Patricia Correcher-Medina

6PUBLICATIONS
45CO-AUTHORS
Food properties (incl. characteristics and health benefits)Medical genetics (excl. cancer genetics)Neurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)Clinical pharmacy and pharmacy practice
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Publications (6)

|Mar 14, 2026
Dietary Patterns in a Nationwide Cohort of Patients with Hereditary Fructose Intolerance.

Elsa Izquierdo-García, Edorta Mora, Dolores García-Arenas

|Apr 12, 2025
Understanding the Natural History and the Effects of Current Therapeutic Strategies on Urea Cycle Disorders: Insights from the UCD Spanish Registry.

Elena Martín-Hernández, Marcello Bellusci, Patricia Pérez-Mohand

|Oct 28, 2023
Clinical Outcomes of Patients with Chronic Neuropathic Form of Gaucher Disease in the Spanish Real-World Setting: A Retrospective Study.

Sinziana Stanescu, Patricia Correcher Medina, Francisco J Del Castillo

|Aug 26, 2023
Breastfeeding and Inborn Errors of Amino Acid and Protein Metabolism: A Spreadsheet to Calculate Optimal Intake of Human Milk and Disease-Specific Formulas.

Isidro Vitoria-Miñana, María-Luz Couce, Domingo González-Lamuño

|Nov 11, 2022
Identification of Clinical Variants beyond the Exome in Inborn Errors of Metabolism.

Alejandro Soriano-Sexto, Diana Gallego, Fátima Leal

|Sep 09, 2022
Switching to Glycerol Phenylbutyrate in 48 Patients with Urea Cycle Disorders: Clinical Experience in Spain.

Elena Martín-Hernández, Pilar Quijada-Fraile, Patricia Correcher

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Frequent Collaborators

5 joint publications

María-Luz Couce

4 joint publications

Luis Peña-Quintana

3 joint publications

Paula Sánchez-Pintos

3 joint publications

Javier de Las Heras Montero