Gaucher Disease
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine
Reference141 articles.
1. Gaucher's disease variant characterised by progressive calcification of heart valves and unique genotype
2. Human β-glucuronidase: In vivo clearance and in vitro uptake by a glycoprotein recognition system on reticuloendothelial cells
3. Treatment of Gaucher's Disease
4. Replacement Therapy for Inherited Enzyme Deficiency — Macrophage-Targeted Glucocerebrosidase for Gaucher's Disease
5. Blaue Pigmentmakrophagen (Sea Blue Histiocytes) und Gaucher-ähnliche Zellen. Vorkommen und Bedeutung
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1. The biochemical basis of interactions between Glucocerebrosidase and alpha‐synuclein inGBA1 mutation carriers;Journal of Neurochemistry;2020-02-03
2. A Neonatal Case With Perinatal Lethal Gaucher Disease Associated With Missense G234E and H413P Heterozygous Mutations;Frontiers in Pediatrics;2019-05-22
3. Cauda equina syndrome in a patient diagnosed with type 1 Gaucher disease: a rare case;Child's Nervous System;2018-08-09
4. Hematopoietic stem cell transplantation for Gaucher disease;Cochrane Database of Systematic Reviews;2017-10-18
5. ETHICAL ISSUES IN MANAGING LYSOSOMAL STORAGE DISORDERS IN CHILDREN IN LOW AND MIDDLE INCOME COUNTRIES;Pakistan Journal of Medical Sciences;2017-08-04
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