Inherited, non-spherocytic haemolysis due to deficiency of glucose-6-phosphate dehydrogenase

Scandinavian Journal of Clinical and Laboratory Investigation

Volumn 67, Issue 1, 2007, Pages 105-111

  Ronquist, G ^a   Theodorsson, E ^b  

^a UPPSALA UNIVERSITY HOSPITAL   (Sweden)

^b LINKÖPING UNIVERSITY HOSPITAL   (Sweden)

Author keywords

G6PD; Glucose 6 phosphate dehydrogenase deficiency; Haemolysis

Indexed keywords

GLUCOSE 6 PHOSPHATE DEHYDROGENASE; GLUTATHIONE; HEMOGLOBIN; NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE;

CLINICAL FEATURE; CYTOPLASM; ENZYME DEFICIENCY; ERYTHROCYTE; FAMILY STUDY; FAVISM; FLUORESCENCE ANALYSIS; GENETIC ANALYSIS; HEINZ BODY; HEMOLYSIS; HEMOLYTIC ANEMIA; HUMAN; LABORATORY DIAGNOSIS; MASS SCREENING; OXIDATION; OXIDATIVE STRESS; POLYMERASE CHAIN REACTION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; REVIEW; SPECTROPHOTOMETRY;

ANEMIA, HEMOLYTIC; GLUCOSEPHOSPHATE DEHYDROGENASE; GLUCOSEPHOSPHATE DEHYDROGENASE DEFICIENCY; HEINZ BODIES; HEMOLYSIS; HUMANS; OXIDATIVE STRESS;

EID: 33846942306     PISSN: 00365513     EISSN: 15027686     Source Type: Journal    
DOI: 10.1080/00365510601047910     Document Type: Review

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