(Phenylketonuria(PKU) ) 臺中榮總全球資訊網Taichung ... | 農藥合法資訊網

苯丙酮尿症，又稱苯酮尿症（英語：Phenylketonuria，縮寫為PKU），是一種遺傳性代謝缺陷，肇因於苯丙胺酸這種胺基酸的代謝能力下降。如果不接受治療，苯 ... Read More

Phenylketonuria (PKU) is an inborn error of metabolism that results in decreased metabolism of the amino acid phenylalanine. ... Untreated, PKU can lead to ... Read More

2021年4月7日 — Phenylketonuria (commonly known as PKU) is an inherited disorder that increases the levels of a substance called phenylalanine in the blood. Read More

苯丙酮尿症(phenylketonuria，PKU)是先天性氨基酸代謝異常的疾病，起源於患者的肝臟缺乏苯丙氨酸羥化酶(phenylalanine hydroxylase，PAH)，以致於無法將 ... Read More

2018年1月27日 — Phenylketonuria (fen-ul-key-toe-NU-ree-uh), also called PKU, is a rare inherited disorder that causes an amino acid called phenylalanine to ... Read More

Phenylketonuria. Phenylketonuria (PKU) is a rare but potentially serious inherited disorder. Our bodies break down the protein in foods ... Read More

由 FJ van Spronsen 著作 · 2021 · 被引用 2 次 — Phenylketonuria (PKU; also known as phenylalanine hydroxylase (PAH, EC 1.14.​16.1) deficiency (OMIM # 261600) and Følling disease) is an ... Read More

Phenylketonuria (PKU) is an inborn error of metabolism that is detectable during the first days of life via routine newborn screening. PKU is characterized by ... Read More

2018年11月5日 — 苯酮尿症(Phenylketonuria)俗稱PKU，此病症，是因為人體必需胺基酸中的苯內胺酸，在代謝成酪胺酸的. 代謝路徑之中發生問題，導致苯丙胺酸 ... Read More