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Connection

ROHINI COORG to Humans

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This is a "connection" page, showing publications ROHINI COORG has written about Humans.
ROHINI COORG
Connection Strength
0.144
Humans
  1. Early Subclinical Status Epilepticus May Contribute to Developmental Delays in Infants With Tuberous Sclerosis Complex. Pediatr Neurol. 2024 Aug; 157:39-41.
    View in: PubMed
    Score: 0.023
  2. Epilepsy Surgery: Monitoring and Novel Surgical Techniques. Neurol Clin. 2021 08; 39(3):723-742.
    View in: PubMed
    Score: 0.019
  3. Successful Treatment of Electrographic Status Epilepticus of Sleep With Felbamate in a Patient With SLC9A6 Mutation. Pediatr Neurol. 2015 Dec; 53(6):527-31.
    View in: PubMed
    Score: 0.013
  4. Clinical neurogenetics: recent advances in the genetics of epilepsy. Neurol Clin. 2013 Nov; 31(4):891-913.
    View in: PubMed
    Score: 0.011
  5. Child Neurology: a case of PMM2-CDG (CDG 1a) presenting with unusual eye movements. Neurology. 2012 Oct 09; 79(15):e131-3.
    View in: PubMed
    Score: 0.010
  6. Filicide-suicide involving children with disabilities. J Child Neurol. 2013 Jun; 28(6):745-51.
    View in: PubMed
    Score: 0.010
  7. Development and Adaptive Function in Individuals With SCN2A-Related Disorders. Neurology. 2025 Aug 12; 105(3):e213868.
    View in: PubMed
    Score: 0.006
  8. Nav1.2 channel mutations preventing fast inactivation lead to SCN2A encephalopathy. Brain. 2025 Jan 07; 148(1):212-226.
    View in: PubMed
    Score: 0.006
  9. Novel Genetic and Phenotypic Expansion in GOSR2-Related Progressive Myoclonus Epilepsy. Genes (Basel). 2023 09 25; 14(10).
    View in: PubMed
    Score: 0.006
  10. Responsive Neurostimulation for the Treatment of Children With Drug-Resistant Epilepsy in Tuberous Sclerosis Complex. Pediatr Neurol. 2023 08; 145:97-101.
    View in: PubMed
    Score: 0.005
  11. An Initial Experience of Completion Hemispherotomy via Magnetic Resonance-Guided Laser Interstitial Therapy. Stereotact Funct Neurosurg. 2023; 101(3):179-187.
    View in: PubMed
    Score: 0.005
  12. KCNA1 gain-of-function epileptic encephalopathy treated with 4-aminopyridine. Ann Clin Transl Neurol. 2023 04; 10(4):656-663.
    View in: PubMed
    Score: 0.005
  13. Epilepsy Surgery in Young Children With Tuberous Sclerosis Complex: A Novel Hybrid Multimodal Surgical Approach. Neurosurgery. 2023 02 01; 92(2):398-406.
    View in: PubMed
    Score: 0.005
  14. Koolen-de Vries syndrome associated with continuous spike-wave in sleep Epileptic Disord. 2022 10 01; 24(5):928-933.
    View in: PubMed
    Score: 0.005
  15. Gain-of-function variants in GABRD reveal a novel pathway for neurodevelopmental disorders and epilepsy. Brain. 2022 05 24; 145(4):1299-1309.
    View in: PubMed
    Score: 0.005
  16. Phenotypic characterization of individuals with SYNGAP1 pathogenic variants reveals a potential correlation between posterior dominant rhythm and developmental progression. J Neurodev Disord. 2019 08 08; 11(1):18.
    View in: PubMed
    Score: 0.004
  17. Intragenic CAMTA1 deletions are associated with a spectrum of neurobehavioral phenotypes. Clin Genet. 2015 May; 87(5):478-82.
    View in: PubMed
    Score: 0.003
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.