Dídac Casas-Alba
7PUBLICATIONS
18CO-AUTHORS
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Publications (7)
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|Aug 28, 2025
Unveiling the Spectrum: Clinical and Molecular Insights from a Spanish Pediatric Cohort with Hypermobility Disorders and Ehlers-Danlos Syndrome.David Foz Felipe, Dídac Casas-Alba, Sara H Sadok
|Jul 14, 2025
Foetal disruptive brain injuries: Diagnosing the underlying pathogenetic mechanisms with cranial ultrasonography.Ana Alarcón, Nuria Carreras, Tobias Muehlbacher
|Jan 11, 2025
MECP2 Duplication Syndrome: AI-Based Diagnosis, Severity Scale Development and Correlation with Clinical and Molecular Variables.Lourdes Vega-Hanna, Dídac Casas-Alba, Sol Balsells
|Mar 07, 2024
Heterozygous MAP3K20 variants cause ectodermal dysplasia, craniosynostosis, sensorineural hearing loss, and limb anomalies.Daniel Brooks, Elizabeth Burke, Sukyeong Lee
|Sep 04, 2018
Hyaline fibromatosis syndrome: Clinical update and phenotype-genotype correlations.Dídac Casas-Alba, Antonio Martínez-Monseny, Rosa M Pino-Ramírez
|Jul 31, 2018
Broadening the spectrum of neonatal hemochromatosis.Dídac Casas-Alba, Jordi Clotet, Emilio J Inarejos
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Frequent Collaborators
3 joint publications
Judith Armstrong
3 joint publications
Antonio F Martínez-Monseny
1 joint publications
Sukyeong Lee
1 joint publications
Melanie O'Leary
1 joint publications
Ikeoluwa Osei-Owusu
1 joint publications
Heidi L Rehm
1 joint publications
Shweta U Dhar
1 joint publications
David Bick
1 joint publications
Carolina Prat
1 joint publications
Francesc Palau
