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 *

198 related articles for article (PubMed ID: 23918208)

  • 1. Learning and memory in children with Noonan syndrome.
    Pierpont EI; Tworog-Dube E; Roberts AE
    Am J Med Genet A; 2013 Sep; 161A(9):2250-7. PubMed ID: 23918208
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genotype differences in cognitive functioning in Noonan syndrome.
    Pierpont EI; Pierpont ME; Mendelsohn NJ; Roberts AE; Tworog-Dube E; Seidenberg MS
    Genes Brain Behav; 2009 Apr; 8(3):275-82. PubMed ID: 19077116
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Molecular and clinical profile of patients referred as Noonan or Noonan-like syndrome in Greece: a cohort of 86 patients.
    Papadopoulos G; Papadopoulou A; Kosma K; Papadimitriou A; Papaevangelou V; Kanaka-Gantenbein C; Bountouvi E; Kitsiou-Tzeli S
    Eur J Pediatr; 2022 Oct; 181(10):3691-3700. PubMed ID: 35904599
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical and molecular characterization of children with Noonan syndrome and other RASopathies in Argentina.
    Chinton J; Huckstadt V; Moresco A; Gravina LP; Obregon MG
    Arch Argent Pediatr; 2019 Oct; 117(5):330-337. PubMed ID: 31560489
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Co-occurring PTPN11 and SOS1 gene mutations in Noonan syndrome: does this predict a more severe phenotype?
    Brasil AS; Malaquias AC; Wanderley LT; Kim CA; Krieger JE; Jorge AA; Pereira AC; Bertola DR
    Arq Bras Endocrinol Metabol; 2010 Nov; 54(8):717-22. PubMed ID: 21340158
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Response to growth hormone in short children with Noonan syndrome: correlation to genotype.
    Binder G
    Horm Res; 2009 Dec; 72 Suppl 2():52-6. PubMed ID: 20029239
    [TBL] [Abstract][Full Text] [Related]  

  • 9. SOS1 and PTPN11 mutations in five cases of Noonan syndrome with multiple giant cell lesions.
    Beneteau C; Cavé H; Moncla A; Dorison N; Munnich A; Verloes A; Leheup B
    Eur J Hum Genet; 2009 Oct; 17(10):1216-21. PubMed ID: 19352411
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The face of Noonan syndrome: Does phenotype predict genotype.
    Allanson JE; Bohring A; Dörr HG; Dufke A; Gillessen-Kaesbach G; Horn D; König R; Kratz CP; Kutsche K; Pauli S; Raskin S; Rauch A; Turner A; Wieczorek D; Zenker M
    Am J Med Genet A; 2010 Aug; 152A(8):1960-6. PubMed ID: 20602484
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. The language phenotype of children and adolescents with Noonan syndrome.
    Pierpont EI; Ellis Weismer S; Roberts AE; Tworog-Dube E; Pierpont ME; Mendelsohn NJ; Seidenberg MS
    J Speech Lang Hear Res; 2010 Aug; 53(4):917-32. PubMed ID: 20543023
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutation analysis of the genes involved in the Ras-mitogen-activated protein kinase (MAPK) pathway in Korean patients with Noonan syndrome.
    Lee ST; Ki CS; Lee HJ
    Clin Genet; 2007 Aug; 72(2):150-5. PubMed ID: 17661820
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Effects of germline mutations in the Ras/MAPK signaling pathway on adaptive behavior: cardiofaciocutaneous syndrome and Noonan syndrome.
    Pierpont EI; Pierpont ME; Mendelsohn NJ; Roberts AE; Tworog-Dube E; Rauen KA; Seidenberg MS
    Am J Med Genet A; 2010 Mar; 152A(3):591-600. PubMed ID: 20186801
    [TBL] [Abstract][Full Text] [Related]  

  • 15. PTPN11 Gain-of-Function Mutations Affect the Developing Human Brain, Memory, and Attention.
    Johnson EM; Ishak AD; Naylor PE; Stevenson DA; Reiss AL; Green T
    Cereb Cortex; 2019 Jul; 29(7):2915-2923. PubMed ID: 30059958
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genotype-phenotype correlation analysis in Japanese patients with Noonan syndrome.
    Shoji Y; Ida S; Niihori T; Aoki Y; Okamoto N; Etani Y; Kawai M
    Endocr J; 2019 Nov; 66(11):983-994. PubMed ID: 31292302
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Transcriptional hallmarks of Noonan syndrome and Noonan-like syndrome with loose anagen hair.
    Ferrero GB; Picco G; Baldassarre G; Flex E; Isella C; Cantarella D; Corà D; Chiesa N; Crescenzio N; Timeus F; Merla G; Mazzanti L; Zampino G; Rossi C; Silengo M; Tartaglia M; Medico E
    Hum Mutat; 2012 Apr; 33(4):703-9. PubMed ID: 22253195
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [SOS1 mutation: a new cause of Noonan syndrome].
    Serrano-Martín MM; Martínez-Aedo MJ; Tartaglia M; López-Siguero JP
    An Pediatr (Barc); 2008 Apr; 68(4):365-8. PubMed ID: 18394382
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. PTPN11 Mutations in the Ras-MAPK Signaling Pathway Affect Human White Matter Microstructure.
    Fattah M; Raman MM; Reiss AL; Green T
    Cereb Cortex; 2021 Feb; 31(3):1489-1499. PubMed ID: 33119062
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.