BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

203 related articles for article (PubMed ID: 36082652)

  • 21. Bannayan-Riley-Ruvalcaba syndrome: a cause of extreme macrocephaly and neurodevelopmental delay.
    Lynch NE; Lynch SA; McMenamin J; Webb D
    Arch Dis Child; 2009 Jul; 94(7):553-4. PubMed ID: 19321504
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. PTEN hamartoma tumor syndrome: an overview.
    Hobert JA; Eng C
    Genet Med; 2009 Oct; 11(10):687-94. PubMed ID: 19668082
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Insights into Clinical Disorders in Cowden Syndrome: A Comprehensive Review.
    Pîrlog LM; Pătrășcanu AA; Militaru MS; Cătană A
    Medicina (Kaunas); 2024 May; 60(5):. PubMed ID: 38792950
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Genetic and phenotypic heterogeneity in the PTEN hamartoma tumour syndrome.
    Orloff MS; Eng C
    Oncogene; 2008 Sep; 27(41):5387-97. PubMed ID: 18794875
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Novel PTEN germline mutation in a family with mild phenotype: difficulties in genetic counseling.
    Busa T; Chabrol B; Perret O; Longy M; Philip N
    Gene; 2013 Jan; 512(2):194-7. PubMed ID: 23124040
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Mutation-positive and mutation-negative patients with Cowden and Bannayan-Riley-Ruvalcaba syndromes associated with distinct 10q haplotypes.
    Pezzolesi MG; Li Y; Zhou XP; Pilarski R; Shen L; Eng C
    Am J Hum Genet; 2006 Nov; 79(5):923-34. PubMed ID: 17033968
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Bannayan-Riley-Ruvalcaba syndrome with gingival hyperpigmentation and facial papules.
    Niklinska EB; Lyons EM; Hicks A; Zwerner JP; Albers SE
    Pediatr Dermatol; 2021 Sep; 38(5):1351-1353. PubMed ID: 34259361
    [TBL] [Abstract][Full Text] [Related]  

  • 30. PTEN Hamartoma tumor syndrome in childhood: A review of the clinical literature.
    Macken WL; Tischkowitz M; Lachlan KL
    Am J Med Genet C Semin Med Genet; 2019 Dec; 181(4):591-610. PubMed ID: 31609537
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Absence of PTEN/MMAC1 germ-line mutations in sporadic Bannayan-Riley-Ruvalcaba syndrome.
    Carethers JM; Furnari FB; Zigman AF; Lavine JE; Jones MC; Graham GE; Teebi AS; Huang HJ; Ha HT; Chauhan DP; Chang CL; Cavenee WK; Boland CR
    Cancer Res; 1998 Jul; 58(13):2724-6. PubMed ID: 9661881
    [TBL] [Abstract][Full Text] [Related]  

  • 32. PTEN hamartoma of soft tissue: a distinctive lesion in PTEN syndromes.
    Kurek KC; Howard E; Tennant LB; Upton J; Alomari AI; Burrows PE; Chalache K; Harris DJ; Trenor CC; Eng C; Fishman SJ; Mulliken JB; Perez-Atayde AR; Kozakewich HP
    Am J Surg Pathol; 2012 May; 36(5):671-87. PubMed ID: 22446940
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Diagnosis and Management of Cancer Risk in the Gastrointestinal Hamartomatous Polyposis Syndromes: Recommendations From the US Multi-Society Task Force on Colorectal Cancer.
    Boland CR; Idos GE; Durno C; Giardiello FM; Anderson JC; Burke CA; Dominitz JA; Gross S; Gupta S; Jacobson BC; Patel SG; Shaukat A; Syngal S; Robertson DJ
    Gastroenterology; 2022 Jun; 162(7):2063-2085. PubMed ID: 35487791
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Thyroid involvement in two patients with Bannayan-Riley-Ruvalcaba syndrome.
    Peiretti V; Mussa A; Feyles F; Tuli G; Santanera A; Molinatto C; Ferrero GB; Corrias A
    J Clin Res Pediatr Endocrinol; 2013; 5(4):261-5. PubMed ID: 24379037
    [TBL] [Abstract][Full Text] [Related]  

  • 35. PTEN: one gene, many syndromes.
    Eng C
    Hum Mutat; 2003 Sep; 22(3):183-98. PubMed ID: 12938083
    [TBL] [Abstract][Full Text] [Related]  

  • 36. PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome.
    Marsh DJ; Kum JB; Lunetta KL; Bennett MJ; Gorlin RJ; Ahmed SF; Bodurtha J; Crowe C; Curtis MA; Dasouki M; Dunn T; Feit H; Geraghty MT; Graham JM; Hodgson SV; Hunter A; Korf BR; Manchester D; Miesfeldt S; Murday VA; Nathanson KL; Parisi M; Pober B; Romano C; Eng C
    Hum Mol Genet; 1999 Aug; 8(8):1461-72. PubMed ID: 10400993
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Bannayan-Riley-Ruvalcaba syndrome and juvenile polyposis in a two-year-old girl].
    Vibede LD; Jensen UB; Sørensen TH; Pedersen LM
    Ugeskr Laeger; 2012 Jun; 174(23):1614-5. PubMed ID: 22673385
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Thyroid Pathology Findings in Cowden Syndrome: A Clue for the Diagnosis of the PTEN Hamartoma Tumor Syndrome.
    Cameselle-Teijeiro J; Fachal C; Cabezas-Agrícola JM; Alfonsín-Barreiro N; Abdulkader I; Vega-Gliemmo A; Hermo JA
    Am J Clin Pathol; 2015 Aug; 144(2):322-8. PubMed ID: 26185318
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Predicting PTEN mutations: an evaluation of Cowden syndrome and Bannayan-Riley-Ruvalcaba syndrome clinical features.
    Pilarski R; Stephens JA; Noss R; Fisher JL; Prior TW
    J Med Genet; 2011 Aug; 48(8):505-12. PubMed ID: 21659347
    [TBL] [Abstract][Full Text] [Related]  

  • 40. PTEN hamartoma tumor syndrome.
    Mester J; Charis E
    Handb Clin Neurol; 2015; 132():129-37. PubMed ID: 26564076
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.