BMC Research Notes, 2018 Objectives Sickle cell anemia is due to a mutations on the betaglobin gene, inducing abnormal hemoglobin. In West Africa the main mutations lead to S or C types of hemoglobin.
Stephane Koui Tossea +8 more
doaj +1 more source
Associated Effect of SLC40A1 and TMPRSS6 Polymorphisms on Iron Overload
Metabolites, 2022 Mutations in the ferroportin (FPN) gene SLC40A1 alter iron recycling and cause disturbances in iron homeostasis. The variants of TMPRSS6 contribute to the development of iron deficiencies.
Lorena Duca +5 more
doaj +1 more source
Following red blood cells in a pulmonary capillary [PDF]
ESAIM: Proc., 2008, Vol. 23, pp. 48-65, 2007 The red blood cells or erythrocytes are biconcave shaped cells and consist mostly in a membrane delimiting a cytosol with a high concentration in hemoglobin. This membrane is highly deformable and allows the cells to go through narrow passages like the capillaries which diameters can be much smaller than red blood cells one. They carry oxygen thanks to
arxiv +1 more source
Blood, 1963 Hereditary persistence of fetal hemoglobin is an anomaly of hemoglobin production apparently caused by a mutant gene that inhibits synthesis of hemoglobins A and A2.
C. Conley +9 more
semanticscholar +1 more source
Alterações hematológicas em Eleginops maclovinus durante uma infestação experimental com Caligus rogercresseyi [PDF]
, 2015 Eleginops maclovinus has been an important fishery resource in Chile since 1957. Caligus rogercresseyi is one of the most prevalent ectoparasite species found on E. maclovinus.
core +1 more source
Hubungan Antara Asupan Zat Gizi (Protein, Zat Besi, Vitamin C) Dan Lama Menstruasi Terhadap Kadar Hemoglobin Pada Remaja Putri Di SMP N 01 Tasikmadu [PDF]
, 2015 Latar belakang: Anemia gizi merupakan salah satu masalah gizi yang sering terjadi di Indonesia khususnya pada remaja putri yang ditandai dengan nilai kadar hemoglobin dibawah nilai normal.
, Dyah Widowati, SKM +2 more
core
32-DFP and 51-Cr for measurement of red cell life span in abnormal hemoglobin syndromes.
Blood, 1969 The red cell life span was measured simultaneously using 51Cr and 32DFP in 21 patients with abnormal hemoglobin β chains and in 7 patients with normal hemoglobin.
P. McCurdy
semanticscholar +1 more source
Effects of the Zanzibar School-Based Deworming Program on Iron Status of Children. [PDF]
, 1998 We evaluated the effects of the Zanzibar school-based deworming program on the iron status of primary school children. Parasitologic and nutritional assessments were carried out at baseline, 6 mo, and 12 mo in 4 nonprogram schools (n = 1002), 4 schools ...
Albonico, M +5 more
core +1 more source
Hemoglobin Levels and Nutrients Intake on Young Soccer Athletes in Yogyakarta
Active: journal of physical education, sport, health and recreation, 2019 The purpose of this study was to know the relationship of nutrients intake and hemoglobin levels in young soccer athletes. This research was an analytical descriptive research with cross-sectional approach.
Yuni Afriani, Desty Ervira Puspaningtyas
doaj +1 more source
beta-thalassemia intermedia in a Brazilian patient with - 101(C > T) and codon 39 (C > T) mutations
São Paulo Medical JournalCONTEXT: We verified molecular alterations in a 72-year-old Brazilian male patient with a clinical course of homozygous beta-thalassemia intermedia, who had undergone splenectomy and was surviving without regular blood transfusions.
Sylvia Morais de Sousa +8 more
doaj +1 more source