Resultats globals: 3 registres trobats en 0.02 segons.
Articles, 3 registres trobats
Articles 3 registres trobats  
1.
26 p, 1.8 MB Molecular and Clinicopathologic Characterization of Intravenous Leiomyomatosis / Ordulu, Zehra (Department of Pathology, Massachusetts General Hospital, Boston, MA, United States) ; Chai, Hongyan (Department of Genetics, Yale University School of Medicine; New Haven, CT) ; Peng, Gang (Department of Biostatistics, Yale School of Public Health, New Haven, CT) ; McDonald, Anna G (Department of Pathology, Wake Forest Baptist Medical Center, Winston Salem, NC) ; De Nictolis, Michele (Department of Pathology, San Salvatore Hospital, Pesaro, Italy) ; Garcia-Fernandez, Eugenia (Department of Pathology, Hospital Universitario La Paz, IdiPAZ, and Faculty of Medicine, Universidad Autónoma de Madrid, Spain) ; Hardisson, David (Department of Pathology, Hospital Universitario La Paz, IdiPAZ, and Faculty of Medicine, Universidad Autónoma de Madrid, Spain) ; Prat, Jaime (Department of Pathology, Hospital de la Sta Creu i Sant Pau, Barcelona, Spain) ; Li, Peining (Department of Genetics, Yale University School of Medicine; New Haven, CT) ; Hui, Pei (Department of Pathology, Yale University School of Medicine; New Haven, CT) ; Oliva, Esther (Department of Pathology, Massachusetts General Hospital, Boston, MA, United States) ; Buza, Natalia (Department of Pathology, Yale University School of Medicine; New Haven, CT)
Intravenous leiomyomatosis (IVL) is an unusual uterine smooth muscle proliferation that can be associated with aggressive clinical behavior despite a histologically benign appearance. It has some overlapping molecular characteristics with both uterine leiomyoma and leiomyosarcoma based on limited genetic data. [...]
2020 - 10.1038/s41379-020-0546-8
Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, Vol. 33 (april 2020) , p. 1844-1860  
2.
22 p, 1.6 MB Primitive Neuroectodermal Tumors of the Female Genital Tract: A Morphologic, Immunohistochemical and Molecular Study of 19 Cases / Chiang, Sarah (Department of Pathology, Memorial Sloan Kettering Cancer Center) ; Snuderl, Matija (Department of Pathology, New York University Langone Medical Center) ; Kojiro-Sanada, Sakiko (Department of Pathology, Kurume University School of Medicine) ; Quer Pi-Sunyer, Ariadna (Institut Germans Trias i Pujol. Hospital Universitari Germans Trias i Pujol) ; Daya, Dean (Department of Pathology, McMaster University, Juravinski Hospital) ; Hayashi, Tohru (Department of Pathology, Junwakai Memorial Hospital) ; Bosincu, Luisanna (Department of Pathology, University of Sassar) ; Ogawa, Fumihiro (Department of Diagnostic Pathology, Sainokuni Higashiomiya Medical Center) ; Rosenberg, Andrew E. (Department of Pathology, Miller School of Medicine, University of Miami) ; Horn, Lars-Christian (Division of Gynecologic, Breast and Perinatal Pathology, University Hospital Leipzig) ; Wang, Lu (Department of Pathology, Memorial Sloan Kettering Cancer Center) ; Iafrate, John (Department of Pathology, Massachusetts General Hospital and Harvard Medical School) ; Oliva, Esther (Department of Pathology, Massachusetts General Hospital and Harvard Medical School) ; Universitat Autònoma de Barcelona
Primary primitive neuroectodermal tumor (PNET) of the female genital tract is rare, and its proper classification remains unclear. The clinical, histologic, and immunophenotypic features as well as EWSR1 rearrangement status of 19 gynecologic PNETs, including 10 ovarian, 8 uterine, and 1 vulvar tumors, are herein reported. [...]
2017 - 10.1097/PAS.0000000000000831
American Journal Of Surgical Pathology, Vol. 41 Núm. 6 (772 2017) , p. 761  
3.
12 p, 3.2 MB Dual loss of the SWI/SNF complex ATPases SMARCA4/BRG1 and SMARCA2/BRM is highly sensitive and specific for small cell carcinoma of the ovary, hypercalcaemic type / Karnezis, Anthony N (University of British Columbia. Department of Pathology and Laboratory Medicine) ; Wang, Yemin (University of British Columbia. Department of Pathology and Laboratory Medicine) ; Ramos, Pilar (Translational Genomics Research Institute (TGen). Division of Integrated Cancer Genomics) ; Hendricks, William PD (Translational Genomics Research Institute (TGen). Division of Integrated Cancer Genomics) ; Oliva, Esther (Massachusetts General Hospital. Department of Pathology) ; D'Angelo, Emanuela (Institut d'Investigació Biomèdica Sant Pau) ; Prat, Jaime (Institut d'Investigació Biomèdica Sant Pau) ; Nucci, Marisa R (Brigham and Women's Hospital. Department of Pathology) ; Nielsen, Torsten O (University of British Columbia. Department of Pathology and Laboratory Medicine) ; Chow, Christine (University of British Columbia. Genetic Pathology Evaluation Centre) ; Leung, Samuel (University of British Columbia. Genetic Pathology Evaluation Centre) ; Kommoss, Friedrich (Synlab MVZ Pathologie) ; Kommoss, Stefan (University Hospital of Tuebingen. Department of Obstetrics and Gynecology) ; Silva, Annacarolina (Harvard Medical School. The James Homer Wright Pathology Laboratories) ; Ronnett, Brigitte M (The Johns Hopkins Hospital. Department of Pathology) ; Rabban, Joseph T (University of California San Francisco. Department of Anatomic Pathology) ; Bowtell, David D (Peter MacCallum Cancer Centre) ; Weissman, Bernard E (University of North Carolina. Department of Pathology and Laboratory Medicine) ; Trent, Jeffrey M (Translational Genomics Research Institute (TGen). Division of Integrated Cancer Genomics) ; Gilks, C Blake (University of British Columbia. Department of Pathology and Laboratory Medicine) ; Huntsman, David G (University of British Columbia. Department of Pathology and Laboratory Medicine) ; Universitat Autònoma de Barcelona
Small cell carcinoma of the ovary, hypercalcaemic type () is a lethal and sometimes familial ovarian tumour of young women and children. We and others recently discovered that over 90% of harbour inactivating mutations in the chromatin remodelling gene with concomitant loss of its encoded protein (), one of two mutually exclusive of the / chromatin remodelling complex. [...]
2015 - 10.1002/path.4633
The Journal of Pathology, Vol. 238, Issue 3 (december 2015) , p. 389-400  

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