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

Teaching NeuroImage: IBA57 Mutation-Associated Infantile Cavitating Leukoencephalopathy.

Neurology - 14 Jun 2022

Cherian Ajith, Yalapalli Manisha K, K P Divya, Vijayaraghavan Asish, Sundaram Soumya

Abstract excerpt

No abstract is available from the source.

Topics

Carrier Proteins
Humans
Leukoencephalopathies
Mutation

Source

Identifiers

PMID

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

35387852

DOI

10.1212/WNL.0000000000200671

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Teaching NeuroImage: IBA57 Mutation-Associated Infantile Cavitating Leukoencephalopathy.PMID 35387852Read ↗

Teaching NeuroImages: Adult-onset leukoencephalopathy with intracranial calcifications and cysts (Labrune syndrome).Semantic proximity Read ↗

Phenotypic spectrum of mutations in IBA57, a candidate gene for cavitating leukoencephalopathy.Semantic proximity Read ↗

Teaching NeuroImage: ROBO3 Mutation Causing Horizontal Gaze Palsy and Brainstem Malformation.Semantic proximity Read ↗

Teaching NeuroImage: Familial Cerebral Cavernous Malformation in PDCD10 Genotype.Semantic proximity Read ↗

Teaching Video NeuroImage: New STUB1 Variant Causes Chorea, Tremor, Dystonia, Myoclonus, Ataxia, Depression, Cognitive Impairment, Epilepsy, and Superficial Siderosis.Semantic proximity Read ↗

Teaching NeuroImages: Adult-onset vanishing white matter disease.Semantic proximity Read ↗

Teaching NeuroImage: A New Imaging Finding in a Boy With Salla Disease Caused by a Pathogenic Variant in the SLC17A5 Gene.Semantic proximity Read ↗

Teaching NeuroImages: Transient cytotoxic edema in a child with a novel ATP1A2 mutation.Semantic proximity Read ↗

Teaching NeuroImage: Primary Familial Brain Calcification in SLC20A2 Genotype.Semantic proximity Read ↗

Teaching Neuro <i>Images</i> : White matter hypomyelination and progressive calcifications in cerebral folate deficiencySemantic proximity Read ↗

Teaching Video NeuroImage: TWNK Mutation Causes Chronic Progressive External Ophthalmoplegia and Cerebellar Ataxia: A POLG-Like Phenotype.Semantic proximity Read ↗

Teaching NeuroImage: Subacute Quadriparesis From Intramedullary Spinal Cord Infiltrating Glioma With TERT Promoter Mutation.Semantic proximity Read ↗

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