Header Logo
Keywords
Last Name
Institution
Announcement

You can now add alternative names! Click here to add other names that you've published under.

Connection

Debopam Samanta to Developmental Disabilities

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

 
Connection Strength
 
 
 
1.845
 
  1. Samanta D, Zarate YA. Widening phenotypic spectrum of GABBR2 mutation. Acta Neurol Belg. 2019 Sep; 119(3):493-496.
    View in: PubMed
    Score: 0.617
  2. 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: 0.486
  3. Samanta D, Willis E, Sharp GB. Absence status after starting clobazam in a patient with syndrome of continuous spike and wave during slow sleep (CSWS). Neurol India. 2014 Nov-Dec; 62(6):685-7.
    View in: PubMed
    Score: 0.460
  4. 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: 0.160
  5. Samanta D. Sinus pericranii and myoclonic epilepsy: novel features of 3q29 microdeletion syndrome. Acta Neurol Belg. 2016 Sep; 116(3):363-4.
    View in: PubMed
    Score: 0.123
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.