Andrea Accogli

16PUBLICATIONS
57CO-AUTHORS
Gene and molecular therapyNeurology and neuromuscular diseasesAdolescent healthOtorhinolaryngologyEpigenetics (incl. genome methylation and epigenomics)
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Publications (16)

|Nov 01, 2022
De novo KCNA6 variants with attenuated KV 1.6 channel deactivation in patients with epilepsy.

Vincenzo Salpietro, Valentina Galassi Deforie, Stephanie Efthymiou

|Jul 26, 2022
Clinical, Endocrine and Neuroimaging Findings in Girls With Central Precocious Puberty.

Daniela Fava, Andrea Calandrino, Maria Grazia Calevo

|Sep 12, 2021
L1CAM variants cause two distinct imaging phenotypes on fetal MRI.

Andrea Accogli, Stacy Goergen, Giana Izzo

|Jul 31, 2021
ZTTK syndrome: Clinical and molecular findings of 15 cases and a review of the literature.

Sulagna Tina Kushary, Anya Revah-Politi, Subit Barua

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