Suzuki K - Search Results

1

Postmortem genetic analysis for a sudden death case complicated with Marfan syndrome.

Takahashi M, Sato T, Nishiguchi M, Suzuki K, Nishio H. Takahashi M, et al. Among authors: suzuki k. Leg Med (Tokyo). 2010 Nov;12(6):305-7. doi: 10.1016/j.legalmed.2010.06.003. Epub 2010 Aug 21. Leg Med (Tokyo). 2010. PMID: 20729124

2

Serum tryptase levels in sudden infant death syndrome in forensic autopsy cases.

Nishio H, Suzuki K. Nishio H, et al. Among authors: suzuki k. Forensic Sci Int. 2004 Jan 6;139(1):57-60. doi: 10.1016/j.forsciint.2003.09.011. Forensic Sci Int. 2004. PMID: 14687774

3

Postmortem molecular screening for cardiac ryanodine receptor type 2 mutations in sudden unexplained death: R420W mutated case with characteristics of status thymico-lymphatics.

Nishio H, Iwata M, Suzuki K. Nishio H, et al. Among authors: suzuki k. Circ J. 2006 Nov;70(11):1402-6. doi: 10.1253/circj.70.1402. Circ J. 2006. PMID: 17062961 Free article.

4

Identification of a novel mutation V2321M of the cardiac ryanodine receptor gene of sudden unexplained death and a phenotypic study of the gene mutations.

Nishio H, Iwata M, Tamura A, Miyazaki T, Tsuboi K, Suzuki K. Nishio H, et al. Among authors: suzuki k. Leg Med (Tokyo). 2008 Jul;10(4):196-200. doi: 10.1016/j.legalmed.2007.12.003. Epub 2008 Feb 11. Leg Med (Tokyo). 2008. PMID: 18262818

5

Identification of an ethnic-specific variant (V207M) of the KCNQ1 cardiac potassium channel gene in sudden unexplained death and implications from a knock-in mouse model.

Nishio H, Kuwahara M, Tsubone H, Koda Y, Sato T, Fukunishi S, Tamura A, Suzuki K. Nishio H, et al. Among authors: suzuki k. Int J Legal Med. 2009 May;123(3):253-7. doi: 10.1007/s00414-009-0321-3. Epub 2009 Feb 7. Int J Legal Med. 2009. PMID: 19198868

6

Identification of malignant hyperthermia-susceptible ryanodine receptor type 1 gene (RYR1) mutations in a child who died in a car after exposure to a high environmental temperature.

Nishio H, Sato T, Fukunishi S, Tamura A, Iwata M, Tsuboi K, Suzuki K. Nishio H, et al. Among authors: suzuki k. Leg Med (Tokyo). 2009 May;11(3):142-3. doi: 10.1016/j.legalmed.2008.12.004. Epub 2009 Feb 14. Leg Med (Tokyo). 2009. PMID: 19223216

7

Postmortem molecular analysis for fatal arrhythmogenic disease in sudden unexplained death.

Nishio H, Suzuki K. Nishio H, et al. Among authors: suzuki k. Leg Med (Tokyo). 2009 Apr;11 Suppl 1:S119-20. doi: 10.1016/j.legalmed.2009.01.031. Epub 2009 Mar 3. Leg Med (Tokyo). 2009. PMID: 19261510

8

Sudden death during exercise in a juvenile with arrhythmogenic right ventricular cardiomyopathy and desmoglein-2 gene substitution: a case report.

Sato T, Nishio H, Suzuki K. Sato T, et al. Among authors: suzuki k. Leg Med (Tokyo). 2011 Nov;13(6):298-300. doi: 10.1016/j.legalmed.2011.08.004. Epub 2011 Oct 13. Leg Med (Tokyo). 2011. PMID: 22000064

9

Sudden death of a child because of an intestinal obstruction caused by a large congenital mesenteric defect.

Sato T, Abe S, Tsuboi K, Iwata M, Tamura A, Tsuchihashi H, Nishio H, Suzuki K. Sato T, et al. Among authors: suzuki k. Leg Med (Tokyo). 2012 May;14(3):157-9. doi: 10.1016/j.legalmed.2012.01.010. Epub 2012 Feb 29. Leg Med (Tokyo). 2012. PMID: 22381353

10

Hypertrophy of lymphoid organs is a possible phenotypic characteristic of R420W mutation of the cardiac ryanodine receptor gene: a study using a knock-in mouse model.

Nishio H, Okudaira N, Matsushita K, Yoshimoto T, Sato T, Suzuki K. Nishio H, et al. Among authors: suzuki k. Leg Med (Tokyo). 2014 Nov;16(6):326-32. doi: 10.1016/j.legalmed.2014.06.008. Epub 2014 Jul 10. Leg Med (Tokyo). 2014. PMID: 25087098

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