2. Infantile-onset spinocerebellar ataxia - MedlinePlus - Health information - Genetics Home Reference
These resources supplement the information in the Genetics Home Reference condition summary on infantile-onset spinocerebellar ataxia.
MedlinePlus (Offsite)

3. Disease Information: Spinocerebellar Ataxia
Spinocerebellar ataxia type 1 (SCA1) is an inherited disorder where a part of the brain (cerebellum) and spinal cord degenerate. This causes ataxia (progressive difficulty with walking and coordination) as well as tremors and difficulty with speec...
patientinfo.ninds.nih.gov

4. Ataxias and Cerebellar or Spinocerebellar Degeneration Information Page: National Institute of Neurological Disorders and Stroke (NINDS)
Ataxia often occurs when parts of the nervous system that control movement are damaged. People with ataxia experience a failure of muscle control in their arms and legs, resulting in a lack of balance and coordination or a disturbance of gait. Whi...
www.ninds.nih.gov

5. ataxia, spinocerebellar ataxia, movement disorders, balance disorders
Ataxia is typically defined as the presence of abnormal, uncoordinated movements. This usage describes signs & symptoms without reference to specific diseases. An unsteady, staggering gait is described as an ataxic gait because walking is uncoordi...
www.hopkinsmedicine.org

6. Spinocerebellar Ataxia
Zuhlke, C., A. Dalski, et al. (2002). "Spinocerebellar ataxia type 1 (SCA1): phenotype-genotype correlation studies in intermediate alleles." Eur J Hum Genet 10 (3): 204-9.
lansbury.bwh.harvard.edu

7. Ataxias and Cerebellar or Spinocerebellar Degeneration Publications: National Institute of Neurological Disorders and Stroke (NINDS)
Sorry, there are no other publications for Ataxias and Cerebellar or Spinocerebellar Degeneration at this time.
accessible.ninds.nih.gov

8. Infantile onset spinocerebellar ataxia
Evidence was critically evaluated at this workshop. Current gaps in knowledge in this area were identified and research priorities were formulated. The workshop summary will provide NICHD and the scientific community a template to address the scie...
rarediseases.info.nih.gov

9. Infantile onset spinocerebellar ataxia
Ophthalmoplegia, hypotonia, ataxia, hypacusis, and athetosis; OHAHA syndrome; IOSCA; Spinocerebellar ataxia 8 (formerly) SCA8 (formerly) Spinocerebellar ataxia infantile with sensory neuropathy; For more information about Infantile onset spinocere.....
www.rarediseases.info.nih.gov

10. JAX Mice Database - Spinocerebellar ataxia
These transgenic mice express a human TATA box binding protein, TBP, containing a 105 polyQ repeat expansion, under the control of the mouse prion protein promoter. The 105 polyQ-expansion is detected by Western blot analysis. At 3 months of age, ...
jaxmice.jax.org