Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Alfredo Vizcaíno-Alarcón"'
Autor:
Jorge Cervantes-Salazar, Juan Calderón-Colmenero, Samuel Ramírez-Marroquín, Alexis Palacios-Macedo, Alejandro Bolio Cerdán, Alfredo Vizcaíno Alarcón, Pedro Curi-Curi, Manuel de la Llata, Julio Erdmenger Orellana, Julieta González, Federico García Soriano, Alejandro Calderón, Luis Casillas, Filiberto Villanueva, Roberto Sánchez Ramírez, Héctor Osnaya, Juan Carlos Necoechea, Carlos Alva Espinoza, Guillermo Prado Villegas
Publikováno v:
Boletín Médico del Hospital Infantil de México, Vol 71, Iss 5, Pp 286-291 (2014)
Background: Currently, there is a spreading worldwide tendency to characterize health issues and to propose alternative solutions via the creation of computerized databases. The aim of this study was to present the results in a computerized database
Externí odkaz:
https://doaj.org/article/d0392e44d1f44609bbfe8acaa04e4cc8
Velocardiofacial syndrome in Mexican patients: Unusually high prevalence of congenital heart disease
Autor:
Claudia Gutiérrez-Camacho, Norma Balderrabano-Saucedo, Paulina María Núñez-Martínez, Jesús Del Bosque-Garza, Dino Pietropaolo-Cienfuegos, Nayely Garibay-Nieto, Verónica Fabiola Morán-Barroso, Arturo Flores-Cuevas, Alejandra Del Pilar Reyes-de la Rosa, Francisco Flores-Ramírez, Constanza García-Delgado, Diana Ibarra-Grajeda, Leticia García-Morales, Patricia G. Medina-Bravo, Luz del Carmen Márquez-Quiróz, Candy Sue Márquez-Ávila, Rocío Sánchez-Urbina, Paola Mendelsberg-Fishbein, Alfredo Vizcaíno-Alarcón, Ariadna Berenice Morales-Jiménez, Salvador Esteva-Solsona
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 79:1886-1891
Introduction Velocardiofacial syndrome (VCFS) is the most common microdeletion syndrome with an incidence of 1:4000 live births. Its phenotype is highly variable with facial, velopharyngeal, cardiac, endocrine, immunologic and psychiatric abnormaliti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8d6f00deaf258b1367b8f131fd69672
https://doi.org/10.1016/j.ijporl.2015.08.038
https://doi.org/10.1016/j.ijporl.2015.08.038
Autor:
Alfredo Vizcaíno Alarcón, Samuel Ramírez-Marroquín, Jorge Cervantes-Salazar, Alejandro Bolio Cerdán, Julieta González, Alejandro Calderón, Julio Erdmenger Orellana, Filiberto Villanueva, Carlos Alva Espinoza, Roberto Sánchez Ramírez, Manuel de la Llata, Juan Carlos Necoechea, Juan Calderón-Colmenero, Alexis Palacios-Macedo, Héctor Osnaya, Guillermo Prado Villegas, Federico García Soriano, Pedro Curi-Curi, Luis Casillas
Publikováno v:
Boletín Médico del Hospital Infantil de México, Vol 71, Iss 5, Pp 286-291 (2014)
Background: Currently, there is a spreading worldwide tendency to characterize health issues and to propose alternative solutions via the creation of computerized databases. The aim of this study was to present the results in a computerized database
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b64cad5e209d5b59fc06ce3ceee9c11b
Autor:
Luis Alexis Arévalo-Salas, Norma Balderrabano-Saucedo, Erika Sandoval-Serrano, Begoña Segura-Stanford, Gonzalo Espinosa-Islas, Francisco Javier Puga-Muñuzuri, Lorenzo Reyes de la Cruz, Alfredo Vizcaíno-Alarcón
Publikováno v:
World Journal for Pediatric and Congenital Heart Surgery. 2:211-218
Pentalogy of Cantrell is a rare disease. Approximately 185 cases have been reported around the world. The authors performed a retrospective study that reviewed the clinical files and pathological samples of 22 cases of pentalogy of Cantrell treated a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0dec8e11ffaa9750503de58f2a39be6
https://doi.org/10.1177/2150135110390528
https://doi.org/10.1177/2150135110390528
Autor:
Begoña Segura-Stanford, Lorenzo Reyes de la Cruz, Gonzalo Espinosa-Islas, Alfredo Vizcaíno-Alarcón, Norma Balderrabano-Saucedo, Alexis Arévalo-Salas
Publikováno v:
Revista Española de Cardiología. 61:1126-1133
Introduccion y objetivos El pronostico para la vida despues de una correccion exitosa de coartacion aortica puede verse afectado por varias complicaciones tardias. Nuestro objetivo fue evaluar la funcion del ventriculo izquierdo en este grupo de paci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3971230f1c3d81e54c9f606f00cf98ac
https://doi.org/10.1157/13127843
https://doi.org/10.1157/13127843
Autor:
Jorge, Cervantes-Salazar, Juan, Calderón-Colmenero, Samuel, Ramírez-Marroquín, Alexis, Palacios-Macedo, Alejandro, Bolio-Cerdán, Alfredo, Vizcaíno Alarcón, Pedro, Curi-Curi, Manuel, de la Llata, Julio, Erdmenger-Orellana, Julieta, González, Federico, García-Soriano, Alejandro, Calderón, Luis, Casillas, Filiberto, Villanueva, Roberto, Sánchez-Ramírez, Héctor, Osnaya, Juan Carlos, Necoechea, Carlos, Alva-Espinoza, Guillermo, Prado-Villegas
Publikováno v:
Revista de investigacion clinica; organo del Hospital de Enfermedades de la Nutricion. 65(6)
Current world tendency is the detection of health problems in order to offer solution alternatives by means of the development of computarized data bases.To present the results of a computerized data base developed for the registry of pediatric cardi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::17a07ab5dbb61270d7f50a12e78b5ae5
https://pubmed.ncbi.nlm.nih.gov/24687354
https://pubmed.ncbi.nlm.nih.gov/24687354
Autor:
Penelope Noriega-Zapata, Rocío Sánchez-Urbina, Diego Arenas-Aranda, Norma Balderrabano-Saucedo, Miguel Klünder-Klünder, Normand García-Hernández, Adriana Sánchez-Boiso, Gabriela Bravo-Hernández, José Alfredo Sierra-Ramírez, Alfredo Vizcaíno-Alarcón
Publikováno v:
Pediatric cardiology. 34(1)
Congenital heart defects (CHD) are the third leading cause of death in children1 year of age in Mexico where there is a high prevalence of the 677C → T polymorphism of the MTHFR gene. This is important because the homozygous 677T/T MTHFR gene and d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9856145704dcb681349b91ecba1f5166
https://pubmed.ncbi.nlm.nih.gov/22660520
https://pubmed.ncbi.nlm.nih.gov/22660520
Autor:
Isabel García-Peláez, Oswaldo M. Aguirre, Alfredo Vizcaíno-Alarcón, Elizabeth Halley-Castillo, Miguel Ángel Villasís-Keever, Manuel Arteaga-Martínez
Publikováno v:
Fetal and pediatric pathology. 28(2)
Our objective was to determine the normal dimensions of the ventricular segment of the human fetal heart between 13 and 20 weeks' gestation. Study Design: 103 hearts obtained by necropsy were dissected and measurements of different portions of ventri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47124860c487af810273651ffb367d53
https://pubmed.ncbi.nlm.nih.gov/19241239
https://pubmed.ncbi.nlm.nih.gov/19241239
Autor:
Gonzalo Espinosa-Islas, Alfredo Vizcaíno-Alarcón, Norma Balderrabano-Saucedo, Alexis Arévalo-Salas, Lorenzo Reyes de la Cruz, Begoña Segura-Stanford
Publikováno v:
Revista espanola de cardiologia. 61(11)
Introduction and objectives. Lifetime prognosis following successful repair of aortic coarctation can be affected by a number of late complications. The objective of this study was to assess left ventricular function in these patients and to identify
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f740650371dd99de4e809ce189350a6
https://pubmed.ncbi.nlm.nih.gov/19000484
https://pubmed.ncbi.nlm.nih.gov/19000484
Autor:
Norma Alicia Balderrábano, Saucedo, Alfredo Vizcaíno, Alarcón, Gonzalo Espinosa, Islas, Lorenzo Reyes, De La Cruz
Publikováno v:
Archivos de cardiologia de Mexico. 78(1)
To evaluate the effect of carvedilol administrated during 8 months in children with heart failure secondary to dilated cardiomyopathy.We initiated carvedilol in patients who, despite optimization of standard treatment, had persistent left ventricular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8ea98089e82ea1e6f53c450e6c3bad48
https://pubmed.ncbi.nlm.nih.gov/18581713
https://pubmed.ncbi.nlm.nih.gov/18581713