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Fatemeh Behmanesh

Researcher at Mashhad University of Medical Sciences

Publications -  29
Citations -  552

Fatemeh Behmanesh is an academic researcher from Mashhad University of Medical Sciences. The author has contributed to research in topics: Primary immunodeficiency & Allergy. The author has an hindex of 10, co-authored 29 publications receiving 444 citations. Previous affiliations of Fatemeh Behmanesh include Shiraz University of Medical Sciences & University of Calgary.

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Primary immunodeficiency disorders in Iran: update and new insights from the third report of the national registry.

TL;DR: Registration of Iranian PID patients increased the awareness of medical community of Iran and developed diagnostic and therapeutic techniques across more parts of the country and better estimation of PID in Iran is presented.
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Fourth Update on the Iranian National Registry of Primary Immunodeficiencies: Integration of Molecular Diagnosis

Hassan Abolhassani, +91 more
TL;DR: Among the genetically different categories of PID patients, the diagnostic rate was highest in defects in immune dysregulation and lowest in predominantly antibody deficiencies and mutations in the MEFV gene were the most frequent genetic disorder in this cohort.
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Pistachio Allergy-Prevalence and In vitro Cross-Reactivity with Other Nuts

TL;DR: Exposure of people to pistachio significantly affects the prevalence of its allergic reactions and it was observed that, among Pistachio allergic subjects, such exposure may affect the co-sensitivities with other nuts, including cashew and almond.
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Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort.

Reza Yazdani, +90 more
TL;DR: First presentations in most patients with Immunodeficiency, Centromeric instability, and Facial dysmorphism were respiratory complications, whereas first presentations in patients with lipopolysaccharides-responsive beige-like anchor deficiency were nonrespiratory complications, highlighting similarities and differences in the clinical and genetic spectrum of the most common PAD-associated gene defects.