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An emerging spectrum of variants and clinical features in KCNMA1-linked channelopathy
Channels, 2021Hans J Moldenhauer +2 more
exaly
Pediatric neuromuscular channelopathies
Pediatric skeletal muscle channelopathies include a spectrum of conditions including nondystrophic myotonias and periodic paralyses. They are rare inherited conditions that can cause significant morbidity. They are characterized by episodic stiffness and weakness. While there is significant phenotypic variability, there are distinct diagnostic features.Vinojini, Vivekanandam +2 more
openaire +2 more sources
Brugada Syndrome: More than a Monogenic Channelopathy
Biomedicines, 2023Antonella Liantonio +2 more
exaly
“Status myotonicus” in Nav1.4-M1592V channelopathy
Neuromuscular Disorders, 2020Sub H Subramony
exaly
Monitoring a Hypothetical Channelopathy in Chronic Fatigue Syndrome
The Journal of Chronic Fatigue Syndrome: Multidisciplinary Innovations in Researchory and Clinical Practice, 2003Jo Nijs
exaly