A. W. Norman & K. Schaefer 
Vitamin D. Basic Research and its Clinical Application [PDF ebook] 
Proceedings of the Fourth Workshop on Vitamin D, Berlin, West Germany, February 1979

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Frontmatter — Foreword — Contents — Chemistry, Structure, Function and Biological Assay — Introduction — Synthesis of Some Side Chain Analogues of Vitamin D3 Metabolites — Structural Transformations on Vitamin D — Distribution and Activity of a Vitamin D3 Compound in Trisetum Flavescens — Synthesis and Biological Activity of 24R-Hydroxy-25-fluorocholecalciferol and 1a, 24R-Dihydroxy-25-fluorocholecalciferol — The Synthesis and Biological Evaluation of Fluorinated Analoges as Probes of Vitamin Da Metabolism — 19-Substituted-10, 19-Dihydrovitamins via Hydrozirconation of Vitamin D3 — The Synthesis of 1a, 3a-Dihydroxy-25Methylcholesta-5, 7-Diene-24-OIC Acid, and of la, 3a-Dihydroxy-25 Methylcholesta-5, 7-Diene — Interconversion of Vitamin D and Trans-Vitamin D by Triplet-Sensitized Isomerization — The Use of UV, CD, 2H-NMR Spectroscopy and Mass Spectrometry for the Investigation of Conformational Mobility of Vitamin D and Previtamin D and their Interconversion — 25 (R), 26 and 25 (S), 26-(OH)2D3: Biological Activity in Intact and Nephrectomized Rats. Comparative Effects of 1, 25, 24 (R), 25-(OH)2D3 and I, 24 (R), 25-(OH)3D3 — Inhibitors of Vitamin D Metabolism and Action — C(1)-Hydroxylation of Vitamin D3 and Related Compounds — Vitamin D3 Sulfate in Lactating normally fed Rats and Suckling Pups After Maternal Administration of 3H Vitamin D3 or 35S Vitamin D3 Sulfate — Synthesis of Vitamin D Analogues and their Covalent Binding to Affinity Chromatographic Media — Osteoporosis — Calcium Absorption and Plasma 1, 25 (OH)2D Levels in Post-Menopausal Osteoporosis — Osteoporosis and Age-Related Osteopenia: Evaluation of Possible Role of Vitamin D Endocrine System in Pathogenesis of Intestinal Calcium Absorption — Two Years Experience of Oral Treatment with 1a-Hydroxyvitamin D and Calcium in Patients with Senile or Postmenopausal Osteoporosis — The Treatment of Osteoporosis with 24, 25 Dihydroxycholecalciferol A Pilot Study — Osteomalacic Factors in the Osteoporosis and the Treatment of Osteoporotic Patients with Vitamin D2 and 1a OHD3 — Transcalciferan/D-Binding Protein(s) — Biologic Significance of Genetic Variation in Human Gc (Vitamin D-Binding Protein) — The Transport of Vitamin D — Structure and Properties of Human Plasma Vitamin D Transport Protein (Group-Specific Component) — Serum Vitamin D Binding and Gc Polymorphism — Sunlight, Skin and Seasonal Effects — Identification of in Vivo Generated Previtamin D3, Vitamin D3 and 25-Hydroxyvitamin D3 in the Vitamin D-Deficient Rats Irradiated by Ultraviolet Light — Response of Plasma 250HD to Standardized Ultra Violet Radiation — Effects of Sunlight Exposure on Blood Concentration of Vitamin D Derivatives in Healthy Japanese Adults — Contribution of Skin Vitamin D3 Synthesis in Patients Receiving Total Parenteral Nutrition — The Photo-Biochemistry of Vitamin D3 in Vivo in the Skin — Assays for Vitamin D Metabolites — Measurement of Plasma 1, 25 (OH)2 Vitamin D by Protein Binding Assay and Radioimmunoassay — Use of Isotope Dilution Mass Fragmentography in Vitamin D Research — Assay of 1, 25-Dihydroxyvitamin D and Other Active Vitamin D Metabolites in Serum: Application to Animals and Humans — 24, 25-Dihydoxyvitamin D in Human Serum — Radioimmunoassay of Vitamin D Metabolites — Assays for Vitamin D and its Metabolites — Radioimmunoassay for Circulating 1, 25- and 25, 26-Dihydroxycholecaliferols in Man — Hemisuccinates of Vitamin D3 and of its Metabolites — Studies on Antisera against Vitamin D Metabolites — The Measurement of Various Vitamin D Derivatives in Plasma Using High-Pressure Liquid Chromatography — Assay of 1, 25- and 24, 25 Dihydoxycholecalciferol in Human Serum – some Technical Considerations — Radiocompetitive Protein Binding Assays for 25-Hydroxy Vitamin D, 24, 25-Dihydroxyvitamin D and 1, 25-Dihydroxy-vitamin D in Human Serum — Steroid Receptors: What do We not Know? — Vitamin D – Parathyroid Hormone — Cholecalcifediol suppression of PTH

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