Terms: = Bone cancer AND STK11, LKB1, 6794, ENSG00000118046, Q15831, PJS AND Diagnosis
8 results:
1. [Cytopathological characteristics of SMARCA4-deficient thoracic undifferentiated tumors in serous effusion].
Wang WN; Liu XT; Liang YM
Zhonghua Bing Li Xue Za Zhi; 2024 Feb; 53(2):143-148. PubMed ID: 38281781
[No Abstract] [Full Text] [Related]
2. Efficacy of aromatase inhibitor therapy in a case with large cell calcifying Sertoli cell tumour-associated prepubertal gynaecomastia.
Kağızmanlı GA; Besci Ö; Acinikli KY; Şeker G; Yaşar E; Öztürk Y; Demir K; Böber E; Abacı A
J Pediatr Endocrinol Metab; 2022 Dec; 35(12):1565-1570. PubMed ID: 36181314
[TBL] [Abstract] [Full Text] [Related]
3. An occult urothelial carcinoma with wide multiorgan metastases and its genetic alteration profiling: Case report and literature review.
Bu K; Shi Z; Lu Y; Zhao J; Li B
Medicine (Baltimore); 2019 Apr; 98(16):e15245. PubMed ID: 31008958
[TBL] [Abstract] [Full Text] [Related]
4. Neuroblastoma cells undergo transcriptomic alterations upon dissemination into the bone marrow and subsequent tumor progression.
Rifatbegovic F; Frech C; Abbasi MR; Taschner-Mandl S; Weiss T; Schmidt WM; Schmidt I; Ladenstein R; Ambros IM; Ambros PF
Int J Cancer; 2018 Jan; 142(2):297-307. PubMed ID: 28921546
[TBL] [Abstract] [Full Text] [Related]
5. Clinical manifestations and stk11 germline mutations in Taiwanese patients with Peutz-Jeghers syndrome.
Chiang JM; Chen TC
Asian J Surg; 2018 Sep; 41(5):480-485. PubMed ID: 28869103
[TBL] [Abstract] [Full Text] [Related]
6. cancer Screening Recommendations and Clinical Management of Inherited Gastrointestinal cancer Syndromes in Childhood.
Achatz MI; Porter CC; Brugières L; Druker H; Frebourg T; Foulkes WD; Kratz CP; Kuiper RP; Hansford JR; Hernandez HS; Nathanson KL; Kohlmann WK; Doros L; Onel K; Schneider KW; Scollon SR; Tabori U; Tomlinson GE; Evans DGR; Plon SE
Clin Cancer Res; 2017 Jul; 23(13):e107-e114. PubMed ID: 28674119
[TBL] [Abstract] [Full Text] [Related]
7. Prepubertal gynecomastia in two monozygotic twins with Peutz-Jeghers syndrome: two years' treatment with anastrozole and genetic study.
Grandone A; del Giudice EM; Cirillo G; Santarpia M; Coppola F; Perrone L
Horm Res Paediatr; 2011; 75(5):374-9. PubMed ID: 21335955
[TBL] [Abstract] [Full Text] [Related]
8. Molecular classification of patients with unexplained hamartomatous and hyperplastic polyposis.
Sweet K; Willis J; Zhou XP; Gallione C; Sawada T; Alhopuro P; Khoo SK; Patocs A; Martin C; Bridgeman S; Heinz J; Pilarski R; Lehtonen R; Prior TW; Frebourg T; Teh BT; Marchuk DA; Aaltonen LA; Eng C
JAMA; 2005 Nov; 294(19):2465-73. PubMed ID: 16287957
[TBL] [Abstract] [Full Text] [Related]
