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[L565.Ebook] Free PDF Inherited Metabolic Disease in Adults: A Clinical Guide (Oxford Monographs on Medical Genetics)From Oxford University Press

Free PDF Inherited Metabolic Disease in Adults: A Clinical Guide (Oxford Monographs on Medical Genetics)From Oxford University Press

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Inherited Metabolic Disease in Adults: A Clinical Guide (Oxford Monographs on Medical Genetics)From Oxford University Press

Inherited Metabolic Disease in Adults: A Clinical Guide (Oxford Monographs on Medical Genetics)From Oxford University Press



Inherited Metabolic Disease in Adults: A Clinical Guide (Oxford Monographs on Medical Genetics)From Oxford University Press

Free PDF Inherited Metabolic Disease in Adults: A Clinical Guide (Oxford Monographs on Medical Genetics)From Oxford University Press

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Inherited Metabolic Disease in Adults: A Clinical Guide (Oxford Monographs on Medical Genetics)From Oxford University Press

As clinical management of inherited metabolic diseases (IMDs) has improved, more patients affected by these conditions are surviving into adulthood. This trend, coupled with the widespread recognition that IMDs can present differently and for the first time during adulthood, makes the need for a working knowledge of these diseases more important than ever.

Inherited Metabolic Disease in Adults offers an authoritative clinical guide to the adult manifestations of these challenging and myriad conditions. These include both the classic pediatric-onset conditions and a number of new diseases that can manifest at any age. It is the first book to give a clear and concise overview of how this group of conditions affects adult patients, a that topic will become a growing imperative for physicians across primary and specialized care.

  • Sales Rank: #1441890 in Books
  • Published on: 2016-08-16
  • Original language: English
  • Number of items: 1
  • Dimensions: 8.40" h x 1.10" w x 11.10" l, .0 pounds
  • Binding: Hardcover
  • 648 pages

About the Author

Carla E. M. Hollak is Professor of Internal Medicine in the Division of Endocrinology and Metabolism at the University of Amsterdam and the Academic Medical Center (AMC). She heads the adult inherited metabolic unit at AMC, including the centers of excellence for Gaucher and Fabry disease and a rapidly growing service for adults with inborn errors of metabolism. Hollak regularly serves as expert for regulatory agencies both at a national and international level. She is chair of the "Erfocentrum" board, treasurer of the European Study Group on Lysosomal Diseases, and involved in activities of the European Working Group on Gaucher Disease and the Adult Metabolic Group for the Society for the Study of Inborn Errors of Metabolism.

Robin Lachmann is Consultant in Metabolic Medicine at the National Hospital for Neurology and Neurosurgery, London, where he heads the Charles Dent Metabolic Unit. He is a member of the British Inherited Metabolic Disease Group and the Society for the Study of Inborn Errors of Metabolism, serving as chair of the latter's adult group. He is Chair of the Scientific Committee of the Recordati Rare Diseases Foundation, organizing training and education in rare diseases; Chair of the Metabolic Disorders Clinical Reference Group, which advises NHS England on metabolic services; and an elected member of Council of the Royal College of Physicians, London.

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