P. Sánchez-Pintos

P. Sánchez-Pintos, J. Cocho, M. Couce, 2016, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Relevance of expanded neonatal screening of medium-chain acyl co-a dehydrogenase deficiency: outcome of a decade in galicia (Spain).

B. Andresen, A. Ribes, P. Sánchez-Pintos, 2011, JIMD reports.

Intravenous branched-chain amino-acid-free solution for the treatment of metabolic decompensation episodes in Spanish pediatric patients with maple syrup urine disease

P. Sánchez-Pintos, M. L. Couce, Á. García-Cazorla, 2022, Frontiers in Pediatrics.

Demonstration of apoptosis in human skin injuries as an indicator of vital reaction

P. Sánchez-Pintos, M. Rodríguez-Calvo, J. Suárez-Peñaranda, 2002, International Journal of Legal Medicine.

Switching to Glycerol Phenylbutyrate in 48 Patients with Urea Cycle Disorders: Clinical Experience in Spain

P. Sánchez-Pintos, M. L. Couce, L. Peña-Quintana, 2022, Journal of clinical medicine.

M. D. de Castro, P. Sánchez-Pintos, M. Couce, 2017, Scientific Reports.

Newborn screening for medium-chain acyl-CoA dehydrogenase deficiency: regional experience and high incidence of carnitine deficiency

A. Ribes, E. Martins, L. Diogo, 2013, Orphanet Journal of Rare Diseases.

Lipid profile status and other related factors in patients with Hyperphenylalaninaemia

P. Sánchez-Pintos, R. Leis, M. Couce, 2016, Orphanet Journal of Rare Diseases.

Treatment adherence in tyrosinemia type 1 patients

P. Sánchez-Pintos, M. L. Couce, F. Andrade, 2021, Orphanet Journal of Rare Diseases.

Evolution of tyrosinemia type 1 disease in patients treated with nitisinone in Spain

P. Sánchez-Pintos, M. Couce, F. Sánchez-Valverde, 2019, Medicine.

Vitamin C and folate status in hereditary fructose intolerance

P. Sánchez-Pintos, M. Couce, A. Cano, 2022, European Journal of Clinical Nutrition.

Transferrin Isoforms, Old but New Biomarkers in Hereditary Fructose Intolerance

P. Sánchez-Pintos, M. Couce, A. Cano, 2021, Journal of clinical medicine.

Vitamin C and folate status in hereditary fructose intolerance

P. Sánchez-Pintos, M. Couce, A. Cano, 2022, European Journal of Clinical Nutrition.

Odimet®: A Pioneering Tele-Health Tool to Empower Dietary Treatment and the Acute Management of Inborn Errors of Metabolism—An Assessment of Its Effectiveness during the COVID Pandemic

P. Sánchez-Pintos, M. Couce, María José Camba-Garea, 2024, Nutrients.

Relevance of expanded neonatal screening of medium-chain acyl co-a dehydrogenase deficiency: outcome of a decade in galicia (Spain).

P. Sánchez-Pintos, J. Cocho, D. Quelhas, 2011, JIMD reports.