Hasil Pencarian - Seyed Alireza Dastgheib

Perbaiki Hasil
  1. 1
    Gender difference in determinant factors of being overweight among the 40–70-year-old population of Kharameh cohort study, Iran

    Gender difference in determinant factors of being overweight among the 40–70-year-old population of Kharameh cohort study, Iran oleh Seyed Alireza Dastgheib, Abbas Rezaianzadeh, Najmeh Maharlouei, Salar Rahimikazerooni, Kamran B. Lankarani

    Diterbitkan 2021-04-01
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  2. 2
    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

    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 oleh Mansour MOGHIMI, Seyed Alireza DASTGHEIB, Naeimeh HEIRANIZADEH, Mohammad ZARE, Elnaz SHEIKHPOUR, Hossein NEAMATZADEH

    Diterbitkan 2020-02-01
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  3. 3
    A thorough analysis of data on the correlation between COL9A1 polymorphisms and the susceptibility to congenital talipes equinovarus: a meta-analysis

    A thorough analysis of data on the correlation between COL9A1 polymorphisms and the susceptibility to congenital talipes equinovarus: a meta-analysis oleh Mohammad Golshan-Tafti, Seyed Alireza Dastgheib, Kamran Alijanpour, Reza Bahrami, Mahta Mazaheri, Hossein Neamatzadeh

    Diterbitkan 2024-06-01
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  4. 4
    Association of MMP-2 -753C>T and MMP-9 -1562C>T Polymorphisms with Chronic/Aggressive Periodontitis Risk: A Systematic Review and Meta-Analysis

    Association of MMP-2 -753C>T and MMP-9 -1562C>T Polymorphisms with Chronic/Aggressive Periodontitis Risk: A Systematic Review and Meta-Analysis oleh Fatemeh MASHHADIABBAS, Hossein NEAMATZADEH, Elnaz FOROUGHI, Seyed Alireza DASTGHEIB, Soudabeh FARAHNAK, Rezvan NASIRI, Shima AHMADI

    Diterbitkan 2019-07-01
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  5. 5
    Association of the IL-6 -174G > C (rs1800795) Polymorphism with Adolescent Idiopathic Scoliosis: Evidence from a Case-Control Study and Meta-Analysis

    Association of the IL-6 -174G > C (rs1800795) Polymorphism with Adolescent Idiopathic Scoliosis: Evidence from a Case-Control Study and Meta-Analysis oleh Mohammad Reza Sobhan, Masoud Mahdinezhad-Yazdi, Seyed Alireza Dastgheib, Hossein Ahrar, Kazem Aghili, Hossein Neamatzadeh

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  6. 6
    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

    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 Met... oleh Mohammad Reza Sobhan, Masoud Mahdinezhad-Yazdi, Seyed Alireza Dastgheib, Mohammadali Jafari, Ali Raee-Ezzabadi, Hossein Neamatzadeh

    Diterbitkan 2020-03-01
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  7. 7
    EPS8 variant causes deafness, autosomal recessive 102 (DFNB102) and literature review

    EPS8 variant causes deafness, autosomal recessive 102 (DFNB102) and literature review oleh Zahra Abbasi, Hossein Jafari Khamirani, Seyed Mohammad Bagher Tabei, Jamal Manoochehri, Mehdi Dianatpour, Seyed Alireza Dastgheib

    Diterbitkan 2023-01-01
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  8. 8
    A single-amino-acid in-frame deletion in CYP17A1 results in combined 17-hydroxylase and 17,20-lyase deficiency in an Iranian family despite the protein mutation site

    A single-amino-acid in-frame deletion in CYP17A1 results in combined 17-hydroxylase and 17,20-lyase deficiency in an Iranian family despite the protein mutation site oleh Ashkan Habib, Alireza Shojazadeh, Mohadeseh Molayemat, Hossein Jafari Khamirani, Sina Zoghi, Seyed Alireza Dastgheib, Asadollah Habib

    Diterbitkan 2021-07-01
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  9. 9
    A novel PTRH2 missense mutation causing IMNEPD: a case report

    A novel PTRH2 missense mutation causing IMNEPD: a case report oleh Hossein Jafari Khamirani, Sina Zoghi, Mehdi Dianatpour, Aria Jankhah, Seyed Sajjad Tabei, Sanaz Mohammadi, Seyed Alireza Dastgheib

    Diterbitkan 2021-06-01
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  10. 10
    Proportion of hematological cancer patients with SARS-CoV-2 infection during the COVID-19 pandemic: A systematic review and meta-analysis

    Proportion of hematological cancer patients with SARS-CoV-2 infection during the COVID-19 pandemic: A systematic review and meta-analysis oleh Mohammadali Jafari, Seyed Alireza Dastgheib, Farzad Ferdosian, Hamid Mirjalili, Hossein Aarafi, Mahmood Noorishadkam, Mahta Mazaheri, Hossein Neamatzadeh

    Diterbitkan 2022-04-01
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  11. 11
    A candidate gene association study of bone mineral density in an Iranian population.

    A candidate gene association study of bone mineral density in an Iranian population. oleh Seyed Alireza Dastgheib, Alison Gartland, Seyed Mohammad Bagher Tabei, Seyed Mohammad Bagher Tabei, Gholamhossein Ranjbar Omrani, Marion Dawn Teare

    Diterbitkan 2016-10-01
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  12. 12
    Association of IL-6 −174 G>C Polymorphism with Susceptibility to Colorectal Cancer and Gastric Cancer: a Systematic Review and Meta-Analysis

    Association of IL-6 −174 G>C Polymorphism with Susceptibility to Colorectal Cancer and Gastric Cancer: a Systematic Review and Meta-Analysis oleh Jamal Jafari-Nedooshan, Seyed Alireza Dastgheib, Saeed Kargar, Mohammad Zare, Ali Raee-Ezzabadi, Naeimeh Heiranizadeh, Jalal Sadeghizadeh-Yazdi, Hossein Neamatzadeh

    Diterbitkan 2020-02-01
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  13. 13
    Association of PAI-1 rs1799889 Polymorphism with Susceptibility to Ischemic Stroke: a Huge Meta-Analysis based on 44 Studies

    Association of PAI-1 rs1799889 Polymorphism with Susceptibility to Ischemic Stroke: a Huge Meta-Analysis based on 44 Studies oleh Mohammadali Jafari, Mohammad Hossein Jarahzadeh, Seyed Alireza Dastgheib, Neda Seifi-Shalamzari, Ali Raee-Ezzabadi, Jalal Sadeghizadeh-Yazdi, Elahe Akbarian, Hossein Neamatzadeh

    Diterbitkan 2020-01-01
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  14. 14
    Clinical and molecular characterization of three patients with Hepatocerebral form of mitochondrial DNA depletion syndrome: a case series

    Clinical and molecular characterization of three patients with Hepatocerebral form of mitochondrial DNA depletion syndrome: a case series oleh Ghazale Mahjoub, Parham Habibzadeh, Hassan Dastsooz, Malihe Mirzaei, Arghavan Kavosi, Laila Jamali, Haniyeh Javanmardi, Pegah Katibeh, Mohammad Ali Faghihi, Seyed Alireza Dastgheib

    Diterbitkan 2019-10-01
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  15. 15
    A novel mutation in SEPN1 causing rigid spine muscular dystrophy 1: a Case report

    A novel mutation in SEPN1 causing rigid spine muscular dystrophy 1: a Case report oleh Fateme Ziyaee, Eslam Shorafa, Hassan Dastsooz, Parham Habibzadeh, Hamid Nemati, Amir Saeed, Mohammad Silawi, Mohammad Ali Farazi Fard, Mohammad Ali Faghihi, Seyed Alireza Dastgheib

    Diterbitkan 2019-01-01
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  16. 16
    Two novel Warburg micro syndrome 1 cases caused by pathogenic variants in RAB3GAP1

    Two novel Warburg micro syndrome 1 cases caused by pathogenic variants in RAB3GAP1 oleh Omid Alavi, Hossein Jafari Khamirani, Sina Zoghi, Afrooz Feili, Seyed Alireza Dastgheib, Seyed Mohammad Bagher Tabei, Jamal Manoochehri, Seyed Mehdi Panahandeh, Majid Kamali, Mehdi Dianatpour

    Diterbitkan 2021-10-01
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  17. 17
    A novel frameshift pathogenic variant in ST3GAL5 causing salt and pepper developmental regression syndrome (SPDRS): A case report

    A novel frameshift pathogenic variant in ST3GAL5 causing salt and pepper developmental regression syndrome (SPDRS): A case report oleh Jamal Manoochehri, Seyed Alireza Dastgheib, Hossein Jafari Khamirani, Maryam Mollaie, Zahra Sharifi, Sina Zoghi, Seyed Mohammad Bagher Tabei, Sanaz Mohammadi, Fatemeh Dehghanian, Zahra Farbod, Mehdi Dianatpour

    Diterbitkan 2021-08-01
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  18. 18
    A pathogenic variant of TULP3 causes renal and hepatic fibrocystic disease

    A pathogenic variant of TULP3 causes renal and hepatic fibrocystic disease oleh Hossein Jafari Khamirani, Vivek Reddy Palicharla, Seyed Alireza Dastgheib, Mehdi Dianatpour, Mehdi Dianatpour, Mohammad Hadi Imanieh, Seyed Sajjad Tabei, Whitney Besse, Saikat Mukhopadhyay, Karel F. Liem

    Diterbitkan 2022-10-01
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  19. 19
    Correction: A novel frameshift pathogenic variant in ST3GAL5 causing salt and pepper developmental regression syndrome (SPDRS): a case report

    Correction: A novel frameshift pathogenic variant in ST3GAL5 causing salt and pepper developmental regression syndrome (SPDRS): a case report oleh Jamal Manoochehri, Seyed Alireza Dastgheib, Hossein Jafari Khamirani, Maryam Mollaie, Zahra Sharifi, Sina Zoghi, Seyed Mohammad Bagher Tabei, Sanaz Mohammadi, Fatemeh Dehghanian, Zahra Farbod, Mehdi Dianatpour

    Diterbitkan 2021-11-01
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  20. 20
    Correlation of TNF-α polymorphisms with susceptibility to lung cancer: evidence from a meta-analysis based on 29 studies

    Correlation of TNF-α polymorphisms with susceptibility to lung cancer: evidence from a meta-analysis based on 29 studies oleh Seyed Masoud HaghighiKian, Ahmad Shirinzadeh-Dastgiri, Reza Ershadi, Mohammad Vakili-Ojarood, Maedeh Barahman, Seyed Alireza Dastgheib, Fatemeh Asadian, Amirmasoud Shiri, Maryam Aghasipour, Amirhossein Rahmani, Kazem Aghili, Hossein Neamatzadeh

    Diterbitkan 2024-09-01
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