Autoimmunity to glutamic acid decarboxylase in the neurodegenerative disorder Batten disease
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Abstract
The pathogenic mechanisms underlying Batten disease are unclear. Patients uniformly possess autoantibodies against glutamic acid decarboxylase (GAD) that are predominantly reactive with a region of GAD (amino acids 1 to 20) distinct from subjects with autoimmune type 1 diabetes or stiff-person syndrome. Batten patients did not possess autoantibodies against other type 1 diabetes-associated autoantigens and human leukocyte antigen genotypes revealed no specific associations with this disease.
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Glutamic acid decarboxylase autoimmunity in Batten disease and other disordersDavid A. Pearce, Mark Atkinson, Danilo A. Tagle et al.Neurology, December 13, 2004 -
Clinical/Scientific Notes
INTERMITTENT PREDNISOLONE AND AUTOANTIBODIES TO GAD65 IN JUVENILE NEURONAL CEROID LIPOFUSCINOSISL. Åberg, M. Talling, T. Härkönen et al.Neurology, March 31, 2008 -
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Anti-GAD antibody syndrome with concomitant cerebellar ataxia, stiff person syndrome, and limbic encephalitisSara M. Schaefer, Jeremy J. Moeller et al.Neurology: Clinical Practice, June 04, 2015 -
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An autoantibody to GAD65 in sera of patients with juvenile neuronal ceroid lipofuscinosesSubrata Chattopadhyay, Elizabeth Kriscenski-Perry, David A. Wenger et al.Neurology, December 10, 2002