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    Prevalence of protein-energy wasting and its various types in Iranian hemodialysis patients: A new classification 

    Hadi Tabibi; Atefeh As'Habi; Behnaz Nozary Heshmati; Mitra Mahdavi-Mazdeh; Mehdi Hedayati (2012-11-01)
    Background: This study was designed to determine the prevalence of protein-energy wasting (PEW) and its various types in hemodialysis (HD) patients in Tehran, Iran. Methods: For this cross-sectional study, 291 HD patients ...
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    Analysis of loss of heterozygsity effect on thyroid tumor with oxyphilia cell locus in familial non medullary thyroid carcinoma in Iranian families 

    Hasti Atashi Shirazi; Mehdi Hedayati; Maryam Sadat Daneshpour; Abdollah Shafiee; Fereidoun Azizi; Fereidoun Azizi; Fereidoun Azizi (2012-09-01)
    Material and Methods: 22 nuclear families (78 persons including 12 patients) with papillary and follicular tumors were selected in a period of six months from Milad hospital. Five microsatellite markers (D19S413, D19S391, ...
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    Dietary assessment of hemodialysis patients in Tehran, Iran 

    Atefeh As'Habi; Hadi Tabibi; Anahita Houshiar Rad; Behnaz Nozary Heshmati; Mitra Mahdavi-Mazdeh; Mehdi Hedayati (2011-10-01)
    Inadequate dietary intakes are a major determinant of malnutrition in hemodialysis (HD) patients. Considering the lack of information available on dietary intakes of HD patients in Iran, the present study was designed to ...
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    Skewed mutational spectrum of RET proto-oncogene Exon10 in Iranian patients with medullary thyroid carcinoma 

    Marjan Zarif Yeganeh; Sara Sheikholeslami; Golnoush Dehbashi Behbahani; Samaneh Farashi; Mehdi Hedayati (2015-07-29)
    © 2015, International Society of Oncology and BioMarkers (ISOBM). Thyroid cancer is the most common endocrine malignant tumor. Medullary thyroid carcinoma (MTC) is an aggressive tumor arising from calcitonin-producing ...
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    Allele frequency distribution for D11S1304, D11S1998, and D11S934 and metabolic syndrome in TLGS 

    Maryam Sadat Daneshpour; Maryam Sadat Daneshpour; Suad Alfadhli; Massoud Houshmand; Sirous Zeinali; Mehdi Hedayati; Maryam Zarkesh; Fereidoun Azizi (2010-12-01)
    Different variant frequencies may lead to different frequencies of the same variants in individuals with drugs resistance and disease susceptibility at the population level. In this study, the allele frequency of three ...
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    Age-specific seroprevalence of hepatitis A infection among children visited in pediatric hospitals of Tehran, Iran 

    Ali Jafari Mehr; Ali Jafari Mehr; Mohammad Javad Ehsani Ardakani; Mehdi Hedayati; Saeed Shahraz; Elnaz Jafari Mehr; Mohammad Reza Zali (2004-04-22)
    Background: Hepatitis A is an enterically transmitted disease that still remains endemic in many developing countries. In some countries improvements in living conditions have recently led to changing in epidemiology of ...
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    Association of Apo E gene polymorphism with HDL level in Tehranian population 

    Maryam S. Daneshpour; Mehdi Hedayati; Parisa Eshraghi; Fereidoun Azizi (2010-07-01)
    The prevalence of cardiovascular risk factors, especially low level of high density lipoprotein cholesterol (HDL-C), is very high in Iran. The associations of apolipoprotein E (Apo E) polymorphism with lipid profile, ...
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    ApoB (XbaI) polymorphism and lipid variation in Teharnian population 

    Maryam S. Daneshpour; Bita Faam; Mehdi Hedayati; Parisa Eshraghi; Fereidoun Azizi (2011-04-01)
    This study examines the association of XbaI apolipoprotein B polymorphism with lipid related variables in Tehran lipid and glucose study. 809 subjects from the TLGS population were selected, anthropometrical and biochemical ...
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    Association of ATP-binding cassette transporter-A1 polymorphism with apolipoprotein AI level in Tehranian population 

    Sohrab Halalkhor; Seyed Alireza Mesbah-Namin; Maryam Sadat Daneshpour; Mehdi Hedayati; Fereidoun Azizi (2011-04-01)
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    A novel succinate dehydrogenase type B mutation in an Iranian family. Its genetic and clinical evaluation 

    Ali A. Ghazi; Ali Mosaddegh Khah; Fereshteh Kamani; Khandan Zare; Alireza Sadeghipour; Mehdi Hedayati; Marjan Zarif Yeganeh; Treena Cranston; Ashley Grossman (2014-01-01)
    © 2014 Hellenic Endocrine Society. All rights reserved. Succinate Dehydrogenase-B (SDH-B) gene mutations constitute one of the most frequent forms of hereditary paragangliomas (PGL). Genetic study is advised in all cases ...

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    Mehdi Hedayati (10)
    Fereidoun Azizi (5)Maryam Sadat Daneshpour (3)Atefeh As'Habi (2)Behnaz Nozary Heshmati (2)Hadi Tabibi (2)Marjan Zarif Yeganeh (2)Maryam S. Daneshpour (2)Mitra Mahdavi-Mazdeh (2)Parisa Eshraghi (2)... View MoreSubject
    Iran (10)
    Hemodialysis (2)ABCA1 (1)Allele frequency (1)Anti-HAV IgG (1)Apo B polymorphism (1)Apo E polymorphism (1)ApoA1 (1)Children (1)Chromosome 11 (1)... View MoreDate Issued2010 - 2015 (9)2004 - 2009 (1)Has File(s)No (10)

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