Sirrs S - Search Results

1

High rate of hypertension in patients with m.3243A>G MELAS mutations and POLG variants.

Pauls AD, Sandhu V, Young D, Nevay DL, Yeung DF, Sirrs S, Tsang MY, Tsang TSM, Lehman A, Mezei MM, Poburko D. Pauls AD, et al. Among authors: sirrs s. Mitochondrion. 2020 Jul;53:194-202. doi: 10.1016/j.mito.2020.05.011. Epub 2020 Jun 2. Mitochondrion. 2020. PMID: 32502631

2

Multisystem disorder in late-onset chronic progressive external ophthalmoplegia.

Pfeffer G, Sirrs S, Wade NK, Mezei MM. Pfeffer G, et al. Among authors: sirrs s. Can J Neurol Sci. 2011 Jan;38(1):119-23. doi: 10.1017/s031716710001115x. Can J Neurol Sci. 2011. PMID: 21156440

3

Echocardiographic Assessment of Patients with Fabry Disease.

Yeung DF, Sirrs S, Tsang MYC, Gin K, Luong C, Jue J, Nair P, Lee PK, Tsang TSM. Yeung DF, et al. Among authors: sirrs s. J Am Soc Echocardiogr. 2018 Jun;31(6):639-649.e2. doi: 10.1016/j.echo.2018.01.016. Epub 2018 Mar 29. J Am Soc Echocardiogr. 2018. PMID: 29606333 Review.

4

Hypogonadotropic Hypogonadism in Males with Glycogen Storage Disease Type 1.

Wong EM, Lehman A, Acott P, Gillis J, Metzger DL, Sirrs S. Wong EM, et al. Among authors: sirrs s. JIMD Rep. 2017;36:79-84. doi: 10.1007/8904_2016_38. Epub 2017 Feb 4. JIMD Rep. 2017. PMID: 28160246 Free PMC article.

5

Increased Prevalence of Hypertension in Young Adults with High Heteroplasmy Levels of the MELAS m.3243A>G Mutation.

Hannah-Shmouni F, Sirrs S, Mezei MM, Waters PJ, Mattman A. Hannah-Shmouni F, et al. Among authors: sirrs s. JIMD Rep. 2014;12:17-23. doi: 10.1007/8904_2013_239. Epub 2013 Jul 12. JIMD Rep. 2014. PMID: 23846908 Free PMC article.

6

Performance of serum and dried blood spot acylcarnitine profiles for detection of fatty acid β-oxidation disorders in adult patients with rhabdomyolysis.

Al-Thihli K, Sinclair G, Sirrs S, Mezei M, Nelson J, Vallance H. Al-Thihli K, et al. Among authors: sirrs s. J Inherit Metab Dis. 2014 Mar;37(2):207-13. doi: 10.1007/s10545-012-9578-7. Epub 2013 Jan 8. J Inherit Metab Dis. 2014. PMID: 23296367

7

Child Neurology: Krabbe disease: a potentially treatable white matter disorder.

Gelinas J, Liao P, Lehman A, Stockler S, Sirrs S. Gelinas J, et al. Among authors: sirrs s. Neurology. 2012 Nov 6;79(19):e170-2. doi: 10.1212/WNL.0b013e3182735c8b. Neurology. 2012. PMID: 23128445 No abstract available.

8

A mitochondrial DNA D loop insertion detected almost exclusively in non-replicating tissues with maternal inheritance across three generations.

Sharma MA, Lee JYJ, Tam A, Sattha B, Mackenzie IR, Vallance HD, Sirrs S, Hannah-Shmouni F, Côté HCF, Mattman A. Sharma MA, et al. Among authors: sirrs s. Mitochondrion. 2019 May;46:298-301. doi: 10.1016/j.mito.2018.08.002. Epub 2018 Aug 13. Mitochondrion. 2019. PMID: 30114489

9

Emphysema in an adult with galactosialidosis linked to a defect in primary elastic fiber assembly.

Lehman A, Mattman A, Sin D, Pare P, Zong Z, d'Azzo A, Campos Y, Sirrs S, Hinek A. Lehman A, et al. Among authors: sirrs s. Mol Genet Metab. 2012 May;106(1):99-103. doi: 10.1016/j.ymgme.2012.02.004. Epub 2012 Feb 8. Mol Genet Metab. 2012. PMID: 22386972

10

Safety of statin therapy in patients with mitochondrial diseases.

Hannah-Shmouni F, Al-Sarraf A, Frohlich J, Mezei MM, Sirrs S, Mattman A. Hannah-Shmouni F, et al. Among authors: sirrs s. J Clin Lipidol. 2013 Mar-Apr;7(2):182. doi: 10.1016/j.jacl.2012.08.003. Epub 2012 Aug 10. J Clin Lipidol. 2013. PMID: 23415441 No abstract available.

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