Oberoi K - Search Results

1

Adult Diagnosis of Type 1 Fiber Predominance Myopathy Caused by Novel Mutations in the RYR1 Gene.

Peddareddygari LR, Oberoi K, Sharer LR, Grewal RP. Peddareddygari LR, et al. Among authors: oberoi k. J Clin Neuromuscul Dis. 2019 Jun;20(4):214-216. doi: 10.1097/CND.0000000000000237. J Clin Neuromuscul Dis. 2019. PMID: 31135626

2

Congenital insensitivity to pain: a case report and review of the literature.

Peddareddygari LR, Oberoi K, Grewal RP. Peddareddygari LR, et al. Among authors: oberoi k. Case Rep Neurol Med. 2014;2014:141953. doi: 10.1155/2014/141953. Epub 2014 Sep 18. Case Rep Neurol Med. 2014. PMID: 25309764 Free PMC article.

3

Factors Affecting Phenotype Variability in a Family with CMT2B: Gender and LRSAM1 Genotype.

Peddareddygari LR, Oberoi K, Vellore JR, Grewal RP. Peddareddygari LR, et al. Among authors: oberoi k. Case Rep Neurol. 2016 Jun 6;8(2):120-6. doi: 10.1159/000446872. eCollection 2016 May-Aug. Case Rep Neurol. 2016. PMID: 27462242 Free PMC article.

4

Clinical and Genetic Analysis of an Asian Indian Family with Charcot-Marie-Tooth Disease Type 4C.

Grewal RP, Oberoi K, Peddareddygari LR. Grewal RP, et al. Among authors: oberoi k. Case Rep Neurol. 2018 Feb 9;10(1):38-44. doi: 10.1159/000486589. eCollection 2018 Jan-Apr. Case Rep Neurol. 2018. PMID: 29515423 Free PMC article.

5

Novel Mutation in Anoctamin 5 Gene Causing Limb-Girdle Muscular Dystrophy 2L.

Peddareddygari LR, Oberoi K, Baisre-De Leon A, Grewal RP. Peddareddygari LR, et al. Among authors: oberoi k. J Clin Neuromuscul Dis. 2018 Jun;19(4):228-231. doi: 10.1097/CND.0000000000000202. J Clin Neuromuscul Dis. 2018. PMID: 29794579

6

Limb Girdle Muscular Dystrophy due to Digenic Inheritance of DES and CAPN3 Mutations.

Peddareddygari LR, Oberoi K, Grewal RP. Peddareddygari LR, et al. Among authors: oberoi k. Case Rep Neurol. 2018 Sep 18;10(3):272-278. doi: 10.1159/000492664. eCollection 2018 Sep-Dec. Case Rep Neurol. 2018. PMID: 30323756 Free PMC article.

7

A Novel Duplication Mutation in the Myelin Protein Zero Gene Causing Mild, Nonprogressive Demyelinating Neuropathy.

Oberoi K, Grewal AS, Peddareddygari LR. Oberoi K, et al. Case Rep Neurol. 2020 Jul 29;12(2):255-259. doi: 10.1159/000509266. eCollection 2020 May-Aug. Case Rep Neurol. 2020. PMID: 32884544 Free PMC article.

8

Novel Titin Gene Mutation Causing Autosomal Dominant Limb-Girdle Muscular Dystrophy.

Peddareddygari LR, Oberoi K, Grewal RP. Peddareddygari LR, et al. Among authors: oberoi k. Cureus. 2022 Oct 21;14(10):e30550. doi: 10.7759/cureus.30550. eCollection 2022 Oct. Cureus. 2022. PMID: 36415435 Free PMC article.

9

Complicated SPG4 presenting with recurrent urinary tract infection.

Oberoi K, Grewal KS, Reddy Peddareddygari L. Oberoi K, et al. J Community Hosp Intern Med Perspect. 2020 Aug 2;10(4):369-370. doi: 10.1080/20009666.2020.1785609. J Community Hosp Intern Med Perspect. 2020. PMID: 32850101 Free PMC article.

10

Bruton's Tyrosine Kinase (BTK) Inhibitors and Autoimmune Diseases: Making Sense of BTK Inhibitor Specificity Profiles and Recent Clinical Trial Successes and Failures.

Ringheim GE, Wampole M, Oberoi K. Ringheim GE, et al. Among authors: oberoi k. Front Immunol. 2021 Nov 3;12:662223. doi: 10.3389/fimmu.2021.662223. eCollection 2021. Front Immunol. 2021. PMID: 34803999 Free PMC article. Review.

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