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Volumn 42, Issue , 2015, Pages 36-40

Cognitive development in females with PCDH19 gene-related epilepsy

Author keywords

Cognitive and behavioral profile; Epilepsy; PCDH19 gene

Indexed keywords

ANTICONVULSIVE AGENT; CADHERIN; PCDH19 PROTEIN, HUMAN;

EID: 84916918835     PISSN: 15255050     EISSN: 15255069     Source Type: Journal    
DOI: 10.1016/j.yebeh.2014.10.019     Document Type: Article
Times cited : (31)

References (14)
  • 1
    • 44349150359 scopus 로고    scopus 로고
    • X-linked protocadherin 19 mutations cause female limited epilepsy and cognitive impairment
    • Dibbens L.M., Tarpey P.S., Hynes K., Bayly M.A., Scheffer I.E., Smith R., et al. X-linked protocadherin 19 mutations cause female limited epilepsy and cognitive impairment. Nat Genet 2008, 40:776-781.
    • (2008) Nat Genet , vol.40 , pp. 776-781
    • Dibbens, L.M.1    Tarpey, P.S.2    Hynes, K.3    Bayly, M.A.4    Scheffer, I.E.5    Smith, R.6
  • 2
    • 84870608256 scopus 로고    scopus 로고
    • Focal seizures with affective symptoms are a major feature of PCDH19 gene-related epilepsy
    • Marini C., Darra F., Specchio N., Mei D., Terracciano, Parmeggiani L., et al. Focal seizures with affective symptoms are a major feature of PCDH19 gene-related epilepsy. Epilepsia 2012, 53:2111-2119.
    • (2012) Epilepsia , vol.53 , pp. 2111-2119
    • Marini, C.1    Darra, F.2    Specchio, N.3    Mei, D.4    Terracciano, P.L.5
  • 3
    • 79959955178 scopus 로고    scopus 로고
    • Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutations
    • Specchio N., Marini C., Terracciano A., Mei D., Trivisano M., Sicca F., et al. Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutations. Epilepsia 2011, 52:1251-1257.
    • (2011) Epilepsia , vol.52 , pp. 1251-1257
    • Specchio, N.1    Marini, C.2    Terracciano, A.3    Mei, D.4    Trivisano, M.5    Sicca, F.6
  • 4
    • 84860650526 scopus 로고    scopus 로고
    • Cognitive and behavioral profile in females with epilepsy with PCDH19 mutation: two novel mutations and review of the literature
    • Camacho A., Simon R., Sanz R., Viñuela A., Martínez-Salio A., Mateos F. Cognitive and behavioral profile in females with epilepsy with PCDH19 mutation: two novel mutations and review of the literature. Epilepsy Behav 2012, 24:134-137.
    • (2012) Epilepsy Behav , vol.24 , pp. 134-137
    • Camacho, A.1    Simon, R.2    Sanz, R.3    Viñuela, A.4    Martínez-Salio, A.5    Mateos, F.6
  • 6
    • 0003465669 scopus 로고
    • The Psychological Corporation, New York, [Tr. It. Scala Wechsler a livello prescolare e di scuola elementare. OS Organizzazioni Speciali, Firenze (1996)]
    • Wechsler D. Wechsler Preschool and Primary Scale of Intelligence - Revised (WPPSI R) 1989, The Psychological Corporation, New York, [Tr. It. Scala Wechsler a livello prescolare e di scuola elementare. OS Organizzazioni Speciali, Firenze (1996)].
    • (1989) Wechsler Preschool and Primary Scale of Intelligence - Revised (WPPSI R)
    • Wechsler, D.1
  • 7
    • 0003664194 scopus 로고
    • The Psychological Corporation, New York, [Tr. It. Scala di Intelligenza Wechsler per Bambini-Terza Edizione OS Organizzazioni Speciali, Firenze (2006)]
    • Wechsler D. Wechsler Intelligence Scale for Children III (WISC III) 1991, The Psychological Corporation, New York, [Tr. It. Scala di Intelligenza Wechsler per Bambini-Terza Edizione OS Organizzazioni Speciali, Firenze (2006)].
    • (1991) Wechsler Intelligence Scale for Children III (WISC III)
    • Wechsler, D.1
  • 8
    • 1642472904 scopus 로고    scopus 로고
    • The Psychological Corporation, New York, Tr. It. Laicardi C, Firenze, Organizzazioni Speciali (1997)
    • Wechsler D. Wechsler Adult Intelligence Scale Revised (WAIS R) 1997, The Psychological Corporation, New York, Tr. It. Laicardi C, Firenze, Organizzazioni Speciali (1997).
    • (1997) Wechsler Adult Intelligence Scale Revised (WAIS R)
    • Wechsler, D.1
  • 11
    • 79951678915 scopus 로고    scopus 로고
    • Cognitive development in Dravet syndrome: a retrospective, multicenter study of 26 patients
    • Ragona F., Granata T., Dalla Bernardina B., Offredi F., Darra F., Battaglia D., et al. Cognitive development in Dravet syndrome: a retrospective, multicenter study of 26 patients. Epilepsia 2011, 52:386-392.
    • (2011) Epilepsia , vol.52 , pp. 386-392
    • Ragona, F.1    Granata, T.2    Dalla Bernardina, B.3    Offredi, F.4    Darra, F.5    Battaglia, D.6
  • 12
    • 78651293102 scopus 로고    scopus 로고
    • Molecular mechanisms of cognitive and behavioral comorbidities of epilepsy in children
    • Brooks-Kayal A. Molecular mechanisms of cognitive and behavioral comorbidities of epilepsy in children. Epilepsia 2011, 52(s1):13-20.
    • (2011) Epilepsia , vol.52 , Issue.S1 , pp. 13-20
    • Brooks-Kayal, A.1
  • 13
    • 84858297870 scopus 로고    scopus 로고
    • PCDH19-related infantile epileptic encephalopathy: an unusual X-linked inheritance disorder
    • Depienne C., Le Guern E. PCDH19-related infantile epileptic encephalopathy: an unusual X-linked inheritance disorder. Hum Mutat 2012, 33:627-634.
    • (2012) Hum Mutat , vol.33 , pp. 627-634
    • Depienne, C.1    Le Guern, E.2
  • 14
    • 84864584881 scopus 로고    scopus 로고
    • Cadherins and neuropsychiatric disorders
    • Redies C., Hertel N., Hubner C.A. Cadherins and neuropsychiatric disorders. Brain Res 2012, 1470:130-144.
    • (2012) Brain Res , vol.1470 , pp. 130-144
    • Redies, C.1    Hertel, N.2    Hubner, C.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.