Detalhe da pesquisa
1.
Amyloid-Forming Corpora Amylacea and Spheroid-Type Amyloid Deposition: Comprehensive Analysis Using Immunohistochemistry, Proteomics, and a Literature Review.
Int J Mol Sci
; 25(7)2024 Apr 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38612850
2.
Development of diagnostic antibodies against immunoglobulin heavy chain variable region for heavy chain amyloidosis (AH amyloidosis).
Pathol Int
; 71(4): 245-254, 2021 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-33713540
3.
Distribution of amyloidosis subtypes based on tissue biopsy site - Consecutive analysis of 729 patients at a single amyloidosis center in Japan.
Pathol Int
; 71(1): 70-79, 2021 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-33112446
4.
Macrophage activation syndrome in adult dermatomyositis: a case-based review.
Rheumatol Int
; 40(7): 1151-1162, 2020 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-32356114
5.
A case of spheroid-type localized lactoferrin amyloidosis in the bronchus.
Pathol Int
; 69(4): 235-240, 2019 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-30779453
6.
Nationwide survey on cerebrotendinous xanthomatosis in Japan.
J Hum Genet
; 63(3): 271-280, 2018 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-29321515
7.
Visualization of multiple organ amyloid involvement in systemic amyloidosis using 11C-PiB PET imaging.
Eur J Nucl Med Mol Imaging
; 45(3): 452-461, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28891012
8.
Hereditary Fibrinogen Aα-Chain Amyloidosis in Asia: Clinical and Molecular Characteristics.
Int J Mol Sci
; 19(1)2018 Jan 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-29361747
9.
[Recurrence of Waldenström macroglobulinemia accompanied by factor X deficiency].
Rinsho Ketsueki
; 57(3): 359-63, 2016 Mar.
Artigo
em Japonês
| MEDLINE | ID: mdl-27076250
10.
Pathological, biochemical, and biophysical characteristics of the transthyretin variant Y114H (p.Y134H) explain its very mild clinical phenotype.
J Peripher Nerv Syst
; 20(4): 372-9, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26306725
11.
Genetic counselling for at-risk family members with hereditary transthyretin amyloidosis: data from a single-centre study.
Amyloid
; : 1-5, 2024 May 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-38795075
12.
Long-term Observation of a Japanese Patient with a Multiple-system Neurodegenerative Disorder with a Uniallelic de novo Missense Variant in KIF1A.
Intern Med
; 62(20): 3047-3051, 2023 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36889712
13.
Severe Cerebral Small Vessel Disease Caused by the Uniallelic p.A252T Variant of HTRA1.
Neurol Genet
; 9(1): e200047, 2023 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-36530220
14.
Ocular findings in patients with acquired ATTRv amyloidosis following domino liver transplantation.
PLoS One
; 18(9): e0291716, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37713404
15.
Lysinuric protein intolerance exhibiting renal tubular acidosis/Fanconi syndrome in a Japanese woman.
JIMD Rep
; 64(6): 410-416, 2023 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-37927490
16.
Cardiac Amyloidosis Associated With Amyloidogenic Transthyretin V122I Variant in an Elderly Japanese Woman.
Circ J
; 81(6): 893-894, 2017 May 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-28090011
17.
CSF/plasma levels, transthyretin stabilisation and safety of multiple doses of tolcapone in subjects with hereditary ATTR amyloidosis.
Amyloid
; 29(3): 190-196, 2022 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-35352593
18.
Giant Hepatomegaly with Spleno-testicular Enlargement in a Patient with Apolipoprotein A-I Amyloidosis: An Uncommon Type of Amyloidosis in Japan.
Intern Med
; 60(4): 575-581, 2021 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-32999221
19.
Localized intestinal AL amyloidosis detected as bright green using autofluorescence endoscopy.
Clin J Gastroenterol
; 14(3): 815-819, 2021 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-33904108
20.
Dialysis-related amyloidosis associated with a novel ß2-microglobulin variant.
Amyloid
; 28(1): 42-49, 2021 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-32875920