Laparoscopic resections of the pancreas in children with hyperinsulinism

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About the authors

Yu. Yu. Sokolov

Russian Medical Academy of Continuous Professional Education, Doletsky Department of Pediatric Surgery

Email: fake@neicon.ru
Moscow, 125993 Россия

M. A. Melikyan

Endocrinology Research Centre

Email: fake@neicon.ru
Moscow, 117036 Россия

A. M. Efremenkov

Russian Medical Academy of Continuous Professional Education, Doletsky Department of Pediatric Surgery

Author for correspondence.
Email: efremart@mail.ru

Artem М. Efremenkov, MD, Cand. Sc.(med), chief of department of pediatric surgery in Central Clinical Hospital with Out-patient Unit; assistant at the chair of pediatric surgery in Russian Medical Academy of Continuous Professional Education

Moscow, 125993

Россия

D. N. Gubaeva

Endocrinology Research Centre

Email: fake@neicon.ru
Moscow, 117036 Россия

V. R. Druzhinin

Bashlaeva Children Hospital

Email: fake@neicon.ru
Moscow, 125373 Россия

I. M. Osmanov

Bashlaeva Children Hospital

Email: fake@neicon.ru
Moscow, 125373 Россия

References

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  3. Меликян М. А., Карева М. А. Врожденный гиперинсулинизм: Пособие для врачей. М.: Практика; 2015.
  4. Palladino A.A., Bennett M.J., Stanley C.A. Hyperinsulinism in infancy and childhood: when an insulin level is not always enough. Ann Biol Clin (Paris). 2009; 67: 3: 245-4.
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  13. Губаева Д.Н., Меликян М.А., Рыжкова Д.В., Пойда М.Д., Баиров В.Г., Сухоцкая А.А., Соколов Ю.Ю., Ефременков А.М., Митрофанова Л.Б., Christesen H., Никитина И.Л. Клинические, генетические и радионуклидные характеристики пациентов с фокальной формой врожденного гиперинсулинизма. Проблемы эндокринологии. 2019. 65 (5); С. 319-29.
  14. Galcheva S, Demirbilek H, Al-Khawaga S, Hussain K. The genetic and molecular mechanisms of congenital hyperinsulinism. Front Endocrinol. 2019; 10: 111.
  15. Thomas P. M., Cote G. J., Wohilk N. et al. Mutations in the sulphonylurea receptor and familial persistent hyperinsulinemic hypoglycemia of infancy. Science. 1995; 268: 426-9.
  16. Thomas P. M., Yuyang Y., Lightner E. Mutation of the pancreatic islet inward rectifier, Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy. Hum Mol Genet. 1996; 5: 1809-12.
  17. Nestorowicz A., Inagaki N., Gonoi T. et al. A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinism. Diabetes. 1997; 46: 1743-8.
  18. Glaser B., Thornton P. S., Otonkoski T., Junien C. The genetics of neonatal hyperinsulinism. Arch Dis Child. 2000; 82: 79-86.
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  20. Kapoor R.R., James C., Hussain K. Advances in the diagnosis and management of hyperinsulinemic hypoglycemia. Nat Clin Pract Endocrinol Metab. 2009; 5(2): 101-12. DOI: https://dx.doi.org/10.18821/1560-9510-2020-24-6-363-369 Original article
  21. Palladino A.A., Bennett M.J., Stanley C.A. Hyperinsulinism in infancy and childhood: when an insulin level is not always enough. Ann Biol Clin (Paris). 2009; 67(3): 245-54.
  22. Сухоцкая А.А., Баиров В.Г., Никитина И.Л., Рыжкова Д.В., Митрофанова Л.Б., Амидхонова С.А. Хирургическое лечение врожденного гиперинсулинизма: предварительный анализ. Детская хирургия. 2019; 23 (3): 124-7.
  23. Banerjee I., Salomon-Estebanez M., Shah P., Nicholson J., Cosgrove K.E., Dunne M.J. Therapies and outcomes of congenital hyperinsulinism-induced hypoglycaemia. Diabet Med J Br Diabet Assoc. 2019; 36(1): 9-21.(in Russian)
  24. Blomberg B.A., Moghbel M.C., Saboury B., Stanley C.A., Alavi A. The value of radiologic interventions and (18)F-DOPA PET in diagnosing and localizing focal congenital hyperinsulinism: Systematic review and meta-analysis. Mol Imaging Biol MIB Off Publ Acad Mol Imaging. 2013;15(1): 97-105.
  25. Salomon-Estebanez M., Flanagan S.E., Ellard S., et al. Conservatively treated Congenital Hyperinsulinism (CHI) due to K-ATP channel gene mutations: reducing severity over time. Orphanet J Rare Dis. 2016; 11: 163.
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  28. Barthlen W., Varol E., Empting S. et al. Surgery in focal congenital hyperinsulinism (CHI) - the “hyperinsulinism Germany international” experience in 30 children. Pediatr Endocrinol Rev. 2016; 14(2): 129-37.

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