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The McArdle Disease Handbook
This handbook explains, in layman's terms, the cause, method of inheritance, history and current and future treatments of McArdle Disease (also known as Glycogen Storage Disease Type V). The handbook puts into plain English the published information relating to the scientific and medical research into McArdle Disease.
One Step at a Time
The account of the author's coming to terms with her diagnosis of a rare muscle disorder. She faces the challenges of a 210 mile long trek across the mountains of Wales. Includes a section on the development of walking courses for people with McArdle Disease and one of guidance for people with the condition who want to follow in her footsteps.
Patient Care in Community Practice
The objectives of this new edition of PATIENT CARE IN COMMUNITY PRACTICE remain the same as in the first: to provide a unique, single-volume, handy reference guide to the background, use and range of non-medicinal products and appliances that may be used in the home. (Preface p. xi).
Oxford Handbook of Primary Care and Community Nursing
This handbook serves as a reference guide for everyday clinical decision-making and provides the organisational knowledge necessary for those nurses who work on the interface of the statutory and voluntary sectors in health, education and social care.
Oxford Handbook of Primary Care and Community Nursing
This Handbook provides easily accessible, contemporary, and evidence-based material, to act a reference or first point of enquiry for practitioners working in the diverse areas of primary and community care
Directory of British Associations & Associations in Ireland
This guide covers the 7000 national associations, chambers of commerce, confederations, federations, institutes, societies and trade unions in all fields of activity. Amongst the information listed is: full name and address; fax, phone and e-mail numbers; web site; contact names; legal status; branches; category and sphere of interest; groups; activities; affiliations; membership; publications; and changes of name (within the last five years).
A Clinical Guide to Inherited Metabolic Diseases
This user-friendly clinical handbook provides a clear and concise overview of how to go about recognizing and diagnosing inherited metabolic diseases. The reader is led through the diagnostic process from the identification of those features of an illness suggesting that it might be metabolic through the selection of appropriate laboratory investigation to a final diagnosis. The book is organized into chapters according to the most prominent presenting problem of patients with inherited metabolic diseases: neurologic, hepatic, cardiac, metabolic acidosis, dysmorphism, and acute catastrophic illness in the newborn. It also includes chapters on general principles, laboratory investigation, neonatal screening, and the principles of treatment. This new edition includes much greater depth on mitochondrial disease and congenital disorders of glycosylation. The chapters on neurological syndrome and newborn screening are greatly expanded, as are those on laboratory investigation and treatment, to take account of the very latest technological developments.
Neuromuscular Disorders in the Adult
A practical handbook for anyone caring for people with progressive disability due to muscle wasting conditions.
Pocket Consultant
There have been significant developments in the fields of gastroenterology and hepatology since the previous edition and this new edition has been entirely revised, updated and considerably expanded. The format and layout have also been updated to include key points at the start of each chapter, bulleted lists and text boxes for tips and warnings. A new author team - which, for the first time, is international - has brought a new global perspective to this book. This is still the leading book for trainees/fellows in gastroenterology and hepatology, as well as junior doctors and general medicine interns. The series title is 'Pocket Consultant' - and that's exactly what the reader gets - the advice and guidance of a consultant on hand when and where they need it.
McArdle Disease - Reference for GPs
This booklet provides referenced information to assist General Practitioners. McArdle Disease (Glycogen Storage Disease V) is an ultra rare metabolic disorder of the muscles. It should be managed in a specialist centre, but this booklet can help with issues arising in the primary care setting.
