Ichimata S, Hata Y, Yoshida K, Hirabayashi K, Nishida N. Exploring the usefulness of prostate tissue in diagnosing transthyretin amyloidosis and predicting cardiac outcomes: an autopsy-based study. Pathology. [in press]
Ichimata S, Kuroda T, Yoshinaga T, Sato M, Katoh N, Kametani F, Onagi S, Yazaki M, Sekijima Y, Ishizawa S. Keratin-derived amyloid deposition associated with silicone granuloma in an older adult: Comprehensive analysis using immunohistochemistry, proteomics, and a literature review. Pathol Int. 2025; 75(1): 46-49. doi: 10.1111/pin.13490.
Yoshida K, Forrest SL, Ichimata S, Tanaka H, Kon T, Kovacs GG. Co-pathologies modify hippocampal protein accumulation patterns in neurodegenerative diseases. Alzheimers Dement. 2025; 21(1): e14355. doi: 10.1002/alz.14355.
2024年
Hirono K, Hata Y, Ichimata S, Nishida N, Imamura T, Asano Y, Kuramoto Y, Tsuboi K, Takarada S, Okabe M, Nakaoka H, Ibuki K, Ozawa S, Muneuchi J, Yasuda K, Urayama K, Oka H, Miyamoto T, Baba K, Kato A, Saiki H, Kuwabara N, Harada M, Baba S, Morikawa M, Iwasaki H, Hirata Y, Ito Y, Sakaguchi H, Urata S, Toda K, Kittaka E, Okada S, Hasebe Y, Hoshino S, Fujii T, Mitsushita N, Nii M, Ogino K, Fujino M, Yoshida Y, Fukuda Y, Iwashima S, Takigiku K, Sakata Y, Inuzuka R, Maeda J, Hayabuchi Y, Fujioka T, Namiki H, Fujita S, Nishida K, Kuraoka A, Kan N, Kido S, Watanabe K, Ichida F. Sarcomere gene variants did not improve cardiac function in pediatric patients with dilated cardiomyopathy from Japanese cohorts. Sci Rep. 2024; 14(1): 30469. doi: 10.1038/s41598-024-77360-3
Hirono K, Hata Y, Imamura T, Tsuboi K, Takarada S, Okabe M, Nakaoka H, Ibuki K, Ozawa S, Ichimata S, Nishida N, Iwasaki H, Urata S, Okada S, Hiratsuji T, Sakaguchi H, Takigiku K, Nakazawa M, Nishihara E, Harada M, Matsuo O, Yasuda K, Yoshida Y, Namiki H, Yasuda K, Ifuku T, Urayama K, Oka H, Ogino K, Kato A, Kan N, Seki S, Seki M, Odanaka Y, Iwashima S, Yoshida S, Miyata T, Miyamoto T, Watanabe K, Kuwabara N, Inuzuka R, Takahashi Y, Sakazaki H, Muneuchi J, Kogaki S, Numano F, Kido S, Nii M, Hoshino S, Ishida H, Maeda J, Hayabuchi Y, Otsubo Y, Ikeda K, Tsukano S, Watanabe M, Momoi N, Fujii T, Fujioka T, Fujino M, Uchiyama H, Baba S, Horigome H, Honda T, Suzuki K, Ichida F. Determination of Genotype and Phenotypes in Pediatric Patients With Biventricular Noncompaction. J Am eart Assoc. 2024; 13(21): e035614. doi: 10.1161/JAHA.124.035614
Ichimata S, Hata Y, Nishida N. Basal vacuolization of renal tubules in hypothermia: A comprehensive pathological study based on 79 forensic autopsy cases. Forensic Sci Int. 2024; 365, December 2024, 1122776. https://doi.org/10.1016/j.forsciint.2024.112277
Ichimata S, Hata Y, Yoshida K, Hirono K, Nishida N. Distinctive Deposition Patterns of Sporadic Transthyretin-Derived Amyloidosis in the Atria: A Forensic Autopsy-Based Study. Int J Mol Sci. 2024; 25(15):8176. https://doi.org/10.3390/ijms25158176
Ichimata S, Hata Y, Yoshida K, Nishida N. Clinicopathological Appearance of Epidermal Growth-Factor-Containing Fibulin-like Extracellular Matrix Protein 1 Deposition in the Lower Gastrointestinal Tract: An Autopsy-Based Study. Int J Mol Sci. 2024; 25(14):7581. https://doi.org/10.3390/ijms25147581
Yoshida K, Hata Y, Ichimata S, Tanaka R, Nishida N. Prevalence and clinicopathological features of primary age-related tauopathy (PART): A large forensic autopsy study. Alzheimers Dement . 202 ;20(8):5411-5420. doi: 10.1002/alz.14037.
Sakai T, Tsuboi K, Takarada S, Okabe M, Nakaoka H, Ibuki K, Ozawa SW, Hata Y, Ichimata S, Nishida N, Hirono K. Tachycardia-Induced Cardiomyopathy in an Infant with Atrial Flutter and Prolonged Recovery of Cardiac Function. J Clin Med. 2024;13(11):3313. https://doi.org/10.3390/jcm13113313.
Ichimata S, Hata Y, Nomoto K, Sato T, Nishida N. Sudden unexpected death after initial infusion of rituximab for Waldenström macroglobulinemia/lymphoplasmacytic lymphoma: an autopsy case. Diagn Pathol. 2024;19(1):89. https://doi.org/10.1186/s13000-024-01519-9.
Yoshida K, Forrest SL, Ichimata S, Tanaka H, Kon T, Tartaglia MC, Tator CH, Lang AE, Nishida N, Kovacs GG. Revisiting the relevance of Hirano bodies in neurodegenerative diseases. Neuropathol Appl Neurobiol. 2024;April 17: e12978. https://doi.org/10.1111/nan.12978.
Ichimata S, Hata Y, Yoshinaga T, Katoh N, Kametani F, Yazaki M, Sekijima Y, Nishida N. Amyloid-Forming Corpora Amylacea and Spheroid-Type Amyloid Deposition: Comprehensive Analysis Using Immunohistochemistry, Proteomics, and a Literature Review. Int J Mol Sci. 2024:25(4):4040. https://doi.org/10.3390/ijms25074040.
Ichimata S, Hata Y, Nomoto K, Nishida N. Transthyretin-derived amyloid (ATTR) and sarcoidosis: Does ATTR deposition cause a granulomatous inflammatory response in older adults with sarcoidosis? Cardiovasc Pathol. 2024 Feb 25:70:107624. https://doi.org/10.1016/j.carpath.2024.107624.
Ichimata S, Aikawa A, Sugishita N, Katoh N, Kametani F, Tagawa H, Handa Y, Yazaki M, Sekijima Y, Ehara T, Nishida N, Ishizawa S. Enterocolic granulomatous phlebitis associated with epidermal growth factor-containing fibulin-like extracellular matrix protein 1 deposition and focal amyloid properties: A case report. Pathol Int. 2024 Mar;74(3):146-153. https://doi.org/10.1111/pin.13405.
Hata Y, Nakase M, Ichimata S, Yoshida K, Nishida N. Neuropathology of patients with preclinical or early clinical Alzheimer's disease with pathogenic PSEN1_p. L392V: Comparison of advanced siblings. Alzheimers Dement. 2024 Mar;20(3):2291-2296. https://doi.org/10.1002/alz.13675.
Ichimata S, Hata Y, Yoshida K, Tanaka R, Nishida N. Sudden unexpected death of a young adult due to subarachnoid hemorrhage associated with polyarteritis nodosa: Clinicopathological appearance and literature review. Cardiovasc Pathol. 2024 March-April;69:107602. https://doi.org/10.1016/j.carpath.2023.107602.
Ichimata S, Yoshida K, Li J, Rogaeva E, Lang AE, Kovacs GG. The molecular spectrum of amyloid-beta (Aβ) in neurodegenerative diseases beyond Alzheimer's disease. Brain Pathol. 2024;34(1):e13210. https://doi.org/10.1111/bpa.13210.
Ogawa K, Hata Y, Ichimata S, Yoshida K, Nishida N. An autopsy case of late-onset spinocerebellar atrophy type 14. Neuropathol Appl Neurobiol. 2023;49(5):e12936. https://doi.org/10.1111/nan.12936.
Hata Y, Ichimata S, Yoshida K, Yamaguchi Y, Hirono K, Nishida N. Comprehensive pathological and genetic investigation of three young adult myotonic dystrophy type 1 patients with sudden unexpected death. J Neurol, 2023;270(11):5380-5391. https://doi.org/10.1007/s00415-023-11850-8.
Ichimata S, Martinez-Valbuena I, Lee S, Li J, Karakani AM, Kovacs GG. Distinct Molecular Signatures of Amyloid-Beta and Tau in Alzheimer's Disease Associated with Down Syndrome. Int J Mol Sci, 2023 Jul 18;24(14):11596. https://doi.org/10.3390/ijms241411596.
Nomoto K, Hata Y, Ichimata S, Mizuno S, Nishida N. An autopsy case of infective aortic aneurysm with Pasteurella multocida infection: clinicopathological appearance and a review of literatures. Ann Clin Microbiol Antimicrob, 2023 Jul 11;22(1):58. https://doi.org/10.1186/s12941-023-00611-0.
Kawamura H, Ikawa M, Hirono K, Kimura J, Okuno T, Kawatani M, Inai K, Hata Y, Nishida N, Yoshida Y. Low-frequency maternal novel MYH7 mosaicism mutation in recurrent fetal-onset severe left ventricular noncompaction: a case report. Front Pediatr, 2023;11:1195222. https://doi.org/10.3389/fped.2023.1195222.
Yoshida K, Hata Y, Ichimata S, Okada K, Nishida N. Argyrophilic grain disease is common in older adults and may be a risk factor for suicide: a study of Japanese forensic autopsy cases. Transl Neurodegener, 2023;12(1):16. https://doi.org/10.1186/s40035-023-00352-2.
Ichimata S, Hata Y, Zaimoku R, Nishida N. Acute benzyl alcohol intoxication: An autopsy case report. Medicine (Baltimore), 2023;102(13):e33395. https://doi.org/10.1097/MD.0000000000033395.
Ichimata S, Kim A, Nishida N, Kovacs GG. Lack of difference between amyloid-beta burden at gyral crests and sulcal depths in diverse neurodegenerative diseases. Neuropathol Appl Neurobiol, 2022;49(1):e12869. https://doi.org/10.1111/nan.12869.
Hata Y, Ichimata S, Hirono K, Yamaguchi Y, Oku Y, Ichida F, Nishida N. Pathological and comprehensive genetic investigation of autopsy cases of idiopathic bradyarrhythmia. Circ J. 2023;87(1):111-119. https://doi.org/10.1253/circj.CJ-22-0397.
2022年
Hata Y, Hachiwaka R, Ichimata S, Yamaguchi Y, Nishida N. An autopsy case of sudden unexpected death of a young adult with progressive intraventricular conduction delay. Pathol Res Pract. 2022;240:154226. doi: 10.1016/j.prp.2022.154226.
Okada K, Hata Y, Ichimata S, Yoshida K, Nishida N. Pathological Appearance of a Case of Preclinical Multiple System Atrophy: A Comparison With Advanced Cases. J Neuropathol Exp Neurol. 2022;81(12):965-974. doi: 10.1093/jnen/nlac096.
Ichimata S, Hata Y, Aikawa A, Ishizawa S, Sato D, Akai T, Nishida N. Calcifying pseudoneoplasm of the neuraxis (CAPNON) associated with neurenteric cyst: an autopsy case showing unusual fatal outcome. Neuropathology. 2022;42(6):548-554. doi: 10.1111/neup.12849.
Ichimata S, Martinez-Valbuena I, Forrest SL, Kovacs GG. Expanding the spectrum of amyloid-β plaque pathology: the Down syndrome associated 'bird-nest plaque'. Acta Neuropathol. 2022;144(6):1171-1174. doi: 10.1007/s00401-022-02500-w.
Hata Y, Tomita N, Shibata A, Yokoyama S, Fukahara K, Nishida N. An autopsy case of sudden unexpected death with Barlow’s disease. Cardiovasc Pathol. 2022 Nov-Dec;61:107462. doi: 10.1016/j.carpath.2022.107462.
Ichimata S, Hata Y, Hirota K, Nishida N. Histopathology of acute colchicine intoxication: novel findings and their association with clinical manifestations. J Toxicol Pathol. 2022;35(3):255-262. doi: 10.1293/tox.2022-0007.
Yamada Y, Yasuda K, Hata Y, Nishida N, Hirono K. A Novel NKX2-5 Variant in a Child with Left Ventricular Noncompaction, Atrial Septal Defect, Atrioventricular Conduction Disorder, and Syncope. J Clin Med. 2022;11(11):3171. doi: 10.3390/jcm11113171.
Yamaguchi Y, Sakamoto T, Hata Y, Nishida N, Mizukami K. Recurrent ventricular fibrillation in a patient with inferolateral early repolarization and higher testosterone level. HeartRhythm Case Rep. 2022;8(5):370-373. doi: 10.1016/j.hrcr.2022.02.015.
Ichimata S, Hata Y, Katoh N, Kametani F, Yazaki M, Sekijima Y, Nishida N. 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. Amyloid. 2022;29(2):139-140. doi: 10.1080/13506129.2021.2020754.
Ichimata S, Yoshida K, Visanji NP, Lang AE, Nishida N, Kovacs GG. Patterns of Mixed Pathologies in Down Syndrome. J Alzheimers Dis. 2022;87:595–607. doi: 10.3233/JAD-215675.
Oka H, Nakau K, Imanishi R, Furukawa T, Tanabe Y, Hirono K, Hata Y, Nishida N, Azuma H. A Case Report of a Rare Heterozygous Variant in the Desmin Gene Associated With Hypertrophic Cardiomyopathy and Complete Atrioventricular Block. CJC Open. 2021;3(9):1195-1198. doi: 10.1016/j.cjco.2021.05.003.
Ichimata S, Katho N, Abe R, Yoshinaga T, Kametani F, Yazaki M, Kusama Y, Sano K, Uehara T, Sekijima Y. Somatostatin-derived amyloid deposition associated with duodenal neuroendocrine tumour (NET): a report of novel localised amyloidosis associated with NET. Amyloid. 2022;29:64–65. doi: 10.1080/13506129.2021.1979513.
Ichimata S, Hata Y, Nishida N. Clinicopathological appearance of advanced ketoacidosis with basal vacuolation in renal tubules: An investigation for forensic autopsy and retrospective analysis. Arch Pathol Lab Med. 2022;146(9):1102-1113. doi: 10.5858/arpa.2021-0226-OA.
2021年
Suzuki T, Saito K, Yoshikawa T, Hirono K, Haya Y, Nishida N, Yasuda K, Nagashima M. A double heterozygous variant in MYH6 and MYH7 associated with hypertrophic cardiomyopathy in a Japanese Family. J Cardiol Cases. 2021;25(4):213-217. doi: 10.1016/j.jccase.2021.09.011. eCollection 2022 Apr.
Hata Y, Ichimata S, Nishida N. Two autopsy cases with injuries to the stomach following cardiopulmonary resuscitation. Leg Med (Tokyo). 2021;53:101916. doi: 10.1016/j.legalmed.2021.101916.
Ichimata S, Hata Y, Nishida N. 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. Pathol Int. 2021;71(8):530-537. doi: 10.1111/pin.13127.
Okada K, Hata Y, Ichimata S, Yoshida K, Oku Y, Asahi T, Nishida N. An autopsy case of pure nigropathy with TUBA4A nonsense mutation. Neurupathol Appl Neurobiol. 2021;47(6):891-893. doi: 10.1111/nan.12712.
Ichimata S, Katoh N, Abe R, Yoshinaga T, Kametani F, Yazaki M, Uehara T, Sekijima Y. A case of novel amyloidosis: glucagon-derived amyloid deposition associated with pancreatic neuroendocrine tumor. Amyloid. 2021; 28(1):72-73. doi: 10.1080/13506129.2020.1785417.
Ichimata S, Hata Y, Yajima N, Katayama Y, Nomoto K, Nishida N. Sex-dependent expression of prostatic markers and hormone receptors in cystic tumor of the atrioventricular node: A histopathological study of three cases. Pathol Int. 2021;71(2):141-146. doi: 10.1111/pin.13052.
Ichimata S, Hata Y, Hirono K, Yamaguchi Y, Nishida N. Clinicopathological features of clinically undiagnosed sporadic transthyretin cardiac amyloidosis: a forensic autopsy-based series. Amyloid. 2021;28(2):125-133. doi: 10.1080/13506129.2021.1882979.
Hirono K, Hata Y, Ozawa SW, Toda T, Momoi N, Fukuda Y, Inuzuka R, Nagamine H, Sakaguchi H, Kurosaki K, Okabe M, Takarada S, Miyao N, Nakaoka H, Ibuki K, Origasa H, Bowles NE, Nishida N, Ichida F, for LVNC study collaborators. A burden of sarcomere gene variants in fetal-onset patients with left ventricular noncompaction. Int J Cardiol. 2021;328:122-129. doi: 10.1016/j.ijcard.2020.12.013.
Oka H, Nakau K, Imanishi R, Furukawa T, Tanabe Y, Hirono K, Hata Y, Nishida N, and Azuma H. A case report of a rare heterozygous variant in the desmin gene associated with hypertrophic cardiomyopathy and complete atrioventricular block. CJC Open. 2021;3(9):1195-1198. doi: 10.1016/j.cjco.2021.05.003.
Nishida N, Hata Y, Otani M, Ichimata S, Yoshida K. Traumatic rupture of circle of Willis with closed head injury: its pathology and possible pathogenesis. J Forensic Leg Med. 2021;78:102114. doi: 10.1016/j.jflm.2020.102114.
2020年
Hirono K, Hata Y, Miyao N, Okabe M, Takarada S, Nakaoka H, Ibuki K, Ozawa S, Origasa H, Nishida N, Ichida F. An Increased Burden of Ion Channel Gene Variants Is Related to Distinct Phenotypes in Pediatric Patients with Left Ventricular Noncompaction. Circ Genom Precis Med. 2020;13(4):e002940.
Ichimata S, Hata Y, Nomoto K, Oshima M, Kato Y, Nishida N. Spheroid-type transthyretin amyloidosis in the gallbladder: a possible histopathological diagnostic clue to prevent overlooking cholecystic latent amyloid deposition. Hum Pathol Case Rep. 2020;21:200407.
Shinohara Y，Iwashima S，Hayano S，Shiozawa R，Satou K，Tanaka Y，Osaki M，Nishida N，Hata Y，Hirono K. Barth Syndrome with Tafazzin Variants Associated with Left Ventricular Noncompaction Cardiomyopathy Estimating on Layer-Specific Two-Dimensional Speckle Tracking Echocardiography: A Case Report. J Pediatr Cardiol Card Surg. 2020;4:22-28.
Hirono K, Hata Y, Miyao N, Okabe M, Takarada S, Nakaoka H, Ibuki K, Ozawa S, Yoshimura N, Nishida N, Ichida F. Left Ventricular Noncompaction and Congenital Heart Disease Increases the Risk of Congestive Heart Failure. J Clin Med. 2020;9(3):785.
Miyao N, Hata Y, Izumi H, Nagaoka R, Oku Y, Takasaki I, Ishikawa T, Takarada S, Okabe M, Nakaoka H, Ibuki K, Ozawa S, Yoshida T, Hasegawa H, Makita N, Nishida N, Mori H, Ichida F, Hirono K. TBX5 R264K acts as a modifier to develop dilated cardiomyopathy in mice independently of T-box pathway. PLoS One. 2020;15(4):e0227393.
Ichimata S, Hata Y, Abe R, Yoshinaga T, Katoh N, Kametani F, Yazaki M, Sekijima Y, Ehara T, Nishida N. An autopsy case of amyloid tubulopathy exhibiting characteristic spheroid-type deposition. Virchows Arch. 2020;477(1):157-163.
Ichimata S, Hata Y, Yoshida K, Nishida N. Autopsy of a multiple lobar hemorrhage case with amyloid β–related angiitis. Neuropathology. 2020;40(3):280-286.
Ozuru R, Wakao S, Tsuji T, Ohara N, Matsuba T, Amuran MY, Isobe J, Iino M, Nishida N, Matsumoto S, Iwadate K, Konishi N, Yasuda K, Tashiro K, Hida M, Yadoiwa A, Kato S, Yamashita E, Matsumoto S, Kurozawa Y, Dezawa M, Fujii J. Rescue from Stx2-Producing E. coli-Associated Encephalopathy by Intravenous Injection of Muse Cells in NOD-SCID Mice. Mol Ther. 2020;28(1):100-118.
Hata Y, Oku Y, Taneichi H, Tanaka T, Igarashi N, Niida Y, Nishida N. Two autopsy cases of sudden unexpected death from Dravet syndrome with novel de novo SCN1A variants. Brain Develop. 2020;42:171-178.
Ichimata S, Hata Y, Nishida N. An autopsy case of sudden unexpected death with loxoprofen sodium-induced allergic eosinophilic coronary periarteritis. Cardiovasc Pathol. 2020 Jan-Feb;44:107154.
2019年
Miyao N, Hirono K, Hata Y, Yoshimura N, Ishida F. Novel compound heterozygous TBX5 variants may induce hypoplastic left heart syndrome. Pediatr Int. 2019 Jun;61(6):607-609.
Yoshida K, Hata Y, Ichimata S, Nishida N. Tau and amyloid-β pathology in Japanese forensic autopsy series under 40 years of age: Prevalence and association with APOE genotype and suicide risk.J Alzheimers Dis, 2019, 72:641-52.
Okada K, Hata Y, Takayanagi Y, Takahashi T, Takayanagi I, Nishida N. An autopsy case of preclinical/early clinical Pick’s disease. J Neuropathol Exp Neurol, 2019, 78:971-974.
Hata Y, Ichimata S, Yamaguchi Y, Hirono K, Oku Y, Ichida F, Nishida N. Clinicopathological and genetic profiles of cases with myocytes disarray- investigation for establishing the autopsy diagnostic criteria for hypertrophic cardiomyopathy. J Clin Med, 2019, 8:463.
Hata Y, HIrono K, Yamaguchi Y, Ichida F, Oku Y, Nishida N. Minimal inflammatory foci of unknown etiology may be a tentative sign of early stage inherited cardiomyopathy. Mod Pathol, 2019, 32(9):1281-1290.
Hata Y, Yoshida K, Nishida N. Sudden unexpected death with rare compound heterozygous variants in PRICKLE1. Neurogenetics. 2019, 20;39-43.
Fujino M, Tsuda E, Hirono K, Nakata M, Ichida F, Hata Y, Nishida N, Kurosaki K. The TNNI3 Arg192His mutation in a 13-year-old girl with left ventricular noncompaction. Journal of Cardiology Cases. 2018, 18;33-36.
Nishida N, Ina S, Hata Y, Nakanishi Y, Ishizawa S, Futatani T. Fetal closed head injuries following maternal motor vehicle accident: A clinicopathologic case report. Medicine, 2018, 97:e13133.
Abe M, Kinoshita K, Matsuoka K, Nakada T, Miura K, Hata Y, Nishida N, Tabata T. Lack of modulatory effect of the SCN5A R1193Q polymorphism on cardiac fast Na+ current at body temperature. PLoS One. 2018, 13;e0202437.
Hirono K, Sakai T, Hata Y, Nishida N. The presence of multiple variants affects the clinical phenotype and prognosis in left ventricular noncompaction after surgery. J Thorac Cardiovasc Surg. 2018, 155:e101-e109.
Hata Y, Ishizawa S, Nishida N. Sudden unexpected death with primary adrenal lymphoma. Leg Med (Tokyo). 2018, 35;25-28.
Takasaki A, Hirono K, Hata Y, Chang B, Wang, C, Nakaoka H, Miyao N, Ibuki K, Ozawa S, Sekine M, Yoshimura N, Nishida N, Adachi Y, Bowles NE, Ichida F. Sarcomere gene variants act as a genetic trigger underlining the development of left ventricular noncompaction. Pediatr Res 2018, 84:733-42.
Hirono K, Hata Y, Nakazawa M, Momoi N, Tsuji T, Matsuoka T, Ayusawa M, Abe Y, Hayashi T, Tsujii N, Abe T, Sakaguchi H, Wang C, Takasaki A, Takarada S, Okabe M, Miyao N, Nakaoka H, Ibuki,K, Saito K, Ozawa S, Nishida N, Bowles Nl; Ichida F. Clinical and echocardiographic impact of TAZ gene variants on the DCM phenotype of LVNC patients during early infancy. Circ J. 2018, 82;2609-18.
Yokoyama R, Kinoshita K, Hata Y, Abe M, Matsuoka K, Hirono K, Kano M, Nakazawa M, Ichida F, Nishida N, Tabata T. A mutant HCN4 channel in a family with bradycardia, left bundle branch block, and left ventricular noncompaction. Heart Vessels. 2018, 33;802-19.
Hata Y, Yoshida K, Nishida N. Autopsy of an Elderly Man with Incidentally Diagnosed TDP-43 Proteinopathy. Alzheimer Dis Assoc Disord. 2018, 32;158-61.
2017年
Yoshida K, Hata Y, Kinoshita K, Nishida N. Argyrophilic grain disease in a 46-year-old male suicide victim. J Neurol Sci. 2017, 380;223-5.
Wang C, Hata Y, Hirono K, Takasaki A, Ozawa S, Nakaoka H, Saito K, Miyao N, Okabe M, Ibuki K, Nishida N, Origasa H, Yu X, Bowles NE, Ichida F. A Wide and specific spectrum of genetic variants and genotype-phenotype correlations revealed by next-generation sequencing in patients with left ventricular noncompaction. JAHA. 2017, 30:6(9).
Nishida N, Hata Y. A case of sudden unexpected death with the presence of multiple myocadial bridges. Int J Clin Cardiol. Int J Clin Cardiol. 2017, 4:099.
Nishida N, Yoshida K. Hata Y. Sudden unexpected death in early Parkinson’s disease: neurogenic or cardiac death? Cardiovasc Pathol. 2017, 30:19-22.
Nishida N. Hata Y, Nomoto K. Intramyocardial bronchogenic cyst: histological appearance and a review of the literature. Cardiovasc Pathol. 2017, 28:64-7.
Hata Y, Kinoshita K, Nishida N. An autopsy case with sudden unexpected death of young adult in hot baths : molecular analysis using next-generation
DNA sequencing. Clin Med Insights Case Rep. 2017, 10:1-6.
Yoshida K, Hata Y, Kinoshita K, Takashima S, Tanaka K, Nishida N. Incipient progressive supranuclear palsy is more common than expected and may comprise clinicopathological subtypes: a forensic autopsy series. Acta Neuropathol. 2017, 133:809-23.
Yamaguchi Y, Mizumaki K, Hata Y, Sakamoto T, Nakatani Y, Kataoka N, Ichida F, Inoue H, Nishida N. Latent pathogenicity of the G38S polymorphism of KCNE1 K+ channel modulator. Heart Vessels. 2017, 32:186-92.
Hata Y, Yoshida K, Kinoshita K, Nishida N. Epilepsy-related sudden unexpected death: molecular analysis using next-generation DNA sequencing. Brain Pathol. 2017, 27:292-304.
2016年
Nishida N, Hata Y, Kinoshita K, Nonomura M. A pseudoaneurysmal defect of mitral-aortic intervalvular fibrosa is likely to be a cerebral embolic source. An autopsy study in remote period from the stroke. Pathol Int. 2016, 66(8):472-4.
Hata Y, Kinoshita K, Mizumaki K, Yamaguchi Y, Hirono K, Ichida F, Takasaki A, Mori H, Nishida N. Postmortem genetic analysis of sudden unexplained death syndrome under 50 years of age : a next-generation sequencing study. Heart Rhythm. 2016, 13(7):1544-51.
Hachiya A, Motoki N, Akazawa Y, Matsuzaki S, Hirono K, Hata Y, Nishida N, Ichida F, Koike K. LVNC revealed by aortic regurgitation due to Kawasaki desease in a boy with LDB3 gene mutation. Pediatr Int. 2016, 58(8):797-800.
Hirono K, Hata Y, Miyao N, Nakaoka H, Saito K, Watanabe K, Ozawa S, Higuma T, Yoshimura N, Nishida N, Ichida F. Anomalous origin of the right coronary evaluated with multidetector computed tomography and its clinical relevance. J Cardiol. 2016, 68(3):196-201.
Kinoshita K, Takahashi H, Hata Y, Nishide K, Kato M, Fujita H, Yoshida S, Murai K, Mizumaki K, Nishida K, Yamaguchi Y, Kano M, Tabata T, Nishida N. SCN5A(K817E), A novel brugada syndrome-associated mutation that alters the activation gating of NaV1.5 channel. Heart Rhythm. 2016, 13(5):1113-20.
Yamaguchi Y, Mizumaki K, Hata Y, Inoue H. Abnormal repolarization dynamics in a patiect with KCNE1(G38S) who presented with torsades de pointes. J Electrocardiol. 2016, 49:94-8.
Yoshida Y, Hirono K, Nakamura K, Suzuki T, Hata Y, Nishida N. A novel ACTC1 mutation in a young boy with left ventricular noncompaction and arrhythmias. Heart Rhythm Case Report. 2016, 2(1):92-7.
2015年
Bunai Y, Ishii A, Akaza K, Nagai A, Nishida N, Yamaguchi S. A case of sudden death after Japanese encephalitis vaccination. Legal Med. 2015, 17:279-82.
西田尚樹 : 腸管出血性大腸菌感染症の病理. 病理と臨床. 文光堂 東京 2015, 832-8.
Hata Y, Chiba T, Ohtani M, Ishizawa S, Nishida N. An autopsy case of pneumococcal Waterhouse-Friderichsen syndrome with possible functional asplenia/hyposplenia. Int J Clin Exp Pathol. 2015, 8:7518-25.
Hisajima N, Hata Y, Kinoshita K, Fukushima T, Nishida N, Kato M, Tabata T. The susceptibilities of human ether-à-go-go-related gene channel with the G487R mutation to arrhythmogenic factors. Biol Pharm Bull. 2015, 38:781-4.
Nishida N, Hata Y, Yoshida K, Kinoshita K. Neuropathological features of suicide victims who presented with acute poststroke depression: Significance of association with neurodegenerative disorders. J Neuropathol Exp Neurol. 2015, 74:401-10.
Nishida N, Yoshida K, Hata Y, Arai Y, Kinoshita K. Pathological features of preclinical or early clinical stages of corticobasal degeneration: a comparison with advanced cases. Neuropathol Appl Neurobiol. 2015, 41:893-905.
Hata Y, Kinoshita K, Kudo K, Ikeda N, Nishida N. Anomalous origin of the right coronary artery from the left coronary sinus with intramural course-comparison between sudden death and non-sudden death cases. Cardiovasc Pathol. 2015, 24:154-9.
Nomura Y, Momoi N, Hirono K, Hata Y, Takasaki A, Nishida N, Ichida F. A novel MYH7 gene mutation in a fetus with left ventricular noncompaction. Can J Cardiol. 2015, 103:e1-3.
2014年
Hirono K, Hata Y, Ibuki K, Yoshimura N. Familial Ebstein's anomaly, left ventricular noncompaction, and ventricular septal defect associated with an MYH7 mutation. J Thorac Cardiovasc Surg. 2014, 148:e223-6.
Tabata T, Yamaguchi Y, Hata Y, Ichida F, Mori H. Modification of KCNH2-encoded cardiac potassium channels by KCNE1 polymorphism. Circ J. 2014, 78:2331.
西田尚樹, 畑由紀子 : 法医解剖と病理. 病理と臨床. 2014, 32:735-42.
Hata Y, Mori H, Tanaka A, Fujita Y, Shimomura T, Tabata T, Kinoshita K, Yamaguchi Y, Ichida F, Kominato Y, Ikeda N, Nishida N. Identification and characterization of a novel genetic mutation with prolonged QT syndrome in an unexplained postoperative death. Int J Legal Med. 2014, 128:105-15.
Hata Y, Takeuchi Y, Kinoshita K, Nishida N. An autopsy case of acute non-alcoholic thiamine-deficient encephalopathy. Eur Neurol. 2014, 71:230-2.
Nishida N, Hata Y, Kinoshita K. High takeoff of the left main coronary artery at autopsy after sudden unexpected death in a male. Pathology. 2014, 46:361-4.
Yamaguchi, Y, Nishide K, Kato M, Hata, Y, Mizumaki K, Kinoshita K, Nonobe Y, Tabata T, Sakamoto T, Kataoka N, Nakatani Y, Ichida F, Mori H, Fukurotani K, Inoue H, Nishida N. Glycine/serine polymorphism at position 38 influences KCNE1 subunit's modulatory actions on rapid and slow delayed rectifier K currents. Circ J. 2014, 78:610-8.
Kinoshita K, Komatsu T, Nishide K, Hata Y, Hisajima N, Takahashi H, Kimoto K, Aonuma K, Tushima E, Tabata T, Yoshida T, Mori H, Nishida K, Yamaguchi Y, Ichida F, Fukurotani K, Inoue H, Nishida N. A590T mutation in KCNQ1 C-terminal helix D decreases IKs channel trafficking and function but not Yotiao interaction. J Mol Cell Cardiol. 2014, 72:273-80.
Hata Y, Yoshida K, Kinoshita K, Nishida N. Sudden unexpected death owing to unilateral medial medullary infarction with early involvement of the respiratory center. Leg Med. 2014, 16:146-9.
Hata Y, Kinoshita K, Miya K, Hirono K, Ichida F, Yoshida K, Nishida N. An autopsy case of infantile-onset vanishing white matter disease related to an EIEF2B2 mutation(V85E) in a hemizygous region. Int J Clin Exp Pathol. 2014, 7:3355-62.
Nishida N, Yamagishi S, Mizukami H, Yagihashi S. Impaired nerve fiber regeneration in axotomized peripheral nerves in streptozotocin-diabetic rats. J Diabetes Invest. 2013, 4:533-539.
Kimoto K, Kinoshita K, Yokoyama T, Hata Y, Komatsu T, Tsushima E, Nishide K, Yamaguchi Y, Mizumaki K, Tabata T, Inoue H, Nishida N, Fukurotani K. Characterization of a novel mutant KCNQ1 channel subunit lacking a large part of the C-terminal domain. Biochem Biophys Res Commun. 2013, 440:283-288.
Chang B, Gorbea C, Lezin G, Li L, Shan L, Sakai N, Kogaki S, Otomo T, Okinaga T, Hamaoka A, Yu X, Hata Y, Nishida N, Yost HJ, Bowles NE, Brunelli L, Ichida F. 14-3-3ε gene variants in a Japanese patient with left ventricular noncompaction and hypoplasia of the corpus callosum. Gene. 2013, 515:173-180.
Hao H, Ishibashi-Ueda H, Nishida N, Kawakami R, Tsukamoto Y, Tsujimoto M, Hirota S. Distribution of myofibroblast and tenascin-C in cystic adventitial disease : Comparison with ganglion. Pathol Int. 2013 Dec;63(12):591-8.
Kinoshita K, Yamaguchi Y, Nishide K, Kimoto K, Nonobe Y, Fujita A, Asano K, Tabata T, Mori H, Inoue H, Hata Y, Fukurotani K, Nishida N. A novel missense mutation causing a G487R substitution in the S2-S3 loop of human ether-à-go-go-related gene channel. J Cardiovasc Electrophysiol. 2012, 23:1246-53.
Uchiyama T, Yoshimura K, Kaneko K, Nemoto S, Ichida F, Hata Y, Nishida N. Surgical repair of left ventricular noncompaction in a patient with a novel mutation of the myosin heavy chain 7 gene. Tohoku J. Exp. Med. 2012, 228:01-4.
Hikiji W, Kudo K, Nishida N, Ishida T, Usumoto Y, Tsuji A, Ikeda N. Acute fatal poisoning with pilsicainide and atenolol. Int J Legal Med. 122(6): 503-6, 2008.
Kage S, Kudo K, Nishida N, Ikeda H, Yoshioka N, Ikeda N. Determination of fluoride in human whole blood and urine by gas chromatography-mass spectrometry. Forensic Toxicol. 26: 23-6, 2008.
Satoh T, Nishida N. Patent ductus arteriosus with infective endocarditis at age 92. Intern Med. 47(4): 263-8, 2008.
Shimada I, Matsui K, Kominato Y, Hata Y, Takizawa H, Nishida N. Immunohistochemical study of thyroid transcription factor-1 and surfactant-associated protein A for investigation of peripheral airway structure in perinatal fatality. Legal Med. 10(2):96-100, 2008.
Ohtani M, Nishida N, Chiba T, Fukuda M, Miyamoto Y, Yoshioka N. Indication and limitations of using palatal rugae for personal identification in edentulous cases. Forensic Sci Int. 176(2-3):178-82, 2008.
Inoue H, Nishida N, Ikeda N, Tsuji A, Kudo K, Hanagama M, Nata M. The sudden and unexpected death of a female-to-male trasnssexual patient. J Forensic and Legal Med. 14: 382-386. 2007.
Ohtani M, Nishida N, Chiba T, Muto H, Yoshioka N. Pathological demonstration of rapid involvement into the subcutaneous tissue in a case of fatal hydrofluoric acid burns. Forensic Sci Int. 167: 49-52. 2007.
Hata Y, Kominato Y, Takizawa H. Identification and characterization of a novel antisense RNA transcribed from the opposite strand of the human blood group ABO gene. Transfusion 47: 842-851, 2007.
2006年
Nishida N, Chiba T, Ohtani M, Ikeda N, Katayama Y, Yoshioka N. Relationship between cardiopulmonary resuscitation and injuries of the cardiac conduction system: Pathological features and pathogenesis of such injuries. Crit Care Med 34: 363-367, 2006.
Kudo K, Ishida T, Nishida N, Yoshioka N, Inoue H, Tsuji A, Ikeda N. Simple and sensitive determination of free and total morphine in human liver and kidney using gas chromatography-mass spectrometry. J Chromatogr B Analyt Technol Bilmed Life Sci 830: 359-363, 2006.
Chiba T, Nishida N, Ohtani M, Suzuki I, Yoshioka N. Fatal hemopericardium caused by retrograde acute abdominal aortic dissection: an autopsy report and morphological consideration. Int J Cardiol 112: 253-255, 2006.
2005年
Nishida N, Chiba T, Ohtani M, Yoshioka N. Sudden unexpected death of a 17-year-old male infected with influenza virus. Legal Med 7: 51-57, 2005.
Chiba T, Yamauchi M, Nishida N, Kaneko T, Yoshizaki K, Yoshizaki N. Risk factors of sudden death in the Japanese hot bath in the senior population. Forensic Sci Int 149:151-158, 2005.
Nishida N, Chiba T, Ohtani M, Yoshioka N. Two adult cases of congenital atresia of the left coronary ostium- Comparison of a sudden death case with a long-term survival case. Virchows Archiv 447: 742-746, 2005.
Chiba T, NIshida N, Ohtami M, Yoshioka N. Acute generalized peritonitis arising from perforation of a Helicobacoter pylori-positive duodenal ulcer: autopsy case of a 12-year-old boy. Res Pract Forens Med 48: 211-216, 2005.
Kominato Y, Hata Y, Takizawa H, Regulation of ABO gene expression. Legal Med 7: 263-265, 2005.
Michino J, Hata Y, Matsui K, Takizawa Y, Tabata S, Nishino K, Yasumura S, Kitajima I. Demonstration of A antigen and Allele of ABO histo-blood group in nail in a case with the absence of Antigen and anti-A antibody in blood. Legal Med 7: 194-197, 2005.
2004年
Inoue H, Ikeda N, Tsuji A, Kudo K, Nishida N. An autopsy case of fatal arrhythmia induced by injuries of the atrioventricular conduction system: A case report. Med Sci Law 44: 353-358, 2004.
Kubo K, Nishida N, Kiyoshima A, Ikeda N. A fata case of poisoning by lidocaine overdosage? Analysis of Lidocaine in formalin-fixed tissue. Med Sci Law 44: 266-271, 2004.
Kominato Y, Matsui K, Hata Y, Matsui K, Kuwayama N, Ishizawa S, Takizawa H. Acute subdural hematoma due to arteriovenous malformation primarily in dura mater: a case report. Legal Med 6: 256-260, 2004.
Kominato Y, Fujikura T, Hata Y, Matsui K, Takizawa H. A case of postoperative hemorrhage after a hysterectomy in which ableeding point of the left uterine artery was identified by postmortem angiography. Legal Med 6: 187-189, 2004.
Kominato Y, Hata Y, Matsui K, Takizawa H, Tsukada J, Nakajima T, Kaneko Y, Kishi K. Transcriptional regulation of the human ABO histo-blood group genes is dependent on the N box upstream of the proximal promoter. Transfusion 44: 1741-1749, 2004.
2003年
Nishida N, Kudo K, Esaki R, Ikeda N. Sudden unexpected death of two obese psychiatric patients with microscopic cardiopulmonary abnormality. Fukuoka Acta Med 94: 66-74, 2003.
Nishida N, Ikeda N, Kudo K, Esaki R. Sudden unexpected death of a methamphetamine abuser with cardiopulmonary abnormalities: A case report. Med Sci Law 43: 267-271, 2003.
Nishida N, Ikeda N, Esaki R, Kudo K, Tsuji A. Conduction system abnormalities in sudden death of alcohol abusers with asymptomatic valvular disease. Legal Med 5: 212-219, 2003.
Nishida N, Ikeda N, Katayama Y, Kudo K, Takasaki T. Subendocardial small infarct in the superior ventricular septum as a cause of sudden death. Forensic Sci Int 138: 62-67,2003.
Takasaki T, Nishida N, Kudo K, Esaki R, Ikeda N. Unexpected death due to right-sided infective endocarditis in a methamphetamine abuser. Legal Med 5: 65-68, 2003.
Chiba T, Nishida N, Gonmori K, Yoshioka N. Interacerebral hemorrhage as the case of death in a severely burned body. Legal Med 5: 108-109, 2003.
Hata Y, Kominato Y, Takizawa H, Tabata S, Michino J, Nishino K, Yasuhara H, Yamamoto F. Transcription starting from an alternative promoter leads to the expression of the human ABO histo-blood group antigen. Transfusion 43: 656-662, 2003.
2002年
Nishida N, Ikeda N, Tsuji A, Esaki R. Acute cerebral infarction caused by congenital hypoplasty of cerebral artery in a severe burn case. Legal Med 4: 119-122, 2002.
Nishida N, Ikeda N, Kudo K, Tsuji A, Kiyoshima A. Forensic significance of the conduction system abnormalities as a precise cause of accidental death. Int J Legal Med: 116: 344-349, 2002.
Kudo K, Ikeda N, Kiyoshima A, Hino Y, Nishida N, Inoue N. Toxicological analysis of chlorhexidine in human serum using HPLC on a polymer-coated ODS colum. J Anal Toxicol 26: 119-122, 2002.
Kiyoshima A, Kudo K, Nishida N, Ikeda N. HPLC simultaneous determination of glycerol and mannitol in human tissues for forensic analysis. Forensic Sci Int 125: 127-133, 2002.
Hata Y, Kominato Y, Yamamoto F, Takizawa H. Characterization of the human ABO gene promoter in erythroid cell lineage. Vox Sang 82: 39-46, 2002.
Kominato Y, Hata Y, Takizawa H, Matusmoto K, Yasui K, Tsukada J, Yamamoto F. Alternative promoter identified between a hypermethylated upstream region of repetitive elements and a CpG island in human ABO histo-blood group genes. J Biol Chem 277: 37936-37948, 2002.
2001年以前
Hino Y, Inoue H, Nishida N, Ikeda N. Distribution of tetracaine and its metabolite in rabbits after high versus normal spinal anesthesia. Forensic Sci Int 124: 130-136, 2001.
Yamamoto M, Lin XH, Kominato Y, Hata Y, Noda R, Saitou N, Yamamoto F. Murine equivalent of the human histo-blood group ABO gene is a cis-AB gene and encodes a glycosyltransferase with both A and B trasnferase activity. J Biol Chem 276: 13701-13708, 2001.
Nishida N, Ogata J, Yutani C, Minematsu K, Yamaguchi T. Cerebral artery thrombosis as a cause of striatocapusular infarction. Cerebrovasc Dis 10: 151-154, 2000.
Nishida N, Ikeda N. Sudden death of an infant with bronchopulmonary dysplasia and bilateral cervical lymph adenopathy-a vagal death? Legal Med 2: 106-109, 2000.
Nishida N, Ikeda N, Tsuji A, Nakanishi K. A case of attempting to induce sudden cardiac death through the use of stungun. Acta Crim Japon 66: 240-244, 2000.
Nishida N, Yutani C, Ishibashi-Ueda H, Tsukamoto Y, Ikeda Y, Nakamura Y. Histopathological characterization of aortic intimal sarcoma with multiple tumor emboli. Pathol Int 50: 923-927, 2000.
Nishida N, Tsuji A, Ikeda N. Traumatic false aneurysm of the descending aorta which reuptured right thoracic cavity. Fukuoka Acta Med 91: 292-296, 2000.
Nishida N, Ikeda N, Tsuji A.Sudden unexpected death with dysplastic change in the atroventricular node artery. Legal Med 2: 216-219, 2000.
Kuroda S, Nishida N, Uzu T, Takeji M, Nishimura M, Fujii T, Nakamura S, Inenaga T, Yutani C, Kimura G. Prevalence of renal artey stenosis in autopsy patients with stroke. Stroke 31: 61-65, 2000.
Kominato Y, Hata Y, Takizawa H, Tsuchiya T, Tsukada J, Yamamoto F. Expression of human histo-blood group ABO genes is dependent upon DNA methylation of the promoter region. J Biol Chem 274: 37240-37250, 1999.
