Resultats globals: 2 registres trobats en 0.02 segons.
Articles, 2 registres trobats
Articles 2 registres trobats  
1.
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  
2.
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 (Hospital de la Santa Creu i Sant Pau. Departament de Patologia) ; Prat, Jaime (Hospital de la Santa Creu i Sant Pau. Departament de Patologia) ; 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  

Vegeu també: autors amb noms similars
1 Oliva, E.
2 Oliva, Esther
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