Skip to search formSkip to main contentSkip to account menu

SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE, WITH AXONAL NEUROPATHY

Known as: SCAN1 
National Institutes of Health

Related topics

Related topics

4 relations

Broader (1)

Spinocerebellar Degeneration
TDP1 geneTDP1 wt AlleleTDP1, HIS493ARG

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
Regional pulmonary function analysis using image registration and 4DCT
  • K. Du
  • 2013
  • Corpus ID: 68683598
Approved: Thesis Supervisor Title and Department 
2012
2012
Spinocerebellar Ataxia with Axonal Neuropathy (SCAN1): A Disorder of Nuclear and Mitochondrial DNA Repair
Spinocerebellar ataxias (SCAs) are a group of progressive and irreversible neurological diseases affecting gait and movement… 
2009
2009
The Dependence of ICA Decomposition on Dimensionality in Functional Connectivity
o, matrix=128×128, 256mm ×256mm FOV, BW=250KHz, Scan 2-4=160 volumes during which time a block-paradigm complex finger tapping… 
Review
2006
Review
2006
[Molecular genetics of inherited neuropathies].
Inherited neuropathies are clinically and genetically heterogeneous. At least 28 genes and 12 loci have been associated with… 
Review
2006
Review
2006
[Molecular genetics of inherited neuropathies].
To clarify the specific features and molecular mechanisms of five diseases that we previously reported, we reviewed recent… 
Review
2004
Review
2004
[Clinical features and molecular genetics of autosomal recessive spinocerebellar degenerations].
The number of patients with spinocerebellar degeneration (SCD) has recently exceeds 20,000 in Japan. Among them, sporadic form is… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)