The new cells can also provide the missing enzyme for someone with a storage disease.

In humans it is the least common type of glycogen storage disease.

Provides emotional support for families affected by any glycoprotein storage disease.

It is used to distinguish different types of glycogen storage diseases.

Glycogen storage disease type I is named for him.

Hunter syndrome is one of several related lysosomal storage diseases.

In 2011, he became a cause ambassador to promote awareness of lysosomal storage disease.

Gaucher's disease is the most common of the lysosomal storage diseases.

It is one of the diseases known as lysosomal storage diseases.

In babies with storage diseases, toxins build up constantly.

Doctors began using bone marrow transplants to treat storage diseases in the 1980's.

Perioperative management of patients with glycogen storage disease type Ia.

This disorder is categorized as a lysosomal storage disease.

These are collectively referred to as glycogen storage diseases.

Unlike most other glycogen storage diseases, it directly affects glycolysis.

Another lysosomal storage disease often confused with the mucopolysaccharidoses is mucolipidosis.

GM-1 storage disease is a recessive deficiency of betagalactosidase.

Fucosidosis is one of nine identified glycoprotein storage diseases.

Furthermore A. pullulans is used in biological control of plant diseases, especially storage diseases.

Morquio syndrome is an inherited disease belonging to the group of mucopolysaccharide storage diseases.

Tay-Sachs disease is one of several related genetic disorders in humans known as lysosomal storage diseases.

Glycogen storage disease is a rare hereditary metabolic disorder.

Like other genetic diseases, individuals inherit lysosomal storage diseases from their parents.

He characterized the condition now known as Glycogen storage disease type II in 1932.

Type I glycogen storage disease is inherited as an autosomal recessive genetic disorder.