Gaucher

Gauch·er

(gō-shā'),
Philippe C.E., French physician, 1854-1918. See: Gaucher cells, Gaucher disease, pseudo-Gaucher cell.
References in periodicals archive ?
Electronic auction: provision of services for the acceptance, recording, storage, packaging, delivery and dispensing of medicines for persons included in the regional segment of the federal register of persons with hemophilia, cystic fibrosis, pituitary nanism, gaucher disease, malignant neoplasms of lymphoid, haematopoietic and related tissues, multiple sclerosis , persons after transplantation of organs and (or) tissues in 2018g
There are around 7000 rare diseases but patients suffering from a particular segment of rare diseases called Lysosomal Storage Disorders (LSDs) like MPS (type I, II, III, IV & VI), Gaucher, Pompe, Fabry, etc.
Ocular manifestations of Gaucher disease: case report and literature review
Bone impairment in patients with Gaucher disease diagnosis).
Mesenteric lymphadenopathy is a rare manifestation of Gaucher disease (GD) with only 26 cases reported worldwide and its outcome remains largely unknown.
Global Markets Direct's, 'Gaucher Disease - Pipeline Review, H1 2016', provides an overview of the Gaucher Disease pipeline landscape.
Background and Objective: Gaucher disease is the most common inherited lysosomal storage disorder.
As the country observes Gaucher's Disease Awareness Month this October, the West Virginia-based National Gaucher Foundation is hosting an online awareness campaign to promote the importance of education and awareness.
M2 EQUITYBITES-May 20, 2015-Genzyme wins NORD innovation award for Cerdelga, a treatment for certain adult Gaucher disease type 1 patients
M2 PHARMA-May 20, 2015-Genzyme wins NORD innovation award for Cerdelga, a treatment for certain adult Gaucher disease type 1 patients
The studies by Chamoles and coworkers were followed by studies from Gelb, Scott, Turecek, and coworkers, who used tandem mass spectrometry (MS/MS) and internal standards to detect multiple enzymatic products in a multiplex analysis of Fabry, Gaucher, Krabbe, mucopolysaccharidosis-I (MPS-I), Niemann-Pick-A/B, and Pompe diseases (16-18).
Gaucher disease is an autosomal-recessive lysosomal storage disorder caused by mutations in the gene encoding acid beta-glucosidase (GBA1).