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Volumn 74, Issue 15, 2010, Pages 1231-1233

Juvenile-onset alpers syndrome: Interpreting MRI findings

Author keywords

[No Author keywords available]

Indexed keywords

ALPERS DISEASE; ARTICLE; BRAIN REGION; EPILEPTIC DISCHARGE; EPILEPTIC STATE; FOCAL EPILEPSY; GRAND MAL EPILEPSY; HUMAN; LEFT HEMISPHERE; NUCLEAR MAGNETIC RESONANCE IMAGING; OCCIPITAL CORTEX; OCCIPITAL LOBE; ONSET AGE; PRIORITY JOURNAL; SYMPTOM; THALAMUS;

EID: 77950961928     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/WNL.0b013e3181d90005     Document Type: Article
Times cited : (11)

References (7)
  • 1
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    • POLG1 mutations cause a syndromic epilepsy with occipital lobe predilection
    • Engelsen BA, Tzoulis C, Karlsen B, et al. POLG1 mutations cause a syndromic epilepsy with occipital lobe predilection. Brain 2008;131:818-828.
    • (2008) Brain , vol.131 , pp. 818-828
    • Engelsen, B.A.1    Tzoulis, C.2    Karlsen, B.3
  • 2
    • 0024999128 scopus 로고
    • Progressive neuronal degeneration of childhood with liver disease (Alpers-Huttenlocher syndrome): A personal review
    • Harding BN. Progressive neuronal degeneration of childhood with liver disease (Alpers-Huttenlocher syndrome): a personal review. J Child Neurol 1990;5:273-287.
    • (1990) J Child Neurol , vol.5 , pp. 273-287
    • Harding, B.N.1
  • 3
    • 33749001168 scopus 로고    scopus 로고
    • Mitochondrial DNA polymerase-gamma and human disease
    • Hudson G, Chinnery PF. Mitochondrial DNA polymerase-gamma and human disease. Hum Mol Genet 2006;15: R244-R252.
    • (2006) Hum Mol Genet , vol.15
    • Hudson, G.1    Chinnery, P.F.2
  • 4
    • 39649120348 scopus 로고    scopus 로고
    • Inherited mitochondrial diseases of DNA replication
    • Copeland WC. Inherited mitochondrial diseases of DNA replication. Annu Rev Med 2008;59:131-146.
    • (2008) Annu Rev Med , vol.59 , pp. 131-146
    • Copeland, W.C.1
  • 5
    • 2142705756 scopus 로고    scopus 로고
    • POLG mutations associated with Alpers' syndrome and mitochondrial DNA depletion
    • Naviaux RK, Nguyen KV. POLG mutations associated with Alpers' syndrome and mitochondrial DNA depletion. Ann Neurol 2004;55:706-712.
    • (2004) Ann Neurol , vol.55 , pp. 706-712
    • Naviaux, R.K.1    Nguyen, K.V.2
  • 6
    • 66849089743 scopus 로고    scopus 로고
    • Status epilepticus in children with Alpers' disease caused by POLG1 mutations: EEG and MRI features
    • Wolf NI, Rahman S, Schmitt B, et al. Status epilepticus in children with Alpers' disease caused by POLG1 mutations: EEG and MRI features. Epilepsia 2008;50:1596-1607.
    • (2008) Epilepsia , vol.50 , pp. 1596-1607
    • Wolf, N.I.1    Rahman, S.2    Schmitt, B.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.