Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Simin, Seyedpour"'
Autor:
Negar Moradian, Samaneh Zoghi, Elham Rayzan, Simin Seyedpour, Raul Jimenez Heredia, Kaan Boztug, Nima Rezaei
Publikováno v:
Allergy, Asthma & Clinical Immunology, Vol 19, Iss 1, Pp 1-8 (2023)
Abstract Background Severe Congenital Neutropenia type 4 (SCN4), is a rare autosomal recessive condition, due to mutations in the G6PC3 gene. The phenotype comprises neutropenia of variable severity and accompanying anomalies. Case presentation We re
Externí odkaz:
https://doaj.org/article/7e4962c5348b4d47934e5e225d7ee5d8
Autor:
Mohammad Dahri, Nima Beheshtizadeh, Nasrin Seyedpour, Amin Nakhostin-Ansari, Faezeh Aghajani, Simin Seyedpour, Moein Masjedi, Fatemeh Farjadian, Reza Maleki, Khosro Adibkia
Publikováno v:
Biomedicine & Pharmacotherapy, Vol 165, Iss , Pp 115048- (2023)
Nowadays, immunotherapy is one of the most essential treatments for various diseases and a broad spectrum of disorders are assumed to be treated by altering the function of the immune system. For this reason, immunotherapy has attracted a great deal
Externí odkaz:
https://doaj.org/article/98f877a9f4a84644b574b16c825018ea
Autor:
Fatemeh Sodeifian, Noosha Samieefar, Sepideh Shahkarami, Elham Rayzan, Simin Seyedpour, Meino Rohlfs, Christoph Klein, Delara Babaie, Nima Rezaei
Publikováno v:
Case Reports in Medicine, Vol 2023 (2023)
Background. Primary ciliary dyskinesia (PCD), also known as the immotile-cilia syndrome, is a clinically and genetically heterogeneous syndrome. Improper function of the cilia causes impaired mucociliary clearance. Neonatal respiratory distress, rhin
Externí odkaz:
https://doaj.org/article/c73f774e21704c209edc96daffcd871f
Autor:
Behzad Khodaei, MD, Simin Seyedpour, MD, MPH, Bahare Gholami, MD, Gholamreza Garmarudi, MD, MCH, MPH, Maryam Nasimi, MD, MSC
Publikováno v:
International Journal of Women's Dermatology, Vol 7, Iss 5, Pp 799-802 (2021)
Objective: We aimed to determine the prevalence of different skin diseases and their seasonal variations at the Razi dermatology hospital from 2019 to 2020.Methods: In this cross-sectional study, we obtained data from the medical records of 3120 pati
Externí odkaz:
https://doaj.org/article/ae3f6eac37bb486998ab563f50012816
Autor:
Ali Asadollahi-Amin, Fereshteh Ghiasvand, Mehrdad Hasibi, Simin Seyedpour, Alireza Barzegary, Fatemeh Ghadimi, Seyed Ahmad SeyedAlinaghi, Omid Dadras
Publikováno v:
Vaccine Research, Vol 7, Iss 2, Pp 9-14 (2020)
We report a case series of nine patients with confirmed coronavirus disease 2019 (COVID-19) in Tehran, Iran. This paper also reports narrative information on the signs and symptoms of the patients and discusses the potential immunologic perspective o
Externí odkaz:
https://doaj.org/article/42288436dc924354b49b1eb815fc5eac
Universal Accreditation System (UAS): An Innovative Education and Research Credit Appraisal by USERN
Autor:
Niloufar Yazdanpanah, Mahsa Keshavarz-Fathi, Heliya Ziaei, Ali Jaberipour, Mona Mirbeyk, Sara Hanaei, Simin Seyedpour, Negar Azami, Milad Akbarzadehmoallemkolaei, Kawthar Mohamed, Noosha Samieefar, Zahra Kolahchi, Sajad Kolahchi, Zahra Rahimi Pirkoohi, Sara Momtazmanesh, Mojdeh Sarzaeim, Negar Moradian, Alireza Sarkar Lotfabadi, Amirhossein Loghman, Saboura Ashkevarian, Nima Rezaei
Publikováno v:
Acta Medica Iranica, Vol 60, Iss 1 (2022)
Externí odkaz:
https://doaj.org/article/043b262901c648f2baef9581a7b0162f
Autor:
Mina Hosseini, Simin Seyedpour, Behzad Khodaei, Amir-Hossein Loghman, Nasrin Seyedpour, Mohammad-Hossein Yazdi, Nima Rezaei
Publikováno v:
Vaccines, Vol 11, Iss 1, p 146 (2023)
Triple-negative breast cancer (TNBC) is the subtype of breast cancer with the poorest outcomes, and is associated with a high risk of relapse and metastasis. The treatment choices for this malignancy have been confined to conventional chemotherapeuti
Externí odkaz:
https://doaj.org/article/7ae8280e4b18476a90f30967657aabbd
Autor:
Nima Rezaei, Hossein Esmaeilzadeh, Arya Aminorroaya, Elham Rayzan, Sepideh Shahkarami, Simin Seyedpour, Samaneh Zoghi, Zahra Aryan, Ido Somekh, Meino Rohlfs, Christoph Klein
Publikováno v:
Endocrine, Metabolic & Immune Disorders - Drug Targets. 23:410-415
Background: Immunodeficiency, centromeric instability, and facial anomalies (ICF) syndrome is a rare autosomal recessive disorder. ICF1 is caused by bi-allelic mutations in the gene encoding deoxyribonucleic acid methyltransferase-3B (DNMT3B). Herein
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a68c89ce00dd8d5d72102b3b502178f
https://doi.org/10.2174/1871530322666220822141722
https://doi.org/10.2174/1871530322666220822141722
Autor:
Mohammadreza Salehi, Fereshteh Ghiasvand, Mohammad Mehdi Feizabadi, Mohammad Zarei, Niloofar Ayoobi Yazdi, Neda Alijani, Mehdi Qaempanah, Simin Seyedpour
Publikováno v:
Iranian Journal of Microbiology, Vol 13, Iss 2 (2021)
This study reports a 43 years-old man diagnosed with piriformis pyomyositis. A literature review was conducted by searching MEDLINE via Pubmed for English language case reports, published from 8th December 2019 to 20th January 2020. Patients' symptom
Externí odkaz:
https://doaj.org/article/22eb150d23aa45fbbc08246f33322482
Autor:
Sara Hanaei, Mojdeh Sarzaeim, Niloufar Yazdanpanah, Zahra Rahimi Pirkoohi, Heliya Ziaei, Kawthar Mohamed, Noosha Samieefar, Mahsa Keshavarz-Fathi, Zahra Kolahchi, Negar Moradian, Sara Momtazmanesh, Simin Seyedpour, Ali Jaberipour, Saboura Ashkevarian, Nima Rezaei
Publikováno v:
Acta Medica Iranica, Vol 59, Iss 1 (2021)
No Absract No Absract No Absract No Absract
Externí odkaz:
https://doaj.org/article/abaacd41009b40618ba09c185fa27846