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AICARDI-GOUTIERES SYNDROME 5 (disorder)

Known as: AGS5, AICARDI-GOUTIERES SYNDROME 5, Aicardi-Goutieres syndrome, autosomal dominant 
National Institutes of Health

Papers overview

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2018
2018
Aicardi–Goutières syndrome, a rare genetic disorder characterized by calcification of basal ganglia, results in psychomotor… 
2014
2014
Innate lymphoid cells, marginal reticular cells and B cell–helper neutrophils interact to promote antibody secretion by B cells… 
2009
2009
Aicardi–Goutières syndrome is a genetic childhood encephalopathy characterized by basal ganglia calcification, chronic… 
2007
2007
According to a theorem by Lagrange, the continued fractions of quadratic surds are periodic. Their periods may have different… 
1997
1997
BACKGROUND The Aicardi syndrome is a complex of congenital anomalies consisting of agenesis of the corpus callosum, infantile… 
1974
1974
Similarities within 220 cases of epileptic myoclonia were computed by the overlapping cluster‐analysis method (Jardine and Sibson… 
1972
1972
A case of Aicardi's syndrome is described. The main features are infantile spasms, pathognomonic chorioretinopathy, evidence of…