LUIS
ALDÁMIZ-ECHEVARRÍA AZUARA
Forscher bis um 2020
M. T.
García Silva
Publikationen, an denen er mitarbeitet M. T. García Silva (3)
2020
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Availability, accessibility and delivery to patients of the 28 orphan medicines approved by the European Medicine Agency for hereditary metabolic diseases in the MetabERN network
Orphanet Journal of Rare Diseases, Vol. 15, Núm. 1
2017
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Genotype and phenotype characterization in a Spanish cohort with isovaleric acidemia
Journal of Human Genetics, Vol. 62, Núm. 3, pp. 355-360
2014
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Urea cycle disorders in Spain: an observational, cross-sectional and multicentric study of 104 cases
Orphanet journal of rare diseases, Vol. 9, pp. 187