The Oxford Specialist Handbook of Paediatric Nephrology helps the reader understand and manage all conditions affecting the kidney in childhood. This concise yet comprehensive guide covers everything from history taking and urinalysis, to electrolyte management, acute kidney injury and transplantation. It is a complete reference for the day to day, bedside, and out-patient management of all conditions dealt with by general paediatricians and specialist paediatric nephrologists. The handbook also offers advice to clinical professionals working with patients in shared care between general hospitals and specialised centres. Paediatric Nephrology benefits from a clear, user-friendly layout, with bullet points and text boxes to highlight key information and colour plates illustrations and photographs. This makes the book a perfect reference for use on-the-go, and easy to navigate during an emergency. The primary focus of the book is investigation and management, but in order to enable a better understanding of conditions such as fluid and electrolytes, it also discusses pathophysiology. Evidence-based recommendations are made where possible, however the authors also provide recommendations informed by their own personal experience and current best practice in areas where high quality evidence is still lacking. Paediatric Nephrology is useful for paediatric consultants and doctors at all levels of their training, including the general paediatrician and the specialist nephrologist. The book has a global appeal, and presents information that is applicable worldwide.

For more than 40 years, this well-regarded reference has bridged the gap between basic and clinical sciences for the many disorders associated with electrolyte imbalances and kidney dysfunction. Authoritative and easy to read, the eighth edition has been thoroughly updated by experts in the field to reflect recent developments in renal pathophysiology. Each chapter first introduces normal physiology, then covers each disorder's clinical features, diagnosis, and treatment. Helpful diagrams, algorithms, and tables further explain the complex concepts. Key Features: A new two-color format throughout promotes easier comprehension and faster navigation. Redrawn and colorized line drawings make complex concepts easier to understand and more visually appealing. New coverage includes: recent developments in disorders of water homeostasis; substantial new information on genetic hypokalemic and hyperkalemic disorders; new content on calcium, phosphorus, vitamin D, and parathyroid hormone activity; a new chapter on the genomic and nongenomic effects of angiotensin and aldosterone in renal and cardiovascular disease; an up-to-date discussion of the pivotal role of the kidney in the pathogenesis of hypertensive states; new advances in our understanding of the glomerulopathies and vasculitides; and much more. Ideal for all members of the nephrology team, including residents and fellows in nephrology, internal medicine, and other specialties, as well as nurses and physician assistants. Your book purchase includes a complimentary download of the enhanced eBook for iOS, Android, PC & Mac. Take advantage of these practical features that will improve your eBook experience: The ability to download the eBook on multiple devices at one time - providing a seamless reading experience online or offline Powerful search tools and smart navigation cross-links allow you to search within this book, or across your entire library of VitalSource eBooks Multiple viewing options offer the ability to scale images and text to any size without losing page clarity as well as responsive design The ability to highlight text and add notes with one click.

This book aims to present a comprehensive classification of hypertensive phenotypes based on underlying target organ involvement. Particular emphasis is placed on review and assessment of clinical presentation, pathophysiologic mechanisms, and possible specific therapeutic options for each hypertension phenotype. Several of these phenotypes are well known and well described in the literature, such as prehypertension, white coat and masked hypertension, isolated systolic hypertension, renovascular hypertension, endocrine hypertension, pediatric hypertension, and gestational hypertension. Other hypertension phenotypes, however, are not widely recognized, being reported only in special reviews; examples include hypertension associated with renal calculus disease and other rarer causes such as Turner syndrome, herbal and medicinal compounds, and pharmacologic agents. A detailed account of the various causes of monogenic hypertension is also included. Finally, a section is devoted to general aspects of hypertension, including the significance of blood pressure indices, the natural course of untreated and treated hypertension, hypertension mechanisms, genetics, and guidelines for blood pressure control.

Critical References Nephrology (Edition 1) contains the essential references for each of 62 topics in adult clinical nephrology. With each reference, the authors have explained how that research study contributed to the clinical topic of interest, providing immediate context. Critical References Nephrology (Edition 1) is an invaluable reference, serving as an easy guide for exam preparation, daily clinical practice and preparation of both research articles and teaching sessions. By summarizing the major findings of the most important research studies, Critical References Nephrology quickly provides the most evidence based information of all major nephrology topics.

This book reviews important aspects of polycystic kidney diseases, the latest scientific understanding of the diseases and syndromes, along with the therapies being developed. Cystic kidney diseases comprise a spectrum of genetic syndromes defined by renal cyst formation and expansion with variable extrarenal manifestations. The most prevalent disorder is the autosomal dominant polycystic kidney disease (ADPKD). It is the most common monogenetic disorder in humans and accounts for 4.4% of end-stage renal disease (ESRD) cases in the U.S. Patients inevitably progress to ESRD and require renal replacement therapy in the form of dialysis or transplantation. Through advancements in genomics and proteomics approaches, novel genes responsible for cystic diseases have been identified, further expanding our understanding of basic mechanisms of disease pathogenesis. The hallmark among all cystic genetic syndromes is the formation and growth of fluid-filled cysts, which originate from tubular epithelia of nephron segments. Cysts are the disease, and treatment strategies are being developed to target prevention or delay of cyst formation and expansion at an early stage, however no such therapy is currently approved.

The two kidneys of mammalian organisms receive around 25 % of the cardiac output at rest, of which only 7 % is distributed to the renal medulla. Despite the low blood flow to the renal medulla, small changes in perfusion to the region can have profound effects on urine-concentrating ability and the excretion of sodium, which in turn affects the chronic regulation of body fluid volumes and arterial blood pressure. Importantly, we know that if blood flow to the renal medulla is not tightly regulated, sodium and water homeostasis is impaired and medullary hypoxia develops. The resultant injury inevitably reduces urine concentrating ability and leads to hypertension. This book will discuss the variety of mechanisms that mammalian organisms have developed to ensure that renal medullary blood flow and oxygen levels are precisely regulated. This book will focus on the unique anatomical arrangement of the medullary circulation, the functional roles of medullary blood flow, as well as the experimental techniques used to assess medullary blood flow and the insight that these studies have provided. The hormonal and non-hormonal control of medullary blood flow will be considered and finally the impact of reduced medullary blood flow on blood pressure is discussed.