Purushottam M - Search Results

1

Duchenne Muscular Dystrophy and Becker Muscular Dystrophy Confirmed by Multiplex Ligation-Dependent Probe Amplification: Genotype-Phenotype Correlation in a Large Cohort.

Vengalil S, Preethish-Kumar V, Polavarapu K, Mahadevappa M, Sekar D, Purushottam M, Thomas PT, Nashi S, Nalini A. Vengalil S, et al. Among authors: purushottam m. J Clin Neurol. 2017 Jan;13(1):91-97. doi: 10.3988/jcn.2017.13.1.91. J Clin Neurol. 2017. PMID: 28079318 Free PMC article.

2

A cross ancestry genetic study of psychiatric disorders from India.

Holla B, Mahadevan J, Ganesh S, Sud R, Janardhanan M, Balachander S, Strom N, Mattheisen M, Sullivan PF, Huang H, Zandi P, Benegal V, Reddy YJ, Jain S; cVEDA collaborators; ADBS-CBM consortium; iPSYCH OCD consortium; NORDiC OCD & Related Disorders Consortium; Purushottam M, Viswanath B. Holla B, et al. Among authors: purushottam m. medRxiv [Preprint]. 2024 Apr 27:2024.04.25.24306377. doi: 10.1101/2024.04.25.24306377. medRxiv. 2024. PMID: 38712191 Free PMC article. Preprint.

3

Whole exome sequencing in dense families suggests genetic pleiotropy amongst Mendelian and complex neuropsychiatric syndromes.

Ganesh S, Vemula A, Bhattacharjee S, Mathew K, Ithal D, Navin K, Nadella RK, Viswanath B, Sullivan PF; ADBS Consortium; Jain S, Purushottam M. Ganesh S, et al. Among authors: purushottam m. Sci Rep. 2022 Dec 7;12(1):21128. doi: 10.1038/s41598-022-25664-7. Sci Rep. 2022. PMID: 36476812 Free PMC article.

4

Paternal inheritance or a de novo mutation in a Duchenne Muscular Dystrophy pedigree from South India.

Purushottam M, Murthy AR, Shubha GN, Gayathri N, Nalini A. Purushottam M, et al. J Neurol Sci. 2008 May 15;268(1-2):179-82. doi: 10.1016/j.jns.2007.10.025. Epub 2007 Nov 26. J Neurol Sci. 2008. PMID: 18031759

5

Deletion analysis of spinal muscular atrophy in southern Indian population.

Swaminathan B, Shylashree S, Purushottam M, Taly AB, Nalini A. Swaminathan B, et al. Among authors: purushottam m. Neurol India. 2008 Jul-Sep;56(3):348-51. doi: 10.4103/0028-3886.43454. Neurol India. 2008. PMID: 18974562 Free article.

6

Duchenne muscular dystrophy: a clinical, histopathological and genetic study at a neurology tertiary care center in Southern India.

Swaminathan B, Shubha GN, Shubha D, Murthy AR, Kiran Kumar HB, Shylashree S, Gayathri N, Jamuna R, Jain S, Purushottam M, Nalini A. Swaminathan B, et al. Among authors: purushottam m. Neurol India. 2009 Nov-Dec;57(6):734-8. doi: 10.4103/0028-3886.59468. Neurol India. 2009. PMID: 20139501 Free article.

7

MLPA identification of dystrophin mutations and in silico evaluation of the predicted protein in dystrophinopathy cases from India.

Deepha S, Vengalil S, Preethish-Kumar V, Polavarapu K, Nalini A, Gayathri N, Purushottam M. Deepha S, et al. Among authors: purushottam m. BMC Med Genet. 2017 Jun 13;18(1):67. doi: 10.1186/s12881-017-0431-6. BMC Med Genet. 2017. PMID: 28610567 Free PMC article.

8

Deep Intronic FGF14 GAA Repeat Expansion in Late-Onset Cerebellar Ataxia.

Pellerin D, Danzi MC, Wilke C, Renaud M, Fazal S, Dicaire MJ, Scriba CK, Ashton C, Yanick C, Beijer D, Rebelo A, Rocca C, Jaunmuktane Z, Sonnen JA, Larivière R, Genís D, Molina Porcel L, Choquet K, Sakalla R, Provost S, Robertson R, Allard-Chamard X, Tétreault M, Reiling SJ, Nagy S, Nishadham V, Purushottam M, Vengalil S, Bardhan M, Nalini A, Chen Z, Mathieu J, Massie R, Chalk CH, Lafontaine AL, Evoy F, Rioux MF, Ragoussis J, Boycott KM, Dubé MP, Duquette A, Houlden H, Ravenscroft G, Laing NG, Lamont PJ, Saporta MA, Schüle R, Schöls L, La Piana R, Synofzik M, Zuchner S, Brais B. Pellerin D, et al. Among authors: purushottam m. N Engl J Med. 2023 Jan 12;388(2):128-141. doi: 10.1056/NEJMoa2207406. Epub 2022 Dec 14. N Engl J Med. 2023. PMID: 36516086 Free PMC article.

9

Psychiatric morbidity and poor follow-up underlie suboptimal functional and survival outcomes in Huntington's disease.

Ratna N, Kamble NL, Venkatesh SD, Purushottam M, Pal PK, Jain S. Ratna N, et al. Among authors: purushottam m. BMC Neurol. 2020 Mar 12;20(1):87. doi: 10.1186/s12883-020-01671-x. BMC Neurol. 2020. PMID: 32164608 Free PMC article.

10

SCA 1, SCA 2 & SCA 3/MJD mutations in ataxia syndromes in southern India.

Krishna N, Mohan S, Yashavantha BS, Rammurthy A, Kiran Kumar HB, Mittal U, Tyagi S, Mukerji M, Jain S, Pal PK, Purushottam M. Krishna N, et al. Among authors: purushottam m. Indian J Med Res. 2007 Nov;126(5):465-70. Indian J Med Res. 2007. PMID: 18160752 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

105 results

Search Page

Filters