Was macht eine gute Führungskraft im Betreuungsdienst aus? Welche Aufgaben und Kompetenzen gehören zum Stellenprofil einer Betreuungsdienstleitung (BDL)? Antworten auf diese und viele weitere Fragen gibt das Arbeitshandbuch der Autorinnen Karger und Klein. Praxisbezogen begleiten Sie das fiktive Ehepaar Fischer bei seinem Einzug ins Pflegeheim und erfahren, wie die Führung des Betreuungsdienstes funktioniert. Auszüge aus Gesetzen, Verordnungen und Richtlinien runden das Handbuch ab. Die Au...

Long-chain fatty acid oxidation disorders (LC-FAODs) are rare, inherited conditions. With an LC-FAOD, the body has trouble breaking down fat for energy, which can lead to symptoms such as low blood sugars, muscle pain/weakness, and heart problems. LC-FAODs are diagnosed by newborn screening or symptoms later in life. Management includes a specialized nutrition plan, and prevention of fasting, especially during illness. A person with an LC-FAOD can live a full, active and healthy life with ...

Disorders affecting the oxidation of long-chain fatty acids are complex, potentially life-threatening, metabolic conditions. A number of genetically distinct conditions exist, depending on the gene and protein affected, but there are some common clinical and biochemical features. Newborn screening, which allows early intervention to prevent long-term morbidity, is not universally available. Even with screening, it is important that health professionals recognize the symptoms that may manif...

The outstanding feature of this publication is that it illustrates in detail the broad range of pancreatic lesions most likely to be encountered on fine needle aspiration of the pancreas, incorporating ancillary testing and differential diagnoses. Detailed descriptions of the cytological features of nonneoplastic entities, ductal and nonductal primary neoplasms, nonneoplastic and neoplastic cystic lesions, and secondary tumors and mesenchymal lesions are included. A multidisciplinary autho...

Disorders affecting the oxidation of long-chain fatty acids are complex, potentially life-threatening, metabolic conditions. A number of genetically distinct conditions exist, depending on the gene and protein affected, but there are some common clinical and biochemical features. Newborn screening, which allows early intervention to prevent long-term morbidity, is not universally available. Even with screening, it is important that health professionals recognize the symptoms that may manif...

Les troubles d’oxydation des acides gras à chaîne longue (TOAG-CL) sont des maladies héréditaires rares. Les TOAG-CL font en sorte que le corps a de la difficulté à convertir les acides gras en énergie, ce qui peut mener à des symptômes tels qu’un taux de sucre sanguin trop bas, des douleurs ou des faiblesses musculaires, et des problèmes cardiaques. Les TOAG-CL sont diagnostiqués à l’aide de tests de dépistage chez les nouveau-nés, ou plus tard, suite à des symptômes. On les traite avec u...

Disorders affecting the oxidation of long-chain fatty acids are complex, potentially life-threatening, metabolic conditions. A number of genetically distinct conditions exist, depending on the gene and protein affected, but there are some common clinical and biochemical features. Newborn screening, which allows early intervention to prevent long-term morbidity, is not universally available. Even with screening, it is important that health professionals recognize the symptoms that may manif...

Les troubles d’oxydation des acides gras à chaîne longue (TOAG-CL) sont des maladies héréditaires rares. Les TOAG-CL font en sorte que le corps a de la difficulté à convertir les acides gras en énergie, ce qui peut mener à des symptômes tels qu’un taux de sucre sanguin trop bas, des douleurs ou des faiblesses musculaires, et des problèmes cardiaques. Les TOAG-CL sont diagnostiqués à l’aide de tests de dépistage chez les nouveau-nés, ou plus tard, suite à des symptômes. On les traite avec u...