Examples of 'storage disorder' in a sentence
Meaning of "storage disorder"
storage disorder ~ a condition characterized by difficulties in organizing or managing personal belongings or items
How to use "storage disorder" in a sentence
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storage disorder
It is a recessively inherited lysosomal storage disorder.
A bladder storage disorder is any factor that increase the frequency of small volume voids.
The result is a lysosomal storage disorder.
AGU is a rare lysosomal storage disorder with autosomal recessive inheritance.
High levels of ferritin can indicate an iron storage disorder.
NPC is a lysosomal storage disorder in which cholesterol accumulates in the brain.
It is a type of lysosomal storage disorder.
Fucosidosis is a lysosomal storage disorder caused by deficiency of the enzyme α-L-fucosidase.
One disclosure relates to a method of treating a subject with a lysosomal storage disorder.
MPS IIIB is a neurodegenerative lysosomal storage disorder caused by mutations in the NAGLU gene.
In one embodiment, the neurological disorder is a storage disorder.
A method of diagnosing a lipid storage disorder in a human subject, the method comprising,.
In a preferred embodiment, the conformational disorder is a lysosomal storage disorder.
In one embodiment, the lysosomal storage disorder is associated with accumulation of glucocerebroside.
Gaucher 's disease is the most prevalent lysosomal storage disorder.
See also
In one embodiment, the lysosomal storage disorder is associated with a deficiency in glucocerebrosidase.
In a specific embodiment, the conformational disorder is a lysosomal storage disorder.
In one embodiment, the lysosomal storage disorder is Fabry disease.
Use of a conjugate of claim 1 in the manufacture of a medicament for treating a lysosomal storage disorder.
It is a lysosomal storage disorder.
The method of claim 4, wherein the patient has been diagnosed with a lysosomal storage disorder.
In another particular embodiment, said lysosomal storage disorder is Metachromatic leukodystrophy.
In a preferred embodiment, the a-galactosidase A is associated with a a lysosomal storage disorder.
NPA is a lysosomal storage disorder caused by a deficiency in acid sphingomyelinase ( ASM ) activity.
In yet another particular embodiment, said lysosomal storage disorder is saposin-deficiency.
Use of a conjugate of E 48 in the manufacture of a medicament for treating a lysosomal storage disorder.
Use of a conjugate of E 48 for treating a lysosomal storage disorder in a subject in need thereof.
The method of claim 1, wherein the a-galactosidase A is associated with a lysosomal storage disorder.
Abstract, Pompe disease is a lysosomal storage disorder characterized by muscle weakness and cardiomyopathy.
In yet another particular embodiment of the present disclosure, said lysosomal storage disorder is saposin-deficiency.
In some aspects, a lysosomal storage disorder protein is " substantially free " of phosphate groups.
In another embodiment of the present invention, the lysosomal storage disorder is mucopolysaccharidosis.
Background of the Invention Gaucher 's disease is the most prevalent lysosomal storage disorder.
Fabry disease is a progressive X-linked lysosomal storage disorder which affects males and females.
Pentosan polysulfate ( PPS ) for use in the treatment of a subject with a lysosomal storage disorder.
Particular aspects include methods of treating a lysosomal storage disorder ( LSD ), including those having a CNS component.
Mucolipidosis type IV ( ML IV ) is an autosomal recessive lysosomal storage disorder.
An IDS deficiency causes the lysosomal storage disorder MPS II ( mucopolysaccharidosis type II ).
The composition of claim 6, wherein the a-galactosidase A is associated with a lysosmal storage disorder.
In a particular embodiment, said lysosomal storage disorder is Niemann-Pick disease type A or B.
So, I was like, okay, this has got to be a glucose storage disorder.
Preferably, said lysosomal storage disorder is Niamann-Pick.
In another particular embodiment of the present disclosure, said lysosomal storage disorder is Sialidosis.
It 's a fatal, genetic lipid storage disorder prevalent upon european Jews.
In another particular embodiment of the present disclosure, said lysosomal storage disorder is Farber disease.
Preferably, said lysosomal storage disorder is Niemann-Pick.
In another particular embodiment of the present disclosure, said lysosomal storage disorder is Krabbe disease.
In one embodiment, the lysosomal storage disorder is Gaucher 's disease.
In another particular embodiment of the present disclosure, said lysosomal storage disorder is Fabry disease.
The method according to claim 1, wherein said lipid storage disorder is a sphingolipidosis.
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