Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Francisco Hevia Urrutia"'
Autor:
Danny Alvarado, Jorge Andres Herrera Corrales, Mildred Jimenez, Karina Hidalgo, Fernanda Vasquez, Francisco Vargas, Jorge Vargas, Francisco Hevia Urrutia
Publikováno v:
Annals of Hepatology, Vol 29, Iss , Pp 101610- (2024)
Conflict of interest: No Introduction and Objectives: In a recent article from the American Journal of Human Genetics, the genetic behavior of variants associated with Wilson's Disease (WD) is analyzed, alongside the worldwide discovery of the respon
Externí odkaz:
https://doaj.org/article/3614c364ecb244f2a0f1f0e3d4bef67f
Autor:
Fernanda Vásquez Carit, Francisco Hevia Urrutia, Jorge Vargas Madrigal, Mildred Jiménez Hernández, Natassia Camacho Matamoros, Danny Alvarado Romero, Jorge Herrera Corrales
Publikováno v:
Annals of Hepatology, Vol 29, Iss , Pp 101628- (2024)
Conflict of interest: No Introduction and Objectives: Alpha-1 antitrypsin (A1AT) levels are normal in up to 20% of liver diseases, and this protein elevates in inflammatory states, causing false negatives. This disease does not follow an autosomal re
Externí odkaz:
https://doaj.org/article/824bb847ba0f4a5f9fbf285a38983804
Autor:
Jorge Andres Herrera Corrales, Francisco Hevia Urrutia, Danny Alvarado, Fernanda Vasquez Carit, Francisco Vargas Navarro, Jorge Eduardo Vargas Madrigal, Karina Hidalgo, Mildred Jimenez
Publikováno v:
Annals of Hepatology, Vol 29, Iss , Pp 101645- (2024)
Conflict of interest: No Introduction and Objectives: Acute liver failure (ALF) can be defined as a complex clinical syndrome characterized by coagulopathy, alteration in liver biochemistry and encephalopathy in a patient without underlying chronic l
Externí odkaz:
https://doaj.org/article/f63b5996385d486e937ef205d4a74b12
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56e1e54a98e467cf1c3bbbc18208a903
https://pubmed.ncbi.nlm.nih.gov/32154060
https://pubmed.ncbi.nlm.nih.gov/32154060
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::55e661bff68901e16817132ed1cd4d7d
https://pubmed.ncbi.nlm.nih.gov/31333228
https://pubmed.ncbi.nlm.nih.gov/31333228
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…
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5a7f3526cfd6716d93625be6526231c
https://doi.org/10.51481/amc.v37i1.623
https://doi.org/10.51481/amc.v37i1.623
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::643e1ffcb9b6fe39cdf862a2201fceca