Sarveswaran N - Search Results

1

Midfacial Toddler Excoriation syndrome (MiTES): case series, diagnostic criteria and evidence for a pathogenic mechanism.

Sarveswaran N, Pamela Y, Reddy AAN, Mustari AP, Parthasarathi A, Mancini AJ, Bishnoi A, Inamadar AC, Olabi B, Browne F, Deshmukh GN, McWilliam K, Vinay K, Srinivas S, Ibbs S, Natarajan S, Rao VR, Zawar V, Gowda VK, Shaikh SS, Moss C, Woods CG, Drissi I. Sarveswaran N, et al. Br J Dermatol. 2024 Apr 9:ljae151. doi: 10.1093/bjd/ljae151. Online ahead of print. Br J Dermatol. 2024. PMID: 38591490

2

Conserved but not critical: Trafficking and function of Na_V1.7 are independent of highly conserved polybasic motifs.

Tyagi S, Sarveswaran N, Higerd-Rusli GP, Liu S, Dib-Hajj FB, Waxman SG, Dib-Hajj SD. Tyagi S, et al. Among authors: sarveswaran n. Front Mol Neurosci. 2023 Mar 16;16:1161028. doi: 10.3389/fnmol.2023.1161028. eCollection 2023. Front Mol Neurosci. 2023. PMID: 37008789 Free PMC article.

3

Depolarizing Na_V and Hyperpolarizing K_V Channels Are Co-Trafficked in Sensory Neurons.

Higerd-Rusli GP, Alsaloum M, Tyagi S, Sarveswaran N, Estacion M, Akin EJ, Dib-Hajj FB, Liu S, Sosniak D, Zhao P, Dib-Hajj SD, Waxman SG. Higerd-Rusli GP, et al. Among authors: sarveswaran n. J Neurosci. 2022 Jun 15;42(24):4794-4811. doi: 10.1523/JNEUROSCI.0058-22.2022. J Neurosci. 2022. PMID: 35589395 Free PMC article.

4

Extending the phenotype of midface toddler excoriation syndrome (MiTES): Five new cases in three families with PR domain containing protein 12 (PRDM12) mutations.

Inamadar AC, Vinay K, Olabi B, Sarveswaran N, Bishnoi A, Woods CG, Moss C. Inamadar AC, et al. Among authors: sarveswaran n. J Am Acad Dermatol. 2019 Dec;81(6):1415-1417. doi: 10.1016/j.jaad.2019.05.036. Epub 2019 May 22. J Am Acad Dermatol. 2019. PMID: 31128170 No abstract available.

5

Midface toddler excoriation syndrome (MiTES) can be caused by autosomal recessive biallelic mutations in a gene for congenital insensitivity to pain, PRDM12.

Moss C, Srinivas SM, Sarveswaran N, Nahorski M, Gowda VK, Browne FM, Woods G. Moss C, et al. Among authors: sarveswaran n. Br J Dermatol. 2018 Nov;179(5):1135-1140. doi: 10.1111/bjd.16893. Epub 2018 Sep 16. Br J Dermatol. 2018. PMID: 29949203

6

Functional SNP allele discovery (fSNPd): an approach to find highly penetrant, environmental-triggered genotypes underlying complex human phenotypes.

Stouffer K, Nahorski M, Moreno P, Sarveswaran N, Menon D, Lee M, Geoffrey Woods C. Stouffer K, et al. Among authors: sarveswaran n. BMC Genomics. 2017 Dec 4;18(1):944. doi: 10.1186/s12864-017-4325-y. BMC Genomics. 2017. PMID: 29202707 Free PMC article.

7

Impaired myocardial flow reserve on rubidium-82 positron emission tomography imaging predicts adverse outcomes in patients assessed for myocardial ischemia.

Ziadi MC, Dekemp RA, Williams KA, Guo A, Chow BJ, Renaud JM, Ruddy TD, Sarveswaran N, Tee RE, Beanlands RS. Ziadi MC, et al. Among authors: sarveswaran n. J Am Coll Cardiol. 2011 Aug 9;58(7):740-8. doi: 10.1016/j.jacc.2011.01.065. J Am Coll Cardiol. 2011. PMID: 21816311 Free article.

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