Текст книги "Нарушения обмена глюкозы у новорожденных детей"

112. Iafusco D., StaziM. A., Cotichini R., Cotellessa М., Martinucci М. E., Mazzella М., Cherubini V, Barbetti F., Martinetti М., Cerutti F., Prisco F. Early Onset Diabetes Study Group of the Italian Society of Paediatric Endocrinology and Diabetology // Diabetologia. 2002. Vol45(6). P. 798–804.

113. Iglesias Platas Thio Lluch М., Pociello Alminana N., Morillo Palomo A., Iriondo SanzM., Krauel Vidal X. Continuous glucose monitoring in infants of very low birth weight. Neonatology. 2009. Vol. 95. P. 217–223.

114. Inder T. How low can I go? The impact of hypoglycemia on the immature brain. Pediatrics. 2008;Vol. 122, N 2. P. 440–441.

115. JonssonJ., Carlsson L., Edlund Т., EdlundH. Insulin-promoter-factor 1 is required for pancreas development in mice // Nature, 1994 Oct 13. Vol. 371, N 6498. P. 606–609.

116. Julier C., Nicolino M. Wolcott-Rallison syndrome // Orphanet. J. Rare Dis. 2010. Vol. 4. P. 5–29.

117. Kalhan S. C., Oliven A., King К. C., Lucero C. Role of glucose in the regulation of endogenous glucose production in the human newborn // Pediatric research. 1986. Vol. 20. P. 49–52.

118. Kalhan S. C., Parimi P. S. Metabolic and endocrine disorders, part one: disorders of carbohydrate metabolism // Neonatal-Perinatal Medicine: Diseases of the Fetus and Newborn.

8. / Martin R. J., Fanaroff A. A., Walsh М. C., editors. Philadelphia: Mosby-Elsevier, 2006. P. 1467–1491.

119. Kalhan S. C., Parimi P., Van Beek R., Gilfillan C., Saker F., Gruca L., Sauer P. J. Estimation of gluconeogenesis in newborn infants // Am. J. Physiol. Endocrinol. Metab. 2001. Vol. 281, N 5. P. 991–997.

120. Kalhan S. C., Savin S. М., Adam P. A. J. Measurement of glucose turnover in the human newborn with glucose-l-13C // Journal of clinical endocrinology and metabolism. 1976. Vol. 43. P. 704–707.

121. KatzL. E., Ferry R. J., Stanley C. A., Collett-SolbergP. F., Baker L., Cohen P. Suppression of insulin oversecretion by subcutaneous recombinant human insulin-like growth factor I in children with congenital hyperinsulinism due to defective beta-cell sulfonylurea receptor//J. Clin. Endocrinol. Metab. 1999. Vol. 84. P. 3117–3124.

122. Kayiran S. М., Giirakan B. Screening of blood glucose levels in healthy neonates // Singapore Med. J. 2010. Vol. 51, N 11. P. 853–835.

123. Kinnala A., Rikalainen H., Lapinleimu H., Parkkola R., Kormano М., Kero P. Cerebral magnetic resonance imaging and ultrasonography findings after neonatal hypoglycemia // Pediatrics. 1999. Vol. 103. P. 724–729.

124. Koivisto М., Blanco-Sequeiros М., Krause U. Neonatal sympomatic and asymptomatic hypoglycaemia: a follow-up study // Developmental medicine and child neurology. 1972. Vol. 14. P. 603–614.

125. Kompare М., Rizzo W. B. Mitochondrial fatty-acid oxidation disorders // Semin. Pediatr. Neurol. 2008. Vol. 15. P. 140–149.

126. Krinsley J. S. Effect of an intensive glucose management protocol on the mortality of critically ill adult patients // Mayo Clin. Proc. 2004. Vol. 79. P. 992–1000.

127. Ktorza A., Bihoreau М. Т., Nurjhan N., Picon L., Girard J. Insulin and glucagon during the perinatal period: secretion and metabolic effects on the liver // Biology of the neonate. 1985. Vol. 48. P. 204–220.

128. Kumari S., Bhargava S. K., Ahmed S. H., Ghosh S. Transient symptomatic hypoglycemia in the newborn // Indian Pediatr. 1971. Vol. 8. P. 762–769.

129. Levitsky L. L., Fisher D. E., Paton J. B. Fasting plasma levels of glucose, acetoacetate, D-hydroxybutyrate, glycerol and lactate in the baboon infant: correlation with cerebral uptake of substrates and oxygen // Pediatric research. 1977. Vol. 11. P. 298–302.

130. Lilien L. D., Pildes R. S., Srinivasan G., Voora S., Yeh T. F. Treatment of neonatal hypoglycemia with minibolus and intraveous glucose infusion // J. Pediatr. 1980. Vol. 97. P. 295–298.

131. Lilien L. D., Rosenfield R. L., Baccaro М. М., Pildes R. S. Hyperglycemia in stressed small premature neonates // J Pediatr. 1979. Vol. 94. P. 454–459.

132. Limesand S. W., Jensen J., Hutton J. C., Hay W. W. Jr. Diminished (3-Cell Replication Contributes to Reduced (3-Cell Mass in Fetal Sheep with Intrauterine Growth Restriction // Am. J. Physiol. Reg. Integr. Comp. Physiol. 2005. Vol. 288. P. 1297–1305.

133. Limesand S. W., Rozance P. J., Zerbe G. O., Hutton J. C., Hay W. W. Jr. Attenuated Insulin Release and Storage in Fetal Sheep Pancreatic Islets with Intrauterine Growth Restriction // Endocrinology. 2006. Vol. 147. P. 1488–1497.

134. Louik C., Mitchell A. A., Epstein M. F., Shapiro S. Risk factors for neonatal hyperglycemia associated with 10 % dextrose infusion//Am. J. Dis. Child., 1985. Vol. 193. P. 783–786.

135. LteifA. N., Schwenk W. F. Hypoglycemia in infants and children // Endocrinol. Metab. Clin. North. Am. 1999. Vol. 28. P. 619–646.

136. Lubchenco L. O., Bard H. Incidence of hypoglycemia in newborn infants classified by birth weight and gestational age // Pediatrics. 1971. Vol. 47. P. 831–838.

137. Lucas A., Boyes S., Bloom S. R., Aynsley-Green A. Metabolic and endocrine responses to a milk feed in six-day-old term infants: differences between breast and cow’s milk formula feeding //Acta paediatrica Scandinavica. 1981. Vol. 70. P. 195–200.

138. Lucas A., Morley R., Cole T. J. Adverse neurodevelopmental outcome of moderate neonatal hypoglycaemia // British medical journal (BMJ). 1988. Vol. 297. P. 1304–1308.

139. van der Lugt N. М., Smits-Wintjens V. E., van Zwieten P. H., Walther F. J. Short and long term outcome of neonatal hyperglycemia in very preterm infants: a retrospective follow-up study // BMC Pediatr. 2010. Vol. 10. P. 52–56.

140. MacMullen C., Fang J., Hsu B. Y., Kelly A., de Lonlay-Debeney P., Saudubray J. М., Ganguly A., Smith T. J., Stanley C. A. Hyperinsulinism/hyperammonemia syndrome in children with regulatory mutations in the inhibitory guanosine triphosphate-bind-ing domain of glutamate dehydrogenase // J. Clin. Endocrinol. Metab. 2001. Vol. 86. P. 1782–1787.

141. Marquis E., Robert J. J., Bouvattier C., Bellanne-Chantelot C., Junien C., Diatloff-Zito C. Major difference in aetiology and phenotypic abnormalities between transient and permanent neonatal diabetes // J. Med. Genet. 2002. Vol. 39, N 5. P. 370–374.

142. McCowen К. C., Malhotra A., Bistrian B. R. Stress-induced hyperglycemia // Crit. Care Clin. 2001. Vol. 17, N 1. P. 107–124.

143. McGowan J. E., Price-Douglas W., Hay W. W. Jr. Glucose homeostasis // Handbook of Neonatal Intensive Care. 6 / Merenstein G., Gardner S., editors. St. Louis: Mosby-Elsevier; 2006. P. 368–390.

144. Meetze W., Bowsher R., Compton J., Moorehead H. Hyperglycemia in extremely-low-birth-weight infants // Biol Neonate. 1998. Vol. 74, N 3. P. 214–221.

145. Mehta A. Hyperinsulinaemic hypoglycaemia in small for dates babies // Archives of disease in childhood. 1991. Vol. 66. P. 749.

146. Mejri A., Dorval V. G., Nuyt A. М., Carceller A. Hypoglycemia in term newborns with a birth weight below the 10th percentile // Paediatr Child Health. 2010. Vol. 15, N 5. P. 271–275.

147. Mesotten D., Wouters P. J., Peeters R. P., Hardman К. V, Holly J. М., Baxter R. C., Van den Berghe G. Regulation of the Somatotropic Axis by Intensive Insulin Therapy during Protracted Critical Illness // The Journal of Clinical Endocrinology & Metabolism. 2004. Vol. 89, N7. P. 3105–3113.

148. Metsvaht Т., Pisarev H., Ilmoja M. L., Parm U., Maipuu L., Merila М., Muiirsepp P., Lut-sar I. Clinical parameters predicting failure of empirical antibacterial therapy in early onset neonatal sepsis, identified by classification and regression tree analysis // BMC Pediatr. 2009. Vol. 24. P. 72–76.

149. Metz C., Cave H., Bertrand A. М., Deffert C., Gueguen-Giroux B., Czernichów P., Polak M. NDM French Study Group. Neonatal diabetes mellitus. Neonatal diabetes mellitus: chromosomal analysis in transient and permanent cases // J. Pediatr. 2002. Vol. 141, N 4. P. 483–489.

150. Miller H. C., Ross R. A. Relation of hypoglycemia to the symptoms observed in infants of diabetic mothers // Journal of pediatrics. 1940. Vol. 16. P. 473–481.

151. Mizock B. A. Alterations in fuel metabolism in critical illness: hyperglycaemia // Best. Pract. Res. Clin. Endocrinol Metab. 2001. Vol. 15, N 4. P. 533–551.

152. Mohnike K., Blankenstein O., MinnH., Mohnike W., Fuchtner F., Otonkoski T. [18FJ-DOPA positron emission tomography for preoperative localization in congenital hyperinsulin-ism // Horm Res. 2008a. Vol. 70. P. 65–72.

153. Mohnike K., Blankenstein O., Pfuetzner A., Potzsch S., Schober E., Steiner S., Hardy О. Т., Grimberg A., van Waarde W. M. Long-term non-surgical therapy of severe persistent congenital hyperinsulinism with glucagon // Horm. Res. 2008b. Vol. 70. P. 59–64.

154. Murad М. H., Coto-Yglesias F., Wang A. Т., Sheidaee N., Mullan R. J., Elamin М. B., Erwin P. J., Montori V. M. Clinical review: Drug-induced hypoglycemia: a systematic review // J. Clin. Endocrinol. Metab. 2009. Vol. 94, N 3. P. 741–745.

155. von Muhlendahl К. E., Herkenhoff H. Long-term course of neonatal diabetes // N. Engl. J. Med. 1995. Vol. 333, N 11. P. 704–708.

156. Nadeem М., Murray D. М., Boylan G. B., Dempsey E. М., Ryan C. A. Early blood glucose profile and neurodevelopmental outcome at two years in neonatal hypoxic-ischaemic encephalopathy // BMC Pediatr., 2011 Feb 4; Vol. 11. P. 10–15.

157. Nehlig A., Pereira de Vasconcelos A. Glucose and ketone body utilisation by the brain of neonatal rats // Progress in Neurobiology. 1993. Vol. 40. P. 163–221.

158. Ng S. М., May J. E., Emmerson A. J. Continuous insulin infusion in hyperglycaemic ex-tremely-low-birth-weight neonates // Biol Neonate. 2005. Vol. 87. P. 269–272.

159. Nicholl R. What is the normal range of blood glucose concentrations in healthy term newborns? // Archives of Disease in Childhood. 2003. Vol. 88. P. 238–239.

160. Nicolino M, Claiborn КС, Senee V, Boland A, Stoffers D. A, Julier C. A novel hypomorphic PDX1 mutation responsible for permanent neonatal diabetes with subclinical exocrine deficiency // Diabetes. 2010. Vol. 59(3). P. 733–740.

161. Nj0lstad P. R., S0vik O., Cuesta-Munoz A., Bj0rkhaug L., Massa O., Barbetti F., Un-dlien D. E., Shiota C., Magnuson M. A., Molven A., Matschinsky F. М., Bell G. I. Neonatal diabetes mellitus due to complete glucokinase deficiency // N Engl J Med. 2001. Vol. 344, N21. P. 1588–1592.

162. Ogata E. S. Carbohydrate homeostasis // Avery’s Neonatology. 6. / MacDonald M. G., Seshia M. М. K, Mullett M. D., editors. Philadelphia: Lippincott Williams & Wilkins, 2005. P. 876–891.

163. Osier F. H., Berkley J. A., Ross A., Sanderson F., Mohammed S., Newton C. R. Abnormal blood glucose concentrations on admission to a rural Kenyan district hospital: prevalence and outcome // Arch Dis Child. 2003. Vol. 88, N 7. P. 621–625.

164. Ostertag S. G., Jovanovic L., Lewis B., Auld P. A. Insulin pump therapy in the very low birth weight infant // Pediatrics. 1986. Vol. 78, N 4. P. 625–630.

165. Otonkoski Т., Nanto-Salonen K., Seppanen М., Veijola R., Huopio H., Hussain K., Tapa-nainen P., Eskola O., Parkkola R., Ekstrom K., Guiot Y., Rahier J., Laakso М., Rintala R., Nuutila P., Minn H. Noninvasive diagnosis of focal hyperinsulinism of infancy with [18F]-DOPA positron emission tomography // Diabetes. 2006. Vol. 55. P. 13–18.

166. Otonkoski Т., Roivainen М., Vaarala O., Dinesen B., Leipala J. A., Hovi Т., Knip M. Neonatal Type I diabetes associated with maternal echovirus 6 infection: a case report // Diabeto-logia. 2000. Vol. 43, N 10. P. 1235–1238.

167. Overfield С. V, Savory J., Heintges M. A. Gycolysis: a re-evaluation of the effect on blood glucose // Clin. Chim. Acta. 1972. Vol. 39. P. 35–40.

168. Ozbek M. N., Senee V., Aydemir S., Kotan L. D., Mungan N. O., Yuksel B., Julier C., To-paloglu A. K. Wolcott-Rallison syndrome due to the same mutation (W522X) in EIF2AK3 in two unrelated families and review of the literature // Pediatric Diabetes. 2010. Vol. 11. P. 279–285.

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.

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.

198. Thorell A., Nygren J., Ljungqvist O. Insulin resistance: a marker of surgical stress // Curr., Opin., Clin., Nutr., Metab., Care. 1999. Vol. 2, N 1. P. 69–78.

199. Tita A. Т., Landon М. B., Spong C. Y., Lai Y., Leveno K. J., Varner M. W., Moawad A. H., Caritis S. N., Meis P. J., Wapner R. J., Sorokin Y., Miodovnik М., Carpenter М., Peace-man A. М., O’Sullivan M. J., Sibai В. М., Langer О., Thorp J. М., Ramin S. М., Mercer В. M. Eunice Kennedy Shriver NICHD Maternal-Fetal Medicine Units Network // Timing of elective repeat cesarean delivery at term and neonatal outcomes // N Engl J Med. 2009. Vol. 360, N 2. P. 111–120.

200. Udani V, Munot P., Ursekar М., Gupta S. Neonatal hypoglycemic brain – injury a common cause of infantile onset remote symptomatic epilepsy // Indian Pediatr. 2009. Vol. 46, N2. P. 127–132 85.

201. Vanhorebeek I., Van den Berghe G. Hormonal and metabolic strategies to attenuate catabolism in critically ill patients // Curr Opin Pharmacol. 2004. Vol. 4, N 6. P. 621–628.

202. Vaucher Y. E., Walson P. D., Morrow G. 3rd. Continuous insulin infusion in hyperglycemic, very low birth weight infants // J. Pediatr. Gastroenterol. Nutr. 1982. Vol. 1, N 2. P. 211–217.

203. Vaulont S., Vasseur-Cognet М., Kahn A. Glucose regulation of gene transcription // J. Biol Chem. 2000. Vol. 275, N 41. P. 31555-31558.

204. Velho G., Froguel P. Genetic, metabolic and clinical characteristics of maturity onset diabetes of the young // Eur. J. Endocrinol. 1998. Vol. 138, N 3. P. 233–239.

205. Wallace J. М., Milne J. S., Aitken R. P., Hay W. W. Jr. Sensitivity to metabolic signals in late gestation growth restricted fetuses from rapidly growing adolescent sheep // Am. J. Physiol. Endo. Metab. 2007. Vol. 293. P. 1233–1241.

206. Weekers F., Van den Berghe G. Endocrine modifications and interventions during critical illness // Proc Nutr Soc. 2004. Vol. 63, N 3. P. 443–450.

207. Wolcott C. D., Rallison М. V. Infancy-onset diabetes mellitus and multiple epiphyseal dysplasia // J. Pediatr. 1972. Vol. 80. P. 292–297.

208. Yamaguchi K., Mishina J., Mitsuishi С., Takamura Т., Nishida H. Follow-up study of neonatal hypoglycemia // Acta Paediatr Jpn. 1997. Vol. 39, suppl 1. P. 51–53.

209. Yorifuji Т., Matsumura М., Okuno Т., Shimizu K., Sonomura Т., Muroi J., Kuno С., Taka-hashi Y., Okuno T. Hereditary pancreatic hypoplasia, diabetes mellitus, and congenital heart disease: a new syndrome? // J. Med. Genet. 1994. Vol. 31, N 4. P. 331–333.