Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Hind Shaker Al-Mamoori"'
Publikováno v:
Iraqi Journal of Hematology, Vol 11, Iss 1, Pp 13-18 (2022)
BACKGROUND: Anemia of β thalassemia results from a combination of ineffective erythropoiesis and hemolysis. This stimulates erythropoietin (EPO) production, which causes expansion of the bone marrow and may lead to serious deformities of the skull a
Externí odkaz:
https://doaj.org/article/6886bcba17a1437b9a12b71e1c2d267d
Publikováno v:
Iraqi Journal of Hematology, Vol 10, Iss 2, Pp 152-157 (2021)
BACKGROUND: Corona virus disease 2019 (COVID-19) is a coronavirus that can produce a variety of symptoms, ranging from asymptomatic carrier status to severe respiratory failure, multiple organ dysfunction, and death, it might be associated with hyper
Externí odkaz:
https://doaj.org/article/a596fc6a03d240548f2bd3e53dea64b0
Publikováno v:
Iraqi Journal of Hematology, Vol 9, Iss 2, Pp 150-154 (2020)
BACKGROUND: Blood group O is transfused as a universal blood group in emergencies. The red cells of blood Group O possess no major ABO antigens, while the blood Group O plasma contains naturally occurring IgM anti-A and anti-B and cross-reacting IgG
Externí odkaz:
https://doaj.org/article/265f650e0d4d4e3a91bbc68e7106fa7d
Publikováno v:
Iraqi Journal of Hematology, Vol 9, Iss 1, Pp 23-29 (2020)
BACKGROUND: Sickle cell disease is a monogenic disease with heterogeneous clinical course. Many genetic factors such as inheritance of α-thalassemia trait and fetal hemoglobin (Hb) level, related to the presence of specific haplotypes, are among the
Externí odkaz:
https://doaj.org/article/5f5aeb9ee4354450931cbe48cddcf994
Publikováno v:
Iraqi Journal of Hematology, Vol 6, Iss 2, Pp 55-59 (2017)
Background: B-chronic lymphocytic leukemia (CLL) is a monoclonal malignancy characterized by an accumulation of small mature-looking B lymphocytes in the blood, bone marrow, and other tissues. It is typically characterized by CD5+, CD23+, CD22−, an
Externí odkaz:
https://doaj.org/article/7560411dfc644386a9251473ad87709d
Publikováno v:
Open Access Macedonian Journal of Medical Sciences. 10:817-823
BACKGROUND: COVID-19 coagulopathy manifests by elevation of certain marker of active coagulation as fibrinogen and this increment associated with increased markers of inflammations. AIM: To measure protein C (PC) level in hospitalized patients with C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e4cd8b81b18e28dbfaa8ebea842bbc2e
https://doi.org/10.3889/oamjms.2022.8937
https://doi.org/10.3889/oamjms.2022.8937
Publikováno v:
Iraqi Journal of Hematology, Vol 9, Iss 1, Pp 23-29 (2020)
BACKGROUND: Sickle cell disease is a monogenic disease with heterogeneous clinical course. Many genetic factors such as inheritance of α-thalassemia trait and fetal hemoglobin (Hb) level, related to the presence of specific haplotypes, are among the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::881a045206413660a134a476317e9020
https://doi.org/10.4103/ijh.ijh_20_19
https://doi.org/10.4103/ijh.ijh_20_19
Publikováno v:
Iraqi Journal of Hematology, Vol 6, Iss 2, Pp 55-59 (2017)
Background: B-chronic lymphocytic leukemia (CLL) is a monoclonal malignancy characterized by an accumulation of small mature-looking B lymphocytes in the blood, bone marrow, and other tissues. It is typically characterized by CD5+, CD23+, CD22−, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fc5f28be34c05eac6c4dfa165a6e82d
https://doi.org/10.4103/ijh.ijh_18_17
https://doi.org/10.4103/ijh.ijh_18_17