SEARCH

SEARCH BY CITATION

REFERENCES

  • 1
    Poza JJ, Saenz A, Martinez-Gil A, et al. Autosomal dominant lateral temporal epilepsy: clinical and genetic study of a large Basque pedigree linked to chromosome 10q. Ann Neurol 1999;42: 1828.DOI: 10.1002/1531-8249(199902)45:2<182::AID-ANA8>3.0.CO;2-G
  • 2
    Winawer MR, Ottman R, Hauser WA, et al. Autosomal dominant partial epilepsy with auditory features: defining the phenotype. Neurology 2000;54: 21736.
  • 3
    Ottman R, Risch N, Hauser WA, et al. Localization of a gene for partial epilepsy to chromosome 10q. Nat Genet 1995;10: 5660.DOI: 10.1038/ng0595-56
  • 4
    Michelucci R, Passarelli D, Pitzalis S, et al. Autosomal dominant partial epilepsy with auditory features: description of a new family. Epilepsia 2000;41: 96770.
  • 5
    Brodtkorb E, Gu W, Nakken KO, et al. Familial temporal lobe epilepsy with aphasic seizures and linkage to chromosome 10q22-q24. Epilepsia 2002;43: 22835.
  • 6
    Michelucci R, Poza JJ, Sofia V, et al. Autosomal dominant lateral temporal epilepsy: clinical spectrum, new epitempin mutations, and genetic heterogeneity in seven European families. Epilepsia 2003;44: 128997.DOI: 10.1046/j.1528-1157.2003.20003.x
  • 7
    Hedera P, Abou-Khalil B, Crunk AE, et al. Autosomal dominant lateral temporal epilepsy: two families with novel mutations in the LGI1 gene. Epilepsia 2004;45: 21822.DOI: 10.1111/j.0013-9580.2004.47203.x
  • 8
    Kanemoto K, Kawasaki J. Familial aphasic episodes: another variant of partial epilepsy with simple inheritance? Epilepsia 2000;41: 10368.
  • 9
    Foldvary N, Acharya V, Luders HO. Auditory auras. In: LudersHO, NoachtarS, eds. Epileptic seizures: pathophysiology and clinical semiology. Philadelphia : Churchill Livingstone, 2000: 30412.
  • 10
    Kalachikov S, Evgrafov O, Ross B, et al. Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features. Nat Genet 2002;30: 33541.DOI: 10.1038/ng832
  • 11
    Morante-Redolat JM, Gorostidi-Pagola A, Piquer-Sirerol S, et al. Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy. Hum Mol Genet 2002;1: 111928.DOI: 10.1093/hmg/11.9.1119
  • 12
    Bisulli F, Tinuper P, Marini C, et al. Partial epilepsy with prominent auditory symptoms not linked to chromosome 10q. Epileptic Disord 2002;4: 1837.
  • 13
    Chernova OB, Somerville RP, Cowell JK. A novel gene, LGI1, from 10q24 is rearranged and downregulated in malignant brain tumors. Oncogene 1998;17: 287381.
  • 14
    Brodtkorb E, Nakken KO, Steinlein OK. No evidence for a seriously increased malignancy risk in LGI1-caused epilepsy. Epilepsy Res 2003;56: 2058.
  • 15
    Kobayashi E, Santos NF, Torres FR, et al. Magnetic resonance imaging abnormalities in familial temporal lobe epilepsy with auditory auras. Arch Neurol 2003;60: 154651.DOI: 10.1001/archneur.60.11.1546
  • 16
    Reutens DC, Howell RA, Gebert KE, et al. Validation of a questionnaire of clinical seizure diagnosis. Epilepsia 1992;33: 106571.
  • 17
    ILAE. Commission on Classification and Terminology of the International League Against Epilepsy: Proposal for revised classification of epilepsies and epileptic syndromes. Epilepsia 1989;30: 38999.
  • 18
    ILAE. Commission of Classification and Terminology of the International League Against Epilepsy: Proposal for revised clinical and electroencephalographic classification of epileptic seizures. Epilepsia 1981;22: 489501.
  • 19
    Raven JC. APM: Advanced progressive matrices: Serie I e II. Firenze , Italy : Organizzazioni Speciali, 1992.
  • 20
    Pruneti C, Fenu, A, Freschi R. Aggiornamento della standardizzazione italiana del test delle Matrici Progressive Colorate di Raven. Boll Psicol Appl 1996;217: 517.
  • 21
    Miceli G, Laudanna, A, Burani C, et al. Analisi dei Deficit Afasici- BADA, Cepsag. Rome : Università Cattolica del Sacro Cuore , 1994.
  • 22
    Sartori G, Job R, Tressoldi PE. Batteria per la valutazione della dislessia e della disortografia evolutiva. Firenze , Italy: Organizzazioni Speciali , 1995.
  • 23
    SpinnlerH, TognoniG, eds. Standardizzazione e taratura italiana di test neuropsicologici. Ital J Neurol Sci 1987;6 suppl:8.
  • 24
    Ferrari E, De Renzi E, Faglioni P, et al. Standardizzazione di una batteria per la valutazione dei disturbi del linguaggio nell'età scolare. Neuropsichiatr Infantile 1981; 2356: 145–58.
  • 25
    Masi G. Unpublished Technical Report of the Italian Ministry of Health. 1996.
  • 26
    Novelli G, Papagno C, Capitani E, et al. Three clinical tests for the assessment of lexical retrieval and production: norms from 320 normal subjects. Arch Psicol Neurol Psichiatry 1986;47: 477506.
  • 27
    Brizzolara D. Unpublished Technical Report of the Italian Ministry of Health, 1989.
  • 28
    Brizzolara D, Pecini C, Brovedani P, et al. Timing and type of congenital brain lesion determine different patterns of language lateralization in hemiplegic children. Neuropsychology 2002;40: 62032.
  • 29
    Wexler BE, Halwes T. Increasing the power of dichotic methods: the fused rhymed words test. Neuropsychology 1983;21: 5966.DOI: 10.1016/0028-3932(83)90100-8
  • 30
    Brizzolara D, Brovedani P, Cioni G, et al. A comparison of two different dichotic tests for the assessment of language lateralization in children. Proceedings of the XXVII International Congress of Psychology, Stockholm, 2000: 238.
  • 31
    Oldfield RC. The assessment and analysis of handedness: the Edinburgh Inventory. Neuropsychology 1971;9: 97113.DOI: 10.1016/0028-3932(71)90067-4
  • 32
    Nakayama J, Hamano K, Iwasaki N, et al. Mutation analysis of the leucine-rich, glioma inactivated 1 gene (LGI1) in Japanese febrile seizure patients. Neuropediatrics 2003;34: 2346.DOI: 10.1055/s-2003-43255