gaucher s disease

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08/14/09
Other - Diseases

Gaucher's Disease is a Lysosomal Storage Disease and is an inherited metabolic disorder that results from malfunctions in the cell's lysosome (which breaks down organelles within the cell), caused...

Latest news about gaucher s disease

Research and Markets: Global Gaucher's Disease Epidemiology and Patient ...
This report provides insights into Gaucher's Disease epidemiology, Gaucher's Disease diagnosed patients, and Gaucher's Disease treatment rate for top seven pharmaceutical markets. The study measures key indicators such as prevalence of Gaucher's
Source: http://www.businesswire.com/news/home/20150122006207/en/Research-Markets-Global-Gauchers-Disease-Epidemiology-Patient
Sanofis Cerdelga Cleared in the EU for Gaucher Disease
The European Commission (EC) has approved Sanofi's (SNY - Analyst Report) first line oral therapy, Cerdelga, for the treatment of certain adults suffering from Gaucher disease type I. The company said that adults who metabolize Cerdelga more rapidly or
Source: http://www.zacks.com/stock/news/161615/sanofis-cerdelga-cleared-in-the-eu-for-gaucher-disease
Pricing uncertainty for orphan drugs and innovative new drugs
Cerezyme is an orphan drug which was approved by the European Medicines Agency in 1997 for the treatment of Gaucher's disease. The disease is considered to be an ultra-orphan disease, meaning that it is prevalent in only one case per 50,000 to
Source: http://www.internationallawoffice.com/newsletters/detail.aspx?g%3Dd6898991-48db-4e51-b604-910a69790d69
FDA approves new drug to treat a form of Gaucher disease
In one randomized, double-blind, placebo-controlled, multicenter clinical trial the safety and effectiveness of Cerdelga were evaluated in 40 participants with Type 1 Gaucher's disease who had not previously received enzyme replacement therapy
Source: http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm410585.htm
Evidence Mounting for Eliglustat in Gaucher's Disease
SAN DIEGO — Eliglustat (Cerdelga, Genzyme), a new oral treatment for type 1 Gaucher's disease, works almost as well as intravenous enzyme replacement therapy with imiglucerase, new research shows. "It provides a new treatment option for our patients,"
Source: http://www.medscape.com/viewarticle/834451

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Gaucher disease is an inherited metabolic disorder in which harmful ...

Gaucher Disease

Gaucher disease, type III

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Other sites on the topic of gaucher s disease

Gaucher's disease - Wikipedia, the free encyclopedia
Gaucher's disease or Gaucher disease is a genetic disease in which fatty substances (sphingolipids) accumulate in cells and certain organs. The disorder is ...
http://en.wikipedia.org/wiki/Gaucher%27s_disease
Gaucher's Disease: MedlinePlus - National Library of ...
Gaucher's disease is a rare, inherited disorder in which you do not have enough of an enzyme called glucocerebrosidase. This causes too much of a fatty substance to ...
http://www.nlm.nih.gov/medlineplus/gauchersdisease.html
Gaucher's disease Definition - Diseases and Conditions ...
Gaucher's disease — Comprehensive overview covers symptoms, causes, treatment of this metabolic disorder.
http://www.mayoclinic.org/diseases-conditions/gauchers-disease/basics/definition/CON-20031396
Gaucher disease (Gaucher's disease)
Gaucher disease, also known as glucocerebrosidase deficiency, occurs when a certain lipid, glucosylceramide, accumulates in the bone marrow, lungs, spleen, liver and ...
http://www.gaucherdisease.org/
Gaucher's Disease - National Institute of Neurological ...
Gaucher's Disease information sheet compiled by the National Institute of Neurological Disorders and Stroke (NINDS).
http://www.ninds.nih.gov/disorders/gauchers/gauchers.htm

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Protalix BioTherapeutics Treats First Gaucher Patient in Phase I Study With PRX-112, an Orally-Administered Enzyme Treatment of Gaucher Disease

Source: Seeking Alpha
the Company's orally-administered enzyme product candidate for the treatment of Gaucher disease. Oral GCD is a plant cell expressed form of the glucocerebrosidase enzyme (GCD) that is naturally encapsulated within carrot cells and administered orally.
Neonatal Gaucher Disease Presenting as Persistent Thrombocytopenia

Source: Nature Publishing group
Current address of S.S.K.: Division of Genetics ... USA Mutations in the -glucocerebrosidase gene cause Gaucher disease with the type 1 variant generally presenting later in life with mild disease and type 2 in infancy with severe neuronopathic symptoms.
Shire’s VPRIV® (velaglucerase alfa for injection) Shows Significant Improvement in Gaucher-Related Bone Disease

Source: Prestige Cars Magazin
Nyon, Switzerland (ots/PRNewswire) – - In a head-to-head trial between VPRIV and Cerezyme(R) (imiglucerase), only patients treated with VPRIV experienced statistically significant improvement in lumbar spine bone mineral density at 9 months Shire plc ...
Update on Protalix Gaucher Study - Analyst Blog

Source: NASDAQ
In addition to its Gaucher disease candidate, Protalix is also developing PRX ... In early 2012, the European Medicines Agency (EMA)'s Committee for Medicinal Products for Human Use (CHMP) had expressed its inability to recommend marketing ...
Gaucher's Disease: A Genetic Disease Detected in Skin Fibroblast Cultures

Source: Science Now
Skin fibroblasts from three adult patients with chronic noncerebral Gaucher's disease, three children of one of the patients, three parents, and six normal individuals were grown in cell culture. Giant fibroblasts containing metachromatic material were ...