Haemolytic anemias 2 , membrane disorders by AO Shittu PDF free download

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

Topics: Simple lipids, Compound lipids, Derived lipids, Lipids complexed compound, Non-Nitrogen Glycerophospholipids, Glycerophospholipids, Phosphate Containing lipids, Phosphatidylcholine, Lecithin, PhosphatidylEthanolamine, Cephalin, Phosphatidylserine, Nitrogen containing Glycerophospholipids, Plasmalogens, Sphingomyelins, Non-Phosphorylated Lipids, Glycosphingolipids, Carbohydrates, Sulfolipids, Sulfatides, Derived Lipids, Fatty Acids, GLYCEROL, Acrolein Test, STEROIDS, STEROLS, CHOLESTEROL, TRIACYL GLYCEROL, Saponification number, Saponification, Rancidity, PHOSPHOLIPIDS, Phosphoinositides, Phospholipids, phospholipases, Lysophospholipids, PLASMALOGENS, SPHINGOMYELINS, Phosphatidyl Sphingosides, Niemann-Pick disease, Cardiolipin, lipotropic action, GANGLIOSIDOSIS, TAY-SACH`S DISEASE, GM-1 Gangliosidosis, GANGLIOSIDES, GAUCHER`S DISEASE, PSYCHOSIN, CEREBROSIDES, GLYCOLIPIDS, Lecithin-Sphingomyelin ratio, Dipalmityl Lecithin, Arachidonic acid

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

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

Topics: ATHEROGENESIS, Endothelial dysfunction, Smooth muscle cell dysfunction, Architectural disruption, LIPOPROTEIN PARTICLES, Primary chylomicronemia, Primary hypertriglyceridemias, Familial hypertriglyceridemia, Familial combined hyperlipoproteinemia, familial dysbetalipoproteinemia, Primary hypercholesterolemias, Familial hypercholesterolemia, Familial ligand-defective Apolipoprotein B, Familial combined hyperlipoproteinemia, hyperlipoproteinemia, Hypercholesterolemias, Hypertriglyceridemias, REDUCTASE INHIBITORS, STATINS, FIBRATES, Fibric acid derivatives, BILE ACID-BINDING RESINS, NICOTINIC ACID, NIACIN, INTESTINAL STEROL ABSORPTION, EZETIMIBE, COMBINATION THERAPY

Topics: Immune haemolytic anaemia, Non-immune acquired haemolytic anaemia, INTRAVASCULAR HAEMOLYSIS, BLACK WATER FEVER, Malaria, haemophagocytic syndrome, Acute intravascular haemolysis, FRAGMENTATION HAEMOLYSIS, MICROANGIOPATHIC HAEMOLYTIC ANAEMIAS, Haemolytic uraemic syndrome, Thrombotic thrombocytopenic purpura, DRUG-INDUCED IMMUNE HAEMOLYTIC ANAEMIA, Drug adsorption mechanism, Membrane modification mechanism, Immune complex innocent bystander mechanism

Topics: IMMUNE HAEMOLYTIC ANAEMIAS, AUTO IMMUNE HAEMOLYTIC ANAEMIAS, immunoglobulin, Red cell destructionComplement mediated destruction, cold AUTO IMMUNE HAEMOLYTIC ANAEMIA, PAROXYMAL COLD HAEMOGLOBINURIA, ALLO IMMUNE HAEMOLYTIC ANAEMIA, DRUG INDUCED HAEMOLYTIC ANAEMIA, RED CELL FRAGMENTATION SYNDROME, MACRO ANGIOPATHIC HAEMOLYTIC ANAEMIA, MICRO ANGIOPATHIC HAEMOLYTIC ANAEMIAS, MARCH HAEMOGLOBINURIA, PAROXYSMAL NOCTURNAL HAEMOGLOBINURA, glycosylphosphatidylinositol

Topics: HAEMOLYSIS, HAEMOLYTIC DISORDERS, COMPENSATED HAEMOLYSIS, red cell production, INHERITED INTRA CORPUSCULAR HAEMOLYTIC DISORDERS, ACQUIRED EXTRA CORPUSCULAR HAEMOLYTIC DISORDERS, ACQUIRED INTRA CORPUSCULAR HAEMOLYTIC DISORDERS, Paroxysmal Nocturnal Haemoglobinuria, Haemosiderinuria, RETICULOCYTOSIS, marked anisocytosis, APLASTIC CRISIS

Topics: PCV Reading, Drabkin solution, red blood cell count, white blood cell count, platelet count, red cell absolute indicies, sickling test, haemoglobin electrophoresis, Coomb's test, haemostasis, blood grouping, blood bag, copper sulphate solution, leishman stain, EDTA

Topics: Child Health Disparities, child health, Global Child Health, Pediatric Care, Neonatal Ethics, Newborn Screening, Genetics, Genomics, Precision Medicine, Adolescent Healthcare, Pediatric Ethics, Pediatric Palliative Care.Domestic Adoption, Intercountry Adoption, Foster care, Kinship Care, immunization, Injury Control, childhood injuries, School Violence, Child Temperament, Child Behavioral Problems, Positive Parenting, Pediatrician, Fetal Growth, fetal Development, Neurologic Development, Middle Childhood, Sleep Medicine, chronobiology, Behavioral Disorder, Psychiatric Disorder, Psychiatric Diagnostic Evaluation, Psychopharmacology, ADHD Medications, Antidepressants, Antipsychotics, Mood Stabilizers, Psychotherapy, Psychiatric Hospitalization, Somatic Symptom, Rumination, Pica, Motor Disorders, Habits, Anxiety Disorders, Mood Disorders, Suicide, Attempted Suicide, eating disorder, Disruptive Disorder, Impulse-Control Disorder, Conduct Disorder, Tantrums, Breath-Holding Spells, Lying, Stealing, Truancy, Aggression, Self-Injurious Behavior, Neurodevelopmental Dysfunction, Executive Function Dysfunction, Attention-Deficit, Hyperactivity Disorder, Dyslexia, Math Learning Disability, Impaired Writing, language disorder, communication disorder, Normal Language Development, Motor Speech Disorder, Hearing Impairment, Hydrocephalus, Language Impairment, Language Delay, Autism Spectrum Disorder, Nutrition, Nutritional Requirements, Dietary Reference Intakes, Soy FormulasProtein Hydrolysate Formulas, Complementary Feeding, Feeding Toddlers, Food Security, Malnutrition, Undernutrition, Severe Acute Malnutrition, Refeeding Syndrome, Malnutrition, Overweight, Obesity, Vitamin A Deficiency, Hypervitaminosis A, Thiamine Deficiency, Thiamine Toxicity, Riboflavin Deficiency, Riboflavin Toxicity, Niacin Deficiency, Niacin Toxicity, Vitamin B6 Deficiency, Vitamin B6 Toxicity, Folate Deficiency, Folate Toxicity, Vitamin B12 Deficiency, Vitamin C Deficiency, Vitamin C Toxicity, Ricket, Vitamin D Disorder, Calcium Deficiency, Phosphorus Deficiency, Distal Renal Tubular Acidosis, Hypervitaminosis

Topics: Immune Hemolytic disorder, Auto-immune Hemolytic anemia, Cold AIHA, Paroxysmal Cold hemoglobinuria, Allo-immune Hemolytic anemia, immune Thrombocytopenic purpura, Evan's syndrome, IMMUNE HEMOLYTIC ANEMIA, Antibody-mediated hemolysis, AUTOIMMUNE HEMOLYTIC ANEMIA, Red cell destruction, cold AIHA syndrome, warm AIHA, ALLOIMMUNE HEMOLYTIC ANEMIA, DRUG-INDUCED HEMOLYTIC ANEMIA, ACQUIRED NON-IMMUNE HEMOLYTIC ANEMIA, INTRAVASCULAR HEMOLYSIS, BLACK WATER FEVER, HEMOPHAGOCYTIC SYNDROME, FRAGMENTATION HEMOLYSIS, MECHANICAL HEMOLYTIC ANEMIA, RED CELL FRAGMENTATION SYNDROME, MICROANGIOPATHIC HEMOLYTIC ANEMIA, HEMOLYTIC UREMIC SYNDROME, THROMBOTIC THROMBOCYTOPENIC PURPURA

Topics: Congenital immunodeficiencies, primary immunodeficiencies, Chronic infection, Opportunistic infection, Recurrent infection, Phagocytic disorders, Complement immunodeficiencies, Phagocytic Disorders, Chronic Granulomatous Disease, Leucocyte Adhesion Deficiency, Chediak Higashi Syndrome, Lazy Leucocyte Syndrome, C1-inactivator deficiency, C3b-inactivator deficiency, C3 deficiency, B cell Deficiency, X-linked Agammaglobulinaemia, Bruton’s Agammaglobulinaemia, Transient hypogammaglobulinaemia, Common variable immunodeficiency, T cell Deficiency, Cellular immunodeficiency, Di George syndrome, T cell lymphopaenia, Chronic mucocutaneous candidiasis, T Lymphocyte Deficiencies, B Lymphocyte Deficiencies, severe combined immunodeficiency, X-linked SCID, Adenine deaminase deficiency SCID, Reticular dysgenesis, Secondary Immunodeficiency, Haemoglobinopathies, Immunosuppressive drugs, Tumour growth

Topics: Haemostatic mechanism, blood vessels, superficial bleeding, petechiae, ecchymosis, non thrombocytopenic purpura, senile purpura, Hereditary haemorrhagic telangiectasia, Osler-Rendu-Weber syndrome, CONNECTIVE TISSUE DISORDERS, Ehlers-Danlos syndrome, Pseudoxanthoma elasticum, Osteogenesis imperfecta, Marfan’s syndrome, ALLERGIC PURPURA, Henoch-Schoenlin purpura, PSYCHOGENIC PURPURA, INFECTIOUS PURPURA, PLATELET ADHESSION, thrombocytopathies, Bernard-Soulier syndrome, Platelet type von-Willibrand, Montreal platelet syndrome, IMMUNE MEDIATED THRONBOCYTOPENIA, Auto Immune Thrombocytopenia, BONE MARROW SUPPRESSION, Thrombotic thrombocytopenic purpura, Haemolytic uraemic syndrome

Topics: Pure red cell aplasia, Diamond-Blackfan anaemia, Congenital pure red cell aplasia, Paroxysmal nocturnal haemoglobinuria

Topics: Glucose-6-phosphate dehydrogenase deficiency, pyruvate kinase deficiency, herediatary spherocytosis, hereditary elliptocytosis

Topics: Decreased hemoglobin oxygen affinity, Haemoglobin oxygen dissociation curve, Redistribution of blood flow, Increased cardiac output, Symptoms of anaemia, Clinical signs of anaemia, RED CELL ABSOLUTE INDICES, MEAN CELL VOLUME, MEAN CELL HAEMOGLOBIN, MEAN CELL HAEMOGLOBIN CONCENTRATION, red cell indices, Polycythaemia, Absolute polycythaemia, Relative Polycythaemia

Topics: LIPID DISORDERS, Serum total cholesterol, Serum triglycerides, Serum HDL-cholesterol, Serum LDL-cholesterol, Lipopoprotein ratios, Apoproteins, Reminant Cholesterol, Non HDL Cholesterol, Hyperlipidaemia, coronary heart disease, anion-exchange resins, cholestyramine, Questran, colestipol, Colestid, Statins, fibric acid drugs, Nicotinic acid

Topics: Myeloid maturation, stem cell, Acute leukaemia

Topics: ENZYMOPATHIES, GLYCOLYSIS, Glutathione, NUCLEOSIDE METABOLISM, G6PD DEFICIENCY, ACUTE HAEMOLYTIC ANAEMIA, Chronic haemolytic anaemia, PYRUVATE KINASE DEFICIENCY

Topics: Low grade lymphoma, Intermediate grade lymphoma, High grade Lymphoma, NK cell Neoplasms, Mature T-cell Neoplasms, FOLLICULAR LYMPHOMA, LARGE CELL LYMPHOMA, MALT Lymphoma, ADULT T-CELL LYMPHOMA, ADULT T-CELL LEUKAEMIA, Mycosis fungoides, SEZARY SYNDROME