Cinzia Bertolin
Queen Square
London, ENG, United Kingdom
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 33 publications
Cerebellar and brainstem MRI alterations in primary brain calcification.
Journal: Neuroradiology
Published: May 25, 2026
White Matter Matters: A Magnetic Resonance Imaging Study with Clinical Correlates in Primary Brain Calcification.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: October 22, 2025
Skin calcium deposits in primary familial brain calcification: A novel potential biomarker.
Journal: Annals of clinical and translational neurology
Published: September 17, 2024
Non-Motor Symptoms in Primary Familial Brain Calcification.
Journal: Journal of clinical medicine
Published: June 01, 2024
Genetic mutations in Parkinson's disease: screening of a selected population from North-Eastern Italy.
Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: February 19, 2024
TP53 DNA binding domain mutational status and rituximabbased treatment are independent prognostic factors for pediatric Burkitt lymphoma patients stratification.
Journal: Haematologica
Published: December 18, 2023
An adult patient with 3-methylglutaconic aciduria type 1 and movement disorders.
Journal: Journal of neurology
Published: November 25, 2021
Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral Sclerosis.
Journal: JAMA neurology
Published: August 30, 2021
Heterozygous frameshift variants in HNRNPA2B1 cause early-onset oculopharyngeal muscular dystrophy.
Journal: Nature communications
Published: April 28, 2021
A novel KRT1 c.1433A>G p.(Glu478Gly) mutation in a newborn with epidermolytic ichthyosis.
Journal: Clinical case reports
Published: July 22, 2020
Last Updated: 09/26/2026