Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Misa Iwata"'
Publikováno v:
Circulation Journal. 70:1402-1406
Background Mutations of the cardiac ryanodine receptor type 2 (RyR2) gene are known to cause effort-induced polymorphic ventricular arrhythmia, syncope and sudden death. Methods and Results The possible mutations in the RyR2 gene were examined in 18
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1623b8e689da68d5f24ccc558e9400a4
https://doi.org/10.1253/circj.70.1402
https://doi.org/10.1253/circj.70.1402
Autor:
Kiyoshi Matsui, Hajime Nishio, Koichi Suzuki, Akiyoshi Tamura, Izumi Takase, Misa Iwata, Tokiko Miyazaki
Publikováno v:
Legal Medicine. 5:161-164
We have detected two unusual alleles at the DXS10011 locus in two paternity trio cases. In one case, one allele of the daughter was found not to have been derived from the mother but the other allele was shared with the father. In the other case, the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ca695f96ed5b089eaadd050ad5914ea
https://doi.org/10.1016/s1344-6223(03)00057-9
https://doi.org/10.1016/s1344-6223(03)00057-9
Publikováno v:
Forensic Science International. 126:53-56
A case of a 40-year-old female who died of amniotic fluid embolism is presented. This case showed typical histological findings of this syndrome. Postmortem serum of this case showed an elevated tryptase level (67.2ng/ml, normal levels
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1c9986d3aa688dd53a6254989a32bfa
https://doi.org/10.1016/s0379-0738(02)00034-8
https://doi.org/10.1016/s0379-0738(02)00034-8
Autor:
Takako Sato, Akiyoshi Tamura, Tokiko Miyazaki, KentoTsuboi, Koichi Suzuki, Misa Iwata, Hajime Nishio
Publikováno v:
Forensic Science International. 194:77-79
Postmortem diagnosis of neuroleptic malignant syndrome (NMS) is difficult to perform, because the clinical symptoms just before death are not usually available. Malignant hyperthermia (MH) is a catastrophic, life-threatening hypermetabolic syndrome t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eecd7319e60d84ac8fdf1ef955c76e76
https://doi.org/10.1016/j.forsciint.2009.10.014
https://doi.org/10.1016/j.forsciint.2009.10.014
Autor:
Hiroko Tsuji, Koichi Suzuki, Akiyoshi Tamura, Kiyofumi Kamiyama, Misa Iwata, Hajime Nishio, Tominori Hashimoto, Tokiko Miyazaki
Publikováno v:
Legal Medicine. 2:189-196
Paternity determination of a fetus whose mother was admitted to an institution for the welfare and health of handicapped persons was requested of us by a doctor and lawyer of the institution. The fetus was recovered by a legal artificial abortion bas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ae1d7f39133bd5fb2a72365507329ba
https://doi.org/10.1016/s1344-6223(00)80039-5
https://doi.org/10.1016/s1344-6223(00)80039-5
Publikováno v:
Legal Medicine. 11:129-131
We investigated a region of repetitive DNA located in intron 40 of the von Willebrand factor (vWF) gene (nucleotides [nt] 1639-2404; i.e., F8VWF). We identified 13 alleles and 33 genotypes in 49 unrelated Japanese individuals. The heterozygosity of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::128e6d45ba8a5b192c4178497811e4d9
https://doi.org/10.1016/j.legalmed.2008.11.004
https://doi.org/10.1016/j.legalmed.2008.11.004
Autor:
Takako Sato, Shuntaro Abe, Hajime Nishio, Masakatsu Nomura, Hitoshi Tsuchihashi, Kento Tsuboi, Koichi Suzuki, Akiyoshi Tamura, Misa Iwata
Publikováno v:
Legal medicine (Tokyo, Japan). 16(2)
Traumatic cerebellar hemorrhagic contusions are infrequent, and the pathogenic mechanism involves a coup injury that is associated with motor vehicle accidents in most cases. Traumatic basal subarachnoid hemorrhage (TBSAH) is commonly reported after
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2de5168c732510a570cf19c59b0c1433
https://pubmed.ncbi.nlm.nih.gov/24411402
https://pubmed.ncbi.nlm.nih.gov/24411402
Autor:
Hajime Nishio, Kiyoshi Matsui, Koichi Suzuki, Akiyoshi Tamura, Misa Iwata, Tokiko Miyazaki, Izumi Takase
Publikováno v:
Legal Medicine. 6:52-54
A population study of the short tandem repeat locus DXS10011 was carried out in a sample of 104 unrelated Japanese individuals (56 males, 48 females). Thirty-six different alleles were distinguished. The power of discrimination was 0.933 (male) and 0
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::822fafcd399647d5dac19ed191be26a2
https://doi.org/10.1016/j.legalmed.2003.09.002
https://doi.org/10.1016/j.legalmed.2003.09.002
Autor:
Koichi Suzuki, Akiyoshi Tamura, Tokiko Miyazaki, Misa Iwata, Hiroko Tsuji, Kiyoshi Matsui, Hajime Nishio
Publikováno v:
International Congress Series. 1239:707-709
Intron 40 of the vWF gene is known to harbor three different STRs, which were separately reported by Kimpton et al. (vWA), by Peake et al. (vWF-P), and by Ploos van Amstel et al. (vWF-A). En bloc detection of the three STRs (F8VWF) and sequencing of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f7e6252c1f6e04e421d69e1ccef4479f
https://doi.org/10.1016/s0531-5131(02)00573-3
https://doi.org/10.1016/s0531-5131(02)00573-3
Autor:
Hajime Nishio, Misa Iwata, Kento Tsuboi, Takako Sato, Shinya Fukunishi, Koichi Suzuki, Akiyoshi Tamura
Publikováno v:
Legal medicine (Tokyo, Japan). 11(3)
Malignant hyperthermia (MH) is a genetic disorder of skeletal muscle in susceptible individuals that is triggered by exposure to anesthetic agents, and can cause death. Mutations in the ryanodine receptor type 1 gene (RYR1) are associated with MH-sus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a432155834e2359e93480bb471325ca
https://pubmed.ncbi.nlm.nih.gov/19223216
https://pubmed.ncbi.nlm.nih.gov/19223216