Rasmussen syndrome combined with IgA deficiency and membranous nephropathy.
暂无分享,去创建一个
S. Ito | S. Takeshita | A. Nezu | K. Ichikawa
[1] F. Andermann,et al. Early onset Rasmussen's syndrome: A malignant, often bilateral form of the disorder , 2006, Epilepsy Research.
[2] J. Freeman. Rasmussen's syndrome: progressive autoimmune multi-focal encephalopathy. , 2005, Pediatric neurology.
[3] Y. Kawasaki,et al. IgA deficiency and membranous glomerulonephritis presenting as nephrotic syndrome , 2005, Pediatric Nephrology.
[4] C. Elger,et al. Pathogenesis, diagnosis and treatment of Rasmussen encephalitis: a European consensus statement. , 2005, Brain : a journal of neurology.
[5] G. Broggi,et al. Experience with immunomodulatory treatments in Rasmussen’s encephalitis , 2003, Neurology.
[6] M. Mishina,et al. Autoantibodies to NMDA receptor in patients with chronic forms of epilepsia partialis continua , 2003, Neurology.
[7] Yukitoshi Takahashi,et al. A patient with epilepsia partialis continua with anti-glutamate receptor epsilon 2 antibodies. , 2003, Pediatric neurology.
[8] R. Spreafico,et al. Antibodies against GluR3 peptides are not specific for Rasmussen's encephalitis but are also present in epilepsy patients with severe, early onset disease and intractable seizures , 2002, Journal of Neuroimmunology.
[9] Charlotte Cunningham-Rundles,et al. Physiology of IgA and IgA Deficiency , 2001, Journal of Clinical Immunology.
[10] R. Nickles,et al. Rasmussen encephalitis: epilepsia partialis continua secondary to chronic encephalitis. , 1990, Pediatric neurology.
[11] Wu-chang Yang,et al. IgA deficiency with membranous glomerulonephritis: a case report and review. , 2003, Journal of nephrology.