These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

144 related articles for article (PubMed ID: 38061703)

  • 1. Acral Pigmentation in Peutz-Jeghers Syndrome: Dermoscopic Findings and Treatment with the Q-Switched Nd:YAG Laser.
    Shin H; Hur K; Lee JS; Seong MW; Mun JH
    Ann Dermatol; 2023 Nov; 35(Suppl 2):S201-S204. PubMed ID: 38061703
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Peutz-Jeghers Syndrome: A Comprehensive Review of Genetics, Clinical Features, and Management Approaches.
    Amru RL; Dhok A
    Cureus; 2024 Apr; 16(4):e58887. PubMed ID: 38800180
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Peutz-Jeghers syndrome: Skin manifestations and endocrine anomalies (Review).
    Sandru F; Petca A; Dumitrascu MC; Petca RC; Carsote M
    Exp Ther Med; 2021 Dec; 22(6):1387. PubMed ID: 34650635
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Novel germline STK11 variants and breast cancer phenotype identified in an Indian cohort of Peutz-Jeghers syndrome.
    Lipsa A; Kowtal P; Sarin R
    Hum Mol Genet; 2019 Jun; 28(11):1885-1893. PubMed ID: 30689838
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [The course and clinical manifestations of Peutz-Jeghers syndrome in the Russian population].
    Savelyeva ТA; Ponomarenko АA; Shelygin YA; Kuzminov АM; Vyshegorodtsev DV; Loginova АN; Pikunov DY; Goncharova ЕP; Likutov АA; Mainovskaya ОA; Tsukanov АS
    Ter Arkh; 2023 Mar; 95(2):145-151. PubMed ID: 37167130
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Hereditary predisposition to cancers of the digestive tract, breast, gynecological and gonadal: focus on the Peutz-Jeghers].
    Turpin A; Cattan S; Leclerc J; Wacrenier A; Manouvrier-Hanu S; Buisine MP; Lejeune-Dumoulin S
    Bull Cancer; 2014 Sep; 101(9):813-22. PubMed ID: 25036236
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A case of sporadic Peutz-Jeghers syndrome presenting as multiple intussusceptions.
    Gorji L; Huish G; Morgan J; Levy P
    J Surg Case Rep; 2022 Mar; 2022(3):rjac070. PubMed ID: 35280052
    [TBL] [Abstract][Full Text] [Related]  

  • 8. An exploration of genotype-phenotype link between Peutz-Jeghers syndrome and STK11: a review.
    Daniell J; Plazzer JP; Perera A; Macrae F
    Fam Cancer; 2018 Jul; 17(3):421-427. PubMed ID: 28900777
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A Case of Solitary Peutz-Jeghers Syndrome Leading to Chronic Small Bowel Obstruction Due to Intussusception From a Large Hamartomatous Polyp.
    Edmondson E; Mihalopulos G; Kwok PE; Dellert A; Olsen L; Zhang ZJ
    Cureus; 2023 Apr; 15(4):e37679. PubMed ID: 37206505
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Role of the Serine/Threonine Kinase 11 (STK11) or Liver Kinase B1 (LKB1) Gene in Peutz-Jeghers Syndrome.
    Altamish M; Dahiya R; Singh AK; Mishra A; Aljabali AAA; Satija S; Mehta M; Dureja H; Prasher P; Negi P; Kapoor DN; Goyal R; Tambuwala MM; Chellappan DK; Dua K; Gupta G
    Crit Rev Eukaryot Gene Expr; 2020; 30(3):245-252. PubMed ID: 32749111
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Chromosome 19p13.3 deletion in a child with Peutz-Jeghers syndrome, congenital heart defect, high myopia, learning difficulties and dysmorphic features: Clinical and molecular characterization of a new contiguous gene syndrome.
    Souza J; Faucz F; Sotomaior V; Filho AB; Rosenfeld J; Raskin S
    Genet Mol Biol; 2011 Oct; 34(4):557-61. PubMed ID: 22215957
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Peutz-Jeghers syndrome.
    Tomlinson IP; Houlston RS
    J Med Genet; 1997 Dec; 34(12):1007-11. PubMed ID: 9429144
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Peutz-Jeghers Syndrome and the Role of Imaging: Pathophysiology, Diagnosis, and Associated Cancers.
    Klimkowski S; Ibrahim M; Ibarra Rovira JJ; Elshikh M; Javadi S; Klekers AR; Abusaif AA; Moawad AW; Ali K; Elsayes KM
    Cancers (Basel); 2021 Oct; 13(20):. PubMed ID: 34680270
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Q-switched Nd:YAG laser treatment for labial lentigines associated with Peutz-Jeghers syndrome.
    Ge Y; Jia G; Lin T
    J Dtsch Dermatol Ges; 2015 Jun; 13(6):551-5. PubMed ID: 26018367
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Must Peutz-Jeghers syndrome patients have the
    Duan FX; Gu GL; Yang HR; Yu PF; Zhang Z
    World J Clin Cases; 2018 Aug; 6(8):224-232. PubMed ID: 30148152
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Peutz-Jeghers syndrome: a new understanding.
    Choi HS; Park YJ; Park JG
    J Korean Med Sci; 1999 Feb; 14(1):2-7. PubMed ID: 10102516
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Somatic mutations in the STK11/LKB1 gene are uncommon in rare gynecological tumor types associated with Peutz-Jegher's syndrome.
    Connolly DC; Katabuchi H; Cliby WA; Cho KR
    Am J Pathol; 2000 Jan; 156(1):339-45. PubMed ID: 10623683
    [TBL] [Abstract][Full Text] [Related]  

  • 18. STK11 Causative Variants and Copy Number Variations Identified in Thai Patients With Peutz-Jeghers Syndrome.
    Chiraphapphaiboon W; Thongnoppakhun W; Limjindaporn T; Sawasdichai S; Roothumnong E; Prangphan K; Pamornpol B; Limwongse C; Pithukpakorn M
    Cureus; 2023 Feb; 15(2):e34495. PubMed ID: 36874343
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Germline mutations of the STK11 gene in Korean Peutz-Jeghers syndrome patients.
    Yoon KA; Ku JL; Choi HS; Heo SC; Jeong SY; Park YJ; Kim NK; Kim JC; Jung PM; Park JG
    Br J Cancer; 2000 Apr; 82(8):1403-6. PubMed ID: 10780518
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.