Results 1 to 10 of about 440 (183)

Familial hypokalemic periodic paralysis: A case series and review

Medical Journal of Dr. D.Y. Patil Vidyapeeth, 2022
The periodic paralyses (PPs) are a group of rare neuromuscular disorders related to muscle ion channels, presenting with episodes of sudden muscle weakness.
Obeid Shafi, Muzamil Latief, Zhahid Hassan, Farhat Abbas, Summyia Farooq   +4 more
doaj   +1 more source

Identification of Mutation in SCN4A, Hot-Spot for Periodic Paralyses, in a Large Chinese Family with a Typical Normokalemic PP Using the Whole-Exome Sequencing [PDF]

Biomedical Journal of Scientific & Technical Research, 2020
Tumor is an abnormal mass of tissue, which could be solid, or fluid filled. Migration Inhibitory Factor (MIF) is a ubiquitously expressed cytokine in tumor. High levels of MIF expression have been observed in several human cancers and expression correlates with tumor grading and clinical prognosis. This experiment was designed to see the size of tumor,
openaire   +1 more source

Molecular cloning of ion channels in Felis catus that are related to periodic paralyses in man: a contribution to the understanding of the genetic susceptibility to feline neck ventroflexion and paralysis

Biology Open, 2014
Neck ventroflexion in cats has different causes; however, the most common is the hypokalemia associated with flaccid paralysis secondary to chronic renal failure.
Marlyn Zapata, Ilda S. Kunii, Rolf M. Paninka, Denise M. N. Simões, Víctor A. Castillo, Archivaldo Reche, Rui M. B. Maciel, Magnus R. Dias da Silva   +7 more
doaj   +1 more source

Muscle channelopathies and electrophysiological approach

Annals of Indian Academy of Neurology, 2008
Myotonic syndromes and periodic paralyses are rare disorders of skeletal muscle characterized mainly by muscle stiffness or episodic attacks of weakness.
Cherian Ajith, Baheti Neeraj, Kuruvilla Abraham   +2 more
doaj  

Genetic diagnosis and treatment progress of primary periodic paralysis

Chinese Journal of Contemporary Neurology and Neurosurgery, 2014
Primary periodic paralysis is autosomal dominant genetic skeletal muscle ion channelopathy. It is characterized by episodes of muscle weakness associated with lower, normal or elevated serum potassium.
Qing KE
doaj  

Paroxysmal limb weakness for ten years

Chinese Journal of Contemporary Neurology and Neurosurgery, 2017
DOI: 10.3969/j.issn.1672-6731.2017.07 ...
Meng-yu ZHANG, Yan XU, Jian-zhong SHEN, Yin-chang YANG, Bin PENG, Li-ying CUI   +5 more
doaj  

A dangerous food binge: a case report of hypokalemic periodic paralysis and review of current literature. [PDF]

Ital J Pediatr, 2022
Colucci MC, Triolo MF, Petrucci S, Pugnaloni F, Corsino M, Evangelisti M, D'Asdia MC, Di Nardo G, Garibaldi M, Terrin G, Parisi P.   +10 more
europepmc   +1 more source

Atypical Fracture of Femur in Association with Familial Hypokalemic Periodic Paralysis: A Case Report. [PDF]

J Orthop Case Rep, 2021
Barwar N, Sharma A, Khatri N, Kumar N.
europepmc   +1 more source

Sporadic adult-onset brainstem hyperkalemic periodic paralysis masquerading as recurrent transient ischemic attacks. [PDF]

Clin Case Rep, 2022
Liang KMA, Liang BC.
europepmc   +1 more source

A Case of Hypokalemic Periodic Paralysis in a Young Athlete. [PDF]

Cureus, 2021
Abdelmasih R, Abdelmaseih R, Hasan M, Nasser H.   +3 more
europepmc   +1 more source