• Home
  • Topics
  • New
  • Q&A
  • Quiz
  • About

Thursday, 30 January 2025

Main

  • Home
  • Topics
  • New
  • Q&A
  • Quiz
  • About

Editor

Here are a few examples of how you can use the search feature:

Entering this and that into the search form will return results containing both "this" and "that".

Entering this not that into the search form will return results containing "this" and not "that".

Entering this or that into the search form will return results containing either "this" or "that".

Search results can also be filtered using a variety of criteria. Select one or more filters below to get started.

Assuming channelopathies is required, the following 8 results were found.

  1. Channelopathieshttps://cnke.org/articles/knowledge-maps/196

    Channelopathies are a group of disorders caused by dysfunctions in ion channels, which are proteins embedded in cell membranes that regulate the flow of ions (such as sodium, potassium, calcium, and chloride) across the membrane. These ion channels are...

    • Type: Article
    • Author: Editor CNKE
    • Category: Knowledge Maps

  2. Channelopathieshttps://cnke.org/topics/channelopathies

    • Type: Tag
    • Author: Editor CNKE

  3. Ion channel disordershttps://cnke.org/articles/231

    Ion channel disorders, or channelopathies, are a group of conditions that involve dysfunctions in ion channels—integral membrane proteins regulating the flow of ions across cellular membranes. In skeletal muscle, these disorders variably produce...

    • Type: Article
    • Author: Editor CNKE
    • Category: Articles

  4. PRRT2-Associated Disordershttps://cnke.org/articles/274

    fully reverted by reintroduction of wild-type PRRT2. Suggests a mechanistic crossover between synapthopathies and channelopathies in paroxysmal neurological disorders. Mutations in SCN8A (encoding Nav1.6) can also cause PxD with epilepsy. Brain...

    • Type: Article
    • Author: Editor CNKE
    • Category: Articles

  5. Schwartz-Jampel Syndrome (SJS)https://cnke.org/articles/328

    Muscular dystrophies (Becker dystrophy, Duchenne dystrophy, congenital muscular dystrophy) Congenital myopathies Channelopathies Mucopolysaccharidosis (Morquio's syndrome) Ehlers-Danlos Syndrome Malignant hyperthermia Blepharospasm Stuve-Wiedemann...

    • Type: Article
    • Author: Editor CNKE
    • Category: Articles

  6. Neuromuscular disorders in childrenhttps://cnke.org/articles/knowledge-maps/195

    Disorders Myotonic Dystrophy Type 1 (DM1, Steinert Disease) Myotonic Dystrophy Type 2 Disorders of Ion Channels (Channelopathies) Periodic Paralyses Hypokalemic Periodic Paralysis Hyperkalemic Periodic Paralysis Andersen-Tawil Syndrome Congenital...

    • Type: Article
    • Author: Editor CNKE
    • Category: Knowledge Maps

  7. Muscle Conditions with Myotonia or Myotonia-like Symptomshttps://cnke.org/articles/knowledge-maps/230

    Muscle Conditions: Myotonic Dystrophy Type 1 (DM1) Myotonic Dystrophy Type 2 (DM2) Non-Dystrophic Muscle Conditions (Channelopathies): Chloride Channel (CLCN1) Disorders: Myotonia Congenita: Thomsen Disease (AD) Becker Disease (AR) Sodium Channel...

    • Type: Article
    • Author: Editor CNKE
    • Category: Knowledge Maps

  8. Peripheral Nerve Hyperexcitability Syndromeshttps://cnke.org/articles/234

    Autoimmune Etiology: Commonly associated with VGKC antibodies. Genetic Contributions: Rare cases linked to ion channelopathies (e.g., SCN4A, KCNA1 mutations). Management Treatment focuses on the underlying etiology and symptom control: Autoimmune...

    • Type: Article
    • Author: Editor CNKE
    • Category: Articles
Results 1 - 8 of 8