Elliptocytosis Books
Author: OO Adesiyun
School: University of Ilorin
Department: Medical, Pharmaceutical and Health science
Course Code: PAEDIATRICS
Topics: Bilirubin Metabolism, Fetal Bilirubin Metabolism, Jaundice, bilirubin excretion, Antibody mediated haemolysis, Red Cell, Red Cell Enzyme defects, Red Cell Membrane defects, ABO Incompatibility, Rh Incompatibility, anti-E & c, anti- Kell, Minor blood group incompatibility, G-6-P-D deficiency, Pyruvate kinase deficiency, Hereditary spherocytosis, Elliptocytosis, EXTRAVASCULAR BLOOD, DRUG INDUCED HEMOLYSIS, Vitamin K3 induced haemolysis, POLYCYTHAEMIA, glucoronosyl transferase, Galactosaemia, Exchange Blood Transfusion, Phototherapy, Chronic Postkernicteric Encephalopathy, Bilirubin Encephalopathy, Bilirubin Toxicity, Encephalopathy, Breast Milk Jaundice, G6PD Deficiency, Iso-immune Haemolytic Diseases
Haemolytic anemias , membrane disorders
Author: Haematology
School: University of Ilorin
Department: Medical, Pharmaceutical and Health science
Course Code: HAEMATOLOGY
Topics: Membrane disorders, MEMBRANOPATHIES, Red cell membrane, hereditary membrane disorders, Hereditary SpherocytosisAplastic crisis, Acute sequestration crisis, Megaloblastic crisis, Gallstones, Hereditary Elliptocytosis, Familial Lecithin-Cholesterol Acyl transferase Deficiency, Echinocytosis, Acanthocytosis, Abetalipoproteinaemia
Haemolytic anemias 2 , membrane disorders
Author: AO Shittu
School: University of Ilorin
Department: Medical, Pharmaceutical and Health science
Course Code: HAEMATOLOGY
Topics: red cell membrane, Protein-Membrane, HEREDITARY SPHEROCYTOSIS, OSMOTIC FRAGILITY TEST, ACIDIFIED GLYCEROL LYSIS TEST, AUTO HAEMOLYSIS, HEREDITARY ELLIPTOCYTOSIS, membrane lipids, Familial Lecithin, Cholesterol Acyltransferase Deficiency, lipoproteinaemia, Echinocytosis, Echinocytes, Acanthocytosis, Acanthocytes
Inherited defects of RBC Enzymes & membrane
Author: Iheanyi Okpala
School: University of Nigeria, Nsukka
Department: Medical, Pharmaceutical and Health science
Course Code: HEM301
Topics: Glucose-6-phosphate dehydrogenase deficiency, pyruvate kinase deficiency, herediatary spherocytosis, hereditary elliptocytosis
Normal red blood cells - membrane cytoskeleton ,overview of RBC disorders
Author: AN Duru
School: University of Nigeria, Nsukka
Department: Medical, Pharmaceutical and Health science
Course Code: HEM301
Topics: RBC Function, RBC membrane, RBC membrane protein, Glycophorin, Spectrin, integral membrane proteins, peripheral proteins, red cell membrane lipids, Phospholipids, Glycolipids, Cholesterol, RBC membrane disorders, Hereditary spherocytosis, Hereditary elliptocytosis, Hereditary pyropoikilocytosis, Hereditary Stomatocytosis Syndromes, Overhydrated Hereditary Stomatocytosis, Dehydrated Hereditary Stomatocytosis
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