Ph. D., Shinshu University

RNA interference in late-stage hereditary transthyretin amyloidosis: a clinicopathological study
Beck G, Yonenobu Y, Kawai M, Ikenaka K, Sera F, Ozono T, Shimada Y, Yamashita R, Sakata Y, Morii E, Yoshinaga T, Ando Y, Murayama S, Mochizuki H
J Neurol, 270((9)), 4544-4548, 2023

Therapeutic Outcome of Lenalidomide-dexamethasone in Patients with Relapsed or Refractory Systemic Immunoglobulin Light Chain (AL) Amyloidosis : A Single-center Analysis and Review of the Literature
Ueno A,Katoh N,Ezawa N,Yoshinaga T,Yazaki M,Sekijima Y
shinshu med J, 70(1), 29-38, 2022

CSF/plasma levels, transthyretin stabilisation and safety of multiple doses of tolcapone in subjects with hereditary ATTR amyloidosis
Takahashi Y, Ohashi N, Takasone K, Yoshinaga T, Yazaki M, Roberts M, Glidden PF, Sekijima Y
Amyloid, 29(3), 190-196, 2022

AH amyloid neuropathy: a novel clinical phenotype confirmed by histopathology and mass spectrometry
Ohashi N, Katoh N, Kasuga K, Yoshinaga T, Kametani F, Yazaki M, Sekijima Y
Amyloid, 29(2), 141-142, 2022

Severe Cerebral Small Vessel Disease Caused by the Uniallelic p.A252T Variant of HTRA1
Kondo Y, Yoshinaga T, Nakamura K, Yamaguchi T, Ishikawa M, Kosho T, Sekijima Y
Neurol Genet, 9(1), e200047, 2022

Somatostatin-derived amyloid deposition associated with duodenal neuroendocrine tumour (NET): a report of novel localised amyloidosis associated with NET
Ichimata S, Katoh N, Abe R, Yoshinaga T, Kametani F, Yazaki M, Kusama Y, Sano K, Uehara T, Sekijima Y
Amyloid, 29(1), 64-65, 2022

Giant hepatomegaly with spleno-testicular enlargement in a patient with apolipoprotein A-I amyloidosis: an uncommon type of amyloidosis in Japan.
Yoshinaga T, Katoh N, Yazaki M, Sato M, Kametani F, Yasuda H, Watanabe K, Kawata K, Nakagawa M, Sekijima Y
Intern Med, 60(4), 575-581, 2021

Localized Gastric Amyloidosis that Displayed Morphological Changes over 10 Years of Observation
Takahashi Y, Hatta W, Koike T, Ogata Y, Fujiya T, Saito M, Jin X, Nakagawa K, Kanno T, Asanuma K, Uno K, Asano N, Imatani A, Fujishima F, Katoh N, Yoshinaga T, Masamune A
Intern Med, 60(4), 539-543, 2021

Hereditary Apolipoprotein A-1 Amyloidosis With Glu34Lys Mutation Treated by Liver Transplantation: A Case Report
Sagawa T, Kogiso T, Ito T, Yasuda H, Katoh N, Yoshinaga T, Yazaki M, Kato T, Omori A, Kotera Y, Egawa H, Yamamoto M, Tokushige K
Transplant Proc, 53(4), 1327-1332, 2021

Development of diagnostic antibodies against immunoglobulin heavy chain variable region for heavy chain amyloidosis (AH amyloidosis)
Nakagawa M, Yazaki M, Kametani F, Katoh N, Yoshinaga T, Higuchi K, Sekijima Y
Pathol Int, 71(4), 245-254, 2021

Dialysis-related amyloidosis associated with a novel β2-microglobulin variant
Mizuno H, Hoshino J, So M, Kogure Y, Fujii T, Ubara Y, Takaichi K, Nakaniwa T, Tanaka H, Kurisu G, Kametani F, Nakagawa M, Yoshinaga T, Sekijima Y, Higuchi K, Goto Y, Yazaki M
Amyloid., 28(1), 42-49, 2021

Localized intestinal AL amyloidosis detected as bright green using autofluorescence endoscopy
Kuroha M, Yoshinaga T, Yazaki M, Fujishima F, Handa T, Suzuki K, Hishinuma K, Masu Y, Shimoyama Y, Naito T, Moroi R, Kanazawa Y, Shiga H, Kakuta Y, Masamune A
Clin J Gastroenterol, 14(3), 815-819, 2021

A case of novel amyloidosis: glucagon-derived amyloid deposition associated with pancreatic neuroendocrine tumour
Ichimata S, Katoh N, Abe R, Yoshinaga T, Kametani F, Yazaki M, Uehara T, Sekijima Y
Amyloid, 28(1), 72-73, 2021

Distribution of amyloidosis subtypes based on tissue biopsy site - Consecutive analysis of 729 patients at a single amyloidosis center in Japan
Abe R, Katoh N, Takahashi Y, Takasone K, Yoshinaga T, Yazaki M, Kametani F, Sekijima Y
Pathol Int, 71(1), 70-79, 2021

Monitoring of Asymptomatic Family Members at Risk of Hereditary Transthyretin Amyloidosis for Early Intervention With Disease-Modifying Therapies
Ueda M, Sekijima Y, Koike H, Yamashita T, Yoshinaga T, Ishii T, Ando Y
J Neurol Sci, 414, 116813, 2020

Limbic Encephalitis with Anti-myelin Oligodendrocyte Glycoprotein Antibody
Takasone K, Usuda M, Yoshinaga T, Sekijima Y
Intern Med, 59(11), 1465-1466, 2020

A Late-onset and Relatively Rapidly Progressive Case of Pure Spinal Form Cerebrotendinous Xanthomatosis with a Novel Mutation in the CYP27A1 Gene.
Takasone K, Morizumi T,Nakamura K,Mochizuki Y, Yoshinaga T,Koyama S,Sekijima Y
Intern Med, 15;59(20), 2587-2591, 2020

Non-invasive detection and differentiation of cardiac amyloidosis using 99m Tc-pyrophosphate scintigraphy and 11 C-Pittsburgh compound B PET imaging
Takasone K, Katoh N, Takahashi Y, Abe R, Ezawa N, Yoshinaga T, Yanagisawa S, Yazaki M, Oguchi K, Koyama J, Sekijima Y.
Amyloid, 27(4), 266-274, 2020

Temporal artery involvement in AL amyloidosis: an important differential diagnosis for giant cell arteritis. A case report and literature review
Oiwa H, Katoh N, Kojo S, Yoshinaga T, Taniguchi K, Shiote Y
Mod Rheumatol, 4(1), 90-94, 2020

Elderly patient with 5q spinal muscular atrophy type 4 markedly improved by Nusinersen
Morizumi T, Ueno A, Takasone K, Ozawa K, Yoshinaga T, Nakamura K, Sekijima Y
J Neurol Sci, 415, 116901, 2020

Macrophage activation syndrome in adult dermatomyositis: a case‑based review
Kishida D, Sakaguchi N, Ueno K, Ushiyama S, Ichikawa T,Yoshinaga T, Shimojima Y, Sekijima Y
Rheumatol Int, 40(7), 1151-1162, 2020

Alteration of BAFF and APRIL in the cerebrospinal fluid based on the therapeutic response in primary central nervous system B-cell lymphoma
Ikeda J, Shimojima Y, Yoshinaga T, Kodaira M , Nishina S, Ito K, Sekijima Y
J Clin Neurosci, 81, 72-75, 2020

An autopsy case of amyloid tubulopathy exhibiting characteristic spheroid-type deposition
Ichimata S, Hata Y, Abe R, Yoshinaga T, Katoh N, Kametani F, Yazaki M, Sekijima Y, Ehara T, Nishida N
Virchows Arch, 477(1), 157-163, 2020

A case of spheroid-type localized lactoferrin amyloidosis in the bronchus
Ichimata, Shojiro; Aoyagi, Daiju; Yoshinaga, Tsuneaki; Katoh, Nagaaki; Kametani, Fuyuki; Yazaki, Masahide; Uehara, Takeshi; Shiozawa, Satoshi;
PATHOLOGY INTERNATIONAL, 69(4), 235-240, Apr. 2019

Monitoring treatment response to tafamidis by serial native T1 and extracellular volume in transthyretin amyloid cardiomyopathy
Shintani, Yasuhiro; Okada, Atsushi; Morita, Yoshiaki; Hamatani, Yasuhiro; Amano, Masashi; Takahama, Hiroyuki; Amaki, Makoto; Hasegawa, Takuya; Ohta-Ogo, Keiko; Kanzaki, Hideaki; Ishibashi-Ueda, Hatsue; Yasuda, Satoshi; Shimazaki, Chihiro; Yoshinaga, Tsuneaki; Yazaki, Masahide; Sekijima, Yoshiki; Izumi, Chisato;
ESC HEART FAILURE, 6(1), 232-236, Feb. 2019

A novel CACNA1A nonsense variant in a patient presenting with paroxysmal exertion-induced dyskinesia
Ogawa, Yuka; Nakamura, Katsuya; Ezawa, Naoki; Yamaguchi, Tomomi; Yoshinaga, Tsuneaki; Miyazak, Daigo; Kosho, Tomoki; Sekijima, Yoshiki;
JOURNAL OF THE NEUROLOGICAL SCIENCES, 399, 214-216, 2019

Late-onset Transthyretin (TTR)-familial Amyloid Polyneuropathy (FAP) with a Long Disease Duration from Non-endemic Areas in Japan
Miyake, Zenshi; Nakamagoe, Kiyotaka; Ezawa, Naoki; Yoshinaga, Tsuneaki; Hashimoto, Ryosuke; Sato, Taiki; Sekijima, Yoshiki; Tamaoka, Akira;
INTERNAL MEDICINE, 58(5), 713-718, 2019

Nationwide survey on cerebrotendinous xanthomatosis in Japan
Sekijima, Yoshiki; Koyama, Shingo; Yoshinaga, Tsuneaki; Koinuma, Masayoshi; Inaba, Yuji;
JOURNAL OF HUMAN GENETICS, 63(3), 271-280, Mar. 2018

Visualization of multiple organ amyloid involvement in systemic amyloidosis using C-11-PiB PET imaging
Ezawa, Naoki; Katoh, Nagaaki; Oguchi, Kazuhiro; Yoshinaga, Tsuneaki; Yazaki, Masahide; Sekijima, Yoshiki;
EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 45(3), 452-461, Mar. 2018

Hereditary Fibrinogen A-Chain Amyloidosis in Asia: Clinical and Molecular Characteristics
Yazaki, Masahide; Yoshinaga, Tsuneaki; Sekijima, Yoshiki; Kametani, Fuyuki; Okumura, Nobuo;
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 19(1), Jan. 2018

膀胱癌の治療後に膀胱限局性ALアミロイドーシスを発症した一例
佐藤 元己;川畑 さゆき;水野 伸彦;大古 美治;柳本 邦雄;江澤 直樹;吉長 恒明;矢崎 正英
日本泌尿器科学会雑誌, 109(3), 140-143, 2018

消化管アミロイドーシスに非閉塞性腸管虚血を併発した1例
伊東 詩織;吉岡 篤史;小倉 祐紀;並木 伸;板垣 信吾;江夏 一彰;吉長 恒明;矢崎 正英;井上 大;藤原 俊;山田 大貴;三浦 夏希;下地 耕平;中園 綾乃;藤木 純子;堀家 英之
消化器内視鏡の進歩：Progress of Digestive Endoscopy, 90(1), 96-97, 2017

第X因子欠乏症を伴って再燃した原発性マクログロブリン血症
大原 慎;萩原 政夫;華 見;井上 盛浩;内田 智之;吉長 恒明;矢崎 正英;関島 良樹;亀谷 富由樹
臨床血液, 57(3), 359-363, 2016

首下がりを主徴とし舌萎縮を呈した全身性強皮症関連ミオパチーの1例
吉長 恒明;宮崎 大吾;福島 和広;下島 恭弘;松田 正之;池田 修一
臨床神経学, 50(10), 732-735, 01 Oct. 2010

Adult or late-onset triple A syndrome Case report and literature review
Nakamura, Katsuya; Yoshida, Kunihiro; Yoshinaga, Tsuneaki; Kodaira, Minori; Shimojima, Yasuhiro; Takei, Yo-ichi; Morita, Hiroshi; Kayanuma, Katsuhiko; Ikeda, Shu-ichi;
JOURNAL OF THE NEUROLOGICAL SCIENCES, 297(1-2), 85-88, 2010

Peer review
BMJ Case Report, 2018