Zobrazeno 1 - 10
of 56
pro vyhledávání: '"Felícitas A. Mateos"'
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:
Rafael Ortega, Juan G. Puig, Felipe Rodriguez, Felícitas A. Mateos, Rafael Dal-Ré, Antonio Buño
Publikováno v:
Journal of Hypertension. 17:1033-1039
OBJECTIVE The influence of angiotensin II AT-1 receptor antagonists on uric acid metabolism, and the potential differences among them with regard to this effect, remains to be precisely established. This study was designed to compare the effects of l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::159d199c06ff5a2a1f40bc61864d4c7e
https://doi.org/10.1097/00004872-199917070-00021
https://doi.org/10.1097/00004872-199917070-00021
Publikováno v:
European Journal of Clinical Investigation. 28:950-957
Background Female carriers of the X-linked recessive disorder hypoxanthine‐guanine phosphoribosyltransferase (HPRT) deficiency show somatic cell mosaicism, and this may cause an increased synthesis of purines. We have examined whether urinary oxypu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09a6004cfe8638499ac70cf548eddb9e
https://doi.org/10.1046/j.1365-2362.1998.00392.x
https://doi.org/10.1046/j.1365-2362.1998.00392.x
Autor:
Carlos Pérez de Ayala, Felícitas A. Mateos, Juan G. Puig, Rosa J. Torres, Antonio Gil, Eugenio de Miguel, Maria Eugenia Miranda
Publikováno v:
The American Journal of Medicine. 97:332-338
purpose: Uncontrolled studies have shown that women with gout have higher serum urate concentrations and similar or lower urinary uric acid excretion rates than do men with gout. These observations suggest a more defective tubular transport of uric a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c88a0f800229986b4374fc7ba9f3644b
https://doi.org/10.1016/0002-9343(94)90299-2
https://doi.org/10.1016/0002-9343(94)90299-2
Publikováno v:
Clinica Chimica Acta. 224:55-63
Methods currently employed for measurement of phosphoribosylpyrophosphate synthetase (ribophosphate pyrophosphokinase; PRPPs) activity are cumbersome and expensive, requiring an auxiliary enzyme reaction, a radioactive nucleobase and multiple incubat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fa906869f70196f33dab20cd5fb200a
https://doi.org/10.1016/0009-8981(94)90120-1
https://doi.org/10.1016/0009-8981(94)90120-1
Autor:
Ma. C. Capitán, Antonio J. Gil, Juan G. Puig, Teresa H. Ramos, Felícitas A. Mateos, Ma Paz Lavilla
Publikováno v:
American Journal of Hypertension. 7:46-51
A prospective randomized, double-blind, double-dummy study investigated the effects of two angiotensin converting enzyme (ACE) inhibitors on urinary albumin excretion in nondiabetic patients with mild to moderate essential hypertension. At the end of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::64518de6b09e650de59646f4d21af59a
https://doi.org/10.1093/ajh/7.1.46
https://doi.org/10.1093/ajh/7.1.46
Autor:
Juan G. Puig, Eugenio de Miguel, Ma. Eugenia Miranda, Ana Espinosa, J. Gijon, Nuria M. Romera, Felícitas A. Mateos
Publikováno v:
Muscle & Nerve. 15:822-828
We report the first case of McArdle's disease (muscle phosphorylase deficiency) and tophaceous gout. To examine the contribution of adenine nucleotide degradation to the disturbance of uric acid metabolism, we labeled the adenine nucleotide pool with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eca7694850e9f475d7c0bfb8d9159eb2
https://doi.org/10.1002/mus.880150711
https://doi.org/10.1002/mus.880150711
Autor:
Felícitas A. Mateos, Rosa J. Torres, R. M. Gundel, J.P. O'Neill, B. S. Gathoff, J. Molano, L. Trombley, Juan G. Puig
Publikováno v:
Purine and Pyrimidine Metabolism in Man X ISBN: 0306465159
Mutations found in Spanish deficient families are heterogeneous: 8 point mutations, 3 deletions and 2 insertions, and are dispersed all over the HPRT gene. There is not a prevalent mutation in the Spanish HPRT deficient population.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5443d628b8877d11ae4033119bf11783
https://doi.org/10.1007/0-306-46843-3_3
https://doi.org/10.1007/0-306-46843-3_3
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