How To Use Pku In A Sentence
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(Unless you have a genetic disease called phenylketonuria (PKU), which prevents you from digesting the amino acid phenylalanine.
Dr. Joseph Mercola: The Deadly Neurotoxin Nearly EVERYONE Uses Daily (VIDEO)
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It would be another quarter of a century before scientists finally identified Carol’s condition she was suffering from phenylketonuria, or PKU, brain degeneration caused by inability in the newborn child to process a chemical called phenyl, a deficiency that can be treated only if detected in its early stages.
PEARL BUCK IN CHINA
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Feb. 26th, 2004: Princess Maha Chakri·Sirindhorn of the Kingdom of Thailand visited PKU. The vice president of PKU Hao Ping met the visitor.
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These conditions include sickle cell anemia, beta thalassemia, phenylketonuria PKU, hypothyroidism,8 and galactosemia.
Pregnancy, Childbirth, and the Newborn
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Virtually the only people who cannot consume the artificial sweetener aspartame are those who have a rare hereditary disease called phenylketonuria PKU—and every product that contains aspartame carries a PKU warning on the label.
The Small Change Diet
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As an example of the power of environmental effects, consider infants with the genetic disorder PKU (phenylketonuria).
The Volokh Conspiracy » Some Scientists’ Openness to the Possibility of Genetic Differences in Mental Traits Among Racial and Ethnic Groups
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I must here also mention a simple little instrument called _keipkūttuk_, being a slender rod of bone nicely rounded, and having a point at one end and a knob or else a laniard at the other.
Journal of the Third Voyage for the Discovery of a North-West Passage
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Years ago all babies were screened for a very rare condition called phenylketonuria PKU with a blood test.
The Official Lamaze® Guide
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PKU is described by scientists as an autosomal recessive genetic disease that is characterized by a deficiency in an enzyme called phenylalanine hydroxylase (PAH).
Medlogs - Recent stories
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The three main laboratory methods used to screen newborns for PKU are the Guthrie bacterial inhibition assay, fluorometric analysis and tandem mass spectrometry.
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Molecular heterogeneity for PKU results in wide phenotypic heterogeneity, which contributes to biochemical individuality.
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Organic acidopathies (propionic acidemia, methylmalonic acidemia, biotinidase deficiency, phenylketonuria (PKU) and other disorders)
Biochemical Genetics-Metabolic Disease
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On Apr. 24 th, the celebration of the 106 th anniversary of Peking University was held in PKU.
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Newborn screening was pioneered in the 1940s by Robert Guthrie, who, having developed a simple blood test for a form of mental retardation called phenylketonuria PKU, proposed the newborn heel stick test to test for PKU and other “inborn errors of metabolism.”
The $1,000 Genome
