Lorenzo Perilli

8PUBLICATIONS
26CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Neurology and neuromuscular diseasesRecordkeeping informaticsMajor global burdens of diseaseCancer genetics
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Publications (8)

|Aug 19, 2026
The genetic architecture of epilepsy across molecular mechanisms and clinical heterogeneity.

|Jul 03, 2026
Expanding the electroclinical spectrum of TANC2-related disorders: Lennox-Gastaut syndrome and related developmental epileptic phenotypes.

|May 04, 2026
Correction: Perilli et al. Early Diagnostic Markers in Crisponi Syndrome: Two Cases and Review. J. Clin. Med. 2025, 14, 7757.

|Mar 04, 2026
Managing Fever and Vaccination Risks in Dravet Syndrome: From Pathophysiology to Clinical Practice.

Alessandro Ferretti, Marco Bianchi, Mattia Costa

|Nov 13, 2025
Early Diagnostic Markers in Crisponi Syndrome: Two Cases and Review.

Lorenzo Perilli, Kamil Dzwilewski, Marta Pietruszka

|Mar 28, 2025
Exploring the Role of IRF6 in Perinatal Arterial Ischemic Stroke: A Case of a Newborn with Craniofacial Malformations.

Lorenzo Perilli, Simona Negro, Samanta Carbone

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Frequent Collaborators

4 joint publications

Pasquale Striano

2 joint publications

Maria Mazurkiewicz-Bełdzinska

2 joint publications

Marta Pietruszka

2 joint publications

Michele Minerva