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Mitsuharu Ueda

Showing results (321-330 of 382) with videos related to

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Journal of the Neurological Sciences|May 30, 2020
Novel dot-blot assay for detection of vascular Notch3 aggregates in patients with CADASILYihong Ma, Mitsuharu Ueda, Akihiko Ueda, et al.
Orphanet Journal of Rare Diseases|April 2, 2026
Six novel SACS mutations expand the autosomal recessive spastic ataxia of Charlevoix-Saguenay spectrumSusumu Ikenoshita, Toshiya Nomura, Haruo Shimazaki, et al.
International Journal of Cardiology. Heart & Vasculature|July 7, 2023
Usefulness of automatic assessment for longitudinal strain to diagnose wild-type transthyretin amyloid cardiomyopathyHiroki Usuku, Eiichiro Yamamoto, Daisuke Sueta, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|December 21, 2011
Aged vervet monkeys developing transthyretin amyloidosis with the human disease-causing Ile122 allele: a valid pathological model of the human diseaseMitsuharu Ueda, Naohide Ageyama, Shinichiro Nakamura, et al.
Journal of Nuclear Cardiology : Official Publication of the American Society of Nuclear Cardiology|December 29, 2021
Amyloid deposit corresponds to technetium-99m-pyrophosphate accumulation in abdominal fat of patients with transthyretin cardiac amyloidosisKoji Takahashi, Daisuke Sasaki, Mina Yamashita, et al.
ESC Heart Failure|December 31, 2020
Plasma growth differentiation factor 15: a novel tool to detect early changes of hereditary transthyretin amyloidosisMasamitsu Okada, Yohei Misumi, Teruaki Masuda, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|April 1, 2026
Development and validation of the modified-comprehensive Kumamoto Score: a multi-organ assessment tool for hereditary transthyretin amyloidosisShiori Yamakawa, Toshiya Nomura, Yohei Misumi, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|June 2, 2022
Guidelines and new directions in the therapy and monitoring of ATTRv amyloidosisYukio Ando, David Adams, Merrill D Benson, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|May 22, 2022
Extracardiac Biopsy Sensitivity in Transthyretin Amyloidosis Cardiomyopathy Patients With Positive <sup>99 m</sup>Tc-Labeled Pyrophosphate Scintigraphy FindingsMasato Nishi, Seiji Takashio, Mami Morioka, et al.
Human Genome Variation|August 16, 2024
The APOA1 p.Leu202Arg variant potentially causes autosomal recessive cardiac amyloidosisShusuke Yagi, Ryosuke Miyamoto, Masayoshi Tasaki, et al.
Pageof 39

Showing results (321-330 of 382) with videos related to

Sort By:
Pageof 39
Journal of the Neurological Sciences|May 30, 2020
Novel dot-blot assay for detection of vascular Notch3 aggregates in patients with CADASILYihong Ma, Mitsuharu Ueda, Akihiko Ueda, et al.
Orphanet Journal of Rare Diseases|April 2, 2026
Six novel SACS mutations expand the autosomal recessive spastic ataxia of Charlevoix-Saguenay spectrumSusumu Ikenoshita, Toshiya Nomura, Haruo Shimazaki, et al.
International Journal of Cardiology. Heart & Vasculature|July 7, 2023
Usefulness of automatic assessment for longitudinal strain to diagnose wild-type transthyretin amyloid cardiomyopathyHiroki Usuku, Eiichiro Yamamoto, Daisuke Sueta, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|December 21, 2011
Aged vervet monkeys developing transthyretin amyloidosis with the human disease-causing Ile122 allele: a valid pathological model of the human diseaseMitsuharu Ueda, Naohide Ageyama, Shinichiro Nakamura, et al.
Journal of Nuclear Cardiology : Official Publication of the American Society of Nuclear Cardiology|December 29, 2021
Amyloid deposit corresponds to technetium-99m-pyrophosphate accumulation in abdominal fat of patients with transthyretin cardiac amyloidosisKoji Takahashi, Daisuke Sasaki, Mina Yamashita, et al.
ESC Heart Failure|December 31, 2020
Plasma growth differentiation factor 15: a novel tool to detect early changes of hereditary transthyretin amyloidosisMasamitsu Okada, Yohei Misumi, Teruaki Masuda, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|April 1, 2026
Development and validation of the modified-comprehensive Kumamoto Score: a multi-organ assessment tool for hereditary transthyretin amyloidosisShiori Yamakawa, Toshiya Nomura, Yohei Misumi, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|June 2, 2022
Guidelines and new directions in the therapy and monitoring of ATTRv amyloidosisYukio Ando, David Adams, Merrill D Benson, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|May 22, 2022
Extracardiac Biopsy Sensitivity in Transthyretin Amyloidosis Cardiomyopathy Patients With Positive <sup>99 m</sup>Tc-Labeled Pyrophosphate Scintigraphy FindingsMasato Nishi, Seiji Takashio, Mami Morioka, et al.
Human Genome Variation|August 16, 2024
The APOA1 p.Leu202Arg variant potentially causes autosomal recessive cardiac amyloidosisShusuke Yagi, Ryosuke Miyamoto, Masayoshi Tasaki, et al.
Pageof 39