✦ LIBER ✦

Gaucher disease

✍ Scribed by Pascal Guggenbuhl; Bernard Grosbois; Gérard Chalès

Book ID: 113684386
Publisher: Elsevier Science
Year: 2008
Tongue: English
Weight: 642 KB
Volume: 75
Category: Article
ISSN: 1297-319X
DOI: 10.1016/j.jbspin.2007.06.006

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

GAUCHER DISEASE

📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 245 KB

Gaucher disease

✍ G. Ya. Wiederschain 📂 Article 📅 2008 🏛 Springer 🌐 English ⚖ 98 KB

Gaucher Disease

✍ Charrow, Joel; Esplin, Joan A.; Gribble, T. John; Kaplan, Paige; Kolodny, Edwin 📂 Article 📅 1998 🏛 American Medical Association 🌐 English ⚖ 95 KB

Neuropathic Gaucher disease

✍ Gregory M. Pastores 📂 Article 📅 2010 🏛 Springer Vienna 🌐 German ⚖ 84 KB

Editorial: Gaucher disease

✍ Peter Mikosch 📂 Article 📅 2010 🏛 Springer Vienna 🌐 German ⚖ 48 KB

Glucocerebrosidase (Gaucher disease)

✍ Ernest Beutler; Terri Gelbart 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 597 KB

Gaucher disease is the most common glycolipid storage disorder, characterized by storage of the glycolipid, glucocerebroside in the liver, spleen, and marrow. The most prevalent form of Gaucher disease is designated type I (MIM 230800). Patients with type I disease may have hepatomegaly, splenomegal