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Perfil clínico y epidemiológico de los niños con cardiopatías congénitas atendidos en el Hospital Infantil de Morelia “Eva Sámano de López Mateos”
(Universidad Michoacana de San Nicolás de Hidalgo, 2011-02)
Congenital malformations generally represent a high incidence in their presentation. Between 3% and 4% of all newborns present an important malformation at birth, with congenital heart defects being the most common ...
Comparación entre las escalas Heart y Grace en relación con hallazgos en la coronariografía de pacientes con síndrome coronario agudo sin elevación del segmento ST
Objetivo: Evaluar comparativamente el rendimiento diagnóstico de las escalas HEART y
GRACE en relación con hallazgos en la coronariografía de pacientes con SCASEST en un
Hospital Universitario de Barranquilla, ...
O miocárdio na tetralogia de Fallot: estudo histológico e morfométrico
(Sociedade Brasileira de Cardiologia - SBC, 2009)
FUNDAMENTO: Pacientes com tetralogia de Fallot freqüentemente cursam com disfunção ventricular no período pós-operatório. A base histológica dessa alteração funcional tem sido pouco estudada. OBJETIVO: Avaliar, em espécimes ...
Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects
(American Society of Human Genetics by Elsevier Inc., 2020-01)
The 22q11.2 deletion syndrome (22q11.2DS) results from non-allelic homologous recombination between low-copy repeats termed LCR22. About 60%-70% of individuals with the typical 3 megabase (Mb) deletion from LCR22A-D have ...
Outcomes of the bidirectional Glenn procedure in patients less than 3 months of age
(Mosby-elsevierNew YorkEUA, 2010)
Función ventricular derecha evaluada por ecocardiografía transtorácica y resonancia magnética nuclear cardiaca
(Ediciones Universidad Simón BolívarFacultad de Ciencias de la Salud, 2019)
La disfunción ventricular derecha constituye un marcador pronóstico de alto riesgo en cardiopatías [3], acompañada de una elevada morbimortalidad. [2]
Los avances en Ecocardiografía y Resonancia magnética nuclear han ...
Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects
(2020)
The 22q11.2 deletion syndrome (22q11.2DS) results from non-allelic homologous recombination between low-copy repeats termed LCR22. About 60%-70% of individuals with the typical 3 megabase (Mb) deletion from LCR22A-D have ...
Estudio del seno coronario y sus tributarias en individuos colombianos: Study of the coronary sinus and its tributaries in colombian subjects
(2010-01-25)
The morphological expression of the coronary sinus is characterized by its great variability, especially with regard to length, caliber, drainage territories and frequency of its tributaries. We assessed the variants in ...
3D whole-heart isotropic-resolution motion-compensated joint T-1/T(2)mapping and water/fat imaging
(2020)
Purpose
To develop a free-breathing isotropic-resolution whole-heart joint T1 and T2 mapping sequence with Dixon-encoding that provides coregistered 3D T1 and T2 maps and complementary 3D anatomical water and fat images ...