Results 31 to 40 of about 40,314 (299)

Hypokalemic periodic paralysis

open access: yesNational Journal of Maxillofacial Surgery, 2012
Hypokalemic periodic paralysis is a rare genetic disorder characterized by recurrent attacks of skeletal muscle weakness with associated hypokalemia which is precipitated by stress, cold, carbohydrate load, infection, glucose infusion, hypothermia, metabolic alkalosis, anesthesia, and steroids.
Abbas, Haider   +2 more
openaire   +3 more sources

DECREMENTAL RESPONSE ON PROLONGED EXERCISE TEST IN A PATIENT WITH THYROTOXIC PERIODIC PARALYSIS

open access: yesMalang Neurology Journal, 2022
Paralysis of acute onset often presents a diagnostic challenge for the assessing physician because of a large number of differential diagnosis and overlap of clinical features among them.
Piyush Ostwal, Maher Alshaheen
doaj   +1 more source

Episodic neurologic disorders: syndromes, genes, and mechanisms. [PDF]

open access: yes, 2013
Many neurologic diseases cause discrete episodic impairment in contrast with progressive deterioration. The symptoms of these episodic disorders exhibit striking variety.
Fu, Ying-Hui   +2 more
core   +2 more sources

Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis [PDF]

open access: yes, 2014
Mutations in the skeletal muscle channel (SCN4A), encoding the Nav1.4 voltage-gated sodium channel, are causative of a variety of muscle channelopathies, including non-dystrophic myotonias and periodic paralysis. The effects of many of these mutations on
Acevedo-Arozena, Abraham   +28 more
core   +2 more sources

Thyrotoxic Periodic Paralysis [PDF]

open access: yesBaylor University Medical Center Proceedings, 2006
Thyrotoxic periodic paralysis (TPP), a disorder most commonly seen in Asian men, is characterized by abrupt onset of hypokalemia and paralysis.
Lien, Lam   +2 more
openaire   +2 more sources

Hypokalemic Periodic Paralysis Precipitated by Thyrotoxicosis and Renal Tubular Acidosis

open access: yesCase Reports in Endocrinology, 2021
Background. Hypokalemic periodic paralysis is a rare neuromuscular disorder characterized by transient episodes of flaccid paralysis due to a defect in muscle ion channels. Most cases are hereditary, but it can be acquired.
Ian Jackson   +9 more
doaj   +1 more source

Histopathological analysis and in situ localisation of Australian tiger snake venom in two clinically envenomed domestic animals [PDF]

open access: yes, 2011
Objective: To assess histopathological changes in clinically envenomed tiger snake patients and identify tissue specific localisation of venom toxins using immunohistochemistry.
Balmer, L.   +5 more
core   +2 more sources

CACNA1S Arg528Cys mutation in a young Chinese man with thyrotoxic hypokalemic periodic paralysis

open access: yesClinical Case Reports, 2020
It has long been believed that the patients with thyrotoxic hypokalemic periodic paralysis (THPP) may harbor genetic mutations commonly found in familial hypokalemic periodic paralysis.
Nader Rezkalla   +5 more
doaj   +1 more source

Thyrotoxic Hypokalemic Periodic Paralysis: A Case Report

open access: yesTurkish Journal of Internal Medicine, 2022
Thyrotoxic hypokalemic periodic paralysis is a rare and fatal complication of hyperthyroidism and is associated with low serum potassium levels and muscle weakness. Herein, we presented a young male patient who did not use the antithyroid drugs given for
Şeyma Esenbuğa   +2 more
doaj   +1 more source

New Aspects of Thromboangiitis obliterans (von Winiwarter-Buerger's Disease) [PDF]

open access: yes, 1984
The existence of thromboangiitis obliterans as a clinical entity has been a matter of debate for many years. In contrast to other immunovasculitides there is no organ involvement while peripheral vessels are affected.
Berlit, Peter   +3 more
core   +1 more source

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