Pediatría
Servicio
Hannover Medical School
Hanóver, AlemaniaPublicaciones en colaboración con investigadores/as de Hannover Medical School (5)
2024
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Brain function in classic galactosemia, a galactosemia network (GalNet) members review
Frontiers in Genetics
2022
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A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy
Communications Biology, Vol. 5, Núm. 1
2021
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Long-term safety and outcomes in hereditary tyrosinaemia type 1 with nitisinone treatment: a 15-year non-interventional, multicentre study
The Lancet Diabetes and Endocrinology, Vol. 9, Núm. 7, pp. 427-435
2014
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Cross-sectional study of 168 patients with hepatorenal tyrosinaemia and implications for clinical practice
Orphanet Journal of Rare Diseases, Vol. 9, Núm. 1
2010
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Management of phenylketonuria in Europe: Survey results from 19 countries
Molecular Genetics and Metabolism, Vol. 99, Núm. 2, pp. 109-115