Mariasavina Severino

IRCCS Istituto Giannina Gaslini

Italy

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Articles (20)

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2025

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2022

Collaborators (10)

András Jakab

Assistant Professor

University of Zurich

SWITZERLAND

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Carlo Augusto Mallio

Università Campus Bio-Medico di Roma

ITALY

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Sara Signa

ITALY

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Lukas Haider

Medical University of Vienna

AUSTRIA

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Renske Oegema

UMC Utrecht

NETHERLANDS

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Martina Resaz

Istituto Giannina Gaslini

ITALY

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GABRIELE ARNULFO

Assistant professor

Università degli Studi di Torino

ITALY

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Dario Paladini

Head - Associate Professor OB/GYN

Istituto Giannina Gaslini

ITALY

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Bruno P. Soares

University of Vermont Medical Center

UNITED STATES

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Isabella Ceccherini

head

Istituto Giannina Gaslini

ITALY

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Mariasavina Severino

Research Interests

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Articles (20)

Neonatal Perforator Stroke: Timing, Risk Factors, and Neurological Outcome from a Single-Center Experience

A STOP‐Gain RNF213 Variant Causes Chorea, Stroke‐Like Episodes, and Leigh Syndrome‐Like Encephalopathy

Biallelic NDUFA9 variants cause a progressive neurodevelopmental disorder with prominent dystonia and mitochondrial complex I deficiency

A hypomorphic FLVCR2 variant resulting in moderate transport deficiency causes hydranencephaly syndrome with brain calcifications

Neuroradiologic, Clinical, and Genetic Characterization of Cerebellar Heterotopia: A Pediatric Multicentric Study

Prenatal assessment of brain malformations on neuroimaging: an expert panel review

Advanced imaging techniques and non-invasive biomarkers in pediatric brain tumors: state of the art

Response assessment in pediatric neurooncology (RAPNO) criteria revisited: a practical navigation guide for neuroradiologists

Arterial Ischemic Stroke in Children

Vein of Galen aneurysmal malformation: does size affect outcome?

Influence of adaptive denoising on Diffusion Kurtosis Imaging at 3T and 7T

Second trimester fetal MRI of the brain: Through the ground glass

Use of gadolinium-based contrast agents in multiple sclerosis: a review by the ESMRMB-GREC and ESNR Multiple Sclerosis Working Group

A PAK1 mutational hotspot within the regulatory CRIPaK domain is associated with severe neurodevelopmental disorders in children

Refining the electroclinical spectrum of NPRL3‐related epilepsy: A novel multiplex family and literature review

Neuroimaging Features of Biotinidase Deficiency

Supratentorial Demyelinating Lesions Following Severe Acute Respiratory Syndrome Coronavirus-2 Infection: A Pediatric Case Report

Imaging characteristics and neurosurgical outcome in subjects with agenesis of the corpus callosum and interhemispheric cysts

An Atypical Case of Aphasia: Transitory Ischemic Attack in a 13-Year-Old Patient with Asymptomatic SARS-CoV-2 Infection

Genotype-Phenotype Correlation and Functional Insights for Two Monoallelic TREX1 Missense Variants Affecting the Catalytic Core

Collaborators (10)

András Jakab

Carlo Augusto Mallio

Sara Signa

Lukas Haider

Renske Oegema

Martina Resaz

GABRIELE ARNULFO

Dario Paladini

Bruno P. Soares

Isabella Ceccherini

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