Download or read book Cystic Fibrosis in the Light of New Research written by Dennis Wat and published by BoD – Books on Demand. This book was released on 2015-08-24 with total page 394 pages. Available in PDF, EPUB and Kindle. Book excerpt: Cystic Fibrosis in the Light of New Research provides the latest research and clinical evidence that will be useful for clinicians, scientists and researchers to further their knowledge around this fascinating condition. The authors have brought along their expertise and wealth of knowledge to produce this book, including the basic science that underlies the disease, the burden of bacterial and viral infections, immunologic aspects of CF, a variety of clinical measurements to predict prognosis and novel therapies including gene therapy. This book will be invaluable and entertaining for anyone who is involved in the care of patients with cystic fibrosis.
Download or read book Cystic Fibrosis Reversed written by Artour Rakhimov and published by Createspace Independent Publishing Platform. This book was released on 2013-06-21 with total page 80 pages. Available in PDF, EPUB and Kindle. Book excerpt: Do not expect your medical doctor to know or teach you about lifestyle factors and how to change automatic breathing (the way we breathe 24/7). Medical schools teach nothing (zero) information about breathing retraining and nearly nothing about lifestyle (how to eat, sleep, exercise, etc.). It is true that cystic fibrosis life expectancy has been steadily growing for many decades. In the late 1930s, most babies with cystic fibrosis died before their first birthday. Later, in the 1950s, cystic fibrosis life expectancy was less than 10 years. Soon after, due to use of various therapies, it increased from 14 years (in the 1980s) up to current 35-37 years. Some researchers predict that babies born with cystic fibrosis during this century can live up to their 50s. However, very few Westerners are aware that there are many Russian people with cystic fibrosis who are over 50 and even 60 years old due to their adherence to one medical therapy that was developed and practiced by over 150 Soviet and Russian doctors. Since the 1960s, these MDs have applied the Buteyko breathing therapy to increase body oxygen levels, and these doctors claim that people with cystic fibrosis can have at least normal (or average) life expectancy. My own experience, in successful elimination of major symptoms of cystic fibrosis in our students, also suggests the same conclusions. The book offers a detailed description of main lifestyle modules from our course. This increases body oxygen naturally and significantly reduce many symptoms of cystic fibrosis (e.g., coughing, too much mucus, wheezing, and various digestive concerns) within days. How and why can these therapies work? Western medical studies clearly proved that tissue hypoxia (low oxygen in cells) creates problems in the work of tiny ionic pumps that transport chemicals (sodium, chlorine, and water) across the epithelial layers. This negative effect of hypoxia is present even in healthy people, but more expressed in people with cystic fibrosis due to the presence of the defective CFTR gene. Each and every study that measured respiratory parameters in people with cystic fibrosis found too fast and deep breathing (hyperventilation) in comparison with the medical norm (that is tiny). Low cellular oxygen causes the formation of too thick and viscous mucus. Cell hypoxia also suppresses the immune system. Both factors promote the growth of pathogens in people with cystic fibrosis in the respiratory and digestive systems, while other organs and body parts are also under physiological and biochemical stress due to low oxygen in cells. Other factors, such as chronic mouth breathing and chest breathing, also reduce body oxygen and make any treatment for cystic fibrosis less effective. Therefore, the suggested medical therapy, in order to increase cystic fibrosis life expectancy, is to slow down automatic breathing back to the medical norm and increase body oxygen naturally. Clinical experience of Buteyko breathing MDs in Russia suggests that results of a simple body oxygen test predict cystic fibrosis life expectancy. People with the moderate degree of cystic fibrosis usually have only about 15-20 seconds or less for their body oxygen test, while the medical norm is 40 seconds. In terminally ill people (with cystic fibrosis and many other disorders) body oxygen is less than 10 seconds. With over 40 seconds for the body-oxygen test, a person with cystic fibrosis can eliminate all symptoms and have an average life expectancy.
Download or read book Cystic Fibrosis written by Prashant Mohite and published by BoD – Books on Demand. This book was released on 2021-06-09 with total page 126 pages. Available in PDF, EPUB and Kindle. Book excerpt: Cystic fibrosis, a genetic disorder in children and young adults, is a multisystemic disease that mainly affects the lungs. Advances and improvements in the diagnosis and management of this condition have led to increased overall and symptom-free survival in cystic fibrosis patients. This book examines recent advances in the field and presents an evidence-based approach to the management of cystic fibrosis.
Download or read book Liver Disease in Children written by Frederick J. Suchy and published by Cambridge University Press. This book was released on 2021-03-18 with total page 875 pages. Available in PDF, EPUB and Kindle. Book excerpt: Liver disease in children is increasing in prevalence, placing a huge burden on healthcare systems and often requiring long-term management. Offering an integrative approach to the science and clinical practice of pediatric hepatology, this is the definitive reference text for improved diagnosis and treatment strategies. In the new edition of this authoritative text, chapters have been thoroughly revised in line with major advances in the field, such as recognizing the increased frequency of fatty liver disease, and how genetic testing has the potential to establish earlier diagnoses for a variety of diseases. Disorders covered include cholestasis, metabolic disorders and hepatitis, with their presentation across the spectrum of infancy, childhood and adolescence discussed. The indications and surgical aspects of liver transplant are explained and post-transplant care is described in detail. This is a valuable resource for pediatricians, hepatologists, gastroenterologists and all clinicians involved in the care of children with liver diseases.
Download or read book Cystic Fibrosis Life Expectancy written by Artour Rakhimov and published by CreateSpace. This book was released on 2013-06-21 with total page 80 pages. Available in PDF, EPUB and Kindle. Book excerpt: Cystic fibrosis is a lifestyle disease. Very few people on the West are aware that there are many Russians with CF (cystic fibrosis) who are over 50 and even 60 years old due to their adherence to one medical therapy that was developed and practiced by over 150 Soviet and Russian medical doctors. Since 1960s, these MDs have applied the Buteyko breathing therapy to increase body oxygen levels, and these doctors claim that people with CF can have at least normal (or average) life expectancy if their maintain high (or normal) body O2 content. You will not find such information in any other cystic fibrosis books. Cystic fibrosis life expectancy has been steadily growing for many decades. In late 1930s, most babies with CF died before their first birthday. Later, in the 1950s, CF life expectancy was less than 10 years. Soon after, due to use of various therapies, it increased from 14 years (in the 1980s) up to current 35-37 years. Some researchers, in their cystic fibrosis books, predict that babies born with CF during this century can live up to their 50s. But a group of Russian doctors claim that main symptoms of CF can be defeated. My own experience, in successful elimination of major symptoms of CF in my students, also suggests the same conclusions. These breathing methods address lifestyle factors that influence body O2 and use breathing exercises to increase body oxygenation. The book offers a detailed description of main lifestyle modules that increase body O2 naturally and significantly reduce many symptoms of CF (e.g., coughing, too much mucus, wheezing, and various digestive concerns) within days. How and why can these therapies work? CF is considered a genetic disease. So is asthma, or Down syndrome. Not all genetic diseases are the same. Many of them, CF included, are also lifestyle diseases meaning that lifestyle choices have a direct impact on quality of life (and CF life expectancy). Western medical studies clearly proved that tissue hypoxia (low O2 in cells) creates problems in the work of tiny ionic pumps that transport chemicals (sodium, chlorine and water) across the epithelial layers. This negative effect of hypoxia is present even in healthy people, but more expressed in people with CF due to the presence of the defective CFTR gene. Each and every study that measured respiratory parameters in people with CF found too fast and deep breathing (hyperventilation) in comparison with the medical norm (that is tiny). There are two long-term scenarios due to overbreathing. Either we get low CO2 levels in the blood (this causes spasm of blood vessels and reduced body O2) or we destroy our airways and lungs due to injurious effects of hypocapnia. In any scenario (with and without lung involvement), hyperventilation leads to low O2 levels in cells. Low cellular O2 causes formation of too thick and viscous mucus. Cell hypoxia also suppresses the immune system. Both factors promote growth of pathogens in people with CF in the respiratory and digestive systems, while other organs and body parts are also under physiological and biochemical stress due to low O2 in cells. Other factors, such as chronic mouth breathing and chest breathing, also reduce body O2 and make any treatment of CF less effective. Therefore, the suggested medical therapy, in order to increase CF life span, is to slow down automatic breathing back to the medical norm and increase body O2 naturally. Clinical experience of Buteyko breathing MDs in Russia suggests that results of a simple body O2 test predict cystic fibrosis life expectancy. People with moderate degree of CF usually have only about 15-20 seconds or less for their body oxygen test, while the medical norm is 40 seconds. In terminally ill people (with CF and many other disorders) body O2 is less than 10 seconds. With over 40 seconds for the body O2 test, a person with CF can eliminate all symptoms and have an average life expectancy.
Download or read book Lung Epithelial Biology in the Pathogenesis of Pulmonary Disease written by Venkataramana K Sidhaye and published by Academic Press. This book was released on 2017-03-09 with total page 276 pages. Available in PDF, EPUB and Kindle. Book excerpt: Lung Epithelial Biology in the Pathogenesis of Pulmonary Disease provides a one-stop resource capturing developments in lung epithelial biology related to basic physiology, pathophysiology, and links to human disease. The book provides access to knowledge of molecular and cellular aspects of lung homeostasis and repair, including the molecular basis of lung epithelial intercellular communication and lung epithelial channels and transporters. Also included is coverage of lung epithelial biology as it relates to fluid balance, basic ion/fluid molecular processes, and human disease. Useful to physician and clinical scientists, the contents of this book compile the important and most current findings about the role of epithelial cells in lung disease. Medical and graduate students, postdoctoral and clinical fellows, as well as clinicians interested in the mechanistic basis for lung disease will benefit from the books examination of principles of lung epithelium functions in physiological condition. Provides a single source of information on lung epithelial junctions and transporters Discusses of the role of the epithelium in lung homeostasis and disease Includes capsule summaries of main conclusions as well as highlights of future directions in the field Covers the mechanistic basis for lung disease for a range of audiences
Download or read book Cystic Fibrosis written by Dennis Wat and published by . This book was released on 2020 with total page 136 pages. Available in PDF, EPUB and Kindle. Book excerpt: Cystic Fibrosis - Heterogeneity and Personalized Treatment provides the latest research and clinical evidence for clinicians, scientists and researchers involved in the care of patients with cystic fibrosis (CF). This book outlines the burden of the CF microbiome, utilisation of CF registries to impact future care, the sequelae of hepatobiliary complication, the use of upcoming technologies to provide patient-centred care, and provides an overview of cystic fibrosis transmembrane regulator (CFTR) modulators. Looking after patients with CF is highly rewarding, allowing those of us to combine our dedication and problem-solving skills to create a personalized approach. This book is invaluable for those involved in the care of CF patients.
Download or read book A Life Course Perspective on Health Trajectories and Transitions written by Claudine Burton-Jeangros and published by Springer. This book was released on 2016-10-22 with total page 213 pages. Available in PDF, EPUB and Kindle. Book excerpt: This open access book examines health trajectories and health transitions at different stages of the life course, including childhood, adulthood and later life. It provides findings that assess the role of biological and social transitions on health status over time. The essays examine a wide range of health issues, including the consequences of military service on body mass index, childhood obesity and cardiovascular health, socio-economic inequalities in preventive health care use, depression and anxiety during the child rearing period, health trajectories and transitions in people with cystic fibrosis and oral health over the life course. The book addresses theoretical, empirical and methodological issues as well as examines different national contexts, which help to identify factors of vulnerability and potential resources that support resilience available for specific groups and/or populations. Health reflects the ability of individuals to adapt to their social environment. This book analyzes health as a dynamic experience. It examines how different aspects of individual health unfold over time as a result of aging but also in relation to changing socioeconomic conditions. It also offers readers potential insights into public policies that affect the health status of a population.
Download or read book Thoracic Medicine written by Peter Emerson and published by Butterworth-Heinemann. This book was released on 1981 with total page 1112 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Nutrition in Cystic Fibrosis written by Elizabeth H. Yen and published by Humana Press. This book was released on 2015-11-28 with total page 288 pages. Available in PDF, EPUB and Kindle. Book excerpt: Nutritional therapies have been key early interventions, and remain central to the well-being and survival of patients with cystic fibrosis. The nature of the disease causes significant alterations in a patient’s ability to process and assimilate nutrients. Furthermore, many factors contribute to higher metabolic demands throughout a patient’s life. In combination, maldigestion, malabsorption, and increased metabolic demands pose a high hurdle for the patient to overcome in order to maintain optimal nutritional status. Nutrition in Cystic Fibrosis: A Guide for Clinicians is an excellent resource for physicians, nurses and dietitians who deliver care for patients with cystic fibrosis. The book provides an introduction to cystic fibrosis and nutritional assessments. It will also serve as a comprehensive guide to the nutritional monitoring and management of patients with cystic fibrosis including special populations within cystic fibrosis that require additional considerations. The chapters are written by experts in their fields and include the most up to date scientific and clinical information. Nutrition in Cystic Fibrosis: A Guide for Clinicians targets pediatric and adult pulmonologists and gastroenterologists, residents and fellows, internists, pediatricians, nurses, dietitians and general practitioners who treat patients with cystic fibrosis.
Download or read book Idiopathic Pulmonary Fibrosis written by Ulrich Costabel and published by European Respiratory Society. This book was released on 2016-03-01 with total page 292 pages. Available in PDF, EPUB and Kindle. Book excerpt: Idiopathic pulmonary fibrosis (IPF) is a steadily progressive and ultimately fatal disease of unknown origin. Recent years have seen advances in our understanding of IPF and a number of guidelines have been published. But many questions remain unanswered, particularly surrounding probable versus definite IPF. This Monograph aims to discuss the latest achievements in IPF, and covers key diagnostic issues, staging of the disease, complications and comorbidities, treatment, unmet patient needs and perspectives for the future. This book will be of interest to all clinicians and researchers in this area.
Download or read book Handbook of Immunohistochemistry and in situ Hybridization of Human Carcinomas written by M. A. Hayat and published by Elsevier. This book was released on 2006-05-23 with total page 609 pages. Available in PDF, EPUB and Kindle. Book excerpt: Classical histology has been augmented by immunohistochemistry (the use of specific antibodies to stain particular molecular species in situ). Immunohistochemistry has allowed the identification of many more cell types than could be visualized by classical histology, particularly in the immune system and among the scattered hormone-secreting cells of the endocrine system. This book discusses all aspects of immunohistochemistry and in situ hybridization technologies and the important role they play in reaching a cancer diagnosis. It provides step-by-step instructions on the methods of additional molecular technologies such as DNA microarrays, and microdissection, along with the benefits and limitations of each method. * The only book available that translates molecular genetics into cancer diagnosis * Methods were developed by internationally-recognized experts and presented in step-by-step manner * Results of each Immunohistochemical and in situ hybridization are presented in the form of color illustrations
Download or read book Cystic Fibrosis written by National Institutes of Health (U.S.). and published by . This book was released on 1979 with total page 108 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Cystic Fibrosis Clinical sciences written by National Institutes of Health (U.S.) and published by . This book was released on 1979 with total page 48 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Cystic Fibrosis Clinical sciences written by and published by . This book was released on 1979 with total page 48 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Cystic Fibrosis New Insights for the Healthcare Professional 2013 Edition written by and published by ScholarlyEditions. This book was released on 2013-07-22 with total page 385 pages. Available in PDF, EPUB and Kindle. Book excerpt: Cystic Fibrosis: New Insights for the Healthcare Professional: 2013 Edition is a ScholarlyEditions™ book that delivers timely, authoritative, and comprehensive information about Diagnosis and Screening. The editors have built Cystic Fibrosis: New Insights for the Healthcare Professional: 2013 Edition on the vast information databases of ScholarlyNews.™ You can expect the information about Diagnosis and Screening in this book to be deeper than what you can access anywhere else, as well as consistently reliable, authoritative, informed, and relevant. The content of Cystic Fibrosis: New Insights for the Healthcare Professional: 2013 Edition has been produced by the world’s leading scientists, engineers, analysts, research institutions, and companies. All of the content is from peer-reviewed sources, and all of it is written, assembled, and edited by the editors at ScholarlyEditions™ and available exclusively from us. You now have a source you can cite with authority, confidence, and credibility. More information is available at http://www.ScholarlyEditions.com/.
Download or read book Diagnostic Molecular Pathology in Practice written by Iris Schrijver and published by Springer Science & Business Media. This book was released on 2011-09-09 with total page 329 pages. Available in PDF, EPUB and Kindle. Book excerpt: This entirely case-based book covers a broad cross-section of the practical issues frequently encountered in the day-to-day activities of a molecular genetic pathologist. The book is divided into four sections on the principal areas addressed in molecular genetic pathology (MGP): inherited diseases, hematopathology, solid tumors, and infectious diseases. The topics covered by the cases in each section include test selection, qualitative and quantitative laboratory techniques, test interpretation, prognostic and therapeutic considerations, ethical considerations, technical troubleshooting, and result reporting. This book will be ideal for trainees in MGP and clinical molecular genetics who require a practice-based preparation for board examinations. It will also be very useful for residents and fellows in medical specialties to which MGP is pertinent, and for practicing pathologists who want to learn more about the current practice of molecular diagnostics.
