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Studies in disorders of muscle. VII. Clinical manifestations and inheritance of a type of periodic paralysis without hypopotassemia.

作者信息

TYLER F H, STEPHENS F E, GUNN F D, PERKOFF G T

出版信息

J Clin Invest. 1951 May;30(5):492-502. doi: 10.1172/JCI102465.

DOI:10.1172/JCI102465
PMID:14832379
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC436282/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0ab/436282/9f454b7f7f4f/jcinvest00418-0064-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0ab/436282/62babba03896/jcinvest00418-0064-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0ab/436282/9f454b7f7f4f/jcinvest00418-0064-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0ab/436282/62babba03896/jcinvest00418-0064-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0ab/436282/9f454b7f7f4f/jcinvest00418-0064-b.jpg

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1
Studies in disorders of muscle. VII. Clinical manifestations and inheritance of a type of periodic paralysis without hypopotassemia.肌肉疾病研究。VII. 一种无低钾血症的周期性麻痹的临床表现及遗传方式
J Clin Invest. 1951 May;30(5):492-502. doi: 10.1172/JCI102465.
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[CO-EXISTENCE OF PERIODIC PARALYSIS AND HYPERTHYROIDISM].
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引用本文的文献

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Periodic paralysis.周期性瘫痪。
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2
Hyperkalemic Periodic Paralysis: Case Report with a SCNA4 Gene Mutation and Literature Review.高钾型周期性麻痹：一例伴有SCN4基因突变的病例报告及文献综述
Case Rep Genet. 2020 Oct 16;2020:8843410. doi: 10.1155/2020/8843410. eCollection 2020.
3
Louis Ptáček receives the 2015 ASCI/Stanley J. Korsmeyer Award. Interview by Sarah Jackson.路易斯·普塔切克荣获2015年美国临床研究学会/斯坦利·J·科尔斯迈耶奖。莎拉·杰克逊采访。

本文引用的文献

1
EXCHANGES OF SODIUM AND POTASSIUM IN FAMILIAL PERIODIC PARALYSIS.家族性周期性麻痹中钠与钾的交换
J Clin Invest. 1948 Jan;27(1):65-73. doi: 10.1172/JCI101925.
2
Studies in disorders of muscle. II Clinical manifestations and inheritance of facioscapulohumeral dystrophy in a large family.肌肉疾病研究。II. 一个大家庭中面肩肱型肌营养不良症的临床表现与遗传方式
Ann Intern Med. 1950 Apr;32(4):640-60. doi: 10.7326/0003-4819-32-4-640.
J Clin Invest. 2015 Apr;125(4):1369-70. doi: 10.1172/JCI81185. Epub 2015 Apr 1.
4
Characterization of hyperkalemic periodic paralysis: a survey of genetically diagnosed individuals.高钾型周期性瘫痪的特征：对基因诊断个体的调查。
J Neurol. 2013 Oct;260(10):2606-13. doi: 10.1007/s00415-013-7025-9. Epub 2013 Jul 25.
5
Histopathology of Voluntary Muscle.随意肌的组织病理学
Postgrad Med J. 1965 Jun;41(476):294-312. doi: 10.1136/pgmj.41.476.294.
6
Targeted mutation of mouse skeletal muscle sodium channel produces myotonia and potassium-sensitive weakness.小鼠骨骼肌钠通道的靶向突变会导致肌强直和钾敏感性肌无力。
J Clin Invest. 2008 Apr;118(4):1437-49. doi: 10.1172/JCI32638.
7
INHERITED DISORDERS OF POTASSIUM METABOLISM.钾代谢的遗传性疾病。
Br Med J. 1964 Aug 1;2(5404):266. doi: 10.1136/bmj.2.5404.266.
8
[ON THE ELECTROLYTE AND ALDOSTERONE METABOLISM IN ADYNAMIA EPISODICA HEREDITARIA, THE HYPERKALEMIC FORM OF PERIODIC PARALYSIS].[遗传性发作性无力症（周期性麻痹的高钾血症形式）中的电解质与醛固酮代谢]
Klin Wochenschr. 1964 Jan 15;42:65-75. doi: 10.1007/BF01478655.
9
[Role of adosterone in paroxysmal paralysis].[醛固酮在阵发性麻痹中的作用]
Klin Wochenschr. 1963 Feb 15;41:178-84. doi: 10.1007/BF01479429.
10
Carbohydrate and sodium metabolism in periodic paralysis.周期性麻痹中的碳水化合物和钠代谢
Br Med J. 1961 Aug 26;2(5251):549-53. doi: 10.1136/bmj.2.5251.549.