Zobrazeno 1 - 10
of 456
pro vyhledávání: '"Christian G Bien"'
Autor:
Annika Lehner, Lucas Hoffmann, Stefan Rampp, Roland Coras, Friedrich Paulsen, Renato Frischknecht, Hajo Hamer, Katrin Walther, Sebastian Brandner, Wiebke Hofer, Tom Pieper, Lea‐Marie Reisch, Christian G. Bien, Ingmar Blumcke
Publikováno v:
Epilepsia Open, Vol 9, Iss 4, Pp 1372-1381 (2024)
Abstract Objective Perineuronal nets (PNN) are specialized extracellular matrix (ECM) components of the central nervous system, frequently accumulating at the surface of inhibitory GABAergic interneurons. While an altered distribution of PNN has been
Externí odkaz:
https://doaj.org/article/3930e1b8c68e483ca7b812230031882d
Autor:
Anna Doll, Martin Wegrzyn, Friedrich G. Woermann, Kirsten Labudda, Christian G. Bien, Johanna Kissler
Publikováno v:
Epilepsia Open, Vol 9, Iss 1, Pp 355-367 (2024)
Abstract Objective Neuroimaging studies reveal frontal lobe (FL) contributions to memory encoding. Accordingly, memory impairments are documented in frontal lobe epilepsy (FLE). Still, little is known about the structural or functional correlates of
Externí odkaz:
https://doaj.org/article/d0182a8d0b474e3980787880d58ca6cc
Autor:
Kirsten Labudda, Stefan Kreisel, Thomas Beblo, Markus Mertens, Oleg Kurlandchikov, Christian G Bien, Martin Driessen, Friedrich G Woermann
Publikováno v:
PLoS ONE, Vol 8, Iss 12, p e83677 (2013)
Results of MRI volumetry in Borderline Personality Disorder (BPD) are inconsistent. Some, but not all, studies reported decreased hippocampus, amygdala, and/or prefrontal volumes. In the current study, we used rater-independent voxel-based morphometr
Externí odkaz:
https://doaj.org/article/dd150049a76e4600a55f1277e436dad3
Autor:
Jonas Honke, Lucas Hoffmann, Roland Coras, Katja Kobow, Costin Leu, Tom Pieper, Till Hartlieb, Christian G. Bien, Friedrich Woermann, Thomas Cloppenborg, Thilo Kalbhenn, Ahmed Gaballa, Hajo Hamer, Sebastian Brandner, Karl Rössler, Arnd Dörfler, Stefan Rampp, Johannes R. Lemke, Sara Baldassari, Stéphanie Baulac, Dennis Lal, Peter Nürnberg, Ingmar Blümcke
Publikováno v:
Acta Neuropathologica Communications, Vol 11, Iss 1, Pp 1-11 (2023)
Abstract Focal cortical dysplasia type II (FCDII) is the most common cause of drug-resistant focal epilepsy in children. Herein, we performed a deep histopathology-based genotype–phenotype analysis to further elucidate the clinico-pathological and
Externí odkaz:
https://doaj.org/article/4bef610997d24176a5d187b82505fdf0
Autor:
Izumi Kuramochi, Takayuki Iwayama, Christian Brandt, Haruo Yoshimasu, Christian G. Bien, Anne Hagemann
Publikováno v:
Epilepsia Open, Vol 8, Iss 3, Pp 946-958 (2023)
Abstract Objective Self‐stigma is the internalization of unfavorable public perceptions, which people with epilepsy (PWE) frequently experience. PWE with strong self‐stigma have low self‐esteem and are less likely to engage in treatment behavio
Externí odkaz:
https://doaj.org/article/ae7dc870a1994e3eafb91dc30e3f4311
Autor:
Lea Hemmeter, Christian G. Bien, Corinna I. Bien, Andrea Tipold, Jasmin Neßler, Andrea Bathen‐Nöthen, Kaspar Matiasek, Maik Dahlhoff, Clare Rusbridge, Carina Rotter Black, Kai Rentmeister, Holger A. Volk, Andrea Fischer
Publikováno v:
Journal of Veterinary Internal Medicine, Vol 37, Iss 4, Pp 1409-1417 (2023)
Abstract Background Autoimmune mechanisms represent a novel category for causes of seizures and epilepsies in humans, and LGI1‐antibody associated limbic encephalitis occurs in cats. Hypothesis/Objectives To investigate the presence of neural antib
Externí odkaz:
https://doaj.org/article/006f3500a9e8409a9f558fb19cebcb0e
Publikováno v:
Epilepsy & Behavior Reports, Vol 28, Iss , Pp 100717- (2024)
Alpha-thalassemia X-linked intellectual disability syndrome (ATRX) is a rare genetic disorder caused by mutations in the ATRX gene. It is characterized by distinct dysmorphic features, alpha thalassemia, varying degrees of intellectual disability, an
Externí odkaz:
https://doaj.org/article/0529a2697f9c403d8267fd7583d42780
Autor:
Ahmed Elshetihy, Lema Nergiz, Thomas Cloppenborg, Friedrich G. Woermann, Birgitt Müffelmann, Christian G. Bien
Publikováno v:
Epilepsy & Behavior Reports, Vol 27, Iss , Pp 100684- (2024)
In this patient, now 42 years old, genetic generalized epilepsy (juvenile myoclonic epilepsy) manifested itself at the age of 13. At the age of 39, she experienced a status episode with prolonged ICU treatment. She was left with a left-sided hippocam
Externí odkaz:
https://doaj.org/article/289d36dd39dd4bacb0858610b94440bf
Publikováno v:
BMC Neurology, Vol 21, Iss 1, Pp 1-5 (2021)
Abstract Background While Covid-19 predominantly affects the respiratory system, neurological manifestations including encephalitis occur in some patients, possibly affecting the course and outcome of the disease. Here, we describe a unique case of a
Externí odkaz:
https://doaj.org/article/6a3453b0f2bb4226b8e288edd628cee0
Publikováno v:
Frontiers in Veterinary Science, Vol 9 (2022)
Autoantibodies against neurotransmitter receptors detected in cerebrospinal fluid (CSF) and serum are increasingly recognized in people with human autoimmune encephalitis causing severe neurological deficits, such as seizures and behavioral abnormali
Externí odkaz:
https://doaj.org/article/d7a13a4b640b4572972ca998b3975a1d