MOLECULAR GENETIC CHARACTERISTICS CHILDREN WITH GROWTHHORMONE DEFICIENCY
- Authors: Berseneva OS1, Glotov AS2, Glotov OS2, Serebryakova EA2, Ivashenko TE2, Bashnina EB1, Baranov VS2
-
Affiliations:
- North-Western State Medical university named after I.I. Mechnikov
- The Research Institute of Obstetrics, Gynecology and Reproductology named after d.O. Ott
- Issue: Vol 9, No 4 (2017)
- Pages: 12-16
- Section: Reviews
- URL: https://journals.rcsi.science/vszgmu/article/view/8593
- DOI: https://doi.org/10.17816/mechnikov20179412-16
- ID: 8593
Cite item
Full Text
Abstract
Keywords
Full Text
##article.viewOnOriginalSite##About the authors
O S Berseneva
North-Western State Medical university named after I.I. Mechnikov
A S Glotov
The Research Institute of Obstetrics, Gynecology and Reproductology named after d.O. Ott
O S Glotov
The Research Institute of Obstetrics, Gynecology and Reproductology named after d.O. Ott
E A Serebryakova
The Research Institute of Obstetrics, Gynecology and Reproductology named after d.O. Ott
T E Ivashenko
The Research Institute of Obstetrics, Gynecology and Reproductology named after d.O. Ott
E B Bashnina
North-Western State Medical university named after I.I. Mechnikov
V S Baranov
The Research Institute of Obstetrics, Gynecology and Reproductology named after d.O. Ott
References
- Эндокринные заболевания у детей и подростков. Руководство для врачей. Под ред. Башниной Е.Б. // ГЭОТАР-Медиа, 2017. - 416 с.
- Alatzoglou K., Kular D., Dattani M. Autosomal Dominant Growth Hormone Deficiency (Type II) // Pediatr Endocrinol Rev. - 2015. - Vol. 2. - № 4. - Р. 347-355.
- Fofanova O., Evgrafov O., Polyakov A. et al. A novel splicing mutation in exon 4 (456G>A) of the GH1 gene in a patient with congenital isolated growth hormone deficiency // Hormones (Athens). - 2006. - Vol. 5. - № 4. - Р. 288-294.
- Дедов И.И., Петеркова В.А. Детская эндокринология, руководство // М.: Универсум паблишинг, 2006. - 595 с.
- Гаврилова А.Е., Нагаева Е.В., Ширяева Т.Ю., Реброва О.Ю., Тюльпаков А.Н., Петеркова В.А., Дедов И.И. Клинико-генетические особенности пациентов с множественным дефицитом гормонов аденогипофиза, обусловленным мутациями в гене PROP1: эффективность терапии рекомбинантным гормоном роста // Проблемы эндокринологии. - 2017. - Т. 63. - № 2. - С. 72-81.