Benakappa N - Search Results

1

Biotin Thiamin Responsive Basal Ganglia Disease in Siblings.

Gowda VK, Srinivasan VM, Bhat M, Benakappa N. Gowda VK, et al. Among authors: benakappa n. Indian J Pediatr. 2018 Feb;85(2):155-157. doi: 10.1007/s12098-017-2471-5. Epub 2017 Nov 4. Indian J Pediatr. 2018. PMID: 29101630

2

Diffuse mesangial sclerosis presenting as infantile nephrotic syndrome.

Umesh L, Prashanth A, Benakappa DG, Govindaraj M, Benakappa N. Umesh L, et al. Among authors: benakappa dg, benakappa n. Indian Pediatr. 2001 Jun;38(6):663-4. Indian Pediatr. 2001. PMID: 11418734 No abstract available.

3

Congenital amastia.

Patil LG, Shivanna NH, Benakappa N, Ravindranath H, Bhat R. Patil LG, et al. Among authors: benakappa n. Indian J Pediatr. 2013 Oct;80(10):870-1. doi: 10.1007/s12098-012-0919-1. Epub 2012 Dec 20. Indian J Pediatr. 2013. PMID: 23255076

4

Role of hematological parameters in predicting retinopathy of prematurity (ROP) in preterm neonates.

Niranjan HS, Bharath Kumar Reddy KR, Benakappa N, Murthy K, Shivananda S, Veeranna V. Niranjan HS, et al. Among authors: benakappa n. Indian J Pediatr. 2013 Sep;80(9):726-30. doi: 10.1007/s12098-013-0986-y. Epub 2013 Feb 23. Indian J Pediatr. 2013. PMID: 23436192

5

Caregiver-reported health-related quality of life of children with cerebral palsy and their families and its association with gross motor function: A South Indian study.

Surender S, Gowda VK, Sanjay KS, Basavaraja GV, Benakappa N, Benakappa A. Surender S, et al. Among authors: benakappa a, benakappa n. J Neurosci Rural Pract. 2016 Apr-Jun;7(2):223-7. doi: 10.4103/0976-3147.178657. J Neurosci Rural Pract. 2016. PMID: 27114652 Free PMC article.

6

Sialidosis Type 1 with a Novel Mutation in the Neuraminidase-1 (NEU1) Gene.

Gowda VK, Srinivasan VM, Benakappa N, Benakappa A. Gowda VK, et al. Among authors: benakappa a, benakappa n. Indian J Pediatr. 2017 May;84(5):403-404. doi: 10.1007/s12098-016-2286-9. Epub 2017 Jan 31. Indian J Pediatr. 2017. PMID: 28138907

7

Homocystinuria with Cerebral Venous Sinus Thrombosis: Excellent Recovery with Intravenous Recombinant Tissue Plasminogen Activator.

Gowda VK, Nanjundappa RC, Pendharkar H, Benakappa N. Gowda VK, et al. Among authors: benakappa n. Iran J Child Neurol. 2017 Summer;11(3):48-52. Iran J Child Neurol. 2017. PMID: 28883877 Free PMC article.

8

Case Series of Infantile Tremor Syndrome in Tertiary Care Paediatric Centre from Southern India.

Gowda VK, Kolli V, Benakappa A, Srinivasan VM, Shivappa SK, Benakappa N. Gowda VK, et al. Among authors: benakappa a, benakappa n. J Trop Pediatr. 2018 Aug 1;64(4):284-288. doi: 10.1093/tropej/fmx062. J Trop Pediatr. 2018. PMID: 28977620

9

Dihydropteridine Reductase Deficiency: A Treatable Neurotransmitter Movement Disorder Masquerading as Refractory Epilepsy Due to Novel Mutation.

Gowda VK, Vegda H, Benakappa N, Benakappa A. Gowda VK, et al. Among authors: benakappa a, benakappa n. Indian J Pediatr. 2018 Sep;85(9):812-813. doi: 10.1007/s12098-018-2671-7. Epub 2018 Mar 28. Indian J Pediatr. 2018. PMID: 29594939 No abstract available.

10

Corticotrophin-ACTH in Comparison to Prednisolone in West Syndrome - A Randomized Study.

Gowda VK, Narayanaswamy V, Shivappa SK, Benakappa N, Benakappa A. Gowda VK, et al. Among authors: benakappa a, benakappa n. Indian J Pediatr. 2019 Feb;86(2):165-170. doi: 10.1007/s12098-018-2782-1. Epub 2018 Sep 19. Indian J Pediatr. 2019. PMID: 30232789 Clinical Trial.

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