Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Andreas Schlotmann"'
Publikováno v:
Frontiers in Human Neuroscience, Vol 15 (2021)
PurposeTo evaluate the prevalence and treatment patterns of speech and language disorders in Germany.MethodsA retrospective analysis of data collected from 32% of the German population, insured by the statutory German health insurance (AOK, Local Hea
Externí odkaz:
https://doaj.org/article/e74041966320460088c57a33aabdf415
Autor:
Michael Porst, Elena von der Lippe, Janko Leddin, Aline Anton, Annelene Wengler, Jan Breitkreuz, Katrin Schüssel, Gabriela Brückner, Helmut Schröder, Heike Gruhl, Dietrich Plaß, Benjamin Barnes, Markus A. Busch, Sebastian Haller, Ulfert Hapke, Hannelore Neuhauser, Lukas Reitzle, Christa Scheidt-Nave, Andreas Schlotmann, Henriette Steppuhn, Julia Thom, Thomas Ziese, Alexander Rommel
Publikováno v:
Dtsch Arztebl Int
BACKGROUND: Summary measures such as disability-adjusted life years (DALY) are becoming increasingly important for the standardized assessment of the burden of disease due to death and disability. The BURDEN 2020 pilot project was designed as an inde
Publikováno v:
Dtsch Arztebl Int
BACKGROUND: Acute liver failure (ALF) is a life-threatening event associated with high mortality. Currently, only estimates are available for its incidence. The aim of the study was to assess the incidence of ALF in Germany, using the accounting data
Autor:
Lena Oevermann, Andrea Daubenbüchel, Andrea Jarisch, Regine Grosse, Stephan Lobitz, Holger Cario, Laura Tagliaferri, Andreas E. Kulozik, Dani Hakimeh, Joachim B. Kunz, Andreas Schlotmann
Publikováno v:
Blood. 138:973-973
Background Worldwide, Sickle Cell Disease (SCD) is the most common single gene disorder affecting >250,000 newborns annually. In Germany, SCD qualifies as a rare disease and almost exclusively affects immigrants from endemic countries and their desce
Autor:
Lena Oevermann, Laura Tagliaferri, Andrea Jarisch, Joachim B. Kunz, Andreas Schlotmann, Andreas E. Kulozik, Dani Hakimeh, Regine Grosse, Andrea Daubenbüchel, Holger Cario, Stephan Lobitz
Publikováno v:
Journal of Clinical Medicine, Vol 10, Iss 4543, p 4543 (2021)
Journal of Clinical Medicine
Volume 10
Issue 19
Journal of Clinical Medicine
Volume 10
Issue 19
Sickle Cell Disease (SCD) is the most common monogenic disorder globally but qualifies as a rare disease in Germany. In 2012, the German Society for Paediatric Oncology and Haematology (GPOH) mandated a consortium of five university hospitals to deve
Autor:
Katharina C. Koltermann, Thomas Reinhold, Stefan N. Willich, Helmut Schröder, Andreas Schlotmann
Publikováno v:
Zeitschrift für Evidenz, Fortbildung und Qualität im Gesundheitswesen. :24-30
Background Until now, there has been little discussion of the costs of the deep infiltrating endometriosis (DIE) of the bowel or the bladder. The aim of the present secondary data analysis was to describe the population affected by this disease and t
Autor:
W. K. Rohrschneider, John H. Clorius, Folker Amelung, Sandra N. Clorius, Andreas Schlotmann, Kristianna Becker
Publikováno v:
Journal of Nuclear Medicine. 49:1196-1203
The significance of delayed tissue tracer transit (TTT) of 99mTc-mercaptoacetyltriglycine (99mTc-MAG3) has not been systematically evaluated in hydronephrosis. We sought to demonstrate that delayed TTT accompanies both functional decline and histomor
Autor:
John H. Clorius, Andreas Schlotmann
Publikováno v:
Journal of Nuclear Medicine. 50:169-169
REPLY: We are thankful for Dr. Piepsz's thoughtful critique. The report presents the first data that show that a parenchymal 99mTc-mercaptoacetyltriglycine (MAG3) transit disturbance, that is, delayed tissue tracer transit (TTT), is accompanied by fu