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

Complicated hereditary spastic paraplegia with thin corpus callosum: variation of phenotypic expression over time.

Journal of neurology - 1 Oct 2004

Sperfeld Anne-Dörte, Kassubek Jan, Crosby Andrew H, Winner Beate, Ludolph Albert C, Uttner Ingo, Hanemann C Oliver

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 Adaptor Proteins, Signal Transducing
Share to Carrier Proteins
Share to Corpus Callosum
Share to Longitudinal Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Magnetic Resonance Imaging

Share to Phenotype

Share to Spastic Paraplegia, Hereditary

Source

Identifiers

PMID: 15503116
DOI: 10.1007/s00415-004-0562-5

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Complicated hereditary spastic paraplegia with thin corpus callosum: variation of phenotypic expression over time.PMID 15503116Read ↗

Hereditary spastic paraplegia with a thin corpus callosum due to SPG11 mutation.Semantic proximity Read ↗

Late-onset hereditary spastic paraplegia with thin corpus callosum caused by a new SPG3A mutation.Semantic proximity Read ↗

Novel SPG11 Mutation in Hereditary Spastic Paraplegia with Thin Corpus Callosum.Semantic proximity Read ↗

Atypical adult onset complicated spastic paraparesis with thin corpus callosum in two patients carrying a novel FA2H mutation.Semantic proximity Read ↗

Atypical hereditary spastic paraplegia with thin corpus callosum in a Korean patient with a novel SPG11 mutation.Semantic proximity Read ↗

Two novel mutations in the SPG11 gene causing hereditary spastic paraplegia associated with thin corpus callosum.Semantic proximity Read ↗

Spastizin mutation in hereditary spastic paraplegia with thin corpus callosum.Semantic proximity Read ↗

Complicated hereditary spastic paraplegia with thin corpus callosum (HSP-TCC) and childhood onset.Semantic proximity Read ↗

A novel locus for hereditary spastic paraplegia with thin corpus callosum and epilepsy.Semantic proximity Read ↗

Rapidly deteriorating course in Dutch hereditary spastic paraplegia type 11 patients.Semantic proximity Read ↗

Novel SPG11 mutations in Chinese families with hereditary spastic paraplegia with thin corpus callosum.Semantic proximity Read ↗

NT5C2 novel splicing variant expands the phenotypic spectrum of Spastic Paraplegia (SPG45): case report of a new member of thin corpus callosum SPG-Subgroup.Semantic proximity Read ↗

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