Diabetic retinopathy in permanent neonatal diabetes due to Kir6.2 gene mutations: the results of a minimum 2-year follow-up after the transfer from insulin to sulphonylurea

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In this Subject: Internal Medicine
By this author: Klupa, T. ;&nbsp; Skupien, J. ;&nbsp; Mirkiewicz-Sieradzka, B. ;&nbsp; Gach, A. ;&nbsp; Noczynska, A. ;&nbsp; Szalecki, M. ;&nbsp; Kozek, E. ;&nbsp; Sieradzki, J. ;&nbsp; Mlynarski, W. ;&nbsp; Malecki, M. T.

Authors: Klupa, T.; Skupien, J.; Mirkiewicz-Sieradzka, B.; Gach, A.¹; Noczynska, A.²; Szalecki, M.³; Kozek, E.; Sieradzki, J.; Mlynarski, W.¹; Malecki, M. T.

Source: Diabetic Medicine, Volume 26, Number 6, June 2009 , pp. 663-664(2)

Publisher: Wiley-Blackwell

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Document Type: Research article

DOI: http://dx.doi.org/10.1111/j.1464-5491.2009.02711.x

Affiliations: 1: Department of Paediatrics, Medical University of Lodz, Lodz 2: Department of Endocrinology and Diabetology for Children and Adolescents, Medical University of Wroclaw, Wroclaw 3: Paediatric Endocrinology Department, Provincial Hospital in Kielce, Kielce, Poland

Publication date: 2009-06-01