Interference of hemoglobin D in hemoglobin A (2) measurement by cation-exchange HPLC
Cotton, F.; Gulbis, B.; Hansen, V.; Vertongen, F.
Clinical Chemistry 45(8 Part 1): 1317-1318
1999
ISSN/ISBN: 0009-9147 PMID: 10430811 Document Number: 504537
Document emailed within 1 workday
Related Documents
Turpeinen, U.; Sipilä, I.; Anttila, P.; Karjalainen, U.; Kuronen, B.; Kalkkinen, N.; Ahola, T.; Stenman, U.H. 1995: Two alpha-chain hemoglobin variants, Hb Broussais and Hb Cemenelum, characterized by cation-exchange HPLC, isoelectric focusing, and peptide sequencing Clinical Chemistry 41(4): 532-536Kruiswijk, T.; Diaz, D.P.; Holtkamp, H.C. 1981: Interference of hemoglobin H in the column-chromatographic assay of glycosylated hemoglobin a Clinical Chemistry 27(4): 641-642
Sanguansermsri, T.; Thanaratanakorn, P.; Steger, H.F.; Tongsong, T.; Sirivatanapa, P.; Wanapirak, C.; Sirichotiyakul, S.; Chanprapas, P.; Flatz, G. 2001: Prenatal diagnosis of hemoglobin Bart's hydrops fetalis by HPLC analysis of hemoglobin in fetal blood samples Southeast Asian Journal of Tropical Medicine and Public Health 32(1): 180-185
Nishiyama, T.; Hanaoka, K. 1997: A simple, lightweight device for measurement of hemoglobin; the HemoCue Blood Hemoglobin Test Masui. Japanese Journal of Anesthesiology 46(2): 284-285
Piomelli, S.; Brickman, A.; Carlos, E. 1976: Rapid diagnosis of iron deficiency by measurement of free erythrocyte porphyrins and hemoglobin: the FEP/hemoglobin ratio Pediatrics 57(1): 136-141
Sumida, I. 1975: Studies of abnormal hemoglobins in western Japan. Frequency of visible hemoglobin variants, and chemical characterization of hemoglobin Sawara (alpha 26Alabeta2) and hemoglobin Mugino (Hb L Ferrara; alpha247Glybeta2) Jinrui Idengaku Zasshi. Japanese Journal of Human Genetics 19(4): 343-363
Togami, D.W.; Poulsen, B.J.; Batalao, C.W.; Rolls, W.A. 1991: Separation of carbohydrates and carbohydrate derivatives by HPLC with cation-exchange columns at high pH Biotechniques 10(5): 650-655
Aleyassine, H. 1979: Low proportions of glycosylated hemoglobin associated with hemoglobin S and hemoglobin C Clinical Chemistry 25(8): 1484-1486
Blank, D.W.; Kroll, M.H.; Ruddel, M.E.; Elin, R.J. 1985: Hemoglobin interference from in vivo hemolysis Clinical Chemistry 31(9): 1566-1569
Salathé, C.; Pugin, P. 2001: Extramedullary hematopoiesis presenting as a chloroma in a patient known for abnormal hemoglobin (Geneva hemoglobin) Revue Medicale de la Suisse Romande 121(8): 585-587
Mcgarrity, M.J.; Er, S.S.; Hsia, J.C. 1987: Hemoglobin-based blood substitutes: characterization of five pyridoxal 5'-phosphate derivatives of hemoglobin Journal of Chromatography 419: 37-50
Nathan, D.M. 1981: Labile glycosylated hemoglobin contributes to hemoglobin A1 as measured by liquid chromatography or electrophoresis Clinical Chemistry 27(7): 1261-1263
Grimaldi, A.; Massin, P.; Bosquet, F.; Thuillier-Juteau, Y.; Delattre, J.; Galli, A. 1987: Overevaluation of glycosylated hemoglobin in a diabetic with "slight" rise of fetal hemoglobin Presse Medicale 16(9): 445
Rotz, S.; Arty, G.; Dall'Amico, R.; De Zen, L.; Zanolli, F.; Bodas, P. 2013: Prevalence of sickle cell disease, hemoglobin S, and hemoglobin C among Haitian newborns American Journal of Hematology 88(9): 827-828
Shamov, I.A.; Kazieva, K.E.; Tokarev, I.N. 1981: New anomalous structural hemoglobin variant: hemoglobin Dagestan (alpha 60 Lys replaced by Glu) Problemy Gematologii i Perelivaniia Krovi 26(12): 3-6
Villanueva, C.L.; Zavala, C.; Alcayaga, M.P. 1995: False high levels glycosylated hemoglobin in 2 diabetic patients with persistence of fetal hemoglobin Revista Medica de Chile 123(9): 1129-1132
Conri, C.; Sanchez, B.; Hombrados, I.; Moreau, F.; Neuzil, E. 1980: Metabolism of hemoglobin A1. no effect of an acute glucose load on the hemoglobin A1 titer in normal subjects La Nouvelle Presse Medicale 9(37): 2741
Egede, L.E.; Obah, E.; Lorch, T.; Oussova, T. 2000: Spurious elevation of hemoglobin A1c by hereditary persistence of fetal hemoglobin Southern Medical Journal 93(1): 62-64
Kimura, H.; Yamato, S.; Murachi, T. 1976: Different susceptibilities to intracellular proteases of hemoglobin and hemoglobin-haptoglobin complex Physiological Chemistry and Physics 8(2): 101-106
Jones, R.T.; Koler, R.D.; Duerst, M.; Stocklen, Z. 1972: Hemoglobin Casper G8 106 leu leads to pro: further evidence that hemoglobin mutations are not random Advances in Experimental Medicine and Biology 28: 79-98