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

Case 20-2021: A 69-Year-Old Man with Ataxia.

The New England journal of medicine - 8 Jul 2021

Khurana Vikram, de Gusmao Claudio M, Glover McKinley, Helgager Jeffrey

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Ataxia
Share to Celiac Disease
Share to Cerebellar Ataxia
Share to Diagnosis, Differential

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Fatal Outcome

Share to Magnetic Resonance Imaging

Share to Supranuclear Palsy, Progressive

Share to Syndrome

Source

Identifiers

PMID: 34233100
DOI: 10.1056/NEJMcpc2004992

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Case 20-2021: A 69-Year-Old Man with Ataxia.PMID 34233100Read ↗

Case 5-2022: A 65-Year-Old Woman with Rapidly Progressive Weakness in the Right Arm and Recurrent Falls.Semantic proximity Read ↗

Familial Cerebellar Ataxia and Amyotrophic Lateral Sclerosis/Frontotemporal Dementia with DAB1 and C9ORF72 Repeat Expansions: An 18‐Year StudySemantic proximity Read ↗

Clinical and Genetic Characterization of Brazilian Patients with Ataxia and Oculomotor Apraxia.Semantic proximity Read ↗

SCA28: Novel Mutation in the AFG3L2 Proteolytic Domain Causes a Mild Cerebellar Syndrome with Selective Type-1 Muscle Fiber Atrophy.Semantic proximity Read ↗

Milestones in Friedreich ataxia: more than a century and still learningSemantic proximity Read ↗

Late onset ataxia: MSA-C or SCA 17? A gene penetrance dilemma.Semantic proximity Read ↗

Capturing clinical progression in multisystemic genetic ataxias: lessons from a prospective study of 884 patients with autosomal recessive or early-onset ataxiaSemantic proximity Read ↗

Different Purkinje cell pathologies cause specific patterns of progressive ataxia in miceSemantic proximity Read ↗

Teaching Video NeuroImages: Spastic ataxia syndrome: The Friedreich-like phenotype of ARSACS.Semantic proximity Read ↗

The pledge, the turn, and the prestige of transient cerebellar alterations in SCA6.Semantic proximity Read ↗

A Comprehensive Scheme for the Objective Upper Body Assessments of Subjects with Cerebellar AtaxiaSemantic proximity Read ↗

Specific Gait Changes in Prodromal Hereditary Spastic Paraplegia Type 4: preSPG4 StudySemantic proximity Read ↗

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