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Novel Mutations in CRLF1: Case Reports with Crisponi Syndrome.
A R, Chandran S, Ghatak AR, Thomas N, Danda S. A R, et al. Among authors: danda s. Indian J Pediatr. 2022 Nov;89(11):1148-1150. doi: 10.1007/s12098-022-04263-4. Epub 2022 Aug 19. Indian J Pediatr. 2022. PMID: 35984556 Review.
Juvenile Sandhoff disease.
Unnikrishnan AG, Danda S, Seshadri MS. Unnikrishnan AG, et al. Among authors: danda s. Indian Pediatr. 2001 Jan;38(1):89-92. Indian Pediatr. 2001. PMID: 11175942 No abstract available.
Fanconi- Bickel Syndrome: mutation in an Indian patient.
Ekbote AV, Mandal K, Agarwal I, Sinha R, Danda S. Ekbote AV, et al. Among authors: danda s. Indian J Pediatr. 2012 Jun;79(6):810-2. doi: 10.1007/s12098-011-0568-9. Epub 2011 Oct 5. Indian J Pediatr. 2012. PMID: 21972075
An Indian boy with additional features in Pallister-Killian syndrome.
Shah K, George R, Balla ES, Oommen SP, Padankatti CS, Srivastava VM, Danda S. Shah K, et al. Among authors: danda s. Indian J Pediatr. 2012 Sep;79(9):1238-40. doi: 10.1007/s12098-011-0585-8. Epub 2011 Oct 20. Indian J Pediatr. 2012. PMID: 22012142
Van der Woude Syndrome: IRF6 Mutations.
Sunny AP, Arunachal G, Danda S. Sunny AP, et al. Among authors: danda s. Indian J Pediatr. 2019 Nov;86(11):1070-1071. doi: 10.1007/s12098-019-03058-4. Epub 2019 Aug 29. Indian J Pediatr. 2019. PMID: 31468312 No abstract available.
156 results