Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Pablo Rodríguez-Doyágüez"'
Autor:
Esperanza Moral Berrio, José C. De La Flor, Minerva Arambarri Segura, Pablo Rodríguez-Doyágüez, Alberto Martínez Calero, Rocío Zamora, Michael Cieza-Terrones, Claudia Yuste-Lozano, María Dolores Sánchez de la Nieta García, Javier Nieto Iglesias, Carmen Vozmediano Poyatos
Publikováno v:
Medicina, Vol 60, Iss 8, p 1198 (2024)
Background and Objectives: Peritoneal dialysis (PD) is a renal replacement therapy modality in which the dialysis dose can be individually adapted according to the patients’ residual kidney function (RKF). RKF is a crucial factor for technique and
Externí odkaz:
https://doaj.org/article/ab197913201b41129bcb4bae2108a7b2
Autor:
Michael Cieza-Terrones, José C. De La Flor, Christian Requejo, Daniel Villa, Jacqueline Apaza, Pablo Rodríguez-Doyágüez, Rocío Zamora, Carmen Asato-Higa, David Rivera-Estrella, Antonio Carrasco-Yalán
Publikováno v:
Medicines, Vol 11, Iss 6, p 13 (2024)
Background: Idiopathic hypereosinophilic syndrome (IHES) is a disorder characterized by abnormal and persistent peripheral blood hypereosinophilia (eosinophil count ≥ 1.5 × 109/L and ≥10% eosinophils) with duration ≥ 6 months, associated organ
Externí odkaz:
https://doaj.org/article/ecc5fc55e2bb4b729039f16202860108
Publikováno v:
Medical Sciences, Vol 12, Iss 2, p 25 (2024)
Phospholipidosis is a rare disorder which consists of an excessive intracellular accumulation of phospholipids and the appearance of zebra bodies or lamellar bodies when looking at them using electron microscopy. This disease is associated with certa
Externí odkaz:
https://doaj.org/article/4fafe11e9f61441fb16a986a180dcf14
Autor:
Xavier E. Guerra-Torres, Pablo Rodríguez Doyágüez, Enrique Ovejero Merino, Alina Valeria Chávez Guillen, Hanane Bouarich, Fuensanta Moreno Barrio
Publikováno v:
Nefrología (English Edition), Vol 42, Iss 2, Pp 213-215 (2022)
Externí odkaz:
https://doaj.org/article/3de769bbac3442faa6bbccccb6cdf1d3
Autor:
Xavier E. Guerra-Torres, Pablo Rodríguez Doyágüez, Enrique Ovejero Merino, Alina Valeria Chávez Guillen, Hanane Bouarich, Fuensanta Moreno Barrio
Publikováno v:
Nefrología, Vol 42, Iss 2, Pp 213-215 (2022)
Externí odkaz:
https://doaj.org/article/11cede73017c403a8915dd4a9ab14611
Autor:
Pablo Rodríguez Doyágüez, Mónica Furlano, Elisabet Ars Criach, Yolanda Arce, Lluís Guirado, Roser Torra Balcells
Publikováno v:
Nefrología.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c59290beaa16f35c8ad0a0597dc01db2
https://doi.org/10.1016/j.nefro.2022.12.001
https://doi.org/10.1016/j.nefro.2022.12.001
Autor:
Hanane Bouarich, Fuensanta Moreno Barrio, Alina Chávez Guillén, Enrique Ovejero Merino, Pablo Rodríguez Doyágüez, X.E. Guerra-Torres
Publikováno v:
Nefrología. 42:213-215
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::820049432103134ba738b4e540629688
https://doi.org/10.1016/j.nefro.2020.09.003
https://doi.org/10.1016/j.nefro.2020.09.003
Autor:
Hernando Trujillo, Justo Sandino, Teresa Cavero, Fernando Caravaca-Fontán, Eduardo Gutiérrez, Ángel M. Sevillano, Amir Shabaka, Gema Fernández-Juárez, Pablo Rodríguez Doyágüez, Rocío Gimena Muñoz, Leonardo Calle García, Virginia Cabello, José Manuel Muñoz-Terol, Ana García Santiago, Oscar Toldos, Juan Antonio Moreno, Manuel Praga
Anticoagulant-related nephropathy (ARN) is a relatively novel recognized entity characterized by hematuria-associated acute kidney injury (AKI) in the context of overanticoagulation. Preexisting or underlying kidney disease seems to be a predisposing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5df2970f74c94801101a3a9a099e762
http://www.kireports.org/article/S2468024922010506/pdf
http://www.kireports.org/article/S2468024922010506/pdf
Autor:
Xavier E. Guerra-Torres, Pablo Rodríguez Doyágüez, Enrique Ovejero Merino, Alina Valeria Chávez Guillen, Hanane Bouarich, Fuensanta Moreno Barrio
Publikováno v:
Nefrologia.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ff3a530491aa7b5e2e653367e2bb43b
https://pubmed.ncbi.nlm.nih.gov/33334593
https://pubmed.ncbi.nlm.nih.gov/33334593
Autor:
Pablo Rodríguez Doyágüez, Mónica Furlano, Elisabet Ars Criach, Yolanda Arce, Lluís Guirado, Roser Torra Balcells
Publikováno v:
Nefrología (English Edition), Vol 43, Iss , Pp 91-95 (2023)
Fabry disease or also called Anderson-Fabry disease (FD) is a rare disease caused by pathogenic variants in the GLA gene, located on the X chromosome. This gene is involved in the metabolism of glycosphingolipids and its pathogenic variants cause a d
Externí odkaz:
https://doaj.org/article/b877b1a662324b6da1d080d28153b1f1