Cargando…

Evaluation of response to hepatitis B vaccine in Iranian 6–18-year-old students

BACKGROUND: Hepatitis B is a dangerous disease with high morbidity and mortality rates all around the world. Vaccination is the most important way to its prevention and control. This cross-sectional study was carried out to study the levels of immunogenicity to hepatitis B vaccine in students. MATER...

Descripción completa

Detalles Bibliográficos
Autores principales:	Jouneghani, Alizamen Salehifard, Chaleshtori, Morteza Hashemzadeh, Khoshdel, Abolfazl, Kheiri, Soleiman, Farrokhi, Effat, Khalafian, Pooran, Aliyari, Zahra
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2017
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5680656/ https://www.ncbi.nlm.nih.gov/pubmed/29184574 http://dx.doi.org/10.4103/jrms.JRMS_204_17

Ejemplares similares

Compound Heterozygosity for Two Novel SLC26A4 Mutations in a Large Iranian Pedigree with Pendred Syndrome
por: Yazdanpanahi, Nasrin, et al.
Publicado: (2013)

Increased levels of miR-124 in human dental pulp stem cells alter the expression of neural markers
por: Mehri-Ghahfarrokhi, Ameneh, et al.
Publicado: (2019)

Association between Interleukin-10-1082 G/A and Tumor Necrosis Factor-α 308 G/A Gene Polymorphisms and Respiratory Distress Syndrome in Iranian Preterm Infants
por: Khoshdel, Abolfazl, et al.
Publicado: (2017)

Examining the solutions to maintain psychological safety and nutritional and physical health of children during war: a review study
por: Salehifardjoneghani, Alizamen, et al.
Publicado: (2019)

Effect of Ramadan Fast on Liver Function Tests
por: Nasiri, Jafar, et al.
Publicado: (2016)

The effect of Ramadan fasting on serum leptin, neuropeptide Y and insulin in pregnant women
por: Khoshdel, Abolfazl, et al.
Publicado: (2014)

rs12480307 and rs6050307 Polymorphisms of VSX1 Gene in Patient with Keratoconusin Southwest Iran Using PCR-RFLP
por: KARAMI ESHKAFTAKI, Raziyeh, et al.
Publicado: (2018)

Study of changes in rs2283265 polymorphisms in dopamine receptor D2 and rs27072 in dopamine transporter gene (SLC6A3) in patients with attention-deficit hyperactivity disorder
por: SAFAVI, Parvin, et al.
Publicado: (2022)

Screening of Myo7A Mutations in Iranian Patients with Autosomal Recessive Hearing Loss from West of Iran
por: ASGHARZADE, Samira, et al.
Publicado: (2017)

Effects of synbiotics on treatment of children with failure to thrive: A triple blind placebo-controlled trial
por: Famouri, Fatemeh, et al.
Publicado: (2014)

Mutations in GJB2 as Major Causes of Autosomal Recessive Non-Syndromic Hearing Loss: First Report of c.299-300delAT Mutation in Kurdish Population of Iran
por: Azadegan-Dehkordi, Fatemeh, et al.
Publicado: (2019)

Tumor microsatellite instability and clinicopathologic features in Iranian colorectal cancer patients at risk for Lynch syndrome
por: Zeinalian, Mehrdad, et al.
Publicado: (2015)

Immunohistochemical Analysis of Mismatch Repair Proteins in Iranian Colorectal Cancer Patients at Risk for Lynch Syndrome
por: Zeinalian, Mehrdad, et al.
Publicado: (2015)

Molecular Genetic Study in a Cohort of Iranian Families Suspected to Maturity-Onset Diabetes of the Young, Reveals a Recurrent Mutation and a High-Risk Variant in the CEL Gene
por: Sarmadi, Akram, et al.
Publicado: (2020)

Novel MYO15A variants are associated with hearing loss in the two Iranian pedigrees
por: Khatami, Somayeh, et al.
Publicado: (2020)

Lack of Association between ESR1 and CYP1A1 Gene Polymorphisms and Susceptibility to Uterine Leiomyoma in Female Patients of Iranian Descent
por: Taghizade Mortezaee, Fatemeh, et al.
Publicado: (2014)

Effect of Oxidized Low Density Lipoprotein on the Expression of Runx2 and SPARC Genes in Vascular Smooth Muscle Cells
por: Farrokhi, Effat, et al.
Publicado: (2015)

Screening of DFNB3 in Iranian families with autosomal recessive non-syndromic hearing loss reveals a novel pathogenic mutation in the MyTh4 domain of the MYO15A gene in a linked family
por: Reiisi, Somayeh, et al.
Publicado: (2016)

Genetic Linkage Analysis of 15 DFNB Loci in a Group of Iranian Families with Autosomal Recessive Hearing Loss
por: Tabatabaiefar, MA, et al.
Publicado: (2011)

Mesenchymal stem cells versus their conditioned medium in the treatment of ischemia/reperfusion injury: Evaluation of efficacy and hepatic specific gene expression in mice
por: Khosravi-Farsani, Somayeh, et al.
Publicado: (2022)

The −514C/T Polymorphism of Hepatic Lipase Gene among Iranian Patients with Coronary Heart Disease
por: Ghatreh Samani, K, et al.
Publicado: (2012)

Mutation analysis of VSX1 and SOD1 in Iranian patients with keratoconus
por: Saee-Rad, Samira, et al.
Publicado: (2011)

Antifungal Effects of Iranian Propolis Extract and Royal jelly Against Candida albicans In-Vitro
por: Moghim, Hassan, et al.
Publicado: (2021)

Iranian research output in pediatrics: 1975-2007
por: Malekahmadi, Mohammad Reza, et al.
Publicado: (2011)

Lack of association between TNF-α gene polymorphisms at position -308 A, -850T and risk of simple febrile convulsion in pediatric patients
por: Khoshdel, Abolfazl, et al.
Publicado: (2012)

Correlation Between Mucosal IL-6 mRNA Expression Level and Virulence Factors of Helicobacter pylori in Iranian Adult Patients With Chronic Gastritis
por: Azadegan-Dehkordi, Fatemeh, et al.
Publicado: (2015)

Screening of 10 DFNB Loci Causing Autosomal Recessive Non-Syndromic Hearing Loss in Two Iranian Populations Negative for GJB2 Mutations
por: KOOHIYAN, Mahbobeh, et al.
Publicado: (2019)

A preliminary study of inherited thrombophilic risk factors in different clinical manifestations of venous thromboembolism in central Iran
por: Karimi, Ali, et al.
Publicado: (2015)

Upregulation of Neuroprogenitor and Neural Markers via Enforced miR-124 and Growth Factor Treatment
por: Mehri Ghahfarrokhi, Ameneh, et al.
Publicado: (2020)

Plasma Level Of miR-21 And miR-451 In Primary And Recurrent Breast Cancer Patients
por: Motamedi, Maryam, et al.
Publicado: (2019)

Analysis of Blood Transfusion Data Using Bivariate Zero-Inflated Poisson Model: A Bayesian Approach
por: Mohammadi, Tayeb, et al.
Publicado: (2016)

Analysis of the Factors Affecting the Interval between Blood Donations Using Log-Normal Hazard Model with Gamma Correlated Frailty
por: Tavakol, Najmeh, et al.
Publicado: (2014)

Artificial Neural Network to Modeling Zero-inflated Count Data: Application to Predicting Number of Return to Blood Donation
por: Haghani, Shima, et al.
Publicado: (2017)

Non-communicable diseases in the southwest of Iran: profile and baseline data from the Shahrekord PERSIAN Cohort Study
por: Ahmadi, Ali, et al.
Publicado: (2021)

Clinical Aspects of Microsatellite Instability Testing in Colorectal Cancer
por: Zeinalian, Mehrdad, et al.
Publicado: (2018)

Genetics of Hearing Loss in North Iran Population: An Update of Spectrum and Frequency of GJB2 Mutations
por: Koohiyan, Mahbobeh, et al.
Publicado: (2019)

Investigation of LRTOMT gene (locus DFNB63) mutations in Iranian patients with autosomal recessive non-syndromic hearing loss
por: Taghizadeh, Seyyed Hossein, et al.
Publicado: (2013)

The protocol of a population-based prospective cohort study in southwest of Iran to analyze common non-communicable diseases: Shahrekord cohort study
por: Khaledifar, Arsalan, et al.
Publicado: (2018)

Small supernumerary marker chromosomes and their correlation with specific syndromes
por: Jafari-Ghahfarokhi, Hamideh, et al.
Publicado: (2015)

Familial Colorectal Cancer Type X in Central Iran: A New Clinicopathologic Description
por: Zeinalian, Mehrdad, et al.
Publicado: (2017)

Cannot write session to /tmp/vufind_sessions/sess_p5q7rc86drc9p06mkdigcbp9g6