J. Serrano-Nieto

Urea cycle disorders in Spain: an observational, cross-sectional and multicentric study of 104 cases

C. Pérez-Cerdá, M. Martínez-Pardo, M. Couce, 2014, Orphanet Journal of Rare Diseases.

Extraintestinal manifestations in inflammatory bowel disease Reactive / non specific Aphthous stomatitis Erythema nodosum Gangrenous pyoderma Sweet syndrome Cutaneous vasculitis Granulomatous cheilits IgA dermatosis Epidermolysis bullosa Specific / granulomatous Direct extension Perianal Peristomal

J. Blasco-Alonso, V. Navas-López, C. Sierra-Salinas, 2022 .

Esophageal multichannel intraluminal impedance and pH testing in the study of apparent life threatening episode incidents in infants.

J. Blasco-Alonso, V. Navas-López, F. Girón Fernández-Crehuet, 2014, Revista espanola de enfermedades digestivas : organo oficial de la Sociedad Espanola de Patologia Digestiva.

Weaning practices in phenylketonuria vary between health professionals in Europe

A. Schlune, A. Macdonald, E. V. D. van der Ploeg, 2018, Molecular genetics and metabolism reports.

Early feeding practices in infants with phenylketonuria across Europe

A. Schlune, A. Macdonald, E. V. D. van der Ploeg, 2018, Molecular genetics and metabolism reports.

Metabolic Serendipities of Expanded Newborn Screening

R. Yahyaoui, Belén Pérez, J. Blasco-Alonso, 2020, Genes.

Vitamin C and folate status in hereditary fructose intolerance

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

International practices in the dietary management of fructose 1-6 biphosphatase deficiency

F. de Boer, M. Dixon, A. Macdonald, 2018, Orphanet Journal of Rare Diseases.

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.