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27 relations: Anticipation (genetics), Ball and chain inactivation, CBS domain, Center for Molecular Neurobiology Hamburg, Dystrophy, Electromyoneurography, Eperisone, Human sexual response cycle, Hyperkalemic periodic paralysis, ICD-10 Chapter VI: Diseases of the nervous system, Index of anatomy articles, List of MeSH codes (C05), List of MeSH codes (C10), List of MeSH codes (C23), Louis Ptáček, Muscular dystrophy, Myopathy, Myotonia congenita, Myotonic dystrophy, Nav1.4, Neuromyotonia, Paramyotonia congenita, Peter Emil Becker, Potassium-aggravated myotonia, Reflex hammer, Schwartz–Jampel syndrome, Scoliosis.
Anticipation (genetics)
In genetics, anticipation is a phenomenon whereby as a genetic disorder is passed on to the next generation, the symptoms of the genetic disorder become apparent at an earlier age with each generation.
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Ball and chain inactivation
In neuroscience, ball and chain inactivation is a model to explain the fast inactivation mechanism of voltage-gated ion channels.
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CBS domain
In molecular biology, the CBS domain is a protein domain found in a range of proteins in all species from bacteria to humans.
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Center for Molecular Neurobiology Hamburg
The Center for Molecular Neurobiology Hamburg (ZMNH), founded in 1988, is an internationally recognized molecular neuroscience research center, part of the University Medical Center Hamburg-Eppendorf (UKE).
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Dystrophy
Dystrophy is the degeneration of tissue, due to disease or malnutrition, most likely due to heredity.
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Electromyoneurography
Electromyoneurography (EMNG) is the combined use of electromyography and electroneurography This technique allows for the measurement of a peripheral nerve’s conduction velocity upon stimulation (electroneurography) alongside electrical recording of muscular activity (electromyography).
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Eperisone
Eperisone (formulated as the eperisone hydrochloride salt) is an antispasmodic drug.
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Human sexual response cycle
The human sexual response cycle is a four-stage model of physiological responses to sexual stimulation, which, in order of their occurrence, are the excitement phase, plateau phase, orgasmic phase and resolution phase.
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Hyperkalemic periodic paralysis
Hyperkalemic periodic paralysis (HYPP, HyperKPP) is a genetic disorder.
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ICD-10 Chapter VI: Diseases of the nervous system
ICD-10 is an international statistical classification used in health care and related industries.
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Index of anatomy articles
Articles related to anatomy include.
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List of MeSH codes (C05)
The following is a list of the "C" codes for MeSH.
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List of MeSH codes (C10)
The following is a list of the "C" codes for MeSH.
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List of MeSH codes (C23)
The following is a list of the "C" codes for MeSH.
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Louis Ptáček
Louis Ptáček is an American neurologist and professor who contributed greatly to the field of genetics and neuroscience.
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Muscular dystrophy
Muscular dystrophy (MD) is a group of muscle diseases that results in increasing weakening and breakdown of skeletal muscles over time.
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Myopathy
Myopathy is a disease of the muscle in which the muscle fibers do not function properly.
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Myotonia congenita
Congenital myotonia, also called myotonia congenita, is a congenital neuromuscular channelopathy that affects skeletal muscles (muscles used for movement).
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Myotonic dystrophy
Myotonic dystrophy is a long term genetic disorder that affects muscle function.
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Nav1.4
Sodium channel protein type 4 subunit alpha is a protein that in humans is encoded by the SCN4A gene.
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Neuromyotonia
Neuromyotonia (NMT) is a form of peripheral nerve hyperexcitability that causes spontaneous muscular activity resulting from repetitive motor unit action potentials of peripheral origin.
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Paramyotonia congenita
Paramyotonia congenita (PC), also known as paramyotonia congenita of von Eulenburg or Eulenburg disease, is a rare congenital autosomal dominant neuromuscular disorder characterized by “paradoxical” myotonia.
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Peter Emil Becker
Peter Emil Becker (23 November 1908 – 7 October 2000) was a German neurologist, psychiatrist and geneticist.
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Potassium-aggravated myotonia
Potassium-aggravated myotonia is a rare genetic disorder that affects skeletal muscle.
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Reflex hammer
A reflex hammer is a medical instrument used by practitioners to test deep tendon reflexes.
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Schwartz–Jampel syndrome
Schwartz–Jampel syndrome (SJS) is a rare genetic disease caused by a mutation in the HSPG2 gene, which makes the protein perlecan, and causes osteochondrodysplasia associated with myotonia.
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Scoliosis
Scoliosis is a medical condition in which a person's spine has a sideways curve.
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Amyotonia, Myatonia, Myotonic, Myotonic disorders, Mytonia, Thomsen Syndrome.
References
[1] https://en.wikipedia.org/wiki/Myotonia
