-
1
-
-
84871995815
-
Standards of medical care in diabetes: 2013
-
American Diabetes Association
-
American Diabetes Association. Standards of medical care in diabetes: 2013. Diabetes Care. 2013;36(suppl 1):S11-S66.
-
(2013)
Diabetes Care
, vol.36
, Issue.SUPPL. 1
-
-
-
2
-
-
41449083279
-
Targeting HbA1c: Standardization and clinical laboratory measurement
-
Molinaro RJ. Targeting HbA1c: standardization and clinical laboratory measurement. MLO Med Lab Obs. 2008;40:10-19.
-
(2008)
MLO Med Lab Obs
, vol.40
, pp. 10-19
-
-
Molinaro, R.J.1
-
3
-
-
0027370108
-
The effect of intensive treatment of diabetes on the development and progression of long-term complications in insulin-dependent diabetes mellitus
-
The Diabetes Control and Complications Trial Research Group
-
The Diabetes Control and Complications Trial Research Group. The effect of intensive treatment of diabetes on the development and progression of long-term complications in insulin-dependent diabetes mellitus. N Engl J Med. 1993;329:977-986.
-
(1993)
N Engl J Med
, vol.329
, pp. 977-986
-
-
-
4
-
-
0032511583
-
Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33)
-
UK Prospective Diabetes Study (UKPDS) Group
-
UK Prospective Diabetes Study (UKPDS) Group. Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33). Lancet. 1998;352:837-853.
-
(1998)
Lancet
, vol.352
, pp. 837-853
-
-
-
5
-
-
48149095259
-
Translating the A1C assay into estimated average glucose values
-
Nathan DM, Kuenen J, Borg R, et al. Translating the A1C assay into estimated average glucose values. Diabetes Care. 2008;31:1473-1478.
-
(2008)
Diabetes Care
, vol.31
, pp. 1473-1478
-
-
Nathan, D.M.1
Kuenen, J.2
Borg, R.3
-
6
-
-
84884266495
-
-
Available at: Accessed November 11, 2013
-
NGSP. HbA1c and estimated average glucose (eAG). Available at: www.ngsp.org/A1ceAG.asp. Accessed November 11, 2013.
-
HbA1c and Estimated Average Glucose (EAG)
-
-
-
7
-
-
84892705157
-
1c values when using assays incapable of detecting hemoglobin variants
-
1c values when using assays incapable of detecting hemoglobin variants. Arch Pathol Lab Med. 2013;137:1788-1791.
-
(2013)
Arch Pathol Lab Med
, vol.137
, pp. 1788-1791
-
-
Rhea, J.M.1
Koch, D.2
Ritchie, J.3
-
8
-
-
84876571521
-
-
Available at Accessed December 2, 2013
-
Centers for Disease Control and Prevention. Sickle cell disease (SCD): data and statistics. Available at http://www.cdc.gov/ncbddd/sicklecell/data. html. Accessed December 2, 2013.
-
Sickle Cell Disease (SCD): Data and Statistics
-
-
-
10
-
-
0014470481
-
32-DFP and 51-Cr for measurement of red cell life span in abnormal hemoglobin syndromes
-
McCurdy PR. 32-DFP and 51-Cr for measurement of red cell life span in abnormal hemoglobin syndromes. Blood. 1969;33:214-224.
-
(1969)
Blood
, vol.33
, pp. 214-224
-
-
McCurdy, P.R.1
-
11
-
-
84864833855
-
Impact of hemoglobin variants on Hb Alc interpretation: Do we assume too much?
-
Rhea JM, Roberts-Wilson TK, Molinaro RJ. Impact of hemoglobin variants on Hb Alc interpretation: do we assume too much? MLO Med Lab Obs. 2012;44:8-20.
-
(2012)
MLO Med Lab Obs
, vol.44
, pp. 8-20
-
-
Rhea, J.M.1
Roberts-Wilson, T.K.2
Molinaro, R.J.3
-
13
-
-
84861362043
-
Contemporary approaches to treatment of beta-thalassemia intermedia
-
Taher AT, Musallam KM, Karimi M, et al. Contemporary approaches to treatment of beta-thalassemia intermedia. Blood Rev. 2012;26(suppl 1):S24-S27.
-
(2012)
Blood Rev
, vol.26
, Issue.SUPPL. 1
-
-
Taher, A.T.1
Musallam, K.M.2
Karimi, M.3
-
14
-
-
0025559637
-
Differences in the pathophysiology of hemolysis of α- and β-thalassemic red blood cells
-
Shinar E, Rachmilewitz EA. Differences in the pathophysiology of hemolysis of α- and β-thalassemic red blood cells. Ann N Y Acad Sci. 1990;612:118-126.
-
(1990)
Ann N Y Acad Sci
, vol.612
, pp. 118-126
-
-
Shinar, E.1
Rachmilewitz, E.A.2
-
15
-
-
0031035526
-
A mild form of Hb S-beta-thalassemia syndrome is assured in Sicilian patients by beta+mutant IVS-I nt 6(T→C)
-
Mirabile E, Testa R, Samperi P, et al. A mild form of Hb S-beta-thalassemia syndrome is assured in Sicilian patients by beta+mutant IVS-I nt 6(T→C). Eur J Haematol. 1997;58:67-69. (Pubitemid 27047135)
-
(1997)
European Journal of Haematology
, vol.58
, Issue.1
, pp. 67-69
-
-
Mirabile, E.1
Testa, R.2
Samperi, P.3
Consalvo, C.4
Romano, V.5
Schiliro, G.6
-
16
-
-
84904512112
-
-
Available at Accessed November 11, 2013
-
Centers for Disease Control and Prevention. Health of black or African American non-Hispanic population. Available at http://www.cdc.gov/nchs/fastats/ black-health.htm. Accessed November 11, 2013.
-
Health of Black or African American Non-Hispanic Population
-
-
-
17
-
-
33846446500
-
-
Available at Accessed November 11, 2013
-
Clinical key. Thalassemia. Available at https://www.clinicalkey.com/ topics/hematology/thalassemia.html. Accessed November 11, 2013.
-
Thalassemia
-
-
-
18
-
-
70349795485
-
Falsely elevated hemoglobin A1c due to S-beta+-thalassemia interference in Bio-Rad Variant II Turbo HbA1c assay
-
Zhu Y, Williams LM. Falsely elevated hemoglobin A1c due to S-beta+-thalassemia interference in Bio-Rad Variant II Turbo HbA1c assay. Clin Chim Acta. 2009;409:18-20.
-
(2009)
Clin Chim Acta
, vol.409
, pp. 18-20
-
-
Zhu, Y.1
Williams, L.M.2
-
19
-
-
48249157956
-
Effects of hemoglobin C and S traits on the results of 14 commercial glycated hemoglobin assays
-
Mongia SK, Little RR, Rohlfing CL, et al. Effects of hemoglobin C and S traits on the results of 14 commercial glycated hemoglobin assays. Am J Clin Pathol. 2008;130:136-140.
-
(2008)
Am J Clin Pathol
, vol.130
, pp. 136-140
-
-
Mongia, S.K.1
Little, R.R.2
Rohlfing, C.L.3
-
20
-
-
0031910842
-
Evaluation and interference study of hemoglobin A(1c) measured by turbidimetric inhibition immunoassay
-
Chang J, Hoke C, Ettinger B, et al. Evaluation and interference study of hemoglobin A1c measured by turbidimetric inhibition immunoassay. Am J Clin Pathol. 1998;109:274-278. (Pubitemid 28110568)
-
(1998)
American Journal of Clinical Pathology
, vol.109
, Issue.3
, pp. 274-278
-
-
Chang, J.1
Hoke, C.2
Ettinger, B.3
Penerian, G.4
-
21
-
-
84862796815
-
Effects of hemoglobin C, D, E, and S traits on measurements of HbA1c by six methods
-
Lin CN, Emery TJ, Little RR, et al. Effects of hemoglobin C, D, E, and S traits on measurements of HbA1c by six methods. Clin Chim Acta. 2012;413:819-821.
-
(2012)
Clin Chim Acta
, vol.413
, pp. 819-821
-
-
Lin, C.N.1
Emery, T.J.2
Little, R.R.3
-
22
-
-
0021931068
-
2 [X-N-Met-1(NA1) Val→Glu]: A new β-chain abnormal hemoglobin observed in a Qatari female
-
2 [X-N-Met-1(NA1)Val→Glu]: a new β-chain abnormal hemoglobin observed in a Qatari female. Biochim Biophys Acta. 1985;831:257-260.
-
(1985)
Biochim Biophys Acta
, vol.831
, pp. 257-260
-
-
Kamel, K.1
El-Najjar, A.2
Webber, B.B.3
-
23
-
-
16244370760
-
Effects of hemoglobin C and S traits on glycohemoglobin measurements by eleven methods
-
DOI 10.1373/clinchem.2004.047142
-
Roberts WL, Safar-Pour S, De BK, et al. Effects of hemoglobin C and S traits on glycohemoglobin measurements by eleven methods. Clin Chem. 2005;51:776-778. (Pubitemid 40463930)
-
(2005)
Clinical Chemistry
, vol.51
, Issue.4
, pp. 776-778
-
-
Roberts, W.L.1
Safar-Pour, S.2
De, B.K.3
Rohlfing, C.L.4
Weykamp, C.W.5
Little, R.R.6
-
26
-
-
77955877141
-
A review of variant hemoglobins interfering with hemoglobin A1c measurement
-
Little RR, Roberts WL. A review of variant hemoglobins interfering with hemoglobin A1c measurement. J Diabetes Sci Technol. 2009;3:446-451.
-
(2009)
J Diabetes Sci Technol
, vol.3
, pp. 446-451
-
-
Little, R.R.1
Roberts, W.L.2
-
28
-
-
36248957657
-
Hb Niigata [beta1(Na1)Val→Leu] in a Romanian individual resulting from another nucleotide substitution than that found in the Japanese
-
DOI 10.1080/03630260701587885, PII 783781324
-
Moradkhani K, Henthom J, Riou J, et al. Hb Niigata [β1(NA1) Val→Leu] in a Romanian individual resulting from another nucleotide substitution than that found in the Japanese. Hemoglobin. 2007;31:477-482. (Pubitemid 350125640)
-
(2007)
Hemoglobin
, vol.31
, Issue.4
, pp. 477-482
-
-
Moradkhani, K.1
Henthorn, J.2
Riou, J.3
Phelan, L.4
Prehu, C.5
Wajcman, H.6
-
29
-
-
0022999118
-
Hemoglobin South Florida: New variant with normal electrophoretic pattern mistaken for glycosylated hemoglobin
-
Shah SC, Malone JI, Boissel JP, et al. Hemoglobin South Florida: new variant with normal electrophoretic pattern mistaken for glycosylated hemoglobin. Diabetes. 1986;35:1073-1076. (Pubitemid 17176947)
-
(1986)
Diabetes
, vol.35
, Issue.10
, pp. 1073-1076
-
-
Shah, S.C.1
Malone, J.I.2
Boissel, J.-P.3
Kasper, T.J.4
-
30
-
-
75549089900
-
Interaction of Hb South Florida (codon 1; GTG→ATG) and HbE, with β-thalassemia (IVS1-1; G→A): Expression of different clinical phenotypes
-
Tan JA, Tan KL, Omar KZ, et al. Interaction of Hb South Florida (codon 1; GTG→ATG) and HbE, with β-thalassemia (IVS1-1; G→A): expression of different clinical phenotypes. Eur J Pediatr. 2009;168:1049-1054.
-
(2009)
Eur J Pediatr
, vol.168
, pp. 1049-1054
-
-
Tan, J.A.1
Tan, K.L.2
Omar, K.Z.3
-
31
-
-
0033694157
-
Hb Watford [beta1(NA1)Val→Gly]: A new, clinically silent hemoglobin variant in linkage with a new neutral mutation
-
Fisher C, Hanslip J, Green BN, et al. Hb Watford [beta1(NA1)Val→Gly] : a new, clinically silent hemoglobin variant in linkage with a new neutral mutation. Hemoglobin. 2000;24:347-353.
-
(2000)
Hemoglobin
, vol.24
, pp. 347-353
-
-
Fisher, C.1
Hanslip, J.2
Green, B.N.3
-
32
-
-
0025041241
-
Hb Fukuoka [beta2(Na2)His→Tyr]: A new mutation at the 2,3-diphosphoglycerate binding site
-
Harano T, Harano K, Ueda S, et al. Hb Fukuoka [beta 2(NA2)His→Tyr]: a new mutation at the 2.3-diphosphoglycerate binding site. Hemoglobin. 1990;14:199-205. (Pubitemid 20256350)
-
(1990)
Hemoglobin
, vol.14
, Issue.2
, pp. 199-205
-
-
Harano, T.1
Harano, K.2
Ueda, S.3
Imai, K.4
Ohkuma, A.5
Koya, Y.6
Takahashi, H.7
-
33
-
-
77950476777
-
Hb Valletta [β-87(F3) Thr→Pro] and Hb Marseille/Long Island [β-2(NA2) His→Pro: (-1)Met-(+1)Val-(+2)Pro-Leu], in a unique compound heterozygote with a normal hemoglobin phenotype
-
Galdies R, Cassar W, Pizzuto M, et al. Hb Valletta [β-87(F3) Thr→Pro] and Hb Marseille/Long Island [β-2(NA2) His→Pro: (-1)Met-(+1)Val-(+2)Pro-Leu], in a unique compound heterozygote with a normal hemoglobin phenotype. Hemoglobin. 2010;34:169-174.
-
(2010)
Hemoglobin
, vol.34
, pp. 169-174
-
-
Galdies, R.1
Cassar, W.2
Pizzuto, M.3
-
34
-
-
0028950238
-
Haemoglobin Graz, a novel haemoglobin variant
-
Schnedl WJ, Reisinger EC, Pieber TR, et al. Haemoglobin Graz, a novel haemoglobin variant. Diabetologia. 1995;38:122.
-
(1995)
Diabetologia
, vol.38
, pp. 122
-
-
Schnedl, W.J.1
Reisinger, E.C.2
Pieber, T.R.3
-
35
-
-
0015306915
-
Hemoglobin Deer Lodge: 2 2 2 His leads to Arg
-
Labossiere A, Vella F, Hiebert J, et al. Hemoglobin Deer Lodge: 2 2 2 His leads to Arg. Clin Biochem. 1972;5:46-50.
-
(1972)
Clin Biochem
, vol.5
, pp. 46-50
-
-
Labossiere, A.1
Vella, F.2
Hiebert, J.3
-
36
-
-
0020966186
-
Hemoglobin Okayama [beta2 (NA 2) His → Gln]: A new 'silent' hemoglobin variant with substituted amino acid residue at the 2,3-diphosphoglycerate binding site
-
DOI 10.1016/0014-5793(83)80239-7
-
Harano T, Harano K, Shibata S, et al. Hemoglobin Okayama [beta 2 (NA 2) His replaced by Gln]: a new 'silent' hemoglobin variant with substituted amino acid residue at the 2,3-diphosphoglycerate binding site. FEBS Lett. 1983;156:20-22. (Pubitemid 13058516)
-
(1983)
FEBS Letters
, vol.156
, Issue.1
, pp. 20-22
-
-
Harano, T.1
Harano, K.2
Shibata, S.3
-
37
-
-
0043173818
-
Two cases in which an abnormal hemoglobin (Hb Kamakura) was identified on the basis of an abnormally low glycohemoglobin levels
-
Saisho Y, Saitoh F, Tabata M, et al. Two cases in which an abnormal hemoglobin (Hb Kamakura) was identified on the basis of an abnormally low glycohemoglobin levels. Intern Med. 2003;42:595-598. (Pubitemid 36926837)
-
(2003)
Internal Medicine
, vol.42
, Issue.7
, pp. 595-598
-
-
Saisho, Y.1
Saitoh, F.2
Tabata, M.3
Imafuku, T.4
Ogihara, T.5
Issiki, I.6
Hattori, Y.7
Yamashiro, Y.8
-
38
-
-
33646124964
-
2 4(A1)Thr→Asn), a new electrophoretically silent variant, by mass spectrometry and molecular modeling studies
-
2 4(A1)Thr→Asn), a new electrophoretically silent variant, by mass spectrometry and molecular modeling studies. J Chromatogr A. 2006;1115:118-124.
-
(2006)
J Chromatogr A
, vol.1115
, pp. 118-124
-
-
Bisse, E.1
Zorn, N.2
Boussert, S.3
-
39
-
-
0037232997
-
25(A2) Pro→Ala], an electrophoretically silent variant with impaired glycation
-
25(A2)Pro→Ala], an electrophoretically silent variant with impaired glycation. Clin Chem. 2003;49:137-143.
-
(2003)
Clin Chem
, vol.49
, pp. 137-143
-
-
Bisse, E.1
Schauber, C.2
Zorn, N.3
-
40
-
-
0028141615
-
A new beta chain variant, Hb Tyne [beta 5(A2)Pro→Ser]
-
Langdown JV, Williamson D, Beresford CH, et al. A new beta chain variant, Hb Tyne [beta 5(A2)Pro→Ser]. Hemogbbin. 1994;18:333-336.
-
(1994)
Hemogbbin
, vol.18
, pp. 333-336
-
-
Langdown, J.V.1
Williamson, D.2
Beresford, C.H.3
-
41
-
-
0021715010
-
Haemoglobin Warwickshire (beta5 [A2] Pro → Arg). A possible 'fine tuning' of 2,3-DPG affinity by beta5 Pro
-
DOI 10.1016/0014-5793(84)81190-4
-
Wilson CI, Cave RJ, Lehmann H, et al. Haemoglobin Warwickshire (β5 [A2] Pro→Arg): a possible 'fine tuning' of 2.3-DPG affinity by β5 Pro. FEBS Lett. 1984;176:331-333. (Pubitemid 15208270)
-
(1984)
FEBS Letters
, vol.176
, Issue.2
, pp. 331-333
-
-
Wilson, C.I.D.1
Cave, R.J.2
Lehmann, H.3
-
42
-
-
79952913254
-
Two new hemoglobin variants: Hb Aix-Les-Bains [β5(A2)Pro→Leu; HBB:C.17 C>T] and Hb Dubai [α122(H5)His→Leu (α2); HBA2:C.368 A>T]
-
Joly P, Garcia C, Lacan P, et al. Two new hemoglobin variants: Hb Aix-Les-Bains [β5(A2)Pro→Leu; HBB:c.17 C>T] and Hb Dubai [α122(H5)His→Leu (α2); HBA2:c.368 A>T]. Hemogbbin. 2011;35:147-151.
-
(2011)
Hemogbbin
, vol.35
, pp. 147-151
-
-
Joly, P.1
Garcia, C.2
Lacan, P.3
-
44
-
-
0020402730
-
Hemoglobin machida [beta6 (A3) Glu → Gln], a new abnormal hemoglobin discovered in a Japanese family: Structure, function and biosynthesis
-
Harano T, Harano K, Ueda S, et al. Hemoglobin Machida [beta 6 (A3) Glu replaced by Gln]: a new abnormal hemoglobin discovered in a Japanese family: structure, function and biosynthesis. Hemoglobin. 1982;6:531-535. (Pubitemid 13242343)
-
(1982)
Hemoglobin
, vol.6
, Issue.5
, pp. 531-535
-
-
Harano, T.1
Harano, K.2
Ueda, S.3
-
45
-
-
0015273346
-
Haemoglobin Siriraj, -7 (A4) Glu leads to Lys, in a Chinese subject in Taiwan
-
Blackwell RQ, Liu CS, Wang CL. Haemoglobin Siriraj, -7 (A4) Glu leads to Lys, in a Chinese subject in Taiwan. Vox Sang. 1972;23:433-438.
-
(1972)
Vox Sang
, vol.23
, pp. 433-438
-
-
Blackwell, R.Q.1
Liu, C.S.2
Wang, C.L.3
-
46
-
-
84865533281
-
A novel β-globin gene mutation HBB.C.22 G>C produces a hemoglobin variant (Hb Vellore) mimicking HbS in HPLC
-
Edison ES, Sathya M, Rajkumar SV, et al. A novel β-globin gene mutation HBB.c.22 G>C produces a hemoglobin variant (Hb Vellore) mimicking HbS in HPLC. Int J Lab Hematol. 2012;34:556-558.
-
(2012)
Int J Lab Hematol
, vol.34
, pp. 556-558
-
-
Edison, E.S.1
Sathya, M.2
Rajkumar, S.V.3
-
48
-
-
0024887555
-
28(A5)Lys→Glu]: A new fast-moving variant with normal stability aqnd oxygen affinity
-
Lena-Russo D, Orsini A, Vovan L, et al. Hb N-Timone [alpha 2 beta 2(8)(A5)Lys→Glu]: a new fast-moving variant with normal stability and oxygen affinity. Hemogbbin. 1989;13:743-747. (Pubitemid 20095930)
-
(1989)
Hemoglobin
, vol.13
, Issue.7-8
, pp. 743-747
-
-
Lena-Russo, D.1
Orsini, A.2
Vovan, L.3
Bardakdjian-Michau, J.4
Lacombe, C.5
Blouquit, Y.6
Craescu, C.T.7
Galacteros, F.8
-
49
-
-
0020539419
-
Hemoglobin Rio Grande [beta8 (A5) Lys→Thr]: A new variant found in a Mexican-American family
-
Moo-Penn WF, Johnson MH, McGuffey JE, et al. Hemoglobin Rio Grande [beta 8 (A5) Lys leads to Thr] a new variant found in a Mexican-American family. Hemoglobin. 1983;7:91-95. (Pubitemid 13113674)
-
(1983)
Hemoglobin
, vol.7
, Issue.1
, pp. 91-95
-
-
Moo, P.W.F.1
Johnson, M.H.2
McGuffey, J.E.3
-
50
-
-
0032820044
-
A novel Indian β-thalassemia mutation: Hb Lucknow [beta8(A5)Lys→Arg]
-
Agarwal S, Hattori Y, Gupta UR, et al. A novel Indian β-thalassemia mutation: Hb Lucknow [beta8(A5)Lys→Arg]]. Hemoglobin. 1999;23:263-265.
-
(1999)
Hemoglobin
, vol.23
, pp. 263-265
-
-
Agarwal, S.1
Hattori, Y.2
Gupta, U.R.3
-
51
-
-
0028826568
-
Hb Nakano [β8Lys→Met]: A new β chain variant found in a Japanese woman
-
Harano K, Harano T, Koide G, et al. Hb Nakano [β8(Lys→Met]: a new β chain variant found in a Japanese woman. Hemoglobin. 1995;19:397-401.
-
(1995)
Hemoglobin
, vol.19
, pp. 397-401
-
-
Harano, K.1
Harano, T.2
Koide, G.3
-
52
-
-
0035543927
-
Hb Limassol [beta8(A5)Lys → Asn]: A new hemoglobin variant
-
DOI 10.1081/HEM-100107880
-
Kyrri A, Felekis X, Kalogerou E, et al. Hb Limassol [beta8(A5) Lys→Asn]: a new hemoglobin variant. Hemoglobin. 2001;25:421-424. (Pubitemid 34037657)
-
(2001)
Hemoglobin
, vol.25
, Issue.4
, pp. 421-424
-
-
Kyrri, A.1
Felekis, X.2
Kalogerou, E.3
Christopoulos, G.4
Makariou, C.5
Loizidou, D.6
Kleanthous, M.7
-
53
-
-
14644431065
-
Two new hemoglobin variants: Hb Brem-sur-Mer [beta9(A6)Ser→Tyr] and Hb Passy [alpha81(F2)Ser→Pro (alpha2)]
-
Lacan P, Moreau M, Becchi M, et al. Two new hemoglobin variants: Hb Brem-sur-Mer [beta9(A6)Ser→Tyr] and Hb Passy [alpha81(F2)Ser→Pro (alpha2)]. Hemoglobin. 2005;29:69-75.
-
(2005)
Hemoglobin
, vol.29
, pp. 69-75
-
-
Lacan, P.1
Moreau, M.2
Becchi, M.3
-
54
-
-
84866406030
-
Heterozygosis for hemoglobin Porto Alegre identified by a combination of laboratory diagnostic methodologies
-
Cataldo MJ, Bonini-Domingos AC, Bonini-Domingos CR. Heterozygosis for hemoglobin Porto Alegre identified by a combination of laboratory diagnostic methodologies. Rev Bras Hematol Hemoter. 2012;34:305-306.
-
(2012)
Rev Bras Hematol Hemoter
, vol.34
, pp. 305-306
-
-
Cataldo, M.J.1
Bonini-Domingos, A.C.2
Bonini-Domingos, C.R.3
-
55
-
-
60749109557
-
1c by routine cation exchange high performance liquid chromatography
-
1c by routine cation exchange high performance liquid chromatography. Hemoglobin. 2009;33:45-50.
-
(2009)
Hemoglobin
, vol.33
, pp. 45-50
-
-
Williams, J.P.1
Jackson, H.2
Green, B.N.3
-
56
-
-
0022617768
-
The survey of abnormal hemoglobins in the Kobe District: HB G-Coushatta [beta22(B4)GLU→ALA], HB Ankara [beta10(A7)ALA→ASP], HB Handa [alpha90(FG2)LYS→MET], and HB J-Habana [alpha71(E20)ALA→GLU]
-
Hidaka K, Iuchi I, Shimasaki S, et al. The survey of abnormal hemoglobins in the Kobe district: Hb G-Coushatta [beta 22(B4)Glu→Ala], Hb Ankara (beta 10(A7)Ala→Asp], Hb Handa [alpha 90(FG2)Lys→Met], and Hb J-Habana [alpha 71(E20)Ala→Glu]. Hemoglobin. 1986;10:65-72. (Pubitemid 16131319)
-
(1986)
Hemoglobin
, vol.10
, Issue.1
, pp. 65-72
-
-
Hidaka, K.1
Iuchi, I.2
Shimasaki, S.3
-
57
-
-
0028064526
-
Hb Washtenaw [beta11(A8)Val->Phe]: An electrophoretically silent, unstable, low oxygen affinity variant associated with anemia and chronic cyanosis
-
Krishnan K, Martinez F, Wille RT, et al. Hb Washtenaw [beta 11(A8)Val→Phe]: an electrophoretically silent, unstable, low oxygen affinity variant associated with anemia and chronic cyanosis. Hemoglobin. 1994;18:285-295. (Pubitemid 24282003)
-
(1994)
Hemoglobin
, vol.18
, Issue.4-5
, pp. 285-295
-
-
Krishnan, K.1
Martinez, F.2
Wille, R.T.3
Jones, R.T.4
Shih, D.T.5
Head, C.6
Fairbanks, V.F.7
Dabich, L.8
-
58
-
-
0024421142
-
Hemoglobin Windsor or beta11 (A8)Val→Asp: A new unstable beta-chain hemoglobin variant producing a hemolytic anemia
-
Gilbert AT, Fleming PJ, Sumner DR, et al. Hemoglobin Windsor or beta 11 (A8)Val→Asp: a new unstable beta-chain hemoglobin variant producing a hemolytic anemia. Hemoglobin. 1989;13:437-453. (Pubitemid 19256521)
-
(1989)
Hemoglobin
, vol.13
, Issue.5
, pp. 437-453
-
-
Gilbert, A.T.1
Fleming, P.J.2
Sumner, D.R.3
Hughes, W.G.4
Holland, R.A.B.5
Tibben, E.A.6
-
59
-
-
0019806564
-
Structural studies of a new hemoglobin: HbJ Lens, beta13(A10) Ala → Asp
-
DOI 10.1016/0014-5793(81)81234-3
-
Djoumessi S, Rousseaux J, Dautrevaux M. Structural studies of a new hemoglobin: HbJ lens, beta 13 (A10) Ala leads to Asp. FEBS Lett. 1981;136:145-147. (Pubitemid 12133492)
-
(1981)
FEBS Letters
, vol.136
, Issue.1
, pp. 145-147
-
-
Djoumessi, S.1
Rousseaux, J.2
Dautrevaux, M.3
-
60
-
-
0035134867
-
Effects of hemoglobin variants and chemically modified derivatives on assays for glycohemoglobin
-
Bry L, Chen PC, Sacks DB. Effects of hemoglobin variants and chemically modified derivatives on assays for glycohemoglobin. Clin Chem. 2001;47:153-163. (Pubitemid 32142912)
-
(2001)
Clinical Chemistry
, vol.47
, Issue.2
, pp. 153-163
-
-
Bry, L.1
Chen, P.C.2
Sacks, D.B.3
-
63
-
-
79959808379
-
HbA1c does not always estimate average glucose
-
Behan KJ, Merschen J. HbA1c does not always estimate average glucose. Clin Lab Sci. 2011;24:71-77.
-
(2011)
Clin Lab Sci
, vol.24
, pp. 71-77
-
-
Behan, K.J.1
Merschen, J.2
|