Molekulyarnaya genetika sakharnogo diabeta u detey i podrostkov (po materialam 32-33 kongressov Mezhdunarodnogo obshchestva po izucheniyu sakharnogo diabeta u detey i podrostkov (ISPAD)
https://doi.org/10.14341/2072-0351-5369
Abstract
About the Authors
M A MelikyanTamara Leonidovna Kuraeva
I A Dubinina
References
1. Barrett T. G. Genetic syndromes and diabetes mellitus. Pediatric Diabetes 2006-vol. 7, S3.
2. Carlsson A., Blom L., Forsander G., Ivarsson S-A., Karlsson A-K., Kernell A., Lernmark A., Lindblad B., Ludvigsson J., Marcus C., Nilsson A., Rastkhani H., Zachrisson I. Better Diabetes Diagnosis (BDD): A countrywide registry of incident patients suggests an altered HLA genotype distribution from 1986-87. Pediatric Diabetes 2006-vol. 7, P27.
3. Galli-Tsinopoulou, Trouva, Klados, Marinou, Sapountzis, Lazidou, Fleva, Daniilidis, Kokaraki, Stylianou, Nousia-Arvanitakis. HLA alleles in children and adolescents with type 1 diabetes mellitus in northern Greece. Pediatric Diabetes 2006-vol. 7, R17.
4. Kantor I. Clinical characteristics of our patient suffering from BETA2/NeuroD1 genetic malformation. Pediatric Diabetes 2006-vol. 7, R19.
5. Mihu M., Mihai C. M., Toringhibel M. Kearns-Sayre Syndrome (KSS). Diagnostic delay in one case. Pediatric Diabetes 2006-vol. 7, R15.
6. Paskova M. Sulfonylurea instead of insulin in PNDM patients with activating mutation in the gene KCNJ11 encoding the Kir6.2 subunit led to significant improvement of DM compensation. Pediatric Diabetes 2006-vol. 7, P34.
7. Peretz A., Israel S., Herschkovitz E., Loewenthal N., Abu-Rabiah Y., Chechik T., Birk O., Leiberman E. Genetic and immunologic basis of diabetes in an extended consanguineous Bedouin family. Pediatric Diabetes 2006-vol. 7, P29.
8. Rami B., Bodamer O., Item B., Heitger A., Haas O., Huber W. D., Schober E. Clinical and molecular findings in an atypical case of IPEXSyndrome. Pediatric Diabetes 2006-vol. 7, P28.
9. Skorka A., Pankowska E., Szypowska A., Choim M., Kostrzewa G., Szalecki M., Korniszewski L., Pioski R. Analysis of genetic factors predisposing to type 1 diabetes in children under 5 years of age. Pediatric Diabetes 2006-vol. 7, P25.
10. Slingerland A. S., Nubour R., Hadders-Algra M., Hattersley A. T., Bruining G. J. Kir6.2 impact of mutation and treatment on diabetes and neurology. Pediatric Diabetes 2006-vol. 7, P30.
11. Datz. N., Nestoris C., Danne T., Driesel A.J. Clinical parameters for molecular testing of maturity onset diabetes in the young (MODY). Pediatric Diabetes 2007-vol. 8, P/WED/52.
12. Jesic M., Sajic S., Zdravkovic V., Maringa M. Maturity onset diabetes of the young type 3: a case report of a female child responsive to a low dose of sulfonylurea. Pediatric Diabetes 2007-vol. 8, P/WED/53
13. Hofer S., Flanagan S., Ellard S., Steichen E. Family report on two siblings affected by transient neonatal diabetes -a novel SUR 1 mutation inherited from the father. Pediatric Diabetes 2007-vol. 8, P/WED/58.
14. Lombardo F., Salzano G., Bruno L., Calabro M. P., F. De Luca. Cardiovascular involvement in Wolfram syndrome. Pediatric Diabetes 2007-vol. 8, P/WED/50.
15. Nakavachara P., Pattaragarn A., Likitmaskul S. A boy with Wolfram syndrome presenting with diabetes mellitus and marked polyuria, bilateral hydronephrosis and hydroureter mimicking obstructive uropathy. Pediatric Diabetes 2007-vol. 8, P/WED/51.
16. Micle I., Marazan M., Marginean O., Pop E., Giurescu R. Permanent neonatal diabetes mellitus - sulphonylureas treatment. Pediatric Diabetes 2007-vol. 8, P/WED/55.
Review
For citations:
Melikyan M.A., Kuraeva T.L., Dubinina I.A. Molekulyarnaya genetika sakharnogo diabeta u detey i podrostkov (po materialam 32-33 kongressov Mezhdunarodnogo obshchestva po izucheniyu sakharnogo diabeta u detey i podrostkov (ISPAD). Diabetes mellitus. 2008;11(3):78-80. (In Russ.) https://doi.org/10.14341/2072-0351-5369

This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (CC BY-NC-ND 4.0).