Results 1 to 10 of about 65 (62)
Health Science Reports, 2023 Background and Aims Major sickle cell syndromes are subjected to a high frequency of hemolysis, infections, oxidative stress, and vasooclusive crises which promote inflammation and iron balance disorders. We aimed to systematically review and analyze the
Prosper Cabral Nya Biapa, TUONO Romaric
exaly +3 more sources
Journal of Thrombosis and Haemostasis, Volume 20, Issue 8, Page 1852-1858, August 2022., 2022 Abstract Background Thrombosis may complicate autoimmune hemolytic anemia (AIHA), but its predictors are still lacking, and no clear‐cut indications for anticoagulant prophylaxis are available. Objectives To characterize frequency and severity of thromboses in AIHA patients and identify risk factors for thrombosis that may advise primary anticoagulant ...
Bruno Fattizzo +5 more
wiley +1 more source
Evidence-Based Complementary and Alternative Medicine, Volume 2022, Issue 1, 2022., 2022 Background. Sickle cell anemia (SCA) or sickle cell disease (SCD) is a genetic disease associated with increased morbidity and mortality in Africa and other developing nations. Therefore, modern and traditional remedies are being introduced for use in the treatment and management of this disease.
Natacha Lena Yembeau +8 more
wiley +1 more source
Hematology Reports, 2010 Sickle Cell Disorder (SCD) is a congenital hemoglobinopathy. There is little in literature regarding the psychological variables affecting individuals living with SCD and all of the significant people around them.
Oluwatoyin Olatundun Ilesanmi
doaj +1 more source
, 2023 HemaSphere, Volume 7, Issue S1, Page 54-55, April 2023.
J.E.M. Maran +9 more
wiley +1 more source
P‐099: ANTI‐SICKLING STUDY OF THE AQUEOUS EXTRACTS OF TINOSPORA CARDIFOLIA AND TERMINALIA BELLIRICA
, 2022 HemaSphere, Volume 6, Issue S4, Page 61-61, August 2022.
PATRA S.
wiley +1 more source
ROLE OF STEM CELL FACTOR IN THE REACTIVATION OF HUMAN FETAL HEMOGLOBIN
Mediterranean Journal of Hematology and Infectious Diseases, 2009 In humans the switch from fetal to adult hemoglobin (HbF→ HbA) takes place in the perinatal and postnatal period, determining the progressive replacement of HbF with HbA synthesis ( i.e., the relative HbF content in red blood cells decreases from 80-90%
Marco Gabbianelli, Ugo Testa
doaj +3 more sources
Renal Thrombotique microangiopathy: An unusual renal involvement in Niemann‐Pick disease type B
Clinical Case Reports, Volume 8, Issue 12, Page 3315-3320, December 2020., 2020 Renal involvement in Niemann‐Pick disease type B is very rare. Kidney check‐up and renal biopsy should be performed in any patient presented with hypertension and kidney disease. Histology identifies the lesion, the prognosis, and guide treatment. Abstract Renal involvement in Niemann‐Pick disease type B is very rare.
Mouna Jerbi +6 more
wiley +1 more source
Evidence-Based Complementary and Alternative Medicine, Volume 2020, Issue 1, 2020., 2020 Background. Sickle cell disease or drepanocytosis is the most known hemoglobin abnormality in the world. Recently, many medicinal plants used in the management of sickle cell disease in African traditional medicine have shown in vitro antisickling activity. Objective.
Jules Munganga Kitadi +7 more
wiley +1 more source