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Volumn 32, Issue 9, 2016, Pages 1567-1568

Excellent response to deep brain stimulation in a young girl with GNAO1-related progressive choreoathetosis

Author keywords

[No Author keywords available]

Indexed keywords

CREATINE KINASE; FENTANYL; GUANINE NUCLEOTIDE BINDING PROTEIN; GUANINE NUCLEOTIDE BINDING PROTEIN ALPHA OTHER; MIDAZOLAM; PIMOZIDE; UNCLASSIFIED DRUG; GNAO1 PROTEIN, HUMAN; INHIBITORY GUANINE NUCLEOTIDE BINDING PROTEIN;

EID: 84973596900     PISSN: 02567040     EISSN: 14330350     Source Type: Journal    
DOI: 10.1007/s00381-016-3139-6     Document Type: Letter
Times cited : (41)

References (5)
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    • (2008) Handb Exp Pharmacol , vol.184 , pp. 207-260
    • Brown, D.A.1    Sihra, T.S.2
  • 2
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    • De novo mutations in GNAO1, encoding a G-alpha-o subunit of heterotrimeric G Proteins, cause epileptic encephalopathy
    • COI: 1:CAS:528:DC%2BC3sXhtlGqsr7M, PID: 23993195
    • Nakamura K, Kodera H, Akita T et al (2013) De novo mutations in GNAO1, encoding a G-alpha-o subunit of heterotrimeric G Proteins, cause epileptic encephalopathy. Am J Hum Genet 93:496–505
    • (2013) Am J Hum Genet , vol.93 , pp. 496-505
    • Nakamura, K.1    Kodera, H.2    Akita, T.3
  • 3
    • 84954142394 scopus 로고    scopus 로고
    • Progressive movement disorder in brothers carrying GNAO1 mutation responsive to deep brain stimulation
    • PID: 26060304
    • Kulkarni N, Tang S, Bhardwaj R et al (2016) Progressive movement disorder in brothers carrying GNAO1 mutation responsive to deep brain stimulation. J Child Neurol 31:211–14
    • (2016) J Child Neurol , vol.31 , pp. 211-214
    • Kulkarni, N.1    Tang, S.2    Bhardwaj, R.3
  • 4
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    • Phenotypic spectrum of GNAO1 variants: epileptic encephalopathy to involuntary movements with severe developmental delay
    • COI: 1:CAS:528:DC%2BC2MXitVenur3E, PID: 25966631
    • Saitsu H, Fukai R, Ben-Zeev B et al (2016) Phenotypic spectrum of GNAO1 variants: epileptic encephalopathy to involuntary movements with severe developmental delay. Eur J Hum Genet 24:129–34
    • (2016) Eur J Hum Genet , vol.24 , pp. 129-134
    • Saitsu, H.1    Fukai, R.2    Ben-Zeev, B.3
  • 5
    • 84974603043 scopus 로고    scopus 로고
    • Clinical course of six children with GNAO1 mutations causing a severe and distinctive movement disorder. Pediatr Neurol. (15)30159-4
    • Ananth AL, Robichaux-Viehoever A, et al (2016) Clinical course of six children with GNAO1 mutations causing a severe and distinctive movement disorder. Pediatr Neurol. (15)30159-4. doi: 10.1016/j.pediatrneurol.2016.02.018.
    • (2016) doi: 10.1016/j.pediatrneurol.2016.02.018
    • Ananth, A.L.1    Robichaux-Viehoever, A.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.