Bone disease in eliglustat treated Gaucher disease type 1 patients: A real-world experience in a tertiary referral hospital

被引：0
|
作者：
Valls-Villalba, Angel [1 ]
Camprodon-Gomez, Maria [2 ]
Moreno-Martinez, Daniel [3 ]
Hernandez-Vara, Jorge [4 ]
Arranz-Amo, Jose Antonio [5 ]
Carnicer-Caceres, Clara [5 ]
机构：
[1] Vall Hebron Univ Hosp, Internal Med, Barcelona, Spain
[2] Vall DHebron Univ Hosp, Unit Rare Dis & Metab Hereditary Disorders, Barcelona, Spain
[3] Vall Hebron Univ Hosp, Dept Radiol, Barcelona, Spain
[4] Vall Hebron Univ Hosp, Dept Neurol, Unit Movement Disorders, Barcelona, Spain
[5] Vall Hebron Univ Hosp, Inborn Error Metab Lab, Barcelona, Spain
来源：
MOLECULAR GENETICS AND METABOLISM | 2023年 / 138卷 / 02期
关键词：
D O I：
10.1016/j.ymgme.2022.107340
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
357
引用
收藏
页码：129 / 129
页数：1
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