Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Kerstin Khalaj Hedayati"'
Age- and sex-related growth patterns of the craniofacial complex in European children aged 3-6 years
Autor:
Stefanie Ritz-Timme, Pasquale Poppa, M. Ratnayake, Arunas Barkus, Cristina Cattaneo, Zuzana Obertová, Kerstin Khalaj-Hedayati, Inge Schroeder, Janina Tutkuviene
Publikováno v:
Annals of human biology. 43(6)
Craniofacial growth changes in young children are not yet completely understood. Up-to-date references for craniofacial measurements are crucial for clinical assessment of orthodontic anomalies, craniofacial abnormalities and subsequent planning of i
Publikováno v:
Nutrition Research. 29:531-541
The BIOPAC indirect calorimeter for measuring resting energy expenditure (REE) is less cumbersome than many other calorimeters. We tested the hypothesis that the BIOPAC calorimeter is as well suited for determining REE in older people as traditional
Autor:
Volkmar Gieselmann, Kerstin Khalaj Hedayati, Hariharasubramanian Ramakrishnan, Hans-Hilmar Goebel, Renate Lüllmann-Rauch, Simon Ngamli Fewou, Matthias Eckhardt, Carsten Wessig, Helena Maier
Publikováno v:
The Journal of Neuroscience. 27:9482-9490
Metachromatic leukodystrophy (MLD) is a lysosomal storage disorder caused by the deficiency of arylsulfatase A (ASA). This results in accumulation of sulfated glycosphingolipids, mainly 3-O-sulfogalactosylceramide (sulfatide), in the nervous system a
Publikováno v:
Ecology of food and nutrition. 49(2)
This study analyzed whether sarcopenia, a risk factor for disability in the aged, also occurs in healthy community-dwelling elders with normal nutritional state. As indicators, body cell mass (BCM) and lean body mass (LBM) were determined in 110 Germ
Publikováno v:
Gerontology. 57(5)
Background: Accurate and comfortable methods are needed to determine resting energy expenditure (REE) in older people who are characterized by a lowered metabolic rate. The portable SenseWear® armband (SWA) body monitor, worn on the right upper arm,
Autor:
Peter Oster, Druck Reinhardt Druck Basel, Lukas Zahner, Judith B. Prins, Peter P. Nawroth, S. Gravenstein, Urs Granacher, Douglas R. McQuoid, Maria Isabella Becerra, Marcel G. M. Olde Rikkert, Manuela Dittmar, Christian Cajochen, Thomas Fleming, Stefanie Heiermann, Y.P.T. Kamsma, Martin Kopp, Gertrudis I. J. M. Kempen, Esther Phielix, Thomas Muehlbauer, Manfred J. Müller, Kerstin Khalaj Hedayati, A. Pop-Vicas, Bernice Simone Elger, Julia Szendroedi, Jung Jae Lee, Michael Schwenk, Angelika Bierhaus, Michael Roden, Reto W. Kressig, Noëlle Junod Perron, G. A. Rixt Zijlstra, Anne Eckert, Roy P.C. Kessels, Liesbeth W.A. Joosten-Weyn Banningh, Steven A. Brown, Klaus Hauer, Satz Mengensatzproduktion, Jin Woo Park, Myrra J.F.J. Vernooij-Dassen, Albert Gollhofer, H Wijnen, Samia Hurst, Chris Todd, David C. Steffens, Seok Bum Lee, Joon Hyuk Park, Ki Woong Kim, Lucia Pagani, Tae Hui Kim, Marieke J. G. van Heuvelen, Nina Beyer, Per M. Humpert, Martin Burtscher, Stéphane Cochet, Lucy Yardley, Elizabeth Weening-Dijksterhuis
Publikováno v:
Gerontology.
Autor:
Heinz Beck, Volkmar Gieselmann, Simon Ngamli Fewou, Matthias Eckhardt, Renate Lüllmann-Rauch, Julika Pitsch, Kerstin Khalaj Hedayati
Metachromatic leukodystrophy is a lysosomal storage disorder caused by deficiency in the sulfolipid degrading enzyme arylsulfatase A (ASA). In the absence of a functional ASA gene, 3-O-sulfogalactosylceramide (sulfatide; SGalCer) and other sulfolipid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db2e807382d88dcf3e84edc1a06b1afe
https://europepmc.org/articles/PMC6672212/
https://europepmc.org/articles/PMC6672212/
Autor:
Ulrich Matzner, Volkmar Gieselmann, Carsten Wessig, Renate Lüllmann-Rauch, Jens Fogh, Stephan Schröder, Carl Eistrup, Christer Möller, Eva Herbst, Kerstin Khalaj Hedayati
Publikováno v:
Human molecular genetics. 14(9)
A deficiency of arylsulfatase A (ASA) causes the lysosomal storage disease metachromatic leukodystrophy, which is characterized by accumulation of the sphingolipid 3-O-sulfogalactosylceramide (sulfatide). Sphingolipid storage results in progressive d