Terms: = Ovarian cancer AND STK11, LKB1, 6794, ENSG00000118046, Q15831, PJS AND Diagnosis
34 results:
1. Detection of FOXL2 C134W Mutation Status by a Novel BaseScope In Situ Hybridization Assay is Highly Sensitive and Specific for Adult Granulosa Cell Tumors.
Hammer PM; Wang A; Beard C; Zdravkovic S; Tenney T; Liang B; Das I; Bremer R; Wang LC; McCluggage WG; Stewart CJR; Howitt BE
Mod Pathol; 2023 Nov; 36(11):100318. PubMed ID: 37634867
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2. stk11 Adnexal Tumor in an Adolescent Female: Diagnostic Pitfalls of a Recently Described Entity.
Sharma AE; Slack JC; Parra-Herran CE; Quade BJ; Shusterman S; Church AJ; Kolin DL; Carreon CK
Pediatr Dev Pathol; 2023; 26(5):486-493. PubMed ID: 37334562
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3. 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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4. 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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5. Extremely high anti-Mullerian hormone levels detected during infertility workup revealing sex cord tumor with annular tubules and underlying Peutz-Jeghers syndrome: A case report.
Yucel Cicek OS; Gezer S; Cakir O; Hekimoglu Gurbuz R
J Obstet Gynaecol Res; 2022 Feb; 48(2):492-496. PubMed ID: 34837285
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6. 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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7. 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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8. 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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9. ovarian Sertoli cell tumours: practical points.
Gheorghisan-Galateanu AA; Carsote M; Terzea D; Valea A; Ghemigian A
J Pak Med Assoc; 2020 Jan; 70(1):129-133. PubMed ID: 31954037
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10. Female adnexal tumors of probable Wolffian origin: morphological, immunohistochemical, and molecular analysis of 15 cases.
Bennett JA; Ritterhouse LL; Furtado LV; Lastra RR; Pesci A; Newell JM; Burandt E; Kooreman L; Van de Vijver K; Krausz T; Felix A; Zannoni GF; Young RH; Oliva E
Mod Pathol; 2020 Apr; 33(4):734-747. PubMed ID: 31591497
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11. Uterine Tumor Resembling ovarian Sex Cord Tumor (UTROSCT): A Morphologic and Molecular Study of 26 Cases Confirms Recurrent NCOA1-3 Rearrangement.
Goebel EA; Hernandez Bonilla S; Dong F; Dickson BC; Hoang LN; Hardisson D; Lacambra MD; Lu FI; Fletcher CDM; Crum CP; Antonescu CR; Nucci MR; Kolin DL
Am J Surg Pathol; 2020 Jan; 44(1):30-42. PubMed ID: 31464709
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12. Genetic Causes of Rare Pediatric ovarian Tumors.
Plevová P; Geržová H
Klin Onkol; 2019; 32(Supplementum2):79-91. PubMed ID: 31409083
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13. Contribution of Massive Parallel Sequencing to diagnosis of Hereditary ovarian cancer in the Czech Republic.
Soukupová J; Lhotová K; Zemánková P; Vočka M; Janatová M; Stolařová L; Borecká M; Kleiblová P; Macháčková E; Foretová L; Koudová M; Lhota F; Tavandzis S; Zikán M; Stránecký V; Veselá K; Panczak A; Kotlas J; Kleibl Z
Klin Onkol; 2019; 32(Supplementum2):72-78. PubMed ID: 31409082
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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. Gastric-type Adenocarcinoma of the Cervix: Tumor With Wide Range of Histologic Appearances.
Pirog EC; Park KJ; Kiyokawa T; Zhang X; Chen W; Jenkins D; Quint W
Adv Anat Pathol; 2019 Jan; 26(1):1-12. PubMed ID: 30234500
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17. 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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18. Peutz-Jeghers Syndrome: Pathobiology, Pathologic Manifestations, and Suggestions for Recommending Genetic Testing in Pathology Reports.
Meserve EE; Nucci MR
Surg Pathol Clin; 2016 Jun; 9(2):243-68. PubMed ID: 27241107
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19. Hereditary non-BRCA gynecological tumors.
Vellone VG; Paudice M; Varesco L
Minerva Ginecol; 2016 Oct; 68(5):579-86. PubMed ID: 26930387
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20. Prevalence of germline mutations in cancer predisposition genes in patients with pancreatic cancer.
Grant RC; Selander I; Connor AA; Selvarajah S; Borgida A; Briollais L; Petersen GM; Lerner-Ellis J; Holter S; Gallinger S
Gastroenterology; 2015 Mar; 148(3):556-64. PubMed ID: 25479140
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