Vengalil S - Search Results

1

Whole-exome analyses of congenital muscular dystrophy and congenital myopathy patients from India reveal a wide spectrum of known and novel mutations.

Sanga S, Ghosh A, Kumar K, Polavarapu K, Preethish-Kumar V, Vengalil S, Nashi S, Bardhan M, Arunachal G, Raju S, Gayathri N, Biswas NK, Chakrabarti S, Nalini A, Roy S, Acharya M. Sanga S, et al. Among authors: vengalil s. Eur J Neurol. 2021 Mar;28(3):992-1003. doi: 10.1111/ene.14616. Epub 2020 Nov 26. Eur J Neurol. 2021. PMID: 33124102

2

Proximal and proximo-distal bimelic amyotrophy: Evidence of cervical flexion induced myelopathy.

Preethish-Kumar V, Polavarapu K, Singh RJ, Vengalil S, Prasad C, Verma A, Nalini A. Preethish-Kumar V, et al. Among authors: vengalil s. Amyotroph Lateral Scler Frontotemporal Degener. 2016 Oct-Nov;17(7-8):499-507. doi: 10.3109/21678421.2016.1167912. Epub 2016 Apr 6. Amyotroph Lateral Scler Frontotemporal Degener. 2016. PMID: 27050119

3

Reverse split hand syndrome: Dissociated intrinsic hand muscle atrophy pattern in Hirayama disease/brachial monomelic amyotrophy.

Singh RJ, Preethish-Kumar V, Polavarapu K, Vengalil S, Prasad C, Nalini A. Singh RJ, et al. Among authors: vengalil s. Amyotroph Lateral Scler Frontotemporal Degener. 2017 Feb;18(1-2):10-16. doi: 10.1080/21678421.2016.1223140. Epub 2016 Aug 30. Amyotroph Lateral Scler Frontotemporal Degener. 2017. PMID: 27575868

4

Muscle MRI in Duchenne muscular dystrophy: Evidence of a distinctive pattern.

Polavarapu K, Manjunath M, Preethish-Kumar V, Sekar D, Vengalil S, Thomas P, Sathyaprabha TN, Bharath RD, Nalini A. Polavarapu K, et al. Among authors: vengalil s. Neuromuscul Disord. 2016 Nov;26(11):768-774. doi: 10.1016/j.nmd.2016.09.002. Epub 2016 Sep 5. Neuromuscul Disord. 2016. PMID: 27666775

5

Ankle-Foot Orthosis in Duchenne Muscular Dystrophy: A 4 year Experience in a Multidisciplinary Neuromuscular Disorders Clinic.

Gupta A, Nalini A, Arya SP, Vengalil S, Khanna M, Krishnan R, Taly AB. Gupta A, et al. Among authors: vengalil s. Indian J Pediatr. 2017 Mar;84(3):211-215. doi: 10.1007/s12098-016-2251-7. Epub 2016 Nov 5. Indian J Pediatr. 2017. PMID: 27815810

6

Duchenne Muscular Dystrophy and Becker Muscular Dystrophy Confirmed by Multiplex Ligation-Dependent Probe Amplification: Genotype-Phenotype Correlation in a Large Cohort.

Vengalil S, Preethish-Kumar V, Polavarapu K, Mahadevappa M, Sekar D, Purushottam M, Thomas PT, Nashi S, Nalini A. Vengalil S, et al. J Clin Neurol. 2017 Jan;13(1):91-97. doi: 10.3988/jcn.2017.13.1.91. J Clin Neurol. 2017. PMID: 28079318 Free PMC article.

7

Ventral longitudinal intraspinal fluid collection: Rare presentation as brachial amyotrophy and intracranial hypotension.

Preethish-Kumar V, Vengalil S, Tiwari S, Polavarapu K, Netravathi M, Ramalingaiah AH, Nalini A. Preethish-Kumar V, et al. Among authors: vengalil s. J Spinal Cord Med. 2019 Jan;42(1):45-50. doi: 10.1080/10790268.2017.1314901. Epub 2017 Apr 12. J Spinal Cord Med. 2019. PMID: 28402198 Free PMC article.

8

MLPA identification of dystrophin mutations and in silico evaluation of the predicted protein in dystrophinopathy cases from India.

Deepha S, Vengalil S, Preethish-Kumar V, Polavarapu K, Nalini A, Gayathri N, Purushottam M. Deepha S, et al. Among authors: vengalil s. BMC Med Genet. 2017 Jun 13;18(1):67. doi: 10.1186/s12881-017-0431-6. BMC Med Genet. 2017. PMID: 28610567 Free PMC article.

9

Fatty acid oxidation defects presenting as primary myopathy and prominent dropped head syndrome.

Vengalil S, Preethish-Kumar V, Polavarapu K, Christopher R, Gayathri N, Natarajan A, Manjunath M, Nashi S, Prasad C, Nalini A. Vengalil S, et al. Neuromuscul Disord. 2017 Nov;27(11):986-996. doi: 10.1016/j.nmd.2017.08.004. Epub 2017 Aug 24. Neuromuscul Disord. 2017. PMID: 28927828

10

Intrafamilial phenotypic variations in familial cases of cervical flexion induced myelopathy/Hirayama disease.

Polavarapu K, Preethish-Kumar V, Nashi S, Vengalil S, Prasad C, Bhattacharya K, Verma A, Pruthi N, Bhat DI, Nalini A. Polavarapu K, et al. Among authors: vengalil s. Amyotroph Lateral Scler Frontotemporal Degener. 2018 Feb;19(1-2):38-49. doi: 10.1080/21678421.2017.1374977. Epub 2017 Sep 22. Amyotroph Lateral Scler Frontotemporal Degener. 2018. PMID: 28938856

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