Hypokalemic periodic paralysis due to CACNA1S gene mutation

Khalid A. Alhasan; Mohammed S. Abdallah; Jameela A. Kari; Fahad A. Bashiri

doi:10.17712/nsj.2018.3.20180005

Article Information

vol. 24 no. 3 225-230

DOI

https://doi.org/10.17712/nsj.2018.3.20180005

PubMed

31380823

Published By

Neurosciences Journal

Online ISSN

1658-3183

History

Received September 20, 2018
Accepted March 24, 2019
Published online November 13, 2020.

Copyright: © Neurosciences Neurosciences is an Open Access journal and articles published are distributed under the terms of the Creative Commons Attribution-NonCommercial License (CC BY-NC). Readers may copy, distribute, and display the work for non-commercial purposes with the proper citation of the original work.

Author Information

Khalid A. Alhasan, MD ⇑,
Mohammed S. Abdallah, MRCPCH,
Jameela A. Kari, FRCPCH and
Fahad A. Bashiri, MD

From the Division of Pediatric Nephrology (Alhasan, Abdallah, Bashiri), Pediatric Department, College of Medicine, King Khalid University Hospital, King Saud University, Riyadh, and from Pediatric Nephrology Center of Excellence and Division of Pediatric Nephrology (Kari), Department of Pediatrics, King Abdulaziz University, Jeddah, Kingdom of Saudi Arabia

Address correspondence and reprint request to: Dr. Khalid A. Alhasan, Division of Pediatric Nephrology, Pediatric Department, College of Medicine, King Khalid University Hospital, King Saud University, Riyadh, Kingdom of Saudi Arabia. E-mail: [email protected], kalhasan28{at}yahoo.com ORICID ID: https://orcid.org/0000-0003-4928-4203

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