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

Double trouble? Progranulin mutation and C9ORF72 repeat expansion in a case of primary non-fluent aphasia.

Journal of the neurological sciences - 15 Jun 2014

Mignarri Andrea, Battistini Stefania, Tomai Pitinca Maria Luigia, Monti Lucia, Burroni Luca, Ginanneschi Federica, Ricci Claudia, Bavazzano Antonio, Federico Antonio, Restagno Gabriella, Dotti Maria Teresa

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 Cerebral Cortex
Share to Fluorodeoxyglucose F18
Share to Intercellular Signaling Peptides and Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Magnetic Resonance Imaging

Share to Positron-Emission Tomography

Share to Progranulins

Share to Radiography

Share to Spin Labels

Source

Identifiers

PMID: 24703252
DOI: 10.1016/j.jns.2014.03.030

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

Double trouble? Progranulin mutation and C9ORF72 repeat expansion in a case of primary non-fluent aphasia.PMID 24703252Read ↗

Case report: coexistence of C9orf72 expansion and progranulin mutation in a case of genetic frontotemporal dementia-clinical features and neuroimaging correlates.Semantic proximity Read ↗

Rapidly progressive primary progressive aphasia and parkinsonism with novel GRN mutation.Semantic proximity Read ↗

Primary progressive aphasia: six questions in search of an answer.Semantic proximity Read ↗

Exome sequencing reveals a novel partial deletion in the progranulin gene causing primary progressive aphasia.Semantic proximity Read ↗

Crossed aphasia in nonfluent variant of primary progressive aphasia carrying a GRN mutation.Semantic proximity Read ↗

One novel GRN null mutation, two different aphasia phenotypes.Semantic proximity Read ↗

Non Fluent Variant of Primary Progressive Aphasia Due to the Novel GRN g.9543delA(IVS3-2delA) Mutation.Semantic proximity Read ↗

Rapidly progressive dementia with psychotic onset in a patient with the C9ORF72 mutation.Semantic proximity Read ↗

A novel granulin mutation in logopenic variant primary progressive aphasias: Case report and literature reviewSemantic proximity Read ↗

Dominant frontotemporal dementia mutations in 140 cases of primary progressive aphasia and speech apraxia.Semantic proximity Read ↗

An update on primary progressive aphasia.Semantic proximity Read ↗

Clinical evolution, neuroimaging, and volumetric analysis of a patient with a CSF1R mutation who presented with progressive nonfluent aphasia.Semantic proximity Read ↗

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