Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Sofia Garces"'
Autor:
Anjanaa Vijayanarayanan, Sa A. Wang, Sofia Garces, Karan Saluja, L. Jeffrey Medeiros, Beenu Thakral
Publikováno v:
eJHaem, Vol 5, Iss 1, Pp 266-268 (2024)
Externí odkaz:
https://doaj.org/article/6e78721b23a640a786ac13d9fc0e145d
Autor:
Nianyi Li, Pei Lin, Zhuang Zuo, M. James You, Wen Shuai, Robert Orlowski, Elisabet E. Manasanch, Shaoying Li, Jie Xu, Sofia Garces, Fatima Zahra Jelloul, Zhenya Tang, Wei Wang, L. Jeffrey Medeiros, C. Cameron Yin
Publikováno v:
Cancer Medicine, Vol 12, Iss 13, Pp 14293-14304 (2023)
Abstract BACKGROUND Mutations in the RAS‐MAPK pathway, such as KRAS, NRAS, and BRAF, are known as high‐risk factors associated with poor prognosis in patients with various cancers, but studies in myeloma have yielded mixed results. METHODS We des
Externí odkaz:
https://doaj.org/article/b57465017f294358af62a22940905108
Autor:
Jiasen He, Faryal Munir, Samanta Catueno, Jeremy S. Connors, Amber Gibson, Lindsay Robusto, David McCall, Cesar Nunez, Michael Roth, Priti Tewari, Sofia Garces, Branko Cuglievan, Miriam B. Garcia
Publikováno v:
Cancers, Vol 16, Iss 5, p 858 (2024)
Childhood acute lymphoblastic leukemia (ALL) has witnessed substantial improvements in prognosis; however, a subset of patients classified as high-risk continues to face higher rates of relapse and increased mortality. While the National Cancer Insti
Externí odkaz:
https://doaj.org/article/2d496f4fe62e424eab5cb0400a617423
Autor:
Adriana Trabal, Amber Gibson, Jiasen He, David McCall, Michael Roth, Cesar Nuñez, Miriam Garcia, Meredith Buzbee, Laurie Toepfer, Aram Bidikian, Naval Daver, Tapan Kadia, Nicholas J. Short, Ghayas C. Issa, Farhad Ravandi, Courtney D. DiNardo, Guillermo Montalban Bravo, Sofia Garces, Andrea Marcogliese, Hana Paek, Zoann Dreyer, Julienne Brackett, Michele Redell, Joanna Yi, Guillermo Garcia-Manero, Marina Konopleva, Alexandra Stevens, Branko Cuglievan
Publikováno v:
Cancers, Vol 15, Iss 7, p 1983 (2023)
The BCL-2 inhibitor venetoclax improves survival for adult patients with acute myeloid leukemia (AML) in combination with lower-intensity therapies, but its benefit in pediatric patients with AML remains unclear. We retrospectively reviewed two Texas
Externí odkaz:
https://doaj.org/article/35c5d62a24de43fd958bda52a78901b4
Publikováno v:
Human Pathology Reports, Vol 27, Iss , Pp 300602- (2022)
Background: Large B-cell lymphoma with IRF4 rearrangement (LBCL-IRF4) is a rare subtype of large B-cell lymphoma characterized by strong and uniform IRF4/MUM1 expression resulting from IRF4 rearrangement, mostly with immunoglobulin heavy chain. LBCL-
Externí odkaz:
https://doaj.org/article/212c815e5ecf4cda8b2a8776e13f4ef5
Publikováno v:
Human Pathology Reports, Vol 27, Iss , Pp 300606- (2022)
Background: Primary testicular follicular lymphoma (TFL) is a rare extranodal variant of follicular lymphoma confined to the testis, almost exclusively occurring in children and young adults. TFL has unique clinicopathologic features and excellent pr
Externí odkaz:
https://doaj.org/article/f9e2001058bf446e967bff907e93bdee
Autor:
Zhuang Zuo, L. Jeffrey Medeiros, Sofia Garces, Mark J. Routbort, Chi Young Ok, Sanam Loghavi, Rashmi Kanagal-Shamanna, Fatima Zahra Jelloul, Guillermo Garcia-Manero, Kelly S. Chien, Keyur P. Patel, Rajyalakshmi Luthra, C. Cameron Yin
Publikováno v:
Biology, Vol 12, Iss 1, p 13 (2022)
It has been reported that gene mutations in SF3B1 and PHF6 are mutually exclusive. However, this observation has never been rigorously assessed. We report the clinicopathologic and molecular genetic features of 21 cases of myeloid neoplasms with doub
Externí odkaz:
https://doaj.org/article/584dd1f056e34ae3afbdf575c030f774
Publikováno v:
Urology Case Reports, Vol 2, Iss 4, Pp 126-128 (2014)
Paratesticular rhabdomyosarcoma (RMS) occurs more frequently in children and is rare in adults. Embryonal RMS is the most common subtype of paratesticular RMS. Spindle cell is a rare variant of embryonal RMS and is associated with a favorable prognos
Externí odkaz:
https://doaj.org/article/30a237d824b8478b87cb3a667011edfa
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Autor:
Wen Shuai, Zhuang Zuo, Nianyi Li, Sofia Garces, Fatima Zahra Jelloul, Chi Young Ok, Shaoying Li, Jie Xu, M. James You, Wei Wang, Catherine Rehder, Elias J. Jabbour, Keyur P. Patel, L. Jeffrey Medeiros, C. Cameron Yin
Publikováno v:
Cancer. 129:878-889
ETNK1 mutation has been suggested as a useful tool to support the diagnosis of atypical chronic myeloid leukemia. ETNK1 mutations, however, occur in other myeloid neoplasms.The authors assessed the clinicopathologic and molecular genetic features of