Glucose-6-phosphate dehydrogenase deficiency and pyruvate kinase deficiency;Hereditäre enzymdefekte der erythrozyten: Glukose-6- phosphatdehydrogenase-mangel und pyruvatkinase-mangel

Therapeutische Umschau

Volumn 63, Issue 1, 2006, Pages 47-56

  Ittig Boo Sedano, I ^a   Rothlisberger B ^a   Huber, Andreas R ^a  

^a CANTONAL HOSPITAL AARAU   (Switzerland)

Author keywords

[No Author keywords available]

Indexed keywords

CYANOCOBALAMIN; FOLIC ACID; GLUCOSE 6 PHOSPHATE DEHYDROGENASE; IRON; PYRUVATE KINASE;

AUTOSOMAL RECESSIVE DISORDER; CLINICAL FEATURE; CYANOCOBALAMIN DEFICIENCY; DIAGNOSTIC ACCURACY; DIFFERENTIAL DIAGNOSIS; ENZYME ACTIVITY; ENZYME DEFICIENCY; FOLIC ACID DEFICIENCY; GENETIC COUNSELING; GENETIC PREDISPOSITION; GLUCOSE 6 PHOSPHATE DEHYDROGENASE DEFICIENCY; HEMOLYSIS; HEMOLYTIC ANEMIA; HUMAN; IRON DEFICIENCY; MEDICAL DECISION MAKING; NEWBORN JAUNDICE; OXIDATIVE STRESS; PATHOGENESIS; PYRUVATE KINASE DEFICIENCY; REVIEW; VICIA FABA; X CHROMOSOMAL INHERITANCE;

ANEMIA, HEMOLYTIC, CONGENITAL; ERYTHROCYTES; GENETIC PREDISPOSITION TO DISEASE; GLUCOSEPHOSPHATE DEHYDROGENASE DEFICIENCY; HEMATOLOGIC TESTS; HUMANS; PHYSICIAN'S PRACTICE PATTERNS; PRACTICE GUIDELINES; PYRUVATE KINASE;

EID: 30744434655     PISSN: 00405930     EISSN: None     Source Type: Journal    
DOI: 10.1024/0040-5930.63.1.47     Document Type: Review

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