Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Hemmat E. El Haddad"'
Autor:
Olfat G. Shaker, Amina M. Alnoury, Gehan A. Hegazy, Hemmat E. El Haddad, Safaa Sayed, Ahmed Hamdy
Publikováno v:
Revista Brasileira de Reumatologia, Vol 56, Iss 5, Pp 414-420
ABSTRACT Background: Rheumatoid arthritis is a widely prevalent autoimmune disorder with suggested genetic predisposition. Objectives: The aim of this study is to detect the pattern of genetic polymorphism of methylene tetrahydrofolate reductase (MTH
Externí odkaz:
https://doaj.org/article/ef8958d7248d4a85bbb91c1c3b9f4290
Autor:
Hany William Z. Hanna, Heba N Baz, Lika'a Fasih Y. Al-Kzayer, Hemmat E El Haddad, Fatma El-Mougy
Publikováno v:
Journal of Applied Biomedicine. 20:141-145
Autor:
Hemmat E El Haddad, Mohamed A Marie, Tarek M Samy, Reem Jan Farid, Mai Sherif, Usama A Sharaf El Din
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 26, Iss 3, Pp 460-467 (2015)
This study evaluates tumor necrosis factor (TNF)-alfa gene expression in patients with end-stage renal disease (ESRD) on regular hemodialysis as an expression of cardiovascular disease (CVD) risk even on a sub-clinical level and its relation to some
Externí odkaz:
https://doaj.org/article/c04d6065e5794add95f443d7cda77470
Autor:
Elham M. Yousief, Ahmed Ramadan, Dalia R. Ibrahim, Heba Sedrak, Hemmat E. El Haddad, Mervat Hussin, Rasha M. Abdel Samie
Publikováno v:
International Journal of Diabetes in Developing Countries. 39:641-646
Irisin is a new myokin and adipokine related to human obesity and insulin resistance status. To investigate whether serum irisin is related to glycemic indicators and micro and macrvascular complications in patients with T2DM. The study included 60 T
Autor:
Randa Salam, Hazem. El-Sayed Abou-youssef, Cristiano Rizzo, Hemmat E. El Haddad, Hany William Z. Hanna, Radwa Marawan Abdel Halim
Publikováno v:
The Journal of Steroid Biochemistry and Molecular Biology. 212:105922
Background Hashimoto's thyroiditis (HT) is considered the predominant cause of hypothyroidism in iodine sufficient countries. The deficiency of 25−OH-vitamin D3 serum level and the variation of vitamin D receptor (VDR) gene were implicated in a num
Autor:
Ahmed Hamdy, Olfat G. Shaker, Hemmat E. El Haddad, Gehan A. Hegazy, Amina M. Alnoury, Safaa Sayed
Publikováno v:
Revista Brasileira de Reumatologia. 56(5):414-420
ResumoAntecedentesA artrite reumatoide é uma doença autoimune amplamente prevalente com sugerida predisposição genética.ObjetivosDetectar o padrão de polimorfismo dos genes metilenotetrahidrofolato redutase (MTHFR C677T e A1298C), fator de cres
Autor:
Safaa Sayed, Amina M. Alnoury, Gehan A. Hegazy, Hemmat E. El Haddad, Olfat G. Shaker, Ahmed Hamdy
Publikováno v:
Revista Brasileira de Reumatologia, Volume: 56, Issue: 5, Pages: 414-420, Published: OCT 2016
Revista Brasileira de Reumatologia v.56 n.5 2016
Revista Brasileira de Reumatologia
Sociedade Brasileira de Reumatologia (SBR)
instacron:SBR
Revista Brasileira de Reumatologia, Vol 56, Iss 5, Pp 414-420
Revista Brasileira de Reumatologia v.56 n.5 2016
Revista Brasileira de Reumatologia
Sociedade Brasileira de Reumatologia (SBR)
instacron:SBR
Revista Brasileira de Reumatologia, Vol 56, Iss 5, Pp 414-420
Background: Rheumatoid arthritis is a widely prevalent autoimmune disorder with suggested genetic predisposition. Objectives: The aim of this study is to detect the pattern of genetic polymorphism of methylene tetrahydrofolate reductase (MTHFR C677 T
Publikováno v:
The Egyptian Journal of Internal Medicine, Vol 28, Iss 1, Pp 9-15 (2016)
Objective This study was performed to estimate the prevalence of Epstein-Barr virus immunoglobulin M virus capsid antigen (EBV IgM VCA) among healthy blood donors and to confirm the real risk of transfusion transmission by detection of virus load usi
Publikováno v:
Endocrine Abstracts.
Publikováno v:
Endocrine Abstracts.