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A Hashiguchi

Showing results (31-40 of 35) with videos related to

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Masui. the Japanese Journal of Anesthesiology|February 1, 1990
[Veno-arterial ECLA (extracorporeal lung assist) for severe respiratory failure due to meconium aspiration]K H Lee, Y Shimizu, T Yano, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|February 24, 2012
Insulinoma may mask the existence of Type 1 diabetesY Oikawa, T Katsuki, M Kawasaki, et al.
European Journal of Neurology|August 4, 2017
Clinical and mutational spectrum of Charcot-Marie-Tooth disease type 2Z caused by MORC2 variants in JapanM Ando, Y Okamoto, A Yoshimura, et al.
Clinical Genetics|April 20, 2017
WNK1/HSN2 founder mutation in patients with hereditary sensory and autonomic neuropathy: A Japanese cohort studyJ-H Yuan, A Hashiguchi, A Yoshimura, et al.
Clinical Genetics|March 1, 2017
Clinical and mutational spectrum of Japanese patients with Charcot-Marie-Tooth disease caused by GDAP1 variantsA Yoshimura, J-H Yuan, A Hashiguchi, et al.
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Showing results (31-40 of 35) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 35 results.
Masui. the Japanese Journal of Anesthesiology|February 1, 1990
[Veno-arterial ECLA (extracorporeal lung assist) for severe respiratory failure due to meconium aspiration]K H Lee, Y Shimizu, T Yano, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|February 24, 2012
Insulinoma may mask the existence of Type 1 diabetesY Oikawa, T Katsuki, M Kawasaki, et al.
European Journal of Neurology|August 4, 2017
Clinical and mutational spectrum of Charcot-Marie-Tooth disease type 2Z caused by MORC2 variants in JapanM Ando, Y Okamoto, A Yoshimura, et al.
Clinical Genetics|April 20, 2017
WNK1/HSN2 founder mutation in patients with hereditary sensory and autonomic neuropathy: A Japanese cohort studyJ-H Yuan, A Hashiguchi, A Yoshimura, et al.
Clinical Genetics|March 1, 2017
Clinical and mutational spectrum of Japanese patients with Charcot-Marie-Tooth disease caused by GDAP1 variantsA Yoshimura, J-H Yuan, A Hashiguchi, et al.
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