UNIOVI-PEDIATRIA
OVIPED
Hospital Severo Ochoa
Madrid, EspañaPublicacións en colaboración con investigadores/as de Hospital Severo Ochoa (7)
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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Familial hypercholesterolaemia in twin brothers born using in-vitro fertilisation with donor semen and ovules
Anales de Pediatria, Vol. 94, Núm. 3, pp. 179-180
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Phenotypic characterization of X-linked hypophosphatemia in pediatric Spanish population
Orphanet Journal of Rare Diseases, Vol. 16, Núm. 1
2017
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A new SLC12A3 founder mutation (p.Val647Met) in Gitelman's syndrome patients of Roma ancestry
Nefrologia, Vol. 37, Núm. 4, pp. 423-428
2007
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Strontium oral load test in children with idiopathic hypercalciuria
Pediatric Nephrology, Vol. 22, Núm. 9, pp. 1303-1307
2003
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IL-1α (-889) promoter polymorphism is a risk factor for osteomyelitis
American Journal of Medical Genetics, Vol. 119 A, Núm. 2, pp. 132-136
1996
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Expression of collagenase-3 in the rat ovary during the ovulatory process
Journal of Endocrinology, Vol. 149, Núm. 3, pp. 405-415