Serena Galosi

9PUBLICATIONS
23CO-AUTHORS
Neurology and neuromuscular diseasesGenetic immunologyMedical virologyGenetics not elsewhere classifiedMajor global burdens of disease
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Publications (9)

|Jul 02, 2026
Pharmacological Treatment of Cerebellar Ataxia in Pediatric Ataxia-Telangiectasia: A Systematic Review.

|Sep 24, 2025
Neurodevelopmental Disorder and Cortical Myoclonus in ZMYM2 Deficiency.

Luca Pollini, Maria Novelli, Lorena Travaglini

|Jan 29, 2025
CAPRIN1 Pro512Leu Variant Causes Childhood Dementia, Myoclonus-Ataxia, and Sensorimotor Neuropathy.

Rossella Bove, Annalaura Torella, Maria Novelli

|Aug 09, 2024
Severe Acute Motor Exacerbations (SAME) across Metabolic, Developmental and Genetic Disorders.

Blas Couto, Serena Galosi, Dora Steel

|Jul 13, 2024
Autosomal Recessive Guanosine Triphosphate Cyclohydrolase I Deficiency: Redefining the Phenotypic Spectrum and Outcomes.

Maria Novelli, Manuela Tolve, Vicente Quiroz

|Apr 30, 2024
Biallelic Variants of MRPS36 Cause a New Form of Leigh Syndrome.

Serena Galosi, Cecilia Mancini, Anna Commone

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Frequent Collaborators

4 joint publications

Luca Pollini

1 joint publications

Simona Balestrini

1 joint publications

Davide Mei

1 joint publications

Federico Melani