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

Clustering of mutations in the 5' tertile of the NF1 gene in Slovakia patients with optic pathway glioma.

Neoplasma - 1 Jan 2013

Bolcekova A, Nemethova M, Zatkova A, Hlinkova K, Pozgayova S, Hlavata A, Kadasi L, Durovcikova D, Gerinec A, Husakova K, Pavlovicova Z, Holobrada M, Kovacs L, Ilencikova D

Abstract excerpt

Optic pathway gliomas (OPG) occur in 15% of patients with neurofibromatosis type 1 (NF1; OMIM 162200). Genotype-phenotype correlations in patients with NF1 may help to determine the risk group for developing complications such as OPG in coincidence with other NF1.features. We evaluated 52 patient...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Child
Share to Child, Preschool

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genes, Neurofibromatosis 1

Share to Genetic Association Studies

Share to Prognosis

Share to Slovakia

Share to Young Adult

Source

Identifiers

PMID: 23906300
DOI: 10.4149/neo_2013_084

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-23906300-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clustering of mutations in the 5' tertile of the NF1 gene in Slovakia patients with optic pathway glioma.PMID 23906300Read ↗

Identification of Mutation Regions on NF1 Responsible for High- and Low-Risk Development of Optic Pathway Glioma in Neurofibromatosis Type ISemantic proximity Read ↗

Clinical signs and genetic evaluation of patients with neurofibromatosis type 1 with and without optic pathway gliomas in a center in Turkey.Semantic proximity Read ↗

A molecular analysis of individuals with neurofibromatosis type 1 (NF1) and optic pathway gliomas (OPGs), and an assessment of genotype-phenotype correlations.Semantic proximity Read ↗

No correlation between NF1 mutation position and risk of optic pathway glioma in 77 unrelated NF1 patients.Semantic proximity Read ↗

Neurofibromatosis Type 1 (NF1)-Related Ocular Signs: New Insights on Their Prevalence, Incidence, and Genotype-Phenotype Correlation in NF1 Children.Semantic proximity Read ↗

An Overview of Optic Pathway Glioma With Neurofibromatosis Type 1: Pathogenesis, Risk Factors, and Therapeutic StrategiesSemantic proximity Read ↗

[Phenotypic and genetic features in neurofibromatosis type 1 in children].Semantic proximity Read ↗

Neurofibromatosis type 1-associated optic pathway gliomas: pathogenesis and emerging treatments.Semantic proximity Read ↗

Mutational spectrum of NF1 gene in 24 unrelated Egyptian families with neurofibromatosis type 1.Semantic proximity Read ↗

Neurological comorbidities and novel mutations in Turkish cases with neurofibromatosis type 1.Semantic proximity Read ↗

Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype-phenotype correlation.Semantic proximity Read ↗

Mutation spectrum of the NF1 gene and genotype-phenotype correlations in Turkish patients: Seventeen novel pathogenic variants.Semantic proximity Read ↗

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