Results 61 to 70 of about 489,393 (127)

Skeletal muscle: molecular structure, myogenesis, biological functions, and diseases

open access: yesMedComm, Volume 5, Issue 7, July 2024.
The article systematically and comprehensively reviews the physiological and pathological processes associated with skeletal muscles from five perspectives: molecule basis, myogenesis, biological function, poststimulation response, and myopathy. We primarily focus on nuclei‐related behaviors of skeletal muscle, cell–cell fusion, and nuclei migration in
Lan‐Ting Feng   +2 more
wiley   +1 more source

Peripheral nervous system and neuromuscular disorders in the emergency department: A review

open access: yesAcademic Emergency Medicine, Volume 31, Issue 4, Page 386-397, April 2024.
Abstract Introduction Acute presentations and emergencies in neuromuscular disorders (NMDs) often challenge clinical acumen. The objective of this review is to refine the reader's approach to history taking, clinical localization and early diagnosis, as well as emergency management of neuromuscular emergencies.
Ajith Sivadasan   +3 more
wiley   +1 more source

Hyperkalemic periodic paralysis (adynamia episodica hereditaria)

open access: yes, 1974
Bu yazıda hipokalemik periyodik paralizinin: klinik ve laboratuar görünümü,tanı ve ayırıcı tanı,tedavi prensipleri ve ilgili literatür gözden geçirildi.In this article, the clinical and laboratory aspects , diagnosis and differential diagnosis, treatment

core  

Altered slow inactivation in sodium channels containing the equine hyperkalemic periodic paralysis mutation

open access: yes, 2002
This thesis examines slow inactivation in human skeletal muscle voltage-gated sodium channels containing the equine hyperkalemic periodic paralysis (HyperPP) mutation.
Ellis, Lee David
core   +1 more source

Allele frequency of hyperkalemic periodic paralysis (HYPP) in quarter horses from Mexico [PDF]

open access: yes, 2015
Hyperkalemic periodic paralysis (HYPP) is an autosomal co-dominant genetic disease of Quarter-mile horses which originated by a point mutation of the gene coding the sodium channel protein in the plasmatic membrane of muscular cells. The mutation affects
Riojas-Valdes, V
core   +1 more source

Clinical, electromyographic, and biophysical characterization of the rare Nav1.4 channel mutation SCN4A L1436P

open access: yesFrontiers in Physiology
IntroductionOur aims were to provide an integrated clinical and biophysical characterization of the rare variant NM_000334.4(SCN4A) c.4307T>C (p.Leu1436Pro; L1436P), affecting the skeletal muscle sodium channel Nav1.4, and to compare its functional ...
François Charles Wang   +10 more
doaj   +1 more source

Andersen's syndrome : a distinct periodic paralysis [PDF]

open access: yes, 1997
A previous study of 4 patients defined Andersen's syndrome (AS) as a triad of potassium-sensitive periodic paralysis, ventricular dysrhythmias, and dysmorphic features.
S. Iannaccone   +11 more
core   +1 more source

Genetic analysis of 37 cases with primary periodic paralysis in Chinese patients

open access: yesOrphanet Journal of Rare Diseases
Background Primary periodic paralysis (PPP) is an inherited disorders of ion channel dysfunction characterized by recurrent episodes of flaccid muscle weakness, which can classified as hypokalemic (HypoPP), normokalemic (NormoPP), or hyperkalemic ...
Xuechao Zhao   +7 more
doaj   +1 more source

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