Padmanabha H - Search Results

1

Genotype-phenotype correlation and natural history study of dysferlinopathy: a single-centre experience from India.

Nashi S, Polavarapu K, Bardhan M, Anjanappa RM, Preethish-Kumar V, Vengalil S, Padmanabha H, Geetha TS, Prathyusha PV, Ramprasad V, Joshi A, Chawla T, Unnikrishnan G, Sharma P, Huddar A, Uppilli B, Thomas A, Baskar D, Mathew S, Menon D, Arunachal G, Faruq M, Thangaraj K, Nalini A. Nashi S, et al. Among authors: padmanabha h. Neurogenetics. 2023 Jan;24(1):43-53. doi: 10.1007/s10048-022-00707-3. Epub 2022 Dec 29. Neurogenetics. 2023. PMID: 36580222

2

Tract-specific myelopathy in myelin oligodendrocyte associated disorder: A novel finding.

Dhar D, Nagaraj AR, Kenchiah R, Mahadevan A, Mahale R, Saini J, Mohanty M, Balgandi S, Padmanabha H. Dhar D, et al. Among authors: padmanabha h. J Clin Neurosci. 2023 Dec;118:23-25. doi: 10.1016/j.jocn.2023.10.003. Epub 2023 Oct 14. J Clin Neurosci. 2023. PMID: 37844490 No abstract available.

3

Vision Loss in an 8-Year-Old Immunocompetent Boy with Cryptococcal Meningitis.

Padmanabha H, Kasinathan A, Kumar A, Zaman K, Suthar R, Suri D, Vyas S, Sankhyan N. Padmanabha H, et al. Pediatr Infect Dis J. 2018 Aug;37(8):e230-e232. doi: 10.1097/INF.0000000000001911. Pediatr Infect Dis J. 2018. PMID: 30004394

4

Syndrome of X linked intellectual disability, epilepsy, progressive brain atrophy and large head associated with SLC9A6 mutation.

Padmanabha H, Saini AG, Sahu JK, Singhi P. Padmanabha H, et al. BMJ Case Rep. 2017 Dec 22;2017:bcr2017222050. doi: 10.1136/bcr-2017-222050. BMJ Case Rep. 2017. PMID: 29275387 Free PMC article.

5

Recurrent encephalopathy in milliary neurocysticercosis: An uncommon manifestation of a common infection.

Sharawat IK, Padmanabha H, Suthar R, Vyas S, Sankhyan N. Sharawat IK, et al. Among authors: padmanabha h. J Infect Public Health. 2018 Nov-Dec;11(6):893-895. doi: 10.1016/j.jiph.2018.02.006. Epub 2018 Mar 9. J Infect Public Health. 2018. PMID: 29530680 Free article.

6

Electrocardiographic Tremor as an Important Diagnostic Aid in Spinal Muscular Atrophy.

Padmanabha H, Kadwa RA, Sahu JK, Singhi PD. Padmanabha H, et al. Indian J Pediatr. 2016 Nov;83(12-13):1506-1507. doi: 10.1007/s12098-016-2202-3. Epub 2016 Jul 27. Indian J Pediatr. 2016. PMID: 27460488 No abstract available.

7

COLQ-Related Congenital Myasthenic Syndrome and Response to Salbutamol Therapy.

Padmanabha H, Saini AG, Sankhyan N, Singhi P. Padmanabha H, et al. J Clin Neuromuscul Dis. 2017 Mar;18(3):162-163. doi: 10.1097/CND.0000000000000160. J Clin Neuromuscul Dis. 2017. PMID: 28221310 No abstract available.

8

Alternating Hemiplegia of Childhood with Novel Features.

Padmanabha H, Goswami JN, Sahu JK, Swaboda KJ, Singhi P. Padmanabha H, et al. Indian J Pediatr. 2017 Jun;84(6):473-474. doi: 10.1007/s12098-017-2290-8. Epub 2017 Jan 31. Indian J Pediatr. 2017. PMID: 28138908 No abstract available.

9

A randomized controlled trial of the ketogenic diet in refractory childhood epilepsy.

Padmanabha H, Suthar R, Sankhyan N. Padmanabha H, et al. Acta Neurol Scand. 2018 Jan;137(1):151. doi: 10.1111/ane.12801. Acta Neurol Scand. 2018. PMID: 29205271 No abstract available.

10

Malar rash in classical homocystinuria.

Saini AG, Padmanabha H, Attri S, Singhi P. Saini AG, et al. Among authors: padmanabha h. BMJ Case Rep. 2017 May 3;2017:bcr2017220296. doi: 10.1136/bcr-2017-220296. BMJ Case Rep. 2017. PMID: 28473367 Free PMC article. No abstract available.

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