Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Carolyn Fein Levy"'
Autor:
Anshul Vagrecha, Mingce Zhang, Suchitra Acharya, Shannon Lozinsky, Aaron Singer, Chana Levine, Maha Al-Ghafry, Carolyn Fein Levy, Randy Q. Cron
Publikováno v:
Biology, Vol 11, Iss 3, p 417 (2022)
Multisystem inflammatory syndrome in children (MIS-C) affects few children previously infected with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). In 2020, 45 children admitted to our hospital for MIS-C underwent genetic screening with
Externí odkaz:
https://doaj.org/article/b19da3dbd46c49bda45704cbad562c86
Autor:
Elizabeth Bellew, Samantha Lee, null Hiren Patel, Carolyn Fein Levy, Rachelle Goldfisher, John Amodio
Publikováno v:
Case Reports in Radiology, Vol 2021 (2021)
We present a 14-year-old boy with peritoneal epithelial malignant mesothelioma (PEMM). While pathology is required to make this diagnosis, radiology plays a crucial role throughout the clinical course of this disease. The key imaging characteristics
Externí odkaz:
https://doaj.org/article/cddb4347b1ee468596fb3313d1b88e7b
Autor:
George Jiao, Carolyn Sommer, Ravneet S. Rai, Sylvia R. Kodsi, Hal R. Schwartzstein, David H. Abramson, Carolyn Fein-Levy
Publikováno v:
Journal of Neuro-Ophthalmology.
Autor:
Kara N. Maxwell, Maureen E. Murphy, Raul C. Ribeiro, Gerard P. Zambetti, Richard W. Kriwacki, Sheri L. Spunt, Carolyn Fein Levy, Morris C. Edelman, Brooke Levin, Fergus J. Couch, Kelly McGoldrick, Stephanie Gutierrez, Jill S. Dolinsky, Kenneth Offit, Vijai Joseph, Judy E. Garber, Jill E. Stopfer, Jeffrey N. Weitzel, Thomas P. Slavin, Susan M. Domchek, Katherine L. Nathanson, Kristin Zelley, Louise C. Pyle, Suzanne P. MacFarland, Marilyn M. Li, Anh N. Le, Gregory Kelly, Ryan Hausler, Heena Desai, Aaron H. Philips, Andrew V. Kossenkov, Tetyana Martynyuk, Jessica C. Leung, Thibaut Barnoud, Emilia M. Pinto, Jacquelyn Powers
Supplementary Figures 1-4. Supplementary Figure S1: Full Pedigrees from TP53 c.1000G>C;p.G334R clinically ascertained families. Fam ID allows reference to Table 1; Supplementary Figure S2: Constructs encoding p53 wild-type (TP53-WT), p53-R175H (TP53-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39c00e89c5b7cf956aea60439d2d5560
https://doi.org/10.1158/0008-5472.22425756
https://doi.org/10.1158/0008-5472.22425756
Autor:
Kara N. Maxwell, Maureen E. Murphy, Raul C. Ribeiro, Gerard P. Zambetti, Richard W. Kriwacki, Sheri L. Spunt, Carolyn Fein Levy, Morris C. Edelman, Brooke Levin, Fergus J. Couch, Kelly McGoldrick, Stephanie Gutierrez, Jill S. Dolinsky, Kenneth Offit, Vijai Joseph, Judy E. Garber, Jill E. Stopfer, Jeffrey N. Weitzel, Thomas P. Slavin, Susan M. Domchek, Katherine L. Nathanson, Kristin Zelley, Louise C. Pyle, Suzanne P. MacFarland, Marilyn M. Li, Anh N. Le, Gregory Kelly, Ryan Hausler, Heena Desai, Aaron H. Philips, Andrew V. Kossenkov, Tetyana Martynyuk, Jessica C. Leung, Thibaut Barnoud, Emilia M. Pinto, Jacquelyn Powers
Germline mutations in TP53 cause a rare high penetrance cancer syndrome, Li–Fraumeni syndrome (LFS). Here, we identified a rare TP53 tetramerization domain missense mutation, c.1000G>C;p.G334R, in a family with multiple late-onset LFS-spectrum canc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29b22083b0736e430d002f93b84e42e5
https://doi.org/10.1158/0008-5472.c.6512130
https://doi.org/10.1158/0008-5472.c.6512130
Autor:
Ryan L Webb, Eleny Romanos-Sirakis, Carolyn Fein Levy, Mark E. Bittman, Derek Hanson, Alex K. Williamson, Morris Edelman, Andrew Doan, Gregory J Riely
Publikováno v:
Journal of Pediatric Hematology/Oncology. 44:e605-e608
Background Thymic carcinomas are rare aggressive mediastinal tumors with a median survival of 2 years. Observation We present a pediatric patient who was diagnosed with metastatic thymic carcinoma and showed continuous improvement of his primary mass
Autor:
Fergus J. Couch, Marilyn M. Li, Tetyana Martynyuk, Kelly McGoldrick, Suzanne P. MacFarland, Judy Garber, Heena Desai, Raul C. Ribeiro, Jessica C. Leung, Katherine L. Nathanson, Stephanie Gutierrez, Kara N. Maxwell, Jeffrey N. Weitzel, Emilia M. Pinto, Richard W. Kriwacki, B. Levin, Louise C. Pyle, Anh N Le, Ryan Hausler, Gerard P. Zambetti, Andrew V. Kossenkov, Maureen E. Murphy, Sheri L. Spunt, Kenneth Offit, Thibaut Barnoud, Aaron H. Philips, Vijai Joseph, Morris Edelman, Jacquelyn Powers, Gregory Kelly, Kristin Zelley, Thomas P. Slavin, Jill S. Dolinsky, Jill E. Stopfer, Susan M. Domchek, Carolyn Fein Levy
Publikováno v:
Cancer Research. 80:3732-3744
Germline mutations in TP53 cause a rare high penetrance cancer syndrome, Li–Fraumeni syndrome (LFS). Here, we identified a rare TP53 tetramerization domain missense mutation, c.1000G>C;p.G334R, in a family with multiple late-onset LFS-spectrum canc
Autor:
Hisham Abdel-Azim, Suchitra S. Acharya, Anurag K. Agrawal, Maha Al-Ghafry, Carl E. Allen, Seema Amin, Mark P. Atlas, Rochelle Bagatell, Lionel Blanc, Francine Blei, James B. Bussel, William L. Carroll, James A. Connelly, Jeffrey S. Dome, Brian M. Dulmovits, Olive S. Eckstein, Caitlin W. Elgarten, Mohamed Tarek Elghetany, Noah Federman, Carolyn Fein Levy, James Feusner, Jonathan D. Fish, Adriana Fonseca, Jason L. Freedman, Debra L. Friedman, Derek Hanson, Nobuko Hijiya, Inga Hofmann, Mary S. Huang, Ionela Iacobas, Cassandra D. Josephson, Rachel Kessel, Eugene Khandros, Julie Krystal, Janet L. Kwiatkowski, Philip Lanzkowsky, Ann Leahey, Jeffrey M. Lipton, Catherine McGuinn, Rajen J. Mody, Amy Nadel, Michelle Nash, Omar Niss, Thomas A. Olson, Pallavi M. Pillai, Jacquelyn M. Powers, Josef T. Prchal, Michael A. Pulsipher, Charles T. Quinn, Miriam Radinsky, Arlene Redner, Susan R. Rheingold, Susmita N. Sarangi, Amish Shah, Jordan A. Shavit, Christine M. Smith, Elizabeth Sokol, Kathryn S. Sutton, Tsewang Tashi, David T. Teachey, Anshul Vagrecha, Adrianna Vlachos, Kelly Walkovich, Anne B. Warwick, Howard J. Weinstein, Katrina Winsnes, Lawrence C. Wolfe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d9ce43d5bfb90ec0781092e5f0e1210
https://doi.org/10.1016/b978-0-12-821671-2.00046-5
https://doi.org/10.1016/b978-0-12-821671-2.00046-5