(Q41104687)

26 September 2017

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title

Channelopathies: the nondystrophic myotonias and periodic paralyses (English)

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26 September 2017

Lehmann-Horn F

1

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26 September 2017

Rüdel R

series ordinal

2

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26 September 2017

publication date

1 June 1996

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Seminars in pediatric neurology

26 September 2017

published in

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26 September 2017

volume

3

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26 September 2017

issue

2

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26 September 2017

page(s)

122-139

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Myotonia induced by chemical agents

26 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Tonische Krämpfe in willkürlich beweglichen Muskeln in Folge von ererbter psychischer Disposition

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

The skeletal muscle chloride channel in dominant and recessive human myotonia

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

AAEE minimonograph #27: differential diagnosis of myotonic syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Muscle pathology of myotonia congenita

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Distinguishing paramyotonia congenita and myotonia congenita by electromyography

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Cable properties of external intercostal muscle fibres from myotonic and nonmyotonic goats

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Multimeric structure of ClC-1 chloride channel revealed by mutations in dominant myotonia congenita (Thomsen)

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Genomic organization of the human muscle chloride channel CIC-1 and analysis of novel mutations leading to Becker-type myotonia.

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

An aspartic acid residue important for voltage-dependent gating of human muscle chloride channels

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Clinical and electrophysiological observations in patients with myotonic muscle disease and the therapeutic effect of N-propyl-ajmalin

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Paramyotonia congenita or hyperkalemic periodic paralysis? Clinical and electrophysiological features of each entity in one family

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Exercise-induced membrane failure in paramyotonia congenita

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Muscle stiffness and electrical activity in paramyotonia congenita

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Genotype-phenotype correlations in human skeletal muscle sodium channel diseases

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Hyperkalemic periodic paralysis and the adult muscle sodium channel alpha-subunit gene

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Paramyotonia congenita and hyperkalemic periodic paralysis are linked to the adult muscle sodium channel gene

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17.

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Primary structure of the adult human skeletal muscle voltage‐dependent sodium channel

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Genomic organization of the human skeletal muscle sodium channel gene

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Destruction of sodium conductance inactivation in squid axons perfused with pronase

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Mutations in an S4 segment of the adult skeletal muscle sodium channel cause paramyotonia congenita

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Temperature-sensitive mutations in the III–IV cytoplasmic loop region of the skeletal muscle sodium channel gene in paramyotonia congenita

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Human sodium channel myotonia: slowed channel inactivation due to substitutions for a glycine within the III-IV linker

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Successuful treatment of paramyotonia congenita (Eulenburg): muscle stiffness and weakness prevented by tocainide

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Paramyotonia congenita: successful treatment with tocainide. Clinical and electrophysiologic findings in seven patients.

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Adynamia episodica and paralysis periodica paramyotonica

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

A novel SCN4A mutation causing myotonia aggravated by cold and potassium

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Sodium channel mutations in acetazolamide-responsive myotonia congenita, paramyotonia congenita, and hyperkalemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

1 reference

7 January 2021

Myotonia fluctuans. A third type of muscle sodium channel disease

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

1 reference

7 January 2021

Acetazolamide-responsive myotonia congenita.

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Linkage of atypical myotonia congenita to a sodium channel locus

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Schwartz-Jampel syndrome: I. Clinical, electromyographic, and histologic studies

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Masseter muscle rigidity associated with glycine1306-to-alanine mutation in the adult muscle sodium channel alpha-subunit gene.

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Studies in disorders of muscle. VII. Clinical manifestations and inheritance of a type of periodic paralysis without hypopotassemia

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Novel mutations in families with unusual and variable disorders of the skeletal muscle sodium channel

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

HYPERKALEMIC PERIODIC PARALYSIS WITH HYPOCALCEMIC EPISODE. ABSENCE OF AN AUTOSOMAL DOMINANT PEDIGREE PATTERN

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Hyperkalemic periodic paralysis: an apparent sporadic case

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

A Met-to-Val mutation in the skeletal muscle Na+ channel alpha-subunit in hyperkalaemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Progressive myopathy in hyperkalemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Identification of a mutation in the gene causing hyperkalemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Non-dystrophic myotonias and periodic paralyses

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Adynamia episodica hereditaria: what causes the weakness?

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

A third type of periodic paralysis, with normokalemia and favourable response to sodium chloride

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

The exercise test in periodic paralysis

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Exercise and rest in hyperkalemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Membrane defects in paramyotonia congenita (Eulenburg)

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Altered gating and conductance of Na+ channels in hyperkalemic periodic paralysis.

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Adynamia episodica hereditaria with myotonia: a non-inactivating sodium current and the effect of extracellular pH

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

A sodium channel defect in hyperkalemic periodic paralysis: potassium-induced failure of inactivation

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Regulation of active Na+-K+ transport in skeletal muscle

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Hyperkalemic periodic paralysis with cardiac dysrhythmia: a novel sodium channel mutation?

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Acetazolamide treatment of hypokalemic periodic paralysis. Prevention of attacks and improvement of persistent weakness

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Treatment of attacks in hyperkalaemic familial periodic paralysis by inhalation of salbutamol

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Mapping of the hypokalaemic periodic paralysis (HypoPP) locus to chromosome 1q31-32 in three European families

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Genetic heterogeneity in hypokalemic periodic paralysis (hypoPP)

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Potential role of acute hypophosphatemia during hypokalemic periodic paralysis attack

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Permanent muscle weakness in familial hypokalaemic periodic paralysis. Clinical, radiological and pathological aspects.

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Familial hypokalemic periodic paralysis with permanent myopathy. A clinical and ultrastructural study

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

A new standardized and effective method of inducing paralysis without administration of exogenous hormone in patients with familial periodic paralysis

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Movement of potassium into skeletal muscle during spontaneous attack in family periodic paralysis

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

The effect of insulin on the transport of sodium and potassium in rat soleus muscle.

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Combined effects of adrenaline and insulin on active electrogenic Na+–K+ transport in rat soleus muscle

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Insulin-mediated hypokalemia and paralysis in familial hypokalemic periodic paralysis.

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

The relationship of insulin receptors to hypokalemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Sodium-potassium adenosine triphosphate n diseased muscle. Studies on periodic paralysis, myasthenia gravis, and Eaton-Lambert syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Potassium movement in patients with familial periodic paralysis: relationship to the defect in muscle function

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Membrane potentials of a single skeletal muscle cell in hypokalemic periodic muscle paralysis

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Hypokalemic periodic paralysis: In vitro investigation of muscle fiber membrane parameters

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Calcium activation of electrically inexcitable muscle fibers in primary hypokalemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Cromakalim (BRL 34915) restores in vitro the membrane potential of depolarized human skeletal muscle fibres

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Enhancement of K+ conductance improves in vitro the contraction force of skeletal muscle in hypokalemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

METABOLIC MYOPATHIES. THE GLYCOGENOSES AFFECTING MUSCLE, AND HYPO- AND HYPERKALEMIC PERIODIC PARALYSIS.

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Hypokalemic periodic paralysis exacerbated by acetazolamide

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Hypokalemic periodic paralysis with unusual responses to acetazolamide and sympathomimetics

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Acetazolamide Prophylaxis in Hypokalemic Periodic Paralysis

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Treatment of "permanent" muscle weakness in familial Hypokalemic Periodic Paralysis

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Assignment of the human gene for the alpha 1 subunit of the skeletal muscle DHP-sensitive Ca2+ channel (CACNL1A3) to chromosome 1q31-q32

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

The gene coding for the alpha 1 subunit of the skeletal dihydropyridine receptor (Cchl1a3 = mdg) maps to mouse chromosome 1 and human 1q32

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Structure and function of voltage-sensitive ion channels

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Voltage sensor of excitation-contraction coupling in skeletal muscle

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

A calcium channel mutation causing hypokalemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Dihydropyridine receptor mutations cause hypokalemic periodic paralysis

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Sodium channel mutations in paramyotonia congenita uncouple inactivation from activation

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

Skeletal muscle DHP receptor mutations alter calcium currents in human hypokalaemic periodic paralysis myotubes

1 reference

https://api.crossref.org/works/10.1016%2FS1071-9091%2896%2980041-6

7 January 2021

10.1016/S1071-9091(96)80041-6

Identifiers

DOI

1 reference

26 September 2017

1 reference