[Unverricht-Lundborg disease (PME1)].

Genton, P

[Unverricht-Lundborg disease (PME1)]. / La maladie d'Unverricht-Lundborg (EPM1).

Genton, P.

Affiliation

Genton P; Centre Saint-Paul--H. Gastaut, Marseille. piergen@aol.com

Rev Neurol (Paris) ; 162(8-9): 819-26, 2006 Sep.

Article in Fr | MEDLINE | ID: mdl-17028542

Subject(s)

Myoclonic Epilepsies, Progressive/physiopathology; Unverricht-Lundborg Syndrome/physiopathology; Adolescent; Adult; Chromosomes, Human, Pair 21; Diagnosis, Differential; Disease Progression; Electroencephalography; Genes, Recessive; Humans; Prevalence; Unverricht-Lundborg Syndrome/diagnosis; Unverricht-Lundborg Syndrome/epidemiology; Unverricht-Lundborg Syndrome/genetics

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Database: MEDLINE Main subject: Myoclonic Epilepsies, Progressive / Unverricht-Lundborg Syndrome Type of study: Diagnostic_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limits: Adolescent / Adult / Humans Language: Fr Year: 2006 Type: Article

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