Nalini A - Search Results

1

Baskar D, Vengalil S, Nashi S, Bardhan M, Srivastava K, Sanka SB, Polavarapu K, Menon D, Preethish-Kumar V, Padmanabha H, Arunachal G, Nalini A. Baskar D, et al. Among authors: nalini a. J Neuromuscul Dis. 2023;10(4):727-730. doi: 10.3233/JND-230017. J Neuromuscul Dis. 2023. PMID: 37154181 Free PMC article.

2

Novel TCAP mutation c.32C>A causing limb girdle muscular dystrophy 2G.

Francis A, Sunitha B, Vinodh K, Polavarapu K, Katkam SK, Modi S, Bharath MM, Gayathri N, Nalini A, Thangaraj K. Francis A, et al. Among authors: nalini a. PLoS One. 2014 Jul 23;9(7):e102763. doi: 10.1371/journal.pone.0102763. eCollection 2014. PLoS One. 2014. PMID: 25055047 Free PMC article.

3

Distal bimelic amyotrophy (DBMA): Phenotypically distinct but identical on cervical spine MR imaging with brachial monomelic amyotrophy/Hirayama disease.

Preethish-Kumar V, Nalini A, Singh RJ, Saini J, Prasad C, Polavarapu K, Thennarasu K. Preethish-Kumar V, et al. Among authors: nalini a. Amyotroph Lateral Scler Frontotemporal Degener. 2015;16(5-6):338-44. doi: 10.3109/21678421.2015.1039546. Epub 2015 May 12. Amyotroph Lateral Scler Frontotemporal Degener. 2015. PMID: 25967543

4

A prospective study on the immunophenotypic characterization of limb girdle muscular dystrophies 2 in India.

Nalini A, Polavarapu K, Sunitha B, Kulkarni S, Gayathri N, Srinivas Bharath MM, Modi S, Preethish-Kumar V. Nalini A, et al. Neurol India. 2015 Jul-Aug;63(4):548-60. doi: 10.4103/0028-3886.162048. Neurol India. 2015. PMID: 26238890 Free article.

5

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: nalini a. 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

6

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: nalini a. 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

7

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: nalini a. 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

8

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: nalini a. 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

9

Missing genetic variations in GNE myopathy: rearrangement hotspots encompassing 5'UTR and founder allele.

Zhu W, Mitsuhashi S, Yonekawa T, Noguchi S, Huei JC, Nalini A, Preethish-Kumar V, Yamamoto M, Murakata K, Mori-Yoshimura M, Kamada S, Yahikozawa H, Karasawa M, Kimura S, Yamashita F, Nishino I. Zhu W, et al. Among authors: nalini a. J Hum Genet. 2017 Feb;62(2):159-166. doi: 10.1038/jhg.2016.134. Epub 2016 Nov 10. J Hum Genet. 2017. PMID: 27829678

10

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. Among authors: nalini a. 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.

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