You may have to Search all our reviewed books and magazines, click the sign up button below to create a free account.
Global Health for All is a deeply historical and ethnographically rich analysis of health at a global scale. It combines sixteen inquiries into actors, institutions, objects, and ideas at the centers and margins of global health, to give a uniquely collaborative account of health's entanglement with development, science, and globalization.
A National Book Award winner’s personal journey through the ethical dilemmas and unsettling choices raised by the new frontier of DNA testing. Several years after Masha Gessen’s mother died of breast cancer, she discovered she too had the BRCA1 gene mutation, which predisposes women to high rates of ovarian and breast cancer. Her doctors gave her narrow options: surgical removal of her breasts and ovaries or living with the likelihood of one day developing cancer. As Gessen wrestled with her own health decisions, she sought more information about the implications of genetic testing from a variety of sources—ranging from others faced with her same dilemma to medical researchers, histori...
Is noninvasive, risk-free prenatal diagnosis of fetal genetic characteristics still a fantasy, or will it soon become reality? The current status of both the leading European research groups as well as the NIH-funded NIFTY study are reported here, indicating that certain fetal genetic traits can now be examined efficiently in a noninvasive manner. Considerable focus is placed on new laser-mediated systems for the effective micro-manipulation of single fetal cells, as well as their analysis by single-cell PCR and the pitfalls to avoid when performing such analyses. Other issues addressed in depth include: novel enrichment techniques, optimal fetal cell recognition, fetal cell culture, as well as the exciting finding that fetal cell traffic is elevated in certain pregnancy-related disorders, most prominently in preeclampsia. This publication is of interest to researchers in the field, genetic counsellors, gynecologists and obstetricians, and researchers in microchimerism, transplantation and transfusion medicine.
Highly Commended in the Obstetrics and Gynaecology category of the 2010 BMA Medical Book Competition Brand new edition of the world's leading text on prenatal diagnosis This 6th Edition of Genetic Disorders and the Fetus maintains it's pre-eminence as the major repository of facts about prenatal diagnosis. It provides a critical analysis and synthesis of established and new knowledge based on the long experience of authorities in their respective fields. A broad international perspective is presented through authoritative contributions from authors in 11 countries. All chapters and guidelines have been updated to reflect contemporary practice. New chapters have been introduced on: The use of...
Cooley's anemia, or thalassemia major, is a blood disorder characterized by a marked increase in F hemoglobin and a decrease in the production of certain oxygen-carrying proteins in red blood cells. Thalassemia major is the most severe form of the chronic familial anemias that result from the premature destruction of red blood cells and is inherited as an autosomal recessive trait. In the years since the Seventh Cooley's Anemia Symposium, held in 1997, major advances have taken place in the understanding and treatment of the disease. The molecular mechanisms responsible for the switch from fetal hemoglobin to adult hemoglobin production have been further clarified, while new drugs to enhance the production of fetal hemoglobin and relieve the anemia of thalassemia have been introduced and studied. Understanding of the relationship between molecular genotype and clinical phenotype has been advanced ...
Periantology is "a new field of medicine--treating the fetus while it is still in the womb." Covers fetal surgery, detecting abnormalities, etc.
None
None
Preimplantation Diagnosis of Genetic Diseases A New Technique in Assisted Reproduction Editors: Yury Verlinsky and Anver M. Kuliev For individuals with hereditary genetic disorders such as cystic fibrosis, muscular dystrophy, or hemophilia, the decision to reproduce can be a profoundly difficult and emotional problem. For specialists in reproductive medicine, this situation can raise a myriad of complex—often conflicting—ethical questions. Recently, a revolutionary approach to screening for genetic disorders has emerged, offering unique possibilities for resolving this dilemma. Preimplantation Diagnosis of Genetic Diseases: A New Technique in Assisted Reproduction details the latest proc...