The Porphyrin Handbook :Medical Aspects of Porphyrins

Publication subTitle :Medical Aspects of Porphyrins

Author: Kadish   Karl;Guilard   Roger;Smith   Kevin M.  

Publisher: Elsevier Science‎

Publication year: 2012

E-ISBN: 9780080923888

P-ISBN(Paperback): 9780123932242

P-ISBN(Hardback):  9780123932242

Subject: O6 Chemistry;O61 Inorganic Chemistry;O62 Organic Chemistry;Q Biological Sciences;Q5 Biochemistry

Language: ENG

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Description

The Porphyrin Handbook, Volume 14: Medical Aspects of Porphyrins provides information pertinent to every aspect of the chemistry, synthesis, spectroscopy, and structure of phthalocyanines. This book examines the biology and medical implications of porphyrin systems.

Organized into 12 chapters, this volume begins with an overview of the underlying diagnostic features, mechanisms, and available treatments of erythropoietic disorders due to defective heme biosynthesis. This text then examines the physiopathology of acute intermittent porphyria, which is transmitted as autosomal dominant disorders with incomplete penetrance. Other chapters consider the main characteristics of congenital erythropoietic porphyria, which includes an increased synthesis, accumulation, ad excretion of porphyrins. This book discusses as well the biochemistry, pathophysiology, and clinical features of variegate porphyria in the light of several essential advances in the understanding, management, and diagnosis of variegate porphyria. The final chapter deals with the legal use of herbal and complementary medicines.

This book is a valuable resource for research scientists, engineers, and clinicians.

Chapter

Front Cover

pp.:  1 – 4

Copyright Page

pp.:  5 – 6

Table of Contents

pp.:  6 – 14

Preface

pp.:  14 – 42

Chapter 85. Erythropoietic Disorders Involving Heme Biosynthesis

pp.:  42 – 64

Chapter 86. Acute Intermittent Porphyria: From Clinical to Molecular Aspects

pp.:  64 – 84

Chapter 87. Congenital Erythropoietic Porphyria

pp.:  84 – 108

Chapter 88. Porphyria Cutanea Tarda and Related Disorders

pp.:  108 – 134

Chapter 89. Variegate Porphyria

pp.:  134 – 162

Chapter 90. Protoporphyria

pp.:  162 – 192

Chapter 91. Miscellaneous Abnormalities in Porphyrin Production and Disposal

pp.:  192 – 210

Chapter 92. Porphyria Caused by Chlorinated AH Receptor Ligands and Associated Mechanisms of Liver Injury

pp.:  210 – 252

Chapter 93. Porphyria: A Diagnostic Approach

pp.:  252 – 288

Chapter 94. Approaches to Treatment and Prevention of Human Porphyrias

pp.:  288 – 326

Chapter 95. Management and Treatment of the Porphyrias

pp.:  326 – 344

Chapter 96. Porphyria: A Toxicogenetic Disease

pp.:  344 – 380

Index

pp.:  380 – 389

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