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Results 1 - 10 of 88 for PHENYLALANINE
  1. Serum phenylalanine screening 
    Serum phenylalanine screening is a blood test to look for signs of the disease phenylketonuria (PKU). The test detects abnormally high levels of an amino acid called phenylalanine.
    https://medlineplus.gov/ency/article/003362.htm - Medical Encyclopedia
  2. PAH gene 
    ... gene provides instructions for making an enzyme called phenylalanine hydroxylase. This enzyme helps process phenylalanine, which is a building block of proteins (amino ...
    https://medlineplus.gov/genetics/gene/pah - Genetics
  3. Sapropterin 
    ... along with a restricted diet to control blood phenylalanine levels in adults and children 1 month of ... have phenylketonuria (PKU; an inborn condition in which phenylalanine may build up in the blood and causes ...
    https://medlineplus.gov/druginfo/meds/a608020.html - Drugs and Supplements
  4. Pegvaliase-pqpz Injection 
    ... along with a specific diet to reduce blood phenylalanine levels in people who have phenylketonuria (PKU; an inborn condition in which phenylalanine may build up in the blood and causes ...
    https://medlineplus.gov/druginfo/meds/a618057.html - Drugs and Supplements
  5. Phenylketonuria (National Library of Medicine)  
    ... you have it, your body can't process phenylalanine (Phe). Phe is an amino acid, a building ...
    https://medlineplus.gov/phenylketonuria.html - Health Topics
  6. Phenylketonuria 
    ... that increases the levels of a substance called phenylalanine in the blood. Phenylalanine is a protein building block (an amino acid) ... some artificial sweeteners. If PKU is not treated, phenylalanine can build up to harmful levels in the ...
    https://medlineplus.gov/genetics/condition/phenylketonuria - Genetics
  7. PCBD1 gene 
    ... body. For example, it works with the enzyme phenylalanine hydroxylase to convert an amino acid called phenylalanine into another amino acid, tyrosine. Tetrahydrobiopterin is also ...
    https://medlineplus.gov/genetics/gene/pcbd1 - Genetics
  8. Sepiapterin reductase deficiency 
    Sepiapterin reductase deficiency is a condition characterized by movement problems, most often a pattern of involuntary, sustained muscle contractions known as dystonia. ...
    https://medlineplus.gov/.../sepiapterin-reductase-deficiency - Genetics
  9. SPR gene 
    The SPR gene provides instructions for making the sepiapterin reductase enzyme. This enzyme is involved in the last of three steps in the production of a ...
    https://medlineplus.gov/genetics/gene/spr - Genetics
  10. Tetrahydrobiopterin deficiency 
    ... levels of several substances in the body, including phenylalanine. Phenylalanine is a building block of proteins (an amino ... and in some artificial sweeteners. High levels of phenylalanine are present from early infancy in people with ...
    https://medlineplus.gov/.../condition/tetrahydrobiopterin-deficiency - Genetics
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