Lucie Pisella

3PUBLICATIONS
28CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Medical infection agents (incl. prions)Neurology and neuromuscular diseases
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Publications (3)

|Apr 25, 2026
Compound heterozygous SLC12A5 variants expand the molecular and functional spectrum of KCC2-developmental and epileptic encephalopathy.

|Sep 04, 2025
Diagnostic Impasse and Wandering in Patients With Rare Neuromuscular Diseases: Insights Into Patient Characteristics From the French National Network for Rare Neuromuscular Diseases (FILNEMUS) and the French National Rare Disease Database (BNDMR).

Rémy Dumas, Anne-Sophie Jannot, Nabila Elarouci

|Oct 17, 2019
Impaired regulation of KCC2 phosphorylation leads to neuronal network dysfunction and neurodevelopmental pathology.

Lucie I Pisella, Jean-Luc Gaiarsa, Diabé Diabira

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Frequent Collaborators

2 joint publications

Jinwei Zhang

2 joint publications

Igor Medina

1 joint publications

Jean-Luc Gaiarsa

1 joint publications

Diabé Diabira