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عضویت
فهرست مطالب نویسنده:

m. r. bordbar

  • H. Bordbar*, M. R. Bordbar, R. A. Borzooei, Y. B. Jun

    In the paper [J. Ghosh and T.K. Samanta, Hyperfuzzy sets and hyperfuzzy group, Int. J. Advanced Sci Tech. 41 (2012), 27–37], Ghosh and Samanta introduced the concept of hyperfuzzy sets as a generalization of fuzzy sets and interval-valued fuzzy sets, and applied it to group theory. The aim of this manuscript is to study N -structures in BCK/BCI-algebras induced from hyperfuzzy structures.

    Keywords: hyperfuzzy set, hyperfuzzy structure, hyperfuzzy subalgebra, N-subalgebra, induced N- function
  • J. Hassanzadeh, R. Mohammadi, Ar Rajaeefard, Mr Bordbar, M. Karimi
    Background
    The causes of childhood leukemia as the most common malignancy in children are vastly unknown. The aim of this study is to evaluate the relationship between maternal birth characteristics with environmental exposures in childhood leukemia.
    Methods
    This is a case-control study which consists of children younger than 18 years old suffering from leukemia who reside at Fars Province of Iran. Patients were individually matched with variables such as age, sex and residence region. In order to evaluate the relationships between each variable and the risk of leukemia, odds ratio(OR) and 95% confidence interval (CI) were estimated using conditional logistic regression.
    Results
    Statistically, the association between risk of childhood leukemia with birth order (OR=6.177, 95%CI: 2.551-14.957), pet ownership (OR=2.565, 95%CI: 1.352-4.868) and history of leukemia in first and second degree relatives (OR=2.667, 95%CI: 1.043-6.815) was significant. However, there was no significant association between daycare attendance, history of miscarriage, number of siblings and history of mother's diagnostic radiology tests with risk of childhood leukemia.
    Conclusion
    Although no definite etiologic factor for acute childhood leukemia has been clearly defined, the contribution of environmental risk factors in the context of genetic predisposition are strongly elucidated.
  • S. Haghbin, Z. Serati, Mr Bordbar, H. Tabesh, F. Asmarian
    Background
    Hyperglycemia and hypocalcemia have separately been attributed to adverse outcomes in critically ill patients. This study aimed to investigate the simultaneous effects of the two conditions on mortality and morbidity in a pediatric intensive care unit.
    Methods
    All children aged 1 month to 18 years, admitted for at least 24 hours to medical pediatric intensive care unit (PICU), Nemazee Hospital, Shiraz, Iran were reviewed over one year period. Those with a history of diabetes mellitus and any calcium disorders were excluded.
    Results
    Data on blood glucose and calcium during the first 6 hours of admission, in-PICU length of stay, need for mechanical ventilation, vassopressor drugs administration, and mortality were assessed. The incidence of hyperglycemia [≥150 mg/dl (8.3mmol/L)] and hypocalcemia [serum calcium < 8.5 mg/dl (2.12mmol/L)] were 26.5% and 43.9%, respectively. Hyperglycemia and hypocalcemia were associated with increased mortality. Among the survivors, hyperglycemia and hypocalcemia had no significant effect on PICU length of stay. The interaction of hyperglycemia and hypocalcemia did not intensify their separate effects on mortality, the need for mechanical ventilation and vasopressor infusion.
    Conclusions
    Although hyperglycemia and hypocalcemia separately increase the mortality rate, their simultaneous presence is not associated with poorer outcomes in critically ill patients.
  • Sh Farjadian, F. Azad, Mr Bordbar, M. Karimi
    Background
    Fanconi anemia (FA) is a chromosomal breakage disorder characterized by familial aplastic anemia (AA), various congenital anomalies, and a characteristic chromosomal response to clastogenic stress.
    Methods
    In this study, chromosome breakage test was performed for 38 patients suspected of having FA and age-matched controls.
    Results
    According to the results, ten patients were considered as FA cases and 15 patients with no chromosomal breaks were considered as AA.
    Conclusion
    Differentiation of FA from AA is very important because the primary treatment is different. This test should be done in every primary presentation of AA.
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