Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Nina-Katharina Walleczek"'
Autor:
Julia Lischka, Klaus Arbeiter, Charlotte de Gier, Andrea Willfort-Ehringer, Nina-Katharina Walleczek, Renata Gellai, Michael Boehm, Albert Wiegman, Susanne Greber-Platzer
Publikováno v:
BMC Pediatrics, Vol 22, Iss 1, Pp 1-8 (2022)
Abstract Background Homozygous familial hypercholesterolemia (hoFH) is a rare genetic disorder leading to extremely increased LDL-cholesterol (LDL-C), resulting in high cardiovascular risk in early childhood. Lipid apheresis (LA) is an effective trea
Externí odkaz:
https://doaj.org/article/10caa512947d4446af3b744b9e199d47
Autor:
Margot Baumgartner, Julia Lischka, Andrea Schanzer, Charlotte de Gier, Nina-Katharina Walleczek, Susanne Greber-Platzer, Maximilian Zeyda
Publikováno v:
Nutrients, Vol 14, Iss 10, p 2133 (2022)
Obesity already causes non-communicable diseases during childhood, but the mechanisms of disease development are insufficiently understood. Myokines such as myostatin and irisin are muscle-derived factors possibly involved in obesity-associated disea
Externí odkaz:
https://doaj.org/article/9a18228dd347454d99370d0ce0554317
Autor:
Julia Lischka, Katharina Lieb, Andrea Schanzer, Azadeh Hojreh, Ahmed Ba-Ssalamah, Charlotte de Gier, Nina-Katharina Walleczek, Maximilian Zeyda, Susanne Greber-Platzer
Publikováno v:
Annals of Nutrition and Metabolism. 78:247-254
Introduction: Early noninvasive detection of incipient liver damage is crucial to prevent long-term adverse health outcomes. A variety of scores to assess liver status have been proposed, mostly for adult populations. Validation of noninvasive hepati
Autor:
Jennifer Kolar, Nadja Kadrnoska, Julia Vodopiutz, Martina Seyr, Kristina Förster, Verena Wasinger-Brandweiner, Nina-Katharina Walleczek
Publikováno v:
Wiener Medizinische Wochenschrift (1946)
Skeletal disorders are inherited disorders with significant skeletal involvement and most of them are rare or extremely rare. Based on the clinical, radiological and genetic phenotype, the group of skeletal disorder comprises more than 450 different
Autor:
Klaus Arbeiter, Albert Wiegman, Julia Lischka, Susanne Greber-Platzer, Andrea Willfort-Ehringer, Michael Boehm, Nina-Katharina Walleczek, Charlotte de Gier, Renata Gellai
Publikováno v:
BMC pediatrics, 22(1):131. BioMed Central
Background Homozygous familial hypercholesterolemia (hoFH) is a rare genetic disorder leading to extremely increased LDL-cholesterol (LDL-C), resulting in high cardiovascular risk in early childhood. Lipid apheresis (LA) is an effective treatment and
Autor:
Susanne Greber-Platzer, Charlotte de Gier, Chike B. Item, Nina-Katharina Walleczek, Ahmed Ba Ssalamah, Ivana Jakober, Thomas F. Metz, Maximilian Zeyda, Andrea Schanzer, Julia Lischka, Azadeh Hojreh
Publikováno v:
Pediatric Obesity
Summary Background Eighty percent of adolescents with severe obesity suffer from non‐alcoholic fatty liver disease (NAFLD). Non‐invasive prediction models have been tested in adults, however, they performed poorly in paediatric populations. Objec
Autor:
Anna Baumgartner, Wolfgang Kristoferitsch, Hamid Assar, Maria-Sophie Hiller, Gabriele Morgenstern, Martin Heine, Markus Mayr, Franz Fazekas, Siegrid Fuchs, Astrid Cisar, Rainer Ehling, Stephan Blechinger, Hermann Moser, Michael Khalil, Christian Enzinger, Helmut Rauschka, Dominic Buchinger, Birgit Meister, Thomas Berger, Herbert Bachler, Gabriel Bsteh, Herburg Liendl, Silvia Parigger, Christoph Birkl, Sandra Rathmaier, Sabine Salhofer-Polanyi, Stefan Koppi, Florian Frommlet, Bettina Raber, Johann Sellner, Fritz Leutmezer, Fahmy Aboulenein-Djamshidian, Christian Eggers, Michael Guger, Jörg Kraus, Ines Kempf, Nina-Katharina Walleczek, Heinrich K Spiss
Publikováno v:
Multiple sclerosis (Houndmills, Basingstoke, England). 25(14)
Background: The month-of-birth-effect (MoBE) describes the finding that multiple sclerosis (MS) patients seem to have been born significantly more frequently in spring, with a rise in May, and significantly less often in autumn and winter with the fe