Terms: = Breast cancer AND STK11, LKB1, 6794, ENSG00000118046, Q15831, PJS AND Diagnosis
35 results:
1. Germline variants of uncertain significance, their frequency, and clinico-pathological features in a cohort of Sri Lankan patients with hereditary breast cancer.
Gunawardena K; Sirisena ND; Anandagoda G; Neththikumara N; Dissanayake VHW
BMC Res Notes; 2023 Jun; 16(1):95. PubMed ID: 37277882
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2. Ovarian Mucinous Tumor Presenting Atypical Lobular Endocervical Glandular Hyperplasia-Like Appearance in a Patient With Germline
Yoshida H; Hiranuma K; Nakahara M; Kobayashi-Kato M; Tanase Y; Uno M; Shiraishi K; Ishikawa M; Kato T
Int J Surg Pathol; 2024 Apr; 32(2):394-400. PubMed ID: 37226494
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3. Pathogenic variants among females with breast cancer and a non-breast cancer reveal opportunities for cancer interception.
Bychkovsky BL; Lo MT; Yussuf A; Horton C; Hemyari P; LaDuca H; Garber JE; Scheib R; Rana HQ
Breast Cancer Res Treat; 2023 Jul; 200(1):63-72. PubMed ID: 36856935
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4. Strong Hereditary Predispositions to Colorectal cancer.
Hryhorowicz S; Kaczmarek-Ryś M; Lis-Tanaś E; Porowski J; Szuman M; Grot N; Kryszczyńska A; Paszkowski J; Banasiewicz T; Pławski A
Genes (Basel); 2022 Dec; 13(12):. PubMed ID: 36553592
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5. cancer risk in patients with Peutz-Jeghers syndrome in Korea: a retrospective multi-center study.
Kim SH; Kim ER; Park JJ; Kim ES; Goong HJ; Kim KO; Nam JH; Park Y; Lee SP; Jang HJ; ;
Korean J Intern Med; 2023 Mar; 38(2):176-185. PubMed ID: 36517957
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6. Prevalence and spectrum of pathogenic variants among patients with multiple primary cancers evaluated by clinical characteristics.
Bychkovsky BL; Lo MT; Yussuf A; Horton C; Richardson M; LaDuca H; Garber JE; Rana HQ
Cancer; 2022 Mar; 128(6):1275-1283. PubMed ID: 34875721
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7. Hereditary pancreatic cancer.
Abe K; Kitago M; Kitagawa Y; Hirasawa A
Int J Clin Oncol; 2021 Oct; 26(10):1784-1792. PubMed ID: 34476650
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8. Gene Sequencing for Pathogenic Variants Among Adults With breast and Ovarian cancer in the Caribbean.
George SHL; Donenberg T; Alexis C; DeGennaro V; Dyer H; Yin S; Ali J; Butler R; Chin SN; Curling D; Lowe D; Lunn J; Turnquest T; Wharfe G; Cerbon D; Barreto-Coelho P; Schlumbrecht MP; Akbari MR; Narod SA; Hurley JE
JAMA Netw Open; 2021 Mar; 4(3):e210307. PubMed ID: 33646313
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9. Genetic Testing and Screening Recommendations for Patients with Hereditary breast cancer.
Bharucha PP; Chiu KE; François FM; Scott JL; Khorjekar GR; Tirada NP
Radiographics; 2020; 40(4):913-936. PubMed ID: 32469631
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10. Radiographic Surveillance of Patients with Non-BRCA1/2 Pathogenic Variants.
Hudson L; Gower N; Lenarcic S; Trufan SJ; White RL
Ann Surg Oncol; 2020 Jul; 27(7):2248-2254. PubMed ID: 31974710
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11. New germline BRCA2 gene variant in the Tuvinian Mongol breast cancer patients.
Gervas P; Klyuch B; Denisov E; Kiselev A; Molokov A; Pisareva L; Malinovskaya E; Choynzonov E; Cherdyntseva N
Mol Biol Rep; 2019 Oct; 46(5):5537-5541. PubMed ID: 31273614
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12. Development and Validation of an Esophageal Squamous Cell Carcinoma Detection Model by Large-Scale MicroRNA Profiling.
Sudo K; Kato K; Matsuzaki J; Boku N; Abe S; Saito Y; Daiko H; Takizawa S; Aoki Y; Sakamoto H; Niida S; Takeshita F; Fukuda T; Ochiya T
JAMA Netw Open; 2019 May; 2(5):e194573. PubMed ID: 31125107
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13. Clinical and Histologic Overlap and Distinction Among Various Hamartomatous Polyposis Syndromes.
Gilad O; Rosner G; Fliss-Isakov N; Aharon-Kaspi S; Strul H; Gluck N; Kariv R
Clin Transl Gastroenterol; 2019 May; 10(5):1-9. PubMed ID: 31107726
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14. Role of ultrasound in advanced peritoneal malignancies.
De Blasis I; Moruzzi MC; Moro F; Mascilini F; Cianci S; Gueli Alletti S; Turco LC; Garganese G; Scambia G; Testa AC
Minerva Med; 2019 Aug; 110(4):292-300. PubMed ID: 31081311
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15. [The French Genetic and cancer Consortium guidelines for multigene panel analysis in hereditary breast and ovarian cancer predisposition].
Moretta J; Berthet P; Bonadona V; Caron O; Cohen-Haguenauer O; Colas C; Corsini C; Cusin V; De Pauw A; Delnatte C; Dussart S; Jamain C; Longy M; Luporsi E; Maugard C; Nguyen TD; Pujol P; Vaur D; Andrieu N; Lasset C; Noguès C;
Bull Cancer; 2018 Oct; 105(10):907-917. PubMed ID: 30268633
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16. Sputum Detection of Predisposing Genetic Mutations in Women with Pulmonary Nontuberculous Mycobacterial Disease.
Philley JV; Hertweck KL; Kannan A; Brown-Elliott BA; Wallace RJ; Kurdowska A; Ndetan H; Singh KP; Miller EJ; Griffith DE; Dasgupta S
Sci Rep; 2018 Jul; 8(1):11336. PubMed ID: 30054559
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17. Associations Between Sentinel Lymph Node Biopsy and Complications for Patients with Ductal Carcinoma In Situ.
Killelea BK; Long JB; Dang W; Mougalian SS; Evans SB; Gross CP; Wang SY
Ann Surg Oncol; 2018 Jun; 25(6):1521-1529. PubMed ID: 29516364
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18. Genetic analysis and clinical description of Greek patients with Peutz-Jeghers syndrome: Creation of a National Registry.
Fostira F; Mollaki V; Lypas G; Alexandrakis G; Christianakis E; Tzouvala M; Zacharopoulou E; Kalfakakou D; Konstantopoulou I; Yannoukakos D
Cancer Genet; 2018 Jan; 220():19-23. PubMed ID: 29310834
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19. Prevalence of deleterious germline variants in risk genes including BRCA1/2 in consecutive ovarian cancer patients (AGO-TR-1).
Harter P; Hauke J; Heitz F; Reuss A; Kommoss S; Marmé F; Heimbach A; Prieske K; Richters L; Burges A; Neidhardt G; de Gregorio N; El-Balat A; Hilpert F; Meier W; Kimmig R; Kast K; Sehouli J; Baumann K; Jackisch C; Park-Simon TW; Hanker L; Kröber S; Pfisterer J; Gevensleben H; Schnelzer A; Dietrich D; Neunhöffer T; Krockenberger M; Brucker SY; Nürnberg P; Thiele H; Altmüller J; Lamla J; Elser G; du Bois A; Hahnen E; Schmutzler R
PLoS One; 2017; 12(10):e0186043. PubMed ID: 29053726
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20. 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
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