Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Evan, Kransdorf"'
Publikováno v:
JACC: Case Reports, Vol 14, Iss , Pp 101825- (2023)
We present 3 heart transplant recipients who developed hypertrophic cardiomyopathy years after transplantation. In all 3 cases, the diagnosis was initially made based on echocardiography and confirmed using cardiac magnetic resonance imaging. (Level
Externí odkaz:
https://doaj.org/article/5fdf9687c4cb4657a093d0814dab945d
Autor:
Hanyu Ni, Elizabeth Jordan, Daniel D. Kinnamon, Jinwen Cao, Garrie J. Haas, Mark Hofmeyer, Evan Kransdorf, Gregory A. Ewald, Alanna A. Morris, Anjali Owens, Brian Lowes, Douglas Stoller, W.H. Wilson Tang, Sonia Garg, Barry H. Trachtenberg, Palak Shah, Salpy V. Pamboukian, Nancy K. Sweitzer, Matthew T. Wheeler, Jane E. Wilcox, Stuart Katz, Stephen Pan, Javier Jimenez, Daniel P. Fishbein, Frank Smart, Jessica Wang, Stephen S. Gottlieb, Daniel P. Judge, Charles K. Moore, Gordon S. Huggins, Ray E. Hershberger
Publikováno v:
Journal of the American College of Cardiology. 81:2059-2071
Autor:
Morcos Atef Awad, Lawrence S. C. Czer, Dominic Emerson, Stanley Jordan, Michele A. De Robertis, James Mirocha, Evan Kransdorf, David H. Chang, Jignesh Patel, Michelle Kittleson, Danny Ramzy, Joshua S. Chung, J. Louis Cohen, Fardad Esmailian, Alfredo Trento, Jon A. Kobashigawa
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 8, Iss 4 (2019)
Background Combined heart and kidney transplantation (HKTx) is performed in patients with severe heart failure and advanced renal insufficiency. We analyzed the long‐term survival after HKTx, the influence of age and dialysis status, the rates of c
Externí odkaz:
https://doaj.org/article/dc61c9b1fecb46e680388602ffd4f8bf
Autor:
Guillaume Coutance, Jon A Kobashigawa, Evan Kransdorf, Alexandre Loupy, Eva Desiré, Michelle Kittleson, Jignesh K. Patel
Publikováno v:
The Journal of Heart and Lung Transplantation.
Autor:
Barry H. Trachtenberg, Javier Jimenez, Alanna A. Morris, Evan Kransdorf, Anjali Owens, Daniel P. Fishbein, Elizabeth Jordan, Daniel D. Kinnamon, Jonathan O. Mead, Gordon S. Huggins, Ray E. Hershberger, Garrie Haas, Daniel Fishbein, Stephen S. Gottlieb, Matthew T. Wheeler, Mark Hofmeyer, W. H. Wilson Tang, Anjali T. Owens, Charles K. Moore, Javier Jimenez Carcamo, Barry Trachtenberg, Nancy K. Sweitzer, Palak Shah, Brian Lowes, Douglas Stoller, Frank Smart, Jane Wilcox, Stuart Katz, Gregory A. Ewald, Keith D. Aaronson, Jessica J. Wang, Salpy Pamboukian, Daniel P. Judge, Evan P. Kransdorf, Sonia Garg, Patrice Desvigne-Nickens, James Troendle, Yi-Ping Fu, Lucia Hindorff
Publikováno v:
Genetics in Medicine. 24:1495-1502
The cardiac phenotype of hereditary transthyretin amyloidosis (hTTR) usually presents as a restrictive or hypertrophic cardiomyopathy, and, although rarely observed as dilated cardiomyopathy (DCM), TTR is routinely included in DCM genetic testing pan
Autor:
Marny Fedrigo, Gerald J Berry, Guillaume Coutance, Elaine F. Reed, Chieh Yu Lin, Alessia Giarraputo, Evan Kransdorf, Olivier Thaunat, Martin Goddard, Annalisa Angelini, Desley Neil, Patrick Bruneval, Jean-Paul Duong Van Huyen, Alexandre Loupy, Dylan Miller
Publikováno v:
SSRN Electronic Journal.
Autor:
Guillaume Coutance, Evan Kransdorf, Olivier Aubert, Guillaume Bonnet, Daniel Yoo, Philippe Rouvier, Jean-Paul Duong Van Huyen, Patrick Bruneval, Jean-Luc Taupin, Pascal Leprince, Shaida Varnous, Jon Kobashigawa, Xavier Jouven, Jignesh Patel, Alexandre Loupy
Publikováno v:
Circulation: Heart Failure. 15
Background: In heart transplantation, antibody-mediated rejection (AMR) is a major contributor to patient morbidity and mortality. Multiple routine endomyocardial biopsies (EMB) remain the gold standard to detect AMR, but this invasive procedure suff
Autor:
Morcos Awad, Lawrence S. C. Czer, Margaret Hou, Sarah S. Golshani, Michael Goltche, Michele De Robertis, Michelle Kittleson, Jignesh Patel, Babak Azarbal, Evan Kransdorf, Fardad Esmailian, Alfredo Trento, Jon A. Kobashigawa
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 5, Iss 11 (2016)
Externí odkaz:
https://doaj.org/article/49f8faad443548dcaf5ebb0ce30b6fe6
Autor:
Gordon S, Huggins, Daniel D, Kinnamon, Garrie J, Haas, Elizabeth, Jordan, Mark, Hofmeyer, Evan, Kransdorf, Gregory A, Ewald, Alanna A, Morris, Anjali, Owens, Brian, Lowes, Douglas, Stoller, W H Wilson, Tang, Sonia, Garg, Barry H, Trachtenberg, Palak, Shah, Salpy V, Pamboukian, Nancy K, Sweitzer, Matthew T, Wheeler, Jane E, Wilcox, Stuart, Katz, Stephen, Pan, Javier, Jimenez, Keith D, Aaronson, Daniel P, Fishbein, Frank, Smart, Jessica, Wang, Stephen S, Gottlieb, Daniel P, Judge, Charles K, Moore, Jonathan O, Mead, Hanyu, Ni, Wylie, Burke, Ray E, Hershberger
Publikováno v:
JAMA. 327(5)
Idiopathic dilated cardiomyopathy (DCM) aggregates in families, and early detection in at-risk family members can provide opportunity to initiate treatment prior to late-phase disease. Most studies have included only White patients, yet Black patient
Autor:
Hanyu Ni, Elizabeth Jordan, Jinwen Cao, Daniel Kinnamon, Stephen Gottlieb, Mark Hofmeyer, Francisco Javier Jimenez Carcamo, Daniel Judge, Alanna Morris, Anjali Owens, Palak Shah, Wai Hong Tang, Jessica Wang, Evan Kransdorf, Ray Hershberger
Publikováno v:
Journal of Cardiac Failure. 29:648