Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Leonardo J Mejía-Marín"'
Autor:
Javier T. Granados Riverón, Maryangel Perea-Cabrera, Leonardo J. Mejía-Marín, Begoña Segura-Stanford, Rocío Sánchez-Urbina, Julio R. Erdmenger-Orellana, Alejandra Contreras-Ramos, Evelyn G. Alvarado-Terrones, Arturo Lopez-Yañez Blanco, Miguel Klünder-Klünder, Norma Balderrabano-Saucedo, Elizabeth Hernández-Carbajal, G. Díaz-Rosas
Publikováno v:
Archives of Medical Research. 49:109-113
The incidence of total anomalous pulmonary venous connection (TAPVC) in the Caucasian population is 2.5/100,000 live births (LB), and the incidence in the Hispanic population is 19.8/100,000 LB. Without knowing the exact etiology for the development
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a447c03af8d40ae06f244f7766a191a
https://doi.org/10.1016/j.arcmed.2018.06.001
https://doi.org/10.1016/j.arcmed.2018.06.001
Autor:
Linda B. Muñoz-Martínez, Verónica Fabiola Morán-Barroso, Luis Enrique Martínez-Barrera, Paola Mendelsberg-Fishbein, Constanza García-Delgado, Mabel Cerrillo-Hinojosa, Leonardo J Mejía-Marín, Maura Robledo-Cayetano
Publikováno v:
Archivos Argentinos de Pediatria. 116
Pallister-Killian syndrome is caused by a tetrasomy 12p mosaicism and is characterized by facial dysmorphism, pigmentary skin anomalies, congenital heart defects, diaphragmatic hernia, epilepsy and mental retardation. The diagnosis is complex as the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::958512c8d2d31b6faf539f2224e10c06
https://doi.org/10.5546/aap.2018.e135
https://doi.org/10.5546/aap.2018.e135
Autor:
Paola, Mendelsberg-Fishbein, Constanza, García-Delgado, Linda B, Muñoz-Martínez, Maura, Robledo-Cayetano, Leonardo J, Mejía-Marín, Luis E, Martínez-Barrera, Mabel, Cerrillo-Hinojosa, Verónica F, Moran-Barroso
Publikováno v:
Archivos argentinos de pediatria. 116(1)
Pallister-Killian syndrome is caused by a tetrasomy 12p mosaicism and is characterized by facial dysmorphism, pigmentary skin anomalies, congenital heart defects, diaphragmatic hernia, epilepsy and mental retardation. The diagnosis is complex as the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b9ae8eb9569bc9b4ec6841cdfdc5341d
https://pubmed.ncbi.nlm.nih.gov/29333839
https://pubmed.ncbi.nlm.nih.gov/29333839