Amaya Belanger-Quintana

9PUBLICATIONS
65CO-AUTHORS
AutoimmunityInfant and child healthNeurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)Medical genetics (excl. cancer genetics)
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Publications (9)

|Aug 13, 2026
Immuno-Inflammatory Profiling and Complement Activation in Fabry Disease: A Cross-Sectional Study.

|Jul 15, 2026
How Well Is Blood Phenylalanine Controlled in Maternal PKU in Europe? Results from 102 Pregnancies.

|Jun 25, 2026
Health Outcomes of Patients with Distal Urea Cycle Disorders Detected by Newborn Screening: Data from the Spanish National Registry.

|Dec 30, 2025
Abnormal Splicing of GALC Transcripts Underlies Unusual Cases of Krabbe Disease.

María Domínguez-Ruiz, Juan Luis Chico, Laura López-Marín

|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

|Sep 14, 2024
Longitudinal Dietary Intake Data in Patients with Phenylketonuria from Europe: The Impact of Age and Phenylketonuria Severity.

Alex Pinto, Kirsten Ahring, Manuela Ferreira Almeida

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Frequent Collaborators

6 joint publications

Sinziana Stanescu

3 joint publications

Francjan van Spronsen

3 joint publications

Júlio César Rocha

3 joint publications

Manuela Ferreira Almeida