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Our understanding of the relationship between genetics and pulmonary disorders is still developing. In 1989, cloning of the gene that, when mutated, causes cystic fibrosis marked a great advance in the study of genetic diseases. Yet, over a decade later, understanding of how this genetic defect leads to colonization by bacteria and inflammation in the lung remains elusive. This is proving to be an engaging area of investigation for many medical professionals, with research into the effects of these genetic variations on various diseases in progress. Genetics for Pulmonologists provides an overview of lung diseases for which the genetic defect has been defined. It is an easy-to-use manual with concise reviews of genetic diseases that pulmonologists might encounter. ... Read more

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During the past decade enormous progress has been made inour understanding of the molecular genetic basis of manycardiovascular disorders, and such information is already beginning toimpact on clinical practice. This book provides cardiologists with aconcise summary of what is presently known about the genetic basis ofmonogenic and polygenic cardiovascular disorders. Each disease isreviewed in identical manner: clinical features, etc. The glossaryprovides a thorough grounding in the fundamentals of geneticterminology and techniques. Aimed primarily at cardiologists, thisbook also provides much of interest to clinical geneticists andgenetic counsellors. With its quick reference format, Genetics forCardiologists will be readily appreciated by busy practitioners. ... Read more

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This digital document is an article from Saturday Evening Post, published by Thomson Gale on January 1, 2007. The length of the article is 1561 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available in your Amazon.com Digital Locker immediately after purchase. You can view it with any web browser.

Citation Details
Title: Bipolar disorder: on the brink of discovery: researchers investigating the genetics of bipolar I disorder report an exciting new study and ask for your help: an interview with Dr. John Nurnberger.(Interview)
Author: Patrick Perry
Publication: Saturday Evening Post (Magazine/Journal)
Date: January 1, 2007
Publisher: Thomson Gale
Volume: 279Issue: 1Page: 78(3)

Article Type: Interview

Distributed by Thomson Gale ... Read more

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Over the past decade advances in molecular biology have transformed our understanding of the genetic basis of a broad range of ophthalmic conditions and of the disease processes that underlie them.

In view of these developments Remedica Publishing presents it’s soon to be published title: Genetics for Ophthalmologists.

As a new addition to the Remedica Publishing Genetics series this book gives a concise summary of the current clinical understanding of genetic ophthalmology and how it may be applied to diagnosis management and counselling of patients with inherited eye diseases. In addition Genetics for Ophthalmologists gives detailed information of recent advances in genetic eye disease and how disease pathophysiology correlates with this molecular genetic information. ... Read more

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National Institute of Mental Health, Bethesda, Maryland. American Psychopathological Association Series. Proceedings of the 82nd Annual Meeting of the American Psychopathological Association, otherwise unidentified. Research on the genetic aspects of psychiatric disorders. 74 contributors, 70 U.S. ... Read more

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The population of the Indian subcontinent consists of a fine amalgamation of people from diverse tribal, cultural, religious and social backgrounds. Mortality and morbidity from a vast number of medical and surgical conditions is significant and well above compared to the developed countries. Although, a large component of the human health problem is related to infection, malnutrition and other preventable causes, a significant proportion is linked to hereditary factors reflecting in the form of chromosomal, single gene and complex medical diseases. Unusual and unique Mendelian disorders are not uncommon and a number of common medical conditions, such as ischemic heart disease and diabetes mellitus are relatively more prevalent among those living in the developing countries of the Indian subcontinent and as well as among the migrant population groups in the western world. However, true burden of the inherited disorders among the Asian Indians is not known, and probably underestimated.This text includes a detailed and concise account of the social and cultural diversity, medical demography, genetic epidemiology, consanguinity and common genetic disorders affecting people from the Indian subcontinent. In addition, specific issues of genetic services in various regions are addressed. This volume also provides a glossary for the benefit of non-genetic professionals, and is aimed at a wide audience including physicians, genetic professionals, public health consultants, medical demographers, medical/ social anthropologists and health administrators. ... Read more

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In 1970, persons in racial and ethnic minority groups accounted for 16 percent of the population; by 1998, this proportion had increased to 27 percent, and it is expected to increase to nearly 50 percent by 2050. Recognition of the disparities in risk for chronic disease has become the foundation for current efforts to improve health care research, delivery, and education to racial and ethnic groups in the United States.

This book provides health information about genetic and chronic diseases that affect ethnic and racial minorities in the United States. Readers will learn about diseases that are prevalent within ethnic and racial groups, the availability of genetic tests and counseling, and the impact of chronic diseases. Information about mental health services, women's health, and tips for improving health are also included, along with a glossary and a list of resources for additional help and information. ... Read more

Customer Reviews (1)

An excellent, basic handbook
World travel and trade have affected public knowledge of international health issues and diseases: Omnigraphics' Ethnic Diseases Sourcebook tells of leading diseases, causes of death, and emerging diseases around the world, discussing behavior patterns associated with the disease and considering the effects of public health on the environment and culture. An excellent, basic handbook. ... Read more

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A large proportion of human disease is caused by faulty genes, but until recently very few of these genes were known. Advances in molecular genetics over the last ten years have made it possible to systematically track down, isolate and begin to understand the function of these disease genes. This book describes the isolation of the genes responsible for a number of important human diseases, including Huntington's disease, muscular dystrophy and cystic fibrosis. ... Read more

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This book is a guide to genetic support groups--what they are, how to begin one, how to keep an existing group operating and successful. Because a support group may be started, run, and joined by genetics professionals or laypeople, the text contains information usable by a range of readers.

The book opens with a brief discussion of why people seek self-help organizations in general and genetic support groups in particular. The bulk of the text then explains how to organize a genetic support group (getting started, finding a leader), how to sustain the group (developing educational materials and newsletters, conducting a meeting, fund-raising), and how to organize peer support training programs. The authors present examples of existing groups' experiences, sample budgets and news releases, tables and checklists, and other specific information to guide readers.

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This work describes the remarkable developments in the detection of inherited or acquired genetic mutations. Focusing on the advances in DNA technology, the book examines new methods for large-scale genome mapping, DNA sequencing and protein structure analysis. The progress of molecular diagnostics in revealing significant human disease genes and in understanding DNA damage and repair is also discussed in the state-of-the-art work. Significant discussions underscore the pervasive and powerful influence of the polymerase chain reaction in all areas of DNA manipulation and analysis. ... Read more

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The purpose of the Symposium was to gain insight into the pathogenesis of Alzheimer's disease from a molecular and genetic point of view. Accordingly, most of the presentations focussed on genetics, amyloid and tangle. Comprising five sections, this volume provides in-depth coverage of a selection of papers presented at the meeting. Section I deals with paired helical filaments and related subjects in which ultrastructure and chemical constituents of PHA and ubiquitin dependent proteolysis of tau protein are discussed. Section II presents the studies on analytical, functional and genetic aspects of beta-amyloid protein and its precursor. Section III concerns trophic activity in the Alzheimer-diseased brain which plays an important role in the understanding of mechanisms involved in processes of neuronal degeneration. Section IV is devoted to molecular and cell biology of prion and addresses the significance of the amino acid sequence of prion protein. Section V provides chromosome restriction maps of human chromosome 21 and the results of linkage studies of familial Alzheimer's disease (FAD). ... Read more

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This text is clinical in orientation and comprehensively covers maternal genetic disease. ... Read more

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This text examines the various techniques available for the treatment of genetic diseases and is aimed at medical geneticists, paediatricians and haematologists. The 66 contributors, from the USA, France, The Netherlands, Japan, Australia and the USSR consider metabolic therapy, bone marrow transplantation, enzyme replacement therapy, gene transfer strategies and in-utero therapy. ... Read more

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In the last few years, dramatic advances in molecular biology have made it possible to analyze human genes directly, providing new insights into human molecular pathology and leading to techniques used for such procedures as the prenatal diagnosis of genetic disorders.Written for nonspecialists by an internationally-known expert, this unique book provides a clear introduction to the new genetics and an in-depth consideration of the impact this technology may have on the future practice of medicine. Weatherall describes recombinant DNA techniques and outlines how they are used to analyze genes; reviews what is known about the molecular pathology of human genetic diseases and about acquired disorders like cancer; and assesses how these methods might be used for preventive genetics and gene therapy.For this new edition, many of the illustrations have been redrawn and revised, and new figures added to clarify the discussion.The book will continue to be a valuable resource for doctors, nurses, and counsellors who need to understand the new molecular tools available to them. ... Read more