𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Gaucher disease

✍ Scribed by G. Ya. Wiederschain


Book ID
110155080
Publisher
Springer
Year
2008
Tongue
English
Weight
98 KB
Volume
73
Category
Article
ISSN
0006-2979

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Gaucher disease
✍ Pascal Guggenbuhl; Bernard Grosbois; GΓ©rard ChalΓ¨s πŸ“‚ Article πŸ“… 2008 πŸ› Elsevier Science 🌐 English βš– 642 KB
GAUCHER DISEASE
πŸ“‚ Article πŸ“… 2008 πŸ› John Wiley and Sons 🌐 English βš– 245 KB
Gaucher Disease
✍ Charrow, Joel; Esplin, Joan A.; Gribble, T. John; Kaplan, Paige; Kolodny, Edwin πŸ“‚ Article πŸ“… 1998 πŸ› American Medical Association 🌐 English βš– 95 KB
Neuropathic Gaucher disease
✍ Gregory M. Pastores πŸ“‚ Article πŸ“… 2010 πŸ› Springer Vienna 🌐 German βš– 84 KB
Editorial: Gaucher disease
✍ Peter Mikosch πŸ“‚ Article πŸ“… 2010 πŸ› Springer Vienna 🌐 German βš– 48 KB
Glucocerebrosidase (Gaucher disease)
✍ Ernest Beutler; Terri Gelbart πŸ“‚ Article πŸ“… 1996 πŸ› John Wiley and Sons 🌐 English βš– 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