Examples of 'pompe disease' in a sentence
Meaning of "pompe disease"
pompe disease: Pompe Disease is a rare genetic disorder that disables the body's ability to break down glycogen, resulting in muscle weakness and other complications. It is named after the Dutch pathologist who first described it, Dr. Joannes Cassianus Pompe
Show more definitions
- Glycogen storage disease type II
How to use "pompe disease" in a sentence
Basic
Advanced
pompe disease
Pompe disease is one of several lysosomal storage disorders.
Then an infantile form of Pompe disease was found.
Pompe disease patients often use mechanical ventilation to help them breathe.
There were some similarities with Pompe disease.
Pompe disease can masquerade as several other neuromuscular disorders due to overlapping signs and symptoms.
Methods and compositions for treatment of Pompe disease.
Infants with Pompe disease may need to use a feeding tube.
I have read all the journal articles on Pompe disease.
Visit our Pompe disease inheritance page for more information.
To characterize and describe the Pompe disease population as a whole.
This meeting will be focused on developing treatments for Pompe disease.
Patients with Pompe disease inherit a gene variant from each of their parents.
I can also promise you a working enzyme for Pompe disease.
The risk factors for developing Pompe disease reside exclusively in the parental genotype.
Nucleic acids and methods for the treatment of Pompe disease.
See also
Current treatment of Pompe disease involves symptomatic treatment of the cardiac and respiratory symptoms.
Myozyme is used to treat patients who have a confirmed diagnosis of Pompe disease.
Lumizyme is now indicated for all patients with Pompe disease regardless of age or phenotype.
Left and right ventricular function were preserved in patients with Pompe disease.
Pompe disease Crowley.
The invention also provides a method for the treatment of Pompe disease.
Types of Pompe disease.
ERT is a useful method of treatment for Pompe disease.
A method for the treatment of pompe disease using 1-deoxynojirimycin and derivatives.
To understand the future market competition in the Pompe Disease market.
Pompe disease causes muscle weakness, but the other symptoms vary widely among people.
The benefits of Myozyme in patients with late onset Pompe disease are not known yet.
Progression of Pompe disease was evaluated in 8 young patients.
Identification and functional characterization of GAA mutations in Colombian patients affected by Pompe disease.
What are your thoughts on Pompe disease research?
People with Pompe disease have low levels of an enzyme called α - glucosidase.
In certain instances, the patient is an adult who has been diagnosed with Pompe disease.
Many patients with later-onset Pompe disease experience long delays in diagnosis.
Abstract, Pompe disease is a lysosomal storage disorder characterized by muscle weakness and cardiomyopathy.
Consequently, glycogen accumulates in the lysosomes of all cells in patients with Pompe disease.
Patients with Pompe disease do not have enough of an enzyme called alpha-glucosidase.
A stable pharmaceutical composition according to claim 4 for use in the treatment of Pompe disease.
People with Pompe disease have low levels of an enzyme called alpha-glucosidase.
What is the clinical presentation of infantile and later-onset paediatric Pompe disease in Canada?
Pompe disease is also known as infantile acid maltase disease ; a variant of GSD type II.
They experimented using a mouse model of Pompe disease called the GAA knockout ( absent ) mouse.
Children with Pompe disease have a defi ciency of the lysosomal enzyme acid alpha-glucosidase GAA.
Described is a pharmaceutical composition for treating Pompe disease comprising an acid alpha-glucosidase and a poloxamer.
This growth reflects the rising number of patients diagnosed with, and treated for, Pompe disease.
Pompe Disease was named after the Dutch doctor who discovered it, Joannes Cassianus Pompe.
These data suggest that vIGF2-rhGAA would be a superior ERT for the treatment of Pompe disease.
Pompe disease - the real story.
A suitable modified recombinant human lysosomal enzyme includes acid a-glucosidase for the treatment of Pompe disease.
How many types of Pompe disease exist?
I can also promise you a working And with the right business plan, enzyme for Pompe disease.
You'll also be interested in:
Examples of using Disease
Show more
A disease caused by a germ found in the environment
Impact of recent major disease outbreaks in aquaculture
Disease and health systems strengthening partners
Examples of using Pompe
Show more
Pompe is known for his fine wood sculpting
Then an infantile form of Pompe disease was found
Pompe disease is one of several lysosomal storage disorders
