Abnormalities of the fast sodium current in myotonic dystrophy, recessive generalized myotonia, and adynamia episodica

No abstract is available for this paper.

• Publication year

  1989

• Venue

  Muscle and Nerve

• Publication date

  1989-04-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1002/mus.880120405PMID 2549413
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• A quantitative description of membrane current and its application to conduction and excitation in nerve. 1952.

  1990cited by this paper
• Hodgkin-Huxley parameters of the sodium channels in human myoballs

  1988cited by this paper
• The membrane lipid and fatty acid composition of erythrocyte ghosts from three patients with paramyotonia congenita

  1988cited by this paper
• Transient weakness and altered membrane characteristic in recessive generalized myotonia (Becker)

  1988cited by this paper
• Adynamia episodica hereditaria with myotonia: A non‐inactivating sodium current and the effect of extracellular pH

  1987cited by this paper
• Membrane defects in paramyotonia congenita (eulenburg)

  1987cited by this paper
• Expression of apamin receptor in muscles of patients with myotonic muscular dystrophy

  1986cited by this paper
• Voltage-dependent channels of human muscle cultures

  1986cited by this paper
• Membrane changes in cells from myotonia patients.

  1985cited by this paper
• Different functional states of tetrodotoxin sensitive and tetrodotoxin resistant Na+ channels occur during the in vitro development of rat skeletal muscle

  1984cited by this paper
• Electrophysiologic properties of aneurally cultured muscle from patients with myotonic muscular atrophy

  1983cited by this paper
• Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches

  1981cited by this paper
• Cultured muscle from myotonic muscular dystrophy patients: altered membrane electrical properties.

  1981cited by this paper
• Voltage‐clamp experiments in normal and denervated mammalian skeletal muscle fibres.

  1980cited by this paper
• A quantitative technique for growing human adult skeletal muscle in culture starting from mononucleated cells.

  1977cited by this paper
• A Biophysical Study of the Human Myotonias

  1973cited by this paper
• The Electrophysiology of Myotonia, with a Review of Congenital Myotonia of Goats

  1973cited by this paper
• A quantitative description of membrane current and its application to conduction and excitation in nerve

  1952cited by this paper

• Myotonie Dystrophy Protein Kinase is Involved in the Modulation of the Ca2+ Homeostasis in Skeletal Muscle Cells

  2017cites this paper
• Ion transport in human skeletal muscle cells : disturbances in myotonic dystrophy and Brody ' s disease

  2017cites this paper
• Properties of voltage-gated Na+ channels in the human rhabdomyosarcoma cell-line SJ-RH30: conventional and automated patch clamp analysis.

  2006cites this paper
• CHAPTER 4 – cis Effects of CTG Expansion in Myotonic Dystrophy Type 1

  2006cites this paper
• Female patient with proximal myotonic myopathy and ventricular tachycardia

  2005cites this paper
• Myocytes from congenital myotonic dystrophy display abnormal Na+ channel activities

  2005cites this paper
• K-Aggravated Myotonia Mutations at Residue G1306 Differentially Alter Deactivation Gating of Human Skeletal Muscle Sodium Channels

  2005cites this paper
• HMG-CoA reductase (HCR) inhibitors are effective cholesterol-lowering agents in the treatment of hypercholesterolemia. Using intracellular microelectrodes, we studied the pathomechanism of rnyotonia experi- mentally induced in rabbits by HCR inhibitors, simvastatin, and pr8av-

  2004cites this paper
• Loss of the muscle-specific chloride channel in type 1 myotonic dystrophy due to misregulated alternative splicing.

  2002cites this paper
• Myotonic Muscular Dystrophy Genetics and Cardiac Sequelae

  2000cites this paper
• Clinical and genetic heterogeneity in myotonic dystrophies

  2000cites this paper
• Carrell-Krusen Symposium Invited Lecture-1997. Myotonic disorders in childhood: diagnosis and treatment.

  1997cites this paper
• Myotonic dystrophy protein kinase is involved in the modulation of the Ca2+ homeostasis in skeletal muscle cells.

  1997cites this paper
• Andersen's syndrome: A distinct periodic paralysis

  1997cites this paper
• Myotonic dystrophy kinase modulates skeletal muscle but not cardiac voltage‐gated sodium channels

  1997cites this paper
• Myotonic Disorders in Childhood: Diagnosis and Treatment

  1997cites this paper
• Age-dependent expression of the apamin-sensitive calcium-activated K+ channel in fast and slow rat skeletal muscle.

  1997cites this paper
• Neural control of the expression of a Ca2+-activated K+ channel involved in the induction of myotonic-like characteristics

  1996cites this paper
• Familial Periodic Paralysis

  1996cites this paper
• Ion transport in human skeletal muscle cells: disturbances in myotonic dystrophy and Brody's disease.

  1996cites this paper
• [Periodic paralysis as the first manifestation of hyperthyroidism].

  1996cites this paper
• Prophylactic efficacy of phenytoin, acetazolamide and hydrochlorothiazide in horses with hyperkalaemic periodic paralysis.

  1995cites this paper
• Structure and function of voltage-gated ion channels.

  1995cites this paper
• Electrical myotonia of rabbit skeletal muscles by HMG‐CoA reductase inhibitors

  1994cites this paper
• Myotonic disorders and periodic paralysis.

  1994cites this paper
• Possible role of apamin‐sensitive K+ channels in myotonic dystrophy

  1994cites this paper
• Anaesthesia and myotonia.

  1994cites this paper
• Genetics and physiology of the myotonic muscle disorders.

  1993cites this paper
• Phenytoin increases specific triacylglycerol fatty esters in skeletal muscle from horses with hyperkalemic periodic paralysis.

  1993cites this paper
• Deficiency of Na+/K(+)-ATPase and sarcoplasmic reticulum Ca(2+)-ATPase in skeletal muscle and cultured muscle cells of myotonic dystrophy patients.

  1993cites this paper
• Mutations in an S4 segment of the adult skeletal muscle sodium channel cause paramyotonia congenita.

  1992cites this paper
• Cellular and molecular biology of voltage-gated sodium channels.

  1992cites this paper
• Single-channel recordings of chloride currents in cultured human skeletal muscle

  1992cites this paper
• Linkage of Thomsen disease to the T-cell-receptor beta (TCRB) locus on chromosome 7q35.

  1992cites this paper
• Effects of phenytoin in two myotonic horses with hyperkalemic periodic paralysis

  1992cites this paper
• Linkage analysis of candidate loci in autosomal dominant myotonia congenita

  1992cites this paper
• Myotonia, periodic paralysis and myopathy.

  1992cites this paper
• Foveal photopigment kinetics--abnormality: an early sign in myotonic dystrophy?

  1992cites this paper
• Hyperkalaemic periodic paralysis and anaesthesia

  1992cites this paper
• Effects of lipid-soluble agents on sodium channel function in normal and MH-susceptible skeletal muscle cultures.

  1991cites this paper
• A sodium channel defect in hyperkalemic periodic paralysis: potassium-induced failure of inactivation.

  1991cites this paper
• Identification of a mutation in the gene causing hyperkalemic periodic paralysis.

  1991cites this paper
• Altered sodium channel behaviour causes myotonia in dominantly inherited myotonia congenita.

  1991cites this paper
• Slow membrane potential changes in skeletal muscle induced in Cl(-)-free medium.

  1991cites this paper
• Different gene loci for hyperkalemic and hypokalemic periodic paralysis.

  1991cites this paper
• Altered Na+ channel activity and reduced Cl− conductance cause hyperexcitability in recessive generalized myotonia (becker)

  1991cites this paper
• Myotonia Congenita

  1991cites this paper
• Analysis in a large hyperkalemic periodic paralysis pedigree supports tight linkage to a sodium channel locus.

  1991cites this paper
• Paramyotonia congenita and hyperkalemic periodic paralysis map to the same sodium-channel gene locus.

  1991cites this paper
• Calcium‐tension relationships of muscle fibers from patients with periodic paralysis

  1991cites this paper
• [Dystrophia myotonica (Steinert disease)--a frequently misdiagnosed disease].

  1990cites this paper
• Electrophysiology of Myotonias and Periodic Paralyses

  1990cites this paper
• Characteristics of Na+ channels and Cl‐ conductance in resealed muscle fibre segments from patients with myotonic dystrophy.

  1990cites this paper
• Electrical myotonia and cataract in X-linked muscular dystrophy (mdx) mouse.

  1990cites this paper
• Schwartz–Jampel syndrome: II. Na+ channel defect causes myotonia

  1990cites this paper
• Electrophysiology of Myotonias and Periodic Paralyses

  1990cites this paper
• The calcium homeostasis and the membrane potential of cultured muscle cells from patients with myotonic dystrophy.

  1990cites this paper
• From Neuron to Action

  1990cites this paper
• Adynamia episodica hereditaria: What causes the weakness?

  1989cites this paper
• Great Britain CHARACTERISTICS OF Na + CHANNELS AND Cl-CONDUCTANCE IN RESEALED MUSCLE FIBRE SEGMENTS FROM PATIENTS WITH MYOTONIC DYSTROPHY

  year unknowncites this paper