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)

|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

5 joint publications

Stefania Paola Corti

4 joint publications

Giacomo Pietro Comi

3 joint publications

Dario Ronchi

2 joint publications

Alessandra Govoni