Kamate M - Search Results

1

Is Herpes Simplex Encephalitis Different in Infants and Toddlers?

Kamate M, Basavanagowda T. Kamate M, et al. Indian J Pediatr. 2023 Dec;90(12):1269. doi: 10.1007/s12098-023-04784-6. Epub 2023 Jul 28. Indian J Pediatr. 2023. PMID: 37505409 No abstract available.

2

Molecular genetic studies in Indian patients with megalencephalic leukoencephalopathy.

Shukla P, Gupta N, Ghosh M, Vasisht S, Gulati S, Balakrishnan P, Sharma R, Gupta AK, Kamate M, Kalra V, Kabra M. Shukla P, et al. Among authors: kamate m. Pediatr Neurol. 2011 Jun;44(6):450-8. doi: 10.1016/j.pediatrneurol.2011.01.003. Pediatr Neurol. 2011. PMID: 21555057

3

Teaching NeuroImage: hemiconvulsion-hemiplegia-epilepsy syndrome: sequential MRI follow-up.

Sankhyan N, Sharma S, Kamate M, Subramanian S. Sankhyan N, et al. Among authors: kamate m. Neurology. 2008 Sep 9;71(11):e28. doi: 10.1212/01.wnl.0000325475.04616.e3. Neurology. 2008. PMID: 18779505 No abstract available.

4

Batten disease: biochemical and molecular characterization revealing novel PPT1 and TPP1 gene mutations in Indian patients.

Sheth J, Mistri M, Bhavsar R, Pancholi D, Kamate M, Gupta N, Kabra M, Mehta S, Nampoothiri S, Thakker A, Jain V, Shah R, Sheth F. Sheth J, et al. Among authors: kamate m. BMC Neurol. 2018 Dec 12;18(1):203. doi: 10.1186/s12883-018-1206-1. BMC Neurol. 2018. PMID: 30541466 Free PMC article.

5

Clinical Profile and Treatment Outcomes of Hypermanganesemia with Dystonia 1 and 2 among 27 Indian Children.

Garg D, Yoganathan S, Shamim U, Mankad K, Gulati P, Bonifati V, Botre A, Kalane U, Saini AG, Sankhyan N, Srivastava K, Gowda VK, Juneja M, Kamate M, Padmanabha H, Panigrahi D, Pachapure S, Udani V, Kumar A, Pandey S, Thomas M, Danda S, Iqbalahmed SA, Subramanian A, Pemde H, Singh V, Faruq M, Sharma S. Garg D, et al. Among authors: kamate m. Mov Disord Clin Pract. 2022 Aug 12;9(7):886-899. doi: 10.1002/mdc3.13516. eCollection 2022 Oct. Mov Disord Clin Pract. 2022. PMID: 36247901 Free PMC article.

6

Lead encephalopathy in an infant mimicking a neurometabolic disorder.

Sahu JK, Sharma S, Kamate M, Kumar A, Gulati S, Kabra M, Kalra V. Sahu JK, et al. Among authors: kamate m. J Child Neurol. 2010 Mar;25(3):390-2. doi: 10.1177/0883073809338625. Epub 2009 Jul 25. J Child Neurol. 2010. PMID: 19633332

7

Parenchymal brain cysts in Schimmelpenning-Feuerstein-Mims syndrome.

Kamate M, Dumale A, Hattiholi V. Kamate M, et al. Neurol India. 2009 Mar-Apr;57(2):225-6. doi: 10.4103/0028-3886.51310. Neurol India. 2009. PMID: 19439869 Free article. No abstract available.

8

Molecular and structural analysis of metachromatic leukodystrophy patients in Indian population.

Shukla P, Vasisht S, Srivastava R, Gupta N, Ghosh M, Kumar M, Sharma R, Gupta AK, Kaur P, Kamate M, Gulati S, Kalra V, Phadke S, Singhi P, Dherai AJ, Kabra M. Shukla P, et al. Among authors: kamate m. J Neurol Sci. 2011 Feb 15;301(1-2):38-45. doi: 10.1016/j.jns.2010.11.007. Epub 2010 Dec 16. J Neurol Sci. 2011. PMID: 21167507

9

Giant axonal neuropathy: a rare inherited neuropathy with simple clinical clues.

Kamate M, Ramakrishna S, Kambali S, Mahadevan A. Kamate M, et al. BMJ Case Rep. 2014 Sep 12;2014:bcr2014204481. doi: 10.1136/bcr-2014-204481. BMJ Case Rep. 2014. PMID: 25216920 Free PMC article.

10

The Genomic Landscape of Wilson Disease in a Pan India Disease Cohort and Population-Scale Data.

Kumar M, Sharma S, Pandey S, Mammayil G, Pala Kuzhiyil A, Sreesh S, Arakkal R, Radhakrishnan DM, Rajan R, Amalnath D, Gulati R, Tayade N, Sadasivan S, Valsan A, Menon J, Kamate M, Mathur SK, Mahadevan R, Dhingra B, Rajan R, Singh K, Shalimar, Geevarghese SK, Kumar VS, Menachery J, Aliyar A, Bhoyar RC, Jolly B, Jain A, Vittal Rangan A, Moitra T, Mhaske A, Gupta V, Senthivel V, Mishra A, Saini A, Gaharwar U, Sivasubbu S, Scaria V, B K B. Kumar M, et al. Among authors: kamate m. Mov Disord Clin Pract. 2024 Nov 13. doi: 10.1002/mdc3.14266. Online ahead of print. Mov Disord Clin Pract. 2024. PMID: 39535360

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