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.
143 related articles for article (PubMed ID: 35989466)
1. Noonan syndrome associated with hypoplastic left heart syndrome. Lawrence KM; Burstein DS; Ahrens-Nicklas R; Gaynor JW; Nuri MA Cardiol Young; 2023 Apr; 33(4):652-654. PubMed ID: 35989466 [TBL] [Abstract][Full Text] [Related]
2. Prenatal diagnosis of hypoplastic left heart syndrome associated with Noonan Syndrome and de novo RAF1 mutation. Schulz S; Fröber R; Kraus C; Schneider U Prenat Diagn; 2012 Oct; 32(10):1016-8. PubMed ID: 22821648 [No Abstract] [Full Text] [Related]
3. Congenital heart defects in Noonan syndrome: Diagnosis, management, and treatment. Linglart L; Gelb BD Am J Med Genet C Semin Med Genet; 2020 Mar; 184(1):73-80. PubMed ID: 32022400 [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. Noonan Syndrome Case Report: PTPN11 and Other Potential Genetic Factors Contributing to Lethal Hypertrophic Right Ventricular Cardiomyopathy. Daoud E; Zwick D Pediatr Dev Pathol; 2019; 22(4):386-390. PubMed ID: 30665336 [TBL] [Abstract][Full Text] [Related]
6. Molecular and clinical studies in 107 Noonan syndrome affected individuals with PTPN11 mutations. Athota JP; Bhat M; Nampoothiri S; Gowrishankar K; Narayanachar SG; Puttamallesh V; Farooque MO; Shetty S BMC Med Genet; 2020 Mar; 21(1):50. PubMed ID: 32164556 [TBL] [Abstract][Full Text] [Related]
7. Congenital Chylothorax as the Initial Presentation of PTPN11-Associated Noonan Syndrome. Ebrahimi-Fakhari D; Freiman E; Wojcik MH; Krone K; Casey A; Winn AS; Roberts AE; Harper BD J Pediatr; 2017 Jun; 185():248-248.e1. PubMed ID: 28363362 [No Abstract] [Full Text] [Related]
8. [Arnold-Chiari malformation in Noonan syndrome and other syndromes of the RAS/MAPK pathway]. Ejarque I; Millán-Salvador JM; Oltra S; Pesudo-Martínez JV; Beneyto M; Pérez-Aytés A Rev Neurol; 2015 May; 60(9):408-12. PubMed ID: 25912702 [TBL] [Abstract][Full Text] [Related]
9. Variants of SOS2 are a rare cause of Noonan syndrome with particular predisposition for lymphatic complications. Lissewski C; Chune V; Pantaleoni F; De Luca A; Capri Y; Brinkmann J; Lepri F; Daniele P; Leenders E; Mazzanti L; Scarano E; Radio FC; Kutsche K; Kuechler A; Gérard M; Ranguin K; Legendre M; Vial Y; van der Burgt I; Rinne T; Andreucci E; Mastromoro G; Digilio MC; Cave H; Tartaglia M; Zenker M Eur J Hum Genet; 2021 Jan; 29(1):51-60. PubMed ID: 32788663 [TBL] [Abstract][Full Text] [Related]
10. [A patient with Noonan syndrome]. Bins A; Gortzak RA Ned Tijdschr Tandheelkd; 2013 Dec; 120(12):671-5. PubMed ID: 24555250 [TBL] [Abstract][Full Text] [Related]
11. Novel association of neurofibromatosis type 1-causing mutations in families with neurofibromatosis-Noonan syndrome. Ekvall S; Sjörs K; Jonzon A; Vihinen M; Annerén G; Bondeson ML Am J Med Genet A; 2014 Mar; 164A(3):579-87. PubMed ID: 24357598 [TBL] [Abstract][Full Text] [Related]
12. Co-occurrence of hypertrophic cardiomyopathy and myeloproliferative disorder in a neonate with Noonan syndrome carrying Thr73Ile mutation in PTPN11. Yagasaki H; Nakane T; Hasebe Y; Watanabe A; Kise H; Toda T; Koizumi K; Hoshiai M; Sugita K Am J Med Genet A; 2015 Dec; 167A(12):3144-7. PubMed ID: 26286251 [TBL] [Abstract][Full Text] [Related]
13. Dilated coronary arteries in a 2-month-old with RIT1-associated Noonan syndrome: a case report. Aniol CV; Prokop JW; Rajasekaran S; Pageau S; Elizer SK; VanSickle EA; Bupp CP BMC Pediatr; 2023 Jan; 23(1):1. PubMed ID: 36593444 [TBL] [Abstract][Full Text] [Related]
14. Multiple giant cell lesions in patients with Noonan syndrome and cardio-facio-cutaneous syndrome. Neumann TE; Allanson J; Kavamura I; Kerr B; Neri G; Noonan J; Cordeddu V; Gibson K; Tzschach A; Krüger G; Hoeltzenbein M; Goecke TO; Kehl HG; Albrecht B; Luczak K; Sasiadek MM; Musante L; Laurie R; Peters H; Tartaglia M; Zenker M; Kalscheuer V Eur J Hum Genet; 2009 Apr; 17(4):420-5. PubMed ID: 18854871 [TBL] [Abstract][Full Text] [Related]
15. Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome. Yamamoto GL; Aguena M; Gos M; Hung C; Pilch J; Fahiminiya S; Abramowicz A; Cristian I; Buscarilli M; Naslavsky MS; Malaquias AC; Zatz M; Bodamer O; Majewski J; Jorge AA; Pereira AC; Kim CA; Passos-Bueno MR; Bertola DR J Med Genet; 2015 Jun; 52(6):413-21. PubMed ID: 25795793 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. Electrocardiography in Noonan syndrome PTPN11 gene mutation--phenotype characterization. Croonen EA; van der Burgt I; Kapusta L; Draaisma JM Am J Med Genet A; 2008 Feb; 146A(3):350-3. PubMed ID: 18203203 [TBL] [Abstract][Full Text] [Related]
18. A novel rasopathy caused by recurrent de novo missense mutations in PPP1CB closely resembles Noonan syndrome with loose anagen hair. Gripp KW; Aldinger KA; Bennett JT; Baker L; Tusi J; Powell-Hamilton N; Stabley D; Sol-Church K; Timms AE; Dobyns WB Am J Med Genet A; 2016 Sep; 170(9):2237-47. PubMed ID: 27264673 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. Mutation and Phenotypic Spectrum of Patients With RASopathies. Lallar M; Bijarnia-Mahay S; Verma IC; Mandal K; Puri RD Indian Pediatr; 2021 Jan; 58(1):30-33. PubMed ID: 33452774 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]