Results 91 to 100 of about 1,313 (165)

Special electromyographic features in a child with paramyotonia congenita: A case report and review of literature. [PDF]

World J Clin Cases
Yi H, Liu CX, Ye SX, Liu YL.
europepmc   +1 more source

Hyperkalemic Periodic Paralysis in Twenty-Two Family Members Over Four Generations: A Rare Case Report. [PDF]

Ann Indian Acad Neurol, 2023
Vivek A, Sengar P, Chaurasia RN, Pathak A, Kumar A, Singh VK.   +5 more
europepmc   +1 more source

A patient with episodic ataxia and paramyotonia congenita due to mutations in KCNA1 and SCN4A. [PDF]

Neurology, 2009
Rajakulendran S, Tan SV, Matthews E, Tomlinson SE, Labrum R, Sud R, Kullmann DM, Schorge S, Hanna MG.   +8 more
europepmc   +1 more source

Propofol Reduces Succinylcholine-induced Muscle Rigidity in a Patient with Paramyotonia Congenita.

Anesth Essays Res, 2017
Elsharydah A, Kaminski AC.
europepmc   +1 more source

Blockers of Skeletal Muscle Na_v1.4 Channels: From Therapy of Myotonic Syndrome to Molecular Determinants of Pharmacological Action and Back. [PDF]

Int J Mol Sci, 2023
De Bellis M, Boccanegra B, Cerchiara AG, Imbrici P, De Luca A.   +4 more
europepmc   +1 more source

[Paramyotonia congenita].

Vojnosanitetski pregled, 1996
D, Marić, V, Ivanisević, S, Petković, V, Martić   +3 more
openaire   +1 more source

Albert Eulenburg (1840-1917). [PDF]

J Neurol
Owecki MK.
europepmc   +1 more source

Myoedema: a forgotten sign in acute colchicine myopathy. [PDF]

BMJ Case Rep, 2023
Le Tri S, Nguyen Vinh K, Dang TQ, Umapathi T.   +3 more
europepmc   +1 more source

Molekularbiologie in der Neurologie [PDF]

, 1994
Borasio, Gian Domenico, Brandt, T., Gasser, T.   +2 more
core  

Skeletal Muscle Channelopathies [PDF]

, 2020
Hanna, M, Matthews, E, Munot, P, Vivekanandam, V   +3 more
core