Eleni Panagiotakaki

5PUBLICATIONS
128CO-AUTHORS
Respiratory diseasesNeurology and neuromuscular diseasesNeurogeneticsCardiology (incl. cardiovascular diseases)Child and adolescent development
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Publications (5)

|Aug 07, 2026
Natural History of Alternating Hemiplegia of Childhood: Vulnerabilities in Early Childhood and Predictive Factors for Long-Term Outcomes.

|Mar 30, 2026
Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies.

Elsa Leitão, Amandine Santini, Benjamin Cogne

|Mar 12, 2026
Missense Variants in the A Isoform of FGF13 as a Novel Cause of Paroxysmal Dyskinesia.

Cyril Mignot, Matthildi Athina Papathanasiou Terzi, Claudia Ravelli

|Sep 10, 2024
Children and Adolescent Patients with Variants in the ATP1A3 -encoded Sodium-Potassium ATPase Alpha-3 Subunit Demonstrate an Impaired QT Response to Bradycardia and Predisposition to Sinus Node Dysfunction.

Meredith K Srour, Minu-Tshyeto K Bidzimou, Padmapriya Muralidharan

|Dec 15, 2018
Alternating hemiplegia of childhood: the gap between paroxysmal manifestations and non-paroxysmal characteristics.

Eleni Panagiotakaki

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Frequent Collaborators

2 joint publications

Gaëtan Lesca

2 joint publications

Jean-Madeleine de Sainte Agathe

2 joint publications

Matthildi Athina Papathanasiou Terzi

2 joint publications

Simona Balestrini