Francesca Magri

8PUBLICATIONS

93CO-AUTHORS

Anthropological geneticsMedical infection agents (incl. prions)Neurology and neuromuscular diseasesGene and molecular therapyMedical bacteriology

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Publications (8)

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|May 21, 2026

Ataxia With Vitamin E Deficiency Syndrome and a Novel TTPA Variant: A Paired Case Report.

|Jan 15, 2026

Clinical and Genotypic Spectrum of Twinkle-Related Disorders: Insights From a Multinational Cohort Study.

Piervito Lopriore, Zeynep Ünlütürk, Thomas Klopstock

|Sep 03, 2025

Single Nucleotide SMN1 Variants in a Cohort of Individuals With Spinal Muscular Atrophy.

Martina Rimoldi, Francesca Magri, Megi Meneri

|Apr 03, 2024

Pathogenic TNNI1 variants disrupt sarcomere contractility resulting in hypo- and hypercontractile muscle disease.

Sandra Donkervoort, Martijn van de Locht, Dario Ronchi

|Jul 26, 2022

MicroRNAs as serum biomarkers in Becker muscular dystrophy.

Delia Gagliardi, Mafalda Rizzuti, Roberta Brusa

|Feb 20, 2021

Diagnostic and prognostic value of CSF neurofilaments in a cohort of patients with motor neuron disease: A cross-sectional study.

Delia Gagliardi, Irene Faravelli, Megi Meneri

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Frequent Collaborators

Stefania Paola Corti

Giacomo Pietro Comi

Dario Ronchi

Alessandra Govoni

Elena Abati

Delia Gagliardi

Sandra Donkervoort

Martijn van de Locht

Daniele Velardo

Catriona A McLean

Frequent Collaborators

Stefania Paola Corti

Giacomo Pietro Comi

Dario Ronchi

Alessandra Govoni