Results 251 to 260 of about 281,357 (305)

AGRN‐, LRP4‐, MUSK‐Related CMS: Clinical, Neurophysiological, Morphological, Genetic and Pathological Mechanisms

open access: yesMuscle &Nerve, EarlyView.
ABSTRACT Congenital myasthenic syndromes (CMS) are inherited disorders caused by mutations in genes encoding proteins essential for neuromuscular junction (NMJ) function. Pathogenic variants have been identified in more than 35 genes, underscoring the complexity of synaptic biology and the wide range of mechanisms that can compromise neuromuscular ...
Rocio‐Nur Villar‐Quiles   +5 more
wiley   +1 more source

Hypokalemic Periodic Paralysis Syndrome. [PDF]

open access: yesCureus
Govil D, Desai S, Singh K, Soueidan A.
europepmc   +1 more source

An evaluation of various parts of face to identify facial paralysis using temporal convolutional neural network model. [PDF]

open access: yesSci Rep
Alshammri GH   +7 more
europepmc   +1 more source

Pontine Hemorrhage Mimicking Bell's Palsy: Isolated Facial Nerve Palsy-A Case Report. [PDF]

open access: yesCase Rep Neurol Med
Takeichi R   +4 more
europepmc   +1 more source

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