Yusuke Takahashi

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

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

Spinal intradural pseudocyst formation in central nervous system superficial siderosis.

Journal: Brain pathology (Zurich, Switzerland)

Published: December 14, 2023

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

Anterior horn damage in brachial multisegmental amyotrophy with superficial siderosis and dural tear: an autopsy case report.

Journal: BMC neurology

Published: December 09, 2022

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.

Journal: Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis

Published: September 16, 2022

CSF/plasma levels, transthyretin stabilisation and safety of multiple doses of tolcapone in subjects with hereditary ATTR amyloidosis.

Journal: Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis

Published: March 30, 2022

Surgical revascularization for quasi-moyamoya disease associated with polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes (POEMS) syndrome: a case report and literature review.

Journal: Nagoya journal of medical science

Published: January 14, 2022

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

Journal: Internal medicine (Tokyo, Japan)

Published: November 08, 2021

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.

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.

Spinal intradural pseudocyst formation in central nervous system superficial siderosis.

Spinal intradural pseudocyst formation in central nervous system superficial siderosis.

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.

Anterior horn damage in brachial multisegmental amyotrophy with superficial siderosis and dural tear: an autopsy case report.

Anterior horn damage in brachial multisegmental amyotrophy with superficial siderosis and dural tear: an autopsy case report.

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.

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.

CSF/plasma levels, transthyretin stabilisation and safety of multiple doses of tolcapone in subjects with hereditary ATTR amyloidosis.

CSF/plasma levels, transthyretin stabilisation and safety of multiple doses of tolcapone in subjects with hereditary ATTR amyloidosis.

Surgical revascularization for quasi-moyamoya disease associated with polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes (POEMS) syndrome: a case report and literature review.

Surgical revascularization for quasi-moyamoya disease associated with polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes (POEMS) syndrome: a case report and literature review.

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.

Absolute quantitative analysis of cardiac amyloidosis using SPECT/CT with 99mTc-pyrophosphate.

Absolute quantitative analysis of cardiac amyloidosis using SPECT/CT with 99mTc-pyrophosphate.

Localized Immunoglobulin Light-Chain Amyloidosis of the Ulnar Nerve.

Localized Immunoglobulin Light-Chain Amyloidosis of the Ulnar Nerve.

Yusuke Takahashi

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.

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.

Spinal intradural pseudocyst formation in central nervous system superficial siderosis.

Spinal intradural pseudocyst formation in central nervous system superficial siderosis.

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.

Anterior horn damage in brachial multisegmental amyotrophy with superficial siderosis and dural tear: an autopsy case report.

Anterior horn damage in brachial multisegmental amyotrophy with superficial siderosis and dural tear: an autopsy case report.

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.

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.

CSF/plasma levels, transthyretin stabilisation and safety of multiple doses of tolcapone in subjects with hereditary ATTR amyloidosis.

CSF/plasma levels, transthyretin stabilisation and safety of multiple doses of tolcapone in subjects with hereditary ATTR amyloidosis.

Surgical revascularization for quasi-moyamoya disease associated with polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes (POEMS) syndrome: a case report and literature review.

Surgical revascularization for quasi-moyamoya disease associated with polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes (POEMS) syndrome: a case report and literature review.

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.

Absolute quantitative analysis of cardiac amyloidosis using SPECT/CT with 99mTc-pyrophosphate.

Absolute quantitative analysis of cardiac amyloidosis using SPECT/CT with 99mTc-pyrophosphate.

Localized Immunoglobulin Light-Chain Amyloidosis of the Ulnar Nerve.

Localized Immunoglobulin Light-Chain Amyloidosis of the Ulnar Nerve.

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.