مرور Volume 3, Issue 4 بر اساس تاریخ انتشار
در حال نمایش موارد 1 - 6 از 6
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Congenital fusion of cervical vertebrae: a review on embryological etiology
(Mashhad University of Medical Sciences, 2016-11-01)Congenital fusion of cervical vertebrae is a rare anomaly. In this condition, two fused vertebrae appear structurally and functionally as one. This anomaly may be symptomatic or asymptomatic. Myelopathy, limitation in neck ...
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The prognostic value of conventional imaging tools to determine how patients with hodgkin lymphoma will respond to treatment
(Mashhad University of Medical Sciences, 2016-11-01)Introduction: This systematic review studies the prognostic value of two conventional imaging tools, sestamibi and gallium scans, for predicting how patients with Hodgkin lymphoma will respond to treatment.
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The role of Toll-Like Receptor Gene Polymorphisms in Tuberculosis Susceptibility: A Systematic Review and Meta-Analysis
(Mashhad University of Medical Sciences, 2016-11-01)Introduction: Susceptibility to tuberculosis (TB) infection varies in individuals and is linked to genetic variations in the toll-like receptors (TLRs) genes. The current study employed a systematic ...
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Atopic dermatitis and the therapeutic methods: a literature review
(Mashhad University of Medical Sciences, 2016-11-01)Atopic dermatitis is an inflammatory skin disease that starts in the early life and usually persists by the end of life in 20% of cases. The disease shows multiple periods of relapse, and significantly affects the patient's ...
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Avian influenza virus and human: pandemic concern and threat?
(Mashhad University of Medical Sciences, 2016-11-01)Type A influenza viruses causes infections in human and animals, especially in birds. Wild aquatic birds are the natural hosts for all known influenza type A viruses. Avian type viruses are divided into two groups: highly ...
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Thyroxin-binding globulin deficiency in a boy with fragile X syndrome: a case report
(Mashhad University of Medical Sciences, 2016-11-01)Fragile X syndrome (FXS) is the most common known genetic cause of male intellectual disability. A wide variety of medical problems has been reported in FXS syndrome including seizures, facial abnormalities, macroorchidism, ...



