Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Amira Elhoufey PhD"'
Autor:
Omnia El-Badawy MD, PhD, Nahla M. Elsherbiny MD, PhD, Doaa Abdeltawab MD, PhD, Doaa M. Magdy MD, PhD, Lamees M. Bakkar MD, PhD, Shimaa A. Hassan MD, PhD, Elham A. Hassan MD, PhD, Ahmed M. Thabet MD, PhD, Ahmed M. Ashmawy MD, PhD, Ehab F. Moustafa MD, PhD, Wael A. Abbas MD, PhD, Ahmad Bahieldeen Ahmad MD, PhD, Amal Rayan MD, PhD, Khaled Saad MD, PhD, Amira Elhoufey PhD, Hosni A. M. Hussein PhD, Ali A. Thabet PhD, Asmaa M. Zahran MD, PhD
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis, Vol 28 (2022)
Aim Our study's objectives were to study the clinical and laboratory characteristics that may serve as biomarkers for predicting disease severity, IL-10 levels, and frequencies of different T cell subsets in comorbid COVID-19 patients. Methods Sixty-
Externí odkaz:
https://doaj.org/article/daa7564817004c06adb966d770e053c4
Autor:
Asmaa M. Zahran MD, Asmaa Nafady MD, Khaled Saad MD, Helal F. Hetta MD, Alam-Eldin M. Abdallah MD, Safwat M. Abdel-Aziz MD, Mostafa M. Embaby MD, Amir M. Abo Elgheet MD, Sanaa F. Darwish PhD, Mohamed Gamil M. Abo-Elela MD, Amira Elhoufey PhD, Khalid I. Elsayh MD
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis, Vol 26 (2020)
Background: Neutrophil-to-lymphocyte ratio (NLR) was introduced as a potential inflammatory marker in sickle cell disease (SCD). This study aimed to evaluate the impact of hydroxyurea (HU) treatment on the value of NLR and some inflammatory mediators
Externí odkaz:
https://doaj.org/article/9fc234b896ba40f580f635718562a4c9
Autor:
Asmaa M. Zahran MD, Khaled Saad MD, Mohamed Gamil Abo-Elela MD, Esraa M. Eloseily MD, Eman F. Gad MD, Amir M. Abo Elgheet MD, Rasha R. Mahmmoud MD, Mervat A. M. Youssef MD, Mona M. Abdelmeguid MD, Bahaa Hawary MD, Sanaa F. Darwish MD, Amira Elhoufey PhD, Khalid I. Elsayh MD
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis, Vol 25 (2019)
Gaucher disease (GD) is one of the most important lysosomal storage disorders. T-lymphocytes perform and regulate many of the immune processes and play a major role in immune homeostasis. Studies have shown that GD causes impairment in T-lymphocyte f
Externí odkaz:
https://doaj.org/article/5c4d23966bd8448db03a3a56cf937fcb
Autor:
Asmaa M. Zahran MD, Khalid I. Elsayh MD, Khaled Saad MD, Mostafa M. Embaby MD, Mervat A. M. Youssef MD, Yasser F. Abdel-Raheem MD, Shaban M. Sror MD, Shereen M. Galal MD, Helal F. Hetta MD, Mohamed Diab Aboul-Khair MD, Mohamd A. Alblihed PhD, Amira Elhoufey PhD
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis, Vol 25 (2019)
Sickle cell disease (SCD) is a genetically inherited hemolytic anemia increasingly appreciated as a chronic inflammatory condition and hypercoagulable state with high thrombotic risk. It is associated with disturbed immune phenotype and function and
Externí odkaz:
https://doaj.org/article/363de7f4fb9543e190dbd3eee057bd4f