Нарушения обмена глюкозы у новорожденных детей

169. Pal D. K., Manandhar D. S., Rajbhandari S., Land J. М., Patel N., de L Costello A. M. Neonatal hypoglycaemia in Nepal 1. Prevalence and risk factors // Arch. Dis. Child. 2000. Vol. 82. P. 46–51.

170. Pati N. K., Maheshwari R., Chellani H., Salhan R. N. Transient Neonatal Hyperglycemia // Indian Pediatrics. 2001. Vol. 38. P. 898–901.

171. Peake J. E., McCrossin R. B., Byrne G., Shepherd R. X-linked immune dysregulation, neonatal insulin dependent diabetes, and intractable diarrhoea // Arch Dis Child Fetal Neonatal Ed. 1996. Vol. 74, N 3. P. 195–199.

172. Persson B., Gentz J. Follow-up of children of insulin-dependent and gestational diabetic mothers: neuropsychological outcome // Acta Paediatr Scand. 1984. Vol. 73. P. 349–358.

173. Pildes R. S. Neonatal hyperglycemia // J. Pediatr. 1986. Vol. 109(5). P. 905–907.

174. Pildes R. S., Cornblath М., Warren I. A prospective controlled study of neonatal hypoglycemia // Pediatrics. 1974. Vol. 54. P. 5–14.

175. Polak М., Cave H. Neonatal diabetes mellitus: a disease linked to multiple mechanisms // Orphanet. J. Rare Dis. 2007. Vol. 9. P. 2–12.

176. Pronicka E., Węglewska-Jurkiewicz A., Taybert J., Pronicki М., Szymańska-Dębińska Т., Karkucińska-Więckowska A., Jakóbkiewicz-Banecka J., Kowalski P., Piekutowska-Abram-czukD., Pajdowska М., Socha P., Sykut-Cegielska J., Węgrzyn 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.