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

High risk of reading disability and speech sound disorder in rolandic epilepsy families: case-control study.

Epilepsia - 1 Dec 2007

Clarke Tara, Strug Lisa J, Murphy Peregrine L, Bali Bhavna, Carvalho Janessa, Foster Suzanne, Tremont Geoffrey, Gagnon Bernadine R, Dorta Nelson, Pal Deb K

Abstract excerpt

PURPOSE: Associations between rolandic epilepsy (RE) with reading disability (RD) and speech sound disorder (SSD) have not been tested in a controlled study. We conducted a case-control study to determine whether (1) RD and SSD odds are higher in RE probands than controls and (2) an RE proband pr...

Read the complete abstract on PubMed

Topics

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

Share to Language Development Disorders
Share to Comorbidity
Share to Dyslexia

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Family

Share to Functional Laterality

Share to International Classification of Diseases

Share to Prevalence

Share to Surveys and Questionnaires

Source

Open in PubMed Open full text

Identifiers

PMID: 17850323
DOI: 10.1111/j.1528-1167.2007.01276.x
PMCID: PMC2150742

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17850323-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

High risk of reading disability and speech sound disorder in rolandic epilepsy families: case-control study.PMID 17850323Read ↗

The genetics of reading disability in an often excluded sample: novel loci suggested for reading disability in Rolandic epilepsy.Semantic proximity Read ↗

The Cleveland Family Speech and Reading Study: A Review of Long-Term Outcomes Linking Phenotypes and Genotypes for Speech Sound Disorders.Semantic proximity Read ↗

Relations among speech, language, and reading disorders.Semantic proximity Read ↗

Evidence of shared genetic risk factors for migraine and rolandic epilepsy.Semantic proximity Read ↗

Literacy outcomes of children with early childhood speech sound disorders: impact of endophenotypes.Semantic proximity Read ↗

Familial epilepsy and developmental dysphasia: description of an Italian pedigree with autosomal dominant inheritance and screening of candidate loci.Semantic proximity Read ↗

Association of the ROBO1 gene with reading disabilities in a family-based analysis.Semantic proximity Read ↗

Association between AVPR1A, DRD2, and ASPM and endophenotypes of communication disorders.Semantic proximity Read ↗

Autosomal dominant inheritance of centrotemporal sharp waves in rolandic epilepsy families.Semantic proximity Read ↗

Family history interview of a broad phenotype in specific language impairment and matched controls.Semantic proximity Read ↗

Heritable risk factors associated with language impairments.Semantic proximity Read ↗

Specific reading disability: a multiplanar view.Semantic proximity Read ↗

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