Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Gregory Cascino"'
Autor:
Aisha Abdulrazaq, Alessandra Ainsworth, Jeffrey Britton, Chandra Shenoy, Samir Babayev, Gregory Cascino, Kelsey Smith
Publikováno v:
Thursday, April 27.
Publikováno v:
Current Treatment Options in Oncology. 22
Improvements in cancer survival have led to the emergence of cardiovascular disease as an important determinant of adverse outcome in survivors. Cancer therapeutics-related cardiac dysfunction is the most well-known form of cardiotoxicity. However, n
Autor:
Gregory Cascino, Nausheen Akhter, Yu Kang, Jessica K. Altman, Peter G. Doukas, Borko Jovanovic, Marielle Scherrer-Crosbie
Publikováno v:
Circulation. 142
Introduction: HF is a major cause of morbidity and mortality in AML patients. This study was designed as an external evaluation of a risk score to determine the risk of HF in patients treated with anthracyclines for AML. Methods: A validation cohort
Publikováno v:
Journal of the American College of Cardiology. 79:3030
Publikováno v:
Journal of the American College of Cardiology. 77:3328
Autor:
Martin S. Tallman, James M. Foran, Jonathan Canaani, Bonnie Ky, Vera H. Rigolin, Jessica K. Altman, Woo Bin Voss, Nausheen Akhter, Selina M. Luger, Gregory Cascino, Nicholas Furiasse, Alfred Rademaker, Mark R. Litzow
Publikováno v:
Echocardiography
Background: Patients with acute myeloid leukemia (AML) are surviving longer. There are no data on changes in myocardial mechanics from standard of care low-dose anthracycline-based induction chemotherapy in older patients with AML. The aim of this st
Publikováno v:
Circulation. 138
Introduction: Pulmonary artery systolic pressure (PASP) can be derived from maximum tricuspid regurgitation velocity (TRV) obtained from echo using a modified Bernoulli equation. However, PASP from an unenhanced echo only modestly correlates to invas
Autor:
Silke Appenzeller, Rudi Balling, Nina Barisic, Stéphanie Baulac, Hande Caglayan, Dana Craiu, Peter De Jonghe, Christel Depienne, Petia Dimova, Tania Djémié, Padhraig Gormley, Renzo Guerrini, Ingo Helbig, Helle Hjalgrim, Dorota Hoffman-Zacharska, Johanna Jähn, Karl Martin Klein, Bobby Koeleman, Vladimir Komarek, Roland Krause, Gregor Kuhlenbäumer, Eric Leguern, Anna-Elina Lehesjoki, Johannes R. Lemke, Holger Lerche, Tarja Linnankivi, Carla Marini, Patrick May, Rikke S. Møller, Hiltrud Muhle, Deb Pal, Aarno Palotie, Manuela Pendziwiat, Angela Robbiano, Filip Roelens, Felix Rosenow, Kaja Selmer, Jose M. Serratosa, Sanjay Sisodiya, Ulrich Stephani, Katalin Sterbova, Pasquale Striano, Arvid Suls, Tiina Talvik, Sarah von Spiczak, Yvonne Weber, Sarah Weckhuysen, Federico Zara, Bassel Abou-Khalil, Brian K. Alldredge, Eva Andermann, Frederick Andermann, Dina Amrom, Jocelyn F. Bautista, Samuel F. Berkovic, Judith Bluvstein, Alex Boro, Gregory Cascino, Damian Consalvo, Patricia Crumrine, Orrin Devinsky, Dennis Dlugos, Michael P. Epstein, Miguel Fiol, Nathan B. Fountain, Jacqueline French, Daniel Friedman, Eric B. Geller, Tracy Glauser, Simon Glynn, Kevin Haas, Sheryl R. Haut, Jean Hayward, Sandra L. Helmers, Sucheta Joshi, Andres Kanner, Heidi E. Kirsch, Robert C. Knowlton, Eric H. Kossoff, Rachel Kuperman, Ruben Kuzniecky, Daniel H. Lowenstein, Shannon M. McGuire, Paul V. Motika, Edward J. Novotny, Ruth Ottman, Juliann M. Paolicchi, Jack Parent, Kristen Park, Annapurna Poduri, Lynette Sadleir, Ingrid E. Scheffer, Renée A. Shellhaas, Elliott Sherr, Jerry J. Shih, Rani Singh, Joseph Sirven, Michael C. Smith, Joe Sullivan, Liu Lin Thio, Anu Venkat, Eileen P.G. Vining, Gretchen K. Von Allmen, Judith L. Weisenberg, Peter Widdess-Walsh, Melodie R. Winawer, Andrew S. Allen, Patrick Cossette, Norman Delanty, Evan E. Eichler, David B. Goldstein, Yujun Han, Erin L. Heinzen, Michael R. Johnson, Anthony G. Marson, Heather C. Mefford, Sahar Esmaeeli Nieh, Terence J. O’Brien, Stephen Petrou, Slavé Petrovski, Elizabeth K. Ruzzo
Publikováno v:
The American journal of human genetics
Møller, R S, EuroEPINOMICS RES Consortium, Epilepsy Phenome/Genome Project & Epi4K Consortium 2014, ' De novo mutations in synaptic transmission genes including DNM1 cause epileptic encephalopathies ', American Journal of Human Genetics, vol. 95, no. 4, pp. 360-370 . https://doi.org/10.1016/j.ajhg.2014.08.013
Møller, R S, EuroEPINOMICS RES Consortium, Epilepsy Phenome/Genome Project & Epi4K Consortium 2014, ' De novo mutations in synaptic transmission genes including DNM1 cause epileptic encephalopathies ', American Journal of Human Genetics, vol. 95, no. 4, pp. 360-370 . https://doi.org/10.1016/j.ajhg.2014.08.013
Emerging evidence indicates that epileptic encephalopathies are genetically highly heterogeneous, underscoring the need for large cohorts of well-characterized individuals to further define the genetic landscape. Through a collaboration between two c
Autor:
Bassel, Abou-Khalil, Brian, Alldredge, Jocelyn, Bautista, Sam, Berkovic, Judith, Bluvstein, Alex, Boro, Gregory, Cascino, Damian, Consalvo, Sabrina, Cristofaro, Patricia, Crumrine, Orrin, Devinsky, Dennis, Dlugos, Michael, Epstein, Robyn, Fahlstrom, Miguel, Fiol, Nathan, Fountain, Kristen, Fox, Jacqueline, French, Catharine, Freyer Karn, Daniel, Friedman, Eric, Geller, Tracy, Glauser, Simon, Glynn, Kevin, Haas, Sheryl, Haut, Jean, Hayward, Sandra, Helmers, Sucheta, Joshi, Andres, Kanner, Heidi, Kirsch, Robert, Knowlton, Eric, Kossoff, Rachel, Kuperman, Ruben, Kuzniecky, Daniel, Lowenstein, Shannon, McGuire, Paul, Motika, Gerard, Nesbitt, Edward, Novotny, Ruth, Ottman, Juliann, Paolicchi, Jack, Parent, Kristen, Park, Annapurna, Poduri, Neil, Risch, Lynette, Sadleir, Ingrid, Scheffer, Renee, Shellhaas, Elliott, Sherr, Jerry J, Shih, Shlomo, Shinnar, Rani, Singh, Joseph, Sirven, Michael, Smith, Joe, Sullivan, Liu Lin, Thio, Anu, Venkat, Eileen, Vining, Gretchen, von Allmen, Judith, Weisenberg, Peter, Widdess-Walsh, Andrew, Yourich
Publikováno v:
Clinical trials (London, England). 10(4)
Background Epilepsy is a common neurological disorder that affects approximately 50 million people worldwide. Both risk of epilepsy and response to treatment partly depend on genetic factors, and gene identification is a promising approach to target