Khadilkar SV - Search Results

1

Clinical and Genomic Evaluation of 207 Genetic Myopathies in the Indian Subcontinent.

Chakravorty S, Nallamilli BRR, Khadilkar SV, Singla MB, Bhutada A, Dastur R, Gaitonde PS, Rufibach LE, Gloster L, Hegde M. Chakravorty S, et al. Among authors: khadilkar sv. Front Neurol. 2020 Nov 5;11:559327. doi: 10.3389/fneur.2020.559327. eCollection 2020. Front Neurol. 2020. PMID: 33250842 Free PMC article.

2

Clinical & genetic analysis of four patients with distal upper limb spinal muscular atrophy.

Hegde MR, Chong B, Stevenson C, Laing NG, Khadilkar S, Love DR. Hegde MR, et al. Indian J Med Res. 2001 Oct;114:141-7. Indian J Med Res. 2001. PMID: 11921836

3

Correlation between deletion patterns of SMN and NAIP genes and the clinical features of spinal muscular atrophy in Indian patients.

Dastur RS, Gaitonde PS, Khadilkar SV, Udani VP, Nadkarni JJ. Dastur RS, et al. Among authors: khadilkar sv. Neurol India. 2006 Sep;54(3):255-9. doi: 10.4103/0028-3886.27147. Neurol India. 2006. PMID: 16936383 Free article.

4

Severe childhood autosomal recessive muscular dystrophy, mental subnormality and chorea.

Khadilkar SV, Menezes KM, Singh RK, Hegde MR. Khadilkar SV, et al. Neurol India. 2006 Sep;54(3):293-5. doi: 10.4103/0028-3886.27157. Neurol India. 2006. PMID: 16936393 Free article.

5

Duchenne and Becker muscular dystrophies: an Indian update on genetics and rehabilitation.

Nadkarni JJ, Dastur RS, Viswanathan V, Gaitonde PS, Khadilkar SV. Nadkarni JJ, et al. Among authors: khadilkar sv. Neurol India. 2008 Jul-Sep;56(3):248-53. doi: 10.4103/0028-3886.43442. Neurol India. 2008. PMID: 18974550 Free article. Review.

6

Becker muscular dystrophy in Indian patients: analysis of dystrophin gene deletion patterns.

Dastur RS, Gaitonde PS, Khadilkar SV, Nadkarni JJ. Dastur RS, et al. Among authors: khadilkar sv. Neurol India. 2008 Jul-Sep;56(3):374-8. doi: 10.4103/0028-3886.40961. Neurol India. 2008. PMID: 18974567 Free article.

7

Twenty-two year follow-up of an Indian family with dysferlinopathy-clinical, immunocytochemical, western blotting and genetic features.

Khadilkar SV, Singh RK, Agarwal P, Krahn M, Levy N. Khadilkar SV, et al. Neurol India. 2008 Jul-Sep;56(3):388-90. doi: 10.4103/0028-3886.43459. Neurol India. 2008. PMID: 18974570 Free article.

8

Spectrum of mutations in sarcoglycan genes in the Mumbai region of western India: high prevalence of 525del T.

Khadilkar SV, Singh RK, Hegde M, Urtizberea A, Love DR, Chong B. Khadilkar SV, et al. Neurol India. 2009 Jul-Aug;57(4):406-10. doi: 10.4103/0028-3886.55603. Neurol India. 2009. PMID: 19770540 Free article.

9

Identification of deletions and duplications in the Duchenne muscular dystrophy gene and female carrier status in western India using combined methods of multiplex polymerase chain reaction and multiplex ligation-dependent probe amplification.

Dastur RS, Kachwala MY, Khadilkar SV, Hegde MR, Gaitonde PS. Dastur RS, et al. Among authors: khadilkar sv. Neurol India. 2011 Nov-Dec;59(6):803-9. doi: 10.4103/0028-3886.91355. Neurol India. 2011. PMID: 22234189 Free article.

10

Ancestral founder mutations in calpain-3 in the Indian Agarwal community: historical, clinical, and molecular perspective.

Ankala A, Kohn JN, Dastur R, Gaitonde P, Khadilkar SV, Hegde MR. Ankala A, et al. Among authors: khadilkar sv. Muscle Nerve. 2013 Jun;47(6):931-7. doi: 10.1002/mus.23763. Epub 2013 May 11. Muscle Nerve. 2013. PMID: 23666804

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