Synonymer & Anagram | Engelska ordet PKU

Exempel på hur man kan använda PKU i en mening

• Phenylketonuria (PKU) is an inborn error of metabolism that results in decreased metabolism of the amino acid phenylalanine.
• Despite the fact that PKU launched its official BBS later on, Wei Ming station, YTHT still managed to burgeon into one of the best and biggest BBS systems in the education network in China with more than 300,000 users, mainly students and well-educated professionals.
• NBS started with the discovery that the amino acid disorder phenylketonuria (PKU) could be treated by dietary adjustment, and that early intervention was required for the best outcome.
• The children, he concluded, had excess phenylpyruvic acid in the urine, the condition which came to be called phenylketonuria (PKU).
• PKU test – Phenylketonuria (PKU) is a metabolic disorder in which the individual is missing an enzyme called phenylalanine hydroxylase.
• Established diagnoses include Down syndrome, Fragile X syndrome, Trisomy 8 mosaic syndrome, Trisomy 13 syndrome, Williams syndrome, Angelman syndrome, Smith–Magenis syndrome, PKU, Tuberous sclerosis, Neurofibromatosis, Sturge–Weber syndrome, Congenital rubella syndrome, the syndrome of hypoxic/ischemic perinatal brain injury, lead encephalopathy, hydrocephalus, prosencephaly, schizencephaly, and other diagnoses.
• Problems in the digestion of phenylalanine (phe) to tyrosine (tyr) lead to the buildup of both phe and phenylpyruvate, in a disease called Phenylketonuria (PKU).
• Manufactured at six industrial zones under government supervision, the models are Super Mandala Jeep from Mandalay Industrial Zone, Myay Latt Jeep from Myingyan Industrial Zone, Htila Jeep from Meikhtila Industrial zone, Chindwin Star Jeep from Monywa Industrial Zone, Shan Star Jeep from Ayethaya Industrial Zone in Taunggyi and PKU Jeep from Pakokku Industrial Zone.
• From 2000 to 2010, Stevens has worked with BioMarin Pharmaceutical to develop Kuvan (tetrahydrobiopterin) and assisted in the design and development of PEG-PAL (pegylated Phenylalanine ammonia-lyase) as treatments for mild and classical phenylketonuria (PKU).
• The most prevalent genetic conditions include Down syndrome, Klinefelter syndrome, Fragile X syndrome (common among boys), neurofibromatosis, congenital hypothyroidism, Williams syndrome, phenylketonuria (PKU), and Prader–Willi syndrome.
• Hyperphenylalaninemia most is commonly diagnosed by newborn screening and must be distinguished from classic PKU by confirmatory testing at an experienced center.
• Among them, the Maternal and Child Safety 120 Action Program covered 10 counties (city, district) in five provinces (municipalities/autonomous regions), and the cumulative number of beneficiaries of the project was about 4,000 person times, and 8 critical and serious pregnant and lying-in woman were rescued; The vision aid program covered 4 counties (cities), 4 provinces, Yucheng District of Ya'an City in Sichuan Province, Chaoyang County in Liaoning Province, Lianyuan City in Hunan Province and Changting County in Fujian Province, benefiting more than 115,000 children; The hearing aid program provided language rehabilitation training for 65 hearing-impaired children and training for 15 parents; Project for two cancer of women screened 750 rural women in Yulong County, Yunnan Province for "two cancer of women"; The PKU program provided special food subsidies for 7 impoverished PKU children in Longde County.
• Richard contributed greatly to identification of the genes for phenylketonuria (PKU) and its variants by conceiving, planning and executing myeloma studies, conceiving affinity adsorbents for PAH (phenylalanine hydroxylase, the enzyme deficient in PKU) & DHPR (di-hydro-folate reductase, also involved in PKU), as well as contributing to tests that are now applied worldwide to all newborns being screened for this disease.
• Levy is an internationally known for his pioneering work in newborn screening for metabolic diseases as well as having established much of current understanding of major biochemical genetic disorders such as homocystinuria, phenylketonuria (PKU), and maternal PKU.
• In September 2021, APR launched a chewable tablet for the treatment of Phenylketonuria, called PKU GOLIKE KRUNCH, in Germany and Italy.

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