Zobrazeno 1 - 10
of 137
pro vyhledávání: '"Maryam, Najafi"'
Autor:
Asadollah Asadi, Mitra Rostami, Radmehr Shafiee, Abbas Ardalani, Atefeh Dehghanitafti, Zakieh Golshadi, Kiarash Kohansal, Fatemeh Ghasemi, Maryam Najafi, Touraj Mahmoudi, Gholamreza Rezamand, Reza Dabiri, Hossein Nobakht, Hamid Farahani, Seidamir Pasha Tabaeian
Publikováno v:
Archives of Endocrinology and Metabolism, Vol 68 (2024)
ABSTRACT Objective: This study was designed to investigate the possible effect of the insulin receptor substrate 1 (IRS1) gene rs1801276 polymorphism on the risk of nonalcoholic fatty liver disease (NAFLD). Subjects and methods: The rs1801276 polymor
Externí odkaz:
https://doaj.org/article/4d5dd597e72b425e828fa9abad01585f
Autor:
Amirreza Veisi, Kimia Daneshvar, Sadid Hooshmandi, Maryam Najafi, Peyman Mohammadi Torbati, Kiana Hassanpour
Publikováno v:
Case Reports in Ophthalmology, Vol 15, Iss 1, Pp 265-272 (2024)
Introduction: Multiple myeloma (MM), a plasma cell malignancy, is a systemic disease affecting various body organs. Plasmacytoma of bone and extramedullary disease (EMD) are presentations of MM. EMD is usually the sign of a more aggressive form of th
Externí odkaz:
https://doaj.org/article/49cadfce0d2d40a1a93a95f8dadcb6bd
Publikováno v:
پژوهشنامه روانشناسی مثبت, Vol 9, Iss 3, Pp 127-148 (2023)
Generalized anxiety disorder is a type of anxiety disorder that is defined as excessive and unreasonable worry about everyday events and activities. The present study was conducted with the aim of determining the effectiveness of positive mindfulness
Externí odkaz:
https://doaj.org/article/d72df2d80fa746cda260f9f5451acc48
Autor:
Mitra Soltani, Shirin Gerami, Zohreh Ghaem Far, Milad Rajabzadeh-Dehkordi, Mohammad Jafar Dehzad, Maryam Najafi, Shiva Faghih
Publikováno v:
International Journal of Nutrition Sciences, Vol 8, Iss 3, Pp 150-157 (2023)
Background: To quantify carbohydrates, various indicators such as glycemic load (GL) and glycemic index (GI) were introduced. In order to address the effect of dietary carbohydrate content on lipid profile, we investigated the relationship between di
Externí odkaz:
https://doaj.org/article/6d7fdef816ce4da5bc921ce58f390fa1
Autor:
Enferadi, Ahmad, Sarani, Saeedeh, Mohammadipour, Shirin, Hasani, Sayyed Jafar, Ajdari, Afshin, Asl, Maryam Najafi, Khademi, Peyman
Publikováno v:
In Infection, Genetics and Evolution March 2024 118
Autor:
Mehran Nouri, Sevda Eskandarzadeh, Maede Makhtoomi, Milad Rajabzadeh-Dehkordi, Niloofar Omidbeigi, Maryam Najafi, Shiva Faghih
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-8 (2023)
Abstract The purpose of this cross-sectional study was to examine the association between ultra-processed foods (UPFs) intake and lipid profile in Iranian people. The study was performed on 236 individuals with the age range of 20–50 years in Shira
Externí odkaz:
https://doaj.org/article/187662caa09b410397c8dad0c0b90e5a
Publikováno v:
Journal of Fundamentals of Mental Health, Vol 25, Iss 2, Pp 111-121 (2023)
مقدمه: پژوهش حاضر به بررسی و مقایسه رفتارهای مثبت کلامی و غیرکلامی با شریک عاطفی در سه دوره نامزدی، نامزدی رسمی و پس از ازدواج پرداخته است.
Externí odkaz:
https://doaj.org/article/1d6b8631bc2a49c4af1ddd76db0d33ae
Publikováno v:
Disease and Diagnosis, Vol 11, Iss 4, Pp 142-146 (2022)
Background: Autosomal recessive primary microcephaly-2 (MCPH2) is a rare genetic disorder with clinical and genetic heterogeneity. This study aimed to perform high-throughput whole-exome sequencing (WES) to facilitate the diagnosis of the genetic var
Externí odkaz:
https://doaj.org/article/6d177938d08141c5910bd8edf58ed533
Autor:
Aboulfazl Rad, Maryam Najafi, Fatemeh Suri, Soheila Abedini, Stephen Loum, Ehsan Ghayoor Karimiani, Narsis Daftarian, David Murphy, Mohammad Doosti, Afrooz Moghaddasi, Hamid Ahmadieh, Hamideh Sabbaghi, Mohsen Rajati, Narges Hashemi, Barbara Vona, Miriam Schmidts
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-9 (2022)
Abstract Background Stickler syndrome (STL) is a rare, clinically and molecularly heterogeneous connective tissue disorder. Pathogenic variants occurring in a variety of genes cause STL, mainly inherited in an autosomal dominant fashion. Autosomal re
Externí odkaz:
https://doaj.org/article/87fa0aea4e584ebbb99125d7d093a01a
Publikováno v:
Archives of Trauma Research, Vol 11, Iss 4, Pp 171-176 (2022)
Background and Objectives: Scaphoid fractures are common fractures of the upper extremity and more than 5% of them progress to nonunion. Nonvascularized bone grafting (NVBG) and vascularized bone grafting (VBG) are used to treat this fracture and the
Externí odkaz:
https://doaj.org/article/6c5d7a43d8f54670b6c707feebd8b3de