Sudden death of a child because of an intestinal obstruction caused by a large congenital mesenteric defect
Sato, Takako, Abe, Shuntaro, Tsuboi, Kento, Iwata, Misa, Tamura, Akiyoshi, Tsuchihashi, Hitoshi, Nishio, Hajime, Suzuki, Koichi
Published in Legal medicine (Tokyo, Japan) (01.05.2012)
Published in Legal medicine (Tokyo, Japan) (01.05.2012)
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Traumatic basal subarachnoid hemorrhage suspected to have been caused by contrecoup cerebellar contusions: A case report
Sato, Takako, Tsuboi, Kento, Nomura, Masakatsu, Iwata, Misa, Abe, Shuntaro, Tamura, Akiyoshi, Tsuchihashi, Hitoshi, Nishio, Hajime, Suzuki, Koichi
Published in Legal medicine (Tokyo, Japan) (01.03.2014)
Published in Legal medicine (Tokyo, Japan) (01.03.2014)
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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, Hajime, Sato, Takako, Fukunishi, Shinya, Tamura, Akiyoshi, Iwata, Misa, Tsuboi, Kento, Suzuki, Koichi
Published in Legal medicine (Tokyo, Japan) (01.05.2009)
Published in Legal medicine (Tokyo, Japan) (01.05.2009)
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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, Hajime, Iwata, Misa, Tamura, Akiyoshi, Miyazaki, Tokiko, Tsuboi, Kento, Suzuki, Koichi
Published in Legal medicine (Tokyo, Japan) (01.07.2008)
Published in Legal medicine (Tokyo, Japan) (01.07.2008)
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Journal Article
Analysis of two types of novel alleles in the DXS10011 locus
Tamura, Akiyoshi, Iwata, Misa, Takase, Izumi, Miyazaki, Tokiko, Matsui, Kiyoshi, Nishio, Hajime, Suzuki, Koichi
Published in Legal medicine (Tokyo, Japan) (01.03.2004)
Published in Legal medicine (Tokyo, Japan) (01.03.2004)
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A de novo recombination in the ABO blood group gene and evidence for the occurrence of recombination products
SUZUKI, K, IWATA, M, TSUJI, H, TAKAGI, T, TAMURA, A, ISHIMOTO, G, ITO, S, MATSUI, K, MIYAZAKI, T
Published in Human genetics (01.04.1997)
Published in Human genetics (01.04.1997)
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Sequence analysis of two de novo mutation alleles at the DXS10011 locus
Tamura, Akiyoshi, Iwata, Misa, Takase, Izumi, Miyazaki, Tokiko, Matsui, Kiyoshi, Nishio, Hajime, Suzuki, Koichi
Published in Legal medicine (Tokyo, Japan) (01.09.2003)
Published in Legal medicine (Tokyo, Japan) (01.09.2003)
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Sibling incest and formulation of paternity probability: case report
Tamura, Akiyoshi, Tsuji, Hiroko, Miyazaki, Tokiko, Iwata, Misa, Nishio, Hajime, Hashimoto, Tominori, Kamiyama, Kiyofumi, Suzuki, Koichi
Published in Legal medicine (Tokyo, Japan) (01.12.2000)
Published in Legal medicine (Tokyo, Japan) (01.12.2000)
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Postmortem molecular screening for mutations in ryanodine receptor type 1 (RYR1) gene in psychiatric patients suspected of having died of neuroleptic malignant syndrome
Sato, Takako, Nishio, Hajime, Iwata, Misa, KentoTsuboi, Tamura, Akiyoshi, Miyazaki, Tokiko, Suzuki, Koichi
Published in Forensic science international (30.01.2010)
Published in Forensic science international (30.01.2010)
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Postmortem molecular screening for cardiac ryanodine receptor type 2 mutations in sudden unexplained death: R420W mutated case with characteristics of status thymico-lymphatics
Nishio, Hajime, Iwata, Misa, Suzuki, Koichi
Published in Circulation journal : official journal of the Japanese Circulation Society (01.11.2006)
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Published in Circulation journal : official journal of the Japanese Circulation Society (01.11.2006)
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A fatal case of amniotic fluid embolism with elevation of serum mast cell tryptase
Nishio, Hajime, Matsui, Kiyoshi, Miyazaki, Tokiko, Tamura, Akiyoshi, Iwata, Misa, Suzuki, Koichi
Published in Forensic science international (28.03.2002)
Published in Forensic science international (28.03.2002)
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Journal Article
Case Report: 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, Hajime, Sato, Takako, Fukunishi, Shinya, Tamura, Akiyoshi, Iwata, Misa, Tsuboi, Kento, Suzuki, Koichi
Published in Legal medicine (Tokyo, Japan) (01.05.2009)
Published in Legal medicine (Tokyo, Japan) (01.05.2009)
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Journal Article
Y Chromosomal Short Tandem Repeat Haplotypes in the Japanese Population
Tamura, Akiyoshi, Iwata, Misa, Takase, Izumi, Miyazaki, Tokiko, Fukunishi, Shinya, Nishio, Hajime, Suzuki, Koichi
Published in Journal of forensic sciences (01.11.2006)
Published in Journal of forensic sciences (01.11.2006)
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Brief Communication: 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, Hajime, Iwata, Misa, Tamura, Akiyoshi, Miyazaki, Tokiko, Tsuboi, Kento, Suzuki, Koichi
Published in Legal medicine (Tokyo, Japan) (01.07.2008)
Published in Legal medicine (Tokyo, Japan) (01.07.2008)
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Journal Article
Novel polymorphisms and haplotypes in the human coagulation factor XIII A-subunit gene
Suzuki, K, Henke, J, Iwata, M, Henke, L, Tsuji, H, Fukunaga, T, Ishimoto, G, Szekelyi, M, Ito, S
Published in Human genetics (01.10.1996)
Published in Human genetics (01.10.1996)
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