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Volumn 120, Issue 5, 1999, Pages 785-786

Bilateral vocal fold paralysis caused by familial hypokalemic periodic paralysis

Author keywords

[No Author keywords available]

Indexed keywords

ACETAZOLAMIDE; ADRENALIN; DIPHENHYDRAMINE; SPIRONOLACTONE; STEROID;

EID: 0032929755     PISSN: 01945998     EISSN: None     Source Type: Journal    
DOI: 10.1053/hn.1999.v120.a86002     Document Type: Article
Times cited : (3)

References (12)
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    • (1992) J Laryngol Otol , vol.106 , pp. 56-57
    • Moralee, S.J.1    Reilly, P.G.2
  • 2
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    • The periodic paralyses
    • Riggs JE. The periodic paralyses. Neurol Clin 1988;6:485-98.
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  • 3
    • 0019831369 scopus 로고
    • Familial periodic paralysis with hypokalemic
    • Johnsen T. Familial periodic paralysis with hypokalemic. Dan Med Bull 1981;28:1-27.
    • (1981) Dan Med Bull , vol.28 , pp. 1-27
    • Johnsen, T.1
  • 4
    • 0026631004 scopus 로고
    • Muscle fiber conduction velocity in the diagnosis of sporadic hypokalemic periodic paralysis
    • Brouwer OF, Zwarts MJ, Links TP, et al. Muscle fiber conduction velocity in the diagnosis of sporadic hypokalemic periodic paralysis. Clin Neurol Neurosurg 1992;94:149-51.
    • (1992) Clin Neurol Neurosurg , vol.94 , pp. 149-151
    • Brouwer, O.F.1    Zwarts, M.J.2    Links, T.P.3
  • 5
    • 0026447672 scopus 로고
    • Diagnosis of familial hypokalemic periodic paralysis: Role of the potassium exercise test
    • Kantola IM, Tarssanen LT. Diagnosis of familial hypokalemic periodic paralysis: role of the potassium exercise test. Neurology 1992;42:2158-61.
    • (1992) Neurology , vol.42 , pp. 2158-2161
    • Kantola, I.M.1    Tarssanen, L.T.2
  • 7
    • 0018387902 scopus 로고
    • Cardiac dysfunction in a patient with familial hypokalemic periodic paralysis
    • Kramer LD, Cole JP, Messenger JC, et al. Cardiac dysfunction in a patient with familial hypokalemic periodic paralysis. Chest 1979;75:189-92.
    • (1979) Chest , vol.75 , pp. 189-192
    • Kramer, L.D.1    Cole, J.P.2    Messenger, J.C.3
  • 8
    • 0028269130 scopus 로고
    • Familial hypokalemic periodic paralysis: Clinical, diagnostic and therapeutic aspects
    • Links TP, Smit AJ, Molenaar WM, et al. Familial hypokalemic periodic paralysis: clinical, diagnostic and therapeutic aspects. J Neurol Sci 1994;122:33-43.
    • (1994) J Neurol Sci , vol.122 , pp. 33-43
    • Links, T.P.1    Smit, A.J.2    Molenaar, W.M.3
  • 9
    • 0027305173 scopus 로고
    • Potassium channels in hypokalemic periodic paralysis: A key to the pathogenesis?
    • Colch
    • Links TP, Smit AJ, Oosterhuis HJ, et al. Potassium channels in hypokalemic periodic paralysis: a key to the pathogenesis? Clin Sci (Colch) 1993;85:319-25.
    • (1993) Clin Sci , vol.85 , pp. 319-325
    • Links, T.P.1    Smit, A.J.2    Oosterhuis, H.J.3
  • 10
    • 0028361074 scopus 로고
    • Mapping of the hypokalemic periodic paralysis (HypoPP) locus to chromosome 1q31-32 in three European families
    • Fontaine B, Vale-Santos JE, Jurkatt-Rott K, et al. Mapping of the hypokalemic periodic paralysis (HypoPP) locus to chromosome 1q31-32 in three European families. Nat Genet 1994;6:267-72.
    • (1994) Nat Genet , vol.6 , pp. 267-272
    • Fontaine, B.1    Vale-Santos, J.E.2    Jurkatt-Rott, K.3
  • 11
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    • Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): Genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 Caucasian families
    • Elbaz A, Vale-Santos J, Jurkat-Rott K, et al. Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 Caucasian families. Am J Hum Genet 1995;56:374-80.
    • (1995) Am J Hum Genet , vol.56 , pp. 374-380
    • Elbaz, A.1    Vale-Santos, J.2    Jurkat-Rott, K.3
  • 12
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    • Electrophysiological properties of the hypokalemic periodic paralysis mutation (R528H) of the skeletal muscle alpha Is subunit as expressed in mouse L cells
    • Lapie P, Goudet C, Nargeot J, et al. Electrophysiological properties of the hypokalemic periodic paralysis mutation (R528H) of the skeletal muscle alpha Is subunit as expressed in mouse L cells. FEBS Lett 1996;382:244-8.
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    • Lapie, P.1    Goudet, C.2    Nargeot, J.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.