Vengalil S - Search Results

1

Novel variants broaden the phenotypic spectrum of PLEKHG5-associated neuropathies.

Chen Z, Maroofian R, Başak AN, Shingavi L, Karakaya M, Efthymiou S, Gustavsson EK, Meier L, Polavarapu K, Vengalil S, Preethish-Kumar V, Nandeesh BN, Gökçe Güneş N, Akan O, Candan F, Schrank B, Zuchner S, Murphy D, Kapoor M, Ryten M, Wirth B, Reilly MM, Nalini A, Houlden H, Sarraf P. Chen Z, et al. Among authors: vengalil s. Eur J Neurol. 2021 Apr;28(4):1344-1355. doi: 10.1111/ene.14649. Epub 2020 Dec 17. Eur J Neurol. 2021. PMID: 33220101

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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