Isbn: 9783662494080 - inherited metabolic diseases: a clinical approach (3 Ergebnisse)

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    • Sprache: Englisch

      Verlag: Berlin, Springer., 2017

      3662494086 / 9783662494080

      • Hardcover

      Anbieter: Universitätsbuchhandlung Herta Hold GmbH, Berlin, DeutschlandUniversitätsbuchhandlung Herta Hold GmbH

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      Verbandsmitglied: VDAGIAQILAB

      Zustand: Gebraucht

      EUR 24,00

      EUR 30,00 Versand 
      Versand von Deutschland nach USA

      Anzahl: 1 verfügbar

      2nd ed. XVII, 605 p. Hardcover. 2nd ed. Versand aus Deutschland / We dispatch from Germany via Air Mail. Einband bestoßen, daher Mängelexemplar gestempelt, sonst sehr guter Zustand. Imperfect copy due to slightly bumped cover, apart from this in very good condition. Stamped. Sprache: Englisch.

    • Sprache: Englisch

      Verlag: Springer Verlag, 2016

      3662494086 / 9783662494080

      • Hardcover

      Anbieter: Revaluation Books, Exeter, Vereinigtes KönigreichRevaluation Books

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      Zustand: Neu

      EUR 225,92

      EUR 23,33 Versand 
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      Hardcover. Zustand: Brand New. 2nd har/psc edition. 605 pages. 10.00x7.00x1.50 inches. In Stock.

    • Sprache: Englisch

      Verlag: Springer Vieweg, 2016

      3662494086 / 9783662494080

      • Hardcover

      Anbieter: AHA-BUCH GmbH, Einbeck, DeutschlandAHA-BUCH GmbH

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      Zustand: Neu

      EUR 320,10

      EUR 40,96 Versand 
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      Buch. Zustand: Neu. Druck auf Anfrage Neuware - Printed after ordering - This book focuses on clinical presentations that may be caused by inherited metabolic diseases. Its symptom- and system-based approach will help clinicians with and without detailed knowledge of human biochemistry in all specialties to reach a correct diagnosis and institute the optimal treatment program. The book summarizes the central elements of inherited metabolic diseases and describes clearly how to carry out an efficient yet complete diagnostic work-up, thereby guiding the clinician from the presenting symptoms and signs through to effective initial management. After an introduction to the different disorders, the book explains when to consider an inborn metabolic error and which initial tests to order. Core aspects such as structured communication, guidelines, transition, pregnancy, maternal care and how to respond to various medical emergencies are covered. Therapeutic concepts such as dietary treatment are delineated and practical advice provided on the quite different treatment approaches required for individual diseases. An extensive section structured according to organ systems outlines the correct approach in the context of specific symptoms and signs. The value of each of the potential investigations is explained, with precise advice on the interpretation of results. The inclusion of algorithms, tables, lists, and charts facilitates rapid decision making and information retrieval, and the appendices include a helpful guide to differential diagnosis based on clinical and biochemical phenotypes. This new updated edition of Inherited Metabolic Diseases will be an invaluable aid for the busy clinician and an excellent quick reference for metabolic and genetic specialists.