Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Progression of microstructural damage in spinocerebellar ataxia type 2: a longitudinal DTI study.

AJNR. American journal of neuroradiology - 1 Jun 2015

Mascalchi M, Toschi N, Giannelli M, Ginestroni A, Della Nave R, Nicolai E, Bianchi A, Tessa C, Salvatore E, Aiello M, Soricelli A, Diciotti S

Abstract excerpt

BACKGROUND AND PURPOSE: The ability of DTI to track the progression of microstructural damage in patients with inherited ataxias has not been explored so far. We performed a longitudinal DTI study in patients with spinocerebellar ataxia type 2. MATERIALS AND METHODS: Ten patients with spinocerebellar ataxia type 2 and 16 healthy age-matched controls were examined twice with DTI (mean time between scans, 3.6 years...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Anisotropy
Share to Brain Mapping

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Diffusion Magnetic Resonance Imaging

Share to Disease Progression

Share to Image Interpretation, Computer-Assisted

Share to Longitudinal Studies

Share to Neurologic Examination

Share to Spinocerebellar Ataxias

Source

Open in PubMed Open full text

Identifiers

PMID: 25882284
DOI: 10.3174/ajnr.A4343
PMCID: PMC8013027

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Progression of microstructural damage in spinocerebellar ataxia type 2: a longitudinal DTI study.PMID 25882284Read ↗

The Pattern and Staging of Brain Atrophy in Spinocerebellar Ataxia Type 2 (SCA2): MRI Volumetrics from ENIGMA-AtaxiaSemantic proximity Read ↗

Progression of corticospinal tract dysfunction in pre-ataxic spinocerebellar ataxia type 2: A two-years follow-up TMS study.Semantic proximity Read ↗

Multimodal MRI and Machine Learning Uncovers Distinct Progression Patterns in Friedreich AtaxiaSemantic proximity Read ↗

In vivo histopathological staging in C9orf72-associated ALS: A tract of interest DTI study.Semantic proximity Read ↗

Tay-Sachs and Sandhoff Diseases: Diffusion tensor imaging and correlational fiber tractography findings differentiate late-onset GM2 GangliosidosisSemantic proximity Read ↗

Brain structural damage in Friedreich's ataxia.Semantic proximity Read ↗

Disentangling Pontine Fiber Geometry and Microstructure in ARSACS Using Advanced MRISemantic proximity Read ↗

Cerebellar Normative Modeling Identifies Neuroanatomical Biotypes Predicting dTMS Response in Spinocerebellar Ataxia Type 3Semantic proximity Read ↗

In Vivo Evaluation of White Matter Abnormalities in Children with Duchenne Muscular Dystrophy Using DTI.Semantic proximity Read ↗

Progression of regional atrophy in the left hemisphere contributes to clinical and cognitive deterioration in multiple sclerosis: A 5-year study.Semantic proximity Read ↗

The progression rate of spinocerebellar ataxia type 2 changes with stage of diseaseSemantic proximity Read ↗

Genotype-specific spinal cord damage in spinocerebellar ataxias: an ENIGMA-Ataxia study.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.