BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

173 related articles for article (PubMed ID: 23877478)

  • 21. Neonatal pulmonary arterial hypertension and Noonan syndrome: two fatal cases with a specific RAF1 mutation.
    Hopper RK; Feinstein JA; Manning MA; Benitz W; Hudgins L
    Am J Med Genet A; 2015 Apr; 167A(4):882-5. PubMed ID: 25706034
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Bilateral cochlear implantation in children with Noonan syndrome.
    Scheiber C; Hirschfelder A; Gräbel S; Peters H; Olze H
    Int J Pediatr Otorhinolaryngol; 2009 Jun; 73(6):889-94. PubMed ID: 19303148
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A Novel Mutation on RAF1 in Association with Fetal Findings Suggestive of Noonan Syndrome.
    Kneitel AW; Norby A; Vettraino I; Treadwell MC
    Fetal Pediatr Pathol; 2015; 34(6):361-4. PubMed ID: 26467173
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Clinical and molecular characterization of 40 patients with Noonan syndrome.
    Ferrero GB; Baldassarre G; Delmonaco AG; Biamino E; Banaudi E; Carta C; Rossi C; Silengo MC
    Eur J Med Genet; 2008; 51(6):566-72. PubMed ID: 18678287
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Leopard syndrome and Chiari type I malformation: a case report and review of the literature.
    Beier AD; Barrett RJ; Burke K; Kole B; Soo TM
    Neurologist; 2009 Jan; 15(1):37-9. PubMed ID: 19131856
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Neurofibromatosis-Noonan syndrome: case report and clinicopathogenic review of the Neurofibromatosis-Noonan syndrome and RAS-MAPK pathway.
    Reig I; Boixeda P; Fleta B; Morenoc C; Gámez L; Truchuelo M
    Dermatol Online J; 2011 Apr; 17(4):4. PubMed ID: 21549079
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Acute lymphoblastic leukemia developing in a patient with Noonan syndrome harboring a PTPN11 germline mutation.
    Sakamoto K; Imamura T; Asai D; Goto-Kawashima S; Yoshida H; Fujiki A; Furutani A; Ishida H; Aoki Y; Hosoi H
    J Pediatr Hematol Oncol; 2014 Mar; 36(2):e136-9. PubMed ID: 24072241
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Germline gain-of-function mutations in SOS1 cause Noonan syndrome.
    Roberts AE; Araki T; Swanson KD; Montgomery KT; Schiripo TA; Joshi VA; Li L; Yassin Y; Tamburino AM; Neel BG; Kucherlapati RS
    Nat Genet; 2007 Jan; 39(1):70-4. PubMed ID: 17143285
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Delineation of LZTR1 mutation-positive patients with Noonan syndrome and identification of LZTR1 binding to RAF1-PPP1CB complexes.
    Umeki I; Niihori T; Abe T; Kanno SI; Okamoto N; Mizuno S; Kurosawa K; Nagasaki K; Yoshida M; Ohashi H; Inoue SI; Matsubara Y; Fujiwara I; Kure S; Aoki Y
    Hum Genet; 2019 Jan; 138(1):21-35. PubMed ID: 30368668
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Mouse model of Noonan syndrome reveals cell type- and gene dosage-dependent effects of Ptpn11 mutation.
    Araki T; Mohi MG; Ismat FA; Bronson RT; Williams IR; Kutok JL; Yang W; Pao LI; Gilliland DG; Epstein JA; Neel BG
    Nat Med; 2004 Aug; 10(8):849-57. PubMed ID: 15273746
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Moyamoya syndrome in a child with Noonan syndrome.
    Hung PC; Wang HS; Wong AM
    Pediatr Neurol; 2011 Aug; 45(2):129-31. PubMed ID: 21763956
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Two cases of Noonan syndrome with severe respiratory and gastroenteral involvement and the SOS1 mutation F623I.
    Fabretto A; Kutsche K; Harmsen MB; Demarini S; Gasparini P; Fertz MC; Zenker M
    Eur J Med Genet; 2010; 53(5):322-4. PubMed ID: 20673819
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Hepatoblastoma in a Noonan syndrome patient with a PTPN11 mutation.
    Yoshida R; Ogata T; Masawa N; Nagai T
    Pediatr Blood Cancer; 2008 Jun; 50(6):1274-6. PubMed ID: 18253957
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Noonan syndrome: introduction and basic clinical features.
    Rohrer T
    Horm Res; 2009 Dec; 72 Suppl 2():3-7. PubMed ID: 20029230
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Noonan syndrome, the SOS1 gene and embryonal rhabdomyosarcoma.
    Jongmans MC; Hoogerbrugge PM; Hilkens L; Flucke U; van der Burgt I; Noordam K; Ruiterkamp-Versteeg M; Yntema HG; Nillesen WM; Ligtenberg MJ; van Kessel AG; Kuiper RP; Hoogerbrugge N
    Genes Chromosomes Cancer; 2010 Jul; 49(7):635-41. PubMed ID: 20461756
    [TBL] [Abstract][Full Text] [Related]  

  • 36. SOS1 mutations are rare in human malignancies: implications for Noonan Syndrome patients.
    Swanson KD; Winter JM; Reis M; Bentires-Alj M; Greulich H; Grewal R; Hruban RH; Yeo CJ; Yassin Y; Iartchouk O; Montgomery K; Whitman SP; Caligiuri MA; Loh ML; Gilliland DG; Look AT; Kucherlapati R; Kern SE; Meyerson M; Neel BG
    Genes Chromosomes Cancer; 2008 Mar; 47(3):253-9. PubMed ID: 18064648
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Noonan syndrome and neurofibromatosis type I in a family with a novel mutation in NF1.
    Nyström AM; Ekvall S; Allanson J; Edeby C; Elinder M; Holmström G; Bondeson ML; Annerén G
    Clin Genet; 2009 Dec; 76(6):524-34. PubMed ID: 19845691
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Investigation of gene dosage imbalances in patients with Noonan syndrome using multiplex ligation-dependent probe amplification analysis.
    Nyström AM; Ekvall S; Thuresson AC; Denayer E; Legius E; Kamali-Moghaddam M; Westermark B; Annerén G; Bondeson ML
    Eur J Med Genet; 2010; 53(3):117-21. PubMed ID: 20302979
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Noonan syndrome associated with neuroblastoma: a case report.
    Lopez-Miranda B; Westra SJ; Yazdani S; Boechat MI
    Pediatr Radiol; 1997 Apr; 27(4):324-6. PubMed ID: 9162899
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Noonan, Costello and cardio-facio-cutaneous syndromes: dysregulation of the Ras-MAPK pathway.
    Tidyman WE; Rauen KA
    Expert Rev Mol Med; 2008 Dec; 10():e37. PubMed ID: 19063751
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.