By Hugo Buhthal and Otto Kurz
First variation, this being the author's annotated interleaved reproduction. Correspondence among the authors and diverse museums are loosely inserted. reviews of the Warburg Institute, vol. 12. Edited through Fritz Saxl. Catalogue of 555 japanese Christian illuminated manuscripts, with chapters dedicated to Syriac, Arabic, Coptic, Nubian, Ethiopian, Armenian, and Georgian manuscripts. comprises record of usually mentioned books and articles. a hundred and twenty pages. fabric with paper backbone label. huge 8vo..
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Mora, PhD R. Mantegazza, MD P. Bernasconi, PhD Address correspondence and reprint requests to Dr. it ABSTRACT Objectives: Juvenile dermatomyositis (JDM), adult dermatomyositis, and polymyositis (PM) are idiopathic inflammatory myopathies (IIMs) characterized by muscle infiltration and specific muscle fiber alterations. They are thought to have an autoimmune etiology, but triggering factors, and how immunologic attack induces muscle weakness, remain unknown. Recent evidence suggests a key role for type I interferon (IFN)-mediated innate immunity in dermatomyositis, which we explored in JDM, dermatomyositis, and PM by gene expression profiling, and other methods.
Cappelletti, Dr. Baggi, Dr. Zolezzi, Dr. Biancolini, Dr. Beretta, and Dr. Severa report no disclosures. Dr. Coccia has received research support from the Fondazione Italiana Sclerosi Multipla. Dr. Confalonieri has received funding for travel from sanofi-aventis and Bayer Schering Pharma; has served as a consultant for Biogen Idec; and has received research support from Merck Serono, Biogen Idec, and sanofi-aventis. Dr. Morandi receives research support from Telethon and the Agenzia Italiana Farmaco (AIFA).
Survival. Two patients died from respiratory failure at the age of 10 years and 22 years. The first patient (patient 21, table e-1) was a girl with obesity and hepatic steatosis who failed to attend her scheduled Neurology 76 June 14, 2011 2075 respiratory follow-up despite her FVC being abnormal at 36% at the age of 10 years. The second patient (patient 33, table e-1) declined the scheduled regular respiratory follow-up and died suddenly at home at the age of 22 years. A postmortem examination showed a mild right ventricular hypertrophy.