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Megi Meneri

5PUBLICATIONS
39CO-AUTHORS
Neurology and neuromuscular diseasesGene mappingOptical technologyEpigenetics (incl. genome methylation and epigenomics)Aged care nursing
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Journal

Publications (5)

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|Sep 03, 2025
Single Nucleotide <i>SMN1</i> Variants in a Cohort of Individuals With Spinal Muscular Atrophy.

Martina Rimoldi, Francesca Magri, Megi Meneri

|Sep 04, 2024
Guanylate Kinase 1 Deficiency: A Novel and Potentially Treatable Mitochondrial DNA Depletion/Deletions Disease.

Agustin Hidalgo-Gutierrez, Jonathan Shintaku, Javier Ramon

|Apr 24, 2023
Ischemic optic neuropathy as first presentation in patient with m.3243 A > G MELAS classic mutation.

Simone Scarcella, Laura Dell'Arti, Delia Gagliardi

|Mar 25, 2022
Biallelic Variants in <i>ENDOG</i> Associated with Mitochondrial Myopathy and Multiple mtDNA Deletions.

Alessia Nasca, Andrea Legati, Megi Meneri

|Aug 21, 2020
COVID-19-Associated PRES-like Encephalopathy with Perivascular Gadolinium Enhancement.

G Conte, S Avignone, M Carbonara

Pageof 1

Frequent Collaborators

2 joint publications

Dario Ronchi

2 joint publications

Giacomo Pietro Comi

1 joint publications

G Conte

1 joint publications

S Avignone

1 joint publications

M Carbonara

1 joint publications

F Ortolano

1 joint publications

C Cinnante

1 joint publications

F Triulzi

1 joint publications

Stefania Corti

1 joint publications

Melisa Emel Ermert

Frequent Collaborators

2 joint publications

Dario Ronchi

2 joint publications

Giacomo Pietro Comi

1 joint publications

G Conte

1 joint publications

S Avignone

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