Нарушения обмена глюкозы у новорожденных детей

Иванов Дмитрий Олегович

176. Pronicka E., Weglewska-Jurkiewicz A., Taybert J., Pronicki М., Szyma'nska-Debi'nska Т., Karkuci'nska-Wieckowska A., Jak'obkiewicz-Banecka J., Kowalski P., Piekutowska-Abram-czukD., Pajdowska М., Socha P., Sykut-Cegielska J., Wegrzyn G. Post mortem identification of deoxyguanosine kinase (DGUOK) gene mutations combined with impaired glucose homeostasis and iron overload features in four infants with severe progressive liver failure // J. Appl. Genet. 2011. Vol. 52, N 1. P. 61–66.

177. Pugh S. K., Doherty D. A., Magann E. F., Chauhan S. P., Hill J. B., Morrison J. C. Does hypoglycemia following a glucose challenge test identify a high risk pregnancy? // Reprod Health. 2009. Vol. 14. P. 6–10.

178. Rahier J., Guiot Y., Sempoux C. Persistent hyperinsulinaemic hypoglycaemia of infancy: a heterogeneous syndrome unrelated to nesidioblastosis // Arch. Dis. Child. Fetal. Neonatal Ed. 2000. Vol. 82. P. 108–112.

179. Rashed M. S., Rahbeeni Z., Ozand P. T. Application of electrospray tandem mass spectrometry to neonatal screening // Semin. Perinatol. 1999. Vol. 23. P. 183–193.

180. Rozance P. J., Hay W. W. Jr. Describing hypoglycemia — definition or operational threshold? // Early Hum. Dev. 2010. Vol. 86, N 5. P. 275–280.

181. Rubio-Cabezas O., Patch A.

М., Minton J. A., Flanagan S. E., Edghill E. L., Hussain K, Balafrej A., Deeb A., Buchanan C. R., Jefferson I. G. Wolcott-Rallison syndrome is the most common genetic cause of permanent neonatal diabetes in consanguineous families // J. Clin. Endocrinol. Metab. 2009. Vol. 94. P. 4162–4170.

182. Satake N., NakanishiМ., OkanoM., Tomizawa K., Ishizaka A., Kojima K., Onodera М., Ariga Т., Satake A., Sakiyama Y. A Japanese family of X-linked auto-immune enteropathy with hae-molytic anaemia and polyendocrinopathy // Eur. J. Pediatr. 1993. Vol. 152, N 4. P. 313–315.

183. Sellick G. S., Barker К. Т., Stolte-Dijkstra I., Fleischmann C., Coleman R. J., Garrett C., Gloyn A. L., Edghill E. L., Hattersley A. Т., Wellauer P. K., Goodwin G., Houlston R. S. Mutations in PTF1A cause pancreatic and cerebellar agenesis // Nat Genet. 2004. Vol. 36, N 12. P. 1301–1305.

184. Senee V, Chelala С., Duchatelet S., Feng D., Blanc H., Cossec J. C., Charon C., Nicoli-no М., Boileau P., Cavener D. R., Bougneres P., Taha D., Julier C. Mutations in GLIS3 are responsible for a rare syndrome with neonatal diabetes mellitus and congenital hypothyroidism // Nat Genet. 2006. Vol. 38, N 6. P. 682–687.

185. Senee V, Vattem К. М., Delepine М., Rainbow L. A., Haton C., Lecoq A., Shaw N. J., Robert J. J., Rooman R., Diatloff-Zito C. Wolcott-Rallison Syndrome: Clinical, Genetic, and Functional Study of EIF2AK3 Mutations and Suggestion of Genetic Heterogeneity // Diabetes. 2004. Vol. 53. P. 1876–1883.

186. Shuman C., Beckwith J. B., Smith A. C., Weksberg R. Beckwith-Wiedemann Syndrome. In: Pagon R. A., Bird T. D., Dolan C. R., Stephens K., editors. GeneReviews [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2000 Mar 3 [updated 2010 Dec 14].

187. Singh

М., Singhal P. K., Paul V. K., Deorari A. K., Sundaram K. R., Ghorpade M. D., Aga-di A. Neurodevelopmental outcome of asymptomatic and symptomatic babies with neonatal hypoglycaemia // Indian journal of medical research [В]. 1991. Vol. 94. P. 6–10.

188. SkovL., Pryds O. Capillary recruitment for preservation of cerebral glucose influx in hypoglycemic preterm newborns: Evidence for a glucose sensor? // Pediatrics. 1992. Vol. 90. P. 193–195.

189. Srinivasan G., Pildes R. S., Cattamanchi G., Voora S., Lilien L. D. Plasma glucose values in normal neonates: A new look // Journal of pediatrics. 1986. Vol. 109. P. 114–117.

190. Steiner D. F., Park S. Y., St0y J., Philipson L. H., Bell G. I. A brief perspective on insulin production // Diabetes. Obes. Metab. 2009. Vol. 11, Suppl 4. P. 189–196.

191. Steward C. G., Newbury-Ecob R. A., Hastings R., Smithson S. F., Tsai-Goodman B., Quar-rell O. W., Kulik W., Wanders R., Pennock М., Williams М., Cresswell J. L., Gonzalez I. L., Brennan P. Barth syndrome: an X-linked cause of fetal cardiomyopathy and stillbirth // Prenat Diagn. 2010. Vol. 30, N 10. P. 970–976.

192. Stoffers D. A., Stanojevic V, Habener J. F. Insulin promoter factor-1 gene mutation linked to early-onset type 2 diabetes mellitus directs expression of a dominant negative isoprotein // J. Clin. Invest. 1998. Vol. 102, N 1. P. 232–241.

193. StoyJ., EdghillE. L., Flanagan S. E., YeH., Paz V. P., Pluzhnikov A, Below J. E., Hayes M. G., CoxN. J., Lipkind G. M. Insulin gene mutations as a cause of permanent neonatal diabetes // Proc. Natl. Acad. Sci. USA. 2007. Vol. 104. P. 15040-15044.

194. Stey J., Steiner D. F., Park S. Y., Ye H., Philipson L. H., Bell G. I. Clinical and molecular genetics of neonatal diabetes due to mutations in the insulin gene // Rev. Endocr. Metab. Disord. 2010. Vol. 11, N 3. P. 205–215.

195. Sunehag A., Gustafsson J., Ewald U. Very immature infants (<30 wk) respond to glucose infusion with incomplete suppression of glucose production // Pediatric research. 1994. Vol. 36. P. 550–555.

196. Temple I. K., Gardner R. J., Mackay D. J., Barber J. C., Robinson D. O., Shield J. P. Transient neonatal diabetes: widening the understanding of the etiopathogenesis of diabetes // Diabetes. 2000. Vol. 49, N 8. P. 1359–1366.

197. Thabet F., Bourgeois. J, Guy B., Putet G. Continuous insulin infusion in hyperglycaemic very-low-birth-weight infants receiving parenteral nutrition // Clin. Nutr. 2003. Vol. 22, N 6. P. 545–547.