Paula Sánchez Pintos
Complejo Hospitalario Universitario de Santiago de Compostela
22 papers found
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Paediatric clinical study of 3D printed personalised medicines for rare metabolic disorders
UploadBeyond genetics: Deciphering the impact of missense variants in CAD deficiency
UploadScreen Time and Bone Status in Children and Adolescents: A Systematic Review
Download from doi.orgTransferrin Isoforms, Old but New Biomarkers in Hereditary Fructose Intolerance
Download from doi.orgTreatment adherence in tyrosinemia type 1 patients
Download from doi.org[Evaluation and perspective of 20 years of neonatal screening in Galicia. Program results.]
UploadClinical Utility of LCT Genotyping in Children with Suspected Functional Gastrointestinal Disorder
Download from doi.orgBone Status in Patients with Phenylketonuria: A Systematic Review
Download from doi.orgEvolution of tyrosinemia type 1 disease in patients treated with nitisinone in Spain
Download from doi.orgAcylcarnitine profile in neonatal hypoxic-ischemic encephalopathy
Download from doi.orgCarbohydrate status in patients with phenylketonuria
Download from link.springer.comSimilarities between acylcarnitine profiles in large for gestational age newborns and obesity
Download from www.nature.comLipid profile status and other related factors in patients with Hyperphenylalaninaemia
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