179 related articles for article (PubMed ID: 1795500)
1. Hypertrophic obstructive cardiomyopathy as a manifestation of a cardiocutaneous syndrome (Noonan syndrome).
Pongratz G; Friedrich M; Unverdorben M; Kunkel B; Bachmann K
Klin Wochenschr; 1991 Dec; 69(20):932-6. PubMed ID: 1795500
[TBL] [Abstract][Full Text] [Related]
2. [Hypertrophic obstructive cardiomyopathy in a patient with Turner syndrome].
Conte MR; Bonfiglio G; Orzan F; Mangiardi L; Camaschella C; Alfarano A; Brusca A
Cardiologia; 1995 Dec; 40(12):947-9. PubMed ID: 8901045
[TBL] [Abstract][Full Text] [Related]
3. A unique case of a 7-year-old with noonan's syndrome, hypertrophic cardiomyopathy, biventricular outflow tract obstruction, and a right ventricular aneurysm.
Tozzi RJ; Abdel-Razek AM; Kipel G; Gardin JM
J Am Coll Cardiol; 2013 Aug; 62(7):643. PubMed ID: 23747783
[No Abstract] [Full Text] [Related]
4. 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]
5. Unusual combination of congenital heart defects in an infant with Noonan syndrome.
Feit LR; Hansen K; Oyer CE; Werner JC
Pediatr Cardiol; 1995; 16(2):95-9. PubMed ID: 7784245
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. [Modern genetic counselling : Practical aspects exemplified by hypertrophic cardiomyopathy].
Czepluch F; Hasenfuß G; Wollnik B
Internist (Berl); 2018 Aug; 59(8):790-798. PubMed ID: 29943241
[TBL] [Abstract][Full Text] [Related]
8. Hypertrophic cardiomyopathy in Noonan syndrome.
Nishikawa T; Ishiyama S; Shimojo T; Takeda K; Kasajima T; Momma K
Acta Paediatr Jpn; 1996 Feb; 38(1):91-8. PubMed ID: 8992870
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Noonan syndrome: a clinical description emphasizing the cardiac findings.
Noonan J; O'Connor W
Acta Paediatr Jpn; 1996 Feb; 38(1):76-83. PubMed ID: 8992867
[No Abstract] [Full Text] [Related]
11. 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]
12. 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]
13. [Hypertrophy of the left ventricle and septum in obstructive and non-obstructive types of hypertrophic cardiomyopathy].
Gregor P; Widimský P; Cervenka V; Sládková T; Vísek V
Vnitr Lek; 1983 Nov; 29(11):1050-9. PubMed ID: 6686390
[No Abstract] [Full Text] [Related]
14. Coronary artery ectasia in Noonan syndrome: Report of an individual with SOS1 mutation and literature review.
Calcagni G; Baban A; De Luca E; Leonardi B; Pongiglione G; Digilio MC
Am J Med Genet A; 2016 Mar; 170(3):665-9. PubMed ID: 26686981
[TBL] [Abstract][Full Text] [Related]
15. Cardiovascular abnormalities in Noonan syndrome: the clinical findings and treatments.
Ishizawa A; Oho S; Dodo H; Katori T; Homma SI
Acta Paediatr Jpn; 1996 Feb; 38(1):84-90. PubMed ID: 8992869
[TBL] [Abstract][Full Text] [Related]
16. Noonan syndrome due to a SHOC2 mutation presenting with fetal distress and fatal hypertrophic cardiomyopathy in a premature infant.
Hoban R; Roberts AE; Demmer L; Jethva R; Shephard B
Am J Med Genet A; 2012 Jun; 158A(6):1411-3. PubMed ID: 22528146
[TBL] [Abstract][Full Text] [Related]
17. Natural History of Hypertrophic Cardiomyopathy in Noonan Syndrome With Multiple Lentigines.
Monda E; Prosnitz A; Aiello R; Lioncino M; Norrish G; Caiazza M; Drago F; Beattie M; Tartaglia M; Russo MG; Colan SD; Calcagni G; Gelb BD; Kaski JP; Roberts AE; Limongelli G
Circ Genom Precis Med; 2023 Aug; 16(4):350-358. PubMed ID: 37199218
[TBL] [Abstract][Full Text] [Related]
18. [Hypertrophic cardiomyopathy associated with Noonan's syndrome and membranous aortic subvalvular stenosis associated with Turner's syndrome. Report of 2 clinical cases].
Perrotta Scaravilli E; Pontillo D; Pennacchia F; Boccanelli A; Greco C; Lo Schiavo P
G Ital Cardiol; 1987 Sep; 17(9):800-6. PubMed ID: 3692082
[TBL] [Abstract][Full Text] [Related]
19. Noonan syndrome and different morphologic expressions of hypertrophic cardiomyopathy.
Martínez-Quintana E; Rodríguez-González F; Junquera-Rionda P
Pediatr Cardiol; 2013; 34(8):1871-3. PubMed ID: 22790361
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]