Two norwegian families illustrating the problem of genotype and phenotype in frontal lobe epilepsy

Acta Neurologica Scandinavica, Supplement

Volumn 102, Issue 175, 2000, Pages 25-27

  Nakken, K O ^a   Brodtkorb, E ^b  

^a National Center for Epilepsy   (Norway)

^b TRONDHEIM UNIVERSITY HOSPITAL   (Norway)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL DOMINANT DISORDER; CLINICAL ARTICLE; DISEASE ASSOCIATION; FEMALE; FRONTAL LOBE EPILEPSY; GENE MUTATION; GENOTYPE; HUMAN; MALE; NORWAY; PEDIGREE; PHENOTYPE; SHORT SURVEY;

EID: 0034522892     PISSN: 00651427     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Short Survey

References (11)

1. Autosomal dominant frontal epilepsy misdiagnosed as sleep disorder
2. Localization of a gene for autosomal dominant nocturnal frontal lobe epilepsy to chromosome 20q13.2
3. Autosomal dominant nocturnal frontal lobe epilepsy: An electroclinical study of a Norwegian family with ten affected members
4. Independent occurrence of the CHRNA4 Ser248Phe mutation in a Norwegian family with nocturnal frontal lobe epilepsy
5. An insertion mutation of the CHRNA4 gene in a family with autosomal dominant nocturnal frontal lobe epilepsy
6. An amino acid exchange in the second transmembrane segment of a neuronal nicotinic receptor causes partial epilepsy by altering its desensitization kinetics
7. Thalamocortical oscillations in the sleeping and aroused brain
8. Autosomal dominant nocturnal frontal lobe epilepsy. A distinctive clinical disorder
9. Nocturnal paroxysmal dystonia
10. Frontal lobe epilepsy: Some clinical characteristics
11. Nocturnal paroxysmal dystonia: A clinical form of focal epilepsy