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Volumn 88, Issue 8, 2009, Pages 815-816
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A rare combination of two inherited disorders in one patient: Pyruvate kinase deficiency and hemochromatosis
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Author keywords
[No Author keywords available]
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Indexed keywords
BILIRUBIN;
DEFEROXAMINE;
FERRITIN;
HEMOGLOBIN;
INSULIN;
ORAL ANTIDIABETIC AGENT;
PYRUVATE KINASE;
TESTOSTERONE;
ADULT;
ARTHRALGIA;
ARTIFICIAL EMBOLISM;
BILIRUBIN BLOOD LEVEL;
CASE REPORT;
CHOLECYSTECTOMY;
CHOLELITHIASIS;
COLIC;
DIABETES MELLITUS;
DIET THERAPY;
ECHOGRAPHY;
ENZYME DEFICIENCY;
FERRITIN BLOOD LEVEL;
FOOT EDEMA;
HEART ARRHYTHMIA;
HEMOCHROMATOSIS;
HEMOGLOBIN BLOOD LEVEL;
HEREDITARY HEMOLYTIC ANEMIA;
HUMAN;
HUMAN TISSUE;
HYPOGONADISM;
IRON OVERLOAD;
JAUNDICE;
LABORATORY TEST;
LAPAROTOMY;
LETTER;
LIVER BIOPSY;
LIVER CELL CARCINOMA;
MALE;
PALLOR;
PHLEBOTOMY;
PRIORITY JOURNAL;
PYRUVATE KINASE DEFICIENCY;
RETICULOCYTE;
SIDEROSIS;
ANEMIA, HEMOLYTIC, CONGENITAL;
HEMOCHROMATOSIS;
HUMANS;
IRON OVERLOAD;
MALE;
MIDDLE AGED;
PHLEBOTOMY;
PYRUVATE KINASE;
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EID: 67649390875
PISSN: 09395555
EISSN: None
Source Type: Journal
DOI: 10.1007/s00277-008-0681-7 Document Type: Letter |
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Times cited : (1)
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References (4)
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