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 *

420 related articles for article (PubMed ID: 29948256)

  • 1. Ocular findings in Noonan syndrome: a retrospective cohort study of 105 patients.
    van Trier DC; van der Burgt I; Draaijer RW; Cruysberg JRM; Noordam C; Draaisma JM
    Eur J Pediatr; 2018 Aug; 177(8):1293-1298. PubMed ID: 29948256
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Ocular Manifestations of Noonan Syndrome: A Prospective Clinical and Genetic Study of 25 Patients.
    van Trier DC; Vos AM; Draaijer RW; van der Burgt I; Draaisma JM; Cruysberg JR
    Ophthalmology; 2016 Oct; 123(10):2137-46. PubMed ID: 27521173
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Ocular manifestations of Noonan syndrome.
    Lee NB; Kelly L; Sharland M
    Eye (Lond); 1992; 6 ( Pt 3)():328-34. PubMed ID: 1446772
    [TBL] [Abstract][Full Text] [Related]  

  • 4. External ear anomalies and hearing impairment in Noonan Syndrome.
    van Trier DC; van Nierop J; Draaisma JMT; van der Burgt I; Kunst H; Croonen EA; Admiraal RJC
    Int J Pediatr Otorhinolaryngol; 2015 Jun; 79(6):874-878. PubMed ID: 25862627
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Ocular manifestations of Noonan syndrome.
    Marin Lda R; da Silva FT; de Sá LC; Brasil AS; Pereira A; Furquim IM; Kim CA; Bertola DR
    Ophthalmic Genet; 2012 Mar; 33(1):1-5. PubMed ID: 21815719
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Ophthalmological findings in children and young adults with genetically verified mitochondrial disease.
    Grönlund MA; Honarvar AK; Andersson S; Moslemi AR; Oldfors A; Holme E; Tulinius M; Darin N
    Br J Ophthalmol; 2010 Jan; 94(1):121-7. PubMed ID: 20385529
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Spectrum of mutations in Noonan syndrome and their correlation with phenotypes.
    Lee BH; Kim JM; Jin HY; Kim GH; Choi JH; Yoo HW
    J Pediatr; 2011 Dec; 159(6):1029-35. PubMed ID: 21784453
    [TBL] [Abstract][Full Text] [Related]  

  • 8. PTPN11, SOS1, KRAS, and RAF1 gene analysis, and genotype-phenotype correlation in Korean patients with Noonan syndrome.
    Ko JM; Kim JM; Kim GH; Yoo HW
    J Hum Genet; 2008; 53(11-12):999-1006. PubMed ID: 19020799
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Expanding the SHOC2 mutation associated phenotype of Noonan syndrome with loose anagen hair: structural brain anomalies and myelofibrosis.
    Gripp KW; Zand DJ; Demmer L; Anderson CE; Dobyns WB; Zackai EH; Denenberg E; Jenny K; Stabley DL; Sol-Church K
    Am J Med Genet A; 2013 Oct; 161A(10):2420-30. PubMed ID: 23918763
    [TBL] [Abstract][Full Text] [Related]  

  • 10. PTPN11 and KRAS gene analysis in patients with Noonan and Noonan-like syndromes.
    Brasil AS; Pereira AC; Wanderley LT; Kim CA; Malaquias AC; Jorge AA; Krieger JE; Bertola DR
    Genet Test Mol Biomarkers; 2010 Jun; 14(3):425-32. PubMed ID: 20578946
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Ophthalmological characteristics in children with Leigh syndrome - A long-term follow-up.
    Åkebrand R; Andersson S; Seyedi Honarvar AK; Sofou K; Darin N; Tulinius M; Grönlund MA
    Acta Ophthalmol; 2016 Sep; 94(6):609-17. PubMed ID: 26893257
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutation analysis of the SHOC2 gene in Noonan-like syndrome and in hematologic malignancies.
    Komatsuzaki S; Aoki Y; Niihori T; Okamoto N; Hennekam RC; Hopman S; Ohashi H; Mizuno S; Watanabe Y; Kamasaki H; Kondo I; Moriyama N; Kurosawa K; Kawame H; Okuyama R; Imaizumi M; Rikiishi T; Tsuchiya S; Kure S; Matsubara Y
    J Hum Genet; 2010 Dec; 55(12):801-9. PubMed ID: 20882035
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A Narrative Review of the Ocular Manifestations in Noonan Syndrome.
    Christou EE; Zafeiropoulos P; Rallis D; Baltogianni M; Asproudis C; Stefaniotou M; Giapros V; Asproudis I
    Semin Ophthalmol; 2022 Feb; 37(2):215-221. PubMed ID: 34280068
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Tumor spectrum in children with Noonan syndrome and SOS1 or RAF1 mutations.
    Denayer E; Devriendt K; de Ravel T; Van Buggenhout G; Smeets E; Francois I; Sznajer Y; Craen M; Leventopoulos G; Mutesa L; Vandecasseye W; Massa G; Kayserili H; Sciot R; Fryns JP; Legius E
    Genes Chromosomes Cancer; 2010 Mar; 49(3):242-52. PubMed ID: 19953625
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Expanding the clinical spectrum of ocular anomalies in Noonan syndrome: Axenfeld-anomaly in a child with PTPN11 mutation.
    Guerin A; So J; Mireskandari K; Jougeh-Doust S; Chisholm C; Klatt R; Richer J
    Am J Med Genet A; 2015 Feb; 167A(2):403-6. PubMed ID: 25425531
    [TBL] [Abstract][Full Text] [Related]  

  • 16. PTPN11 gene analysis in 74 Brazilian patients with Noonan syndrome or Noonan-like phenotype.
    Bertola DR; Pereira AC; Albano LM; De Oliveira PS; Kim CA; Krieger JE
    Genet Test; 2006; 10(3):186-91. PubMed ID: 17020470
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Dermatological manifestations in Noonan syndrome: a prospective multicentric study of 129 patients positive for mutation.
    Bessis D; Miquel J; Bourrat E; Chiaverini C; Morice-Picard F; Abadie C; Manna F; Baumann C; Best M; Blanchet P; Bursztejn AC; Capri Y; Coubes C; Giuliano F; Guillaumont S; Hadj-Rabia S; Jacquemont ML; Jeandel C; Lacombe D; Mallet S; Mazereeuw-Hautier J; Molinari N; Pallure V; Pernet C; Philip N; Pinson L; Sarda P; Sigaudy S; Vial Y; Willems M; Geneviève D; Verloes A; Cavé H
    Br J Dermatol; 2019 Jun; 180(6):1438-1448. PubMed ID: 30417923
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Visual function in Noonan and LEOPARD syndrome.
    Alfieri P; Cesarini L; Zampino G; Pantaleoni F; Selicorni A; Salerni A; Vasta I; Cerutti M; Dickmann A; Colitto F; Staccioli S; Leoni C; Ricci D; Brogna C; Tartaglia M; Mercuri E
    Neuropediatrics; 2008 Dec; 39(6):335-40. PubMed ID: 19568997
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Congenital ectropion in Noonan syndrome.
    Dorronsoro M; Bertino M; Suarez JM; Morocho GJ; Vivante SJ; Aldecoa JP
    Arch Soc Esp Oftalmol (Engl Ed); 2024 Apr; 99(4):169-172. PubMed ID: 38309657
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 21.