Vademecum Metabolicum
Diagnosis and Treatment of Inborn Errors of Metabolism Forword by William L. Nyhan, San Diego, USA
Seiten
2011
|
1st reprint 2014 of the 3rd, revised ed. 2011
Schattauer (Verlag)
978-3-7945-2816-5 (ISBN)
Schattauer (Verlag)
978-3-7945-2816-5 (ISBN)
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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.
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.
Johannes Zschocke Univ.-Prof. Dr. med. Ph. D., Facharzt für Humangenetik und Medizinische Genetik; Professor für Humangenetik, Direktor der Division für Humangenetik, Ärztlicher Leiter des Zentrums Medizinische Genetik Innsbruck, Medizinische Universität Innsbruck
Diagnosis and management of metabolic disease
Essential basic laboratory tests
General clinical situations: metabolic emergency, epileptic encephalopathy, sudden infant death, unusual clinical and laboratory findings, post-mortem investigations, etc.
Special metabolic investigations
Function tests
Newborn screening
Metabolic pathways and their disorders
| Zusatzinfo | 29 Abb., 40 Tab. |
|---|---|
| Sprache | englisch |
| Maße | 120 x 185 mm |
| Gewicht | 249 g |
| Einbandart | kartoniert |
| Themenwelt | Medizin / Pharmazie ► Medizinische Fachgebiete |
| Schlagworte | Allgemeinmedizin • Pädiatrie • Stoffwechselkrankheiten |
| ISBN-10 | 3-7945-2816-6 / 3794528166 |
| ISBN-13 | 978-3-7945-2816-5 / 9783794528165 |
| Zustand | Neuware |
| Informationen gemäß Produktsicherheitsverordnung (GPSR) | |
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