Hossein Neámatzadeh

ORCID: 0000-0003-1031-9288
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About
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Research Areas
  • Pregnancy and preeclampsia studies
  • Cytokine Signaling Pathways and Interactions
  • Neonatal Respiratory Health Research
  • DNA Repair Mechanisms
  • Folate and B Vitamins Research
  • COVID-19 and healthcare impacts
  • Genetic factors in colorectal cancer
  • BRCA gene mutations in cancer
  • Birth, Development, and Health
  • COVID-19 Impact on Reproduction
  • Cleft Lip and Palate Research
  • Congenital Diaphragmatic Hernia Studies
  • Reproductive System and Pregnancy
  • Blood Coagulation and Thrombosis Mechanisms
  • Gestational Diabetes Research and Management
  • Protease and Inhibitor Mechanisms
  • Osteoarthritis Treatment and Mechanisms
  • Cancer-related Molecular Pathways
  • Estrogen and related hormone effects
  • Cancer-related molecular mechanisms research
  • Helicobacter pylori-related gastroenterology studies
  • Acute Lymphoblastic Leukemia research
  • Streptococcal Infections and Treatments
  • Growth Hormone and Insulin-like Growth Factors
  • Scoliosis diagnosis and treatment

Shahid Sadoughi University of Medical Sciences and Health Services
2016-2025

Iran University of Medical Sciences
2016-2021

Shiraz University of Medical Sciences
2020-2021

Background: The tumorigenesis of lung cancer is complicated, and genetic factor may have the role in malignant transformation cells. IL-10 gene polymorphisms been evaluated for their potential roles cancer. However, those studies results are controversial. To clarify effects rs1800871, rs1800872 rs1800896 on risk cancer, a meta-analysis was performed with eligible individual studies. Methods: Eligible publications were gathered by retrieving PubMed, Web Science, Embase, Wan Fang, CNKI up to...

10.31557/apjcp.2024.25.1.287 article EN cc-by Asian Pacific Journal of Cancer Prevention 2024-01-01

Breast cancer is a serious health problem. Early detection crucial for optimal treatment and reducing mortality.The aim of this study was to evaluate beliefs concerning performance breast self- examination (BSE) mammography in sample Iranian female workers.This cross-sectional performed among 441 care workers (physicians=88, nurses=163, midwives=38, officers=68, others=84) 3 different centers Yazd, Iran. Data were collected using self administered questionnaire which included demographic...

10.7314/apjcp.2014.15.22.9817 article EN cc-by Asian Pacific Journal of Cancer Prevention 2014-12-18

Studies on the CXCL12 rs1801157 polymorphism show that this is involved in development of breast cancer, but its specific relationships or effects are not consistent. The purpose meta-analysis was to investigate association between and susceptibility cancer. PubMed, Scopus, Embase, Cochrane Library, Web Science, CNKI were searched for eligible studies through February 01, 2023. A total ten with 2093 cases 2302 controls included meta-analysis. Overall, there a significant risk cancer under...

10.31557/apjcp.2024.25.3.767 article EN cc-by Asian Pacific Journal of Cancer Prevention 2024-03-01

The coronavirus disease 2019 (COVID-19) pandemic is the main challenges to public health systems worldwide now. Cancer patients are considered as a high risk group during COVID-19 pandemic. Considering evidence so far, cancer underlying comorbidities might increase of death in with COVID-19. Many increased contracting than general population regularly visit facilities for treatment and surveillance. Thus, has profound impact on care treatment. Here, we attempted summarize current suggestions...

10.18502/acta.v61i8.14900 article EN cc-by-nc ACTA MEDICA IRANICA 2024-02-18

BackgroundInsulin-like growth factor-II (IGF-II) has a prominent role in fetal and development. The aim of this study was to investigate the association IGF-II Apa1 MspI polymorphisms with intrauterine restriction (IUGR) risk. Methods: A total 45 infants IUGR appropriate for gestational (AGA) were enrolled. Genotyping assayed by PCR-RFLP approach. Results: heterozygote genotype (AG) CT associated an increased risk IUGR. Genotypes alleles polymorphism had no significant susceptibility (P >...

10.1080/15513815.2020.1745970 article EN Fetal and Pediatric Pathology 2020-04-05

<title>Abstract</title> Background This study aims to perform a comprehensive meta-analysis of existing literature elucidate the associations between genetic variations in XPD gene and risk prostate cancer development. Methods A systematic search multiple databases, including PubMed, Scopus, EMBASE, CNKI, was executed up until January 1, 2025, collect pertinent information. The utilized relevant keywords MeSH terms pertaining factors. Inclusion criteria were established for original...

10.21203/rs.3.rs-5770719/v1 preprint EN cc-by Research Square (Research Square) 2025-01-10

<title>Abstract</title> Background Idiopathic short stature (ISS) poses substantial challenges in pediatric growth assessment due to its multifactorial origins. This meta-analysis explores the relationship between IGF1R polymorphisms and risk of ISS children. Methods A comprehensive literature review was performed utilizing PubMed, Web Knowledge, CNKI, culminating on January 1, 2025, focusing studies published before this date. The search employed relevant keywords MeSH terms related...

10.21203/rs.3.rs-5865273/v1 preprint EN cc-by Research Square (Research Square) 2025-01-24
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