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Monday, 06 January 2025

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Editor

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Assuming effects is required, the following 69 results were found.

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

    Mechanism of action is poorly understood, possibly related to protection against oxidative stress and antiapoptotic effects in neurons deprived of nerve growth factor (Ferrari 1995, Hurd 1996). Electroencephalographic (EEG) recordings: Abnormal even...

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  2. Valproic acid and Lamotrigine combinationhttps://cnke.org/articles/312

    [DOI: 10.1111/bcp.12984] 2. Gidal BE, Sheth R, Parnell J, Maloney K, Sale M. Evaluation of VPA dose and concentration effects on lamotrigine pharmacokinetics: implications for conversion to lamotrigine monotherapy. Epilepsy Res. 2003 Dec;57(2-3):85-93....

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  3. Fragile X Syndromehttps://cnke.org/articles/578

    FMRP disrupts synaptic plasticity, neuronal connectivity, and normal regulation of protein translation. Key physiological effects: Increased neuronal excitation Reduced GABAergic activity Brain-specific impacts: Decreased cerebellar size Hypoplasia of...

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  4. Kufor-Rakeb Syndrome https://cnke.org/articles/255

    Overview Kufor-Rakeb Syndrome (KRS), also known as PARK9, is a rare neurodegenerative disorder caused by mutations in the ATP13A2 gene. It was first reported by Nisipeanu et al. in 1994. Clinical Features The initial symptoms of KRS typically include:...

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  5. Illness Anxiety Disorder (IAD)https://cnke.org/articles/281

    Overview Definition: Illness Anxiety Disorder (IAD), formerly known as hypochondriasis, is characterized by excessive worry about having a serious illness despite having little or no medical evidence to support such concerns. Prevalence: Less common in...

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  6. 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...

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    • Author: Editor CNKE
    • Category: Articles

  7. Benign Paroxysmal Torticollis of Infancyhttps://cnke.org/articles/270

    Etymology and Definition The name "torticollis" comes from the Latin words "tortus" (twisted) and "collum" (neck). Torticollis typically involves the head being tilted to one side and rotated so that the chin points to the opposite side. It is a common...

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  8. Developmental Milestones (Birth to 8 Years)https://cnke.org/articles/166

    Newborn (0–1 Month) Gross Motor: Flexed posture Turns head to side while lying prone Momentary head control in upright position Fine Motor: Hands predominantly fisted Reflexive grasp Social/Emotional: Prefers human faces Cries to communicate needs...

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  9. Guidelines for becoming an Editor on CNKE.ORGhttps://cnke.org/about/199

    CNKE.org is committed to maintaining a high standard of quality, accuracy, and depth in its content. To uphold these standards, we welcome contributors who demonstrate dedication and expertise in child neurology to join our editorial team. Below are...

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  10. Speech and Language developmental disordershttps://cnke.org/articles/243

    Definition and Components of Language and Speech Language: A communication system acquired through use, involving symbols sequenced to share attention and ideas. Speech: One mechanism for expressing language, but other methods like gestures, sign...

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  11. Landau-Kleffner Syndromehttps://cnke.org/articles/169

    Landau-Kleffner syndrome (LKS), or acquired epileptiform aphasia, is an epilepsy syndrome involving progressive neuropsychological impairment related to the appearance of paroxysmal electroencephalograph (EEG) activity. History Frank R Kleffner...

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  12. 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...

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  13. Night Terrors https://cnke.org/articles/230

    Night terrors, also known as sleep terrors, are an early childhood parasomnia characterized by screams or cries, behavioral manifestations of extreme fear, difficulty waking and inconsolability upon awakening[1].Parasomnias can often occur during any...

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  14. William G. Lennoxhttps://cnke.org/articles/51

    Early Life and Education Dr. William G. Lennox, born on July 15, 1884, in Boston, Massachusetts, was a pioneering neurologist known for his groundbreaking work in epilepsy research. Lennox pursued his undergraduate studies at Harvard University, where...

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    • Author: Editor CNKE
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  15. 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...

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

    Zika virus is a mosquito-borne flavivirus primarily transmitted by Aedes aegypti mosquitoes (Hayes, 2009; CDC, 2016 ) and to a lesser extent by Aedes albopictus mosquitoes. Aedes aegypti and Aedes albopictus mosquitoes, found throughout much of the...

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  17. MED12L Variant and Its Role in Human Diseasehttps://cnke.org/articles/360

    MED12L is a gene that plays a crucial role in transcriptional coactivation of nearly all RNA polymerase II-dependent genes. It is highly conserved across eukaryotes and contains 43 exons. The protein encoded by MED12L is a component of the Mediator...

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  18. Mucopolysaccharidoses (MPS)https://cnke.org/articles/468

    Overview Mucopolysaccharidoses (MPS) are lysosomal storage disorders due to enzyme deficiencies impairing degradation of glycosaminoglycans (GAGs), also known as mucopolysaccharides. GAGs are complex sugar molecules found in connective tissues, skin,...

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  19. The Diagnosis of Rett Syndromehttps://cnke.org/articles/154

    The Diagnosis of Rett Syndrome (RTT) Introduction Definition: Rett Syndrome (RTT) is a rare neurodevelopmental disorder, primarily affecting females, characterized by developmental regression, loss of acquired skills, and stereotypic hand movements....

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  20. Privacy statementhttps://cnke.org/about/privacy

    Privacy Statement for CNKE.ORG Effective Date: Feb 14, 2024 At CNKE.ORG, the Child Neurology Knowledge Environment, we are committed to protecting your privacy and ensuring that your personal information is handled securely and responsibly. This...

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Results 41 - 60 of 69