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Infantile onset spinocerebellar ataxia

mutation in C10ORF2
Also Known As:
Infantile-Onset Spinocerebellar Ataxia; OHAHA Syndrome; Ophthalmoplegia, hypotonia, ataxia, hypacusis, and athetosis; Spinocerebellar Ataxia, Infantile, with Sensory Neuropathy; Spinocerebellar ataxia infantile with sensory neuropathy
Networked: 18 relevant articles (1 outcomes, 0 trials/studies)

Relationship Network

Disease Context: Research Results

Related Diseases

1. Chronic Progressive External Ophthalmoplegia (Progressive External Ophthalmoplegia)
2. Mitochondrial Myopathies (Mitochondrial Myopathy)
3. Mitochondrial Diseases (Mitochondrial Disease)
4. Sensory Partial Epilepsy
5. Parkinsonian Disorders (Parkinsonism)

Experts

1. Suomalainen, Anu: 6 articles (12/2018 - 10/2005)
2. Lönnqvist, Tuula: 5 articles (12/2018 - 10/2005)
3. Paetau, Anders: 4 articles (04/2016 - 12/2008)
4. Spelbrink, Johannes N: 3 articles (01/2009 - 10/2005)
5. Ahola, Sofia: 2 articles (12/2018 - 04/2016)
6. Buzkova, Jana: 2 articles (12/2018 - 04/2016)
7. Carroll, Christopher J: 2 articles (12/2018 - 04/2016)
8. Hakonen, Anna H: 2 articles (12/2018 - 12/2008)
9. Nikkanen, Joni: 2 articles (12/2018 - 04/2016)
10. Velagapudi, Vidya: 2 articles (12/2018 - 04/2016)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Infantile onset spinocerebellar ataxia:
1. Valproic Acid (Depakote)FDA LinkGeneric
2. Mitochondrial DNA (mtDNA)IBA
3. Mitochondrial Proteins (Mitochondrial Protein)IBA
4. Inositol 1,4,5-Trisphosphate Receptors (Inositol Triphosphate Receptor)IBA
5. Complementary DNA (cDNA)IBA
6. Proteins (Proteins, Gene)FDA Link
7. NucleotidesIBA
8. Niacinamide (Nicotinamide)FDA LinkGeneric
9. CreatineIBA
10. DNA Polymerase gammaIBA