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The Biochemical Basis for Red Blood Cell Disorders 599
Carlo Brugnara M D
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abnormalities ACTH activity acute adolescents adrenal adults amino acids androgen anemia antibodies antigens assay assessment associated autosomal bilirubin binding biochemical blood cardiac carnitine cause childhood cholesterol chromosome chronic clinical congenital cortisol creatinine decreased defects deficiency diabetes diagnosis digoxin disorders dose drug effects enzyme erythrocyte evaluation excretion factors fatty acids function gene genetic globin glucose growth half-life hemoglobin hemolysis hepatic hormone hypocalcemia hypoglycemia hypoparathyroidism increased infants infection inherited insulin intestinal laboratory Leu Leu levels lipids lipoprotein liver disease markers measurement membrane metabolic metabolites mg/dL mmol/L molecular molecules monitoring muscle mutations neonatal neuroblastoma newborn normal nutritional occur patients Pediatr phenytoin plasma porphyria present protein puberty pulmonary receptor red cell renal respiratory response salicylate screening secretion serum serum concentrations specific steroid symptoms syndrome synthesis Table thalassemia therapeutic therapy thyroid tion tissue toxicity treatment triglyceride tumors Type urinary urine vitamin