Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Francisco Hevia-Urrutia"'
Autor:
Daniela Hernández-Castro, Wagner Ramírez-Quesada, Carolina Gutiérrez-Ramírez, Sylvia Álvarez-Umaña, José Pablo Cortes-Navarrete, Aldo Carvajal-González, Francisco Hevia-Urrutia, Ana Lorena Madrigal-Méndez, Jorge Vargas-Madrigal
Publikováno v:
Annals of Hepatology, Vol 28, Iss , Pp 100978- (2023)
Introduction and Objectives: Endoscopic ultrasound-guided liver biopsy (EUS-LB) has been proposed as a novel technique that could offer some advantages over traditional methods, especially regarding specimen adequacy. A systematic review that include
Externí odkaz:
https://doaj.org/article/34c5872b0fb24642889c28fee60c0540
Autor:
Monica Penon‐Portmann, Stephanie Lotz‐Esquivel, Alejandra Chavez Carrera, Mildred Jiménez‐Hernández, Danny Alvarado‐Romero, Sharon Segura‐Cordero, Fiorella Rimolo‐Donadio, Francisco Hevia‐Urrutia, Alfredo Mora‐Guevara, Manuel Saborío‐Rocafort, Gabriela Jiménez‐Arguedas, Ramsés Badilla‐Porras
Publikováno v:
JIMD Reports, Vol 52, Iss 1, Pp 55-62 (2020)
Abstract Introduction The prevalence of Wilson disease (WD) in Costa Rica is among the highest reported in the world, 4.9:100 000. Previous investigators have also described a burden of autosomal recessive conditions in this country. Genetic testing
Externí odkaz:
https://doaj.org/article/1a193398fcd844faa43ef76b7306a0b8
Autor:
Ricardo Barahona-García, Francisco Hevia-Urrutia, Marianella Madrigal-Borloz, Wagner Ramírez-Quesada
Publikováno v:
Acta Médica Costarricense, Volume: 62, Issue: 4, Pages: 187-195, Published: DEC 2020
Resumen Introducción: Costa Rica es un país con un sistema de salud pública que ha permitido detectar oportunamente a los pacientes con hepatitis C, y ofrecer un tratamiento con base en antivirales de acción directa (AAD) de última generación.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57ad425789a736ddc9ec0efa6b982ef4
http://www.scielo.sa.cr/scielo.php?script=sci_arttext&pid=S0001-60022020000400187&lng=en&tlng=en
http://www.scielo.sa.cr/scielo.php?script=sci_arttext&pid=S0001-60022020000400187&lng=en&tlng=en
Autor:
Mildred Jiménez-Hernández, Alejandra Chavez Carrera, Sharon Segura‐Cordero, Francisco Hevia-Urrutia, Monica Penon-Portmann, Danny Alvarado-Romero, Alfredo Mora‐Guevara, Gabriela Jiménez‐Arguedas, Stephanie Lotz-Esquivel, Ramsés Badilla‐Porras, Fiorella Rimolo‐Donadio, Manuel Saborío-Rocafort
Publikováno v:
JIMD Reports, Vol 52, Iss 1, Pp 55-62 (2020)
JIMD Reports
JIMD Reports
Introduction The prevalence of Wilson disease (WD) in Costa Rica is among the highest reported in the world, 4.9:100 000. Previous investigators have also described a burden of autosomal recessive conditions in this country. Genetic testing for WD be
Autor:
Wagner, Ramírez-Quesada, Francisco, Hevia-Urrutia, Marlon, Rojas-Alvarado, Fernando, Brenes-Pino, Eduardo, Alfaro-Alcocer, Johanna, Sauma-Rodríguez, Manuel, Saborío-Rocafort, Mildred, Jiménez-Hernández, Natassia, Camacho-Matamoros, Danny, Alvarado-Romero
Publikováno v:
Revista de gastroenterologia del Peru : organo oficial de la Sociedad de Gastroenterologia del Peru. 39(2)
Alfa 1-antitrypsin deficiency is one of the most prevalent genetic diseases in the human being, sadly it is not a commonly suspected clinical entity. With more than 100 known mutations, those associated with hepatic disease are the Z homocygote allel
Publikováno v:
Acta Médica Costarricense. 37
Los síndromes de malabsorción constituyen una entidad compleja de etiopatogenia multifactorial. Clásicamente se describe el sprue tropical, entidad con predisposición genética…
Autor:
Cecilia Monge-Bonilla, Marcela Barguil-Gallardo, Marta Sánchez-Molina, Oscar Méndez-Blanca, Álvaro Sánchez-Siles, Ileana Alvarado-Echeverría, Luis Meza-Sierra, Alexander Parajeles-Vindas, Francisco Hevia-Urrutia, Manuel Saborío-Rocafort, Iliana Chavarría-Quirós, Alfredo Sanabria-Castro
Publikováno v:
Hepatology, Medicine and Policy
Hepatology, Medicine and Policy, Vol 2, Iss 1, Pp 1-6 (2016)
Hepatology, Medicine and Policy, Vol 2, Iss 1, Pp 1-6 (2016)
Wilson’s disease is an inherited disorder in which defective biliary excretion of copper leads to its accumulation, particularly in the liver and brain. Mutations in the ATP7B gene on chromosome 13 cause Wilson’s disease. If left untreated it wil
Publikováno v:
Acta Médica Costarricense, Vol 50, Iss suppl 3, Pp 03-04 (2008)
Externí odkaz:
https://doaj.org/article/052380e89d6f45d5945c63e19500f2ec