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Connection

Co-Authors

This is a "connection" page, showing publications co-authored by Debopam Samanta and Raghu Hosahalli Ramakrishnaiah.

 
Connection Strength
 
 
 
5.234
 
  1. Harada Y, Ramakrishnaiah R, Arya K, Samanta D. Extensive reversible myelopathy secondary to acute quadriventricular noncommunicating hydrocephalus. Childs Nerv Syst. 2019 11; 35(11):2023-2026.
    View in: PubMed
    Score: 0.723
  2. Samanta D, Ramakrishnaiah R, Frye RE. Complex Heterozygous Polymerase Gamma Mutation and Cerebral Folate Deficiency in a Child with Refractory Partial Status. Neurol India. 2022 Sep-Oct; 70(5):2265-2267.
    View in: PubMed
    Score: 0.448
  3. Samanta D, Ramakrishnaiah R. Intravenous Immunoglobulin in the Treatment of Alternating Hemiplegia of Childhood. Clin Neuropharmacol. 2021 Jan-Feb 01; 44(1):23-26.
    View in: PubMed
    Score: 0.399
  4. Samanta D, Ramakrishnaiah R. Early-Onset Parkinsonism and Halo Sign: Beta-propeller Proteinassociated Neurodegeneration. J Pediatr Neurosci. 2020 Jul-Sep; 15(3):325-327.
    View in: PubMed
    Score: 0.395
  5. Samanta D, Ramakrishnaiah R. Recurrent Oral Ulcers in a Child With Seizures. Pediatr Neurol. 2020 02; 103:89-90.
    View in: PubMed
    Score: 0.355
  6. Samanta D, Ramakrishnaiah R, Schaefer B. The neurological aspects related to POGZ mutation: case report and review of CNS malformations and epilepsy. Acta Neurol Belg. 2020 Apr; 120(2):447-450.
    View in: PubMed
    Score: 0.352
  7. Samanta D, Ramakrishnaiah R, Crary SE, Sukumaran S, Burrow TA. Multiple Autoimmune Disorders in Aicardi-Gouti?res Syndrome. Pediatr Neurol. 2019 07; 96:37-39.
    View in: PubMed
    Score: 0.350
  8. Samanta D, Ramakrishnaiah R. Recurrent Encephalopathy with Spinal Cord Involvement: An Atypical Manifestation of Aicardi-Gouti?res Syndrome. Ann Indian Acad Neurol. 2019 Jan-Mar; 22(1):111-115.
    View in: PubMed
    Score: 0.347
  9. Samanta D, Ramakrishnaiah R, Frye RE. Complex heterozygous polymerase gamma mutation and cerebral folate deficiency in a child with refractory partial status. Neurol India. 2019 Jan-Feb; 67(1):259-260.
    View in: PubMed
    Score: 0.347
  10. Samanta D, Ramakrishnaiah R. Neuroimaging Findings in a Child With SensorineuralHearing Loss. Pediatr Neurol. 2018 11; 88:75-76.
    View in: PubMed
    Score: 0.338
  11. Samanta D, Ramakrishnaiah R. Diffuse Carotid Arteriosclerosis and Stroke in a Patient With Schimke Immuno-osseous Dysplasia. Pediatr Neurol. 2017 Jun; 71:82-83.
    View in: PubMed
    Score: 0.307
  12. Samanta D, Ramakrishnaiah R. De novo R853Q mutation of SCN2A gene and West syndrome. Acta Neurol Belg. 2015 Dec; 115(4):773-6.
    View in: PubMed
    Score: 0.267
  13. Samanta D, Ramakrishnaiah R. Novel brain magnetic resonance imaging finding in a patient with trisomy 9p syndrome. Acta Neurol Belg. 2015 Sep; 115(3):431-2.
    View in: PubMed
    Score: 0.263
  14. Samanta D, Ramakrishnaiah R, Willis E, Frye RE. Myoclonic epilepsy evolved into West syndrome: a patient with a novel de novo KCNQ2 mutation. Acta Neurol Belg. 2015 Sep; 115(3):475-8.
    View in: PubMed
    Score: 0.256
  15. Malatesta LM, Samanta D, Ramakrishnaiah R. An Unusual Cause of Recurrent Facial Nerve Palsy. Pediatr Neurol. 2019 02; 91:68-69.
    View in: PubMed
    Score: 0.086
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.