Periodic paralysis in quarter horses: a sodium channel mutation disseminated by selective breeding.

Inheritance of myotonic discharges in American quarter horses and the relationship to hyperkalemic periodic paralysis.

Analysis in a large hyperkalemic periodic paralysis pedigree supports tight linkage to a sodium channel locus.

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

Paramyotonia congenita and hyperkalemic periodic paralysis map to the same sodium-channel gene locus.

Mice with an NaV1.4 sodium channel null allele have latent myasthenia, without susceptibility to periodic paralysis.

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

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

Hypokalemic periodic paralysis: an omega pore mutation affects inactivation.

Periodic hypokalemic paralysis transmitted by an unaffected male with negative family history: a delayed mutation?

Sodium channel gene defects in the periodic paralyses.

Transient Fanconi syndrome in Quarter horses.

Altered ionic permeability in skeletal muscle from horses with hyperkalemic periodic paralysis.

Effects of phenytoin in two myotonic horses with hyperkalemic periodic paralysis.

New territory opened by periodic paralysis associated with mitochondrial DNA mutation.

Thyrotoxic periodic paralysis in a pediatric patient.

Hyperthyroid hypokalemic periodic paralysis.

Domain III S4 in closed-state fast inactivation: insights from a periodic paralysis mutation.

Propofol in hyperkalaemic periodic paralysis.

Identification of a mutation in the gene causing hyperkalemic periodic paralysis.

A rare case of thyrotoxic periodic paralysis precipitated by hydrocortisone.

Hypokalaemic periodic paralysis complicating thyrotoxicosis.

[Hypokalemic periodic paralysis. A case report].

In vivo and in vitro sodium pump activity in subjects with thyrotoxic periodic paralysis.

[Thyrotoxic hypokalemic periodic paralysis. A case report].

Suggest Documents

Inheritance of myotonic discharges in American quarter horses and the relationship to hyperkalemic periodic paralysis.

Analysis in a large hyperkalemic periodic paralysis pedigree supports tight linkage to a sodium channel locus.

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

Paramyotonia congenita and hyperkalemic periodic paralysis map to the same sodium-channel gene locus.

Mice with an NaV1.4 sodium channel null allele have latent myasthenia, without susceptibility to periodic paralysis.

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

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

Hypokalemic periodic paralysis: an omega pore mutation affects inactivation.

Periodic hypokalemic paralysis transmitted by an unaffected male with negative family history: a delayed mutation?

Sodium channel gene defects in the periodic paralyses.

Transient Fanconi syndrome in Quarter horses.

Altered ionic permeability in skeletal muscle from horses with hyperkalemic periodic paralysis.

Effects of phenytoin in two myotonic horses with hyperkalemic periodic paralysis.

New territory opened by periodic paralysis associated with mitochondrial DNA mutation.

Thyrotoxic periodic paralysis in a pediatric patient.

Hyperthyroid hypokalemic periodic paralysis.

Domain III S4 in closed-state fast inactivation: insights from a periodic paralysis mutation.

Propofol in hyperkalaemic periodic paralysis.

Identification of a mutation in the gene causing hyperkalemic periodic paralysis.

A rare case of thyrotoxic periodic paralysis precipitated by hydrocortisone.

Hypokalaemic periodic paralysis complicating thyrotoxicosis.

[Hypokalemic periodic paralysis. A case report].

In vivo and in vitro sodium pump activity in subjects with thyrotoxic periodic paralysis.

[Thyrotoxic hypokalemic periodic paralysis. A case report].

Periodic paralysis in quarter horses: a sodium channel mutation disseminated by selective breeding.

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