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Journal of Clinical Medicine
|
April 10, 2019
Clinicopathological and Genetic Profiles of Cases with Myocytes Disarray-Investigation for Establishing the Autopsy Diagnostic Criteria for Hypertrophic Cardiomyopathy
Yukiko Hata, Shojiro Ichimata, Yoshiaki Yamaguchi, et al.
Pathology International
|
January 16, 2014
Distribution of myofibroblast and tenascin-C in cystic adventitial disease: comparison with ganglion
Hiroyuki Hao, Hatsue Ishibashi-Ueda, Naoki Nishida, et al.
Journal of Alzheimer'S Disease : JAD
|
March 21, 2022
Patterns of Mixed Pathologies in Down Syndrome
Shojiro Ichimata, Koji Yoshida, Naomi P Visanji, et al.
Molecules (Basel, Switzerland)
|
October 31, 2014
Field performance test of an air-cleaner with photocatalysis-plasma synergistic reactors for practical and long-term use
Tsuyoshi Ochiai, Erina Ichihashi, Naoki Nishida, et al.
Journal of Cardiology Cases
|
October 4, 2018
The <i>TNNI3</i> Arg192His mutation in a 13-year-old girl with left ventricular noncompaction
Mitsuhiro Fujino, Etsuko Tsuda, Keiichi Hirono, et al.
Plos One
|
November 13, 2018
Lack of modulatory effect of the SCN5A R1193Q polymorphism on cardiac fast Na+ current at body temperature
Masayoshi Abe, Koshi Kinoshita, Kenta Matsuoka, et al.
International Journal of Molecular Sciences
|
April 13, 2024
Amyloid-Forming Corpora Amylacea and Spheroid-Type Amyloid Deposition: Comprehensive Analysis Using Immunohistochemistry, Proteomics, and a Literature Review
Shojiro Ichimata, Yukiko Hata, Tsuneaki Yoshinaga, et al.
Journal of Cardiology Cases
|
August 1, 2022
A double heterozygous variant in <i>MYH6</i> and <i>MYH7</i> associated with hypertrophic cardiomyopathy in a Japanese Family
Takanori Suzuki, Kazuyoshi Saito, Tetsushi Yoshikawa, et al.
CJC Open
|
October 29, 2021
A Case Report of a Rare Heterozygous Variant in the <i>Desmin</i> Gene Associated With Hypertrophic Cardiomyopathy and Complete Atrioventricular Block
Hideharu Oka, Kouichi Nakau, Rina Imanishi, et al.
Heart and Vessels
|
June 4, 2016
Latent pathogenicity of the G38S polymorphism of KCNE1 K<sup>+</sup> channel modulator
Yoshiaki Yamaguchi, Koichi Mizumaki, Yukiko Hata, et al.
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of 15
Search research articles
Search
Showing results (101-110 of 144) with videos related to
Sort By:
Page
of 15
Journal of Clinical Medicine
|
April 10, 2019
Clinicopathological and Genetic Profiles of Cases with Myocytes Disarray-Investigation for Establishing the Autopsy Diagnostic Criteria for Hypertrophic Cardiomyopathy
Yukiko Hata, Shojiro Ichimata, Yoshiaki Yamaguchi, et al.
Pathology International
|
January 16, 2014
Distribution of myofibroblast and tenascin-C in cystic adventitial disease: comparison with ganglion
Hiroyuki Hao, Hatsue Ishibashi-Ueda, Naoki Nishida, et al.
Journal of Alzheimer'S Disease : JAD
|
March 21, 2022
Patterns of Mixed Pathologies in Down Syndrome
Shojiro Ichimata, Koji Yoshida, Naomi P Visanji, et al.
Molecules (Basel, Switzerland)
|
October 31, 2014
Field performance test of an air-cleaner with photocatalysis-plasma synergistic reactors for practical and long-term use
Tsuyoshi Ochiai, Erina Ichihashi, Naoki Nishida, et al.
Journal of Cardiology Cases
|
October 4, 2018
The <i>TNNI3</i> Arg192His mutation in a 13-year-old girl with left ventricular noncompaction
Mitsuhiro Fujino, Etsuko Tsuda, Keiichi Hirono, et al.
Plos One
|
November 13, 2018
Lack of modulatory effect of the SCN5A R1193Q polymorphism on cardiac fast Na+ current at body temperature
Masayoshi Abe, Koshi Kinoshita, Kenta Matsuoka, et al.
International Journal of Molecular Sciences
|
April 13, 2024
Amyloid-Forming Corpora Amylacea and Spheroid-Type Amyloid Deposition: Comprehensive Analysis Using Immunohistochemistry, Proteomics, and a Literature Review
Shojiro Ichimata, Yukiko Hata, Tsuneaki Yoshinaga, et al.
Journal of Cardiology Cases
|
August 1, 2022
A double heterozygous variant in <i>MYH6</i> and <i>MYH7</i> associated with hypertrophic cardiomyopathy in a Japanese Family
Takanori Suzuki, Kazuyoshi Saito, Tetsushi Yoshikawa, et al.
CJC Open
|
October 29, 2021
A Case Report of a Rare Heterozygous Variant in the <i>Desmin</i> Gene Associated With Hypertrophic Cardiomyopathy and Complete Atrioventricular Block
Hideharu Oka, Kouichi Nakau, Rina Imanishi, et al.
Heart and Vessels
|
June 4, 2016
Latent pathogenicity of the G38S polymorphism of KCNE1 K<sup>+</sup> channel modulator
Yoshiaki Yamaguchi, Koichi Mizumaki, Yukiko Hata, et al.
Page
of 15