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From the Department of Neurological Rehabilitation (Drs. Nemni and Gironi), Don C. Gnocchi Foundation, University of Milan, Italy; Department of Neurology (Dr. Caniatti), S. Anna Hospital, University of Ferrara, Italy; Diagnostic Laboratory (E. Bazzigaluppi), San Raffaele Scientific Institute, Milan, Italy; and Department of Neurology (Dr. De Grandis), Rovigo Civic Hospital, Italy.
Address correspondence and reprint requests to Dr. Raffaello Nemni, Department of Neurological Rehabilitation, Don C. Gnocchi Foundation, University of Milan, 20148 Milan, Italy; e-mail: raffaello.nemni{at}unimi.it
The authors report the presence of high titer antibodies to glutamic acid decarboxylase (anti-GAD65) until age 24 months in two asymptomatic newborns of a woman with stiff-person syndrome (SPS). No signs of SPS were detectable in the two children at ages 6 and 8 years. This observation indicates that other cofactors are involved in the pathogenesis of SPS.
Received November 17, 2003. Accepted in final form February 3, 2004.
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T. M. Burns, L. H. Phillips II, H. R. Jones, R. Nemni, L.M. Caniatti, M. Gironi, E. Bazzigaluppi, and D. D. Grandis Stiff person syndrome does not always occur with maternal passive transfer of GAD65 antibodies Neurology, January 25, 2005; 64(2): 399 - 400. [Full Text] [PDF] |
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