Results 61 to 70 of about 51,565 (192)

A Case of Thyrotoxic Hypokalemia Periodic Paralysis

open access: yesMedicine Science, 2014
Hypokalemic periodic paralysis is a rare disease characterized by reversible attacks of muscle weakness accompanied by episodic hypokalemia. The most common causes of Hypokalemic periodic paralysis are familial periodic paralysis, thyrotoxic periodic ...
Mazhar Muslum Tuna   +8 more
doaj   +1 more source

Resistance Training in a Patient With Hypokalemic Periodic Paralysis and Permanent Weakness: A Case Report

open access: yes
Muscle &Nerve, Volume 74, Issue 1, Page 265-268, July 2026.
Jeppe Moesgaard Rasmussen   +5 more
wiley   +1 more source

“Hashitoxicosis” and possible acquired Gitelman syndrome: dual pathology leading to a catastrophic hypokalemic periodic paralysis

open access: yesAsian Journal of Internal Medicine
Thyrotoxic periodic paralysis (TPP) is more commonly seen in Graves’ disease. But TPP can occur in any condition leading to a hyperthyroid state. It’s important to identify the underlying aetiology of the thyrotoxic state as the management differs with ...
M. S. N. Padmasiri   +4 more
doaj   +1 more source

STIM1 Reduction Prevents Tubular Aggregate Formation and Compromises Muscle Performance in Ageing Mice

open access: yesJournal of Cachexia, Sarcopenia and Muscle, Volume 16, Issue 6, December 2025.
ABSTRACT Background Ageing is an irreversible process involving the gradual decline of cellular functions in all tissues. In male mice, age‐related loss of muscle force is accompanied by the formation of tubular aggregates, which are honeycomb‐like structures composed of membrane tubules, proteins and Ca2+ deposits. Tubular aggregates are also found in
Laura Pérez‐Guàrdia   +3 more
wiley   +1 more source

Thyrotoxic Periodic Paralysis with Hypokalemia in an Adult Male from Nepal: A Case Report

open access: yesJournal of Nepal Medical Association, 2019
Thyrotoxic periodic paralysis is rare complication of hyperthyroidism characterized by the sudden onset of hypokalemia and muscle paralysis. It is typically present in young Asian males.
Sabina Khadka   +4 more
doaj   +1 more source

Unmasking Idiopathic Inflammatory Myopathy: A Case of Proximal Weakness in a Young Male With Co‐Occurring Vitamin D Deficiency

open access: yesClinical Case Reports, Volume 13, Issue 11, November 2025.
ABSTRACT Idiopathic inflammatory myopathy (IIM) encompasses rare autoimmune disorders causing muscle inflammation and weakness, with subtypes including dermatomyositis, necrotizing myopathy, antisynthetase syndrome, and inclusion body myositis. This case report details a 25‐year‐old South Asian male presenting with a 60‐day history of progressive ...
Ibrahim Khalil   +3 more
wiley   +1 more source

Etiological Spectrum of patients with Hypokalemic Paralysis [PDF]

open access: yes
Objective:  To determine the etiological spectrum of patients with Hypokalemic paralysis. Materials & Methods:  A descriptive Cross-Sectional study was conducted in the Department of Neurology, Mayo Hospital Lahore.
Khawaja Muhammad Ali   +4 more
core   +1 more source

A Case of Hypokalemic Periodic Paralysis in a Young Athlete.

open access: yes, 2021
Hypokalemic periodic paralysis (HPP) is one of the group muscle disorders that can cause sudden onset paresis or paralysis. It is a quite rare, yet, potentially life-threatening condition that, if appropriately and promptly diagnosed and treated, can be ...
Nasser, Hesham   +3 more
core   +1 more source

Sjögren's Syndrome With Distal Renal Tubular Acidosis and Hypokalemic Myopathy in Pregnancy: A Rare Case

open access: yesClinical Case Reports, Volume 13, Issue 11, November 2025.
Case timeline. ABSTRACT Sjogren's syndrome may rarely present with distal renal tubular acidosis (dRTA), causing severe hypokalemia and myopathy. A 27‐year‐old primigravida at 15 weeks gestation presented with progressive proximal weakness and myalgia.
Nabiha Khan   +5 more
wiley   +1 more source

Voltage Sensors in Hypokalemic Periodic Paralysis

open access: yes, 2009
Researchers at the National Hospital, Queen Square, London, UK, conducted automated DNA sequencing of the S4 regions of CACNA1S and SCN4A in 83 patients with hypokalemic periodic paralysis (HypoPP)
J Gordon Millichap
core   +1 more source

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