A new clinical entity in T704M mutation in periodic paralysis-Reference-Cited by-同舟云学术

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A new clinical entity in T704M mutation in periodic paralysis

Published:2020-08 Issue: Volume:78 Page:203-206
ISSN:0967-5868
Container-title:Journal of Clinical Neuroscience
language:en
Short-container-title:Journal of Clinical Neuroscience

Author:

Gun Bilgic Dilek,Aydin Gumus Aydeniz,Gerik Celebi Hamide Betul,Bilgic Abdulkadir,Unaltuna Erginel Nihan,Cam Fethi Sirri

Publisher

Elsevier BV

Subject

Physiology (medical),Clinical Neurology,Neurology,General Medicine,Surgery

Reference19 articles.

1. Primary periodic paralyses;Finsterer;Acta Neurol Scand.,2008

2. Different gene loci for hyperkalemic and hypokalemic periodic paralysis;Fontaine;Neuromuscul Disord,1991

3. Familial hypokalemic periodic paralysis in Finland;Kantola;J Neurol Neurosurg Psychiatry,1992

4. Hypokalemic paralyses: a review of the etiologies, pathophysiology, presentation, and therapy;Stedwell;Am J Emerg Med,1992

5. Severe infantile hyperkalaemic periodic paralysis and paramyotonia congenita: broadening the clinical spectrum associated with the T704M mutation in SCN4A;Brancati;J Neurol Neurosurg Psychiatry,2003

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Familial Hypokalemic Periodic Paralysis with Mutation in a Voltage-gated Calcium Channel;Erciyes Medical Journal;2022

2. Inherited Neuromuscular Disorders: Which Role for Serum Biomarkers?;Brain Sciences;2021-03-21

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