Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Joaquín, Arcas"'
Autor:
Gabriela, Pesántez-Ríos, Antonio, Martínez-Bermejo, Joaquín, Arcas, Milagros, Merino-Andreu, Arturo, Ugalde-Canitrot
Publikováno v:
Revista de neurologia. 61(3)
The development of atypical features in rolandic epilepsy is part of a clinical spectrum of phenotypes that are variable, idiopathic and age-dependent, as well as having a genetically determined predisposition.To study the electroclinical characteris
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8404f966fa11fe2d5f0dbf4dcb0732cd
https://pubmed.ncbi.nlm.nih.gov/26178515
https://pubmed.ncbi.nlm.nih.gov/26178515
Autor:
Patrick O'Neill, Teresa H. Ramos, Joaquín Arcas, Juan G. Puig, Felícitas A. Mateos, Antonio Buño, Rosa J. Torres
Publikováno v:
Medicine. 80:102-112
The enzyme hypoxanthine-guanine phosphoribosyltransferase (HPRT) catalyzes the reutilization of hypoxanthine and guanine to the purine nucleotides IMP and GMP, respectively. HPRT deficiency is an X-linked disorder characterized by uric acid overprodu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65fd32188a795401dde9dcda99503971
https://doi.org/10.1097/00005792-200103000-00003
https://doi.org/10.1097/00005792-200103000-00003
Autor:
Felícitas A. Mateos, Juan G. Puig, Antonio Buño, Joaquín Arcas, Teresa H. Ramos, Rosa J. Torres
Publikováno v:
Purine and Pyrimidine Metabolism in Man X ISBN: 0306465159
Summary The enzyme hypoxanthine-guanine phosphoribo-syltransferase (HPRT) catalyzes the reutilization ofhypoxanthine and guanine to the purine nucleotidesIMP and GMP, respectively. HPRT deficiency is an X-linked disorder characterized by uric acid o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d8f3041163d9e9c326280c34e5236868
https://doi.org/10.1007/0-306-46843-3_4
https://doi.org/10.1007/0-306-46843-3_4
Autor:
Felícitas A. Mateos, Antonio Buño, Juan G. Puig, Ignacio Pascual-Castroviejo, Joaquín Arcas, Rosa J. Torres
Publikováno v:
Advances in Experimental Medicine and Biology ISBN: 9781461374565
Patients with HGPRT deficiency may be phenotypically classified into two differentiated entities: (a) Lesch-Nyhan syndrome, also named “complete HGPRT deficiency”, characterized by spasticity, choreoathetosis, mental retardation, and self-mutilat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::499120f49af6d0031d686aaecdc27c31
https://doi.org/10.1007/978-1-4615-5381-6_5
https://doi.org/10.1007/978-1-4615-5381-6_5
Autor:
Antonio Martínez Bermejo, Isabel Polanco Allué, Alfredo Royo, Valentín López Martín, Joaquín Arcas Martínez, Adrián Tendero Gormaz, Alberto Fernández Jaén, Ignacio Pascual Castroviejo
Publikováno v:
Revista de Neurología. 29:105
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::73c6e194a349723513d603a704559d25
https://doi.org/10.33588/rn.2902.99144
https://doi.org/10.33588/rn.2902.99144
Autor:
Sánchez-Arcilla Bernal, José
Desde hace algunos años los autores de los trabajos de investigación que componen este libro hemos venido estudiando documentación judicial conservada en archivos de lugares muy diferentes y en períodos relativamente diversos, con el objetivo de
th th This volume comprizes articles presented at the joint IX International and 6 Euro pean Symposium on Purine and Pyrimidine Metabolism in Man held in Gmunden, Austria, June 1 through 7, 1997. Since the first of this series of meetings was held
Autor:
Esther Zoref-Shani, Oded Sperling
th This volume contains articles presented at the X International Symposium on Purines and Pyrimidines in Man, held on May 14 19, 2000 in Tel Aviv, Israel. The first symposium in this series took place in Tel Aviv in 1973. Since then, the symposium h