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

Epidemiology and characteristics of occipital brain infarcts in young adults in southwestern Finland.

Journal of neurology - 1 Feb 2010

Martikainen Mika H, Majamaa Kari

Abstract excerpt

Occipital stroke and occipital epilepsy are possible manifestations of mitochondrial diseases. A previous study in northern Finland suggested a frequency of 10% for mitochondrial disorder in young patients with stroke. Here we studied the epidemiology of occipital brain infarcts in a defined population in southwestern Finland. Patients diagnosed with brain infarct or visual field defect with onset at the ages of...

Read the complete abstract on PubMed

Topics

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

Share to Brain Infarction
Share to DNA-Directed DNA Polymerase
Share to DNA Polymerase gamma

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

Share to Finland

Share to Migraine Disorders

Share to Mutation, Missense

Share to Occipital Lobe

Share to Sex Factors

Source

Identifiers

PMID: 19730927
DOI: 10.1007/s00415-009-5305-1

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Epidemiology and characteristics of occipital brain infarcts in young adults in southwestern Finland.PMID 19730927Read ↗

Mitochondrial DNA haplogroup U as a risk factor for occipital stroke in migraineSemantic proximity Read ↗

Frequency of MELAS main mutation in a phenotype-targeted young ischemic stroke patient population.Semantic proximity Read ↗

Phylogenetic analysis of mitochondrial DNA in patients with an occipital stroke. Evaluation of mutations by using sequence data on the entire coding region.Semantic proximity Read ↗

Mitochondrial DNA haplogroups and risk of transient ischaemic attack and ischaemic stroke: a genetic association study.Semantic proximity Read ↗

Forecasting stroke-like episodes and outcomes in mitochondrial disease.Semantic proximity Read ↗

Pediatric Cerebral Infarction Unraveled: A Case of MTHFR Mutation and Hyperhomocysteinemia-Case ReportSemantic proximity Read ↗

Inherited thrombophilic disorders in young adults with ischemic stroke and patent foramen ovale.Semantic proximity Read ↗

Mitochondrial DNA haplogroups and short-term neurological outcomes of ischemic stroke.Semantic proximity Read ↗

MTHFR homozygous mutation and additional risk factors for cerebral infarction in a large Italian family.Semantic proximity Read ↗

Do common prothrombotic mutations influence the risk of cerebral ischaemia in patients with patent foramen ovale? Systematic review and meta-analysis.Semantic proximity Read ↗

Mitochondrial haplogroup H1 is protective for ischemic stroke in Portuguese patients.Semantic proximity Read ↗

Factor V Leiden, prothrombin gene G20210A variant, and methylenetetrahydrofolate reductase C677T genotype in young adults with ischemic stroke.Semantic proximity Read ↗

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