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About 121 results

ALLMedicine™ Periodic Paralyses Center

Research & Reviews  59 results

Next-generation sequencing application to investigate skeletal muscle channelopathies i...
https://doi.org/10.1016/j.nmd.2020.12.003
Neuromuscular Disorders : NMD; Brugnoni R, Maggi L et. al.

Feb 12th, 2021 - Non-dystrophic myotonias and periodic paralyses are a heterogeneous group of disabling diseases classified as skeletal muscle channelopathies. Their genetic characterization is essential for prognostic and therapeutic purposes; however, several ge...

Familial periodic paralysis associated with a rare KCNJ5 variant that supposed to have ...
https://doi.org/10.1016/j.braindev.2020.10.010
Brain & Development; Hiraide T, Fukumura S et. al.

Nov 17th, 2020 - The periodic paralyses are a group of skeletal muscle channelopathies caused by variants in several ion channel genes. Potassium Inwardly Rectifying Channel Subfamily J Member 5 (KCNJ5) encodes the G-protein-activated inwardly rectifying potassium...

Prolonged Exercise Test in Patients With History of Thyrotoxicosis.
https://doi.org/10.1097/WNP.0000000000000766
Journal of Clinical Neurophysiology : Official Publicatio... Tan HT, Tan CY et. al.

Aug 10th, 2020 - Thyrotoxic periodic paralysis is characterized by recurrent episodes of reversible, severe proximal muscle weakness associated with hypokalemia and hyperthyroidism. Prolonged exercise test is an easy, noninvasive method of demonstrating abnormal m...

Skeletal Muscle Channelopathies.
https://doi.org/10.1016/j.ncl.2020.04.003
Neurologic Clinics; Vivekanandam V, Munot P et. al.

Jul 24th, 2020 - Skeletal muscle channelopathies are rare genetic neuromuscular conditions that include the nondystrophic myotonias and periodic paralyses. They cause disabling muscle symptoms and can limit educational potential, work opportunities, socialization,...

A new clinical entity in T704M mutation in periodic paralysis.
https://doi.org/10.1016/j.jocn.2020.04.061
Journal of Clinical Neuroscience : Official Journal of Th... Gun Bilgic D, Aydin Gumus A et. al.

Apr 27th, 2020 - Periodic paralyses (PPs) are a group of rare disorders characterized by episodic, sudden-onset, flaccid paralysis of skeletal muscles usually resulting in complete recovery after the attacks. PPs are caused by abnormal, mostly potassium-sensitive ...

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Clinicaltrials.gov  61 results

Next-generation sequencing application to investigate skeletal muscle channelopathies i...
https://doi.org/10.1016/j.nmd.2020.12.003
Neuromuscular Disorders : NMD; Brugnoni R, Maggi L et. al.

Feb 12th, 2021 - Non-dystrophic myotonias and periodic paralyses are a heterogeneous group of disabling diseases classified as skeletal muscle channelopathies. Their genetic characterization is essential for prognostic and therapeutic purposes; however, several ge...

Familial periodic paralysis associated with a rare KCNJ5 variant that supposed to have ...
https://doi.org/10.1016/j.braindev.2020.10.010
Brain & Development; Hiraide T, Fukumura S et. al.

Nov 17th, 2020 - The periodic paralyses are a group of skeletal muscle channelopathies caused by variants in several ion channel genes. Potassium Inwardly Rectifying Channel Subfamily J Member 5 (KCNJ5) encodes the G-protein-activated inwardly rectifying potassium...

Prolonged Exercise Test in Patients With History of Thyrotoxicosis.
https://doi.org/10.1097/WNP.0000000000000766
Journal of Clinical Neurophysiology : Official Publicatio... Tan HT, Tan CY et. al.

Aug 10th, 2020 - Thyrotoxic periodic paralysis is characterized by recurrent episodes of reversible, severe proximal muscle weakness associated with hypokalemia and hyperthyroidism. Prolonged exercise test is an easy, noninvasive method of demonstrating abnormal m...

Skeletal Muscle Channelopathies.
https://doi.org/10.1016/j.ncl.2020.04.003
Neurologic Clinics; Vivekanandam V, Munot P et. al.

Jul 24th, 2020 - Skeletal muscle channelopathies are rare genetic neuromuscular conditions that include the nondystrophic myotonias and periodic paralyses. They cause disabling muscle symptoms and can limit educational potential, work opportunities, socialization,...

A new clinical entity in T704M mutation in periodic paralysis.
https://doi.org/10.1016/j.jocn.2020.04.061
Journal of Clinical Neuroscience : Official Journal of Th... Gun Bilgic D, Aydin Gumus A et. al.

Apr 27th, 2020 - Periodic paralyses (PPs) are a group of rare disorders characterized by episodic, sudden-onset, flaccid paralysis of skeletal muscles usually resulting in complete recovery after the attacks. PPs are caused by abnormal, mostly potassium-sensitive ...

see more →

News  1 results

Periodic Paralysis: Shedding Light on a Rare Neurologic Disorder
https://www.medscape.com/viewarticle/903922

Oct 28th, 2018 - Like many rare disorders, periodic paralysis can go undiagnosed and be easily misinterpreted as a wide variety of neurologic or other disorders. But with increased awareness of the unique symptoms of this disorder and how to manage them, patients ...

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