• Home
  • Topics
  • New
  • Forum
  • Quiz
  • About

Saturday, 04 January 2025

Main

  • Home
  • Topics
  • New
  • Forum
  • 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 icas is required, the following 188 results were found.

  1. Infantile Spasms Syndromehttps://cnke.org/articles/269

    Terminology The Infantile Spasms Syndrome (ISs) belongs to the group of “early epileptic encephalopathies” (EEE), characterized by severe, drug-resistant epileptic disorders, with onset in early life, associated to persistent EEG abnormalities and...

    • Type: Article
    • Author: Editor
    • Category: Home

  2. Charcot–Marie–Tooth disease (CMT)https://cnke.org/articles/214

    Charcot–Marie–Tooth disease (CMT) refers to a group of genetically heterogeneous disorders affecting peripheral nerve function. Charcot–Marie–Tooth disease (CMT) Definition: Charcot–Marie–Tooth disease (CMT) refers to a group of genetically...

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

  3. Lennox-Gastaut Syndrome (LGS)https://cnke.org/articles/247

    Lennox-Gastaut Syndrome (LGS) was first characterized by Dr. William G. Lennox as a form of epilepsy known as a "Petit mal variant." In 1966, the Marseille School in France provided a more detailed description of the syndrome. Dr. Henri Gastaut and his...

    • Type: Article
    • Author: Editor
    • Category: Home

  4. Progressive myoclonus epilepsy https://cnke.org/articles/258

    Introduction Progressive Myoclonus Epilepsy (PME) with onset between late childhood and late adolescence includes several conditions: Neuronal ceroid lipofuscinosis Type I sialidosis Myoclonic epilepsy with ragged red fibers Most common forms of PME in...

    • Type: Article
    • Author: Editor
    • Category: Home

  5. Metabolic derangements and Autismhttps://cnke.org/articles/126

    Disruption at any of the stages in metabolism could contribute to primary and/or secondary contributions to ASD Possible Role for Metabolism in the Pathogenesis of ASD Overview of Metabolism: Metabolism encompasses biochemical processes for: Converting...

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

  6. Migraine in childhoodhttps://cnke.org/articles/358

    Review of acute and preventative pharmacologic and non-pharmacologic treatment of pediatric migraine, including recent or ongoing clinical trials. Index Acute Treatment of Migraine in Pediatrics: Guidelines and Recommendations Guidelines Overview...

    • Type: Article
    • Author: Editor
    • Category: Home

  7. Dravet syndromehttps://cnke.org/articles/180

    Severe myoclonic epilepsy in infancy (SME) was described by Charlotte Dravet in 1978. In the Revised ILAE classification of epilepsies, the SMEI is named “Dravet syndrome” because of the lack of myoclonic seizures in many patients and is considered...

    • Type: Article
    • Author: Editor
    • Category: Home

  8. Dravet syndromehttps://cnke.org/articles/265

    Severe myoclonic epilepsy in infancy (SME) was described by Charlotte Dravet in 1978. In the Revised ILAE classification of epilepsies, the SMEI is named “Dravet syndrome” because of the lack of myoclonic seizures in many patients and is considered...

    • Type: Article
    • Author: Editor
    • Category: Home

  9. Zika Virus Infectionhttps://cnke.org/articles/353

    Aedes albopictus mosquitoes. Aedes aegypti and Aedes albopictus mosquitoes, found throughout much of the Region of the Americas, including parts of the United States, also transmit dengue and chikungunya viruses (CDC, 2015). Zika virus infections result...

    • Type: Article
    • Author: Editor
    • Category: Home

  10. The Normal EEG in Childrenhttps://cnke.org/articles/25

    Introduction Paediatric EEG Normal Awake 3-12 months 14 months-2years 3-4 years 5-10 years 11-16 years Hyperventilation Normal Drowsiness, Sleep, Arousal Drowsy patterns Burst Drowsy Patterns V Waves Spindles V Waves and Spindles Positive Occipital...

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

  11. Neurofibromatosishttps://cnke.org/articles/283

    Introduction Forms of Neurofibromatosis: Neurofibromatosis Type 1 (NF1): Previously known as von Recklinghausen disease, the most common type. NF2-related Schwannomatosis (NF2): Formerly neurofibromatosis type 2. Schwannomatoses: Related to genetic...

    • Type: Article
    • Author: Editor
    • Category: Home

  12. Aicardi-Goutières syndromehttps://cnke.org/articles/175

    Aicardi-Goutieres syndrome (AGS) is a genetic encephalopathy characterized by the inappropriate induction of a type I interferon-mediated immune response and usually results in severe cognitive and physical morbidities. It is named after Jean Aicardi...

    • Type: Article
    • Author: Editor
    • Category: Home

  13. Migrainehttps://cnke.org/articles/234

    Overview Migraines are severe, often bilateral, throbbing headaches commonly located in the temples or frontal regions of the head. They affect different age groups with varying prevalence rates: 2-5% in preschool children, 10% in school-aged children,...

    • Type: Article
    • Author: Editor
    • Category: Home

  14. Hereditary ataxias due to repeat expansionshttps://cnke.org/articles/186

    Hereditary ataxias are caused by repeat expansions in specific genes. Testing for repeat expansions is recommended before Next-Generation Sequencing (NGS) analysis. Key clinical features often include cerebellar ataxia and other systemic...

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

  15. Familial (Autosomal Dominant) Focal Epilepsieshttps://cnke.org/articles/357

    Overview: Temporal lobe epilepsy was traditionally considered an acquired condition. Causes include lesions such as: Hippocampal sclerosis Tumours Trauma Vascular malformations Malformations of cortical development Recent research has highlighted the...

    • Type: Article
    • Author: Editor
    • Category: Home

  16. Comparitive genomic hybridization (CGH) https://cnke.org/articles/288

    Comparitive genomic hybridization (CGH) or Chromosomal microarray analysis(CMA) is a modern cytogenetic technique for analyzing variations in DNA copy-number. Alteration in DNA copy number is one of the many ways in which modification of gene...

    • Type: Article
    • Author: Editor
    • Category: Home

  17. Classification of the Epilepsieshttps://cnke.org/articles/knowledge-maps/263

    The ILAE Classification of the Epilepsies was updated in 2017[1][2] to reflect the advances made in recent years in the understanding of the epilepsies and their pathophysiologies since the classification was last ratified in 1989[3]. The current...

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

  18. ADCY5 Dyskinesiahttps://cnke.org/articles/213

    ADCY5 dyskinesia is a hyperkinetic movement disorder characterized by infantile to late-adolescent onset of chorea, athetosis, dystonia, myoclonus, or a combination of these. Overview Hyperkinetic movement disorder, more prominent in the face and arms...

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

  19. Chronic Daily Headache Disorderhttps://cnke.org/articles/236

    Definition and Prevalence Chronic daily headache is diagnosed based on the presence of headaches occurring for 15 or more days per month, over a period of three consecutive months, without any underlying organic pathology. These headaches last for more...

    • Type: Article
    • Author: Editor
    • Category: Home

  20. The History of Rett Syndromehttps://cnke.org/historical-vignettes/162

    Rett syndrome, a rare neurodevelopmental disorder predominantly affecting females, is characterized by profound physical and cognitive impairments. It was first described in 1966 by Dr. Andreas Rett, an Austrian pediatrician whose tireless work has...

    • Type: Article
    • Author: Biju Hameed
    • Category: Historical Vignettes
Results 1 - 20 of 188