Rare Diseases and Orphan Drugs: Keys to Understanding and Treating the Common Diseases by Jules J. Berman
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Overview: Jules Berman received two baccalaureate degrees from MIT; in Mathematics, and in Earth and Planetary Sciences. He received the Ph.D. from Temple University, and the M.D. from the U. of Miami. He received post-doctoral training at NIH and residency training at Geo. Washington U Med Ctr. He is board certified in anatomic pathology and in cytopathology. He served as Chief of Anatomic Pathology, Surgical Pathology and Cytopathology at the Veterans Administration Medical Center in Baltimore, Maryland, where he held joint appointments at the University of Maryland Medical Center and the Johns Hopkins Medical Institutions. In 1998, he became a Medical Officer at the U.S. National Cancer Institute and served as the Program Director for Pathology Informatics in the Institute’s Cancer Diagnosis Program. In 2006, Jules Berman was President of the Association for Pathology Informatics. In 2011 he received the Lifetime Achievement Award from the Association for Pathology Informatics. Today, Jules Berman is a free-lance writer. He has first-authored 100+ articles and 14 book titles in science and medicine.
Genre: Non-Fiction > Educational
Rare Diseases and Orphan Drugs shows that much of what we now know about common diseases has been achieved by studying rare diseases. It proposes that future advances in the prevention, diagnosis, and treatment of common diseases will come as a consequence of our accelerating progress in the field of rare diseases.
Understanding the complex steps in the development of common diseases, such as cancer, cardiovascular disease, and metabolic diseases, has proven a difficult problem. Rare diseases, however, are often caused by aberrations of a single gene. In rare diseases, we may study how specific genetic defects can trigger a series of events that lead to the expression of a particular disease. Often, the disease process manifested in a certain rare disease is strikingly similar to the disease process observed in a common disease.
This work ties the lessons learned about rare diseases to our understanding of common ones. Chapters covering the number of common diseases are minimized, while rare diseases are introduced as single diseases or as members of diseases classes. After reading this book, readers will appreciate how further research into the rare diseases may lead to new methods for preventing, diagnosing, and treating all diseases, rare or common.
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