Yusuke Mochizuki

Matsumoto, Japan

Last Updated: 09/26/2026

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Found 11 publications

Pyrophosphate Scintigraphy Changes After Tafamidis Therapy　- Proposed Novel Index From Quantitative Single-Photon Emission Computed Tomography.

Pyrophosphate Scintigraphy Changes After Tafamidis Therapy　- Proposed Novel Index From Quantitative Single-Photon Emission Computed Tomography.

Journal: Circulation journal : official journal of the Japanese Circulation Society
Published: February 15, 2026

Involvement of bile acid in diarrhoea and therapeutic effect of colestimide in hereditary ATTR amyloidosis.

Involvement of bile acid in diarrhoea and therapeutic effect of colestimide in hereditary ATTR amyloidosis.

Journal: Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis
Published: November 20, 2024

Neurofilament light chain as a biomarker for hereditary ATTR amyloidosis - correlation between neurofilament light chain and nerve conduction study.

Neurofilament light chain as a biomarker for hereditary ATTR amyloidosis - correlation between neurofilament light chain and nerve conduction study.

Journal: Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis
Published: October 08, 2024

Two Cases of Alice in Wonderland Syndrome with a Right Occipital Lobe Lesion Caused by Isolated Cortical Venous Thrombosis.

Two Cases of Alice in Wonderland Syndrome with a Right Occipital Lobe Lesion Caused by Isolated Cortical Venous Thrombosis.

Journal: Internal medicine (Tokyo, Japan)
Published: December 03, 2023

Neurofilament light chain as a biomarker for monitoring response to change in treatment in hereditary ATTR amyloidosis.

Neurofilament light chain as a biomarker for monitoring response to change in treatment in hereditary ATTR amyloidosis.

Journal: Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis
Published: March 13, 2023

Light and heavy chain deposition disease with focal amyloid deposition diagnosed with mass spectrometry: a case report.

Light and heavy chain deposition disease with focal amyloid deposition diagnosed with mass spectrometry: a case report.

Journal: BMC nephrology
Published: December 30, 2022

Distribution and progression of cerebral amyloid angiopathy in early-onset V30M (p.V50M) hereditary ATTR amyloidosis.

Distribution and progression of cerebral amyloid angiopathy in early-onset V30M (p.V50M) hereditary ATTR amyloidosis.

Journal: Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis
Published: September 30, 2022

Reduction of cardiac AL amyloid deposition after complete response visualised by PiB-PET imaging.

Reduction of cardiac AL amyloid deposition after complete response visualised by PiB-PET imaging.

Journal: Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis
Published: September 16, 2022

Delayed Detection of Hydrocephalus following Mildly Traumatic Subarachnoid Hemorrhage in Corticobasal Degeneration: A Case Report.

Delayed Detection of Hydrocephalus following Mildly Traumatic Subarachnoid Hemorrhage in Corticobasal Degeneration: A Case Report.

Journal: Case reports in neurology
Published: March 15, 2022

Moyamoya Disease-like Cerebrovascular Stenotic Lesions Are an Important Phenotype of POEMS Syndrome-associated Vasculopathy.

Moyamoya Disease-like Cerebrovascular Stenotic Lesions Are an Important Phenotype of POEMS Syndrome-associated Vasculopathy.

Journal: Internal medicine (Tokyo, Japan)
Published: November 08, 2021

A Late-onset and Relatively Rapidly Progressive Case of Pure Spinal Form Cerebrotendinous Xanthomatosis with a Novel Mutation in the CYP27A1 Gene.

A Late-onset and Relatively Rapidly Progressive Case of Pure Spinal Form Cerebrotendinous Xanthomatosis with a Novel Mutation in the CYP27A1 Gene.

Journal: Internal medicine (Tokyo, Japan)
Published: June 26, 2020
Showing 1-11 of 11

Last Updated: 09/26/2026