Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Lidia Castro-Feijoó"'
Autor:
Raquel Corripio, Leandro Soriano-Guillén, Francisco-Javier Herrero, Lidia Castro-Feijoó, Aránzazu Escribano, Paula Sol-Ventura, Rafael Espino, Amaia Vela, José-Ignacio Labarta, The Spanish PUBERE Group, Jesús Argente, Ignacio Díez López, Rafael Ruiz Cano, José Pastor Rosado, Diego Esteban de Sotto, Nuria Cabrinety Perez, Diego Yeste Fernández, Larisa Suárez Ortega, Mariona Bonet Alcaina, Rosa Martín Ramos, Gertrudis Martí Aromir, Rosangela Tomasini, Gemma Carreras González, María Victoria Borrás Pérez, Meritxell Torrabías Rodas, Montserrat Roqueta Sureda, Marta Murillo Valles, Francisco Javier Arroyo Díez, Jesús González de Buitrago, José Luis Lechuga Campoy, Alfonso Lechuga Sancho, Ramón Cañete Estrada, Lidia Castro Feijóo, Jesús Barreiro Conde, Paloma Cabanas Rodríguez, Jordi Bosch Muñoz, Alicia Cepedano Dans, Mª Teresa Muñoz Calvo, Julio Guerrero Fernández, Rafael Yturriaga Matarranz, Elena Gallego Gómez, Jaime Sánchez del Pozo, Purificación Ros Pérez, Joaquín Ramírez Fernández, Mª Dolores Rodríguez Arnao, Amparo Rodríguez Sánchez, Juan Pedro López Siguero, Maria Jose Martinez-Aedo Ollero, Antonio Gutiérrez Macias, José María Martos Tello, María Chueca Guindulain, Cristina Azcona Sanjulián, Pablo Guerrero, Isolina Riaño Galán, Sofía Quinteiro González, José Manuel Rial Rodríguez, Juan Pedro González Díaz, Rafael Espino Aguilar, Luis López-Canti, Raquel Monné Gelonch, Jesús Martín Calama, Lidia Blasco Gonzalez, Juan Alcón SáezJosé, Amparo Plasencia Couchoud, Luis Castaño González, Pedro Martul Tobío, Itxaso Rica Etxebarría, Concepción Fernández Ramos, Mª. Zaragoza Lou Francés Gracia, Manuel Ruiz-Echarri Zalaya, Gloria Bueno Lozano
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
ObjectiveIdiopathic central precocious puberty (CPP) precipitates epiphyseal fusion of growth plates in long bones, leading to reduced adult stature. Gonadotropin-releasing hormone analogues (GnRHa) are the treatment of choice for idiopathic CPP, but
Externí odkaz:
https://doaj.org/article/867c62e98a744977af47cfe8cacfc68d
Autor:
Alberto Gómez-Carballa, María Cerezo, Emilia Balboa, Claudia Heredia, Lidia Castro-Feijóo, Itxaso Rica, Jesús Barreiro, Jesús Eirís, Paloma Cabanas, Isabel Martínez-Soto, Joaquín Fernández-Toral, Manuel Castro-Gago, Manuel Pombo, Ángel Carracedo, Francisco Barros, Antonio Salas
Publikováno v:
PLoS ONE, Vol 6, Iss 4, p e18348 (2011)
BACKGROUND: There are several known autosomal genes responsible for Ras/MAPK pathway syndromes, including Noonan syndrome (NS) and related disorders (such as LEOPARD, neurofibromatosis type 1), although mutations of these genes do not explain all cas
Externí odkaz:
https://doaj.org/article/b8063b8f143b4d779742046bb25b7b6c
Autor:
Francisco Sousa-Santos, Helder Simões, Lidia Castro-Feijóo, Paloma Cabanas Rodríguez, Ana Fernández-Marmiesse, Rebeca Saborido Fiaño, Teresa Rego, Ángel Carracedo, Jesús Barreiro Conde
Publikováno v:
Archives of Endocrinology and Metabolism, Vol 62, Iss 5, Pp 560-565
SUMMARY Congenital hyperinsulinism (CHI) is a heterogenous disease caused by insulin secretion regulatory defects, being ABCC8/KCNJ11 the most commonly affected genes. Therapeutic options include diazoxide, somatostatin analogues and surgery, which i
Externí odkaz:
https://doaj.org/article/5f848febb63447a59a29afe718a2628b