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Comment
. 2011 Nov;34(11):e170; author's reply e171.
doi: 10.2337/dc11-1440.

Comment on: Wilson et al. Persistence of individual variations in glycated hemoglobin: analysis of data from the juvenile diabetes research foundation continuous glucose monitoring randomized trial. Diabetes Care 2011;34:1315-1317

Comment

Comment on: Wilson et al. Persistence of individual variations in glycated hemoglobin: analysis of data from the juvenile diabetes research foundation continuous glucose monitoring randomized trial. Diabetes Care 2011;34:1315-1317

James M Hempe et al. Diabetes Care. 2011 Nov.
No abstract available

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Comment on

References

    1. Wilson DM, Xing D, Cheng J, et al. ; Juvenile Diabetes Research Foundation Continuous Glucose Monitoring Study Group Persistence of individual variations in glycated hemoglobin: analysis of data from the Juvenile Diabetes Research Foundation Continuous Glucose Monitoring Randomized Trial. Diabetes Care 2011;34:1315–1317 - PMC - PubMed
    1. Wilson DM, Kollman C, Xing D, et al. ; Diabetes Research in Children Network (DirecNet) Study Group Relationship of A1C to glucose concentrations in children with type 1 diabetes: assessments by high-frequency glucose determinations by sensors. Diabetes Care 2008;31:381–385 - PMC - PubMed
    1. Hempe JM, Gomez R, McCarter RJ, Jr, Chalew SA. High and low hemoglobin glycation phenotypes in type 1 diabetes: a challenge for interpretation of glycemic control. J Diabetes Complications 2002;16:313–320 - PubMed
    1. McCarter RJ, Hempe JM, Gomez R, Chalew SA. Biological variation in HbA1c predicts risk of retinopathy and nephropathy in type 1 diabetes. Diabetes Care 2004;27:1259–1264 - PubMed
    1. Cohen RM, Holmes YR, Chenier TC, Joiner CH. Discordance between HbA1c and fructosamine: evidence for a glycosylation gap and its relation to diabetic nephropathy. Diabetes Care 2003;26:163–167 - PubMed

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