Background And Objectives: Magnetic resonance imaging (MRI) in dysferlinopathy has consistently demonstrated a particular pattern of affliction. We aimed to study muscle MRI characteristics of lower limbs in limb girdle muscular dystrophy (LGMD)-R2 phenotypes and correlate them with the gait pattern.
Methods: Forty genetically and/or biopsy-proven cases of dysferlinopathy underwent muscle MRI of the lower limbs.
Epileptic Disord
March 2025
Objectives: New-onset refractory status epilepticus (NORSE), a subtype of status epilepticus, poses a critical neurological emergency marked by considerable morbidity and mortality. This study aimed to characterize NORSE phenotypically and assess its outcomes, interleukin levels, and miRNA levels.
Methods: Over a 3-year period, patients presenting with NORSE were enrolled.
Objectives: GAA- ataxia (SCA27B) is a recently reported late-onset ataxia caused by a GAA repeat expansion in intron 1 of the gene. After the clinical observation of superior cerebellar peduncle (SCP) involvement in some affected patients, we sought to verify the prevalence of this finding in our cohort and 4 additional independent cohorts of patients with SCA27B.
Methods: We performed a retrospective review of the brain MRI scans of a total of 87 patients (median age at MRI 69 years; range 28-88 years) from different independent cohorts to assess the presence of SCP involvement, defined as abnormally high T2 signal along the SCP tract.
Aim: In this study, we explore the role of FA maps in predicting the histopathological subtypes of meningioma using a qualitative ordinal scale and quantitative histogram features.
Material & Methods: Retrospective analysis of grey-scale FA maps of 96 cases of meningioma was done by two observers blinded to the histopathological diagnosis. An ordinal scale of 1-4 was used to grade the degree of FA in each lesion.