Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Nashwa M Al Azizi"'
Publikováno v:
Minerva pediatrics.
Background Assessment of the left ventricular function in the dialysis children and explore its association with vitamin D level and markers reflecting calcium and phosphate metabolism. Methods In this case-control study, we enrolled forty children o
Autor:
Mayy A.N. Allah, Mohammed E. Hamed, Hind M. Abdelrahman, Eman A. Bendary, Maha A. Noah, Rehab M. Nabil, Salah F. Alsayed, Ahmed R. Ahmed, Lamiaa M. Kamel, Ghada M. Al-Akad, Ahmed A. Emam, Nasser I. Abdelsalam, Heba H. Gawish, Mustafa I.A. Hashem, Seham F. Azab, Nashwa M Al Azizi, Dalia S. Fahmy, Yasser F Ali, Mohsen A.A. Farghaly
Publikováno v:
Medicine
Systemic lupus erythematosus (SLE) is a multisystemic autoimmune disease. The vitamin D receptor (VDR) gene is a candidate gene for susceptibility to autoimmune disorders. To date, only a few studies concerned the association of the VDR gene polymorp
Autor:
Asmaa Esh, Ebtesam E. Khalil, Maha Atfy, Mohamed M. El Naggar, Layla Sherief, Nashwa M Al Azizi
Publikováno v:
Indian Journal of Hematology and Blood Transfusion. 27:18-25
Impaired apoptosis is mediated by members of the inhibitor of apoptosis proteins (IAP) family such as survivin. Survivin was described in number of different tumors and found to correlate with poor prognosis in a variety of cancers including hematolo
Publikováno v:
Nucleosides, Nucleotides and Nucleic Acids. 29:228-236
In order to assess the potential biochemical markers in the development, diagnosis, and prognosis of diabetic patient with microvascular complication represented with retinopathy, we analyzed the levels of cell-free DNA by two different techniques. T
Publikováno v:
OncoTargets and therapy
Ebtesam I Ahmad, Heba H Gawish, Nashwa MA Al Azizi, Ashraf M ElhefniClinical Pathology Department, Hematology and Oncology Unit of Internal Medicine Department, Faculty of Medicine, Zagazig University, Sharkia, EgyptBackground: Activating point mutat
Publikováno v:
Leukemia research. 35(10)
Background Philadelphia-chromosome positive acute myeloid leukemia (Ph+ AML) is a rare entity and patient prognosis is poor, with short median survival. Biphenotypic acute leukemia (BAL) is a rare disorder that is difficult to diagnose and it display
Autor:
Mayy A.N. Allah, Nasser I. Abdelsalam, Dalia S. Fahmy, Rehab M. Nabil, Nashwa M Al Azizi, Heba H. Gawish, Ahmed R. Ahmed, Hind M. Abdelrahman, Heba Gamal Anany, Hany E. Ibrahim, Salah F. Alsayed, Hosam F. Elsaadany, Boshra R. Ibrahim, Shaimaa S. A. Elashkar, Mohsen A.A. Farghaly, Sanaa M. Ismail, Manar Fathy, Ghada M. Al-Akad, Maha A. Noah, Mohammed E. Hamed, Yasser F Ali
Publikováno v:
Italian Journal of Pediatrics
Background Juvenile Idiopathic Arthritis (JIA) is the most common chronic arthritis in children worldwide. Among anti-inflammatory cytokines, interleukin-10 (IL-10) is a key immunosuppressive cytokine involved in the pathogenesis of JIA. To date, onl