Kamate M - Search Results

1

A Low-Excretor Biochemical Phenotype of Glutaric Aciduria Type I: Identification of Novel Mutations in the Glutaryl CoA Dehydrogenase Gene and Review of Literature from India.

Shaik M, Kamate M, Kruthika-Vinod TP, Vedamurthy AB. Shaik M, et al. Among authors: kamate m. Ann Indian Acad Neurol. 2020 Sep-Oct;23(5):724-726. doi: 10.4103/aian.AIAN_188_19. Epub 2020 Dec 8. Ann Indian Acad Neurol. 2020. PMID: 33623287 Free PMC article. No abstract available.

2

Central nervous system inflammatory demyelinating disorders of childhood.

Kamate M, Chetal V, Tonape V, Mahantshetti N, Hattiholi V. Kamate M, et al. Ann Indian Acad Neurol. 2010 Oct;13(4):289-92. doi: 10.4103/0972-2327.74204. Ann Indian Acad Neurol. 2010. PMID: 21264138 Free PMC article.

3

Authors' reply.

Kamate M, Chetal V, Tonape V, Mahantshetti N, Hattiholi V. Kamate M, et al. Ann Indian Acad Neurol. 2011 Jul;14(3):222-3. Ann Indian Acad Neurol. 2011. PMID: 22028545 Free PMC article. No abstract available.

4

Glutaric aciduria type I: A treatable neurometabolic disorder.

Kamate M, Patil V, Chetal V, Darak P, Hattiholi V. Kamate M, et al. Ann Indian Acad Neurol. 2012 Jan;15(1):31-4. doi: 10.4103/0972-2327.93273. Ann Indian Acad Neurol. 2012. PMID: 22412270 Free PMC article.

5

A case of hereditary sensory autonomic neuropathy type IV.

Prashanth GP, Kamate M. Prashanth GP, et al. Among authors: kamate m. Ann Indian Acad Neurol. 2012 Apr;15(2):134-6. doi: 10.4103/0972-2327.94999. Ann Indian Acad Neurol. 2012. PMID: 22566729 Free PMC article.

6

Single Lysis-Salting Out Method of Genomic DNA Extraction From Dried Blood Spots.

Shaik M, Shivanna DK, Kamate M, Ab V, Tp KV. Shaik M, et al. Among authors: kamate m. J Clin Lab Anal. 2016 Nov;30(6):1009-1012. doi: 10.1002/jcla.21972. Epub 2016 Apr 13. J Clin Lab Anal. 2016. PMID: 27074880 Free PMC article.

7

Acute encephalopathy: A novel presentation of mineralizing microangiopathy of childhood.

Kamate M, Malhotra M, Gangamma DH, Hattiholi V. Kamate M, et al. Ann Indian Acad Neurol. 2016 Oct-Dec;19(4):528-530. doi: 10.4103/0972-2327.194465. Ann Indian Acad Neurol. 2016. PMID: 27994370 Free PMC article. No abstract available.

8

Genetic Screening of Selected Disease-Causing Mutations in Glutaryl-CoA Dehydrogenase Gene among Indian Patients with Glutaric Aciduria Type I.

Tp KV, Muntaj S, Devaraju KS, Kamate M, Vedamurthy AB. Tp KV, et al. Among authors: kamate m. J Pediatr Genet. 2017 Sep;6(3):142-148. doi: 10.1055/s-0037-1599202. Epub 2017 Mar 7. J Pediatr Genet. 2017. PMID: 28794906 Free PMC article.

9

Cysts in White Matter: A Novel Neuroimaging Finding in Infantile GM1 Gangliosidosis.

Kamate M. Kamate M. Ann Indian Acad Neurol. 2018 Jan-Mar;21(1):82-83. doi: 10.4103/aian.AIAN_343_17. Ann Indian Acad Neurol. 2018. PMID: 29720806 Free PMC article. No abstract available.

10

Is Expanded Newborn Screening Adequate to Detect Indian Biochemical Low Excretor Phenotype Patients of Glutaric Aciduria Type I?

Shaik M, T P KV, Kamate M, A B V. Shaik M, et al. Among authors: kamate m. Indian J Pediatr. 2019 Nov;86(11):995-1001. doi: 10.1007/s12098-019-03017-z. Epub 2019 Jul 13. Indian J Pediatr. 2019. PMID: 31302874

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