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ALAT
ALT
Alanine aminotransferase
Alanine transaminase
Biotin-dependent carboxylase deficiency
Deficiency
Deficiency of phosphoenolpyruvate carboxykinase
Dehydrogenase
Early-onset multiple carboxylase deficiency
GPT
Glutamic-pyruvic transaminase
Hexokinase deficiency
PK
Pyruvate carboxylase
Pyruvate carboxylase measurement
Pyruvate kinase
Pyruvic acid imbecility
Pyruvic acid oligophrenia
SPGT
Serum alanine aminotransferase
Serum glutamic pyruvic transaminase
Triose-phosphate isomerase deficiency

Vertaling van "pyruvate carboxylase " (Engels → Nederlands) :



Pyruvate carboxylase measurement

bepalen van pyruvaatcarboxylase


Deficiency of:phosphoenolpyruvate carboxykinase | pyruvate:carboxylase | dehydrogenase |

deficiëntie van | fosfo-enolpyruvaatcarboxykinase | deficiëntie van | pyruvaat | carboxylase | deficiëntie van | pyruvaat | dehydrogenase


pyruvic acid imbecility | pyruvic acid oligophrenia

oligophrenia phenylpyruvica | syndroom van Foelling | ziekte van Foelling


alanine aminotransferase | alanine transaminase | glutamic-pyruvic transaminase | serum alanine aminotransferase | serum glutamic pyruvic transaminase | ALAT [Abbr.] | ALT [Abbr.] | GPT [Abbr.] | SPGT [Abbr.]

alanineaminotransferase | glutamaatpyruvaattransaminase | serumglutamaatpyruvaattransaminase | ALAT [Abbr.]


Congenital lactic acidosis is defined by the presence of a metabolic acidosis due to the accumulation of lactic acid in blood. Congenital defects of any one of the multiple enzymatic steps of pyruvate utilization induce accumulation of pyruvate and l

fatale infantiele lactaatacidose gelijktijdig met methylmalonacidurie


Early-onset multiple carboxylase deficiency

meervoudige carboxylasedeficiëntie met vroege aanvang


Biotin-dependent carboxylase deficiency

deficiëntie van biotineafhankelijke carboxylase


Anaemia:haemolytic nonspherocytic (hereditary), type II | hexokinase deficiency | pyruvate kinase [PK] deficiency | triose-phosphate isomerase deficiency

anemie (door) | deficiëntie van | pyruvaatkinase [PK] | anemie (door) | deficiëntie van | triosefosfaatisomerase | anemie (door) | hemolytisch niet-sferocytair (hereditair), type II | anemie (door) | deficiëntie van | hexokinase


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