tyrosinemia oor Fins
tyrosinemia
en
(medicine) A metabolic disorder characterized by the presence of excess tyrosine in the blood
Vertalings in die woordeboek Engels - Fins
Tyrosinemia
en
amino acid metabolic disorder that involves impaired break down of the amino acid tyrosine
tyrosiinin aineenvaihduntahäiriö
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Restriction of tyrosine and phenylalanine in the diet should limit the toxicity associated with this type of tyrosinemia (see section
Mr.Irving, joka tienasi tarkastuksia, sir?EMEA0.3 EMEA0.3
Restriction of tyrosine and phenylalanine in the diet should limit toxicity associated with this type of tyrosinemia
Tuen tarkoitusEMEA0.3 EMEA0.3
Treatment with Orfadin should be started and monitored by doctors who are experienced in the treatment of hereditary tyrosinemia type # (HT-#) patients
Koeta kestää, kaveriEMEA0.3 EMEA0.3
The biochemical defect in hereditary tyrosinemia type # (HT-#) is a deficiency of fumarylacetoacetate hydrolase, which is the final enzyme of the tyrosine catabolic pathway
Mikä joukkue teillä on?EMEA0.3 EMEA0.3
Treatment of patients with confirmed diagnosis of hereditary tyrosinemia type # (HT-#) in combination with dietary restriction of tyrosine and phenylalanine
Näin hirvittäviä painajaisia, joissa olitte kuin öljy ja vesi- ja vihasitte toisianne joka hetkiEMEA0.3 EMEA0.3
Orfadin is used to treat hereditary tyrosinemia type # (HT-#), a rare childhood disease
Luen tämän vieläEMEA0.3 EMEA0.3
Orfadin is used for treatment of a disease called hereditary tyrosinemia type I
Tanssimme häissämme.- Ei se ollut tanssimistaEMEA0.3 EMEA0.3
Diagnoselist > Tyrosinemia type 2 - Rarelink.en
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