Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Mona Fathey Abdel Fattah Hassan"'
Autor:
Rawda Ahmed Alaaeldin Ahmed Mohamed Saad, Amany Ahmed Osman, Mona Fathey Abdel Fattah Hassan, Shereen Abdel Monem Ibrahim, Yasmin Nabil El-Sakhawy
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 22, Iss 1, Pp 1-11 (2021)
Abstract Background Acute myeloid leukemia (AML) is a disorder characterized by a rapid onset of symptoms attributable to bone marrow failure due to clonal proliferation of primitive hematopoietic stem cells or progenitor cells. Epigenetic abnormalit
Externí odkaz:
https://doaj.org/article/c502983aa2484b83a047184a999ed1b9
Autor:
Amany Ahmed Osman, Yasmin N El-Sakhawy, Rawda Ahmed Alaa Eldin, Mona Fathey Abdel Fattah Hassan, Shereen Abdel-Monem Ibrahim
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 22, Iss 1, Pp 1-11 (2021)
Background Acute myeloid leukemia (AML) is a disorder characterized by a rapid onset of symptoms attributable to bone marrow failure due to clonal proliferation of primitive hematopoietic stem cells or progenitor cells. Epigenetic abnormalities play
Autor:
Mona Fathey Abdel Fattah Hassan, Marwa G Ibrahim, Nayera Hazaa Khalil Elsherif, Sara M. Makkeyah
Publikováno v:
QJM: An International Journal of Medicine. 114
Background Autoimmune cytopenias are characterized by the production of autoantibodies against differentiated hematopoietic cells because of defects in central and/or peripheral tolerance. It includes autoimmune hemolytic anemia (AIHA), immune thromb
Autor:
Eldin, Rawda Ahmed Alaa1 (AUTHOR) rawdaalaa_12@yahoo.com, Osman, Amany Ahmed1 (AUTHOR), Hassan, Mona Fathey Abdel Fattah1 (AUTHOR), Ibrahim, Shereen Abdel Monem1 (AUTHOR), El-Sakhawy, Yasmin Nabil1 (AUTHOR)
Publikováno v:
Egyptian Journal of Medical Human Genetics. 5/3/2021, Vol. 22 Issue 1, p1-11. 11p.