A Common Polymorphism in SCN5A is Associated with Lone Atrial Fibrillation von Chen, LY, Ballew, JD, Herron, KJ, Rodeheffer, RJ, Olson, TM

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Cardiac troponin T mutation in familial cardiomyopathy with variable remodeling and restrictive physiology von Menon, SC, Michels, VV, Pellikka, PA, Ballew, JD, Karst, ML, Herron, KJ, Nelson, SM, Rodeheffer, RJ, Olson, TM

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Altered expression of glomerular heat shock protein 27 in experimental nephrotic syndrome von Smoyer, W E, Gupta, A, Mundel, P, Ballew, J D, Welsh, M J

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Sodium Channel Mutations and Susceptibility to Heart Failure and Atrial Fibrillation von Olson, Timothy M, Michels, Virginia V, Ballew, Jeffrey D, Reyna, Sandra P, Karst, Margaret L, Herron, Kathleen J, Horton, Steven C, Rodeheffer, Richard J, Anderson, Jeffrey L

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Familial atrial fibrillation is a genetically heterogeneous disorder von Darbar, Dawood, Herron, Kathleen J, Ballew, Jeffrey D, Jahangir, Arshad, Gersh, Bernard J, Shen, Win-K, Hammill, Stephen C, Packer, Douglas L, Olson, Timothy M

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ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic K ATP channel gating von Terzic, Andre, Bienengraeber, Martin, Olson, Timothy M, Selivanov, Vitaliy A, Kathmann, Eva C, O'Cochlain, Fearghas, Gao, Fan, Karger, Amy B, Ballew, Jeffrey D, Hodgson, Denice M, Zingman, Leonid V, Pang, Yuan-Ping, Alekseev, Alexey E

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von Willebrand disease in the RIIIS/J mouse is caused by a defect outside of the von Willebrand factor gene von Nichols, W C, Cooney, K A, Mohlke, K L, Ballew, J D, Yang, A, Bruck, M E, Reddington, M, Novak, E K, Swank, R T, Ginsburg, D

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Procalcitonin Test in the Diagnosis of Bacteremia: A Meta-analysis von Jones, Alan E., MD, Fiechtl, James F., MD, Brown, Michael D., MD, Ballew, Jason J., MD, Kline, Jeffrey A., MD

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von Willebrand disease in the RIIIS/J mouse is caused by a defect outside of the von Willebrand factor gene von Nichols, W C, Cooney, K A, Mohlke, K L, Ballew, J D, Yang, A, Bruck, M E, Reddington, M, Novak, E K, Swank, R T, Ginsburg, D

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A common polymorphism in SCN5A is associated with lone atrial fibrillation. Commentary von CARLQUIST, J. F, ANDERSON, J. L, CHEN, L. Y, BALLEW, J. D, HERRON, K. J, RODEHEFFER, R. J, OLSON, T. M

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ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic K sub(ATP) channel gating von Bienengraeber, M, Olson, T M, Selivanov, V A, Kathmann, E C, O'Cochlain, F, Gao, F, Karger, AB, Ballew, J D, Hodgson, D M, Zingman, LV, Pang, Y-P, Alekseev, A E, Terzic, A

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von Willebrand disease in the RIIIS/J mouse is caused by a defect outside of the von Willebrand factor gene [published erratum appears in Blood 1995 Sep 15;86(6):2461] von Nichols, WC, Cooney, KA, Mohlke, KL, Ballew, JD, Yang, A, Bruck, ME, Reddington, M, Novak, EK, Swank, RT, Ginsburg, D

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von Willebrand disease in the RIIS/J mouse is caused by a defect outside of the von Willebrand factor gene von NICHOLS, W. C, COONEY, K. A, MOHLKE, K. L, BALLEW, J. D, YANG, A, BRUCK, M. E, REDDINGTON, M, NOVAK, E. K, SWANK, R. T, GINSBURG, D

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Evaluating Glomerular Filtration Rate Slope as a Surrogate End Point for ESKD in Clinical Trials: An Individual Participant Meta-Analysis of Observational Data von Grams, Morgan E, Sang, Yingying, Ballew, Shoshana H, Matsushita, Kunihiro, Astor, Brad C, Carrero, Juan Jesus, Chang, Alex R, Inker, Lesley A, Kenealy, Timothy, Kovesdy, Csaba P, Lee, Brian J, Levin, Adeera, Naimark, David, Pena, Michelle J, Schold, Jesse D, Shalev, Varda, Wetzels, Jack F M, Woodward, Mark, Gansevoort, Ron T, Levey, Andrew S, Coresh, Josef

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New Creatinine- and Cystatin C–Based Equations to Estimate GFR without Race von Inker, Lesley A, Eneanya, Nwamaka D, Coresh, Josef, Tighiouart, Hocine, Wang, Dan, Sang, Yingying, Crews, Deidra C, Doria, Alessandro, Estrella, Michelle M, Froissart, Marc, Grams, Morgan E, Greene, Tom, Grubb, Anders, Gudnason, Vilmundur, Gutiérrez, Orlando M, Kalil, Roberto, Karger, Amy B, Mauer, Michael, Navis, Gerjan, Nelson, Robert G, Poggio, Emilio D, Rodby, Roger, Rossing, Peter, Rule, Andrew D, Selvin, Elizabeth, Seegmiller, Jesse C, Shlipak, Michael G, Torres, Vicente E, Yang, Wei, Ballew, Shoshana H, Couture, Sara J, Powe, Neil R, Levey, Andrew S

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Decline in Estimated Glomerular Filtration Rate and Subsequent Risk of End-Stage Renal Disease and Mortality von Coresh, Josef, Turin, Tanvir Chowdhury, Matsushita, Kunihiro, Sang, Yingying, Ballew, Shoshana H, Appel, Lawrence J, Arima, Hisatomi, Chadban, Steven J, Cirillo, Massimo, Djurdjev, Ognjenka, Green, Jamie A, Heine, Gunnar H, Inker, Lesley A, Irie, Fujiko, Ishani, Areef, Ix, Joachim H, Kovesdy, Csaba P, Marks, Angharad, Ohkubo, Takayoshi, Shalev, Varda, Shankar, Anoop, Wen, Chi Pang, de Jong, Paul E, Iseki, Kunitoshi, Stengel, Benedicte, Gansevoort, Ron T, Levey, Andrew S

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Predicting timing of clinical outcomes in patients with chronic kidney disease and severely decreased glomerular filtration rate von Grams, Morgan E., Sang, Yingying, Ballew, Shoshana H., Carrero, Juan Jesus, Djurdjev, Ognjenka, Heerspink, Hiddo J.L., Ho, Kevin, Ito, Sadayoshi, Marks, Angharad, Naimark, David, Nash, Danielle M., Navaneethan, Sankar D., Sarnak, Mark, Stengel, Benedicte, Visseren, Frank L.J., Wang, Angela Yee-Moon, Köttgen, Anna, Levey, Andrew S., Woodward, Mark, Eckardt, Kai-Uwe, Hemmelgarn, Brenda, Coresh, Josef

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Hoyeraal-Hreidarsson syndrome caused by a germline mutation in the TEL patch of the telomere protein TPP1 von Kocak, Hande, Ballew, Bari J, Bisht, Kamlesh, Eggebeen, Rebecca, Hicks, Belynda D, Suman, Shalabh, O'Neil, Adri, Giri, Neelam, Maillard, Ivan, Alter, Blanche P, Keegan, Catherine E, Nandakumar, Jayakrishnan, Savage, Sharon A

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A Meta-analysis of the Association of Estimated GFR, Albuminuria, Age, Race, and Sex With Acute Kidney Injury von Grams, Morgan E., MD, PhD, Sang, Yingying, MS, Ballew, Shoshana H., PhD, Gansevoort, Ron T., MD, PhD, Kimm, Heejin, MD, PhD, Kovesdy, Csaba P., MD, Naimark, David, MD, MSc, Oien, Cecilia, MD, PhD, Smith, David H., RPh, PhD, Coresh, Josef, MD, PhD, Sarnak, Mark J., MD, MS, Stengel, Benedicte, MD, Tonelli, Marcello, MD, SM

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Past Decline Versus Current eGFR and Subsequent ESRD Risk von Kovesdy, Csaba P, Coresh, Josef, Ballew, Shoshana H, Woodward, Mark, Levin, Adeera, Naimark, David M J, Nally, Joseph, Rothenbacher, Dietrich, Stengel, Benedicte, Iseki, Kunitoshi, Matsushita, Kunihiro, Levey, Andrew S

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