176 related articles for article (PubMed ID: 36003032)
1. Coexisting lipomatous meningioma and glioblastoma in Cowden syndrome: A unique tumor association.
Prieto R; Hofecker V; Corbacho C
Neuropathology; 2023 Feb; 43(1):110-116. PubMed ID: 36003032
[TBL] [Abstract][Full Text] [Related]
2. Hidden association of Cowden syndrome, PTEN mutation and meningioma frequency.
Yakubov E; Ghoochani A; Buslei R; Buchfelder M; Eyüpoglu IY; Savaskan N
Oncoscience; 2016; 3(5-6):149-55. PubMed ID: 27489861
[TBL] [Abstract][Full Text] [Related]
3. Brain magnetic resonance imaging in patients with Cowden syndrome.
Lok C; Viseux V; Avril MF; Richard MA; Gondry-Jouet C; Deramond H; Desfossez-Tribout C; Courtade S; Delaunay M; Piette F; Legars D; Dreno B; Saïag P; Longy M; Lorette G; Laroche L; Caux F;
Medicine (Baltimore); 2005 Mar; 84(2):129-136. PubMed ID: 15758842
[TBL] [Abstract][Full Text] [Related]
4. Lhermitte-Duclos Disease in association with Cowden Syndrome.
Nielson C; Fischer T; Fischer R; Donald J; Rajpara A
Dermatol Online J; 2016 May; 22(5):. PubMed ID: 27617518
[TBL] [Abstract][Full Text] [Related]
5. PTEN inactivation by germline/somatic c.950_953delTACT mutation in patients with Lhermitte-Duclos disease manifesting progressive phenotypes.
Chen XY; Lu F; Wang YM; Yang Y; Wei GQ; Wu D; Wang LF; Wu YM
Clin Genet; 2014 Oct; 86(4):349-54. PubMed ID: 24102544
[TBL] [Abstract][Full Text] [Related]
6. Cowden syndrome and the associated Lhermitte-Duclos disease--Case presentation.
Stępniak I; Trojanowski T; Drelich-Zbroja A; Willems P; Zaremba J
Neurol Neurochir Pol; 2015; 49(5):339-43. PubMed ID: 26377987
[TBL] [Abstract][Full Text] [Related]
7. Lhermitte-Duclos and Cowden diseases: breast cancer as an unusual initial presentation of these overlapping conditions.
Walsh S; Carter M; Tubridy N; McDermott EW
BMJ Case Rep; 2011 Oct; 2011():. PubMed ID: 22675060
[TBL] [Abstract][Full Text] [Related]
8. Association between Cowden syndrome and Lhermitte-Duclos disease: report of two cases and review of the literature.
Derrey S; Proust F; Debono B; Langlois O; Layet A; Layet V; Longy M; Fréger P; Laquerrière A
Surg Neurol; 2004 May; 61(5):447-54; discussion 454. PubMed ID: 15120218
[TBL] [Abstract][Full Text] [Related]
9. Mutation of the PTEN (MMAC1) tumor suppressor gene in a subset of glioblastomas but not in meningiomas with loss of chromosome arm 10q.
Boström J; Cobbers JM; Wolter M; Tabatabai G; Weber RG; Lichter P; Collins VP; Reifenberger G
Cancer Res; 1998 Jan; 58(1):29-33. PubMed ID: 9426052
[TBL] [Abstract][Full Text] [Related]
10. Multiple primary malignancies and subtle mucocutaneous lesions associated with a novel PTEN gene mutation in a patient with Cowden syndrome: case report.
Vasovčák P; Senkeříková M; Hatlová J; Křepelová A
BMC Med Genet; 2011 Mar; 12():38. PubMed ID: 21406108
[TBL] [Abstract][Full Text] [Related]
11. Germline inactivation of PTEN and dysregulation of the phosphoinositol-3-kinase/Akt pathway cause human Lhermitte-Duclos disease in adults.
Zhou XP; Marsh DJ; Morrison CD; Chaudhury AR; Maxwell M; Reifenberger G; Eng C
Am J Hum Genet; 2003 Nov; 73(5):1191-8. PubMed ID: 14566704
[TBL] [Abstract][Full Text] [Related]
12. Utility of PTEN protein dosage in predicting for underlying germline PTEN mutations among patients presenting with thyroid cancer and Cowden-like phenotypes.
Ngeow J; He X; Mester JL; Lei J; Romigh T; Orloff MS; Milas M; Eng C
J Clin Endocrinol Metab; 2012 Dec; 97(12):E2320-7. PubMed ID: 23066114
[TBL] [Abstract][Full Text] [Related]
13. Genodermatosis Affecting the Skin and Mucosa of the Head and Neck: Clinicopathologic, Genetic, and Molecular Aspect--PTEN-Hamartoma Tumor Syndrome/Cowden Syndrome.
Nosé V
Head Neck Pathol; 2016 Jun; 10(2):131-8. PubMed ID: 26975628
[TBL] [Abstract][Full Text] [Related]
14. Germline PTEN, SDHB-D, and KLLN alterations in endometrial cancer patients with Cowden and Cowden-like syndromes: an international, multicenter, prospective study.
Mahdi H; Mester JL; Nizialek EA; Ngeow J; Michener C; Eng C
Cancer; 2015 Mar; 121(5):688-96. PubMed ID: 25376524
[TBL] [Abstract][Full Text] [Related]
15. Lhermitte-Duclos Disease (Dysplastic Gangliocytoma of the Cerebellum) and Cowden Syndrome: Clinical Experience From a Single Institution with Long-Term Follow-Up.
Jiang T; Wang J; Du J; Luo S; Liu R; Xie J; Wang Y; Li C
World Neurosurg; 2017 Aug; 104():398-406. PubMed ID: 28479525
[TBL] [Abstract][Full Text] [Related]
16. Novel PTEN mutation in Cowden syndrome: case report with late diagnosis and non-malignant course.
Martínez-Doménech A; García-Legaz Martínez M; Magdaleno-Tapial J; Pérez-Pastor G; Rodríguez-López R; Pérez-Ferriols A
Dermatol Online J; 2019 May; 25(5):. PubMed ID: 31220904
[TBL] [Abstract][Full Text] [Related]
17. Germline PTEN mutation Cowden syndrome: an underappreciated form of hereditary kidney cancer.
Shuch B; Ricketts CJ; Vocke CD; Komiya T; Middelton LA; Kauffman EC; Merino MJ; Metwalli AR; Dennis P; Linehan WM
J Urol; 2013 Dec; 190(6):1990-8. PubMed ID: 23764071
[TBL] [Abstract][Full Text] [Related]
18. Skin abnormalities in individuals with macrocephaly: Cowden disease from a dermatologist's point of view.
van der Velden JJ; Vreeburg M; Smeets EE; Schrander-Stumpel CT; van Steensel MA
Int J Dermatol; 2008 Nov; 47 Suppl 1():45-8. PubMed ID: 18986487
[TBL] [Abstract][Full Text] [Related]
19. Germline epigenetic regulation of KILLIN in Cowden and Cowden-like syndrome.
Bennett KL; Mester J; Eng C
JAMA; 2010 Dec; 304(24):2724-31. PubMed ID: 21177507
[TBL] [Abstract][Full Text] [Related]
20. Clinical and genetic diagnosis of Cowden syndrome: A case report of a rare PTEN germline variant and diverse clinical presentation.
Arai H; Akagi K; Nakagawa A; Onai Y; Utsu Y; Masuda S; Aotsuka N
Medicine (Baltimore); 2023 Jan; 102(1):e32572. PubMed ID: 36607858
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
