Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Alyaa Al-Ibraheemi"'
Autor:
Alanna J. Church, Laura B. Corson, Pei-Chi Kao, Alma Imamovic-Tuco, Deirdre Reidy, Duong Doan, Wenjun Kang, Navin Pinto, Luke Maese, Theodore W. Laetsch, AeRang Kim, Susan I. Colace, Margaret E. Macy, Mark A. Applebaum, Rochelle Bagatell, Amit J. Sabnis, Daniel A. Weiser, Julia L. Glade-Bender, Alan C. Homans, John Hipps, Haley Harris, Danielle Manning, Alyaa Al-Ibraheemi, Yvonne Li, Hersh Gupta, Andrew D. Cherniack, Ying-Chun Lo, Gianna R. Strand, Lobin A. Lee, R. Seth Pinches, Lorena Lazo De La Vega, Maegan V. Harden, Niall J. Lennon, Seong Choi, Hannah Comeau, Marian H. Harris, Suzanne J. Forrest, Catherine M. Clinton, Brian D. Crompton, Junne Kamihara, Laura E. MacConaill, Samuel L. Volchenboum, Neal I. Lindeman, Eliezer Van Allen, Steven G. DuBois, Wendy B. London, Katherine A. Janeway
Publikováno v:
Nature Medicine. 28:1581-1589
To evaluate the clinical impact of molecular tumor profiling (MTP) with targeted sequencing panel tests, pediatric patients with extracranial solid tumors were enrolled in a prospective observational cohort study at 12 institutions. In the 345-patien
Autor:
Alyaa Al-Ibraheemi, Siddharth Srivastava, Aristotelis Filippidis, Alfred P. See, Katie Pricola Fehnel, Hart G.W. Lidov, Darren B. Orbach
Publikováno v:
American Journal of Medical Genetics Part A. 188:907-910
Gain of function PIK3CA pathogenic variants have been identified in overgrowth syndromes collectively termed "PIK3CA-related overgrowth spectrum" (PROS). There are no previously reported cases of cerebrovascular venous malformations in PROS syndromes
Autor:
Brandon T. Larsen, Alyaa Al-Ibraheemi, Jessica L. Davis, Yajuan J. Liu, Tanaya Neff, Michael Michal, Karen Fritchie, Carol Beadling, Christina M. Lockwood, Soo-Jin Cho, Erin R. Rudzinski, Alyssa J. Penning, Christopher L. Corless, Vera A. Paulson, Lukáš Plank
Publikováno v:
Modern Pathology. 34:1530-1540
Infantile fibrosarcoma (IFS)/cellular congenital mesoblastic nephroma (cCMN) commonly harbors the classic ETV6-NTRK3 translocation. However, there are recent reports of mesenchymal tumors with IFS-like morphology harboring fusions of other receptor t
Autor:
Anne Piche-Schulman, Sanda Alexandrescu, Alanna J. Church, Kristen Gill, Alyaa Al-Ibraheemi, Raja Shaikh, Rosemarie Tavares Proulx, R. Seth Pinches, Christopher B. Weldon, Sara O. Vargas, Monica Hollowell, Andrew L. Hong, Antonio R. Perez-Atayde, Suzanne J. Forrest, Catherine Clinton, Gianna R. Strand, Abigail Ward, Marian H. Harris, Brian D. Crompton, Allison F. O'Neill, Stephanie C. Meyer, Tamara Restrepo, Katherine A. Janeway, Hillary Detert
Publikováno v:
Pediatric Blood & Cancer. 67
Introduction Tissue from pediatric solid tumors is in high demand for use in high-impact research studies, making the allocation of tissue from an anatomic pathology laboratory challenging. We designed, implemented, and assessed an interdepartmental
Autor:
Abigail Ward, Nicole R. LeBoeuf, Duong Doan, Alyaa Al-Ibraheemi, Patrick J. Leavey, Steven G. DuBois, Catherine Clinton, Susan N. Chi, Natalie B. Collins, Alanna J. Church, Elizabeth Mullen, Suzanne J. Forrest, Juan Putra, R. Seth Pinches, Cigall Kadoch, Katherine A. Janeway
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 26(12)
Purpose:Several aggressive pediatric cancers harbor alterations in SMARCB1, including rhabdoid tumors, epithelioid sarcoma, and chordoma. As tumor profiling has become more routine in clinical care, we investigated the relationship between SMARCB1 ge
Publikováno v:
Pediatric Dermatology. 38:299-300
Lipoblastoma typically occurs in childhood and is associated with rearrangements of the PLAG1 gene. We present a patient with an isolated mass thought to be a lipoblastoma clinically, radiographically, and histologically. The lesion was diagnosed as
Publikováno v:
International Journal of Clinical Medicine. :478-480
The commonest pathologic diagnosis of large prolapsed polyps is leiomyoma. Benign or malignant adenomyomatous polyps follow. Adenomyotic cyst is a rare form of adenomyosis. To our knowledge, a recurrent prolapsed giant uterine polyp comprised of aden