Front Cover -- Advances in Clinical Chemistry, Volume 5 -- Copyright Page -- Contents -- Contributors to Volume 5 -- Foreword to the Series -- Preface to Volume 5 -- Contents -- List of Tables -- Chapter 1. Inherited Metabolic Disorders: Galactosemia -- 1. Introduction -- 2. Clinical Features -- 3. Biochemical Aspects -- 4. Laboratory Diagnostic Procedures -- 5. Genetics of Galactosemia -- 6. Treatment of Galactosemia -- 7. Conditions Mimicking Galactosemia -- Acknowledgments -- References.
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3. Haptoglobin and Its Hemoglobin Complexes -- 4. Methods for Determination of Concentration and of Type -- 5. Homeostasis of Haptoglobin in Health and in Disease -- 6. Haptoglobin in Animals -- References -- Chapter 5. Microbiological Assay Methods for Vitamins -- 1. Introduction -- 2. Thiamine -- 3. Pantothenic Acid -- 4. Nicotinic Acid and Amide -- 5. Biotin -- 6. Inositol -- 7. Vitamin B6 -- 8. Folic Acid -- 9. Vitamin B12 -- 10. Conclusions -- References.
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Chapter 2. The Malabsorption Syndrome, with Special Reference to the Effects of Wheat Gluten -- 1. Introduction -- 2. Diagnosis -- 3. Differentiation of the ""Sprue Group"" -- 4. The Mechanism of the Effects of Gluten in the Malabsorption Syndrome -- References -- Chapter 3. Peptides in Human Urine -- 1. Introduction -- 2. Principal Methods of Analysis -- 3. Results of Studies on Urinary Peptides -- 4. Concluding Remarks -- References -- Chapter 4. Haptoglobins -- 1. Introduction -- 2. Genetically Controlled Variation.
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Chapter 6. Dehydrogenases: Glucose-6-Phosphate Dehydrogenase, 6-Phosphogluconate Dehydrogenase, Glutathione Reductase, Methemoglobin Reductase, Polyol Dehydrogenase -- 1. Introduction -- 2. Glucose-6-phosphate Dehydrogenase and 6-Phosphogluconate Dehydrogenase -- 3. Glutathione Reductase -- 4. Methemoglobin Reductase -- 5. Sorbitol (Polyol) Dehydrogenase -- Addendum -- List of Abbreviations -- References -- Author Index -- Subject Index -- Index of Contributors-Vols. 1-5 -- Cumulative Topical Index-Vols. 1-5.