Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Héctor Silva-Báez"'
Autor:
Eduardo Sotelo-Anaya, Pedro Coello-Ramírez, Héctor Silva-Báez, Eddy Mizraím Ixtabalán-Escalante, Victor Hugo Sainz-Escárrega, Mariana Gallo-Morales, Eduardo Cordero-Estrada, C.F. Ploneda-Valencia
Publikováno v:
Annals of Medicine and Surgery
Background Choledochal cyst (CC) is a rare congenital anomaly of the bile duct that approximately 75% of the patients are diagnosed in childhood. Without a standardized surgical procedure for the biliary reconstruction, we present our experience over
Autor:
Antonio Heliodoro, Chávez-Aguilar, Héctor, Silva-Báez, Yamid Brajin, Sáchez-Rodríguez, Carlos, Esparza-Ponce, Miguel Ángel, Zatarain Ontiveros, Juan Carlos, Barrere-de León
Publikováno v:
Gaceta medica de Mexico. 151(5)
Autor:
Eloy López-Marure, J. Román Corona-Rivera, Héctor Silva-Báez, Valérie Cormier-Daire, María Inés Estrada-Solorio, Pedro Coello-Ramírez, Nathalie Dagoneau, Carmen O. Romo-Huerta, Liuba M. Aguirre-Salas
Publikováno v:
European Journal of Medical Genetics. 52:242-246
Stüve-Wiedemann syndrome (SWS) is an autosomal recessive bone dysplasia (OMIM #601559) characterized by bowing of long bones, camptodactyly, respiratory insufficiency, hyperthermic episodes, and neonatal death from hyperthermia or apnea. We describe
Autor:
Antonio Heliodoro, Chávez-Aguilar, Héctor, Silva-Báez, Yamid Brajin, Sánchez-Rodríguez, Carlos, Esparza-Ponce, Miguel Ángel, Zatarain-Ontiveros, Juan Carlos, Barrera de León
Publikováno v:
Gaceta medica de Mexico. 151(3)
To describe the early complications of esophageal replacement with colon in children.Descriptive cross-sectional study from 2005 to 2011 in pediatric patients diagnosed with alkali intake, esophageal atresia or esophageal injury traumatic esophageal