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As clinical management of inherited metabolic diseases (IMDs) has improved, more patients affected by these conditions are surviving into;
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that this is an inherited metabolic disease, and where one goes from here to establish a diagnosis. The well-illustrated text is organised;
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Inherited Metabolic Diseases are common enough for health, social service and education professionals to encounter them periodically, but;
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expanded new edition of the first book to bridge clinical epilepsy with inherited metabolic diseases brings together leading authorities to present;
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and pathogenesis, treatment and prognosis of inherited metabolic diseases, along with essential information on clinical presentation.
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clinical workload. Endocrine and Metabolic Medical Emergencies: A Clinician's Guide provides a singular reference to help endocrinologists, acute;
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cases, diagnosis of inherited disease is delayed or missed owing to a lack of awareness, and an even greater number of relatives are exposed to;
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with a detailed knowledge of inherited cardiovascular diseases, from the fundamentals of molecular biology and genetic testing to the detailed;
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different. This book thoroughly covers various neonatal and pediatric liver and metabolic diseases through a unique clinical case based approach via;
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procedures to treat metabolic diseases, especially, Type 2 diabetes. This book is a guide to techniques in bariatric and metabolic surgery;
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Clinical Paediatric Dietetics, Fifth Edition continues to provide a very practical approach to dietary management of children with an;
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discussion to diseases associated with metabolic syndrome. The development of drug therapies for these diseases and complications is extensively;
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Primer on the Metabolic Bone Diseases and Disorders of Mineral Metabolism offers an updated and comprehensive guide to bone and mineral health;
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previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder.;
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previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder.;
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previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder.;
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previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder.;
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This new edition is a comprehensive guide to ocular syndromes and systemic diseases, for clinicians. Presented alphabetically for;
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experience providing nutrition management of patients with an inherited metabolic disorder (IMD), Nutrition Management of Patients with Inherited;
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pathophysiology of cardiovascular and metabolic diseases Written in a concise and easy to read manner, allowing readers to quickly understand;
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theory illuminate and explain the origin of these diseases, development of this theory logically leads to a novel and revolutionary metabolic and;
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This concise, case-based text discusses the current state of the art for the diagnosis and management of metabolic bones diseases. Each;
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disorders, and inherited metabolic diseases. This expertly written reference provides current information on methods and outcomes in a wide range;
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Practical Developments in Inherited Metabolic Disease is een boek van Springer;
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diseases associated with nucleic acids metabolism such as gout and Lesch-Nyhan syndrome. The last two chapters are dedicated to concise but useful;
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our understanding of both the scientific and the clinical basis of these diseases. Lysosomal Storage Disorders: A Practical Guide is the fruit;
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awareness, the metabolic basis of the manifestation will not be recognized at all.This book offers a guide on how to diagnose the metabolic;
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