Genotype and Phenotype Analysis of Patients With Sporadic Periodic Paralysis
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference35 articles.
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2. Hypokalemia and paralysis;Lin;QJM,2001
3. Hypokalemia: a practical approach to diagnosis and its genetic basis;Lin;Curr Med Chem,2007
4. Laboratory tests to determine the causes for hypokalemia and paralysis;Lin;Arch Intern Med,2004
5. Thyrotoxic periodic paralysis;Lin;Mayo Clin Proc,2005
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1. Periodic paralysis;Handbook of Clinical Neurology;2024
2. Gene panel analysis of 119 index patients with suspected periodic paralysis in Japan;Frontiers in Neurology;2023-01-26
3. Case report: SCN4A p.R1135H gene variant in combination with thyrotoxicosis causing hypokalemic periodic paralysis;Frontiers in Neurology;2023-01-17
4. Short-Communication: Variable Expression of Clinical Symptoms and an Unexpected Finding of Vacuolar Myopathy Related to a Pathogenic Variant in the CACNA1S Gene in a Previous Case Report;Cureus;2022-04-02
5. Genetic Screening of Patients with Thyrotoxic Hypokalemic Periodic Paralysis: An Experience from a Tertiary Care Hospital in the Northeast of Brazil;Endocrine, Metabolic & Immune Disorders - Drug Targets;2021-12
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