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This up-to-date reference on the nutrition management of inherited metabolic diseases (IMD) covers a wide range of these disorders, including phenylketonuria and other aminoacidopathies, organic acidemias, urea cycle disorders, fatty acid oxidation disorders, galactosemia and glycogen storage diseases. Guidance is also provided on laboratory evaluations and biochemical testing and monitoring. Topics such as newborn screening for IMD, as well as nutrition management during pregnancy and transplantation, are addressed. The book is based on 7 years of lectures delivered through Metabolic University – an interactive, didactic program designed to provide training to dietitians who work with individuals with IMD. This book provides the basic information required to manage nutrition care and is a resource for clinicians new to this complex field.
Families will love this. Simple yet creative ideas for making a variety of meals from a few basic low protein foods. Fran Rohr, MS, RD, LDN. Clinical Nutrition Specialist. Boston Children's Hospital Laurie Bernstein and her team have put together another great educational booklet! This guide will help our families feel more comfortable in the kitchen and create low protein delicious dishes for the whole family! Mary Sowa, MS, RD CHOC Children's Hospital Setting Up Your Low Protein Kitchen is a practical...and fun... resource for anyone following a low protein diet. Sandy van Calcar, M.S., RD University of Wisconsin
This captivating book is a story of the friendship between a genius physicist Wolfgang Pauli and Charlotte Houtermans whose career in physics was not as glamorous. They met in the late 1920s in Germany, at the very onset of the quantum era and personally knew all the major players in the emergent quantum world that was very much part of central Europe: Germany, Austria, Hungary, Denmark and Switzerland. And Charlotte was a student at Göttingen that was right at the heart.Caught between two evils — Soviet Communism and German National Socialism — she would have probably perished if it were not for the brotherhood of physicists: Niels Bohr, Wolfgang Pauli, Albert Einstein, James Franck, M...
Named one of the "Ten must-read science histories" by Science Magazine In a lifetime of practice, most physicians will never encounter a single case of PKU. Yet every physician in the industrialized world learns about the disease in medical school and, since the early 1960s, the newborn heel stick test for PKU has been mandatory in many countries. Diane B. Paul and Jeffrey P. Brosco’s beautifully written book explains this paradox. PKU (phenylketonuria) is a genetic disorder that causes severe cognitive impairment if it is not detected and treated with a strict and difficult diet. Programs to detect PKU and start treatment early are deservedly considered a public health success story. Some...
Drawing on ethnographic studies of the lived experiences of people with rare diseases, this volume critically examines rare, chronic diseases in the context of care, kinship, and technologies, providing in-depth analyses of local worlds that usually remain at the peripheries of medical anthropological inquiry.
Geographical listing of treatment programs in the United States and Puerto Rico as surveyed during Jan-Aug, 1988. Also includes introductory and statistical information. Entries give identifying information and key contact persons, with telephone numbers. Also contains directory of parent support groups.
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