Davide Tonduti

Assistant Professor

Università degli Studi di Torino

Italy

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About

Davide Tonduti is an Assistant Professor at Università degli Studi di Milano, Italy. His research primarily focuses on neurogenetics, including diagnostic imaging for neurological disorders, the role of epigenetics in leukodystrophies, and the long-term efficacy of treatments for various conditions. Recent publications reflect his contributions to understanding leukodystrophies, movement disorders, and the management of autoinflammatory diseases.

Articles (12)

Year:

2024

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2024

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2023

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2022

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2022

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2022

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2022

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2022

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2022

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2022

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2022

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2021

Collaborators (11)

Gaetano Cantalupo

Associate Professor

University of Verona

ITALY

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Santosh Mordekar

Consultant Paediatric Neurologist / Honorary Senior Lecturer

UNITED KINGDOM

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Alireza Tavasoli

Pediatric Headache Fellowship

Phoenix Children's Hospital

UNITED STATES

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Federica Rey

University of Milan

ITALY

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Stephana Carelli

University of Milan

ITALY

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Nina-Maria Wilpert

Charité - Universitätsmedizin Berlin

GERMANY

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Krishna Chatterjee

University of Cambridge

UNITED KINGDOM

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odile boespflug-tanguy

Professor

Université Paris Diderot

FRANCE

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Erica L T van den Akker

NETHERLANDS

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Marco Spada

University of Turin

ITALY

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Carmelo Rizzari

ITALY

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Davide Tonduti

Research Interests

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Articles (12)

Role of epigenetics and alterations in RNA metabolism in leukodystrophies

Brainstem Chipmunk Sign: A Diagnostic Imaging Clue across All Subtypes of Alexander Disease

Expanding the Spectrum of NUBPL-Related Leukodystrophy

Correspondence on “Expanded phenotype of AARS1-related white matter disease” by Helman et al

How to look for intracranial calcification in children with neurological disorders: CT, MRI, or both of them?

Mucopolysaccharidosis-Plus Syndrome, a Rapidly Progressive Disease: Favorable Impact of a Very Prolonged Steroid Treatment on the Clinical Course in a Child

Corrigendum: Parental Somatic Mosaicism Uncovers Inheritance of an Apparently De Novo GFAP Mutation (Front. Genet., (2021), 12, 744068, 10.3389/fgene.2021.744068)

Long-Term Efficacy of T3 Analogue Triac in Children and Adults with MCT8 Deficiency: A Real-Life Retrospective Cohort Study

Movement disorders in MCT8 deficiency/Allan-Herndon-Dudley Syndrome

The 2021 European Alliance of Associations for Rheumatology/American College of Rheumatology Points to Consider for Diagnosis and Management of Autoinflammatory Type I Interferonopathies: CANDLE/PRAAS, SAVI, and AGS

The 2021 Eurpean Alliance of Associations for Rheumatology/American College of Rheumatology points to consider for diagnosis and management of autoinflammatory type i interferonopathies: CANDLE/PRAAS, SAVI and AGS

Spinal cord involvement and paroxysmal events in “Infantile Onset Transient Hypomyelination” due to TMEM63A mutation

Collaborators (11)

Gaetano Cantalupo

Santosh Mordekar

Alireza Tavasoli

Federica Rey

Stephana Carelli

Nina-Maria Wilpert

Krishna Chatterjee

odile boespflug-tanguy

Erica L T van den Akker

Marco Spada

Carmelo Rizzari

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