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酷似原发性多肌炎的原发性醛固酮增多症二例 被引量:5

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作者 陆亚华
出处 《中华风湿病学杂志》 CAS CSCD 2005年第10期635-636,共2页 Chinese Journal of Rheumatology
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  • 1[1]Buruma OJ, Bots GT, Went LW. Familial hypokalemic periodic paralysis, 50-year follow-up of a large family. Arch Neurol, 1985, 42(1):28
  • 2[2]Links TP, Smie AJ, Molenaar WM, et al. Familial hypokalemic periodic paralysis. clinical, diagnostic and therapeutic aspects. J Neurol Sci, 1994, 122(1):33
  • 3[3]Kramer LD, Cole JP, Messeager JL, et al. Cardiac dysfunction in a patient with familial hypokalemic periodic paralysis. Chest, 1979, 75(2):189
  • 4[4]Toglia UJ, Mandel S, Kosmorsky G. Multiple sclerosis and hypokalemic periodic paralysis in the same patient. Arch Neurol, 1982, 39(8):530
  • 5[5]Bohan A, peter JB. Polymyositis and dermatomyositis. N engl J Med, 1975, 292(4):344
  • 6[6]Jukat-Rott K, Mitrovic N, hang C, et al. Novel voltage sensor sodium channel mutations causr hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current. Proc Natl Acad Sci USA, 2000,97(17):9549
  • 7[7]Sterberg D, Maisonobe T, Jurkat-Kott, et al. Hypokalemic periodic patalysis type 2 caused by mutatuons at codon 672 in the muscle sodium channel gene SCN4A. Brain, 2001, 1249(Pt6):1091
  • 8[8]Ogawa T, Kamikubo K. Hypokalemic periodic paralysis associated with hypophosphatemia in apatient with hyperinsulinemia. Am J Med Sci, 1999, 318(1):69
  • 9[9]Tricarico D, Servidei S, Tonali P, et al. Impariment of skeletal muscle adenosin triphospnate-sensitive K+ channels in patients eith hypokalemic periodic paralysis. J Clin Invesl, 1999, 103(6):675
  • 10彭超英,蒲传强.周期性麻痹110例临床分析[J].中国神经免疫学和神经病学杂志,1999,6(4):259-262. 被引量:48

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