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Page 1
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: suroliya v. 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
Tumor necrosis factor-alpha (- 308G/A, + 488G/A, - 857C/T and -1031 T/C) gene polymorphisms and risk of ischemic stroke in north Indian population: A hospital based case-control study.
Kumar P, Kumar A, Misra S, Sagar R, Faruq M, Suroliya V, Vivekanandhan S, Srivastava AK, Prasad K. Kumar P, et al. Among authors: suroliya v. Meta Gene. 2015 Nov 17;7:34-9. doi: 10.1016/j.mgene.2015.11.003. eCollection 2016 Feb. Meta Gene. 2015. PMID: 26862479 Free PMC article.
Mitochondrial DNA haplogroups and age at onset of Machado-Joseph disease/spinocerebellar ataxia type 3: a study in patients from multiple populations.
Ramos A, Planchat M, Vieira Melo AR, Raposo M, Shamim U, Suroliya V, Srivastava AK, Faruq M, Morino H, Ohsawa R, Kawakami H, Bannach Jardim L, Saraiva-Pereira ML, Vasconcelos J, Santos C, Lima M. Ramos A, et al. Among authors: suroliya v. Eur J Neurol. 2019 Mar;26(3):506-512. doi: 10.1111/ene.13860. Epub 2018 Dec 7. Eur J Neurol. 2019. PMID: 30414314
C9orf72 hexanucleotide repeat expansion in Indian patients with ALS: a common founder and its geographical predilection.
Shamim U, Ambawat S, Singh J, Thomas A, Pradeep-Chandra-Reddy C, Suroliya V, Uppilli B, Parveen S, Sharma P, Chanchal S, Nashi S, Preethish-Kumar V, Vengalil S, Polavarapu K, Keerthipriya M, Mahajan NP, Reddy N, Thomas PT, Sadasivan A, Warrier M, Seth M, Zahra S, Mathur A, Vibha D, Srivastava AK, Nalini A, Faruq M. Shamim U, et al. Among authors: suroliya v. Neurobiol Aging. 2020 Apr;88:156.e1-156.e9. doi: 10.1016/j.neurobiolaging.2019.12.024. Epub 2020 Jan 3. Neurobiol Aging. 2020. PMID: 32035847
Genomic analysis of patients in a South Indian Community with autosomal dominant cortical tremor, myoclonus and epilepsy suggests a founder repeat expansion mutation in the SAMD12 gene.
Mahadevan R, Bhoyar RC, Viswanathan N, Rajagopal RE, Essaki B, Suroliya V, Chelladurai R, Sankaralingam S, Shanmugam G, Vayanakkan S, Shamim U, Mathur A, Jain A, Imran M, Faruq M, Scaria V, Sivasubbu S, Kalyanaraman S. Mahadevan R, et al. Among authors: suroliya v. Brain Commun. 2020 Dec 19;3(1):fcaa214. doi: 10.1093/braincomms/fcaa214. eCollection 2021. Brain Commun. 2020. PMID: 33501421 Free PMC article.
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