Seyed Alireza Dastgheib

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 7

Top Topics

Systematic Review

Muscular Dystrophy

Nitric Oxide Synthase

Top Venues

Revista brasileira de ortopedia

BMC medical genetics

Archives of gynecology and obstetrics

Fetal and pediatric pathology

This page only lists publications with an associated author ORCID identifier.

Publications

Mohammad Golshan-Tafti, Reza Bahrami, Seyed Alireza Dastgheib, Mohamad Hosein Lookzadeh, Seyed Reza Mirjalili, Maryam Yeganegi, Zahra Marzban Rad, Maryam Aghasipour, Amirhossein Shahbazi, Ali Masoudi, Mahmood Noorishadkam, Hossein Neamatzadeh
A Comprehensive Compilation of Data on the Relationship Between Surfactant Protein-B (SFTPB) Polymorphisms and Susceptibility to Neonatal Respiratory Distress Syndrome. Fetal and pediatric pathology (2024)
Hossein Golestanpour, Reza Bahrami, Seyed Alireza Dastgheib, Razieh Sadat Tabatabaei, Atiyeh Javaheri, Mojgan Karimi-Zarchi, Seyed Reza Mirjalili, Hossein Neamatzadeh
A meta-analysis for association of eNOS VNTR 4b/a, - 786 T > C and + 894G > T polymorphisms with risk of recurrent pregnancy loss. Archives of gynecology and obstetrics 304 (5) (2021)
Mansour Moghimi, Seyed Alireza Dastgheib, Naeimeh Heiranizadeh, Mohammad Zare, Elnaz Sheikhpour, Hossein Neamatzadeh
ASSOCIATION OF IL-8 -251T>A (RS4073) POLYMORPHISM WITH SUSCEPTIBILITY TO GASTRIC CANCER: A SYSTEMATIC REVIEW AND META-ANALYSIS BASED ON 33 CASE-CONTROL STUDIES. Arquivos de gastroenterologia 57 (1) (2020)
Mohammad Reza Sobhan, Masoud Mahdinezhad-Yazdi, Seyed Alireza Dastgheib, Mohammadali Jafari, Ali Raee-Ezzabadi, Hossein Neamatzadeh
Association of ESRα XbaI A > G, ESRα PvuII T > C and ESRβ AlwNI T > C Polymorphisms with the Risk of Developing Adolescent Idiopathic Scoliosis: A Systematic Review and Genetic Meta-analysis. Revista brasileira de ortopedia 55 (1) (2020)
Mohammad Reza Sobhan, Masoud Mahdinezhad-Yazdi, Seyed Alireza Dastgheib, Hossein Ahrar, Kazem Aghili, Hossein Neamatzadeh
Association of the IL-6 -174G > C (rs1800795) Polymorphism with Adolescent Idiopathic Scoliosis: Evidence from a Case-Control Study and Meta-Analysis. Revista brasileira de ortopedia 55 (1) (2019)
Ghazale Mahjoub, Parham Habibzadeh, Hassan Dastsooz, Malihe Mirzaei, Arghavan Kavosi, Laila Jamali, Haniyeh Javanmardi, Pegah Katibeh, Mohammad Ali Faghihi, Seyed Alireza Dastgheib
Clinical and molecular characterization of three patients with Hepatocerebral form of mitochondrial DNA depletion syndrome: a case series. BMC medical genetics 20 (1) (2019)
Fateme Ziyaee, Eslam Shorafa, Hassan Dastsooz, Parham Habibzadeh, Hamid Nemati, Amir Saeed, Mohammad Silawi, Mohammad Ali Farazi Fard, Mohammad Ali Faghihi, Seyed Alireza Dastgheib
A novel mutation in SEPN1 causing rigid spine muscular dystrophy 1: a Case report. BMC medical genetics 20 (1) (2019)