spinocerebellar ataxia , SCA (skrót)

The following is a list of some, not all, types of Spinocerebellar ataxia.

These include neuromuscular problems such as spinocerebellar ataxia and myopathies.

The theory that Lincoln was afflicted with type 5 spinocerebellar ataxia is no longer accepted.

There is no known prevention of spinocerebellar ataxia.

It is associated with Spinocerebellar ataxia type 5.

It's the same for another neurological disease we study in my lab, spinocerebellar ataxia Type 1, which is also inherited.

It has also been associated with cerebellar degeneration in spinocerebellar ataxia type 16.

Important examples of polyglutamine diseases are spinocerebellar ataxia and Huntington's disease.

This can also result in excitotoxicity, as may occur in some cases of spinocerebellar ataxia type-6.

He was medically discharged in 2005 following a 2004 diagnosis of spinocerebellar ataxia, a hereditary disease.

Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia 8.

Mdf mice model human spinocerebellar ataxia type disorders.

KCNC3 is associated with spinocerebellar ataxia type 13.

Crouzon specialized in hereditary neurological diseases, especially spinocerebellar ataxia.

Spinocerebellar ataxia type 2.

The related diseases, which are also inherited, include spinocerebellar ataxia and spinal and bulbar muscular atrophy.

A similar mechanism, involving triplet repeats, underlies myotonic dystrophy, spinocerebellar ataxia and Huntington's disease.

Her work has helped uncover genes and mechanisms responsible for Rett syndrome and spinocerebellar ataxia neurological disorders.

Machado-Joseph disease is a type of spinocerebellar ataxia and is the most common cause of autosomal-dominant ataxia.

Spinocerebellar ataxia (SCA) is a progressive, degenerative, genetic disease with multiple types, each of which could be considered a disease in its own right.

A large protein of unknown function, ataxin-2, associated with the neurodegenerative disease spinocerebellar ataxia type 2, also has a N-terminal LSm domain.

Persons who have been diagnosed with autosomal dominant spinocerebellar ataxia (SCAs) also exhibit dysmetria.

There is no currently known cure for spinocerebellar ataxia, which is considered to be a progressive and irreversible disease, although not all types cause equally severe disability.

Important It is possible that the main title of the report Spinocerebellar Ataxia with Axonal Neuropathy is not the name you expected.

Drosophila is being used as a genetic model for several human diseases including the neurodegenerative disorders Parkinson's, Huntington's, spinocerebellar ataxia and Alzheimer's disease.