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Phenylketonuria (pronounced fee-nill-key-toe-NURR-ee-uh) or PKU is a rare, inherited metabolic disorder. Each year, approximately 1 in 14,000 newborn babies are diagnosed with PKU. If you have PKU, your body cannot break down, or metabolize, the essential amino acid, phenylalanine (Phe). Amino acids are the building blocks of protein. The primary treatment for PKU is a special metabolic formula and the restriction of foods high in Phe (protein), such as meats, cheeses, milk, bread and pasta. Life-long dietary compliance is a critical component for proper growth and development in children and...

Fenylketonuri, ogsa kalt PKU, er en sjelden og arvelig stoffskiftesykdom. Hvert ar blir rundt 5 nyfodte diagnostisert med PKU i Norge. Hvis du har PKU, klarer ikke kroppen din a bryte ned, eller omdanne, den essensielle aminosyren fenylalanin (Phe). Aminosyrer er det som proteiner er bygget opp av. Hovedbehandlingen av PKU er en diett bestaende av proteinerstatning og begrenset mengde av mat med mye Phe (protein) som kjott, ost, melk, brod og pasta. Det a holde fast ved dietten hele livet ut, er helt grunnleggende for at barn skal vokse og utvikle seg normalt og for god livskvalitet hos...

Revolutionary Russia: A History in Documents provides a visually stimulating survey of revolutionary Russia, from the collapse of the autocracy in 1917 to the consolidation of the Stalinist system in the 1930s. Authors Robert Weinberg and Laurie Bernstein have collected far-flung documents--many available in English for the first time--and woven them into a narrative that focuses on the effort to build communism in Russia and its effects on the lives of ordinary people. Providing introductions to each chapter and document along with sidebars and detailed photo captions, the main text...