212 related articles for article (PubMed ID: 19795160)
1. PTPN11 mutation associated with aortic dilation and hypertrophic cardiomyopathy in a pediatric patient with Noonan syndrome.
Jefferies JL; Belmont JW; Pignatelli R; Towbin JA; Craigen WJ
Pediatr Cardiol; 2010 Jan; 31(1):114-6. PubMed ID: 19795160
[TBL] [Abstract][Full Text] [Related]
2. [Gene mutation and clinical phenotype analysis of patients with Noonan syndrome and hypertrophic cardiomyopathy].
Liu XH; Ding WW; Han L; Liu XR; Xiao YY; Yang J; Mo Y
Zhonghua Er Ke Za Zhi; 2017 Oct; 55(10):780-784. PubMed ID: 29050118
[No Abstract] [Full Text] [Related]
3. 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]
4. Combined PTPN11 and MYBPC3 Gene Mutations in an Adult Patient with Noonan Syndrome and Hypertrophic Cardiomyopathy.
Caiazza M; Rubino M; Monda E; Passariello A; Fusco A; Cirillo A; Esposito A; Pierno A; De Fazio F; Pacileo R; Evangelista E; Pacileo G; Russo MG; Limongelli G
Genes (Basel); 2020 Aug; 11(8):. PubMed ID: 32824488
[TBL] [Abstract][Full Text] [Related]
5. Pediatric patients with RASopathy-associated hypertrophic cardiomyopathy: the multifaceted consequences of PTPN11 mutations.
Calcagni G; Digilio MC; Marino B; Tartaglia M
Orphanet J Rare Dis; 2019 Jul; 14(1):163. PubMed ID: 31277675
[TBL] [Abstract][Full Text] [Related]
6. Lessons From a Genotype-Phenotype Study About the Clinical Spectrum of Hypertrophic Cardiomyopathy Associated With Noonan Syndrome With Multiple Lentigines and PTPN11-Mutations.
Östman-Smith I
Circ Genom Precis Med; 2023 Aug; 16(4):359-362. PubMed ID: 37325916
[No Abstract] [Full Text] [Related]
7. 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]
8. 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]
9. PTPN11 gene mutation and severe neonatal hypertrophic cardiomyopathy: what is the link?
Faienza MF; Giordani L; Ferraris M; Bona G; Cavallo L
Pediatr Cardiol; 2009 Oct; 30(7):1012-5. PubMed ID: 19582499
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Cardiovascular disease in Noonan syndrome.
Pierpont ME; Digilio MC
Curr Opin Pediatr; 2018 Oct; 30(5):601-608. PubMed ID: 30024444
[TBL] [Abstract][Full Text] [Related]
12. A novel mutation in the PTPN11 gene in a patient with Noonan syndrome and rapidly progressive hypertrophic cardiomyopathy.
Takahashi K; Kogaki S; Kurotobi S; Nasuno S; Ohta M; Okabe H; Wada K; Sakai N; Taniike M; Ozono K
Eur J Pediatr; 2005 Aug; 164(8):497-500. PubMed ID: 15889278
[TBL] [Abstract][Full Text] [Related]
13. Hotspots in PTPN11 Gene Among Indian Children With Noonan Syndrome.
Narayanan DL; Pandey H; Moirangthem A; Mandal K; Gupta R; Puri RD; Patil SJ; Phadke SR
Indian Pediatr; 2017 Aug; 54(8):638-643. PubMed ID: 28607217
[TBL] [Abstract][Full Text] [Related]
14. PTPN11 mutations and genotype-phenotype correlations in Noonan and LEOPARD syndromes.
Ogata T; Yoshida R
Pediatr Endocrinol Rev; 2005 Jun; 2(4):669-74. PubMed ID: 16208280
[TBL] [Abstract][Full Text] [Related]
15. Coronary artery dilatation in LEOPARD syndrome. A child case and literature review.
Iwasaki Y; Horigome H; Takahashi-Igari M; Kato Y; Razzaque MA; Matsuoka R
Congenit Heart Dis; 2009; 4(1):38-41. PubMed ID: 19207402
[TBL] [Abstract][Full Text] [Related]
16. Duplication of chromosome band 12q24.11q24.23 results in apparent Noonan syndrome.
Shchelochkov OA; Patel A; Weissenberger GM; Chinault AC; Wiszniewska J; Fernandes PH; Eng C; Kukolich MK; Sutton VR
Am J Med Genet A; 2008 Apr; 146A(8):1042-8. PubMed ID: 18348260
[TBL] [Abstract][Full Text] [Related]
17. 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]
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. Cardiac features of Noonan syndrome in Japanese patients.
Ichikawa Y; Kuroda H; Ikegawa T; Kawai S; Ono S; Kim KS; Yanagi S; Kurosawa K; Aoki Y; Ueda H
Cardiol Young; 2023 Apr; 33(4):564-569. PubMed ID: 35475426
[TBL] [Abstract][Full Text] [Related]
20. Bilateral coronary artery dilatation and supravalvular pulmonary stenosis in a child with noonan syndrome.
Uçar T; Atalay S; Tekin M; Tutar E
Pediatr Cardiol; 2005; 26(6):848-50. PubMed ID: 16088418
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
