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Journal of Diabetes Investigation
|
October 17, 2018
In silico and in vitro analyses of the pathological relevance of the R258H mutation of hepatocyte nuclear factor 4α identified in maturity-onset diabetes of the young type 1
Kenji Sugawara, Kazuhiro Nomura, Yuko Okada, et al.
Molecular Genetics and Metabolism Reports
|
June 4, 2020
Need for strict clinical management of patients with carnitine palmitoyltransferase II deficiency: Experience with two cases detected by expanded newborn screening
Ryosuke Bo, Ikuma Musha, Kenji Yamada, et al.
Internal Medicine (Tokyo, Japan)
|
December 17, 2013
Rapid progression of neuromuscular disorder related cardiomyopathy in a young patient
Mayuko Hayashi, Hidekazu Tanaka, Tetsushi Yamamoto, et al.
The American Journal of Cardiology
|
January 1, 2013
Utility of transmural myocardial strain profile for prediction of early left ventricular dysfunction in patients with Duchenne muscular dystrophy
Tetsushi Yamamoto, Hidekazu Tanaka, Kensuke Matsumoto, et al.
Journal of Diabetes Investigation
|
February 25, 2018
Treatment of a case of severe insulin resistance as a result of a PIK3R1 mutation with a sodium-glucose cotransporter 2 inhibitor
Tetsushi Hamaguchi, Yushi Hirota, Takehito Takeuchi, et al.
Journal of Infection and Chemotherapy : Official Journal of the Japan Society of Chemotherapy
|
April 28, 2016
A pediatric patient with interstitial pneumonia due to enterovirus D68
Masaaki Matsumoto, Hiroyuki Awano, Miki Ogi, et al.
The Journal of Dermatology
|
October 23, 2025
Multidisciplinary Management of Plexiform Neurofibromas in Pediatric Patients With Neurofibromatosis 1: Insights From Advisory Board-Guided Clinical Experience in Japan
Yuko Ehara, Tohru Okanishi, Yoshiko Suyama, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society
|
October 24, 2017
Renal insufficiency mimicking glutaric acidemia type 1 on newborn screening
Masaaki Matsumoto, Hiroyuki Awano, Ryosuke Bo, et al.
Circulation. Genomic and Precision Medicine
|
June 7, 2018
Cardiac Dysfunction in Duchenne Muscular Dystrophy Is Less Frequent in Patients With Mutations in the Dystrophin Dp116 Coding Region Than in Other Regions
Tetsushi Yamamoto, Hiroyuki Awano, Zhujun Zhang, et al.
Molecular Genetics and Metabolism Reports
|
March 4, 2022
Early clinical signs and treatment of Menkes disease
Chie Fujisawa, Hiroko Kodama, Yasuhiro Sato, et al.
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of 16
Search research articles
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Showing results (101-110 of 152) with videos related to
Sort By:
Page
of 16
Journal of Diabetes Investigation
|
October 17, 2018
In silico and in vitro analyses of the pathological relevance of the R258H mutation of hepatocyte nuclear factor 4α identified in maturity-onset diabetes of the young type 1
Kenji Sugawara, Kazuhiro Nomura, Yuko Okada, et al.
Molecular Genetics and Metabolism Reports
|
June 4, 2020
Need for strict clinical management of patients with carnitine palmitoyltransferase II deficiency: Experience with two cases detected by expanded newborn screening
Ryosuke Bo, Ikuma Musha, Kenji Yamada, et al.
Internal Medicine (Tokyo, Japan)
|
December 17, 2013
Rapid progression of neuromuscular disorder related cardiomyopathy in a young patient
Mayuko Hayashi, Hidekazu Tanaka, Tetsushi Yamamoto, et al.
The American Journal of Cardiology
|
January 1, 2013
Utility of transmural myocardial strain profile for prediction of early left ventricular dysfunction in patients with Duchenne muscular dystrophy
Tetsushi Yamamoto, Hidekazu Tanaka, Kensuke Matsumoto, et al.
Journal of Diabetes Investigation
|
February 25, 2018
Treatment of a case of severe insulin resistance as a result of a PIK3R1 mutation with a sodium-glucose cotransporter 2 inhibitor
Tetsushi Hamaguchi, Yushi Hirota, Takehito Takeuchi, et al.
Journal of Infection and Chemotherapy : Official Journal of the Japan Society of Chemotherapy
|
April 28, 2016
A pediatric patient with interstitial pneumonia due to enterovirus D68
Masaaki Matsumoto, Hiroyuki Awano, Miki Ogi, et al.
The Journal of Dermatology
|
October 23, 2025
Multidisciplinary Management of Plexiform Neurofibromas in Pediatric Patients With Neurofibromatosis 1: Insights From Advisory Board-Guided Clinical Experience in Japan
Yuko Ehara, Tohru Okanishi, Yoshiko Suyama, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society
|
October 24, 2017
Renal insufficiency mimicking glutaric acidemia type 1 on newborn screening
Masaaki Matsumoto, Hiroyuki Awano, Ryosuke Bo, et al.
Circulation. Genomic and Precision Medicine
|
June 7, 2018
Cardiac Dysfunction in Duchenne Muscular Dystrophy Is Less Frequent in Patients With Mutations in the Dystrophin Dp116 Coding Region Than in Other Regions
Tetsushi Yamamoto, Hiroyuki Awano, Zhujun Zhang, et al.
Molecular Genetics and Metabolism Reports
|
March 4, 2022
Early clinical signs and treatment of Menkes disease
Chie Fujisawa, Hiroko Kodama, Yasuhiro Sato, et al.
Page
of 16