Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Sepideh Borhan-Dayani"'
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
Publikováno v:
J Diabetes Metab Disord
PURPOSE: Personal medicine is a new notion for individualizing treatment in the future. Studying pathogenic markers including genetic variants would be beneficial in better diagnosis and management of complex diseases such as diabetes and obesity. Ad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d0876350c8930cfd0945fe141e66d5b
https://doi.org/10.1007/s40200-022-00978-5
https://doi.org/10.1007/s40200-022-00978-5
Autor:
Rahim Vakili, Solmaz Heidari, Sepideh Borhan-Dayani, Sian Ellard, Peyman Eshraghi, Farzaneh Abbasi, Saba Vakili, Andrew T. Hattersley, Timothy J. McDonald, Ali Rabbani, Kashyap A. Patel, K Colclough, Samaneh Enayati, Nosrat Ghaemi, Hanieh Yaghootkar, Matthew Wakeling, Fatemeh Sayarifard, Mahsa M. Amoli
Publikováno v:
Diabetic Medicine
Aim To examine the extent to which discriminatory testing using antibodies and Type 1 diabetes genetic risk score, validated in European populations, is applicable in a non‐European population. Methods We recruited 127 unrelated children with diabe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08ea7969d60d6aa7e90967091d7f502e
https://doi.org/10.1111/dme.14071
https://doi.org/10.1111/dme.14071
Publikováno v:
Molecular biology reports. 48(10)
Cardiovascular diseases (CVDs) are the most common and the first cause of death worldwide. While some studies have investigated the association of the Adenosine Deaminase (ADA) gene with CDVs, its roles on in-stent restenosis (ISR) has not been studi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6e2471d323815426e54958cb4d71c5e5
https://pubmed.ncbi.nlm.nih.gov/34510320
https://pubmed.ncbi.nlm.nih.gov/34510320
Autor:
Farzaneh Abbasi, Samaneh Enayati, Ali Rabbani, Babak Saadati, Reihaneh Mohsenipour, Fatemeh Sayarifard, Aria Setoodeh, Sepideh Borhan-Dayani, Hanieh Yaghootkar, Mahsa M. Amoli, Solmaz Heidari
Publikováno v:
Meta Gene. 21:100599
H syndrome is a hereditary disease transmitted in an autosomal recessive pattern.It consists of two major clusters of cutaneous and systemic manifestations [1,2].The symptoms include short stature, hyperpigmentation of skin, hypertrichosis, deafness,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f81bdab2444806ce4b7d201857306dc6
https://doi.org/10.1016/j.mgene.2019.100599
https://doi.org/10.1016/j.mgene.2019.100599