Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Alejandro del Castillo-Rueda"'
Autor:
Ana Lopez Aparicio, Alejandro García-Espona-Pancorbo, Marta Clavero-Olmos, Inmaculada Muñoz-Roldán, Alejandro del Castillo-Rueda
Publikováno v:
European Journal of Case Reports in Internal Medicine, Vol 2, Iss 6 (2015)
Background and objectives: Significantly elevated serum ferritin levels are associated with both iron overload and some inflammatory conditions. Hepcidin is a protein that interferes with iron absorption in inflammatory states and acts as an acute-ph
Externí odkaz:
https://doaj.org/article/02d105971d684c4f8cf23d72982314fd
Autor:
Alejandro del Castillo Rueda
Publikováno v:
Atención Primaria Práctica, Vol 3, Iss 4, Pp 100106- (2021)
Externí odkaz:
https://doaj.org/article/5a9000eff6b74ca8be5ad13af973ebf7
Autor:
Alejandro del Castillo Rueda
Publikováno v:
Medicina Clínica (English Edition). 159:e30-e31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::12714dfbd9edb53ffc6012cb336f95ea
https://doi.org/10.1016/j.medcle.2022.02.026
https://doi.org/10.1016/j.medcle.2022.02.026
Autor:
Alejandro del Castillo Rueda
Publikováno v:
Medicina Clínica. 159:e30-e31
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe5a124baf5ee9c91a2705c1ddad1de1
https://doi.org/10.1016/j.medcli.2022.02.019
https://doi.org/10.1016/j.medcli.2022.02.019
Autor:
María-Josefa Morán-Jiménez, María José Hernández-Alfaro, Manuel Méndez, Juan-Antonio Muñoz-Muñoz, María-Isabel Moreno-Carralero, Rafaela López-Rodríguez, Nuria Cuadrado-Grande, Rafael Enríquez-de-Salamanca, Alejandro del-Castillo-Rueda
Publikováno v:
American Journal of Hematology. 89:689-694
Ferroportin disease is an inherited disorder of iron metabolism and is caused by mutations in the ferroportin gene (SLC40A1). We present a patient with hyperferritinemia, iron overload in the liver with reticuloendothelial distribution and also in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e87186bf52d56acbc36da9cf54bf6f8
https://doi.org/10.1002/ajh.23714
https://doi.org/10.1002/ajh.23714
Autor:
Priscilla Sugianto, Eileen Fung, Tomas Ganz, Bo Qiao, María-Josefa Morán-Jiménez, Elizabeta Nemeth, Alejandro del-Castillo-Rueda
Publikováno v:
Cell Metabolism. 15:918-924
Summary Ferroportin exports iron into plasma from absorptive enterocytes, erythrophagocytosing macrophages, and hepatic stores. The hormone hepcidin controls cellular iron export and plasma iron concentrations by binding to ferroportin and causing it
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ccbd2516cb6ae9b61c5634c6276895d3
https://doi.org/10.1016/j.cmet.2012.03.018
https://doi.org/10.1016/j.cmet.2012.03.018
Autor:
Alejandro del-Castillo-Rueda, Nuria Cuadrado-Grande, Emilio Álvarez-Fernández, Rafael Enríquez-de-Salamanca, Luis Antonio Álvarez-Sala, María Josefa Morán-Jiménez
Publikováno v:
Revista Espanola de Enfermedades Digestivas, Vol 103, Iss 7, Pp 379-382 (2011)
Iron overload disease has a wide variety of genotypes. The genetic study of this disease confirms its hereditary nature and enables us to provide genetic counseling for first-degree relatives. We performed magnetic resonance imaging and liver biopsy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::3cbe0ada8bf6f04bfa0ffed00865022f
http://scielo.isciii.es/scielo.php?script=sci_arttext&pid=S1130-01082011000700010
http://scielo.isciii.es/scielo.php?script=sci_arttext&pid=S1130-01082011000700010
Autor:
María Josefa Morán Jiménez, Luis Antonio Alvarez Sala, Alejandro del Castillo Rueda, Nuria Cuadrado Grande, Emilio Alvarez Fernández, Rafael Enríquez de Salamanca
Publikováno v:
Revista Española de Enfermedades Digestivas v.103 n.7 2011
SciELO España. Revistas Científicas Españolas de Ciencias de la Salud
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SciELO España. Revistas Científicas Españolas de Ciencias de la Salud
instname
Iron overload disease has a wide variety of genotypes. The genetic study of this disease confirms its hereditary nature and enables us to provide genetic counseling for first-degree relatives. We performed magnetic resonance imaging and liver biopsy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29520fe9d05f5b1383c088a9c7ba95ed
https://doi.org/10.4321/s1130-01082011000700010
https://doi.org/10.4321/s1130-01082011000700010
Autor:
María-Josefa Morán-Jiménez, Nuria Cuadrado-Grande, María Isabel Moreno-Carralero, Alejandro del Castillo-Rueda, Manuel Méndez
Publikováno v:
Medicina Clínica. 137:68-72
Resumen Fundamento y objetivo La hiperferritinemia es un hallazgo comun en la practica clinica diaria que puede ser congenita o adquirida y no siempre se asocia con sobrecarga ferrica. La hiperferritinemia genetica puede acompanarse de sobrecarga, co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c0f92003791f9b7ce38191e40247fce
https://doi.org/10.1016/j.medcli.2011.02.023
https://doi.org/10.1016/j.medcli.2011.02.023
Autor:
Manuel Méndez, María-Isabel Moreno-Carralero, Luis-Antonio Álvarez-Sala-Walther, María-Josefa Morán-Jiménez, Nuria Cuadrado-Grande, Rafael Enríquez-de-Salamanca, Alejandro del-Castillo-Rueda
Publikováno v:
European Journal of Haematology. 86:260-264
The most common form of hemochromatosis is caused by mutations in the HFE gene. Rare forms of the disease are caused by mutations in other genes. We present a patient with hyperferritinemia and iron overload, and facial flushing. Magnetic resonance i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6ad7963da5d79c10cf388b0674096ca9
https://doi.org/10.1111/j.1600-0609.2010.01565.x
https://doi.org/10.1111/j.1600-0609.2010.01565.x