Mimaki M - Search Results

1

Rapid Detection of Candida auris Based on Loop-Mediated Isothermal Amplification (LAMP).

Yamamoto M, Alshahni MM, Tamura T, Satoh K, Iguchi S, Kikuchi K, Mimaki M, Makimura K. Yamamoto M, et al. Among authors: mimaki m. J Clin Microbiol. 2018 Aug 27;56(9):e00591-18. doi: 10.1128/JCM.00591-18. Print 2018 Sep. J Clin Microbiol. 2018. PMID: 29950329 Free PMC article. No abstract available.

2

NDUFAF3 variants that disrupt mitochondrial complex I assembly may associate with cavitating leukoencephalopathy.

Ishiyama A, Muramatsu K, Uchino S, Sakai C, Matsushima Y, Makioka N, Ogata T, Suzuki E, Komaki H, Sasaki M, Mimaki M, Goto YI, Nishino I. Ishiyama A, et al. Among authors: mimaki m. Clin Genet. 2018 May;93(5):1103-1106. doi: 10.1111/cge.13215. Epub 2018 Feb 11. Clin Genet. 2018. PMID: 29344937

3

Cyclosporine A C_1.5 monitoring reflects the area under the curve in children with nephrotic syndrome: a single-center experience.

Nishino T, Takahashi K, Tomori S, Ono S, Mimaki M. Nishino T, et al. Among authors: mimaki m. Clin Exp Nephrol. 2022 Feb;26(2):154-161. doi: 10.1007/s10157-021-02139-z. Epub 2021 Sep 24. Clin Exp Nephrol. 2022. PMID: 34559341

4

Two patients with 19p13.2 deletion (Malan syndrome) involving NFIX and CACNA1A with overgrowth, developmental delay, and epilepsy.

Kuroda Y, Mizuno Y, Mimaki M, Oka A, Sato Y, Ogawa S, Kurosawa K. Kuroda Y, et al. Among authors: mimaki m. Clin Dysmorphol. 2017 Oct;26(4):224-227. doi: 10.1097/MCD.0000000000000185. Clin Dysmorphol. 2017. PMID: 28557812 No abstract available.

5

A double mutation (G11778A and G12192A) in mitochondrial DNA associated with Leber's hereditary optic neuropathy and cardiomyopathy.

Mimaki M, Ikota A, Sato A, Komaki H, Akanuma J, Nonaka I, Goto Y. Mimaki M, et al. J Hum Genet. 2003;48(1):47-50. doi: 10.1007/s100380300005. J Hum Genet. 2003. PMID: 12560876

6

Cochlear damage due to germanium-induced mitochondrial dysfunction in guinea pigs.

Yamasoba T, Goto Y, Komaki H, Mimaki M, Sudo A, Suzuki M. Yamasoba T, et al. Among authors: mimaki m. Neurosci Lett. 2006 Feb 27;395(1):18-22. doi: 10.1016/j.neulet.2005.10.045. Epub 2005 Nov 9. Neurosci Lett. 2006. PMID: 16289317

7

A case of primary erythermalgia, wintry hypothermia and encephalopathy.

Takahashi K, Saitoh M, Hoshino H, Mimaki M, Yokoyama Y, Takamizawa M, Mizuguchi M, Lin ZM, Yang Y, Igarashi T. Takahashi K, et al. Among authors: mimaki m. Neuropediatrics. 2007 Jun;38(3):157-9. doi: 10.1055/s-2007-990265. Neuropediatrics. 2007. PMID: 17985268

8

Different effects of novel mtDNA G3242A and G3244A base changes adjacent to a common A3243G mutation in patients with mitochondrial disorders.

Mimaki M, Hatakeyama H, Ichiyama T, Isumi H, Furukawa S, Akasaka M, Kamei A, Komaki H, Nishino I, Nonaka I, Goto Y. Mimaki M, et al. Mitochondrion. 2009 Apr;9(2):115-22. doi: 10.1016/j.mito.2009.01.005. Epub 2009 Jan 21. Mitochondrion. 2009. PMID: 19460299

9

Reversible infantile respiratory chain deficiency: a clinical and molecular study.

Mimaki M, Hatakeyama H, Komaki H, Yokoyama M, Arai H, Kirino Y, Suzuki T, Nishino I, Nonaka I, Goto Y. Mimaki M, et al. Ann Neurol. 2010 Dec;68(6):845-54. doi: 10.1002/ana.22111. Ann Neurol. 2010. PMID: 21194154

10

Cyclic Vomiting Syndrome in Infants and Children: A Clinical Follow-Up Study.

Hikita T, Kodama H, Ogita K, Kaneko S, Nakamoto N, Mimaki M. Hikita T, et al. Among authors: mimaki m. Pediatr Neurol. 2016 Apr;57:29-33. doi: 10.1016/j.pediatrneurol.2016.01.001. Epub 2016 Jan 7. Pediatr Neurol. 2016. PMID: 26861170

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