Glucose 6 phosphate (G-6-P) deficiency and pyruvate kinase deficiency by PAT PDF free download

Topics: Autoimmune diseases, Warm type Autoimmune, Cold type Autoimmune, immune Hemolytic anaemia, autoimmune haemolysis, extravascular haemolysis, cold Autoimmune Hemolytic anaemia, intravascular haemolysis, cold antibody Autoimmune Hemolytic anaemia, cold haemagglutin disease, paroxysmal cold haemoglobinuria, alloimmune Hemolytic anaemia

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: 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: Hypercholesterolaemia, lipoprotein metabolism, Hypertriglyceridaemia, Hyperalphalipoproteinaemia, Hypoalphalipoproteinaemia, LIPOPROTEIN DISORDERS

Topics: Lipoproteins, Apolipoproteins, Exogenous lipid pathway, Endogenous lipid pathway, Reverse cholesterol transport pathway, lipid pathway

Topics: VITAMIN B12 METABOLISM, COBALAMIN MALABSORPTION, Pernicious anaemia, MEGALOBLASTIC ANAEMIA, MACROCYTES, HYPERSEGMENTED NEUTROPHIL, cobalamin deficiency

Topics: Anaemia

Topics: Catalytic Activity, Isoenzymes, enzymology, enzyme activity, Liver Enzymes, Aspartate Transaminase, Alkaline Phosphatase, Gamma-glutamyl transferase, Lactate Dehydrogenase, CREATINE KINASE, creatine phosphokinase, Aldolase, Amylase, Macroamylasemia, lipase, Acid Phosphatase, Tumour markers

Topics: Glycolysis, Hexokinase, Pyruvate kinase, pyruvate, Alcoholic Fermentation, Hexokinase, fructose, mannose, galactose, citric acid cycle, Glycogen Metabolism, glycogen metabolism, glycogenolysis, Glycogenesis, Pentose Phosphate Pathway, Hexose Monophosphate Shunt, Phosphogluconate Pathway, Cori cycle, Calvin cycle, respiratory chain, electron transport chain, oxidative phosphorylation, cynaide, carbon monoxide, iodine, chromium, manganese, selenium, copper, zinc, iron, trace elements, cyanocobalamin, Pyridoxine, folic acid, niacin, riboflavin, thiamine

Topics: Monoclonal antibodies, PROTEIN TYROSINE KINASE INHIBITORS, Imatinib, Dasatinib, Nilotinib, IMATINIB MESYLATE, DASATINIB, SPRYCEL, NILOTINIB, TASIGNA, Gefitinib, Iressa, Erlotinib, TARCEVA, Lapatinib, Tyverb, Trastuzumab, HERCEPTIN, Cetuximab, ERBITUX

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: Alanine Cycle, gluconeogenesis organ, Cori Cycle, adipose, tissue, Hexokinase, Phosphofructokinase-1, Pyruvate kinase (PyrK), Fructose 1, 6-bisphosphatase

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

Topics: Antibody-mediated immunity, humoral immunity, antibodies, Immunoglobulin Structure, Human Immunoglobulin Classes, Monoclonal Antibody, immunological memory, antibody binding

Topics: Antigen Recognition, Haptens, Epitopes, Immunogen, antigen, epitope, hapten, Tumor antigen, Autoantigen, ABO system, Alloantigen, Heterophile antigen, forssman antigen, Immune serum, Exotoxin, toxoid, Common antigen

Topics: autoimmune disease, Autoimmune thrombocytopenic purpura, Autoimmune haemolytic anaemia, cold haemagglutinin disease, paroxysmal cold haemoglobinuria, Autoimmune neutropenia

Topics: Autophagy, Reversible cell injury, Hydropic swelling, Pyknosis, Karyorrhexis, necrosis, Coagulative necrosis, Acute tubular necrosis, patchy tubular necrosis, Dry gangrenous necrosis, gangrenous necrosis, Liquefactive necrosis, Caseous necrosis, Traumatic fat necrosis, Enzymatic fat necrosis, Fibrinoid necrosis, Haemorrhagic necrosis, Testicular torsion, Autopsy Case, Apoptosis, colonic crypts, Apoptosis control, Apoptosis integration, Effector pathway, executionary pathway, Extrinsic apoptosis

Topics: laboratory test, biochemical profile, dynamic function test, urgent test, routine test, specimen collection, chemica pathology investigation cycle, case history, gaussian distribution

Topics: DNA split, human karyogram, mutation, Genetic disorder, CYTOGENETIC DISORDER, AUTOSOMAL CYTOGENETIC DISORDER, down syndrome, EDWARD SYNDROME, PATAU SYNDROME, Lyonization, X-chromosome, Y-chromosome, Klinefelter's Syndrome, Testicular Dysgenesis, Male hypogonadism, Klinefelter Syndrome, Turner Syndrome, MENDELIAN DISORDER, Autosomal Dominant Disorder, Marfan Syndrome, Achondroplasia, Osteogenesis imperfecta, brittle bone disease, Ehlers-Danlos Syndrome, Autosomal recessive disorder, X-LINKED DISORDER, Multifactorial disorder, Hereditary Cancer Syndrome, DEFECTIVE DNA REPAIR, Single-Gene Disorder, TRIPLET-REPEAT MUTATION, FRAGILE-X SYNDROME, LEBER HEREDITARY OPTIC NEUROPATHY, GENOMIC IMPRINTING

Topics: Bone marrow trephine biopsy, massice splenomegaly, bone marrow reticulin, fibrous tissue