Hanada H

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 : Increased level of pericardial insulin-like growth factor-1 in patients with left ventricular dysfunction and advanced heart failure - Abe_2006_J.Am.Coll.Cardiol_48_1387
Author(s) : Abe N , Matsunaga T , Kameda K , Tomita H , Fujiwara T , Ishizaka H , Hanada H , Fukui K , Fukuda I , Osanai T , Okumura K
Ref : J Am Coll Cardiol , 48 :1387 , 2006
Abstract :
PubMedSearch : Abe_2006_J.Am.Coll.Cardiol_48_1387
PubMedID: 17010800