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

Polyradiculoneuritis on MRI: An Overlooked Feature of Biallelic POLG Gene Mutations in Infancy.

Neurology - 1 Jun 2024

Roux Charles-Joris, Dufeu-Berat Claire-Marine, Hully Marie, Rotig Agnes, Schiff Manuel, De Lonlay Pascale, Aubart Mélodie, Alison Marianne, Jaroussie Marianne, Levy Raphaël, Dangouloff-Ros Volodia, Barcia Giulia, Desguerre Isabelle, Munnich Arnold, Gitiaux Cyril, Boddaert Nathalie

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 DNA Polymerase gamma
Share to POLG gene
Share to Infant

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Magnetic Resonance Imaging

Share to Mutation

Source

Identifiers

PMID: 38754044
DOI: 10.1212/WNL.0000000000209356

Genes

POLG

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Polyradiculoneuritis on MRI: An Overlooked Feature of Biallelic POLG Gene Mutations in Infancy.PMID 38754044Read ↗

Recognisable Neuroradiological Findings in Five Neurogenetic Disorders.Semantic proximity Read ↗

Spectrum of Neuroradiologic Findings Associated with Monogenic Interferonopathies.Semantic proximity Read ↗

'The phenotypic conundrum of Trp748Ser variant in POLG gene: a report of two patients'.Semantic proximity Read ↗

Typical MRI features of PLA2G6 mutation-related phospholipase-associated neurodegeneration (PLAN)/infantile neuroaxonal dystrophy (INAD).Semantic proximity Read ↗

Leukodystrophy Imaging: Insights for Diagnostic DilemmasSemantic proximity Read ↗

Striatal Variant of POLR3A: Report of Two Indian Cases.Semantic proximity Read ↗

Novel insights into the clinico-radiological spectrum of phenotypes associated to PIGN mutations.Semantic proximity Read ↗

Neuroimaging patterns in paediatric onset hereditary spastic paraplegias.Semantic proximity Read ↗

Cranial nerve and cervical root enhancement in an infant with polymerase gamma mutation mitochondrial disease.Semantic proximity Read ↗

Two Cases of CLIPPERS-like Syndrome Sharing a Hypomorphic UNC13D Variant.Semantic proximity Read ↗

Novel imaging findings in pyruvate dehydrogenase complex ( PDHc ) deficiency—Results from a nationwide population‐based studySemantic proximity Read ↗

Brain and spine MRI features of Hunter disease: frequency, natural evolution and response to therapy.Semantic proximity Read ↗

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