Examples of 'spinocerebellar ataxia' in a sentence
Meaning of "spinocerebellar ataxia"
spinocerebellar ataxia: A group of rare, genetic disorders characterized by progressive problems with movement, such as walking, speaking, and eye movements
How to use "spinocerebellar ataxia" in a sentence
Basic
Advanced
spinocerebellar ataxia
Your daughter is suffering from spinocerebellar ataxia.
Spinocerebellar ataxia is often misdiagnosed is MS as well.
New chapter section on various forms of spinocerebellar ataxia.
Eventually, spinocerebellar ataxia type 1 even leads to cognitive impairment and memory issues.
X-linked recessive spinocerebellar ataxia.
The Machado-Joseph disease MJD is a degenerative disease, which is considered the most frequent spinocerebellar ataxia.
Suffered from spinocerebellar ataxia.
Crouzon specialized in hereditary neurological diseases, especially spinocerebellar ataxia.
The result was important because spinocerebellar ataxia 1 is a devastating inherited disorder with no cure.
Presymptomatic testing for autosomal dominant spinocerebellar ataxia type 1.
Spinocerebellar ataxia type 7, Report of an Indian family.
Autosomal dominant - episodic ataxia and some cases of spinocerebellar ataxia are inherited in this way.
Spinocerebellar Ataxia ( SCA ) and Friedreich 's Ataxia ( FRDA ) are its most common forms.
It is also alternatively known as Spinocerebellar ataxia type 3.
In certain embodiments, the neurodegenerative disease Huntington 's Disease or spinocerebellar ataxia.
See also
Ataxic cerebral palsy Spinocerebellar ataxia Bruns apraxia dystaxia . n . d.
This experimental therapy is in development as a treatment for spinocerebellar ataxia ( SCA ).
A possible transmission of Spinocerebellar Ataxia type 3, blah, blah, blah . Indirect research in three generations.
Her work helped elucidate mechanisms of Rett syndrome and spinocerebellar ataxia type 1.
Machado-Joseph disease ( MJD ), which is also called spinocerebellar ataxia type 3, is a rare hereditary ataxia.
My mother, Addison Garber . Remember her? Suffered from spinocerebellar ataxia.
He has a rare disease called Spinocerebellar Ataxia ( SCA ), check out his blog at,.
Mutations in the TBP gene are responsible for HDL4 ( also known as spinocerebellar ataxia type 17 ).
In addition, results from the patient 's Spinocerebellar Ataxia Functional Index ( SCAFI ) analysis were,.
Ataxin 7 is a protein associated with both olivopontocerebellar atrophy type 3 ( OPCA3 ) and spinocerebellar ataxia type 7 SCA7.
There is currently no cure for Spinocerebellar ataxia type 1.
The researchers used a mouse model of a particular form of spinocerebellar ataxia known as SCA7.
Important examples of polyglutamine diseases are spinocerebellar ataxia and Huntington 's disease.
These features have not been systematically assessed in spinocerebellar ataxia type 10 sca10.
At first glance, patients with a type of ataxia, called spinocerebellar ataxia type 2, appear drunk.
However, no one showed olfactory deficit in spinocerebellar ataxia type 10 sca10.
You'll also be interested in:
Examples of using Ataxia
Show more
The ataxia must be affecting your work
The child with ataxia can not do it
Ataxia and myoclonus may also be seen
Examples of using Spinocerebellar
Show more
The spinocerebellar tract is involved to a lesser extent
Your daughter is suffering from spinocerebellar ataxia
Spinocerebellar tract transmitting sensory information
