𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Lessons from glucosylceramide and Gaucher’s disease

✍ Scribed by Friedrich C. Luft


Publisher
Springer
Year
1998
Tongue
English
Weight
33 KB
Volume
76
Category
Article
ISSN
0946-2716

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Gaucher's disease and portal hypertensio
✍ J. E. L. Sales; A. H. Hunt 📂 Article 📅 1970 🏛 John Wiley and Sons 🌐 English ⚖ 478 KB

## Abstract Two cases of Gaucher's disease with portal hypertension are dscribed, of which one was relieved by splenectomy and the other, which had recurrent bleeding from oesophageal varices, by portacaval anastomosis. These cases demonstrate that portal hypertension in this condition may be due t

Gaucher's disease and chronic lymphocyti
✍ Henry Fox; Philip McCarthy; Janine André-Schwartz; Yehuda Shoenfeld; Kenneth B. 📂 Article 📅 1984 🏛 John Wiley and Sons 🌐 English ⚖ 417 KB

The authors report a case of Gaucher's disease with chronic lymphocytic leukemia. The diagnosis of Gaucher's disease was confirmed by electron microscopy and glucocerebrosidase assay. There may be a pathogenetic

Lysosomal storage disorders and Parkinso
✍ Tamar Shachar; Christophe Lo Bianco; Alessandra Recchia; Christoph Wiessner; Ann 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 343 KB

Parkinson's disease is associated with mutations in the glucocerebrosidase gene, which result in the enzyme deficiency causing Gaucher disease, the most common lysosomal storage disorder. We have performed an exhaustive literature search and found that additional lysosomal storage disorders might be

Gaucher disease: The effects of phosphat
✍ Francis Y. M. Choy 📂 Article 📅 1984 🏛 Springer 🌐 English ⚖ 564 KB

Glucocerebroside beta-glucosidase (glucocerebrosidase) activity was assayed from cultured fibroblasts of normal individuals, and patients with type 1 (non-neuropathic), type 2 (acute neuropathic), and type 3 (subacute neuropathic) form of Gaucher disease. Residual glucocerebrosidase activity of pati