All Stories

  1. Distinctive Deposition Patterns of Sporadic Transthyretin-Derived Amyloidosis in the Atria: A Forensic Autopsy-Based Study
  2. Distinctive Deposition Patterns of Sporadic Transthyretin-Derived Amyloidosis in the Atria: A Forensic Autopsy–Based Study
  3. Clinicopathological Appearance of Epidermal Growth-Factor-Containing Fibulin-like Extracellular Matrix Protein 1 Deposition in the Lower Gastrointestinal Tract: An Autopsy-Based Study
  4. Prevalence and clinicopathological features of primary age‐related tauopathy (PART): A large forensic autopsy study
  5. Revisiting the relevance of Hirano bodies in neurodegenerative diseases
  6. Novel MYH7 Variant in the Neonate of a Mother with Gestational Diabetes Mellitus Showing Left Ventricular Hypertrophy and Noncompaction
  7. Sudden unexpected death of a young adult due to subarachnoid hemorrhage associated with polyarteritis nodosa: Clinicopathological appearance and literature review
  8. Sarcomere gene variants did not improve cardiac function in pediatric patients with dilated cardiomyopathy from Japanese cohorts
  9. Neuropathology of patients with preclinical or early clinical Alzheimer's disease with pathogenic PSEN1_p. L392V: Comparison of advanced siblings
  10. An autopsy case of late‐onset spinocerebellar atrophy type 14
  11. An autopsy case of infective aortic aneurysm with Pasteurella multocida infection: clinicopathological appearance and a review of literatures
  12. Comprehensive pathological and genetic investigation of three young adult myotonic dystrophy type 1 patients with sudden unexpected death
  13. Low-frequency maternal novel MYH7 mosaicism mutation in recurrent fetal-onset severe left ventricular noncompaction: a case report
  14. Argyrophilic grain disease is common in older adults and may be a risk factor for suicide: a study of Japanese forensic autopsy cases
  15. Benzyl Alcohol Intoxication: Autopsy Findings and Lessons
  16. Lack of difference between amyloid‐beta burden at gyral crests and sulcal depths in diverse neurodegenerative diseases
  17. Pathological and Comprehensive Genetic Investigation of Autopsy Cases of Idiopathic Bradyarrhythmia
  18. An autopsy case of sudden unexpected death of a young adult with progressive intraventricular conduction delay
  19. An autopsy case of sudden unexpected death with Barlow's disease
  20. Pathological Appearance of a Case of Preclinical Multiple System Atrophy: A Comparison With Advanced Cases
  21. Calcifying pseudoneoplasm of the neuraxis ( CAPNON ) associated with neurenteric cyst. An autopsy case showing unusual fatal outcome
  22. A double heterozygous variant in MYH6 and MYH7 associated with hypertrophic cardiomyopathy in a Japanese Family
  23. Novel histopathological deposition patterns of EGF-containing fibulin-like extracellular matrix protein 1 amyloidosis: an autopsy case exhibiting a possible association between AEFEMP1 amyloidosis and elastic fibres
  24. Histopathology of acute colchicine intoxication: novel findings and their association with clinical manifestations
  25. Two autopsy cases with injuries to the stomach following cardiopulmonary resuscitation
  26. Effects of sporadic transthyretin amyloidosis frequently on the gallbladder and the correlation between amyloid deposition in the gallbladder and heart: A forensic autopsy‐based histopathological evaluation
  27. An autopsy case of pure nigropathy with TUBA4A nonsense mutation
  28. Calcifying pseudoneoplasm of the neuraxis (CAPNON) associated with neurenteric cyst: an autopsy case showing unusual fatal outcome
  29. Clinicopathological features of clinically undiagnosed sporadic transthyretin cardiac amyloidosis: a forensic autopsy-based series
  30. Traumatic rupture of the circle of Willis with closed head injury: Its pathology and possible pathogenesis
  31. Sex‐dependent expression of prostatic markers and hormone receptors in cystic tumor of the atrioventricular node: A histopathological study of three cases
  32. Increased Burden of Ion Channel Gene Variants Is Related to Distinct Phenotypes in Pediatric Patients With Left Ventricular Noncompaction
  33. Left Ventricular Noncompaction and Congenital Heart Disease Increases the Risk of Congestive Heart Failure
  34. Autopsy of a multiple lobar hemorrhage case with amyloid‐β‐related angiitis
  35. An autopsy case of amyloid tubulopathy exhibiting characteristic spheroid-type deposition
  36. An autopsy case of sudden unexpected death with loxoprofen sodium–induced allergic eosinophilic coronary periarteritis
  37. Rescue from Stx2-Producing E. coli-Associated Encephalopathy by Intravenous Injection of Muse Cells in NOD-SCID Mice
  38. Tau and Amyloid-β Pathology in Japanese Forensic Autopsy Series Under 40 Years of Age: Prevalence and Association with APOE Genotype and Suicide Risk
  39. Minimal inflammatory foci of unknown etiology may be a tentative sign of early stage inherited cardiomyopathy
  40. An Autopsy Case of Preclinical/Early Clinical Pick Disease
  41. Clinicopathological and Genetic Profiles of Cases with Myocytes Disarray—Investigation for Establishing the Autopsy Diagnostic Criteria for Hypertrophic Cardiomyopathy
  42. Sudden unexpected death with rare compound heterozygous variants in PRICKLE1
  43. Lack of modulatory effect of the SCN5A R1193Q polymorphism on cardiac fast Na+ current at body temperature
  44. Fetal closed head injuries following maternal motor vehicle accident
  45. Sudden unexpected death with primary adrenal lymphoma
  46. Clinical and Echocardiographic Impact of Tafazzin Variants on Dilated Cardiomyopathy Phenotype in Left Ventricular Non-Compaction Patients in Early Infancy
  47. Sarcomere gene variants act as a genetic trigger underlying the development of left ventricular noncompaction
  48. The TNNI3 Arg192His mutation in a 13-year-old girl with left ventricular noncompaction
  49. Autopsy of an Elderly Man With Incidentally Diagnosed TDP-43 Proteinopathy
  50. A mutant HCN4 channel in a family with bradycardia, left bundle branch block, and left ventricular noncompaction
  51. A pedigree of hereditary hyperekplexia
  52. Endothelin-1 may play an important role in the Fontan circulation
  53. Argyrophilic grain disease in a 46-year-old male suicide victim
  54. Sudden unexpected death in early Parkinson's disease: neurogenic or cardiac death?
  55. A Wide and Specific Spectrum of Genetic Variants and Genotype–Phenotype Correlations Revealed by Next‐Generation Sequencing in Patients with Left Ventricular Noncompaction
  56. A Case of Sudden Unexpected Death with the Presence of Multiple Myocardial Bridges
  57. Intramyocardial bronchogenic cyst: histological appearance and a review of the literature
  58. Incipient progressive supranuclear palsy is more common than expected and may comprise clinicopathological subtypes: a forensic autopsy series
  59. An Autopsy Case of Sudden Unexpected Death of a Young Adult in a Hot Bath: Molecular Analysis Using Next-Generation DNA Sequencing
  60. Anomalous origin of the right coronary artery evaluated with multidetector computed tomography and its clinical relevance
  61. Left ventricular non-compaction revealed by aortic regurgitation due to Kawasaki disease in a boy withLDB3mutation
  62. Postmortem genetic analysis of sudden unexplained death syndrome under 50 years of age: A next-generation sequencing study
  63. Epilepsy-related sudden unexpected death: targeted molecular analysis of inherited heart disease genes using next-generation DNA sequencing
  64. Latent pathogenicity of the G38S polymorphism of KCNE1 K+ channel modulator
  65. Pseudoaneurysmal defect of mitral-aortic intervalvular fibrosa is likely to be a cerebral embolic source. An autopsy study in remote period from the stroke
  66. SCN5A(K817E), a novel Brugada syndrome–associated mutation that alters the activation gating of NaV1.5 channel
  67. A novel ACTC1 mutation in a young boy with left ventricular noncompaction and arrhythmias
  68. A case of sudden death after Japanese encephalitis vaccination
  69. Pathological features of preclinical or early clinical stages of corticobasal degeneration: a comparison with advanced cases
  70. Neuropathologic Features of Suicide Victims Who Presented With Acute Poststroke Depression
  71. Anomalous origin of the right coronary artery from the left coronary sinus with an intramural course: comparison between sudden-death and non-sudden-death cases
  72. A Novel MYH7 Gene Mutation in a Fetus With Left Ventricular Noncompaction
  73. The Susceptibilities of Human Ether-à-Go-Go-Related Gene Channel with the G487R Mutation to Arrhythmogenic Factors
  74. A590T mutation in KCNQ1 C-terminal helix D decreases IKs channel trafficking and function but not Yotiao interaction
  75. High takeoff of the left main coronary artery at autopsy after sudden unexpected death in a male
  76. Sudden unexpected death owing to unilateral medial medullary infarction with early involvement of the respiratory center
  77. An Autopsy Case of Acute and Nonalcoholic Thiamine-Deficient Encephalopathy
  78. Glycine/Serine Polymorphism at Position 38 Influences KCNE1 Subunit’s Modulatory Actions on Rapid and Slow Delayed Rectifier K<sup>+</sup> Currents
  79. Distribution of myofibroblast and tenascin-C in cystic adventitial disease: Comparison with ganglion
  80. Characterization of a novel mutant KCNQ1 channel subunit lacking a large part of the C-terminal domain
  81. Impaired nerve fiber regeneration in axotomized peripheral nerves in streptozotocin-diabetic rats
  82. Identification and characterization of a novel genetic mutation with prolonged QT syndrome in an unexplained postoperative death
  83. 14-3-3ε Gene variants in a Japanese patient with left ventricular noncompaction and hypoplasia of the corpus callosum
  84. A Novel Missense Mutation Causing a G487R Substitution in the S2-S3 Loop of Humanether-à-go-go-Related Gene Channel
  85. Surgical Repair of Left Ventricular Noncompaction in a Patient with a Novel Mutation of the Myosin Heavy Chain 7 Gene
  86. Acute fatal poisoning with pilsicainide and atenolol
  87. Robust Design Optimization Approach by Combination of Sensitivity Analysis and Sigma Level Estimation
  88. Determination of fluoride in human whole blood and urine by gas chromatography-mass spectrometry
  89. Indication and limitations of using palatal rugae for personal identification in edentulous cases
  90. Immunohistochemical study of thyroid transcription factor-1 and surfactant-associated protein A for investigation of peripheral airway structure in perinatal fatality
  91. Patent Ductus Arteriosus with Infective Endocarditis at Age 92
  92. The sudden and unexpected death of a female-to-male transsexual patient
  93. Application of Stepwise Multiple Regression to Design Optimization of Electric Machine
  94. Pathological demonstration of rapid involvement into the subcutaneous tissue in a case of fatal hydrofluoric acid burns
  95. Selective obstruction of lateral striate capsular arteries due to a small cardiogenic embolus as a cause of acute cerebral infarction limited to unilateral putamen
  96. Fatal hemopericardium caused by retrograde acute abdominal aortic dissection: An autopsy report and morphological consideration
  97. Relationship between cardiopulmonary resuscitation and injuries of the cardiac conduction system: Pathological features and pathogenesis of such injuries*
  98. Simple and sensitive determination of free and total morphine in human liver and kidney using gas chromatography–mass spectrometry
  99. Two adult cases of congenital atresia of the left coronary ostium—comparison of a sudden death case with a long-term survival case
  100. Advanced photomask repair technology for 65nm lithography (3)
  101. Risk factors of sudden death in the Japanese hot bath in the senior population
  102. Sudden unexpected death of a 17-year-old male infected with the influenza virus
  103. 1. An Autopsy Case of Fatal Arrhythmia Induced by Injuries of the Atrioventricular Conduction System: A case report
  104. 3. A Fatal Case of Poisoning by Lidocaine Overdosage – Analysis of Lidocaine in Formalin-Fixed Tissues
  105. Conduction system abnormalities in alcoholics with asymptomatic valvular disease who suffer sudden death
  106. Subendocardial small infarct in the superior ventricular septum as a cause of sudden death
  107. Sudden Unexpected Death of a Methamphetamine Abuser with Cardiopulmonary Abnormalities
  108. Intracerebral hemorrhage as the cause of death in a severely burned body
  109. Unexpected death due to right-sided infective endocarditis in a methamphetamine abuser
  110. Forensic significance of conduction system abnormalities as a precise cause of accidental death
  111. Acute cerebral infarction caused by congenital hypoplasty of cerebral artery in a severe burn case
  112. HPLC simultaneous determination of glycerol and mannitol in human tissues for forensic analysis
  113. Distribution of tetracaine and its metabolite in rabbits after high versus normal spinal anesthesia
  114. Identification of reddish alcoholic beverages by GC/MS using aroma components as indicators
  115. Sudden unexpected death with dysplastic change in the atrioventricular node artery
  116. Histopathological characterization of aortic intimal sarcoma with multiple tumor emboli
  117. Sudden death of an infant with bronchopulmonary dysplasia and bilateral cervical lymphadenopathy—a vagal death?
  118. Recurrent incompetence of repaired floppy mitral valves and the severity of myxomatous degeneration
  119. Prevalence of Renal Artery Stenosis in Autopsy Patients With Stroke
  120. Cerebral Artery Thrombosis as a Cause of Striatocapsular Infarction
  121. A Case of Interleukin-6-producing Malignant Fibrous Histiocytoma Originating in the Heart
  122. Sutured Wound in Myxomatous Mitral Valve One Month After Repair Surgery: Report of Two Cases
  123. Coronary atherosclerosis and interventions: Pathological sequences and restenosis
  124. Two cases of mesotheliaI/monocytic incidental cardiac excrescences of the heart
  125. Valproate Metabolites in High‐Dose Valproate Plus Phenytoin Therapy
  126. Metabolite profiles in patients on high-dose valproate monotherapy
  127. Expression of nitric oxide synthase in macula densa in streptozotocin diabetic rats
  128. A technique for measuring partial erasure
  129. Reye-like syndrome associated with valproic acid