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Highly Commended, BMA Medical Book Awards 2013Sarcoidosis represents a major challenge for physicians-not just in respiratory medicine, but across a range of specialties. This book, with a multidisciplinary authorship of the highest standard, presents the most up-to-date thinking on all aspects of the condition, from epidemiology to clinical manife
Pulmonary Sarcoidosis: A Guide for the Practicing Clinician is a valuable resource for clinicians of varied disciplines concerning the care of the sarcoidosis patient. Sarcoidosis is a multi-system disorder and represents a major challenge to physicians. Although any organ may be involved with sarcoidosis, the lung is the most common organ affected. Chapters are written by distinguished authors who have extensive experience in caring for these patients. Detailed figures and tables are provided to guide the practicing clinician through all aspects of the condition, from clinical manifestations to treatment options. Pulmonary Sarcoidosis: A Guide for the Practicing Clinician is fully comprehensive and evidence-based and will be an essential addition to the bookshelves of all whose practice involves the care and treatment of patients with sarcoidosis.
In this issue of Clinics in Chest Medicine, guest editors Drs. Robert P. Baughman, Elyse E. Lower, and Marc A. Judson bring their considerable expertise to the topic of Sarcoidosis. Top experts in the field discuss the role of bronchoscopy in diagnosis of sarcoidosis; monitoring pulmonary sarcoidosis; ocular sarcoidosis; biomarkers in sarcoidosis; cutaneous sarcoidosis; neurologic sarcoidosis; and more. - Contains 15 relevant, practice-oriented topics including sarcoidosis-associated pulmonary hypertension; predictors of mortality from sarcoidosis; hematologic manifestations of sarcoidosis; quality of life; anti-inflammatory therapy for sarcoidosis; and more. - Provides in-depth clinical reviews on sarcoidosis, offering actionable insights for clinical practice. - Presents the latest information on this timely, focused topic under the leadership of experienced editors in the field. Authors synthesize and distill the latest research and practice guidelines to create clinically significant, topic-based reviews.
This issue of Clinics in Chest Medicine focuses on Sarciodosis. Drs. Baughman and Culver have put together an expert roster of authors for articles concerning: Etiology of sarcoidosis, Immunology of sarcoidosis, Genetics of Sarcoidosis, Diagnosis of sarcoidosis, Chest imaging, Biomarkers and genetic profiles, Pulmonary Sarcoidosis, Neurosarcoidosis, Cardiac Sarcoidosis, Ocular Sarcoidosis, Quality of life assessments, and more!
Since the first edition of this book in 1967, interest in sarcoidosis has increased world-wide, leading to increasing numbers of published clinical, epidemiological and laboratory studies, notably in immunology and in the pathogenesis of granulomatous inflammation. Aseries of international con ferences which started as an informal gathering in London in. 1958 has continued at approximately three-yearly intervals with increasing numbers of participants and more formal organisation, and the proceedings of all but the first have been published. When the preparation of a second edition was suggested to me, I consi dered several questions. ls there still a piace for a comprehensive, clinically or...
- Comprehensive illustrative encyclopedia containg many rare images - Includes clinical analysis for the physician - Designed to complement and provide a visual supplement to already existing texts on sarcoidosis - Only atlas of sarcoidosis which reviews the multisystmeic nature of sarcoidosis on the context of clinical medicine - Written by world reknown experts in sarcoidosis
Get a quick, expert overview of the etiology, diagnosis, and management of pulmonary and extra pulmonary sarcoidosis with this concise, practical resource. Drs. Robert B. Baughman and Dominique Valeyre fully cover the recent advances in various aspects of this disease, including new genetic studies and new diagnostic techniques. It's an ideal resource for pulmonologists and respiratory medicine specialists, as well as primary care physicians and pulmonary/respiratory care nurses. Provides a comprehensive discussion of the various facets of sarcoidosis, including common manifestations of the lung, skin, and eyes, as well as other important aspects such as cardiac and neurologic disease. Covers newer diagnostic techniques for the lungs and elsewhere in the body, each discussed in detail and compared to older diagnostic techniques. Discusses treatment options including anti-inflammatory drugs, and management of other aspects of the disease, such as pulmonary hypertension, fatigue, and small fiber neuropathy. Consolidates today's available information and experience in this important area into one convenient resource.
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.
Sarcoidosis is a rare condition that causes small patches of red and swollen tissue, called granulomas, to develop in the organs of the body. It most often affects the lungs and skin. Typical symptoms include tender, red bumps on the skin, shortness of breath and a persistent cough. There is no cure for sarcoidosis, but the condition often improves without treatment within a few months or years. Sarcoidosis is estimated to affect about 1 in every 10,000 people in the UK (NHS Choices). Part of the Clinical Focus Series, this book provides trainees with an overview of this complex condition. Beginning with an introduction and guidance on recognising pulmonary granulomas, the following chapters...