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Connection

Debopam Samanta to Mutation

This is a "connection" page, showing publications Debopam Samanta has written about Mutation.

 
Connection Strength
 
 
 
3.247
 
  1. Samanta D, Zarate YA. Widening phenotypic spectrum of GABBR2 mutation. Acta Neurol Belg. 2019 Sep; 119(3):493-496.
    View in: PubMed
    Score: 0.451
  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. 2019 Jan-Feb; 67(1):259-260.
    View in: PubMed
    Score: 0.449
  3. Samanta D. Contactin-associated protein-like (CNTNAP) 2 gene mutation in a patient with bilateral schizencephaly. Acta Neurol Belg. 2017 03; 117(1):403-404.
    View in: PubMed
    Score: 0.375
  4. Samanta D. Severe developmental delay and complete agenesis of corpus callosum in a Noonan syndrome patient with SOS1 mutation. Acta Neurol Belg. 2016 Jun; 116(2):223-4.
    View in: PubMed
    Score: 0.355
  5. 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: 0.345
  6. Samanta D, Willis E. Electroencephalographic findings in KBG syndrome: a child with novel mutation in ANKRD11 gene. Acta Neurol Belg. 2015 Dec; 115(4):779-82.
    View in: PubMed
    Score: 0.340
  7. Samanta D. GRIN2A-related epilepsy and speech disorders: A comprehensive overview with a focus on the role of precision therapeutics. Epilepsy Res. 2023 Jan; 189:107065.
    View in: PubMed
    Score: 0.147
  8. 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: 0.145
  9. Samanta D. Reply to Cerebral Infarction in CARS2 Mutation. Pediatr Neurol. 2019 04; 93:66.
    View in: PubMed
    Score: 0.112
  10. Samanta D, Gokden M. PEHO syndrome: KIF1A mutation and decreased activity of mitochondrial respiratory chain complex. J Clin Neurosci. 2019 Mar; 61:298-301.
    View in: PubMed
    Score: 0.111
  11. Samanta D. Epileptic spasm and de novo KCNB1 mutation: if it is not one potassium channel, it is another! Acta Neurol Belg. 2020 Apr; 120(2):417-420.
    View in: PubMed
    Score: 0.108
  12. Samanta D, Bosanko KB, Zarate YA. An infant with ash-leaf and café au lait spots: a case of double phakomatosis. Acta Neurol Belg. 2017 03; 117(1):323-324.
    View in: PubMed
    Score: 0.093
  13. Samanta D. A 15-year-old with seizures: late diagnosis of pyridoxine-dependent epilepsy. Acta Neurol Belg. 2016 Dec; 116(4):667-669.
    View in: PubMed
    Score: 0.092
  14. Samanta D. Epilepsy with PCDH19 mutation masquerading as benign partial epilepsy in infancy. Neurol India. 2016 Mar-Apr; 64(2):327-8.
    View in: PubMed
    Score: 0.092
  15. Binaafar S, Garshasbi M, Tavasoli AR, Badv RS, Hosseiny SMM, Samanta D, Rabbani B, Mahdieh N. Nonsyndromic Early-Onset Epileptic Encephalopathies: Two Novel KCTD7 Pathogenic Variants and a Literature Review. Dev Neurosci. 2021; 43(6):348-357.
    View in: PubMed
    Score: 0.034
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.