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1.
A standard echocardiographic and tissue Doppler study of morphological and functional findings in children with hypertrophic cardiomyopathy compared to those with left ventricular hypertrophy in the setting of Noonan and LEOPARD syndromes.
Cardiol Young
; 18(6): 575-80, 2008 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-18842161
2.
Global and regional left ventricular function in patients undergoing transcatheter closure of secundum atrial septal defect.
Am J Cardiol
; 96(3): 439-42, 2005 Aug 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-16054478
3.
Impact of pulmonary regurgitation and age at surgical repair on textural and functional right ventricular myocardial properties in patients with tetralogy of Fallot.
Ital Heart J
; 6(9): 745-50, 2005 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-16212077
4.
Analysis of right ventricular Doppler tissue imaging and load dependence in patients undergoing percutaneous closure of atrial septal defect.
Am J Cardiol
; 94(9): 1202-5, 2004 Nov 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-15518625
5.
Myocardial ultrasound tissue characterization in patients with hypertrophic cardiomyopathy: noninvasive evidence of electrical and textural substrate for ventricular arrhythmias.
J Am Soc Echocardiogr
; 16(8): 803-7, 2003 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-12878988
6.
Time-course of cardiac remodeling following transcatheter closure of atrial septal defect.
Int J Cardiol
; 112(3): 348-52, 2006 Oct 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-16303193
7.
Timed mutation and cell-fate mapping reveal reiterated roles of Tbx1 during embryogenesis, and a crucial function during segmentation of the pharyngeal system via regulation of endoderm expansion.
Development
; 132(19): 4387-95, 2005 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-16141220
8.
Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery development.
Development
; 132(23): 5307-15, 2005 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-16284121
9.
Familial aggregation of genetically heterogeneous hypertrophic cardiomyopathy: a boy with LEOPARD syndrome due to PTPN11 mutation and his nonsyndromic father lacking PTPN11 mutations.
Birth Defects Res A Clin Mol Teratol
; 70(2): 95-8, 2004 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-14991917
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