Immune Responses In Patients With Lysosomal Storage Disorders Treated With Enzyme Replacement Therapy And Haemopoietic Stem Cell Transplantation
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Author | : Michelle Kenyon |
Publisher | : Springer |
Total Pages | : 318 |
Release | : 2018-03-14 |
Genre | : Medical |
ISBN | : 3319500260 |
This book is open access under a CC BY 4.0 license. This textbook, endorsed by the European Society for Blood and Marrow Transplantation (EBMT), provides adult and paediatric nurses with a full and informative guide covering all aspects of transplant nursing, from basic principles to advanced concepts. It takes the reader on a journey through the history of transplant nursing, including essential and progressive elements to help nurses improve their knowledge and benefit the patient experience, as well as a comprehensive introduction to research and auditing methods. This new volume specifically intended for nurses, complements the ESH-EBMT reference title, a popular educational resource originally developed in 2003 for physicians to accompany an annual training course also serving as an educational tool in its own right. This title is designed to develop the knowledge of nurses in transplantation. It is the first book of its kind specifically targeted at nurses in this specialist field and acknowledges the valuable contribution that nursing makes in this area. This volume presents information that is essential for the education of nurses new to transplantation, while also offering a valuable resource for more experienced nurses who wish to update their knowledge.
Author | : National Research Council |
Publisher | : National Academies Press |
Total Pages | : 74 |
Release | : 1999-05-06 |
Genre | : Medical |
ISBN | : 0309173051 |
The American Anti-Vivisection Society (AAVS) petitioned the National Institutes of Health (NIH) on April 23, 1997, to prohibit the use of animals in the production of mAb. On September 18, 1997, NIH declined to prohibit the use of mice in mAb production, stating that "the ascites method of mAb production is scientifically appropriate for some research projects and cannot be replaced." On March 26, 1998, AAVS submitted a second petition, stating that "NIH failed to provide valid scientific reasons for not supporting a proposed ban." The office of the NIH director asked the National Research Council to conduct a study of methods of producing mAb. In response to that request, the Research Council appointed the Committee on Methods of Producing Monoclonal Antibodies, to act on behalf of the Institute for Laboratory Animal Research of the Commission on Life Sciences, to conduct the study. The 11 expert members of the committee had extensive experience in biomedical research, laboratory animal medicine, animal welfare, pain research, and patient advocacy (Appendix B). The committee was asked to determine whether there was a scientific necessity for the mouse ascites method; if so, whether the method caused pain or distress; and, if so, what could be done to minimize the pain or distress. The committee was also asked to comment on available in vitro methods; to suggest what acceptable scientific rationale, if any, there was for using the mouse ascites method; and to identify regulatory requirements for the continued use of the mouse ascites method. The committee held an open data-gathering meeting during which its members summarized data bearing on those questions. A 1-day workshop (Appendix A) was attended by 34 participants, 14 of whom made formal presentations. A second meeting was held to finalize the report. The present report was written on the basis of information in the literature and information presented at the meeting and the workshop.
Author | : Steven U. Walkley |
Publisher | : |
Total Pages | : 496 |
Release | : 2004 |
Genre | : Medical |
ISBN | : |
Lysosomal storage diseases are inherited metabolic disorders characterized by severe pathology, typically involving the brain. Although individually rare, they collectively represent a significant group of diseases that primarily present in early infancy or childhood. In recent yearsconsiderable progress has been made in understanding the molecular mechanisms that lead to disordered function of the lysosomal system and to lysosomal storage. Unravelling the basis for these diseases is providing unique insight into the normal biology of cells and pointing the way to thedevelopment of therapeutic strategies for their treatment. Lysosomal Disorders of Brain details recent advances in the molecular and cellular pathologies of these diseases and in the development of effective therapies. After an overview of the biology of the endosomal-lysosomal system and the types of diseases resulting from defects in this system, thebook describes in detail the molecular mechanisms of storage, model systems and pathophysiological mechanisms, and finally, new advances toward treatment. With each chapter written by leading experts in their field, this book will be valuable for scientists and clinicians in helping them understandthe role of lysosomes in normal cells and mechanisms underlying these disorders, how they can be diagnosed, and the treatment options that are currently available.
Author | : John A. Barranger |
Publisher | : Springer Science & Business Media |
Total Pages | : 563 |
Release | : 2007-10-16 |
Genre | : Science |
ISBN | : 0387709096 |
The knowledge of lysosomal biology and the consequences of its dysfunction have increased dramatically in the past 60 years. This book describes the nature of the lysosomal dysfunction and diseases as well as potential future treatments and therapies. Disease specific chapters provide thorough reviews of the clinical features of lysosomal storage disorders, their molecular basis and the commercial or experimental therapeutic approaches sought in this area. This is an invaluable resource for researchers in biochemical and molecular genetics, enzyme therapy, and gene transfer.
Author | : Frederick J. Suchy |
Publisher | : Cambridge University Press |
Total Pages | : 995 |
Release | : 2007-05-07 |
Genre | : Medical |
ISBN | : 1139464035 |
Completely revised new edition of the premier reference on pediatric liver disease. Liver Disease in Children, 3rd Edition provides authoritative coverage of every aspect of liver disease affecting infants, children, and adolescents. The book offers an integrated approach to the science and clinical practice of pediatric hepatology and charts the substantial progress in understanding and treating these diseases. Chapters are written by international experts and address the unique pathophysiology, manifestations, and management of these disorders in the pediatric population. The third edition has been thoroughly updated and features new contributions on liver development, cholestatic and autoimmune disorders, fatty liver disease, and inborn errors of metabolism. With the continued evolution of pediatric hepatology as a discipline, this text remains an essential reference for all physicians involved in the care of children with liver disease.
Author | : YP Munjal |
Publisher | : JP Medical Ltd |
Total Pages | : 1450 |
Release | : 2015-08-30 |
Genre | : Medical |
ISBN | : 9351524159 |
This is the tenth edition of the authoritative API Textbook of Medicine, completely revised, updated and expanded, with 28 brand new chapters. The textbook is comprised of two volumes, divided into 29 sections. Beginning with an introduction to the practice of medicine, and a disease profile and epidemiology of communicable and non-communicable diseases, each subsequent section covers a separate medical specialty. The second section on ‘Clinical Approach to Key Manifestation’ has been expanded with six new chapters, including the appropriate selection of imaging modalities. Other new topics in this edition include advanced cardiac life support system, life-style changes in the management of diabetes, diabetes in the elderly, prevention of cardiovascular disease, acute and chronic pancreatitis, and tumours of the liver. Chapters on chronic and sleep-related pulmonary disorders have been completely re-written to highlight their increased prevalence, and a new chapter on pulmonary rehabilitation has been added. An entirely new section on the ‘Future of Medicine’ including regenerative medicine, nanotechnology and nanomedicine, robotic surgery, and an introduction to ‘space medicine’, brings the API Textbook of Medicine to its conclusion. With 1090 full colour images and illustrations, spanning over 3000 pages, this all-encompassing textbook is a comprehensive guide to the practice of medicine, brought fully up-to-date for physicians, surgeons and post-graduate medical students. Key Points New edition of this comprehensive, two volume textbook Fully revised, updated and expanded with 28 new chapters New section on the future of medicine 1090 full colour images and illustrations Previous edition published 2012
Author | : Carla E. M. Hollak |
Publisher | : Oxford University Press |
Total Pages | : 657 |
Release | : 2016 |
Genre | : Medical |
ISBN | : 0199972133 |
As clinical management of inherited metabolic diseases (IMDs) has improved, more patients affected by these conditions are surviving into adulthood. This trend, coupled with the widespread recognition that IMDs can present differently and for the first time during adulthood, makes the need for a working knowledge of these diseases more important than ever. Inherited Metabolic Disease in Adults offers an authoritative clinical guide to the adult manifestations of these challenging and myriad conditions. These include both the classic pediatric-onset conditions and a number of new diseases that can manifest at any age. It is the first book to give a clear and concise overview of how this group of conditions affects adult patients, a that topic will become a growing imperative for physicians across primary and specialized care.
Author | : Aubrey Milunsky |
Publisher | : John Wiley & Sons |
Total Pages | : 1392 |
Release | : 2021-03-30 |
Genre | : Science |
ISBN | : 1119676975 |
"The time is fast approaching when virtually all the culprit genes and their mutations for 7,000 rare monogenic disorders1 will be known. Thus far causal single genes and their mutations have been determined for 5,6732 genetic disorders, enabling pre-implantation genetic testing or prenatal genetic diagnosis. These advances using chromosomal microarrays, whole exome sequencing and even whole genome sequencing together with fetal imaging, and non-invasive prenatal testing, expand the era in which all couples have the option of avoiding or preventing having children with irreversible, irremediable, crippling, or lethal monogenic disorders. Primary care physicians, and those in all medical specialties, will need to inform their patients of this key option. This imperative is already partly in current practice. Missing is the requirement of physicians to request and obtain the precise name of the genetic disorder in question or an existing DNA report on a family member, for prospective parents to benefit from available options"--
Author | : Juan M. Pascual |
Publisher | : Cambridge University Press |
Total Pages | : 507 |
Release | : 2017-04-20 |
Genre | : Medical |
ISBN | : 1107042054 |
A review of childhood neurodegenerative and other progressive but non-degenerative disorders to guide their diagnosis and management.
Author | : Jennifer G. Treleaven |
Publisher | : Elsevier Health Sciences |
Total Pages | : 568 |
Release | : 2008-09-02 |
Genre | : Medical |
ISBN | : 0702033537 |
A guide to the practice of stem cell transplantation, its status in the treatment of various disorders and the problems that arise after transplantation, aimed at the whole transplant team. - An up to date guide to best practice in the use of stem cell transplantation, covering current status in the treatment of malignant and non-malignant conditions, practical aspects and problems such as infection and graft versus host disease. - Has a practical, accessible approach with free use of algorithms, list tables. - Aimed at the whole transplant team - this is an interdisciplinary field. - International contributor team with editors in the UK and USA. - Illustrated in colour throughout.