Verma S - Search Results

1

Phenotypic continuum of NFU1-related disorders.

Kaiyrzhanov R, Zaki MS, Lau T, Sen S, Azizimalamiri R, Zamani M, Sayin GY, Hilander T, Efthymiou S, Chelban V, Brown R, Thompson K, Scarano MI, Ganesh J, Koneev K, Gülaçar IM, Person R, Sadykova D, Maidyrov Y, Seifi T, Zadagali A, Bernard G, Allis K, Elloumi HZ, Lindy A, Taghiabadi E, Verma S, Logan R, Kirmse B, Bai R, Khalaf SM, Abdel-Hamid MS, Sedaghat A, Shariati G, Issa M, Zeighami J, Elbendary HM, Brown G, Taylor RW, Galehdari H, Gleeson JJ, Carroll CJ, Cowan JA, Moreno-De-Luca A, Houlden H, Maroofian R. Kaiyrzhanov R, et al. Among authors: verma s. Ann Clin Transl Neurol. 2022 Dec;9(12):2025-2035. doi: 10.1002/acn3.51679. Epub 2022 Oct 18. Ann Clin Transl Neurol. 2022. PMID: 36256512 Free PMC article.

2

Expanding the genotype-phenotype correlation of childhood sensory polyneuropathy of genetic origin.

Chakravorty S, Logan R, Elson MJ, Luke RR, Verma S. Chakravorty S, et al. Among authors: verma s. Sci Rep. 2020 Sep 30;10(1):16184. doi: 10.1038/s41598-020-73219-5. Sci Rep. 2020. PMID: 32999401 Free PMC article.

3

Georgia state spinal muscular atrophy newborn screening experience: Screening assay performance and early clinical outcomes.

Elkins K, Wittenauer A, Hagar AF, Logan R, Sekul E, Xiang Y, Verma S, Wilcox WR. Elkins K, et al. Among authors: verma s. Am J Med Genet C Semin Med Genet. 2022 Jun;190(2):187-196. doi: 10.1002/ajmg.c.32003. Epub 2022 Sep 26. Am J Med Genet C Semin Med Genet. 2022. PMID: 36164257

4

Childhood-Onset Hereditary Spastic Paraplegia (HSP): A Case Series and Review of Literature.

Panwala TF, Garcia-Santibanez R, Vizcarra JA, Garcia AG, Verma S. Panwala TF, et al. Among authors: verma s. Pediatr Neurol. 2022 May;130:7-13. doi: 10.1016/j.pediatrneurol.2022.02.007. Epub 2022 Mar 3. Pediatr Neurol. 2022. PMID: 35303589 Review.

5

PEBAT, an Intriguing Neurodegenerative Tubulinopathy Caused by a Novel Homozygous Variant in TBCD: A Case Series and Literature Review.

Ocampo-Chih C, Dennis H, Lall N, Pham N, Liang B, Verma S, Neira Fresneda J. Ocampo-Chih C, et al. Among authors: verma s. Pediatr Neurol. 2023 Feb;139:59-64. doi: 10.1016/j.pediatrneurol.2022.11.006. Epub 2022 Nov 23. Pediatr Neurol. 2023. PMID: 36527993 Review.

6

COL6A and LAMA2 Mutation Congenital Muscular Dystrophy: A Clinical and Electrophysiological Study.

Verma S, Goyal P, Guglani L, Peinhardt C, Pelzek D, Barkhaus PE. Verma S, et al. J Clin Neuromuscul Dis. 2018 Mar;19(3):108-116. doi: 10.1097/CND.0000000000000198. J Clin Neuromuscul Dis. 2018. PMID: 29465610

7

Novel PLEC gene variants causing congenital myasthenic syndrome.

Gonzalez Garcia A, Tutmaher MS, Upadhyayula SR, Sanchez Russo R, Verma S. Gonzalez Garcia A, et al. Among authors: verma s. Muscle Nerve. 2019 Dec;60(6):E40-E43. doi: 10.1002/mus.26703. Epub 2019 Oct 23. Muscle Nerve. 2019. PMID: 31509265 No abstract available.

8

Superficial fibular nerve sensory nerve conduction study in children.

Verma S, Pochiraju S. Verma S, et al. Muscle Nerve. 2016 Oct;54(4):808-9. doi: 10.1002/mus.25181. Epub 2016 May 27. Muscle Nerve. 2016. PMID: 27158948 No abstract available.

9

Jitter values in infants.

Verma S, Lin J. Verma S, et al. Muscle Nerve. 2017 Jan;55(1):140. doi: 10.1002/mus.25239. Epub 2016 Jul 19. Muscle Nerve. 2017. PMID: 27386822 No abstract available.

10

Amifampridine phosphate in congenital myasthenic syndrome.

Verma S, Mazell SN, Shah DA. Verma S, et al. Muscle Nerve. 2016 Oct;54(4):809-10. doi: 10.1002/mus.25230. Epub 2016 Jul 19. Muscle Nerve. 2016. PMID: 27348204 No abstract available.

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