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

Pediatric Leigh Syndrome: Neuroimaging Features and Genetic Correlations.

Annals of neurology - 1 Aug 2020

Alves Cesar A P F, Teixeira Sara R, Martin-Saavedra Juan S, Guimarães Gonçalves Fabrício, Lo Russo Francesco, Muraresku Colleen, McCormick Elizabeth M, Falk Marni J, Zolkipli-Cunningham Zarazuela, Ganetzky Rebecca, Vossough Arastoo, Goldstein Amy, Zuccoli Giulio

Abstract excerpt

The neurodiagnostic criteria of Leigh syndrome have not yet been clearly redefined based on the expanding of molecular etiologies. We aimed to analyze 20 years of clinical, genetic, and magnetic resonance studies from our Leigh syndrome cohort to provide a detailed description of central nervous system lesions in Leigh syndrome and their biological evolution in view of their genetic and clinical findings. Our...

Read the complete abstract on PubMed

Topics

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

Share to Child
Share to DNA, Mitochondrial

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Follow-Up Studies

Share to Genetic Variation

Share to Leigh Disease

Share to Magnetic Resonance Imaging

Share to Neuroimaging

Source

Identifiers

PMID: 32445240
DOI: 10.1002/ana.25789

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Pediatric Leigh Syndrome: Neuroimaging Features and Genetic Correlations.PMID 32445240Read ↗

Molecular basis of Leigh syndrome: a current look.Semantic proximity Read ↗

Leigh syndrome: Resolving the clinical and genetic heterogeneity paves the way for treatment options.Semantic proximity Read ↗

[Clinical and genetic characteristics of children with Leigh syndrome].Semantic proximity Read ↗

Leigh Syndrome: A Study of 209 Patients at the Beijing Children's Hospital.Semantic proximity Read ↗

The magnetic resonance imaging of Leigh syndrome in a child.Semantic proximity Read ↗

Atypical Leigh Syndrome Diagnosed in an Infant with Prominent Cardiac Hypertrophy as Initial Symptom: A Case Report with Novel LRPPRC VariantsSemantic proximity Read ↗

Genetic heterogeneity in Leigh syndrome: Highlighting treatable and novel genetic causes.Semantic proximity Read ↗

Leigh syndrome: an adult presentation of a paediatric disease.Semantic proximity Read ↗

Multimodal MRI in Leigh syndrome due to m.13513G > A.Semantic proximity Read ↗

The Fetus with Ganglionic Eminence Abnormality: Head Size and Extracranial Sonographic Findings Predict Genetic Diagnoses and Postnatal OutcomesSemantic proximity Read ↗

Complex I deficiency and Leigh syndrome through the eyes of a clinician.Semantic proximity Read ↗

Clinical Spectrum, Heteroplasmy-Phenotype Correlation, and Prognosis of the MT-ND3 m.10191 T > C Mutation.Semantic proximity Read ↗

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