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Periodic paralysis
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19185183
retrieved
30 July 2017
review article
1 reference
stated in
Europe PubMed Central
title
Periodic paralysis.
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19185183
retrieved
30 July 2017
author name string
Bertrand Fontaine
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19185183
retrieved
30 July 2017
publication date
1 January 2008
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19185183
retrieved
30 July 2017
published in
Advances in Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19185183
retrieved
30 July 2017
volume
63
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19185183
retrieved
30 July 2017
page(s)
3-23
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19185183
retrieved
30 July 2017
cites work
MiRP2 forms potassium channels in skeletal muscle with Kv3.4 and is associated with periodic paralysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
In vivo and in vitro functional characterization of Andersen's syndrome mutations.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Progressive myopathy in hyperkalemic periodic paralysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
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inferred from DOI database lookup
Severe infantile hyperkalaemic periodic paralysis and paramyotonia congenita: broadening the clinical spectrum associated with the T704M mutation in SCN4A
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel sodium channel mutation in a family with hypokalemic periodic paralysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Myopathy in familial hypokalaemic periodic paralysis independent of paralytic attacks
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Severe prognosis in a large family with hypokalemic periodic paralysis.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Pathomechanisms in channelopathies of skeletal muscle and brain
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Functional expression of sodium channel mutations identified in families with periodic paralysis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Theoretical reconstruction of myotonia and paralysis caused by incomplete inactivation of sodium channels
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Gating defects of a novel Na+ channel mutant causing hypokalemic periodic paralysis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Normokalemic periodic paralysis revisited: does it exist?
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Impaired slow inactivation in mutant sodium channels
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Treatment of "permanent" muscle weakness in familial Hypokalemic Periodic Paralysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mutation in the KCNE3 potassium channel gene is associated with susceptibility to thyrotoxic hypokalemic periodic paralysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Calcium activation of electrically inexcitable muscle fibers in primary hypokalemic periodic paralysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hyperkalemic periodic paralysis: rapid molecular diagnosis and relationship of genotype to phenotype in 12 families
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hyperkalemic periodic paralysis and the adult muscle sodium channel alpha-subunit gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31-32 in three European families
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hypokalemic periodic paralysis: a model for a clinical and research approach to a rare disorder
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genotype-phenotype correlations of DHP receptor alpha 1-subunit gene mutations causing hypokalemic periodic paralysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Electromyography guides toward subgroups of mutations in muscle channelopathies.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Acetazolamide treatment of hypokalemic periodic paralysis. Prevention of attacks and improvement of persistent weakness
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Defective slow inactivation of sodium channels contributes to familial periodic paralysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The anesthetic myopathies and malignant hyperthermias.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Periodic paralysis mutation MiRP2-R83H in controls: Interpretations and general recommendation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genotype-phenotype correlation and therapeutic rationale in hyperkalemic periodic paralysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A calcium channel mutation causing hypokalemic periodic paralysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A family of hypokalemic periodic paralysis with CACNA1S gene mutation showing incomplete penetrance in women
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Paramyotonia congenita and hyperkalemic periodic paralysis associated with a Met 1592 Val substitution in the skeletal muscle sodium channel alpha subunit--a large kindred with a novel phenotype
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Phenotypic variation of a Thr704Met mutation in skeletal sodium channel gene in a family with paralysis periodica paramyotonica
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical review: Thyrotoxic periodic paralysis: a diagnostic challenge
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Exercise test in muscle channelopathies and other muscle disorders
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Electrophysiological properties of the hypokalaemic periodic paralysis mutation (R528H) of the skeletal muscle alpha 1s subunit as expressed in mouse L cells.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Are myotonias and periodic paralyses associated with susceptibility to malignant hyperthermia?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Muscle fiber conduction velocity in arg1239his mutation in hypokalemic periodic paralysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Improvement of muscle strength in familial hypokalaemic periodic paralysis with acetazolamide
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Permanent muscle weakness in familial hypokalaemic periodic paralysis. Clinical, radiological and pathological aspects.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial hypokalemic periodic paralysis. Clinical, diagnostic and therapeutic aspects
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Surface EMG and muscle fibre conduction during attacks of hypokalaemic periodic paralysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The exercise test in periodic paralysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Comparative efficacy of repetitive nerve stimulation, exercise, and cold in differentiating myotonic disorders
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Correlating phenotype and genotype in the periodic paralyses
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Malignant-hyperthermia susceptibility is associated with a mutation of the alpha 1-subunit of the human dihydropyridine-sensitive L-type voltage-dependent calcium-channel receptor in skeletal muscle
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Effects of mutations causing hypokalaemic periodic paralysis on the skeletal muscle L-type Ca2+ channel expressed in Xenopus laevis oocytes.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hyperkalemic periodic paralysis and paramyotonia congenita--a novel sodium channel mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Paramyotonia congenita: genotype to phenotype correlations in two families and report of a new mutation in the sodium channel gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a mutation in the gene causing hyperkalemic periodic paralysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Sodium channel mutations in paramyotonia congenita and hyperkalemic periodic paralysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dihydropyridine receptor mutations cause hypokalemic periodic paralysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Acetazolamide Prophylaxis in Hypokalemic Periodic Paralysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Adynamia episodica and paralysis periodica paramyotonica
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A Met-to-Val mutation in the skeletal muscle Na+ channel alpha-subunit in hyperkalaemic periodic paralysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hypokalemic periodic paralysis: In vitro investigation of muscle fiber membrane parameters
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Calcium-tension relationships of muscle fibers from patients with periodic paralysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Insulin acts in hypokalemic periodic paralysis by reducing inward rectifier K+ current
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Slow inactivation: slow but not dull
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of mutations in the CACNL1A3 gene in 13 families of Scandinavian origin having hypokalemic periodic paralysis and evidence of a founder effect in Danish families.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lack of association of the potassium channel–associated peptide MiRP2-R83H variant with periodic paralysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Temperature-sensitive sodium channelopathy with heat-induced myotonia and cold-induced paralysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
No mutation in the KCNE3 potassium channel gene in Chinese thyrotoxic hypokalaemic periodic paralysis patients.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Andersen's syndrome: potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Randomized trials of dichlorphenamide in the periodic paralyses. Working Group on Periodic Paralysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hypokalemic periodic paralysis exacerbated by acetazolamide
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Impairment of skeletal muscle adenosine triphosphate-sensitive K+ channels in patients with hypokalemic periodic paralysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Acetazolamide opens the muscular K Ca 2+ channel: A novel mechanism of action that may explain the therapeutic effect of the drug in hypokalemic periodic paralysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
SCN4A-associated hypokalemic periodic paralysis merits a trial of acetazolamide
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The primary periodic paralyses: diagnosis, pathogenesis and treatment
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel sodium channel mutation causing a hyperkalemic paralytic and paramyotonic syndrome with variable clinical expressivity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Muscle Na+ channelopathies: MRI detects intracellular 23Na accumulation during episodic weakness
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The muscle fiber conduction velocity and power spectra in familial hypokalemic periodic paralysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0065-2660%2808%2901001-8
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0065-2660(08)01001-8
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19185183
retrieved
30 July 2017
PubMed publication ID
19185183
1 reference
stated in
Europe PubMed Central
PubMed publication ID
19185183
retrieved
30 July 2017
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