Srivastava A - Search Results

1

Novel PANK2 Variant in Asian Indians with Atypical Pantothenate Kinase Associated Neurodegeneration.

Saini A, Holla VV, Kalikavil Puthanveedu D, Mehta S, Elavarasi A, Pillai KS, Mohapatra P, Kumari R, Bari S, Singh I, Cherian A, Krishnan S, Radhakrishnan DM, Agarwal A, Garg D, Garg K, Singh M, Garg A, Muthusamy B, Lal V, Kishore A, Pal PK, Srivastava A, Faruq M, Rajan R. Saini A, et al. Among authors: srivastava a. Mov Disord. 2024 May;39(5):920-923. doi: 10.1002/mds.29737. Epub 2024 Mar 20. Mov Disord. 2024. PMID: 38506547 No abstract available.

2

SCA-LSVD: a repeat-oriented locus-specific variation database for genotype to phenotype correlations in spinocerebellar ataxias.

Faruq M, Scaria V, Singh I, Tyagi S, Srivastava AK, Mukerji M. Faruq M, et al. Hum Mutat. 2009 Jul;30(7):1037-42. doi: 10.1002/humu.21006. Hum Mutat. 2009. PMID: 19370769

3

North and South Indian populations share a common ancestral origin of Friedreich's ataxia but vary in age of GAA repeat expansion.

Singh I, Faruq M, Mukherjee O, Jain S, Pal PK, Srivastav MV, Behari M, Srivastava AK, Mukerji M. Singh I, et al. Ann Hum Genet. 2010 May;74(3):202-10. doi: 10.1111/j.1469-1809.2010.00569.x. Epub 2010 Mar 31. Ann Hum Genet. 2010. PMID: 20374234

4

Effect of successful epilepsy surgery on subjective and objective sleep parameters--a prospective study.

Zanzmera P, Shukla G, Gupta A, Goyal V, Srivastava A, Garg A, Bal CS, Suri A, Behari M. Zanzmera P, et al. Among authors: srivastava a. Sleep Med. 2013 Apr;14(4):333-8. doi: 10.1016/j.sleep.2012.11.017. Epub 2013 Feb 6. Sleep Med. 2013. PMID: 23395512

5

Novel mutations in typical and atypical genetic loci through exome sequencing in autosomal recessive cerebellar ataxia families.

Faruq M, Narang A, Kumari R, Pandey R, Garg A, Behari M, Dash D, Srivastava AK, Mukerji M. Faruq M, et al. Among authors: srivastava ak. Clin Genet. 2014 Oct;86(4):335-41. doi: 10.1111/cge.12279. Epub 2013 Oct 13. Clin Genet. 2014. PMID: 24102492

6

Identification of FXTAS presenting with SCA 12 like phenotype in India.

Faruq M, Srivastava AK, Suroliya V, Kumar D, Garg A, Shukla G, Behari M. Faruq M, et al. Among authors: srivastava ak. Parkinsonism Relat Disord. 2014 Oct;20(10):1089-93. doi: 10.1016/j.parkreldis.2014.07.001. Epub 2014 Jul 17. Parkinsonism Relat Disord. 2014. PMID: 25085749

7

Spinocerebellar ataxia 7 (SCA7) in Indian population: predilection of ATXN7-CAG expansion mutation in an ethnic population.

Faruq M, Srivastava AK, Singh S, Gupta R, Dada T, Garg A, Behari M, Mukerji M. Faruq M, et al. Among authors: srivastava ak. Indian J Med Res. 2015 Feb;141(2):187-98. doi: 10.4103/0971-5916.155556. Indian J Med Res. 2015. PMID: 25900954 Free PMC article.

8

Investigation of mitochondrial DNA variations among Indian Friedreich's ataxia (FRDA) patients.

Singh I, Faruq M, Padma MV, Goyal V, Behari M, Grover A, Mukerji M, Srivastava AK. Singh I, et al. Among authors: srivastava ak. Mitochondrion. 2015 Nov;25:1-5. doi: 10.1016/j.mito.2015.08.003. Epub 2015 Aug 29. Mitochondrion. 2015. PMID: 26321457

9

Iron related hemochromatosis (HFE) gene mutations in Friedreich Ataxia patients.

Singh I, Shakya S, Singh RK, Ahmad I, Goyal V, Shukla G, Srivastava MV, Faruq M, Srivastava AK. Singh I, et al. Parkinsonism Relat Disord. 2017 Jan;34:71-72. doi: 10.1016/j.parkreldis.2016.10.015. Epub 2016 Oct 19. Parkinsonism Relat Disord. 2017. PMID: 27814974 No abstract available.

10

Clinical behaviour of spinocerebellar ataxia type 12 and intermediate length abnormal CAG repeats in PPP2R2B.

Srivastava AK, Takkar A, Garg A, Faruq M. Srivastava AK, et al. Brain. 2017 Jan;140(1):27-36. doi: 10.1093/brain/aww269. Epub 2016 Nov 17. Brain. 2017. PMID: 27864267

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

7,371 results

Search Page

Filters