132 related articles for article (PubMed ID: 23866578)
1. Turcot syndrome. Rare observation and literature review.
Ozerov SS; Zakharov IV; Talypov SR; Konovalov DM; Kisliakov AN; Kachanov DIu; Zheludkova OG; Varfolomeeva SR; Rachkov VE
Zh Vopr Neirokhir Im N N Burdenko; 2013; 77(3):49-53; discussion 53. PubMed ID: 23866578
[TBL] [Abstract][Full Text] [Related]
2. Two different primary brain tumors, glioblastoma multiforme and pituitary adenoma, in association with colorectal carcinoma: an unusual case of nonfamilial Turcot's syndrome?
Naydenov E; Marinov M; Nachev S
J Neurol Surg A Cent Eur Neurosurg; 2012 Nov; 73(6):410-2. PubMed ID: 21735373
[No Abstract] [Full Text] [Related]
3. Gastrointestinal stromal tumor in Turcot syndrome.
Bulus H; Tas A; Koklu S
Gastroenterol Nurs; 2015; 38(2):126-7. PubMed ID: 25831251
[No Abstract] [Full Text] [Related]
4. Turcot syndrome type 2: medulloblastoma with multiple colorectal adenomas.
Skomorowski M; Taxier M; Wise W
Clin Gastroenterol Hepatol; 2012 Oct; 10(10):A24. PubMed ID: 22732270
[No Abstract] [Full Text] [Related]
5. A potential life-saving diagnosis--recognizing Turcot syndrome.
Gorovoy IR; de Alba Campomanes A
J AAPOS; 2014 Apr; 18(2):186-8. PubMed ID: 24698620
[TBL] [Abstract][Full Text] [Related]
6. A novel APC gene mutation associated with a severe phenotype in a patient with Turcot syndrome.
Fritch Lilla SA; Yi JS; Hall BA; Moertel CL
J Pediatr Hematol Oncol; 2014 Apr; 36(3):e177-9. PubMed ID: 24309598
[TBL] [Abstract][Full Text] [Related]
7. Glioblastomas with giant cell and sarcomatous features in patients with Turcot syndrome type 1: a clinicopathological study of 3 cases.
Lusis EA; Travers S; Jost SC; Perry A
Neurosurgery; 2010 Sep; 67(3):811-7; discussion 817. PubMed ID: 20657316
[TBL] [Abstract][Full Text] [Related]
8. [Turcot syndrome and Gardner's syndrome in a female patient with familial colon adenomatosis. A case report and literature review].
Kuz'minov AM; Vyshegorodtsev DV; Toboeva MK; Korolik VY; Gavryushin AV; Maynovskaya OA; Tsukanov AS
Zh Vopr Neirokhir Im N N Burdenko; 2019; 83(6):72-77. PubMed ID: 32031170
[TBL] [Abstract][Full Text] [Related]
9. Ovarian neoplasm and endometrioid carcinoma in a patient with Turcot syndrome.
Shalon L; Markowitz J; Bialer M; Kahn E; Weinblatt M; Giardiello FM; Luce MC; Daum F
J Pediatr Gastroenterol Nutr; 1997 Aug; 25(2):224-7. PubMed ID: 9252914
[No Abstract] [Full Text] [Related]
10. Muir-Torre Syndrome and founder mismatch repair gene mutations: A long gone historical genetic challenge.
Ponti G; Manfredini M; Tomasi A; Pellacani G
Gene; 2016 Sep; 589(2):127-32. PubMed ID: 26143115
[TBL] [Abstract][Full Text] [Related]
11. Diplopia as presenting sign of Turcot syndrome.
Ninclaus VG; Walraedt S; Baert E; Laureys G; Leroy BP; De Zaeytijd J
Int Ophthalmol; 2017 Feb; 37(1):275-278. PubMed ID: 27143045
[TBL] [Abstract][Full Text] [Related]
12. Identification of a novel PMS2 alteration c.505C>G (R169G) in trans with a PMS2 pathogenic mutation in a patient with constitutional mismatch repair deficiency.
Mork ME; Borras E; Taggart MW; Cuddy A; Bannon SA; You YN; Lynch PM; Ramirez PT; Rodriguez-Bigas MA; Vilar E
Fam Cancer; 2016 Oct; 15(4):587-91. PubMed ID: 27017610
[TBL] [Abstract][Full Text] [Related]
13. Teenage colorectal polyposis and cancer may be caused by constitutional mismatch repair deficiency (CMMRD).
Soplepmann J; Laidre P
Acta Oncol; 2016 Dec; 55(12):1503-1505. PubMed ID: 27723366
[No Abstract] [Full Text] [Related]
14. Turcot syndrome: case report and nosological aspects.
Fracasso P; Caviglia R; Grassi A; Lapenta R; Stigliano V; Franco D; Casale V
J Exp Clin Cancer Res; 1997 Dec; 16(4):433-5. PubMed ID: 9505220
[TBL] [Abstract][Full Text] [Related]
15. Late-Onset Biallelic Mismatch Repair Deficiency Syndrome.
Ebner DW; Al-Bawardy B; Sweetser S
Clin Gastroenterol Hepatol; 2018 Mar; 16(3):e31-e32. PubMed ID: 28602968
[No Abstract] [Full Text] [Related]
16. [Turban tumour with intracranial invasion].
Lauritzen E; Ibrahim RM; Schmidt G
Ugeskr Laeger; 2018 Jun; 180(23):. PubMed ID: 29809129
[TBL] [Abstract][Full Text] [Related]
17. Clinical genetics of hereditary colorectal cancer.
Power DG; Gloglowski E; Lipkin SM
Hematol Oncol Clin North Am; 2010 Oct; 24(5):837-59. PubMed ID: 20816577
[TBL] [Abstract][Full Text] [Related]
18. Diagnosis of Constitutional Mismatch Repair-Deficiency Syndrome Based on Microsatellite Instability and Lymphocyte Tolerance to Methylating Agents.
Bodo S; Colas C; Buhard O; Collura A; Tinat J; Lavoine N; Guilloux A; Chalastanis A; Lafitte P; Coulet F; Buisine MP; Ilencikova D; Ruiz-Ponte C; Kinzel M; Grandjouan S; Brems H; Lejeune S; Blanché H; Wang Q; Caron O; Cabaret O; Svrcek M; Vidaud D; Parfait B; Verloes A; Knappe UJ; Soubrier F; Mortemousque I; Leis A; Auclair-Perrossier J; Frébourg T; Fléjou JF; Entz-Werle N; Leclerc J; Malka D; Cohen-Haguenauer O; Goldberg Y; Gerdes AM; Fedhila F; Mathieu-Dramard M; Hamelin R; Wafaa B; Gauthier-Villars M; Bourdeaut F; Sheridan E; Vasen H; Brugières L; Wimmer K; Muleris M; Duval A;
Gastroenterology; 2015 Oct; 149(4):1017-29.e3. PubMed ID: 26116798
[TBL] [Abstract][Full Text] [Related]
19. Genomic alterations in Turcot syndrome: Insights from whole exome sequencing.
Karschnia P; Erson-Omay EZ; Huttner AJ; Kaulen LD; Duran D; Fulbright RK; Günel M; Baehring JM
J Neurol Sci; 2020 Oct; 417():117056. PubMed ID: 32739502
[No Abstract] [Full Text] [Related]
20. Phenotypic and genotypic characterisation of biallelic mismatch repair deficiency (BMMR-D) syndrome.
Durno CA; Sherman PM; Aronson M; Malkin D; Hawkins C; Bakry D; Bouffet E; Gallinger S; Pollett A; Campbell B; Tabori U;
Eur J Cancer; 2015 May; 51(8):977-83. PubMed ID: 25883011
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]