Substitutions of the S4DIV R2 residue (R1451) in NaV1.4 lead to complex forms of paramyotonia congenita and periodic paralyses. [PDF]
Poulin H +9 more
europepmc +1 more source
A Detailed Clinical Approach to Non-dystrophic Myotonia: A Case Report of Two Brothers With Myotonia Congenita. [PDF]
Gilitwala Z, Satpute S, Patil S.
europepmc +1 more source
Anaesthesia for Paramyotonia Congenita: A Narrative Review. [PDF]
Chee M +3 more
europepmc +1 more source
Special electromyographic features in a child with paramyotonia congenita: A case report and review of literature. [PDF]
Yi H, Liu CX, Ye SX, Liu YL.
europepmc +1 more source
A patient with episodic ataxia and paramyotonia congenita due to mutations in KCNA1 and SCN4A. [PDF]
Rajakulendran S +8 more
europepmc +1 more source
Hyperkalemic Periodic Paralysis in Twenty-Two Family Members Over Four Generations: A Rare Case Report. [PDF]
Vivek A +5 more
europepmc +1 more source
Lifestyle and dietary measures in Periodic Paralyses. [PDF]
Politano L.
europepmc +1 more source
Propofol Reduces Succinylcholine-induced Muscle Rigidity in a Patient with Paramyotonia Congenita.
Elsharydah A, Kaminski AC.
europepmc +1 more source
Blockers of Skeletal Muscle Nav1.4 Channels: From Therapy of Myotonic Syndrome to Molecular Determinants of Pharmacological Action and Back. [PDF]
De Bellis M +4 more
europepmc +1 more source

