Masuda D

References (2)

Title : A Case of Familial Chylomicronemia Syndrome Caused by a Novel Homozygous GPIHBP1 Mutation Successfully Treated with the Selective PPARalpha Modulator Pemafibrate - Otsuki_2026_J.Atheroscler.Thromb__
Author(s) : Otsuki T , Chung Y , Kawachi Y , Komuku S , Yamanishi M , Takano T , Yamaguchi A , Hanada H , Masuda D , Miyashita K , Yamashita S
Ref : J Atheroscler Thromb , : , 2026
Abstract :
PubMedSearch : Otsuki_2026_J.Atheroscler.Thromb__
PubMedID: 42309774

Title : Comparison of effects of anagliptin and alogliptin on serum lipid profile in type 2 diabetes mellitus patients - Kurozumi_2018_J.Diabetes.Investig_9_360
Author(s) : Kurozumi A , Okada Y , Arao T , Kobayashi T , Masuda D , Yamashita S , Tanaka Y
Ref : J Diabetes Investig , 9 :360 , 2018
Abstract :
PubMedSearch : Kurozumi_2018_J.Diabetes.Investig_9_360
PubMedID: 28853228