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Assuming autism is required, the following 28 results were found.

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

    liver & kidney toxicity, adrenal insufficiency Cannabidiol Anxiolytic properties may decrease behavioral problems in autism Core ASD symptoms Not yetb Hypervigilence, sleep disturbances, irritability, loss of appetite, psychosis (rare) aBenefits might...

    • Type: Article
    • Author: Editor CNKE
    • Category: Home
  2. Self Injurious Behaviour (SIB) https://cnke.org/articles/229

    be indicative of coexisting psychiatric disorders in individuals with intellectual disabilities, as well as those with autism spectrum disorders. Conducting a functional behavior assessment (FBA) can help identify any behavioral factors that may be...

    • Type: Article
    • Author: Editor
    • Category: Home
  3. Transcranial Magnetic Stimulation (TMS) in Autism Spectrum Disordershttps://cnke.org/articles/182

    presents a promising, non-invasive intervention for modulating neurophysiological abnormalities associated with ASD. Autism Spectrum Disorder (ASD) ASD is a neurodevelopmental disorder characterized by: Difficulties in social communication and...

    • Type: Article
    • Author: Editor
    • Category: Home
  4. Autism, nutritional supplementshttps://cnke.org/topics/nutritional-supplements-in-autism

    • Type: Tag
    • Author: Editor CNKE
  5. Autism, Cannabidiol inhttps://cnke.org/topics/cannabidiol-in-autism

    • Type: Tag
    • Author: Editor CNKE
  6. Autism, metabolic interventions inhttps://cnke.org/topics/metabolic-interventions-in-autism

    • Type: Tag
    • Author: Editor CNKE
  7. Autism Spectrum Disorderhttps://cnke.org/topics/autism-spectrum-disorder

    • Type: Tag
    • Author: Editor
  8. Fragile X Syndromehttps://cnke.org/articles/578

    FXS is the most prevalent inherited cause of mild-to-severe intellectual disability and the most common monogenic cause of autism spectrum disorder. Overview Fragile X Syndrome (FXS), also known historically as Martin-Bell syndrome, is a non-Mendelian...

    • Type: Article
    • Author: Editor
    • Category: Home
  9. 1p21.3 microdeletion syndromehttps://cnke.org/articles/153

    is an extremely rare chromosomal anomaly characterized by severe speech and language delay, intellectual deficiency, autism spectrum disorder Definition 1p21.3 microdeletion syndrome is a rare chromosomal anomaly characterized by: Severe speech and...

    • Type: Article
    • Author: Editor
    • Category: Home
  10. Infantile Spasms Syndromehttps://cnke.org/articles/269

    spasms and the hypsarrhythmia pattern [93–95]. Cognitive and Behavioral Associations: Cognitive/Intellectual Disability and Autism Spectrum Disorder (ASD): Often associated with or preceding the onset of ISs. Deletions of SCN2A and SCN3A genes found in...

    • Type: Article
    • Author: Editor
    • Category: Home
  11. Psychometric measureshttps://cnke.org/articles/197

    (SCARED) Motor Skills Bruininks-Oseretsky Test of Motor Proficiency (BOT-2) Peabody Developmental Motor Scales (PDMS-2) Autism Spectrum Disorder Autism Diagnostic Observation Schedule (ADOS-2) Autism Diagnostic Interview-Revised (ADI-R) Gilliam Autism...

    • Type: Article
    • Author: Editor CNKE
    • Category: Articles
  12. Genes implicated in neurotransmitter disordershttps://cnke.org/articles/279

    PTPS deficiency GABAergic Pathway Disorders GABRA1 (Gamma-aminobutyric acid type A receptor alpha1 subunit) Epilepsy, autism GABRB3 (Gamma-aminobutyric acid type A receptor beta3 subunit) Epilepsy, autism GABRG2 (Gamma-aminobutyric acid type A receptor...

    • Type: Article
    • Author: Editor
    • Category: Home
  13. MED12L Variant and Its Role in Human Diseasehttps://cnke.org/articles/360

    expression are the root cause of these conditions. Common features include: Intellectual disability Behavior abnormalities Autism spectrum disorders Corpus callosum anomalies Macrocephaly Tall forehead Hypotonia MED13 Variants in MED13 have been...

    • Type: Article
    • Author: Editor
    • Category: Home
  14. The Diagnosis of Rett Syndromehttps://cnke.org/articles/154

    Gait abnormalities (e.g., ataxia, dyspraxia). Seizures: High prevalence but variable severity. Behavioral Features: Initial autism-like behaviors, followed by anxiety and mood instability. Inappropriate laughing/screaming (supportive diagnostic...

    • Type: Article
    • Author: Editor
    • Category: Home
  15. Comparitive genomic hybridization (CGH) https://cnke.org/articles/288

    Several microdeletions and microduplications have been recently described in children with unexplained mental retardation, autism, or congenital anomalies and in unaffected persons. These imbalances remain undetectable using routine karyotype...

    • Type: Article
    • Author: Editor
    • Category: Home
  16. The History of Rett Syndromehttps://cnke.org/historical-vignettes/162

    Ovidio Ramos, Dr. Hagberg published a landmark paper in the Annals of Neurology in 1983 titled "A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett’s syndrome: report of 35 cases." This publication...

    • Type: Article
    • Author: Biju Hameed
    • Category: Historical Vignettes
  17. Biochemical investigations in Urinehttps://cnke.org/articles/167

    acid storage disease. 100-fold increase in sialuria Succinyl purines (Bratton-Marshall trst) Neonatal seizures, delay, autism, Angelman-like, + dysmorphism Freeze random morning urine; purine reference laboratory will confirm ↑ in adenylosuccinate lyase...

    • Type: Article
    • Author: Editor
    • Category: Home
  18. Insomnia in childrenhttps://cnke.org/articles/242

    in circadian rhythms, leading to severe disruption of family life. Conditions associated with these disturbances include: Autism Spectrum Disorders Angelman Syndrome Smith-Magenis Syndrome Severe Cerebral Palsy Blindness Treatment Melatonin: Found to be...

    • Type: Article
    • Author: Editor
    • Category: Home
  19. Common Epilepsy Geneshttps://cnke.org/articles/277

    SYN1 X-linked epilepsy LGI1 Autosomal dominant lateral temporal lobe epilepsy NRXN1 Schizophrenia and epilepsy NLGN1 Autism spectrum disorders and epilepsy Metabolic Pathway Genes ALDH7A1 Pyridoxine-dependent epilepsy PANK2 Pantothenate...

    • Type: Article
    • Author: Editor
    • Category: Home
  20. Neurofibromatosishttps://cnke.org/articles/283

    Disability: 4 to 8%, slightly higher than the general population (2 to 3%). Associated Conditions: Increased frequency of autism spectrum disorder. Learning Disabilities: Up to 65% of children with NF1, poor performance on tasks involving nonverbal...

    • Type: Article
    • Author: Editor
    • Category: Home
Results 1 - 20 of 28