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Volumn 25, Issue 8, 1996, Pages 832-835

Gamstorp's disease and pregnancy. A case report;Maladie de Gamstorp et grossesse. A propos d'un cas

Author keywords

hyperkaliemic periodic paralysis; malignant hyperthermia; pregnancy

Indexed keywords

ADULT; ARTICLE; CASE REPORT; DISEASE COURSE; FEMALE; HUMAN; HYPERKALEMIA; PERIODIC PARALYSIS; PREGNANCY;

EID: 0030453448     PISSN: 03682315     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (4)

References (9)
  • 1
    • 75949140831 scopus 로고
    • Les crises récidivantes de faiblesse musculaire à caractère héréditaire
    • Gamstorp I. Les crises récidivantes de faiblesse musculaire à caractère héréditaire. Rev Prat 1964;4:527-45.
    • (1964) Rev Prat , vol.4 , pp. 527-545
    • Gamstorp, I.1
  • 2
    • 12644252264 scopus 로고
    • Paralysies périodiques
    • Harisson TR, ed. Paris : Flammarion
    • e édition américaine). Paris : Flammarion, 1992:2121-2.
    • (1992) e Édition Américaine) , pp. 2121-2122
    • Griggs, R.C.1
  • 5
    • 0014440985 scopus 로고
    • Hyperkaliemic periodic paralysis (intracellular electromyographic studies)
    • Brooks JE. Hyperkaliemic periodic paralysis (intracellular electromyographic studies). Arch Neurol 1969;20:13-8.
    • (1969) Arch Neurol , vol.20 , pp. 13-18
    • Brooks, J.E.1
  • 6
    • 0025062007 scopus 로고
    • Progressive myopathy in hyperkaliemic periodic paralysis
    • Bradley WG, Taylor R, Rice DR. Progressive myopathy in hyperkaliemic periodic paralysis. Arch Neurol 1990;47:1013-7.
    • (1990) Arch Neurol , vol.47 , pp. 1013-1017
    • Bradley, W.G.1    Taylor, R.2    Rice, D.R.3
  • 8
    • 0028221445 scopus 로고
    • Mutations in the muscle sodium channel gene (SCN4A) in 13 French families with hyperkaliemic periodic paralysis and paramyotonia congenita: Phenotype to genotype correlations and demonstration of the predominance of two mutations
    • Plassart E, Reboul J, Rime CS, Recan D, Millasseau P, Desnuelle C et al. Mutations in the muscle sodium channel gene (SCN4A) in 13 French families with hyperkaliemic periodic paralysis and paramyotonia congenita: phenotype to genotype correlations and demonstration of the predominance of two mutations. Eur J Hum Genet 1994;2:110-24.
    • (1994) Eur J Hum Genet , vol.2 , pp. 110-124
    • Plassart, E.1    Reboul, J.2    Rime, C.S.3    Recan, D.4    Millasseau, P.5    Desnuelle, C.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.