BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

205 related articles for article (PubMed ID: 37442961)

  • 1. Diagnosis of PTEN mosaicism: the relevance of additional tumor DNA sequencing. A case report and review of the literature.
    Cavaillé M; Crampon D; Achim V; Bubien V; Uhrhammer N; Privat M; Ponelle-Chachuat F; Gay-Bellile M; Lepage M; Ouedraogo ZG; Jones N; Bidet Y; Sevenet N; Bignon YJ
    BMC Med Genomics; 2023 Jul; 16(1):166. PubMed ID: 37442961
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Looking for the hidden mutation: Bannayan-Riley-Ruvalcaba syndrome caused by constitutional and mosaic 10q23 microdeletions involving PTEN and BMPR1A.
    Golas MM; Auber B; Ripperger T; Pabst B; Schmidt G; Morlot M; Diebold U; Steinemann D; Schlegelberger B; Morlot S
    Am J Med Genet A; 2019 Jul; 179(7):1383-1389. PubMed ID: 31062505
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cowden syndrome and the PTEN hamartoma tumor syndrome: systematic review and revised diagnostic criteria.
    Pilarski R; Burt R; Kohlman W; Pho L; Shannon KM; Swisher E
    J Natl Cancer Inst; 2013 Nov; 105(21):1607-16. PubMed ID: 24136893
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Catch them if you are aware: PTEN postzygotic mosaicism in clinically suspicious patients with PTEN Hamartoma Tumour Syndrome and literature review.
    Hendricks LAJ; Schuurs-Hoeijmakers J; Spier I; Haadsma ML; Eijkelenboom A; Cremer K; Mensenkamp AR; Aretz S; Vos JR; Hoogerbrugge N
    Eur J Med Genet; 2022 Jul; 65(7):104533. PubMed ID: 35640862
    [TBL] [Abstract][Full Text] [Related]  

  • 5. PTEN mosaicism with features of Cowden syndrome.
    Gammon A; Jasperson K; Pilarski R; Prior T; Kuwada S
    Clin Genet; 2013 Dec; 84(6):593-5. PubMed ID: 23240978
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. Novel dermatological and skeletal features associated with PTEN variant in PTEN hamartoma tumor syndrome.
    Comeau D; Allain V; Maillet-Lebel N; Ben Amor M
    Eur J Med Genet; 2023 Aug; 66(8):104798. PubMed ID: 37307869
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A mosaic PTEN mutation causing Cowden syndrome identified by deep sequencing.
    Pritchard CC; Smith C; Marushchak T; Koehler K; Holmes H; Raskind W; Walsh T; Bennett RL
    Genet Med; 2013 Dec; 15(12):1004-7. PubMed ID: 23619277
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. A novel mutation of PTEN gene in a patient with Cowden syndrome with excessive papillomatosis of the lips, discrete cutaneous lesions, and gastrointestinal polyposis.
    Vasovcak P; Krepelova A; Puchmajerova A; Spicak J; Voska L; Musilova A; Mestak J; Martinek J
    Eur J Gastroenterol Hepatol; 2007 Jun; 19(6):513-7. PubMed ID: 17489063
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. PTEN hamartoma tumour syndrome: case report based on data from the Iranian hereditary colorectal cancer registry and literature review.
    Rahmatinejad Z; Goshayeshi L; Bergquist R; Goshayeshi L; Golabpour A; Hoseini B
    Diagn Pathol; 2023 Apr; 18(1):43. PubMed ID: 37016356
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cowden disease and Lhermitte-Duclos disease: characterization of a new phakomatosis.
    Robinson S; Cohen AR
    Neurosurgery; 2000 Feb; 46(2):371-83. PubMed ID: 10690726
    [TBL] [Abstract][Full Text] [Related]  

  • 15. PTEN hamartoma tumor syndromes in childhood: description of two cases and a proposal for follow-up protocol.
    Piccione M; Fragapane T; Antona V; Giachino D; Cupido F; Corsello G
    Am J Med Genet A; 2013 Nov; 161A(11):2902-8. PubMed ID: 24123798
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A case of Cowden syndrome diagnosed from multiple gastric polyposis.
    Ha M; Chung JW; Hahm KB; Kim YJ; Lee W; An J; Kim DK; Kim MG
    World J Gastroenterol; 2012 Feb; 18(8):861-4. PubMed ID: 22371648
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Imaging of PTEN-related abnormalities in the central nervous system.
    Dhamija R; Hoxworth JM
    Clin Imaging; 2020 Apr; 60(2):180-185. PubMed ID: 31927175
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Considerations on diagnosis and surveillance measures of PTEN hamartoma tumor syndrome: clinical and genetic study in a series of Spanish patients.
    Pena-Couso L; Ercibengoa M; Mercadillo F; Gómez-Sánchez D; Inglada-Pérez L; Santos M; Lanillos J; Gutiérrez-Abad D; Hernández A; Carbonell P; Letón R; Robledo M; Rodríguez-Antona C; Perea J; Urioste M;
    Orphanet J Rare Dis; 2022 Feb; 17(1):85. PubMed ID: 35227301
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Colonic manifestations of PTEN hamartoma tumor syndrome: case series and systematic review.
    Stanich PP; Pilarski R; Rock J; Frankel WL; El-Dika S; Meyer MM
    World J Gastroenterol; 2014 Feb; 20(7):1833-8. PubMed ID: 24587660
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Ovarian Clear Cell Carcinoma in Cowden Syndrome.
    Yauy K; Imbert-Bouteille M; Bubien V; Lindet-Bourgeois C; Rathat G; Perrochia H; MacGrogan G; Longy M; Bessis D; Tinat J; Baert-Desurmont S; Blanluet M; Perre PV; Baudry K; Pujol P; Corsini C
    J Natl Compr Canc Netw; 2019 Jan; 17(1):7-11. PubMed ID: 30659124
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.