Question: How old was Napoleon Bonaparte during the Napoleonic Wars? Passage 1:The phenomenon of a government in exile predates the formal utilization of the term. In periods of monarchical government, exiled monarchs or dynasties sometimes set up exile courts—as the House of Stuart did when driven from their throne by Oliver Cromwell and again at the Glorious Revolution (see ). The House of Bourbon would be another example because it continued to be recognized by other countries at the time as the legitimate government of France after it was overthrown by the populace during the French Revolution. This continued to last through the rule of Napoleon Bonaparte and the Napoleonic Wars from 1803–04 to 1815. With the spread of constitutional monarchy, monarchical governments which were exiled started to include a prime minister, such as the Dutch government during World War II headed by Pieter Sjoerds Gerbrandy.
 Passage 2:He attended the Pennsylvania State University and obtained his M.D. degree from Harvard Medical School in 1947. He interned at the Hospital of the University of Pennsylvania. From 1948 to 1952 he was a post-doctoral fellow in the Department of Physiological Chemistry at the University of Pennsylvania School of Medicine and fellow in clinical medicine in the Department of Medicine. In collaboration with Samuel Gurin at the University of Pennsylvania, Brady discovered the enzyme system for the biosynthesis of long chain fatty acids, and later discovered the role of malonate coenzyme A in this process. After two and one-half years on active duty in the U.S. Naval Medical Corps, he joined the National Institutes of Health in 1954. He was Chief of the Developmental and Metabolic Neurology Branch in the National Institute of Neurological Disorders and Stroke from 1972 to 2006. Dr. Brady and his colleagues identified the enzymatic defects in Gaucher's disease, Niemann–Pick disease, Fabry disease and the specific metabolic abnormality in Tay–Sachs disease. He and his associates developed diagnostic, carrier detection, prenatal tests for these conditions, and effective enzyme replacement therapy for patients with Gaucher disease and Fabry disease. These were the first-ever enzyme replacement therapy (ERT) treatments for lysosomal diseases, and directly led to great advances in the development of enzyme replacement therapies for some of the other lysosomal diseases, by many different researchers who were inspired by Dr. Brady. (An international research and development effort for new ERT for several devastating lysosomal diseases continues today at an intense pace, and numerous ERT clinical trials are underway.) Late in his life, Dr. Brady was investigating substrate depletion, molecular chaperone therapy, and gene therapy for patients with metabolic storage disorders.
 Passage 3:Achille Honoré Van Acker was born into a working class family in Bruges, Belgium in 1898 as the youngest of 12 children. He only attended school until the age of 11. Despite entering the workforce, Van Acker read widely and joined several social associations in Bruges. At the outbreak of World War I, he was refused by the Belgian Army because he suffered from astigmatism. While the Germans occupied most of Belgium, Van Acker fled into the small section of unoccupied territory behind the Yser Front where he worked in various menial capacities. Mixing with Belgian soldiers during the war, Van Acker became involved in socialist politics, developing a distinctive ideology based on moderate social democracy. After the end of the war, he returned to Bruges and joined the Belgian Labour Party (Belgische Werkliedenpartij, POB–BWP) and became active in socialist groups, trade unions, and cooperatives.

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