with atherosclerotic coronary artery disease: evidence for adrenergically mediated alterations in coronary artery tone von WINNIFORD, M. D, WHEELAN, K. R, KREMERS, M. S, UGOLINI, V, VAN DEN BERG, E, NIGGEMANN, E. H, JANSEN, D. E, HILLIS, L. D

Volltext

Reversible segmental left ventricular dysfunction after coronary angioplasty von VAN DEN BERG, E. K, POPMA, J. J, DEHMER, G. J, SNOW, F. R, LEWIS, S. A, VETROVEC, G. W, NIXON, J. V

Volltext

Plasma Serotonin Concentrations: Validation of a Sampling Technique Using Long Catheters von Van Den Berg, Egerton K., Schmitz, James M., Benedict, Claude R., Prewitt, Jacquin B., Malloy, Craig R., Willerson, James T., Dehmer, Gregory J.

Volltext

Measurement of cardiac output without right heart catheterization: reliability, advantages, and limitations of a left-sided indicator dilution technique von VAN DEN BERG, E. JR, PACIFICO, A, LANGE, R. A, WHEELAN, K. R, WINNIFORD, M. D, HILLIS, L. D

Volltext

Cisplatin-induced changes in sodium, chloride, and urea transport by the frog skin von van den berg, Egerton K., Brazy, Peter C., Huang, Andrew T., Dennis, Vincent W.

Volltext

Mutations in the profilin 1 gene cause familial amyotrophic lateral sclerosis von Wu, Chi-Hong, Fallini, Claudia, Ticozzi, Nicola, Keagle, Pamela J., Sapp, Peter C., Piotrowska, Katarzyna, Lowe, Patrick, Koppers, Max, McKenna-Yasek, Diane, Baron, Desiree M., Kost, Jason E., Gonzalez-Perez, Paloma, Fox, Andrew D., Adams, Jenni, Taroni, Franco, Tiloca, Cinzia, Leclerc, Ashley Lyn, Chafe, Shawn C., Mangroo, Dev, Moore, Melissa J., Zitzewitz, Jill A., Xu, Zuo-Shang, van den Berg, Leonard H., Glass, Jonathan D., Siciliano, Gabriele, Cirulli, Elizabeth T., Goldstein, David B., Salachas, Francois, Meininger, Vincent, Rossoll, Wilfried, Ratti, Antonia, Gellera, Cinzia, Bosco, Daryl A., Bassell, Gary J., Silani, Vincenzo, Drory, Vivian E., Brown Jr, Robert H., Landers, John E.

Volltext

X-ray structure of a protein-conducting channel von Berg, Bert van den, Clemons, William M., Collinson, Ian, Modis, Yorgo, Hartmann, Enno, Harrison, Stephen C., Rapoport, Tom A.

Volltext

Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degeneration von Simpson, Claire L., Lemmens, Robin, Miskiewicz, Katarzyna, Broom, Wendy J., Hansen, Valerie K., van Vught, Paul W.J., Landers, John E., Sapp, Peter, Van Den Bosch, Ludo, Knight, Joanne, Neale, Benjamin M., Turner, Martin R., Veldink, Jan H., Ophoff, Roel A., Tripathi, Vineeta B., Beleza, Ana, Shah, Meera N., Proitsi, Petroula, Van Hoecke, Annelies, Carmeliet, Peter, Horvitz, H. Robert, Leigh, P. Nigel, Shaw, Christopher E., van den Berg, Leonard H., Sham, Pak C., Powell, John F., Verstreken, Patrik, Brown, Robert H., Robberecht, Wim, Al-Chalabi, Ammar

Volltext

C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: A genome-wide meta-analysis von Diekstra, Frank P., Van Deerlin, Vivianna M., van Swieten, John C., Al-Chalabi, Ammar, Ludolph, Albert C., Weishaupt, Jochen H., Hardiman, Orla, Landers, John E., Brown Jr, Robert H., van Es, Michael A., Pasterkamp, R. Jeroen, Koppers, Max, Andersen, Peter M., Estrada, Karol, Rivadeneira, Fernando, Hofman, Albert, Uitterlinden, André G., van Damme, Philip, Melki, Judith, Meininger, Vincent, Shatunov, Aleksey, Shaw, Christopher E., Leigh, P. Nigel, Shaw, Pamela J., Morrison, Karen E., Fogh, Isabella, Chiò, Adriano, Traynor, Bryan J., Czell, David, Weber, Markus, Heutink, Peter, de Bakker, Paul I. W., Silani, Vincenzo, Robberecht, Wim, van den Berg, Leonard H., Veldink, Jan H.

Volltext

Age is the main determinant of COVID-19 related in-hospital mortality with minimal impact of pre-existing comorbidities, a retrospective cohort study von Henkens, M T H M, Raafs, A G, Verdonschot, J A J, Linschoten, M, van Smeden, M, Wang, P, van der Hooft, B H M, Tieleman, R, Janssen, M L F, Ter Bekke, R M A, Hazebroek, M R, van der Horst, I C C, Asselbergs, F W, Magdelijns, F J H, Heymans, S R B

Volltext

Exome-wide Rare Variant Analysis Identifies TUBA4A Mutations Associated with Familial ALS von Smith, Bradley N., Ticozzi, Nicola, Fallini, Claudia, Gkazi, Athina Soragia, Topp, Simon, Kenna, Kevin P., Scotter, Emma L., Kost, Jason, Keagle, Pamela, Miller, Jack W., Calini, Daniela, Vance, Caroline, Danielson, Eric W., Troakes, Claire, Tiloca, Cinzia, Al-Sarraj, Safa, Lewis, Elizabeth A., King, Andrew, Colombrita, Claudia, Pensato, Viviana, Castellotti, Barbara, de Belleroche, Jacqueline, Baas, Frank, ten Asbroek, Anneloor LMA, Sapp, Peter C., McKenna-Yasek, Diane, McLaughlin, Russell L., Polak, Meraida, Asress, Seneshaw, Esteban-Pérez, Jesús, Muñoz-Blanco, José Luis, Simpson, Michael, D’Alfonso, Sandra, Mazzini, Letizia, Comi, Giacomo P., Del Bo, Roberto, Ceroni, Mauro, Gagliardi, Stella, Querin, Giorgia, Bertolin, Cinzia, van Rheenen, Wouter, Diekstra, Frank P., Lauria, Giuseppe, Duga, Stefano, Corti, Stefania, Cereda, Cristina, Corrado, Lucia, Sorarù, Gianni, Morrison, Karen E., Williams, Kelly L., Nicholson, Garth A., Blair, Ian P., Dion, Patrick A., Leblond, Claire S., Rouleau, Guy A., Hardiman, Orla, Veldink, Jan H., van den Berg, Leonard H., Al-Chalabi, Ammar, Pall, Hardev, Shaw, Pamela J., Turner, Martin R., Talbot, Kevin, Taroni, Franco, García-Redondo, Alberto, Wu, Zheyang, Glass, Jonathan D., Gellera, Cinzia, Ratti, Antonia, Brown, Robert H., Silani, Vincenzo, Shaw, Christopher E., Landers, John E.

Volltext

The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder von Smith, Bradley N, Newhouse, Stephen, Shatunov, Aleksey, Vance, Caroline, Topp, Simon, Johnson, Lauren, Miller, Jack, Lee, Younbok, Troakes, Claire, Scott, Kirsten M, Jones, Ashley, Gray, Ian, Wright, Jamie, Hortobágyi, Tibor, Al-Sarraj, Safa, Rogelj, Boris, Powell, John, Lupton, Michelle, Lovestone, Simon, Sapp, Peter C, Weber, Markus, Nestor, Peter J, Schelhaas, Helenius J, Asbroek, Anneloor Alm Ten, Silani, Vincenzo, Gellera, Cinzia, Taroni, Franco, Ticozzi, Nicola, Van den Berg, Leonard, Veldink, Jan, Van Damme, Phillip, Robberecht, Wim, Shaw, Pamela J, Kirby, Janine, Pall, Hardev, Morrison, Karen E, Morris, Alex, de Belleroche, Jacqueline, Vianney de Jong, J M B, Baas, Frank, Andersen, Peter M, Landers, John, Brown, Jr, Robert H, Weale, Michael E, Al-Chalabi, Ammar, Shaw, Christopher E

Volltext

Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS von Diekstra, Frank P, Saris, Christiaan G J, van Rheenen, Wouter, Franke, Lude, Jansen, Ritsert C, van Es, Michael A, van Vught, Paul W J, Blauw, Hylke M, Groen, Ewout J N, Horvath, Steve, Estrada, Karol, Rivadeneira, Fernando, Hofman, Albert, Uitterlinden, Andre G, Robberecht, Wim, Andersen, Peter M, Melki, Judith, Meininger, Vincent, Hardiman, Orla, Landers, John E, Brown, Jr, Robert H, Shatunov, Aleksey, Shaw, Christopher E, Leigh, P Nigel, Al-Chalabi, Ammar, Ophoff, Roel A, van den Berg, Leonard H, Veldink, Jan H

Volltext

Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis von van Es, Michael A., Schelhaas, Helenius J., van Vught, Paul W. J., Ticozzi, Nicola, Andersen, Peter M., Groen, Ewout J. N., Schulte, Claudia, Blauw, Hylke M., Koppers, Max, Diekstra, Frank P., Fumoto, Katsumi, LeClerc, Ashley Lyn, Keagle, Pamela, Bloem, Bastiaan R., Scheffer, Hans, van Nuenen, Bart F. L., van Blitterswijk, Marka, van Rheenen, Wouter, Wills, Anne-Marie, Lowe, Patrick P., Hu, Guo-fu, Yu, Wenhao, Kishikawa, Hiroko, Wu, David, Folkerth, Rebecca D., Mariani, Claudio, Goldwurm, Stefano, Pezzoli, Gianni, Van Damme, Philip, Lemmens, Robin, Dahlberg, Caroline, Birve, Anna, Fernández-Santiago, Rubén, Waibel, Stefan, Klein, Christine, Weber, Markus, van der Kooi, Anneke J., de Visser, Marianne, Verbaan, Dagmar, van Hilten, Jacobus J., Heutink, Peter, Hennekam, Eric A. M., Cuppen, Edwin, Berg, Daniela, Brown Jr, Robert H., Silani, Vincenzo, Gasser, Thomas, Ludolph, Albert C., Robberecht, Wim, Ophoff, Roel A., Veldink, Jan H., Pasterkamp, R. Jeroen, de Bakker, Paul I. W., Landers, John E., van de Warrenburg, Bart P., van den Berg, Leonard H.

Volltext

A large-scale international meta-analysis of paraoxonase gene polymorphisms in sporadic ALS von WILLS, A.-M, CRONIN, S, ROULEAU, G. A, FISHER, E. M. C, SHAW, P. J, MORRISON, K. E, PAMPHLETT, R, VAN DEN BERG, L. H, FIGLEWICZ, D. A, ANDERSEN, P. M, AL-CHALABI, A, HARDIMAN, O, SLOWIK, A, PURCELL, S, LANDERS, J. E, BROWN, Rh, KASPERAVICIUTE, D, VAN ES, M. A, MORAHAN, J. M, VALDMANIS, P. N, MEININGER, V, MELKI, J, SHAW, C. E

Volltext

A meta-analysis of Hodgkin lymphoma reveals 19p13.3 TCF3 as a novel susceptibility locus von Cozen, W., Timofeeva, M. N., Li, D., Diepstra, A., Hazelett, D., Delahaye-Sourdeix, M., Edlund, C. K., Franke, L., Rostgaard, K., Van Den Berg, D. J., Cortessis, V. K., Smedby, K. E., Glaser, S. L., Westra, H.-J., Robison, L. L., Mack, T. M., Ghesquieres, H., Hwang, A. E., Nieters, A., de Sanjose, S., Lightfoot, T., Becker, N., Maynadie, M., Foretova, L., Roman, E., Benavente, Y., Rand, K. A., Nathwani, B. N., Glimelius, B., Staines, A., Boffetta, P., Link, B. K., Kiemeney, L., Ansell, S. M., Bhatia, S., Strong, L. C., Galan, P., Vatten, L., Habermann, T. M., Duell, E. J., Lake, A., Veenstra, R. N., Visser, L., Liu, Y., Urayama, K. Y., Montgomery, D., Gaborieau, V., Weiss, L. M., Byrnes, G., Lathrop, M., Cocco, P., Best, T., Skol, A. D., Adami, H.-O., Melbye, M., Cerhan, J. R., Gallagher, A., Taylor, G. M., Slager, S. L., Brennan, P., Coetzee, G. A., Conti, D. V., Onel, K., Jarrett, R. F., Hjalgrim, H., van den Berg, A., McKay, J. D.

Volltext

Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study von Shatunov, Aleksey, PhD, Mok, Kin, MSc, Newhouse, Stephen, PhD, Weale, Michael E, PhD, Smith, Bradley, PhD, Vance, Caroline, PhD, Johnson, Lauren, PhD, Veldink, Jan H, MD, van Es, Michael A, MD, van den Berg, Leonard H, Prof, Robberecht, Wim, Prof, Van Damme, Philip, MD, Hardiman, Orla, Prof, Farmer, Anne E, Prof, Lewis, Cathryn M, Prof, Butler, Amy W, PhD, Abel, Olubunmi, MSc, Andersen, Peter M, Prof, Fogh, Isabella, PhD, Silani, Vincenzo, Prof, Chiò, Adriano, MD, Traynor, Bryan J, MD, Melki, Judith, Prof, Meininger, Vincent, Prof, Landers, John E, PhD, McGuffin, Peter, Prof, Glass, Jonathan D, MD, Pall, Hardev, MD, Leigh, P Nigel, Prof, Hardy, John, Prof, Brown, Robert H, Prof, Powell, John F, DPhil, Orrell, Richard W, MD, Morrison, Karen E, Prof, Shaw, Pamela J, Prof, Shaw, Christopher E, Prof, Al-Chalabi, Ammar, Prof

Volltext

Comprehensive molecular characterization of urothelial bladder carcinoma von Weinstein, John N, Akbani, Rehan, Broom, Bradley M, Wang, Wenyi, Verhaak, Roeland G. W, McConkey, David

Volltext

fMRI Activities in the Emotional Cerebellum: A Preference for Negative Stimuli and Goal-Directed Behavior von Schraa-Tam, Caroline K. L., Rietdijk, Willem J. R., Verbeke, Willem J. M. I., Dietvorst, Roeland C., van den Berg, Wouter E., Bagozzi, Richard P., De Zeeuw, Chris I.

Volltext

Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis von Dewan, Ramita, Keagle, Pamela, Bacikova, Dagmar, Soltis, Anthony R., Kost, Jason, Colombrita, Claudia, Lewis, Elizabeth A., Pensato, Viviana, Castellotti, Barbara, McLaughlin, Russell L., Comi, Giacomo P., Ceroni, Mauro, Gagliardi, Stella, van Blitterswijk, Marka, Corrado, Lucia, Sorarù, Gianni, Williams, Kelly L., Morrison, Karen E., Veldink, Jan H., Brown, Robert H., Ambrose, John C., Brittain, H., Elgar, Greg, Halai, Dina, Holman, James E., Jackson, Rob, Leong, Ivonne U.S., Maleady-Crowe, Fiona, Mason, Joanne, Riesgo-Ferreiro, Pablo, Rogers, Tim, Watters, Sarah A., Arepalli, Sampath, Chiò, Adriano, Dunckley, Travis L., Faghri, Faraz, Feldman, Eva, Floeter, Mary Kay, Gerhard, Glenn, Jansson, Lilja, Kirby, Janine, Mora, Gabriele, Nalls, Mike A., Pulst, Stefan M., Ravits, John M., Renton, Alan E., Robberecht, Wim, Robey, Ian, Dols-Icardo, Oriol, Illán-Gala, Ignacio, Lleó, Alberto, Khoshnood, Behzad, Sorbi, Sandro, Pastor, Pau, Bigio, Eileen H., Black, Sandra E., Brunetti, Maura, Canosa, Antonio, Gan-Or, Ziv, Goate, Alison, Hupalo, Daniel, Infante, Jon, Kaufmann, Horacio, Kim, Ronald C., Krüger, Rejko, Logroscino, Giancarlo, Love, Seth, Mao, Qinwen, Masliah, Eliezer, Pletnikova, Olga, Reynolds, Regina H., Scherzer, Clemens R., Serrano, Geidy E., Xiromerisiou, Georgia, Phatnani, Hemali, Kwan, Justin, Broach, James R., Arcila-Londono, Ximena, Malaspina, Andrea, Thompson, Leslie M., Dardiotis, Efthimios, Chandran, Siddharthan, Butovsky, Oleg, Dubnau, Joshua, Harms, Matt, Poss, Mary, Phillips-Cremins, Jennifer, Altschuler, Steven, Hu, Michele T.M., Leigh, P. Nigel, Massey, Luke A., Pavese, Nicola, Vaughan, Jenny, Rowe, James B., Ghidoni, Roberta, Ryten, Mina, Tanaka, Toshiko, Ferrucci, Luigi, Vonsattel, Jean Paul, Landers, John E.

Volltext