Terms: = Germ cell tumor AND RAF1, Raf-1, 5894, P04049, ENSG00000132155, c-Raf, CRAF AND Diagnosis
15 results:
1. Spitz tumor with raf1 fusion: A report of 3 cases.
Donati M; Nosek D; Olivares S; Lemahieu J; Loontiens S; Mansour B; Gerami P; Kazakov DV
Ann Diagn Pathol; 2023 Dec; 67():152215. PubMed ID: 37856952
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2. Recurrent TRAK1::raf1 Fusions in pediatric low-grade gliomas.
Benhamida JK; Harmsen HJ; Ma D; William CM; Li BK; Villafania L; Sukhadia P; Mullaney KA; Dewan MC; Vakiani E; Karajannis MA; Snuderl M; Zagzag D; Ladanyi M; Rosenblum MK; Bale TA
Brain Pathol; 2023 Sep; 33(5):e13185. PubMed ID: 37399073
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3. Atypical Molecular Features of Pediatric Tectal Glioma: A Single Institutional Series.
Yakir MJ; Elster JD; Paul MR; Khanna PC; Malicki DM; Levy ML; Crawford JR
J Pediatr Hematol Oncol; 2023 Apr; 45(3):e410-e414. PubMed ID: 36730386
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4. Infantile metastatic ependymoma with a novel molecular profile and favorable outcome to intensive chemotherapy without irradiation: Case-based review.
De Faria FW; Schieffer KM; Pierson CR; Boue DR; LaHaye S; Miller KE; Amayiri N; Koboldt DC; Lichtenberg T; Leraas K; Brennan P; Kelly B; White P; Magrini V; Wilson RK; Mardis ER; Cottrell CE; Rusin J; Finlay JL; Osorio DS
Genes Chromosomes Cancer; 2023 Jan; 62(1):39-46. PubMed ID: 35716171
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5. A juvenile case of epilepsy-associated, isocitrate dehydrogenase wild-type/histone 3 wild-type diffuse glioma with a rare BRAF
Sadashima S; Suzuki SO; Haruyama H; Mukae N; Fujioka Y; Hata N; Mizoguchi M; Ishimatsu K; Hiwatashi A; Iwaki T
Neuropathology; 2020 Dec; 40(6):646-650. PubMed ID: 32996219
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6. Molecularly defined diffuse leptomeningeal glioneuronal tumor (DLGNT) comprises two subgroups with distinct clinical and genetic features.
Deng MY; Sill M; Chiang J; Schittenhelm J; Ebinger M; Schuhmann MU; Monoranu CM; Milde T; Wittmann A; Hartmann C; Sommer C; Paulus W; Gärtner J; Brück W; Rüdiger T; Leipold A; Jaunmuktane Z; Brandner S; Giangaspero F; Nozza P; Mora J; Morales la Madrid A; Cruz Martinez O; Hansford JR; Pietsch T; Tietze A; Hernáiz-Driever P; Stoler I; Capper D; Korshunov A; Ellison DW; von Deimling A; Pfister SM; Sahm F; Jones DTW
Acta Neuropathol; 2018 Aug; 136(2):239-253. PubMed ID: 29766299
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7. Copy number alterations determined by single nucleotide polymorphism array testing in the clinical laboratory are indicative of gene fusions in pediatric cancer patients.
Busse TM; Roth JJ; Wilmoth D; Wainwright L; Tooke L; Biegel JA
Genes Chromosomes Cancer; 2017 Oct; 56(10):730-749. PubMed ID: 28597942
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8. Disseminated glioneuronal tumors occurring in childhood: treatment outcomes and BRAF alterations including V600E mutation.
Dodgshun AJ; SantaCruz N; Hwang J; Ramkissoon SH; Malkin H; Bergthold G; Manley P; Chi S; MacGregor D; Goumnerova L; Sullivan M; Ligon K; Beroukhim R; Herrington B; Kieran MW; Hansford JR; Bandopadhayay P
J Neurooncol; 2016 Jun; 128(2):293-302. PubMed ID: 26994902
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9. In vivo assessment of optical properties of melanocytic skin lesions and differentiation of melanoma from non-malignant lesions by high-definition optical coherence tomography.
Boone MA; Suppa M; Dhaenens F; Miyamoto M; Marneffe A; Jemec GB; Del Marmol V; Nebosis R
Arch Dermatol Res; 2016 Jan; 308(1):7-20. PubMed ID: 26563265
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10. Correlation of somatic mutations and clinical outcome in melanoma patients treated with Carboplatin, Paclitaxel, and sorafenib.
Wilson MA; Zhao F; Letrero R; D'Andrea K; Rimm DL; Kirkwood JM; Kluger HM; Lee SJ; Schuchter LM; Flaherty KT; Nathanson KL
Clin Cancer Res; 2014 Jun; 20(12):3328-37. PubMed ID: 24714776
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11. Calcium/Calmodulin-dependent protein kinase II and its endogenous inhibitor α in medullary thyroid cancer.
Russo E; Salzano M; De Falco V; Mian C; Barollo S; Secondo A; Bifulco M; Vitale M
Clin Cancer Res; 2014 Mar; 20(6):1513-20. PubMed ID: 24449826
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12. Overdiagnosis of a typical carcinoid tumor as an adenocarcinoma of the lung: a case report and review of the literature.
Demirci I; Herold S; Kopp A; Flaßhove M; Klosterhalfen B; Janßen H
World J Surg Oncol; 2012 Jan; 10():19. PubMed ID: 22269186
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13. Melanoma mimic: a case of multiple pagetoid Spitz nevi.
Harris K; Florell SR; Papenfuss J; Kohlmann W; Jahromi M; Schiffman JD; Quackenbush J; Cassidy P; Leachman S
Arch Dermatol; 2012 Mar; 148(3):370-4. PubMed ID: 22105811
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14. [Pheochromocytoma, first manifestation of Von Hippel-Lindau disease: a possibility to be considered].
Richard S; Resche F; Vermesse B; Fendler JP; Francillard M; Laroche F; Luton JP; Méry JP; Proye C; Redondo A
Arch Mal Coeur Vaiss; 1992 Aug; 85(8):1153-6. PubMed ID: 1482250
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15. Mapping of the von Hippel-Lindau disease locus to a small region of chromosome 3p by genetic linkage analysis.
Maher ER; Bentley E; Yates JR; Latif F; Lerman M; Zbar B; Affara NA; Ferguson-Smith MA
Genomics; 1991 Aug; 10(4):957-60. PubMed ID: 1680799
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