Titlebook: Whole Body Ultrasonography in the Critically Ill; Daniel A. Lichtenstein Book 2010 Springer-Verlag Berlin Heidelberg 2010 Critical Ultraso

MURKY

Lung and Interstitial Syndromes, demonstrating that the diagnosis of pleural effusion or alveolar disorders was just an appetizer. If lung ultrasound is a raison d’être of critical ultrasound, the potential of interstitial syndrome is the raison d’être of lung ultrasound. Based on artifact analysis, it changes the approach to th

prediabetes

巡回

Peritoneumas dealt with before the lung chapters, which standardize this semiotic of air. Meanwhile, one practical suggested label for designating the abdominal gas structures is the term “G-lines” – . for gut.

注視

Liver probes. Their only use seems to be for accurate measurement of hepatic size, which is a tool of interest for the radiologist but not yet a tool for the intensivist. Unexpected uses may emerge from knowing the size of the liver, but this can be achieved using our probe.

Texture

微不足道

in a variety of settings, including unexplained shock, management of hemodynamic instability, acute respiratory failure (the BLUE protocol), and the critically ill neonate, is carefully explained. Interventiona978-3-642-42307-9978-3-642-05328-3

Gudgeon

Daniel A. Lichtensteinowledge regarding human β-cell replication. It seems clear that unlike in rodents, spontaneous replication of adult human β cells is uncommon. Further, standard manipulations, nutrients, and growth factors that induce rodent β-cell replication fail to do so in human β cells. In this chapter we focus

Notorious

Desert

Myocarditis

Daniel A. Lichtensteinst-translationally modified by deamidation in its loop domain in human liver tissues; deamidated Bcl-xL is a major form in normal liver tissues, whereas the level of deamidated Bcl-xL is lower than that of unmodified Bcl-xL in the majority of HCC tissues. As protein deamidation of Bcl-xL leads to a