Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Siroos Karimdadi"'
Autor:
Maryam Razzaghy-Azar, Saeedeh Saeedi, Sepideh Borhan Dayani, Samaneh Enayati, Farzaneh Abbasi, Somayyeh Hashemian, Peyman Eshraghi, Siroos Karimdadi, Parisa Tajdini, Rahim Vakili, Mahsa M. Amoli, Hanieh Yaghootkar
Publikováno v:
JCRPE, Vol 14, Iss 1, Pp 87-95 (2022)
INTRODUCTION: Congenital hyperinsulinism (CHI) is the most frequent cause of severe and persistent hypoglycaemia from birth. Understanding the pathophysiology and genetic defects behind hyperinsulinism and its complications provides clues to timely d
Externí odkaz:
https://doaj.org/article/cc986b66066b476cbc4115fdd2b9bbee
Autor:
Somayyeh Hashemian, Reza Jafarzadeh Esfehani, Siroos Karimdadi, Nosrat Ghaemi, Peyman Eshraghi, Najmeh Malekzadeh Gonabadi, Amirhossein Sahebkar, Rahim Vakili, Mohammad Reza Abbaszadegan
Publikováno v:
Case Reports in Endocrinology, Vol 2021 (2021)
Background. Congenital hyperinsulinism (CHI) is a heterogeneous disease with various underlying genetic causes. Among different genes considered effective in the development of CHI, ABCC8, KCNJ11, and HADH genes are among the important genes, especia
Externí odkaz:
https://doaj.org/article/997f836e832f42b8b9150aede057f01e
Autor:
Somayyeh Hashemian, Reza Jafarzadeh Esfehani, Siroos Karimdadi, Rahim Vakili, Daniel Zamanfar, Amirhossein Sahebkar
Publikováno v:
International Journal of Endocrinology, Vol 2020 (2020)
Background. Congenital hyperinsulinism (CHI) is a rare and life-threatening genetic disorder. Sirolimus as a mammalian target of rapamycin inhibitor may be helpful in patients with CHI who do not respond well to other treatments including diazoxide a
Externí odkaz:
https://doaj.org/article/a30e9a73c9e849fa9dfd87cf0757d787
Publikováno v:
Patient Safety and Quality Improvement Journal, Vol 6, Iss 3, Pp 0-0 (2018)
Introduction: To investigate the value of procalcitonin (PCT) in lobar and non-lobar pneumonia in children. Materials and Methods: 80 children with pneumonia were included. 20 healthy children were selected as control. Lobar and non-lobar pneumonia w
Externí odkaz:
https://doaj.org/article/8fa2e4343336473ab018a8db6fbf7c7d
Autor:
Reza Jafarzadeh Esfehani, Peyman Eshraghi, Amirhossein Sahebkar, Najmeh Malekzadeh Gonabadi, Mohammad Reza Abbaszadegan, Nosrat Ghaemi, Siroos Karimdadi, Rahim Vakili, Somayyeh Hashemian
Publikováno v:
Case Reports in Endocrinology, Vol 2021 (2021)
Case Reports in Endocrinology
Case Reports in Endocrinology
Background. Congenital hyperinsulinism (CHI) is a heterogeneous disease with various underlying genetic causes. Among different genes considered effective in the development of CHI, ABCC8, KCNJ11, and HADH genes are among the important genes, especia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b313208b3248018bda5961e6820b49d
https://doaj.org/article/997f836e832f42b8b9150aede057f01e
https://doaj.org/article/997f836e832f42b8b9150aede057f01e
Autor:
Reza Jafarzadeh Esfehani, Rahim Vakili, Amirhossein Sahebkar, Somayyeh Hashemian, Siroos Karimdadi, Daniel Zamanfar
Publikováno v:
International Journal of Endocrinology
International Journal of Endocrinology, Vol 2020 (2020)
International Journal of Endocrinology, Vol 2020 (2020)
Background. Congenital hyperinsulinism (CHI) is a rare and life-threatening genetic disorder. Sirolimus as a mammalian target of rapamycin inhibitor may be helpful in patients with CHI who do not respond well to other treatments including diazoxide a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f55adde5b3f0a70cfd7f163156b56d0
http://europepmc.org/articles/PMC7396056
http://europepmc.org/articles/PMC7396056