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Hideyuki Takeuchi

Showing results (211-220 of 214) with videos related to

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Circulation Journal : Official Journal of the Japanese Circulation Society|November 3, 2017
Echocardiographic Assessment of Cardiac Structural and Functional Abnormalities in Patients With End-Stage Renal Disease Receiving Chronic HemodialysisHiroshi Matsuo, Kaoru Dohi, Hirofumi Machida, et al.
Nature Genetics|July 24, 2019
Long-read sequencing identifies GGC repeat expansions in NOTCH2NLC associated with neuronal intranuclear inclusion diseaseJun Sone, Satomi Mitsuhashi, Atsushi Fujita, et al.
Neurobiology of Disease|June 24, 2019
Ataxic phenotype with altered Ca<sub>V</sub>3.1 channel property in a mouse model for spinocerebellar ataxia 42Shunta Hashiguchi, Hiroshi Doi, Misako Kunii, et al.
Science Advances|March 25, 2021
De novo ATP1A3 variants cause polymicrogyriaSatoko Miyatake, Mitsuhiro Kato, Takuma Kumamoto, et al.
Pageof 22

Showing results (211-220 of 214) with videos related to

Sort By:
Pageof 22
You have reached the last page of results.This site can display upto 214 results.
Circulation Journal : Official Journal of the Japanese Circulation Society|November 3, 2017
Echocardiographic Assessment of Cardiac Structural and Functional Abnormalities in Patients With End-Stage Renal Disease Receiving Chronic HemodialysisHiroshi Matsuo, Kaoru Dohi, Hirofumi Machida, et al.
Nature Genetics|July 24, 2019
Long-read sequencing identifies GGC repeat expansions in NOTCH2NLC associated with neuronal intranuclear inclusion diseaseJun Sone, Satomi Mitsuhashi, Atsushi Fujita, et al.
Neurobiology of Disease|June 24, 2019
Ataxic phenotype with altered Ca<sub>V</sub>3.1 channel property in a mouse model for spinocerebellar ataxia 42Shunta Hashiguchi, Hiroshi Doi, Misako Kunii, et al.
Science Advances|March 25, 2021
De novo ATP1A3 variants cause polymicrogyriaSatoko Miyatake, Mitsuhiro Kato, Takuma Kumamoto, et al.
Pageof 22