Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Rebecca Kulbida"'
Autor:
Lutz Priebe, Franziska Degenhardt, Jana Strohmaier, René Breuer, Stefan Herms, Stephanie H Witt, Per Hoffmann, Rebecca Kulbida, Manuel Mattheisen, Susanne Moebus, Andreas Meyer-Lindenberg, Henrik Walter, Rainald Mössner, Igor Nenadic, Heinrich Sauer, Dan Rujescu, Wolfgang Maier, Marcella Rietschel, Markus M Nöthen, Sven Cichon
Publikováno v:
PLoS ONE, Vol 8, Iss 7, p e64035 (2013)
Large rare copy number variants (CNVs) have been recognized as significant genetic risk factors for the development of schizophrenia (SCZ). However, due to their low frequency (1∶150 to 1∶1000) among patients, large sample sizes are needed to det
Externí odkaz:
https://doaj.org/article/aa40682df3914b2a8a019f4252c725a5
Publikováno v:
Journal of Integrative Medicine. 17:383-386
We report about hirudotherapy in a patient with chronic complex regional pain syndrome (CRPS) in the right hand. CRPS is a multifactorial disease associated with disabling pain as well as sensory and motor deficits. The optimal therapeutic management
Autor:
Rebecca Kulbida, Johannes Loeser, Christopher Plata, Brigitte Layer, Klaus-Maria Perrar, Tim Hucho
Publikováno v:
Journal of integrative medicine. 18(5)
Objective Osteoarthritis is a degenerative disease that affects synovial joints. Micro-injuries of articular structures initiate inflammatory processes, leading to persistent pain. Due to various risk factors, osteoarthritis is often diagnosed in mul
Autor:
Sanjay P. Singh, Dervla O'Malley, Jennifer Manning, Deniz Yilmazer-Hanke, Lindsay Jensen, Rebecca Kulbida, Prerana Rai, Judith E. Bouma
Publikováno v:
Experimental Physiology. 99:1370-1386
New Findings What is the central question of this study? Individuals suffering from Duchenne muscular dystrophy show progressive deterioration of muscle function associated with muscle inflammation and are susceptible to anxiety and depression. The c
Autor:
Albert J. Becker, Christina Schaub, Thoralf Opitz, Dana Ekstein, Karen M.J. van Loo, Julika Pitsch, Horst Urbach, Susanne Schoch, Adam Dalal, Yoel Yaari, Heinz Beck, Rebecca Kulbida
Publikováno v:
Nature Communications
Temporal lobe epilepsy (TLE) is the most common focal seizure disorder in adults. In many patients, transient brain insults, including status epilepticus (SE), are followed by a latent period of epileptogenesis, preceding the emergence of clinical se
Autor:
Susanne Schoch, Albert J. Becker, Rebecca Kulbida, Karen M.J. van Loo, Eva-Maria Mandelkow, Yipeng Wang
Publikováno v:
Brain structure & function 220(5), 3067-3073 (2014). doi:10.1007/s00429-014-0801-1
Brain Structure & Function
Brain Structure & Function
Focal epilepsies often originate in the hippocampal formation of the temporal lobe (temporal lobe epilepsy) and are generally acquired after transient brain insults. Such insults induce cellular and structural reorganization processes of the hippocam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec9b83da84f19ca61e2a77103efbe30e
https://pub.dzne.de/record/138074
https://pub.dzne.de/record/138074
Autor:
Jennifer, Manning, Rebecca, Kulbida, Prerana, Rai, Lindsay, Jensen, Judith, Bouma, Sanjay P, Singh, Dervla, O'Malley, Deniz, Yilmazer-Hanke
Publikováno v:
Experimental physiology. 99(10)
Mutations in the structural protein dystrophin underlie muscular dystrophies characterized by progressive deterioration of muscle function. Dystrophin-deficient mdx mice are considered a model for Duchenne muscular dystrophy (DMD). Individuals with D
Autor:
Franziska Degenhardt, Wolfgang Maier, Susanne Moebus, Jana Strohmaier, Igor Nenadic, Per Hoffmann, Rebecca Kulbida, Lutz Priebe, René Breuer, Marcella Rietschel, Heinrich Sauer, Stephanie H. Witt, Sven Cichon, Markus M. Nöthen, Henrik Walter, Stefan Herms, Andreas Meyer-Lindenberg, Dan Rujescu, Manuel Mattheisen, Rainald Mössner
Publikováno v:
PLOS ONE 8(7), e64035 (2013). doi:10.1371/journal.pone.0064035
PLoS one 8(7), e64035-(2013). doi:10.1371/journal.pone.0064035
Priebe, L, Degenhardt, F, Strohmaier, J, Breuer, R, Herms, S, Witt, S H, Hoffmann, P, Kulbida, R, Mattheisen, M, Moebus, S, Meyer-Lindenberg, A, Walter, H, Mössner, R, Nenadic, I, Sauer, H, Rujescu, D, Maier, W, Rietschel, M, Nöthen, M M & Cichon, S 2013, ' Copy number variants in german patients with schizophrenia ', P L o S One, vol. 8, no. 7, pp. e64035 . https://doi.org/10.1371/journal.pone.0064035
PLoS ONE
PLoS ONE; Vol 8
PLoS ONE, Vol 8, Iss 7, p e64035 (2013)
PLoS one 8(7), e64035-(2013). doi:10.1371/journal.pone.0064035
Priebe, L, Degenhardt, F, Strohmaier, J, Breuer, R, Herms, S, Witt, S H, Hoffmann, P, Kulbida, R, Mattheisen, M, Moebus, S, Meyer-Lindenberg, A, Walter, H, Mössner, R, Nenadic, I, Sauer, H, Rujescu, D, Maier, W, Rietschel, M, Nöthen, M M & Cichon, S 2013, ' Copy number variants in german patients with schizophrenia ', P L o S One, vol. 8, no. 7, pp. e64035 . https://doi.org/10.1371/journal.pone.0064035
PLoS ONE
PLoS ONE; Vol 8
PLoS ONE, Vol 8, Iss 7, p e64035 (2013)
Large rare copy number variants (CNVs) have been recognized as significant genetic risk factors for the development of schizophrenia (SCZ). However, due to their low frequency (1:150 to 1:1000) among patients, large sample sizes are needed to detect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f07ca2464a601ed9e85014134c4fe935
https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&origin=inward&scp=84879746391
https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&origin=inward&scp=84879746391