Deconstructing surgical education-teacher quality really matters : Implications for attracting medical students to surgical careers von EHRLICH, Peter F, SEIDMAN, P. A

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Anaesthetic complications of acromegaly von Seidman, P A, Kofke, W A, Policare, R, Young, M

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Monitoring intraoperative effectiveness of caudal analgesia through skin temperature variation von Ehrlich, P.F., Vedulla, G., Cottrell, N., Seidman, P.A.

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Sharps disposal in the operating room : Current clinical practices and costs von SEIDMAN, P. A, PARKER, B. M

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Successful Intraoperative Spinal Cord Monitoring During Scoliosis Surgery Using a Total Intravenous Anesthetic Regimen Including Dexmedetomidine von Anschel, David J, Aherne, Andrew, Soto, Roy G, Carrion, Wesley, Hoegerl, Carl, Nori, Palgun, Seidman, Peggy A

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Complications of pediatric trauma: effects on pediatric trauma anesthesia von Cottrell, D J, Seidman, P A

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Monitoring intraoperative effectiveness of caudal analgesia through skin temperature variation. Discussion von EHRLICH, P. F, VEDULLA, G, COTTRELL, N, SEIDMAN, P. A

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Anawsthetic complications of acromegaly von Seidman, P A, Kofke, W A, Policare, R, Young, M

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Stress Profiles and Their Implications for Intervention von Franco, Kathleen N., Tamburrino, Marijo B., Carroll, Brendan, Seidman, Peggy A., Evans, Cynthia L.

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Anaesthetic Complications of Acromegaly von SEIDMAN, P. A., KOFKE, W. A., POLICARE, R., YOUNG, M.

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Glycogen Storage Diseases Presenting as Hypertrophic Cardiomyopathy von Arad, Michael, Maron, Barry J, Gorham, Joshua M, Johnson, Walter H, Saul, J. Philip, Perez-Atayde, Antonio R, Spirito, Paolo, Wright, Gregory B, Kanter, Ronald J, Seidman, J.G, Seidman, Christine E

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Genetic and Phenotypic Landscape of Peripartum Cardiomyopathy von Goli, Rahul, Li, Jian, Brandimarto, Jeff, Levine, Lisa D., Riis, Valerie, McAfee, Quentin, DePalma, Steven, Haghighi, Alireza, Seidman, J. G., Seidman, Christine E., Jacoby, Daniel, Macones, George, Judge, Daniel P., Rana, Sarosh, Margulies, Kenneth B., Cappola, Thomas P., Alharethi, Rami, Damp, Julie, Hsich, Eileen, Elkayam, Uri, Sheppard, Richard, Alexis, Jeffrey D., Boehmer, John, Kamiya, Chizuko, Gustafsson, Finn, Damm, Peter, Ersbøll, Anne S., Goland, Sorel, Hilfiker-Kleiner, Denise, McNamara, Dennis M., Arany, Zolt

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Mutations in Sarcomere Protein Genes as a Cause of Dilated Cardiomyopathy von Kamisago, Mitsuhiro, Sharma, Pankaj, Sharma, Sapna D, DePalma, Steven R, Solomon, Scott, McDonough, Barbara, Smoot, Leslie, Mullen, Mary P, Woolf, Paul K, Wigle, E. Douglas, Seidman, Christine E, Seidman, J.G, Jarcho, John, Shapiro, Lawrence R

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Dilated Cardiomyopathy and Heart Failure Caused by a Mutation in Phospholamban von Schmitt, Joachim P., Kamisago, Mitsuhiro, Asahi, Michio, Li, Guo Hua, Ahmad, Ferhaan, Mende, Ulrike, Kranias, Evangelia G., MacLennan, David H., Seidman, J. G., Seidman, Christine E.

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Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes von Flannick, Jason, Beer, Nicola L, Bick, Alexander G, Agarwala, Vineeta, Molnes, Janne, Gupta, Namrata, Burtt, Noël P, Florez, Jose C, Meigs, James B, Taylor, Herman, Lyssenko, Valeriya, Irgens, Henrik, Fox, Ervin, Burslem, Frank, Johansson, Stefan, Brosnan, M Julia, Trimmer, Jeff K, Newton-Cheh, Christopher, Tuomi, Tiinamaija, Molven, Anders, Wilson, James G, O'Donnell, Christopher J, Kathiresan, Sekar, Hirschhorn, Joel N, Njølstad, Pål R, Rolph, Tim, Seidman, J G, Gabriel, Stacey, Cox, David R, Seidman, Christine E, Groop, Leif, Altshuler, David

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Genome sequencing as a first-line genetic test in familial dilated cardiomyopathy von Minoche, Andre E., Horvat, Claire, Johnson, Renee, Gayevskiy, Velimir, Morton, Sarah U., Drew, Alexander P., Woo, Kerhan, Statham, Aaron L., Lundie, Ben, Bagnall, Richard D., Ingles, Jodie, Semsarian, Christopher, Seidman, J. G., Seidman, Christine E., Dinger, Marcel E., Cowley, Mark J., Fatkin, Diane

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Paternal-age-related de novo mutations and risk for five disorders von Taylor, Jacob L., Debost, Jean-Christophe P. G., Morton, Sarah U., Wigdor, Emilie M., Heyne, Henrike O., Lal, Dennis, Howrigan, Daniel P., Bloemendal, Alex, Larsen, Janne T., Kosmicki, Jack A., Weiner, Daniel J., Homsy, Jason, Seidman, Jonathan G., Seidman, Christine E., Agerbo, Esben, McGrath, John J., Mortensen, Preben Bo, Petersen, Liselotte, Daly, Mark J., Robinson, Elise B.

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A common genetic variant within SCN10A modulates cardiac SCN5A expression von van den Boogaard, Malou, Smemo, Scott, Burnicka-Turek, Ozanna, Arnolds, David E, van de Werken, Harmen J G, Klous, Petra, McKean, David, Muehlschlegel, Jochen D, Moosmann, Julia, Toka, Okan, Yang, Xinan H, Koopmann, Tamara T, Adriaens, Michiel E, Bezzina, Connie R, de Laat, Wouter, Seidman, Christine, Seidman, J G, Christoffels, Vincent M, Nobrega, Marcelo A, Barnett, Phil, Moskowitz, Ivan P

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Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy von Esslinger, Ulrike, Garnier, Sophie, Korniat, Agathe, Proust, Carole, Kararigas, Georgios, Müller-Nurasyid, Martina, Empana, Jean-Philippe, Morley, Michael P, Perret, Claire, Stark, Klaus, Bick, Alexander G, Prasad, Sanjay K, Kriebel, Jennifer, Li, Jin, Tiret, Laurence, Strauch, Konstantin, O'Regan, Declan P, Marguiles, Kenneth B, Seidman, Jonathan G, Boutouyrie, Pierre, Lacolley, Patrick, Jouven, Xavier, Hengstenberg, Christian, Komajda, Michel, Hakonarson, Hakon, Isnard, Richard, Arbustini, Eloisa, Grallert, Harald, Cook, Stuart A, Seidman, Christine E, Regitz-Zagrosek, Vera, Cappola, Thomas P, Charron, Philippe, Cambien, François, Villard, Eric

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Transgenic mice overexpressing mutant PRKAG2 define the cause of wolff-parkinson-white syndrome in glycogen storage cardiomyopathy von ARAD, Michael, MOSKOWITZ, Ivan P, STAPLETON, David, SCHMITT, Joachim P, GUO, X. X, PIZARD, Anne, KUPERSHMIDT, Sabina, RODEN, Dan M, BERUL, Charles I, SEIDMAN, Christine E, SEIDMAN, J. G, PATEL, Vickas V, AHMAD, Ferhaan, PEREZ-ATAYDE, Antonio R, SAWYER, Douglas B, WALTER, Mark, LI, Guo H, BURGON, Patrick G, MAGUIRE, Colin T

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