(Q34566685)

3 August 2017

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title

Periodic paralysis: understanding channelopathies (English)

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3 August 2017

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2

Karin Jurkat-Rott

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author name string

Frank Lehmann-Horn

series ordinal

1

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3 August 2017

Reinhardt Rüdel

series ordinal

3

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3 August 2017

publication date

1 January 2002

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Current Neurology and Neuroscience Reports

3 August 2017

published in

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3 August 2017

volume

2

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3 August 2017

issue

1

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3 August 2017

page(s)

61-69

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https://scigraph.springernature.com/pub.10.1007/s11910-002-0055-9

3 August 2017

exact match

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cites work

Identification of a mutation in the gene causing hyperkalemic periodic paralysis

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11910-002-0055-9

A novel sodium channel mutation causing a hyperkalemic paralytic and paramyotonic syndrome with variable clinical expressivity

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS11910-002-0055-9

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

21 January 2018

1 reference

12 December 2020

A novel sodium channel mutation in a family with hypokalemic periodic paralysis

1 reference

12 December 2020

Defective slow inactivation of sodium channels contributes to familial periodic paralysis

1 reference

12 December 2020

Structural parts involved in activation and inactivation of the sodium channel

1 reference

12 December 2020

The role of K+ channels in the force recovery elicited by Na+-K+ pump stimulation in Ba2+-paralysed rat skeletal muscle

1 reference

12 December 2020

Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current

1 reference

12 December 2020

Andersen's syndrome: potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features

1 reference

12 December 2020

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

1 reference

12 December 2020

Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome

1 reference

12 December 2020

Sodium channel inactivation defects are associated with acetazolamide-exacerbated hypokalemic periodic paralysis

1 reference

12 December 2020

Atomic scale movement of the voltage-sensing region in a potassium channel measured via spectroscopy

1 reference

12 December 2020

Voltage-gated ion channels and hereditary disease

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Surface EMG and muscle fibre conduction during attacks of hypokalaemic periodic paralysis

1 reference

12 December 2020

A peptide segment critical for sodium channel inactivation functions as an inactivation gate in a potassium channel

1 reference

12 December 2020

Molecular basis of charge movement in voltage-gated sodium channels

1 reference

12 December 2020

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

1 reference

12 December 2020

Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A.

1 reference

12 December 2020

Effects of mutations causing hypokalaemic periodic paralysis on the skeletal muscle L-type Ca2+ channel expressed in Xenopus laevis oocytes.

1 reference

12 December 2020

Electrophysiological properties of the hypokalaemic periodic paralysis mutation (R528H) of the skeletal muscle alpha 1s subunit as expressed in mouse L cells.

1 reference

12 December 2020

Calcium currents and transients of native and heterologously expressed mutant skeletal muscle DHP receptor alpha1 subunits (R528H)

1 reference

12 December 2020

A novel syndrome of episodic muscle weakness maps to xp22.3.

1 reference

12 December 2020

MiRP2 forms potassium channels in skeletal muscle with Kv3.4 and is associated with periodic paralysis

1 reference

12 December 2020

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

1 reference

12 December 2020

Activation and inactivation of the voltage-gated sodium channel: role of segment S5 revealed by a novel hyperkalaemic periodic paralysis mutation.

1 reference

12 December 2020

A double mutation in families with periodic paralysis defines new aspects of sodium channel slow inactivation

1 reference

12 December 2020

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

12 December 2020

Defective slow inactivation of sodium channels contributes to familial periodic paralysis

1 reference

12 December 2020

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

1 reference

12 December 2020

Expression and functional characterization of the cardiac L-type calcium channel carrying a skeletal muscle DHP-receptor mutation causing hypokalaemic periodic paralysis

1 reference

12 December 2020

Functional expression of sodium channel mutations identified in families with periodic paralysis

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12 December 2020

Insulin acts in hypokalemic periodic paralysis by reducing inward rectifier K+ current

1 reference

12 December 2020

The human skeletal muscle Na channel mutation R669H associated with hypokalemic periodic paralysis enhances slow inactivation.

1 reference

12 December 2020

Gating of the L-type Ca channel in human skeletal myotubes: an activation defect caused by the hypokalemic periodic paralysis mutation R528H

1 reference

12 December 2020

Dihydropyridine receptor mutations cause hypokalemic periodic paralysis

1 reference

12 December 2020

Impairment of skeletal muscle adenosine triphosphate-sensitive K+ channels in patients with hypokalemic periodic paralysis

1 reference

12 December 2020

Andersen's syndrome: A distinct periodic paralysis

1 reference

12 December 2020

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

1 reference

12 December 2020

A calcium channel mutation causing hypokalemic periodic paralysis

1 reference

12 December 2020

10.1007/S11910-002-0055-9

Identifiers

DOI

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Dimensions Publication ID

3 August 2017

1011248951

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1 reference