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Benedetta Piccolo

Biographic Data

ID8260960
NAMEBenedetta Piccolo
GIVEN NAMESBenedetta
FAMILY NAMEPiccolo
SIGNATUREPICCOLO B
AFFILIATIONSOspedale di Parma
ORCID0000-0002-2919-7447
VERIFIEDYes
TOTAL WORKS2
TOTAL CITATIONS0
WORKS AS AUTHOR2
WORKS AS EDITOR0
FIRST PUBLICATION YEAR2024
LATEST PUBLICATION YEAR2025
H-INDEX0
  • Early Predictors of Outcome in Pediatric Acquired Demyelinating Syndromes

    Open Access•Emanuela Claudia Turco, Martina Gnazzo et al.•ARTICLE•Children•2025

    Background/Objectives : Pediatric acquired demyelinating syndromes (ADSs) encompass a heterogeneous group of disorders, including multiple sclerosis (MS), MOG antibody-associated disease (MOGAD), and neuromyelitis optica spectrum disorder (NMOSD), with distinct clinical trajectories and prognoses. While analyzed collectively at baseline to reflect real-world diagnostic uncertainty, outcome predictors were also examined according to final diagnosi…

  • FLAIR Hyperintense Cortical Lesions in a 4-Year-Old Child with Myelin Oligodendrocyte Glycoprotein (MOG)-Associated Encephalitis and Seizures

    Open Access•Luca Bernardi, Nicole Mussi et al.•ARTICLE•Children•2024

    Myelin oligodendrocyte glycoprotein (MOG)-IgG-associated disease (MOGAD) is a relatively uncommon autoantibody demyelinating disorder of the central nervous system (CNS) with heterogeneous clinical manifestations and magnetic resonance imaging (MRI) findings. In recent years, a rare MOGAD subtype characterized by distinct clinical and MRI findings has been described. Seizures and cortical hyperintensities best seen on MRI T2-weighted fluid-attenu…

No prominent works on this page.

  • FLAIR Hyperintense Cortical Lesions in a 4-Year-Old Child with Myelin Oligodendrocyte Glycoprotein (MOG)-Associated Encephalitis and Seizures

    Open Access•Luca Bernardi, Nicole Mussi et al.•ARTICLE•Children•2024

    Myelin oligodendrocyte glycoprotein (MOG)-IgG-associated disease (MOGAD) is a relatively uncommon autoantibody demyelinating disorder of the central nervous system (CNS) with heterogeneous clinical manifestations and magnetic resonance imaging (MRI) findings. In recent years, a rare MOGAD subtype characterized by distinct clinical and MRI findings has been described. Seizures and cortical hyperintensities best seen on MRI T2-weighted fluid-attenu…

  • Early Predictors of Outcome in Pediatric Acquired Demyelinating Syndromes

    Open Access•Emanuela Claudia Turco, Martina Gnazzo et al.•ARTICLE•Children•2025

    Background/Objectives : Pediatric acquired demyelinating syndromes (ADSs) encompass a heterogeneous group of disorders, including multiple sclerosis (MS), MOG antibody-associated disease (MOGAD), and neuromyelitis optica spectrum disorder (NMOSD), with distinct clinical trajectories and prognoses. While analyzed collectively at baseline to reflect real-world diagnostic uncertainty, outcome predictors were also examined according to final diagnosi…

Medicine (2 works) · Multiple Sclerosis Research Studies (2 works) · Peripheral Neuropathies and Disorders (2 works) · Autoimmune Neurological Disorders and Treatments (1 work) · Disease (1 work) · Encephalitis (1 work) · Fluid-attenuated inversion recovery (1 work) · Hereditary Neurological Disorders (1 work) · Hyperintensity (1 work) · Immunology (1 work)

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