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You searched for: Author/Creator Awano, Hiroyuki

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1. 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. Issue 3 (10th December 2018)

2. Treatment of a case of severe insulin resistance as a result of a PIK3R1 mutation with a sodium–glucose cotransporter 2 inhibitor. Issue 5 (25th March 2018)

3. Resonant Hall effect under generation of a self-sustaining mode of spin current in nonmagnetic bipolar conductors with identical characters between holes and electrons. (8th February 2018)

5. Renal insufficiency mimicking glutaric acidemia type 1 on newborn screening. Issue 1 (14th December 2017)

6. Acute rhabdomyolysis following viral infection with coxsackie A4 in a 50-day-old infant with Fukuyama congenital muscular dystrophy. Issue 5 (May 2020)

7. Early phase 2 trial of TAS‐205 in patients with Duchenne muscular dystrophy. Issue 2 (20th January 2020)

8. FKRP mutations cause congenital muscular dystrophy 1C and limb-girdle muscular dystrophy 2I in Asian patients. (October 2021)