All Stories

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