Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Cesar Loris"'
Autor:
Félix Claverie-Martín, Víctor García-Nieto, Cesar Loris, Gema Ariceta, Inmaculada Nadal, Laura Espinosa, Ángeles Fernández-Maseda, Montserrat Antón-Gamero, Africa Avila, Álvaro Madrid, Hilaria González-Acosta, Elizabeth Córdoba-Lanus, Fernando Santos, Marta Gil-Calvo, Mar Espino, Elena García-Martinez, Ana Sanchez, Rafael Muley, RenalTube Group
Publikováno v:
PLoS ONE, Vol 8, Iss 1, p e53151 (2013)
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis is an autosomal recessive tubular disorder characterized by excessive renal magnesium and calcium excretion and chronic kidney failure. This rare disease is caused by mutations in the C
Externí odkaz:
https://doaj.org/article/2c3ebfb9b36c483bb8d72f29164232c0
Autor:
Félix Claverie-Martín, Víctor García-Nieto, Cesar Loris, Gema Ariceta, Inmaculada Nadal, Laura Espinosa, Ángeles Fernández-Maseda, Montserrat Antón-Gamero, África Avila, Álvaro Madrid, Hilaria González-Acosta, Elizabeth Córdoba-Lanus, Fernando Santos, Marta Gil-Calvo, Mar Espino, Elena García-Martinez, Ana Sanchez, Rafael Muley
Publikováno v:
PLoS ONE, Vol 8, Iss 10 (2013)
Externí odkaz:
https://doaj.org/article/1552117235a14ab3833cbe4a2ee7ddaf
Autor:
Pablo, César Loris
Publikováno v:
In Anales de pediatria continuada November-December 2014 12(6):355-361
Autor:
Julián Rodríguez, Helena Gil-Peña, José David Herrero-Morín, Eliecer Coto, L. Espinosa, Victoria Alvarez, Fernando Santos, Cesar Loris, Marta Gil-Calvo
Publikováno v:
Nephrology Dialysis Transplantation. 26:151-155
Background. Gitelman syndrome is a primary tubular disorder causing hypokalaemic metabolic alkalosis with hypocalciuria. Its prevalence is high in Gypsies, who harbour an identical mutation, intron 9 + 1 G>T, in the SLC12A3 gene. Methods. To better d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1987589258bc2045d5f36cc1e83e03d
https://doi.org/10.1093/ndt/gfq352
https://doi.org/10.1093/ndt/gfq352
Autor:
Serafín Málaga, Gema Ariceta, Mercedes Navarro, Isolina Riaño-Galán, Cesar Loris, Luis Rajmil, Alfredo Vallo
Publikováno v:
Pediatric Nephrology. 24:1561-1568
The health-related quality of life (HRQOL) of adolescents with end-stage renal disease (ESRD) is an important marker of disease burden. Our aims were to investigate HRQOL in a group of children and adolescents with ESRD and to compare them with the r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a701d462da32e04184fdcfcb09526646
https://doi.org/10.1007/s00467-009-1175-0
https://doi.org/10.1007/s00467-009-1175-0
Autor:
Irma Carballo‐Trujillo, Francisco J. Moya‐Angeler, Cesar Loris, Sebastián Méndez-Álvarez, Montserrat Antón-Gamero, Felix Claverie-Martin, Víctor García-Nieto
Publikováno v:
Nephrology Dialysis Transplantation. 18:717-723
Background. Dent’s disease is characterized by lowmolecular-weight proteinuria, hypercalciuria, nephrocalcinosis, nephrolithiasis, rickets and eventual renal failure. The disease is caused by mutations in the Xlinked chloride channel CLCN5 gene, wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e410de1ee02b1e6ea6fe9b2c85b1b02a
https://doi.org/10.1093/ndt/gfg016
https://doi.org/10.1093/ndt/gfg016
Autor:
Félix, Claverie-Martín, Víctor, García-Nieto, Cesar, Loris, Gema, Ariceta, Inmaculada, Nadal, Laura, Espinosa, Ángeles, Fernández-Maseda, Montserrat, Antón-Gamero, Africa, Avila, Álvaro, Madrid, Hilaria, González-Acosta, Elizabeth, Córdoba-Lanus, Fernando, Santos, Marta, Gil-Calvo, Mar, Espino, Elena, García-Martinez, Ana, Sanchez, Rafael, Muley, Mireia, Aguirre Meñica
Publikováno v:
PLoS ONE
PLoS ONE, Vol 8, Iss 1, p e53151 (2013)
PLoS ONE, Vol 8, Iss 1, p e53151 (2013)
Journal Article; Research Support, Non-U.S. Gov't; Familial hypomagnesemia with hypercalciuria and nephrocalcinosis is an autosomal recessive tubular disorder characterized by excessive renal magnesium and calcium excretion and chronic kidney failure
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea7d7895cca58a0afa669374b78496f0
https://pubmed.ncbi.nlm.nih.gov/23301036
https://pubmed.ncbi.nlm.nih.gov/23301036
Autor:
Eliecer Coto, Michel Fischbach, Rosario Stone, Julián Rodríguez, Victoria Alvarez, Fernando Santos, Hannsjörg W. Seyberth, Luis M. Rodríguez, Nikola Jeck, Cesar Loris
Publikováno v:
Kidney international. 65(1)
A new mutation (intron 9 +1 G>T) in the SLC12A3 gene is linked to Gitelman syndrome in Gypsies. Background Gitel syndrome is an inherited tubular disorder characterized by metabolic alkalosis, hypokalemia, and hypomagnesemia of renal origin and hypoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79868af069c94951a08380f84b32dd86
https://pubmed.ncbi.nlm.nih.gov/17882248
https://pubmed.ncbi.nlm.nih.gov/17882248
Autor:
Rafael Pardo, Ruth Alvarez, Mercedes Navarro, Cesar Loris, Victoria Alvarez, L. Espinosa, Alfredo Vallo, Serafín Málaga, Eliecer Coto, Socorro Braga
Publikováno v:
Pediatric nephrology (Berlin, Germany). 18(2)
The purpose of the study was to determine whether DNA polymorphisms at the renin-angiotensin-aldosterone (RAS) genes were associated with evolution to renal scar formation and, consequently, with reflux nephropathy (RN) in patients with vesicouretera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::795fcb739417932ee0c14f58ee4c440e
https://pubmed.ncbi.nlm.nih.gov/12579398
https://pubmed.ncbi.nlm.nih.gov/12579398
Autor:
L Callis, J Martin-Govantes, Serafín Málaga, Cesar Loris, I Riaño, Alfredo Vallo, Mercedes Navarro
Publikováno v:
Scopus-Elsevier
There are few data describing the current practices of treatment selection for children with end-stage renal disease (ESRD). In an effort to establish a consensus among Spanish pediatric nephrologists for inclusion and exclusion criteria for renal re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0774bf6179cbdcfddfa8c595957930fd
https://pubmed.ncbi.nlm.nih.gov/11095035
https://pubmed.ncbi.nlm.nih.gov/11095035