HELENA
GIL PEÑA
Investigador/a
Laura
Espinosa Román
Publicaciones en las que colabora con Laura Espinosa Román (3)
2021
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Correction to: Phenotypic characterization of X-linked hypophosphatemia in pediatric Spanish population (Orphanet Journal of Rare Diseases, (2021), 16, 1, (104), 10.1186/s13023-021-01729-0)
Orphanet Journal of Rare Diseases
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Phenotypic characterization of X-linked hypophosphatemia in pediatric Spanish population
Orphanet Journal of Rare Diseases, Vol. 16, Núm. 1
2011
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Gitelman syndrome in Gypsy paediatric patients carrying the same intron 9 + 1 G>T mutation. Clinical features and impact on quality of life
Nephrology Dialysis Transplantation, Vol. 26, Núm. 1, pp. 151-155