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

Autosomal dominant cortical tremor, myoclonus and epilepsy: many syndromes, one phenotype.

Acta neurologica Scandinavica - 1 Apr 2005

Striano P, Zara F, Striano S

Abstract excerpt

The association of cortical tremor, myoclonus and epileptic seizures has been reported in many Japanese and European families with different acronyms. We reviewed the familial cases presenting the clinical picture of autosomal dominant cortical tremor, myoclonus and epilepsy and analysed the phenotypic differences between the pedigrees, according to the recent genetic acquisitions. We concluded that BAFME, FAME,...

Read the complete abstract on PubMed

Topics

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

Share to Chromosomes, Human, Pair 2
Share to Chromosomes, Human, Pair 8
Share to Electrocardiography

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Epilepsies, Myoclonic

Share to Syndrome

Share to Tremor

Source

Identifiers

PMID: 15740570
DOI: 10.1111/j.1600-0404.2005.00385.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Autosomal dominant cortical tremor, myoclonus and epilepsy: many syndromes, one phenotype.PMID 15740570Read ↗

Familial Cortical Myoclonic Tremor and Epilepsy, an Enigmatic Disorder: From Phenotypes to Pathophysiology and Genetics. A Systematic Review.Semantic proximity Read ↗

Familial Cortical Myoclonic Tremor and Epilepsy, an Enigmatic Disorder: From Phenotypes to Pathophysiology and Genetics. A Systematic ReviewSemantic proximity Read ↗

Familial adult myoclonic epilepsy: recognition of mild phenotypes and refinement of the 2q locus.Semantic proximity Read ↗

Familial Cortical Myoclonic Tremor with Epilepsy and Cerebellar Changes: Description of a New Pathology Case and Review of the LiteratureSemantic proximity Read ↗

Rational search for genes in familial cortical myoclonic tremor with epilepsy, clues from recent advances.Semantic proximity Read ↗

Familial cortical myoclonic tremor with epilepsySemantic proximity Read ↗

Absence of linkage to 8q24 in a European family with familial adult myoclonic epilepsy (FAME)Semantic proximity Read ↗

Benign adult familial myoclonic epilepsy: genetic heterogeneity and allelism with ADCME.Semantic proximity Read ↗

Benign adult familial myoclonic epilepsy (BAFME): evidence of an extended founder haplotype on chromosome 2p11.1-q12.2 in five Italian families.Semantic proximity Read ↗

Familial cortical myoclonic tremor with epilepsy: TTTCA/TTTTA repeat expansions and expanding phenotype in two Chinese families.Semantic proximity Read ↗

Remapping and mutation analysis of benign adult familial myoclonic epilepsy in a Japanese pedigree.Semantic proximity Read ↗

A new benign adult familial myoclonic epilepsy (BAFME) pedigree suggesting linkage to chromosome 2p11.1-q12.2.Semantic proximity Read ↗

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