Tekijä: Georg. F. Hoffmann; William L. Nyhan; Johannes Zschocke; Stephen G. Kahler; Ertan Mayatepek Kustantaja: Lippincott Williams & Wilkins (2001) Saatavuus: Loppuunmyyty.
Tekijä: Georg F Hoffmann; Michael J Lentze; Jürgen Spranger; Fred Zepp Kustantaja: Springer-Verlag Berlin and Heidelberg GmbH & Co. KG (2014) Saatavuus: Noin 17-20 arkipäivää
Tekijä: Georg F Hoffmann; Professor Michael J Lentze; Jurgen Spranger; Fred Zepp Kustantaja: Springer-Verlag Berlin and Heidelberg GmbH & Co. KG (2014) Saatavuus: Ei tiedossa
Tekijä: Georg F Hoffmann; Michael J Lentze; Jurgen Spranger; Fred Zepp; Reinhard Berner Kustantaja: Springer-Verlag Berlin and Heidelberg GmbH & Co. KG (2020) Saatavuus: Noin 17-20 arkipäivää
Tekijä: Georg F. Hoffmann (ed.); Michael J. Lentze (ed.); Jürgen Spranger (ed.); Fred Zepp (ed.); Reinhard Berner (ed.) Kustantaja: Springer (2020) Saatavuus: Noin 17-20 arkipäivää
Tekijä: Burkhard Tonshoff; Sabine Kopf; Reiner Singer; Georg F Hoffmann Kustantaja: Springer-Verlag Berlin and Heidelberg GmbH & Co. KG (2002) Saatavuus: | Arvioimme, että tuote lähetetään meiltä noin 1-3 viikossa
Tekijä: Georg F. Hoffmann; Johannes Zschocke; William L. Nyhan Kustantaja: Springer-Verlag Berlin and Heidelberg GmbH & Co. KG (2016) Saatavuus: Noin 17-20 arkipäivää
Taylor & Francis Ltd Sivumäärä: 888 sivua Asu: Kovakantinen kirja Painos: 3rd New edition Julkaisuvuosi: 2011, 30.12.2011 (lisätietoa) Kieli: Englanti
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 third edition of this highly regarded book, authored by three of the foremost authorities in pediatric metabolic medicine, fulfils this need by providing an invaluable insight into the problems associated with metabolic diseases.
The Atlas of Metabolic Disease is divided into sections of related disorders, such as disorders of amino acid metabolism, lipid storage disorders and mitochondrial diseases, with an introductory outline where appropriate summarizing the biochemical features and general management issues. Within sections each chapter deals with an individual disease, starting with a useful summary of major phenotypic expression and including clear and helpful biochemical pathways, identifying for the reader exactly where the defect is occurring.
Throughout the book, plentiful photographs, often showing extremely rare disorders, are an invaluable aid to diagnosis.
