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Diagnosis and Therapy of Porphyrias and Lead Intoxication

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Table of Contents

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    Book Overview
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    Chapter 1 Regulation of Heme Biosynthesis in Hepatic and Erythroid Cells: A Brief Introduction to the Pathobiochemistry of Human Porphyrias
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    Chapter 2 Differential Patterns of Heme and Prophyrin Biosynthesis in Liver and Kidney: Metal Ion Blockade of δ-Aminolevulinate Synthetase Introduction by Porphyrinogenic Agents
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    Chapter 3 The Regulatory Function of the Mitochondrial Inner Membrane in the Overall Ferrochelatase Reaction
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    Chapter 4 Permissive Effects of Hormones on the Induction of δ-Aminolevulinic Acid Synthase in Cultured Chick-Embryo Liver Cells
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    Chapter 5 Biochemical and Clinical Transitions Between the Hereditary Hepatic Porphyrias: New Concepts
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    Chapter 6 A New Approach to Porphyria
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    Chapter 7 The Clinical Chemistry of Variegate Porphyria with Special Reference to the Identification of a New Plasma-Marker Porphyrin
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    Chapter 8 Expression of the Gene Defects of Acute Intermittent Porphyria (AIP) and Erythropoietic Protoporphyria (EPP) in Mitogen-Stimulated Lymphocytes
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    Chapter 9 Uroporphyrinogen-Synthase (Uro-S) in Erythrocytes in Acute Intermittent Porphyria (AIP)
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    Chapter 10 Hereditary Coproporphyria: Demonstration of a Genetic Defect in Coproporphyrinogen Metabolism
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    Chapter 11 A Case of Acute Intermittent Porphyria, Relapsing Acute Pancreatitis, and Unconjugated Hyperbilirubinemia (Gilbert’s Syndrome)
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    Chapter 12 Acute Intermittent Porphyria; EEG Changes and Their Relationship to the Biochemical Manifestation
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    Chapter 13 Family Studies of Patients with Acute Intermittent Porphyria (AIP): Neurological, Biochemical, and Genetic Investigations
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    Chapter 14 The Effect of Hematin in “Inducible” Hepatic Porphyria
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    Chapter 15 Therapy of Acute Intermittent Porphyria With Ovulation Inhibitors in Women
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    Chapter 16 Clinical Observation, Diagnostics, and Therapy for Symptomatic and Hereditary Porphyria Cutanea Tarda
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    Chapter 17 Uroporphyrinogen Decarboxylase (Uro-D) Defect in Erythrocytes in Chronic Hepatic Porphyrias
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    Chapter 18 The Problem of Possible Etiological Factors in the Origin and Development of PCT
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    Chapter 19 Incidence of Porphyria in Slovenia
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    Chapter 20 Chronic Hepatic Porphyrias and the Role of Iron in These Disorders
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    Chapter 21 Chloroquine in the Treatment of Porphyria Cutanea Tarda
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    Chapter 22 Chloroquine Treatment of Porphyria Cutanea Tarda
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    Chapter 23 Clinical Importance of Suburoporphyrins
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    Chapter 24 Current Diagnostic Problems in the Cutaneous Porphyrias in Infancy. Presentation of Unusual Cases
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    Chapter 25 Influence of Environmental Factors on Porphyrin Metabolism
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    Chapter 26 Porphyrinogenic Action of Polyhalogenated Aromatic Compounds, With Special Reference to Porphyria and Environmental Impact
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    Chapter 27 Lead Poisoning Attributable to Automobile Traffic
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    Chapter 28 Neoplasms and Metabolic Disturbances of Porphyrins in Rats With Chronic Experimental Lead Poisoning
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    Chapter 29 Time Course and Compartment Relations of Heme-Synthesis Disturbances Induced by Inorganic Lead Compounds in Humans
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    Chapter 30 Urinary Porphyrin Profiles in Acute Lead Poisoning: Relation to Differentiation From Acute Intermittent Porphyria
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    Chapter 31 Determination of Lead and Cadmium in Whole Blood by Electrothermal Atomic Absorption Spectroscopy
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    Chapter 32 Biochemical Behavior of Delta-Aminolevulinic Acid Dehydratase During Chronic Oral Lead Poisoning in Sheep
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    Chapter 33 Diagnostic Criteria of Increased Lead Absorption in Occupational Medicine
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    Chapter 34 Analysis of the Diagnostically Relevant Heme Precursors (5-Aminolevulinic Acid, Coproporphyrin, and Protoporphyrin) in Lead Poisoning by Use of Thinlayer Chromatography
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    Chapter 35 Comparison of Fluorometric Micromethods for Analyzing Erythrocytic Porphyrins (EP)
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    Chapter 36 Therapy for Lead Poisoning
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    Chapter 37 Subclinical Effects of a Ubiquitous Poison: Lead
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    Chapter 38 Correlations Between Chronic Exposure to Lead and Excretion of Heme Precursors in Ceramics Industry Workers
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    Chapter 39 Modification of Radiosensitivity by Porphyrins: Studies of Tumors and Other Systems
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    Chapter 40 Meso-Tetra (p-Sulfophenyl) Porphine as a Potential Tumor-Localizing Agent
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    Chapter 41 Frequency of Occurrence of Hepatocellular Carcinoma in Patients With Porphyria Cutanea Tarda in Long-term Follow-up
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    Chapter 42 Organ Porphyrins in Human Circulatory Disorders and Neoplastic Disease
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    Chapter 43 Characterization of the Defect in Heme Metabolism in Patients With Erythropoietic Protoporphyria
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    Chapter 44 Biochemical and Morphologic Changes in Early Phases of Experimental Protoporphyria
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    Chapter 45 Hereditary Bovine Protoporphyria, a “Total Body” Deficiency of Ferrochelatase: Some Basic Distinctions From Hypochromic Anemias
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    Chapter 46 Treatment of Erythropoietic Porphyrias
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    Chapter 47 Interactions of Porphyrins With Proteins
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    Chapter 48 Hemopexin and Albumin Metabolism in Porphyria Cutanea Tarda
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    Chapter 49 Photodynamic Modification of Erythrocyte Membrane Proteins Induced by Protoporphyrin
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    Chapter 50 New Aspects of Hematin Excretion in Rats
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    Chapter 51 Hematin Therapy in Acute Porphyria and Observations on Hemopexin
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    Chapter 52 Das Wirken Hans Fischers für die Porphyrinforschung
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    Chapter 53 Thudichum und der Purpur
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Title
Diagnosis and Therapy of Porphyrias and Lead Intoxication
Published by
Springer Berlin Heidelberg, December 2012
DOI 10.1007/978-3-642-67002-2
ISBNs
978-3-54-008863-9, 978-3-64-267002-2
Editors

Doss, Manfred

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The data shown below were compiled from readership statistics for 3 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 3 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 1 33%
Student > Doctoral Student 1 33%
Student > Master 1 33%
Readers by discipline Count As %
Agricultural and Biological Sciences 1 33%
Chemistry 1 33%
Medicine and Dentistry 1 33%