Zobrazeno 1 - 6
of 6
pro vyhledávání: '"M. C., Valero"'
Autor:
C Benavent Garcia, A Romero Valero, A Garcia Suarez, F Peris Castello, F M Rodriguez Santiago, M Del Rio Lopez, N Vicente Ibarra, A Garcia Honrubia, M C Valero Medrano, M M Quintana Aguilar, M Martinez Moreno, M Gomez Martinez, E Castilla Cabanes, A S Tamayo Obregon, P Morillas Blasco
Publikováno v:
European Heart Journal. 43
Background Iron deficiency in patients with heart failure with reduced left ventricular ejection fraction (LVEF) confers a poor prognosis in terms of hospital admissions and mortality, worsening functional class and quality of life. Its replacement w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cdcb73808b07e7cb87522a6bf1c782c0
https://doi.org/10.1093/eurheartj/ehac544.072
https://doi.org/10.1093/eurheartj/ehac544.072
Autor:
J., Blanch, X., Nogués, M. J., Moro, M. C., Valero, D., del Pino-Montes, L., Canals, L., Lizán
Publikováno v:
Journal of Osteoporosis & Mineral Metabolism / Revista de Osteoporosis y Metabolismo Mineral (English edition); Apr-Jun2017, Vol. 9 Issue 2, p62-70, 9p
Autor:
J., Blanch, X., Nogués, M. J., Moro, M. C., Valero, del Pino-Montes, D., L., Canals, L., Lizán
Publikováno v:
Journal of Osteoporosis & Mineral Metabolism / Revista de Osteoporosis y Metabolismo Mineral (Spanish edition); abr-jun2017, Vol. 9 Issue 2, p62-71, 10p
Publikováno v:
Human genetics. 99(6)
Neurofibromatosis type 1 (NF1) is a common autosomal dominant disorder. To date, a relatively small number of NF1 mutations have been characterized, thus precluding genotype-phenotype correlations. By genotyping 75 NF1 families, we have detected six
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6beb5a7cbf1095d6fe23ba7a6e262d6c
https://pubmed.ncbi.nlm.nih.gov/9187663
https://pubmed.ncbi.nlm.nih.gov/9187663
Autor:
Felipe Moreno, Jesús Cruces, García-Patiño E, Eladio Velasco, Concepción Hernández-Chico, M C Valero, de la Puente A, Antonio Coloma, del Castillo I
Publikováno v:
Human molecular genetics. 3(8)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6c6d071604d59fa71bb0f3e28b809b0
https://pubmed.ncbi.nlm.nih.gov/7987335
https://pubmed.ncbi.nlm.nih.gov/7987335
Publikováno v:
Human molecular genetics. 3(4)
Neurofibromatosis type 1 (NF1) is one of the most common inherited disorders. The gene responsible for the disease has a very high mutation rate, approximately fifty per cent of NF1 patients appear to have a de novo mutation. The search for mutations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5167069794d497c61eada9d83baea711
https://pubmed.ncbi.nlm.nih.gov/8069310
https://pubmed.ncbi.nlm.nih.gov/8069310