Work

156. Enzyme replacement therapy with velaglucerase alfa improves key clinical parameters in a pediatric subgroup with type 1 Gaucher disease

Year: 2010

Type: article

Source: Molecular Genetics and Metabolism

DOI: 10.1016/j.ymgme.2009.10.173

Authors: Ari Zimran, Derlis Gonzalez, Eric Crombez, Kiran Bhirangi

Institution: Shaare Zedek Medical Center

Language: English

Topic: Lysosomal Storage Disorders Research

Subfield: Genetics (clinical)

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W1997272292

FWCI: 0.218

Cites:

Cited by: 2

Related to: 10