Zobrazeno 1 - 10
of 115
pro vyhledávání: '"K. Eberlein"'
Autor:
Maximilian Deest, Jelte Wieting, Maximilian Michael Jakob, Stephanie Deest-Gaubatz, Adrian Groh, Johanna Seifert, Sermin Toto, Stefan Bleich, Helge Frieling, Christian K. Eberlein
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-8 (2022)
Abstract Background Prader–Willi syndrome (PWS) is a rare neurodevelopmental disorder based on a loss of paternally expressed genes in chromosome segment 15q11-13. Behavioral traits such as temper outbursts, stereotypic, and ritualistic behavior, a
Externí odkaz:
https://doaj.org/article/400fe37ecfb946909614b20b9a1f56e5
Autor:
Hannah M. Heseding, Kirsten Jahn, Christian K. Eberlein, Jelte Wieting, Hannah B. Maier, Phileas J. Proskynitopoulos, Alexander Glahn, Stefan Bleich, Helge Frieling, Maximilian Deest
Publikováno v:
Translational Psychiatry, Vol 12, Iss 1, Pp 1-10 (2022)
Abstract Prader-Willi syndrome (PWS) is a rare neurodevelopmental disorder caused by a loss of usually paternally expressed, maternally imprinted genes located on chromosome 15q11-q13. Individuals with PWS display a specific behavioral phenotype and
Externí odkaz:
https://doaj.org/article/fc7e7b943f0e4d5e8631edc777c05481
Autor:
Johanna Seifert, Christian Ihlefeld, Tristan Zindler, Christian K. Eberlein, Maximilian Deest, Stefan Bleich, Sermin Toto, Catharina Meissner
Publikováno v:
Psychiatry International, Vol 2, Iss 3, Pp 310-324 (2021)
Studies have consistently determined that patients with acute psychosis are more likely to be involuntarily admitted, although few studies examine specific risk factors of involuntary admission (IA) among this patient group. Data from all patients pr
Externí odkaz:
https://doaj.org/article/859a0193d3e3439890226e689d2a934c
Autor:
Jelte Wieting, Kirsten Jahn, Christian K. Eberlein, Stefan Bleich, Helge Frieling, Maximilian Deest
Publikováno v:
Behavioural Brain Research. 450:114494
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8a31fe7e88e45ad868dc5df167efd5f0
https://doi.org/10.1016/j.bbr.2023.114494
https://doi.org/10.1016/j.bbr.2023.114494
Akademický článek
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Autor:
Jelte Wieting, Kirsten Jahn, Vanessa Buchholz, Ralf Lichtinghagen, Stefan Bleich, Christian K. Eberlein, Maximilian Deest, Helge Frieling
Prader-Willi syndrome (PWS) is a rare neurodevelopmental disorder based on a loss of paternally expressed but maternally imprinted genes in chromosome region 15q11-13. During child development, PWS usually results in insatiable appetite with subseque
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::220bb304c63053b5178bdab1e75e4cda
https://doi.org/10.1101/2021.12.15.21267839
https://doi.org/10.1101/2021.12.15.21267839
Autor:
Hannah M. Heseding, Kirsten Jahn, Christian K. Eberlein, Jelte Wieting, Hannah B. Maier, Phileas J. Proskynitopoulos, Alexander Glahn, Stefan Bleich, Helge Frieling, Maximilian Deest
BackgroundPrader-Willi syndrome (PWS) is a rare neurodevelopmental disorder caused by a loss of usually paternally expressed, maternally imprinted genes located on chromosome 15q11-q13. Individuals with PWS display a specific behavioral phenotype and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58ebb6620316024f04e008aaa7ab1713
https://doi.org/10.1101/2021.12.14.21267765
https://doi.org/10.1101/2021.12.14.21267765
Electroconvulsive therapy and adiposity-related parameters in treatment-resistant depressed patients
Autor:
Hannah Benedictine Maier, Christoph Pollak, Nicole Moschny, Sermin Toto, Colin Schlatt, Christian K. Eberlein, Wolfgang Sperling, Johannes Kornhuber, Kai G. Kahl, Stefan Bleich, Alexandra Neyazi, Helge Frieling
Publikováno v:
Journal of neural transmission (Vienna, Austria : 1996). 129(3)
Obesity is often accompanied by major depressive disorder (MDD), and vice versa. Latest research findings suggest the body mass index (BMI) to play a role in antidepressant treatment response in general. Our study aims to examine whether adiposity-re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4fa0a6fccd2ff229e2a557deef659936
https://pubmed.ncbi.nlm.nih.gov/35212862
https://pubmed.ncbi.nlm.nih.gov/35212862
Autor:
Jelte, Wieting, Kirsten, Jahn, Vanessa, Buchholz, Ralf, Lichtinghagen, Stephanie, Deest-Gaubatz, Stefan, Bleich, Christian K, Eberlein, Maximilian, Deest, Helge, Frieling
Publikováno v:
Psychoneuroendocrinology. 143:105857
Prader-Willi syndrome (PWS) is a rare neurodevelopmental disorder based on a loss of paternally expressed but maternally imprinted genes in chromosome region 15q11-13. PWS individuals typically show insatiable appetite with subsequent obesity represe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96067891ae4c6499c6ecf38f70bad49f
https://doi.org/10.1016/j.psyneuen.2022.105857
https://doi.org/10.1016/j.psyneuen.2022.105857
Autor:
Alexandra Kleimann, Sermin Toto, Christian K Eberlein, Jan T Kielstein, Stefan Bleich, Helge Frieling, Marcel Sieberer
Publikováno v:
PLoS ONE, Vol 9, Iss 7, p e101839 (2014)
In May 2011 an outbreak of Shiga toxin-producing enterohaemorrhagic E. coli (STEC) O104:H4 in Northern Germany led to a high number of in-patients, suffering from post-enteritis haemolytic-uraemic syndrome (HUS) and often severe affection of the cent
Externí odkaz:
https://doaj.org/article/87345bd60fad47a5a960b0e3c5032ad8