Grewal RP - 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: grewal rp. J Clin Neuromuscul Dis. 2019 Jun;20(4):214-216. doi: 10.1097/CND.0000000000000237. J Clin Neuromuscul Dis. 2019. PMID: 31135626

2

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: grewal rp. J Clin Neuromuscul Dis. 2018 Jun;19(4):228-231. doi: 10.1097/CND.0000000000000202. J Clin Neuromuscul Dis. 2018. PMID: 29794579

3

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

Peddareddygari LR, Oberoi K, Grewal RP. Peddareddygari LR, et al. Among authors: grewal rp. 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.

4

Identification of Novel Mutations in Spatacsin and Apolipoprotein B Genes in a Patient with Spastic Paraplegia and Hypobetalipoproteinemia.

Peddareddygari LR, Grewal RP. Peddareddygari LR, et al. Among authors: grewal rp. Case Rep Genet. 2015;2015:219691. doi: 10.1155/2015/219691. Epub 2015 May 7. Case Rep Genet. 2015. PMID: 26064709 Free PMC article.

5

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: grewal rp. 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.

6

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. 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.

7

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: grewal rp. 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.

8

Genotype phenotype analysis in a family carrying truncating mutations in the titin gene.

Peddareddygari LR, Baisre-de León A, Grewal RP. Peddareddygari LR, et al. Among authors: grewal rp. Acta Myol. 2021 Mar 31;40(1):61-65. doi: 10.36185/2532-1900-043. eCollection 2021 Mar. Acta Myol. 2021. PMID: 33870097 Free PMC article.

9

Clinical and Genetic Analysis of a Patient with CMT4J.

Peddareddygari LR, Grewal RP. Peddareddygari LR, et al. Among authors: grewal rp. Neurol Int. 2022 Feb 10;14(1):207-211. doi: 10.3390/neurolint14010017. Neurol Int. 2022. PMID: 35225887 Free PMC article.

10

Intrafamilial Phenotypic Variability Associated with the I1739V Mutation in the SCN9A Gene.

Peddareddygari LR, Grewal RP. Peddareddygari LR, et al. Among authors: grewal rp. Case Rep Neurol. 2021 Feb 25;13(1):135-139. doi: 10.1159/000513561. eCollection 2021 Jan-Apr. Case Rep Neurol. 2021. PMID: 35949357 Free PMC article.

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