Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Christoph Schrade"'
Autor:
Robert Peach, Maximilian Friedrich, Lara Fronemann, Muthuraman Muthuraman, Sebastian R. Schreglmann, Daniel Zeller, Christoph Schrader, Joachim K. Krauss, Alfons Schnitzler, Matthias Wittstock, Ann-Kristin Helmers, Steffen Paschen, Andrea Kühn, Inger Marie Skogseid, Wilhelm Eisner, Joerg Mueller, Cordula Matthies, Martin Reich, Jens Volkmann, Chi Wang Ip
Publikováno v:
npj Digital Medicine, Vol 7, Iss 1, Pp 1-11 (2024)
Abstract Dystonia is a neurological movement disorder characterised by abnormal involuntary movements and postures, particularly affecting the head and neck. However, current clinical assessment methods for dystonia rely on simplified rating scales w
Externí odkaz:
https://doaj.org/article/0fbad953609640cea57e36f47712b111
Publikováno v:
Journal of the London Mathematical Society. 101:659-681
Adjoint functor theorems give necessary and sufficient conditions for a functor to admit an adjoint. In this paper, we prove general adjoint functor theorems for functors between ∞‐categories. One of our main results is an ∞‐categorical gener
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b76390b18d76e6fe7009f8ebf5cf62c8
https://doi.org/10.1112/jlms.12282
https://doi.org/10.1112/jlms.12282
We prove general adjoint functor theorems for weakly (co)complete $n$-categories. This class of $n$-categories includes the homotopy $n$-categories of (co)complete $\infty$-categories, so these $n$-categories do not admit all small (co)limits in gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81cee745f8db25be9c1ed550a3c78c72
http://arxiv.org/abs/2103.06003
http://arxiv.org/abs/2103.06003
Autor:
Lan Ye, Sam Sadeghi Sani, Linda Veith Sanches, Lea Farina Magdalena Krey, Florian Wegner, Matthias Höllerhage, Christoph Schrader, Günter Höglinger, Martin Klietz
Publikováno v:
Brain Sciences, Vol 14, Iss 10, p 991 (2024)
The acute levodopa challenge is widely used to distinguish Parkinson’s disease (PD) from atypical parkinsonian syndromes (APSs) such as multiple system atrophy (MSA) and progressive supranuclear palsy (PSP). In APSs, very few patients present a cli
Externí odkaz:
https://doaj.org/article/0981210e93614e8c8f561db0d770b4de
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-7 (2020)
Abstract Background Charcot-Marie-Tooth disease (CMT) is one of the most commonly inherited neurological disorders. A growing number of genes, involved in glial and neuronal functions, have been associated with different subtypes of CMT leading to im
Externí odkaz:
https://doaj.org/article/fcf40c8636684ab7983bc0c7c2a59581
Autor:
Martin Klietz, Amelie Tulke, Lars H. Müschen, Lejla Paracka, Christoph Schrader, Dirk W. Dressler, Florian Wegner
Publikováno v:
Frontiers in Neurology, Vol 9 (2018)
BackgroundParkinson’s disease (PD) is the second most frequent neurodegenerative disease of the elderly. Patients suffer from various motor and non-motor symptoms leading to reduced health-related quality of life (HRQOL) and an increased mortality.
Externí odkaz:
https://doaj.org/article/dc856044f8a9411099ca576c776831b7