Vedanarayanan V - Search Results

1

Novel mutations in collagen VI genes: expansion of the Bethlem myopathy phenotype.

Scacheri PC, Gillanders EM, Subramony SH, Vedanarayanan V, Crowe CA, Thakore N, Bingler M, Hoffman EP. Scacheri PC, et al. Among authors: vedanarayanan v. Neurology. 2002 Feb 26;58(4):593-602. doi: 10.1212/wnl.58.4.593. Neurology. 2002. PMID: 11865138

2

A novel ryanodine receptor gene mutation causing both cores and rods in congenital myopathy.

Scacheri PC, Hoffman EP, Fratkin JD, Semino-Mora C, Senchak A, Davis MR, Laing NG, Vedanarayanan V, Subramony SH. Scacheri PC, et al. Among authors: vedanarayanan v. Neurology. 2000 Dec 12;55(11):1689-96. doi: 10.1212/wnl.55.11.1689. Neurology. 2000. PMID: 11113224

3

Tick paralysis in children: electrophysiology and possibility of misdiagnosis.

Vedanarayanan VV, Evans OB, Subramony SH. Vedanarayanan VV, et al. Neurology. 2002 Oct 8;59(7):1088-90. doi: 10.1212/wnl.59.7.1088. Neurology. 2002. PMID: 12370471

4

Tick paralysis.

Vedanarayanan V, Sorey WH, Subramony SH. Vedanarayanan V, et al. Semin Neurol. 2004 Jun;24(2):181-4. doi: 10.1055/s-2004-830905. Semin Neurol. 2004. PMID: 15257515 Review.

5

CINRG randomized controlled trial of creatine and glutamine in Duchenne muscular dystrophy.

Escolar DM, Buyse G, Henricson E, Leshner R, Florence J, Mayhew J, Tesi-Rocha C, Gorni K, Pasquali L, Patel KM, McCarter R, Huang J, Mayhew T, Bertorini T, Carlo J, Connolly AM, Clemens PR, Goemans N, Iannaccone ST, Igarashi M, Nevo Y, Pestronk A, Subramony SH, Vedanarayanan VV, Wessel H; CINRG Group. Escolar DM, et al. Among authors: vedanarayanan vv. Ann Neurol. 2005 Jul;58(1):151-5. doi: 10.1002/ana.20523. Ann Neurol. 2005. PMID: 15984021 Clinical Trial.

6

Sequence variation in GAA repeat expansions may cause differential phenotype display in Friedreich's ataxia.

McDaniel DO, Keats B, Vedanarayanan VV, Subramony SH. McDaniel DO, et al. Among authors: vedanarayanan vv. Mov Disord. 2001 Nov;16(6):1153-8. doi: 10.1002/mds.1210. Mov Disord. 2001. PMID: 11748752

7

Treatment of childhood dermatomyositis with high dose intravenous immunoglobulin.

Vedanarayanan V, Subramony SH, Ray LI, Evans OB. Vedanarayanan V, et al. Pediatr Neurol. 1995 Nov;13(4):336-9. doi: 10.1016/0887-8994(95)00195-6. Pediatr Neurol. 1995. PMID: 8771171

8

Lethal neonatal autosomal recessive axonal sensorimotor polyneuropathy.

Vedanarayanan VV, Smith S, Subramony SH, Bock GO, Evans OB. Vedanarayanan VV, et al. Muscle Nerve. 1998 Nov;21(11):1473-7. doi: 10.1002/(sici)1097-4598(199811)21:11<1473::aid-mus16>3.0.co;2-1. Muscle Nerve. 1998. PMID: 9771672

9

Missed diagnosis of lambert-eaton syndrome.

Chandler A, Wee A, Vedanarayanan V, Subramony SH. Chandler A, et al. Among authors: vedanarayanan v. J Clin Neuromuscul Dis. 2002 Mar;3(3):135-6. doi: 10.1097/00131402-200203000-00007. J Clin Neuromuscul Dis. 2002. PMID: 19078668 No abstract available.

10

Confirmation of the severe phenotypic effect of serine at codon 41 of the superoxide dismutase 1 gene.

Subramony SH, Ashizawa T, Langford L, McKenna R, Avvaru B, Siddique T, Vedanarayanan V. Subramony SH, et al. Among authors: vedanarayanan v. Muscle Nerve. 2011 Oct;44(4):499-502. doi: 10.1002/mus.22117. Epub 2011 Jul 13. Muscle Nerve. 2011. PMID: 21755517

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