Zobrazeno 1 - 10
of 12
pro vyhledávání: '"César Loris"'
Publikováno v:
Gaceta Sanitaria, Vol 31, Iss 3, p 276 (2017)
Externí odkaz:
https://doaj.org/article/14918da76d5744978dbf23b323826b7d
Autor:
Pablo, César Loris
Publikováno v:
In Anales de pediatria continuada November-December 2014 12(6):355-361
Publikováno v:
Gaceta Sanitaria, Vol 31, Iss 3, p 276 (2017)
Gaceta Sanitaria v.31 n.3 2017
SciELO España. Revistas Científicas Españolas de Ciencias de la Salud
instname
Gaceta Sanitaria v.31 n.3 2017
SciELO España. Revistas Científicas Españolas de Ciencias de la Salud
instname
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b15cdb6a74006c32c2a1daddc068beb9
Autor:
César Loris Pablo
Publikováno v:
Anales de Pediatría Continuada. 12:355-361
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d3f261c91883aea08ab87637183ad3d
https://doi.org/10.1016/s1696-2818(14)70217-3
https://doi.org/10.1016/s1696-2818(14)70217-3
Publikováno v:
Anales de Pediatría Continuada. 7:353-357
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee8e8e626236b1eccceec08a644194a0
https://doi.org/10.1016/s1696-2818(09)73205-6
https://doi.org/10.1016/s1696-2818(09)73205-6
Predictors of Final Adult Height after Renal Transplantation during Childhood: A Single-Center Study
Publikováno v:
Nephron. 86:266-273
Aim: Assessment of final adult height and its predictive factors in children transplanted (RTx) and followed up in a single center. Methods: A cohort of 32 patients (17 boys, 15 girls) who received RTx before the age of 15 years and had reached a fin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a810fc74c3108b86711d45a46fa18ef9
https://doi.org/10.1159/000045780
https://doi.org/10.1159/000045780
Publikováno v:
Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia. 34(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2f44c88686c0124b2d908627fe84eda7
https://pubmed.ncbi.nlm.nih.gov/24463860
https://pubmed.ncbi.nlm.nih.gov/24463860
Autor:
Bettina Lorenz-Depiereux, Mustapha Amyere, Ursula Müller-Barth, Miikka Vikkula, Stephanie M Kaiser, Janine Wagenstaller, José L. Olivares, Roger S. Rittmaster, Alan H Shlossberg, Klaus Badenhoop, Tim M. Strom, Harald Jüppner, César Loris, Feliciano J. Ramos, Anna Benet-Pagès, Murat Bastepe, Francis H. Glorieux
Publikováno v:
Nature Genetics, Vol. 38, no. 11, p. 1248-1250 (2006)
Hypophosphatemia is a genetically heterogeneous disease. Here, we mapped an autosomal recessive form (designated ARHP) to chromosome 4q21 and identified homozygous mutations in DMP1 (dentin matrix protein 1), which encodes a non-collagenous bone matr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8747576acc94c7999b447cf86f08bfe8
https://pubmed.ncbi.nlm.nih.gov/17395654
https://pubmed.ncbi.nlm.nih.gov/17395654
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