Examples of 'huntington disease' in a sentence
Meaning of "huntington disease"
Huntington disease, also known as Huntington's disease, is a hereditary neurodegenerative disorder characterized by progressive movement, cognitive, and psychiatric symptoms. It is caused by a mutation in the huntingtin gene. Symptoms usually appear in adulthood and worsen over time, leading to significant functional and cognitive decline
How to use "huntington disease" in a sentence
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huntington disease
Huntington disease will continue to be a part of their life.
Anaplerotic therapy of huntington disease and other polyglutamine diseases.
Huntington disease gradually gets worse over time.
Learning more about Huntington disease is important.
Huntington disease is a genetic disorder that is inherited in the autosomal dominant gene mutation.
Addresses psychological consequences of genetic testing for Huntington disease.
Huntington disease has responded to EPA.
Individuals decide to request predictive testing for Huntington disease.
Huntington Disease is in the striatum.
Other examples include cystic fibrosis and Huntington disease.
Juvenile Huntington disease.
We have also identified the first reliable biomarker in Huntington disease.
Huntington disease is a progressive disorder of motor, cognitive, and psychiatric disturbances.
Predictive testing and the social construction of risk for Huntington disease.
Several Huntington disease ( HD ) clinical trials are in progress and on the horizon.
See also
But there is no way to know when you will develop Huntington disease.
Huntington disease ( HD ) is an inherited brain disorder affecting the nervous system.
The condition is now better known as Huntington chorea or Huntington disease.
Huntington disease ( HD ) is a devastating inherited neurodegenerative disease without curative treatment.
Non-disclosing preimplantation genetic diagnosis for Huntington disease.
About Huntington disease HD is a monogenetic hereditary neurodegenerative disease caused by a defective gene on chromosome 4.
Drug therapies are an attractive solution to clinical treatment of Huntington disease ( HD ).
Huntington disease ( HD ) is a lethal inherited disorder that affects the central nervous system.
Hayden, who has conducted extensive genetic research on Huntington disease.
In rare cases, an individual with Huntington disease does not have a parent with the disorder.
Individuals have played an essential role in all aspects of Huntington disease ( HD ) research.
Juvenile Huntington disease tends to progress more quickly than the adult-onset form.
The use according to claim 1, wherein the polyglutamine disease is Huntington disease.
Juvenile-onset Huntington disease progresses more quickly than the adult-onset form.
In a preferred embodiment of the present invention, the polyglutamine disease is Huntington disease.
In both cases, the mutant Huntington disease proteins aggregated less and fewer neurons died.
November is amaryllis month, named after the emblem of the fight against Huntington disease.
Motor dysfunction is evaluated with the Unified Huntington disease rating scale, UHDRS Siesling et al.
It does not, however, say anything about her current health with respect to Huntington disease.
Huntington disease is caused by a change, or mutation, in a gene.
Food substance for use according to claim 5, wherein the polyglutamine disease is Huntington disease.
Huntington disease ( HD ) is a strong candidate for siRNA-based therapy.
Drugs being tested now have been specifically designed for Huntington disease ( HD ).
For example, the root of Huntington disease is a gene lying on chromosome 4.
HSC 's goal is for a world that is free from Huntington Disease.
Huntington disease ( HD ) is an inherited, debilitating brain disorder that is fatal and incurable.
Consequently, plasma BCAA can be considered as relevant biomarkers for Huntington disease.
Most cases of Huntington disease are diagnosed between the ages of 30 and 50 years of age.
Mystery solved, Tiny protein-activator responsible for brain cell damage in Huntington disease.
Improvement reported in a patient with Huntington disease following fetal neural transplantation ( Madrazo 1991 ).
Precursor of propionyl-CoA for use according to claim 1, wherein the polyglutamine disease is Huntington disease.
Her father, John, has Huntington disease.
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