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

Progress towards understanding the neurobiology of Batten disease or neuronal ceroid lipofuscinosis.

Current opinion in neurology - 1 Apr 2003

Cooper Jonathan D

Abstract excerpt

PURPOSE OF REVIEW: The identification of genes mutated in the neuronal ceroid lipofuscinoses has accelerated research into the mechanisms that underlie these fatal autosomal recessive storage disorders, which are often referred to as Batten disease. This review summarizes progress in this field since October 2001, describing advances in cell biology, the characterization of new animal models of neuronal ceroid...

Read the complete abstract on PubMed

Topics

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

Share to Cell Death
Share to Disease Models, Animal
Share to Lysosomal Storage Diseases

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Lysosomal Storage Disorders Research

Share to Mutation

Share to Neuroglia

Share to Neuronal Ceroid-Lipofuscinoses

Share to Protein Transport

Source

Identifiers

PMID: 12644737
DOI: 10.1097/01.wco.0000063762.15877.9b

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Progress towards understanding the neurobiology of Batten disease or neuronal ceroid lipofuscinosis.PMID 12644737Read ↗

Progress towards understanding the neurobiology of Batten disease or neuronal ceroid lipofuscinosisSemantic proximity Read ↗

Neurodegenerative disease: the neuronal ceroid lipofuscinoses (Batten disease).Semantic proximity Read ↗

Batten disease: clinical aspects, molecular mechanisms, translational science, and future directions.Semantic proximity Read ↗

Molecular basis of the neuronal ceroid lipofuscinoses: mutations in CLN1, CLN2, CLN3, and CLN5.Semantic proximity Read ↗

Autophagy in the Neuronal Ceroid Lipofuscinoses (Batten Disease)Semantic proximity Read ↗

The neuronal ceroid-lipofuscinoses.Semantic proximity Read ↗

The neuronal ceroid lipofuscinoses: the same, but different?Semantic proximity Read ↗

The neuronal ceroid‐lipofuscinoses (Batten disease): A new class of lysosomal storage diseasesSemantic proximity Read ↗

Current Insights in Elucidation of Possible Molecular Mechanisms of the Juvenile Form of Batten Disease.Semantic proximity Read ↗

The genetic spectrum of human neuronal ceroid-lipofuscinoses.Semantic proximity Read ↗

Targeted disruption of the Cln3 gene provides a mouse model for Batten disease. The Batten Mouse Model Consortium [corrected].Semantic proximity Read ↗

Genetic basis and phenotypic correlations of the neuronal ceroid lipofusinoses.Semantic proximity Read ↗

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