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Transthyretin: Its function and amyloid formation

Neurochemistry international, 2022-05, Vol.155, p.105313-105313, Article 105313

Ueda, Mitsuharu

2022

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JCS 2020 Guideline on Diagnosis and Treatment of Cardiac Amyloidosis

Circulation Journal, 2020/08/25, Vol.84(9), pp.1610-1671

2020

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Diagnosis and management of transthyretin familial amyloid polyneuropathy in Japan: red-flag symptom clusters and treatment algorithm

Orphanet journal of rare diseases, 2018-01, Vol.13 (1), p.6-6, Article 6

2018

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Early transverse tubule involvement in cardiomyocytes in hereditary transthyretin amyloidosis: a possible cause of cardiac events

Cardiovascular pathology, 2022-11, Vol.61, p.107458-107458, Article 107458

2022

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Metformin attenuates vascular pathology by increasing expression of insulin-degrading enzyme in a mixed model of cerebral amyloid angiopathy and type 2 diabetes mellitus

Neuroscience letters, 2021-09, Vol.762, p.136136-136136, Article 136136

2021

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First Nationwide Survey of 199 Patients with Amyloid A Amyloidosis in Japan

Internal Medicine, 2018/12/01, Vol.57(23), pp.3351-3355

2018

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Current Management and Therapeutic Strategies for Cerebral Amyloid Angiopathy

International journal of molecular sciences, 2021-04, Vol.22 (8), p.3869

2021

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Autoimmune Polyglandular Syndrome with Refractory Gait Disturbance

Internal Medicine, 2023/07/15, Vol.62(14), pp.2133-2137

2023

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Miller Fisher Syndrome Following Vaccination against SARS-CoV-2

Internal Medicine, 2022/04/01, Vol.61(7), pp.1067-1069

2022

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Early onset Congo red‐positive fibrillary glomerulonephritis associated with glomerular DNAJB9 deposits mimicking renal amyloidosis

Pathology international, 2023-02, Vol.73 (2), p.106-108

2023

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Two autopsy cases of wild-type transthyretin cardiac amyloidosis who died 10 days after technetium-99m-pyrophosphate scintigraphy

Journal of nuclear cardiology, 2023-10, Vol.30 (5), p.2215-2221

2023

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Possible Cerebral Vasculitis in a Case with Rheumatoid Arthritis

Internal Medicine, 2021/03/15, Vol.60(6), pp.935-940

2021

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EGF‐containing fibulin‐like extracellular matrix protein 1 (EFEMP1) amyloid deposits in the lower rectum from aged patient with bloody stools

Pathology international, 2022-03, Vol.72 (3), p.217-218

2022

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Guidelines and new directions in the therapy and monitoring of ATTRv amyloidosis

Amyloid, 2022-07, Vol.29 (3), p.143-155

2022

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Trends in Diagnostic Imaging of Cardiac Amyloidosis: Emerging Knowledge and Concepts

Radiographics, 2020-07, Vol.40 (4), p.190069-981

2020

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SIRT7 Deficiency Protects against Aβ42-Induced Apoptosis through the Regulation of NOX4-Derived Reactive Oxygen Species Production in SH-SY5Y Cells

International journal of molecular sciences, 2022-08, Vol.23 (16), p.9027

2022

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Feasibility Study of Dendrimer-Based TTR-CRISPR pDNA Polyplex for Ocular Amyloidosis in Vitro

Biological and Pharmaceutical Bulletin, 2022/11/01, Vol.45(11), pp.1660-1668

2022

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Human amyloidosis, still intractable but becoming curable: The essential role of pathological diagnosis in the selection of type‐specific therapeutics

Pathology international, 2020-04, Vol.70 (4), p.191-198

2020

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Myopathic changes caused by protein aggregates in adult-onset spinal muscular atrophy

Neuropathology, 2023-10, Vol.43 (5), p.408-412

2023

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Nationwide Survey of 741 Patients with Systemic Amyloid Light-chain Amyloidosis in Japan

Internal Medicine, 2018/01/15, Vol.57(2), pp.181-187

2018

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Identification and Assessment of Cardiac Amyloidosis by Myocardial Strain Analysis of Cardiac Magnetic Resonance Imaging

Circulation Journal, 2017/06/23, Vol.81(7), pp.1014-1021

2017

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Myocarditis in Myasthenia Gravis　― Multiparametric Evaluation Using Cardiac Magnetic Resonance Imaging

Circulation Journal, 2022/10/25, Vol.86(11), pp.1788

2022

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Treatment response to Tafamidis quantitatively assessed by serial bone scintigraphy in transthyretin amyloid cardiomyopathy

Journal of nuclear cardiology, 2023-02, Vol.30 (1), p.403-404

2023

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Delayed cerebral complications associated with endovascular catheter coil embolization for pulmonary venous shunts mimicking cerebral inflammatory diseases

Heliyon, 2024-07, Vol.10 (13), p.e33541, Article e33541

2024

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Transthyretin: Its function and amyloid formation

JCS 2020 Guideline on Diagnosis and Treatment of Cardiac Amyloidosis

Patisiran, an RNAi Therapeutic, for Hereditary Transthyretin Amyloidosis

Diagnosis and management of transthyretin familial amyloid polyneuropathy in Japan: red-flag symptom clusters and treatment algorithm

Early transverse tubule involvement in cardiomyocytes in hereditary transthyretin amyloidosis: a possible cause of cardiac events

Metformin attenuates vascular pathology by increasing expression of insulin-degrading enzyme in a mixed model of cerebral amyloid angiopathy and type 2 diabetes mellitus

First Nationwide Survey of 199 Patients with Amyloid A Amyloidosis in Japan

Current Management and Therapeutic Strategies for Cerebral Amyloid Angiopathy

Autoimmune Polyglandular Syndrome with Refractory Gait Disturbance

Miller Fisher Syndrome Following Vaccination against SARS-CoV-2

Early onset Congo red‐positive fibrillary glomerulonephritis associated with glomerular DNAJB9 deposits mimicking renal amyloidosis

Two autopsy cases of wild-type transthyretin cardiac amyloidosis who died 10 days after technetium-99m-pyrophosphate scintigraphy

Possible Cerebral Vasculitis in a Case with Rheumatoid Arthritis

EGF‐containing fibulin‐like extracellular matrix protein 1 (EFEMP1) amyloid deposits in the lower rectum from aged patient with bloody stools

Guidelines and new directions in the therapy and monitoring of ATTRv amyloidosis

Trends in Diagnostic Imaging of Cardiac Amyloidosis: Emerging Knowledge and Concepts

SIRT7 Deficiency Protects against Aβ42-Induced Apoptosis through the Regulation of NOX4-Derived Reactive Oxygen Species Production in SH-SY5Y Cells

Feasibility Study of Dendrimer-Based TTR-CRISPR pDNA Polyplex for Ocular Amyloidosis in Vitro

Human amyloidosis, still intractable but becoming curable: The essential role of pathological diagnosis in the selection of type‐specific therapeutics

Myopathic changes caused by protein aggregates in adult-onset spinal muscular atrophy

Nationwide Survey of 741 Patients with Systemic Amyloid Light-chain Amyloidosis in Japan

Identification and Assessment of Cardiac Amyloidosis by Myocardial Strain Analysis of Cardiac Magnetic Resonance Imaging

Myocarditis in Myasthenia Gravis　― Multiparametric Evaluation Using Cardiac Magnetic Resonance Imaging

Treatment response to Tafamidis quantitatively assessed by serial bone scintigraphy in transthyretin amyloid cardiomyopathy

Delayed cerebral complications associated with endovascular catheter coil embolization for pulmonary venous shunts mimicking cerebral inflammatory diseases

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