Daniel Natera-de Benito

32PUBLICATIONS
192CO-AUTHORS
Neurology and neuromuscular diseasesInfant and child healthHaematological tumoursGene expression (incl. microarray and other genome-wide approaches)Gene and molecular therapy
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Publications (32)

|Aug 27, 2026
Clinical Variability and Genotype-Driven Outcomes in CHRND-Related Congenital Myasthenic Syndrome.

|Jul 28, 2026
Expanding the phenotypic spectrum of COL6-related diseases: Motor neuropathy-like and neuromyopathy associated with COL6A3 c.7447A>G.

|Jul 06, 2026
IMU-based workspace area as a promising complementary tool to assess upper limb function in Neuromuscular diseases: A one-year follow-up.

|Jun 26, 2026
The International Consortium for Arthrogryposis: A Collaborative Framework for Early Detection, Care, Research, and Education.

|Sep 26, 2025
Expanding Hereditary Spastic Paraplegias Limits: Biallelic SPAST Variants in Cerebral Palsy Mimics.

Gregorio A Nolasco, Mònica Roldán, Yalda Jamshidi

|Sep 09, 2025
The Solve-RD Solvathons as a pan-European interdisciplinary collaboration to diagnose patients with rare disease.

Vicente A Yépez, German Demidov, Kornelia Ellwanger

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Frequent Collaborators

6 joint publications

Berta Estévez-Arias

5 joint publications

Francesc Palau

5 joint publications

Laura Carrera-García

4 joint publications

German Demidov