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Journal Abstract Search
519 related items for PubMed ID: 24503755
1. SMARCB1 (INI1)-negative rhabdoid carcinomas of the gastrointestinal tract: clinicopathologic and molecular study of a highly aggressive variant with literature review. Agaimy A, Rau TT, Hartmann A, Stoehr R. Am J Surg Pathol; 2014 Jul; 38(7):910-20. PubMed ID: 24503755 [Abstract] [Full Text] [Related]
2. SWI/SNF Complex-deficient Undifferentiated/Rhabdoid Carcinomas of the Gastrointestinal Tract: A Series of 13 Cases Highlighting Mutually Exclusive Loss of SMARCA4 and SMARCA2 and Frequent Co-inactivation of SMARCB1 and SMARCA2. Agaimy A, Daum O, Märkl B, Lichtmannegger I, Michal M, Hartmann A. Am J Surg Pathol; 2016 Apr; 40(4):544-53. PubMed ID: 26551623 [Abstract] [Full Text] [Related]
6. The expanding family of SMARCB1(INI1)-deficient neoplasia: implications of phenotypic, biological, and molecular heterogeneity. Agaimy A. Adv Anat Pathol; 2014 Nov; 21(6):394-410. PubMed ID: 25299309 [Abstract] [Full Text] [Related]
7. SMARCB1/INI1 protein expression in round cell soft tissue sarcomas associated with chromosomal translocations involving EWS: a special reference to SMARCB1/INI1 negative variant extraskeletal myxoid chondrosarcoma. Kohashi K, Oda Y, Yamamoto H, Tamiya S, Oshiro Y, Izumi T, Taguchi T, Tsuneyoshi M. Am J Surg Pathol; 2008 Aug; 32(8):1168-74. PubMed ID: 18580682 [Abstract] [Full Text] [Related]
9. Pediatric extra-renal rhabdoid tumors with unusual morphology: a diagnostic pitfall for small biopsies. Alaggio R, Boldrini R, Di Venosa B, Rosolen A, Bisogno G, Magro G. Pathol Res Pract; 2009 Aug; 205(7):451-7. PubMed ID: 19243895 [Abstract] [Full Text] [Related]
12. Conventional chondrosarcoma in a survivor of rhabdoid tumor: enlarging the spectrum of tumors associated with SMARCB1 germline mutations. Forest F, David A, Arrufat S, Pierron G, Ranchere-Vince D, Stephan JL, Clemenson A, Delattre O, Bourdeaut F. Am J Surg Pathol; 2012 Dec; 36(12):1892-6. PubMed ID: 23154773 [Abstract] [Full Text] [Related]
15. Extrarenal rhabdoid tumors of soft tissue: clinicopathological and molecular genetic review and distinction from other soft-tissue sarcomas with rhabdoid features. Oda Y, Tsuneyoshi M. Pathol Int; 2006 Jun; 56(6):287-95. PubMed ID: 16704491 [Abstract] [Full Text] [Related]
17. SMARCB1 (INI-1)-deficient Sinonasal Carcinoma: A Series of 39 Cases Expanding the Morphologic and Clinicopathologic Spectrum of a Recently Described Entity. Agaimy A, Hartmann A, Antonescu CR, Chiosea SI, El-Mofty SK, Geddert H, Iro H, Lewis JS, Märkl B, Mills SE, Riener MO, Robertson T, Sandison A, Semrau S, Simpson RH, Stelow E, Westra WH, Bishop JA. Am J Surg Pathol; 2017 Apr; 41(4):458-471. PubMed ID: 28291122 [Abstract] [Full Text] [Related]