Jain R - Search Results

1

Alexander disease with periventricular calcification: a novel mutation of the GFAP gene.

Jefferson RJ, Absoud M, Jain R, Livingston JH, VAN DER Knaap MS, Jayawant S. Jefferson RJ, et al. Among authors: jain r. Dev Med Child Neurol. 2010 Dec;52(12):1160-3. doi: 10.1111/j.1469-8749.2010.03784.x. Epub 2010 Oct 21. Dev Med Child Neurol. 2010. PMID: 20964669 Free article.

2

Homozygous mutations in the SCN1A gene associated with genetic epilepsy with febrile seizures plus and Dravet syndrome in 2 families.

Brunklaus A, Ellis R, Stewart H, Aylett S, Reavey E, Jefferson R, Jain R, Chakraborty S, Jayawant S, Zuberi SM. Brunklaus A, et al. Among authors: jain r. Eur J Paediatr Neurol. 2015 Jul;19(4):484-8. doi: 10.1016/j.ejpn.2015.02.001. Epub 2015 Feb 21. Eur J Paediatr Neurol. 2015. PMID: 25795284

3

WITHDRAWN: Nemaline myopathy presenting as a stiff baby.

Jain RK, Jayawant S. Jain RK, et al. Neuromuscul Disord. 2010 Mar 20. doi: 10.1016/j.nmd.2010.02.014. Online ahead of print. Neuromuscul Disord. 2010. PMID: 20304646

4

Nemaline myopathy with stiffness and hypertonia associated with an ACTA1 mutation.

Jain RK, Jayawant S, Squier W, Muntoni F, Sewry CA, Manzur A, Quinlivan R, Lillis S, Jungbluth H, Sparrow JC, Ravenscroft G, Nowak KJ, Memo M, Marston SB, Laing NG. Jain RK, et al. Neurology. 2012 Apr 3;78(14):1100-3. doi: 10.1212/WNL.0b013e31824e8ebe. Epub 2012 Mar 21. Neurology. 2012. PMID: 22442437 No abstract available.

5

Electroclinical outcome of children referred with suspected absence seizures.

Anand G, Padeniya A, Jain R, Hasan N, Jayawant S, Pike M, McShane T, Zaiwalla Z. Anand G, et al. Among authors: jain r. Arch Dis Child. 2011 Oct;96(10):987-8. doi: 10.1136/archdischild-2011-300531. Epub 2011 Sep 8. Arch Dis Child. 2011. PMID: 21908420 No abstract available.

6

Video EEG outcome on children referred following a single unprovoked afebrile seizure.

Anand G, Padeniya A, Jain R, Hasan N, Pike M, Jayawant S, McShane T, Zaiwalla Z. Anand G, et al. Among authors: jain r. Arch Dis Child. 2012 Jan;97(1):90. doi: 10.1136/archdischild-2011-300960. Epub 2011 Oct 6. Arch Dis Child. 2012. PMID: 21979135 No abstract available.

7

An unusual cause of head drops.

Jain RK, Anslow P, Pike MG. Jain RK, et al. Eur J Paediatr Neurol. 2011 Jan;15(1):78-80. doi: 10.1016/j.ejpn.2010.03.008. Epub 2010 May 15. Eur J Paediatr Neurol. 2011. PMID: 20472477

8

Exploring the Connection: Moyamoya Disease and Its Implications for Cardiovascular Health.

Walters BP, Trivedi YV, Katoch T, Gupta V, Jain R. Walters BP, et al. Among authors: jain r. Cardiol Rev. 2025 Jan 15. doi: 10.1097/CRD.0000000000000794. Online ahead of print. Cardiol Rev. 2025. PMID: 39812469

9

Learning from the CFTR modulator baby boom.

Jain R, Goralski JL. Jain R, et al. J Cyst Fibros. 2025 Jan 9:S1569-1993(24)01857-5. doi: 10.1016/j.jcf.2024.12.003. Online ahead of print. J Cyst Fibros. 2025. PMID: 39794183 No abstract available.

10

A comprehensive multicenter analysis of clinical, molecular, and imaging characteristics and outcomes of H3 K27-altered diffuse midline glioma in adults.

Sim Y, McClelland AC, Choi K, Han K, Park YW, Ahn SS, Chang JH, Kim SH, Gardner S, Lee SK, Jain R. Sim Y, et al. Among authors: jain r. J Neurosurg. 2025 Jan 10:1-12. doi: 10.3171/2024.8.JNS241180. Online ahead of print. J Neurosurg. 2025. PMID: 39793011

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