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Year Number of Results
1963 1
1988 1
1991 1
1993 5
1994 1
1995 1
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1997 7
1999 5
2000 3
2001 8
2002 4
2004 2
2007 4
2008 6
2010 2
2012 3
2013 2
2014 1
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65 results

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Page 1
Review of the Diagnosis and Treatment of Periodic Paralysis.
Statland JM, Fontaine B, Hanna MG, Johnson NE, Kissel JT, Sansone VA, Shieh PB, Tawil RN, Trivedi J, Cannon SC, Griggs RC. Statland JM, et al. Muscle Nerve. 2018 Apr;57(4):522-530. doi: 10.1002/mus.26009. Epub 2017 Nov 29. Muscle Nerve. 2018. PMID: 29125635 Free PMC article. Review.
Periodic paralyses (PPs) are rare neuromuscular disorders caused by mutations in skeletal muscle sodium, calcium, and potassium channel genes. PPs include hypokalemic paralysis, hyperkalemic paralysis, and Andersen-Tawil syndrome. Common features of PP
Periodic paralyses (PPs) are rare neuromuscular disorders caused by mutations in skeletal muscle sodium, calcium, and potassium chann
Muscle channelopathies.
Vivekanandam V, Jayaseelan D, Hanna MG. Vivekanandam V, et al. Handb Clin Neurol. 2023;195:521-532. doi: 10.1016/B978-0-323-98818-6.00006-6. Handb Clin Neurol. 2023. PMID: 37562884 Review.
The myotonic conditions, characterized predominantly by stiffness, include myotonia congenita, paramyotonia congenita, and sodium channel myotonia. The periodic paralysis conditions include hypokalemic periodic paralysis, hyperkalemic periodi
The myotonic conditions, characterized predominantly by stiffness, include myotonia congenita, paramyotonia congenita, and sodium channel my …
Periodic paralysis.
Fialho D, Griggs RC, Matthews E. Fialho D, et al. Handb Clin Neurol. 2018;148:505-520. doi: 10.1016/B978-0-444-64076-5.00032-6. Handb Clin Neurol. 2018. PMID: 29478596 Review.
The periodic paralyses are a group of skeletal muscle channelopathies characterizeed by intermittent attacks of muscle weakness often associated with altered serum potassium levels. ...
The periodic paralyses are a group of skeletal muscle channelopathies characterizeed by intermittent attacks of muscle weakness often …
Episodic Muscle Disorders.
Sansone VA. Sansone VA. Continuum (Minneap Minn). 2019 Dec;25(6):1696-1711. doi: 10.1212/CON.0000000000000802. Continuum (Minneap Minn). 2019. PMID: 31794467 Review.
PURPOSE OF REVIEW: This article reviews the episodic muscle disorders, including benign cramp-fasciculation syndrome, the periodic paralyses, and the nondystrophic myotonias. The core diagnostic criteria for a diagnosis of primary periodic paralysis, includin …
PURPOSE OF REVIEW: This article reviews the episodic muscle disorders, including benign cramp-fasciculation syndrome, the periodic pa …
Periodic paralysis.
Fontaine B. Fontaine B. Adv Genet. 2008;63:3-23. doi: 10.1016/S0065-2660(08)01001-8. Adv Genet. 2008. PMID: 19185183 Review.
It is thus usual to differentiate hypokalemic, normokalemic, and hyperkalemic periodic paralysis. Except for thyrotoxic hypokalemic periodic paralysis and periodic paralyses secondary to permanent changes of blood potassium levels, all of …
It is thus usual to differentiate hypokalemic, normokalemic, and hyperkalemic periodic paralysis. Except for thyrotoxic …
Sodium Channelopathies of Skeletal Muscle.
Cannon SC. Cannon SC. Handb Exp Pharmacol. 2018;246:309-330. doi: 10.1007/164_2017_52. Handb Exp Pharmacol. 2018. PMID: 28939973 Free PMC article. Review.
Consequently, mutations of SCN4A encoding Na(V)1.4 produce pure skeletal muscle phenotypes that now include six allelic disorders: sodium channel myotonia, paramyotonia congenita, hyperkalemic periodic paralysis, hypokalemic periodic paralysis, …
Consequently, mutations of SCN4A encoding Na(V)1.4 produce pure skeletal muscle phenotypes that now include six allelic disorders: sodium ch …
Endocrine myopathies.
Ruff RL, Weissmann J. Ruff RL, et al. Neurol Clin. 1988 Aug;6(3):575-92. Neurol Clin. 1988. PMID: 3065602 Review.
Adrenal insufficiency produces generalized weakness, muscle cramping, and fatigue in 50 per cent of patients. Some patients also develop hyperkalemic paralysis. The treatment is hormone replacement. Thyrotoxicosis produces myopathy caused by net protein catabolism, …
Adrenal insufficiency produces generalized weakness, muscle cramping, and fatigue in 50 per cent of patients. Some patients also develop …
Genotype-phenotype correlation and therapeutic rationale in hyperkalemic periodic paralysis.
Jurkat-Rott K, Lehmann-Horn F. Jurkat-Rott K, et al. Neurotherapeutics. 2007 Apr;4(2):216-24. doi: 10.1016/j.nurt.2007.02.001. Neurotherapeutics. 2007. PMID: 17395131 Free article. Review.
Familial hyperkalemic periodic paralysis (PP) is a dominantly inherited muscle disease characterized by attacks of flaccid weakness and intermittent myotonia. ...In this review, the functional and clinical consequences of the mutations and therapeutic strateg …
Familial hyperkalemic periodic paralysis (PP) is a dominantly inherited muscle disease characterized by attacks of flac …
Muscle channelopathies.
Saperstein DS. Saperstein DS. Semin Neurol. 2008 Apr;28(2):260-9. doi: 10.1055/s-2008-1062262. Semin Neurol. 2008. PMID: 18351527 Review.
Myopathic channelopathies include two main groups: nondystrophic myotonias and periodic paralyses. This article reviews the clinical features, diagnostic approach, molecular causes, and management of patients with nondystrophic myotonias and periodic paralyses....
Myopathic channelopathies include two main groups: nondystrophic myotonias and periodic paralyses. This article reviews the clinical …
The nondystrophic myotonias.
Heatwole CR, Moxley RT 3rd. Heatwole CR, et al. Neurotherapeutics. 2007 Apr;4(2):238-51. doi: 10.1016/j.nurt.2007.01.012. Neurotherapeutics. 2007. PMID: 17395134 Free article. Review.
These diseases are divided into those with chloride channel dysfunction (the myotonia congenita disorders) and those with sodium channel dysfunction (paramyotonia congenita, potassium-aggravated myotonia, and hyperkalemic periodic paralysis with myotonia). Th …
These diseases are divided into those with chloride channel dysfunction (the myotonia congenita disorders) and those with sodium channel dys …
65 results