Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Behnaz Bazrafshan"'
Publikováno v:
Journal of Clinical and Basic Research, Vol 7, Iss 4, Pp 15-19 (2023)
Background: Neurodegenerative diseases (NDDs) cause progressive neuronal loss, resulting in morbidity and mortality. Research is continued on treatment strategies that can tackle the disease's pathophysiology and cease its progression. Considering th
Externí odkaz:
https://doaj.org/article/81a9526981aa4bb3bb552482b1b5412c
The Association between Prolonged Jaundice and UGT1A1 Gene Polymorphism (G71R) in Gilbert's Syndrome
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 10, Iss 11, Pp GC05-GC08 (2016)
Introduction: Jaundice is a common condition during the neonatal period. Prolonged jaundice occurs in a large number of breastfed infants. Considering the impact of genetic factors on the incidence of jaundice present study was conducted. Aim: Th
Externí odkaz:
https://doaj.org/article/d8445d12130a433386be6c04dd378e25
Autor:
Seyyed-Mohsen Hosseininejad, Fateme-Sadat Hosseininejad, Amirhossein SalimiKordasiabi, Fateme-Sadat Tabatabaei, Firouzeh Derakhshanpour, Behnaz Bazrafshan, Mostafa Moin
Publikováno v:
International Journal of Pediatrics, Vol 5, Iss 12, Pp 6699-6702 (2017)
Acute disseminated encephalomyelitis (ADEM) is a monophasic clinical syndrome, characterized by immune-mediated demyelination of central nervous system neurons, which yield extensive damage in the brain and spinal cord.It usually affects children and
Autor:
Behnaz Bazrafshan, Abdolreza Fazel, Seyed Payam Shirangi, Masoomeh Rostami, Payam Sarmadi, Akram Sanagoo, Leila Jouybari, Mohammad Reza Hashempour
Publikováno v:
Journal of Nursing and Midwifery Sciences, Vol 3, Iss 4, Pp 56-59 (2016)
Adrenal gland cysts are rare indications of adrenal diseases, which are commonly asymptomatic. In radiological studies, these cysts, known as incidentalomas, are often detected by coincidence accounting for 6% of the population. Adrenal incidentaloma
Publikováno v:
Frontiers of Medicine. 10:345-350
Asthma is the most common chronic disease among children, and its incidences are often imminent among elementary schoolchildren. This study aimed to examine the prevalence of asthma symptoms in Golestan schoolchildren aged 6–7 and 13–14 years in
Autor:
Javad Tavakkoly-Bazzaz, Seyedhossein Hekmatimoghaddam, A Sarli, Mohammad Ali Zaimy, A Abdalaian, Bahram Kazemi, Ali Jebali, Behnaz Bazrafshan, A Tavakoli, S Shabani, Azadeh Shojaei, Hakim Azizi, S Mehrtashfar, Pantea Izadi
Publikováno v:
Cancer Gene Therapy. 23:315-320
The aim of this study was to evaluate an engineered nanostructure to silence five important oncogenes, including BAG1, MDM2, Bcl-2, BIRC5 (survivin) and XIAP, in acute myeloid leukemia subtype 2 (AML-M2). The smart nanostructures were functionalized
Autor:
Behnaz Bazrafshan, Hamidreza Bazrafshan, Mamak Eftekharie, Mehrdad Aghaei, Fatemeh Mousavi, Gunter Stalla, Payam Sarmadi, Hossien Shadpourdashti
Publikováno v:
Endocrine Abstracts.
Publikováno v:
Endocrine Abstracts.
The Association between Prolonged Jaundice and UGT1A1 Gene Polymorphism (G71R) in Gilbert's Syndrome
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 10, Iss 11, Pp GC05-GC08 (2016)
Introduction: Jaundice is a common condition during the neonatal period. Prolonged jaundice occurs in a large number of breastfed infants. Considering the impact of genetic factors on the incidence of jaundice present study was conducted. Aim: The ai
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 10, Iss 2, Pp SD03-SD05 (2016)
As a rare multisystem congenital anomaly disorder, Cornelia de Lange syndrome (CdLS) is featured by delayed growth and development, distinct facial dimorphism, limb malformations and multiple organ defects. CdLS is a genetic syndrome affecting 1/1000