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PUBMED FOR HANDHELDS

Journal Abstract Search


556 related items for PubMed ID: 29981911

  • 21. Pediatric Rhabdoid Meningioma with Extension to the Heart: A First Case Report and Literature Review.
    Khairy S, Al-Ahmari AN, Saeed MA, Azzubi M.
    World Neurosurg; 2019 Sep; 129():445-450. PubMed ID: 31247353
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  • 22. BAP1 and BRAFV600E expression in benign and malignant melanocytic proliferations.
    Piris A, Mihm MC, Hoang MP.
    Hum Pathol; 2015 Feb; 46(2):239-45. PubMed ID: 25479927
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  • 23. Malignant Peripheral Nerve Sheath Tumor in a Patient With BAP1 Tumor Predisposition Syndrome.
    Kaszuba MC, Pulido JS, Folpe AL, Pichurin PN, Goodenberger ML, Spinner RJ.
    World Neurosurg; 2018 Jan; 109():362-364. PubMed ID: 29061454
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  • 29. Histomorphologic spectrum of germline-related and sporadic BAP1-inactivated melanocytic tumors.
    Garfield EM, Walton KE, Quan VL, VandenBoom T, Zhang B, Kong BY, Isales MC, Panah E, Kim G, Gerami P.
    J Am Acad Dermatol; 2018 Sep; 79(3):525-534. PubMed ID: 29753057
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  • 30. Multiple Cutaneous Melanomas and Clinically Atypical Moles in a Patient With a Novel Germline BAP1 Mutation.
    Gerami P, Yélamos O, Lee CY, Obregon R, Yazdan P, Sholl LM, Guitart GE, Njauw CN, Tsao H.
    JAMA Dermatol; 2015 Nov; 151(11):1235-9. PubMed ID: 26154183
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  • 31. Rhabdoid Meningioma Arising Concurrent in Pulmonary and Intracranial with a Rare Malignant Clinical Progression: Case Report and Literature Review.
    Zhao P, Li N, Cao J, Lin X, Liang C.
    World Neurosurg; 2017 Nov; 107():1046.e17-1046.e22. PubMed ID: 28797981
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  • 32. Exon scanning for mutations of the NF2 gene in pediatric ependymomas, rhabdoid tumors and meningiomas.
    Slavc I, MacCollin MM, Dunn M, Jones S, Sutton L, Gusella JF, Biegel JA.
    Int J Cancer; 1995 Aug 22; 64(4):243-7. PubMed ID: 7657387
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  • 33. Intrahepatic cholangiocarcinoma development in a patient with a novel BAP1 germline mutation and low exposure to asbestos.
    Brandi G, Deserti M, Palloni A, Turchetti D, Zuntini R, Pedica F, Frega G, De Lorenzo S, Abbati F, Rizzo A, Di Marco M, Massari F, Tavolari S.
    Cancer Genet; 2020 Oct 22; 248-249():57-62. PubMed ID: 33093002
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  • 39. CDKN2A and BAP1 germline mutations predispose to melanoma and mesothelioma.
    Betti M, Aspesi A, Biasi A, Casalone E, Ferrante D, Ogliara P, Gironi LC, Giorgione R, Farinelli P, Grosso F, Libener R, Rosato S, Turchetti D, Maffè A, Casadio C, Ascoli V, Dianzani C, Colombo E, Piccolini E, Pavesi M, Miccoli S, Mirabelli D, Bracco C, Righi L, Boldorini R, Papotti M, Matullo G, Magnani C, Pasini B, Dianzani I.
    Cancer Lett; 2016 Aug 10; 378(2):120-30. PubMed ID: 27181379
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  • 40. BAP1 cancer syndrome: malignant mesothelioma, uveal and cutaneous melanoma, and MBAITs.
    Carbone M, Ferris LK, Baumann F, Napolitano A, Lum CA, Flores EG, Gaudino G, Powers A, Bryant-Greenwood P, Krausz T, Hyjek E, Tate R, Friedberg J, Weigel T, Pass HI, Yang H.
    J Transl Med; 2012 Aug 30; 10():179. PubMed ID: 22935333
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