Examples of 'storage diseases' in a sentence
Meaning of "storage diseases"
storage diseases: Refers to a group of disorders characterized by the accumulation of substances in cells leading to cell damage and dysfunction. These diseases often affect organs such as the liver, spleen, or brain
How to use "storage diseases" in a sentence
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storage diseases
All of the lysosomal storage diseases are hereditary.
These are collectively referred to as glycogen storage diseases.
Lipid storage diseases are due to abnormal fat processing.
Gene therapy for lysosomal storage diseases.
These lysosomal storage diseases include Gaucher disease.
Examples of such are the lysosomal storage diseases.
Glycogen storage diseases.
It is used to distinguish different types of glycogen storage diseases.
Metabolic storage diseases.
It is the most common of the glycogen storage diseases.
Glycogen storage diseases - inability to properly utilize sugars.
This can diagnose storage diseases.
Examples of therapeutic agents include the enzymes that are deficient in lysosomal storage diseases.
Metabolic pathways related to glycogen storage diseases and to galactose and fructose disorders.
Intraventricular enzyme delivery for lysosomal storage diseases.
See also
The lysosomal storage diseases are, as outlined herein above, caused by a defective enzyme.
Investigation and management of the hepatic glycogen storage diseases.
This however does not mean other glycogen storage diseases should not be distinguished as well.
This invention is related to the area of lysosomal storage diseases.
Treatment and / or prophylaxis of storage diseases of harvested material.
Fabry disease is one of a group of conditions known as lysosomal storage diseases.
Enzyme replacement therapy for lysosomal storage diseases ( ISDs ) is being actively pursued.
Methods and compositions for the treatment of lysosomal storage diseases.
As a result, individuals suffering from lysosomal storage diseases have accumulated materials in lysosomes.
Enzyme replacement therapy has been used for other lysosomal storage diseases.
More than thirty distinct, inherited lysosomal storage diseases have been characterized in humans.
A similar principle is now used for the treatment of other lysosomal storage diseases.
The lysosomal storage diseases affecting the operation of a vital part of the cell, the lysosome.
Clarifying lysosomal storage diseases.
Storage diseases - Inherited metabolic diseases that are caused due to lack of certain enzymes.
All the cells in the body can be affected by lysosomal storage diseases or glycogenosis.
Representative lysosomal storage diseases and the associated defective enzymes are listed in Table 1.
Excessive hepatic glycogen stores are found in patients with some glycogen storage diseases.
Table 4 provides a list of representative storage diseases and the enzymatic defect associated with the diseases.
Enzyme replacement therapy is particularly effective when treating certain lysosomal storage diseases.
Exemplary lysosomal storage diseases are listed in Table 1.
Also described herein are compositions and methods for the treatment of lysosomal storage diseases.
Interactions of 1MCP and storage diseases need to be studied.
This is where AD differs from other lysosomal storage diseases.
Other examples of lysosomal storage diseases are provided in Table 1.
FBPase inhibitors may also be used to treat excess glycogen storage diseases.
Some of the more prominent lysosomal storage diseases are Gaucher 's disease and Fabry disease.
Availability and use of disease pest management approaches for Canadian apple production storage diseases.
Lysosomal storage diseases having a CNS etiology or component, includes Hunter syndrome.
Hunter syndrome is one of several related lysosomal storage diseases called the MPS diseases.
Exemplary lysosomal storage diseases include mucopolysaccharidosis type II ( Hunter Syndrome ).
Rare diseases such as Wilson disease and Glycogen storage diseases.
Table I . Lysosomal storage diseases and associated enzymatic defects.
As known in the art, there are a multitude of lysosomal storage diseases.
Background, the hepatic glycogen storage diseases ( gsd ) are relatively common genetic disorders.
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