Hoffmann georg f (59 Ergebnisse)

Zustand: good. Befriedigend/Good: Durchschnittlich erhaltenes Buch bzw. Schutzumschlag mit Gebrauchsspuren, aber vollständigen Seiten. / Describes the average WORN book or dust jacket that has all the pages present.

Zustand: very good. Gut/Very good: Buch bzw. Schutzumschlag mit wenigen Gebrauchsspuren an Einband, Schutzumschlag oder Seiten. / Describes a book or dust jacket that does show some signs of wear on either the binding, dust jacket or pages.

Softcover. Zustand: As New. Leichte Kratzer / Abnutzungen / Druckstellen. This pocket size clinical reference provides concise information on diagnosis and management of inherited metabolic diseases. Topics in this handy guide cover approaches to metabolic diseases, specialized investigations of metabolic diseases, functional tests and additional diagnostic procedures, a system and symptom based approach to patients, and commonalities of therapy. Numerous tables and figures provide rapid access to individual items aiding in diagnostic and therapeutic decisions. This valuable resource is a useful tool for pediatricians, internists, neurologists, and clinical geneticists.…

Paperback. Zustand: Brand New. 5th edition. 264 pages. 7.17x4.72x0.55 inches. In Stock.

Zustand: New.

Zustand: New. In German.

Zustand: Very Good. 1st Edition. Pages intact with possible writing/highlighting. Binding strong with minor wear. Dust jackets/supplements may not be included. Stock photo provided. Product includes identifying sticker. Better World Books: Buy Books. Do Good.

0. Gr. 8°.141 S., VI, 192 S., VII, 227 S., Orig.-Halblederband. Einband leicht berieben. Schönes Exemplar. de Band.

Taschenbuch. Zustand: Neu. Neuware - Immediate access to expert advice .Every so often a physician will be confronted with a patient who has an inborn error of metabolism. This can be a challenging situation, particularly in an emergency when rapid, specific investigations and effective treatment are essential for a good outcome. It is exactly then that it is good to have the Vademecum Metabolicum at hand. This concise book - explains the typical presentation patterns of the various metabolic disease groups; - describes essential differential diagnostic procedures; - summarises the main features of all metabolic diseases from the clinician s point of view.With its unique approach, easy accessibility, and availability in 10 different Languages, Vademecum Metabolicum is the most successful book on inborn errors of metabolism worldwide! Highly valued by practitioners in all specialities (particularly paediatricians, geneticists, general physicians, neurologists, laboratory physicians) as well as midwives, nurses and medical students.…

Paperback. Zustand: Brand New. 64 pages. German language. 8.27x5.83x0.15 inches. In Stock.

Zustand: New. Immediate access to expert advice .Every so often a physician will be confronted with a patient who has an inborn error of metabolism. This can be a challenging situation, particularly in an emergency when rapid, specific invest.

Taschenbuch. Zustand: Gut. 128 S. Besitzereintrag innen. Innerhalb Deutschlands Versand je nach Größe/Gewicht als Großbrief bzw. Bücher- und Warensendung mit der Post oder per DHL. Rechnung mit MwSt.-Ausweis liegt jeder Lieferung bei. Sprache: Englisch Gewicht in Gramm: 454.

Softcover. Zustand: Gut. 106 S. Ehem. Bibliotheksexemplar mit Signatur und Stempel. GUTER Zustand, ein paar Gebrauchsspuren. Ex-library with stamp and library-signature. GOOD condition, some traces of use. w20391 3857914432 Sprache: Deutsch Gewicht in Gramm: 350.

Zustand: Good. 2010th Edition. Former library copy. Pages intact with minimal writing/highlighting. The binding may be loose and creased. Dust jackets/supplements are not included. Includes library markings. Stock photo provided. Product includes identifying sticker. Better World Books: Buy Books. Do Good. …

Zustand: New. This is a Brand-new US Edition. This Item may be shipped from US or any other country as we have multiple locations worldwide.

Zustand: New. This is a Brand-new US Edition. This Item may be shipped from US or any other country as we have multiple locations worldwide.

Zustand: Used. pp. xviii + 416.

Zustand: Used. pp. xviii + 416.

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

Zustand: New. pp. 896.

Taschenbuch. Zustand: Neu. Inherited Metabolic Diseases | A Clinical Approach | Georg F. Hoffmann (u. a.) | Taschenbuch | xvii | Englisch | 2018 | Springer | EAN 9783662570081 | Verantwortliche Person für die EU: Springer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg, juergen[dot]hartmann[at]springer[dot]com | Anbieter: preigu. …

Taschenbuch. 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.…

Gebunden. Zustand: New. William L. Nyhan, MD, PhD, is Professor of Pediatrics and Founding Director of The William L. Nyhan Biochemical Genetics and Metabolomics Laboratory at the University of California, San Diego.Georg F. Hoffmann, MD.

Buch. Zustand: Neu. Neuware - In a field where even experts may find that years have elapsed since they last encountered a child with a given disorder, it is essential for the clinician to have a comprehensive source of practical and highly illustrated information covering the whole spectrum of metabolic disease to refer to.The content is divided into sections of related disorders, including disorders of amino acid metabolism, lipid storage disorders, and mitochondrial diseases for ease of reference, with an introductory outline where appropriate summarizing the biochemical features and general management issues. Within the sections, each chapter deals with an individual disease, opening with a useful summary of major phenotypic expression including clear and helpful biochemical pathways, identifying for the reader exactly where the defect occurs.Throughout the book, plentiful photographs, often showing extremely rare disorders, are an invaluable aid to diagnosis.Key Features¿ Fully updated to incorporate all new developments in the field¿ Brand new chapters cover methylmalonic aciduria of ACSF3 deficiency, branched chain keto acid dehydrogenase deficiency, serine deficiencies, purine nucleoside phosphorylase deficiency, antiquitin deficiency, and others¿ Excellent and detailed clinical descriptions, with numerous valuable hints and suggestions for management¿ Helpful explanatory algorithms and decision trees, and high-quality illustrative material including biochemical pathways and an unrivaled photographic collection, which enhance clinical applicabilityThe fourth edition of this highly regarded book, authored by two of the foremost authorities in pediatric metabolic medicine, continues to provide incomparable insight into the problems associated with metabolic diseases and remains invaluable to pediatricians, geneticists, and general clinicians worldwide.…

Softcover. Zustand: gut. Erbliche Stoffwechselkrankheiten Differentialdiagnose akut kranker Kinder chronische Erkrankungen Bandbreite der Krankheiten Vademecum Metabolicum Kliniken Praxen Diagnose Therapie Stoffwechselkrankheiten differentialdiagnostisches Vorgehen Indikation Durchführung Potential Stoffwechselanalysen metabolische Funktionstests Stoffwechselwege Störungen Klinische Merkmale Krankheitsgruppen Imbecillitas phenylpyruvica Phenylketonurie PKU Behandlung PKU-Diät Phenylalanin-Stoffwechsel Guthrie Massenscreening aller Neugeborenen Forschungsarbeiten Biochemie Molekulargenetik Störung charakteristisches Krankheitsbild Behandlungsmöglichkeiten phenylalaninfreien Aminosäuremischung Tetrahydrobiopterin Stoffwechsel Humanmediziner Ernährungswissenschaftler Diätetiker Stoffwechselstörung Pädiater, Stoffwechsel-Experten und Biochemiker, Klinische Psychologen, Neurologen, Medizinhistoriker, Studierende der Medizin, Ökotrophologen und Diätassistentinnen, Universitätsinstitute und Lehranstalten auf den Gebieten Ernährungswissenschaft und Diätetik, Gesundheitsbehörden und Krankenkassen, Hebammen und Kinderkrankenschwestern, SelbsthilfegruppenHumanmediziner, Pädiater, Stoffwechsel-Experten und Biochemiker, Klinische Psychologen, Neurologen, Medizinhistoriker, Studierende der Medizin, Ökotrophologen und Diät assistentinnen, Universitätsinstitute und Lehranstalten auf den Gebieten Ernährungswissenschaft und Diätetik, Gesundheitsbehörden und Krankenkassen, Hebammen und Kinderkrankenschwestern, Selbsthilfegruppen.Kinderheilkunde und Kinderkrankenpflege für Schwestern. Mit 500 Fragen für Examen und Fortbildung Michael Hertl In deutscher Sprache. 176 pages. 18 x 12 x 1,2 cm Auflage: 3., veränd. A. (September 2004).…

104 pp.; 29.7 x 21 cm.; staple bound; black-and-white; edition size unknown; unsigned and unnumbered; offset-printed The first issue of "NYB : An Arts Magazine" published in 1985. Contributors include Mimi Gross, Peter Werner, Gerhard Ullmann, Peter Hoffmann, Bernd Weyergraf, Michael Glassmeier, Timothy F. Rub, Georg C. Bertsch, Thomas Hoffmann, Thomas Wulffen, Henry Ries, B.H. Friedman, Bernhard Schulz, Barry Neuman, John Ashbery, John Yau, Tony Towle, Jean Holabird, Taylor Mead, Tama Janowitz, Doris Nadja Wiewiorra, Peter Schneider, Lutze, Klaus Stiller, Karis Kiwus, Anne Jud, Joan Jonas, Lil Picard, Anne Wehrer, Renate Ponsold, Jackie Curtis, Peter Feinauer, William Hellermann and Julius, and an interview with John Cage by Thomas Wulffen. Fine. Covers and contents clean and unmarked. …

Erstausgabe Gr.8°, Orig.Halbledereinband, reichlich goldverziert 4 Bll., 141 Seiten mit 14 Holzschnitten/ VI + 192 Seiten/ VII + 232 Seiten, 1 Bl., rundum Rotschnitt Ecken und Kanten berieben, Rücken unten mit kleiner Fehlstelle, sonst durchaus gutes Exemplar Specielle Pathologie und Therapie. Hrsg.v. Prof.Dr. Hermann Nothnagel. XIV.Band, II.Hälfte, I.Abtheilung. …

kart. Zustand: Sehr gut. 106 S. : Ill. ; 21 cm Sprache: Deutsch Gewicht in Gramm: 158.

Zustand: New.

279 x 210 mm gebundene Ausgabe. Zustand: Gut. 4., vollst. überarb. Aufl. 2245 Seiten Flecken auf dem Einband hinten und vorne. Einband leicht berieben. Schrammen auf dem Einband. Schnitt dezent fleckig. Zustand insgesamt gut. Seiten sauber. Ein schonend gelesenes Exemplar. Seiten ohne Eintragungen oder Markierungen. 121 Sprache: Deutsch Gewicht in Gramm: 3370.…