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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-Lymphaticus

Circulation Journal, 2006, Vol.70(11), pp.1402-1406

2006

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

Legal medicine (Tokyo, Japan), 2012-05, Vol.14 (3), p.157-159

2012

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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

Legal medicine (Tokyo, Japan), 2009-05, Vol.11 (3), p.142-143

2009

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Traumatic basal subarachnoid hemorrhage suspected to have been caused by contrecoup cerebellar contusions: A case report

Legal medicine (Tokyo, Japan), 2014-03, Vol.16 (2), p.92-94

2014

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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

Legal medicine (Tokyo, Japan), 2008-07, Vol.10 (4), p.196-200

2008

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Identification of newly polymorphic intron 40 markers of the von Willebrand factor gene in a Japanese population

Legal medicine (Tokyo, Japan), 2009-05, Vol.11 (3), p.129-131

2009

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Analysis of two types of novel alleles in the DXS10011 locus

Legal medicine (Tokyo, Japan), 2004-03, Vol.6 (1), p.52-54

2004

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A de novo recombination in the ABO blood group gene and evidence for the occurrence of recombination products

Human genetics, 1997-04, Vol.99 (4), p.454-461

1997

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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

Forensic science international, 2010-01, Vol.194 (1), p.77-79

2010

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Sequence analysis of two de novo mutation alleles at the DXS10011 locus

Legal medicine (Tokyo, Japan), 2003-09, Vol.5 (3), p.161-164

2003

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Sibling incest and formulation of paternity probability: case report

Legal medicine (Tokyo, Japan), 2000-12, Vol.2 (4), p.189-196

2000

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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

Circulation journal : official journal of the Japanese Circulation Society, 2006-11, Vol.70 (11), p.1402-1406

2006

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A fatal case of amniotic fluid embolism with elevation of serum mast cell tryptase

Forensic science international, 2002-03, Vol.126 (1), p.53-56

2002

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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

Legal medicine (Tokyo, Japan), 2009-05, Vol.11 (3), p.142-143

2009

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Y Chromosomal Short Tandem Repeat Haplotypes in the Japanese Population

Journal of forensic sciences, 2006-11, Vol.51 (6), p.1431-1433

2006

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FOR THE RECORD: Y Chromosomal Short Tandem Repeat Haplotypes in the Japanese Population

Journal of forensic sciences, 2006-11, Vol.51 (6), p.1431-1433

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

Legal medicine (Tokyo, Japan), 2008-07, Vol.10 (4), p.196-200

2008

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Sequence analysis of two de novo mutation alleles at the Y-STR locus

Forensic science international. Genetics supplement series, 2008-08, Vol.1 (1), p.250-251

2008

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Novel polymorphisms and haplotypes in the human coagulation factor XIII A-subunit gene

Human genetics, 1996-10, Vol.98 (4), p.393-395

1996

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Molecular basis for subtypic differences of the a subunit of coagulation factor XIII with description of the genesis of the subtypes

Human genetics, 1994-08, Vol.94 (2), p.129-135

1994

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Allele 14 of vWA is characterized by 3′-flanking nucleotide substitutions and a TTAT insertion

International Congress series, 2003, Vol.1239, p.707-709

2003

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A Pilot Study of Tranilast for Cardiomyopathy of Muscular Dystrophy

Internal Medicine, 2018/02/01, Vol.57(3), pp.311-318

2018

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Porphyromonas gingivalis, the most influential pathogen in red‐complex bacteria: A cross‐sectional study on the relationship between bacterial count and clinical periodontal status in Japan

Journal of periodontology (1970), 2021-12, Vol.92 (12), p.1719-1729

2021

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Perception of overseas experiences among medical students in Japan: a national online survey

BMC medical education, 2023-06, Vol.23 (1), p.461-461, Article 461

2023

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Effect of Thiophene π-Conjugation Spacers on the Performance of Photosensitized Dyes Having Trifluoromethylthiazole-5-carboxylic Acid as an Acceptor-anchor Moiety

Chemistry letters, 2021-10, Vol.50 (10), p.1791-1793

2021

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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-Lymphaticus

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

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

Traumatic basal subarachnoid hemorrhage suspected to have been caused by contrecoup cerebellar contusions: A case report

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

Identification of newly polymorphic intron 40 markers of the von Willebrand factor gene in a Japanese population

Analysis of two types of novel alleles in the DXS10011 locus

A de novo recombination in the ABO blood group gene and evidence for the occurrence of recombination products

Postmortem molecular screening for mutations in ryanodine receptor type 1 (RYR1) gene in psychiatric patients suspected of having died of neuroleptic malignant syndrome

Sequence analysis of two de novo mutation alleles at the DXS10011 locus

Sibling incest and formulation of paternity probability: case report

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

A fatal case of amniotic fluid embolism with elevation of serum mast cell tryptase

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

Y Chromosomal Short Tandem Repeat Haplotypes in the Japanese Population

FOR THE RECORD: Y Chromosomal Short Tandem Repeat Haplotypes in the Japanese Population

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

Sequence analysis of two de novo mutation alleles at the Y-STR locus

Novel polymorphisms and haplotypes in the human coagulation factor XIII A-subunit gene

Molecular basis for subtypic differences of the a subunit of coagulation factor XIII with description of the genesis of the subtypes

Allele 14 of vWA is characterized by 3′-flanking nucleotide substitutions and a TTAT insertion

A Pilot Study of Tranilast for Cardiomyopathy of Muscular Dystrophy

Porphyromonas gingivalis, the most influential pathogen in red‐complex bacteria: A cross‐sectional study on the relationship between bacterial count and clinical periodontal status in Japan

Perception of overseas experiences among medical students in Japan: a national online survey

Effect of Thiophene π-Conjugation Spacers on the Performance of Photosensitized Dyes Having Trifluoromethylthiazole-5-carboxylic Acid as an Acceptor-anchor Moiety

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