UID:
edocfu_9958128225502883
Umfang:
1 online resource (388 p.)
ISBN:
9786613931917
,
1-283-61946-6
,
9786613931993
,
1-283-61954-7
,
0-08-092388-7
,
9786613931948
,
1-283-61949-0
Serie:
The porphyrin handbook ; v. 14
Inhalt:
The Porphyrin Handbook
Anmerkung:
Description based upon print version of record.
,
Front Cover; The Porphyrin Handbook: Medical Aspects of Porphyrins; Copyright Page; Table of Contents; Preface; Chapter 85. Erythropoietic Disorders Involving Heme Biosynthesis; I. Introduction; II. Sideroblastic Anemias; III. Lead Poisoning; IV. Porphyrias; V. Iron-Deficient Erythropoiesis; VI. Animal Models; References; Chapter 86. Acute Intermittent Porphyria: From Clinical to Molecular Aspects; I. Introduction and Classification of Human Porphyrias; II. Acute Intermittent Porphyria; III. Treatment of Acute Attacks; IV. Summary; References; Chapter 87. Congenital Erythropoietic Porphyria
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I. IntroductionII. Clinical Findings in CEP; III. Enzymology and Biochemical Findings; IV. Molecular Biology and Pathology; V. Physiopathology; VI. Diagnosis; VII. Treatment; References; Chapter 88. Porphyria Cutanea Tarda and Related Disorders; I. Introduction; II. The Human UROD Locus; III. Human Uroporphyrinogen Decarboxylase (UROD); IV. Molecular Pathology and Classification of UROD Deficiency Disorders; V. Porphyria Cutanea Tarda; VI. Hepatoerythropoietic Porphyria; References; Chapter 89. Variegate Porphyria; I. Introduction; II. History and Prevalence
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III. Heme Biosynthetic Enzymes in Variegate Porphyria (VP)IV. Diagnosis of VP; V. Clinical Features of VP; VI. Homozygous VP; VII. Conclusion; References; Chapter 90. Protoporphyria; I. Protoporphyria; II. Definition and History; III. Prevalence of Protoporphyria; IV. Clinical Features; V. Pathological Features of Protoporphyria; VI. Biochemical Abnormalities; VII. Pathogenesis; VIII. Clinical and Molecular Genetics of Protoporphyria; IX. Diagnosis of Protoporphyria; X. Treatment; XI. Future Directions in Protoporphyria Research; XII. Summary; References
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Chapter 91. Miscellaneous Abnormalities in Porphyrin Production and DisposalI. Introduction; II. Porphyrin Excretion in Bile and Urine; III. Secondary Porphyrinopathies; IV. The Bronze Baby Syndrome; V. The Multiple Chemical Sensitivity Syndrome; VI. Porphyrin Abnormalities in Response to Lead and Other Industrial Toxins; VII. Pseudoporphyria; VIII. Disturbances in Porphyrin Metabolism and Excretion Associated with Renal Disease; IX. Porphyrin Disturbances in Carcinomatosis; X. Familial Conjugated Hyperbilirubinaemias; References
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Chapter 92. Porphyria Caused by Chlorinated AH Receptor Ligands and Associated Mechanisms of Liver InjuryI. Introduction; II. Known Porphyrogenic Polyhalogenated Aromatic Chemicals; III. Porphyria and Porphyrinuria in Man; IV. Experimental Porphyria in Animals by Polyhalogenated Aromatic Chemical; V. Metabolic Responses; VI. Mechanistic Hypotheses of Uroporphyria; VII. Liver Injury and Cancer Associated with Porphyria; VIII. Summary; References; Chapter 93. Porphyria: A Diagnostic Approach; I. Introduction; II. Approach to the Diagnosis of the Porphyrias
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III. Quantitation of Biochemical Parameters in the Porphyrias
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English
Weitere Ausg.:
ISBN 0-12-393220-3
Weitere Ausg.:
ISBN 0-12-393224-6
Sprache:
Englisch
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