@phdthesis{Walter2011,
  author    = {Walter, Lena},
  title     = {Ergebnisse der Behandlung mit Bevacizumab bei altersabh{\"a}ngiger Makuladegeneration mit subfovealer Neovaskularisationsmembran {\"u}ber 3 bis 12 Monate},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-65918},
  school      = {Universit{\"a}t W{\"u}rzburg},
  year      = {2011},
  abstract  = {Therapieergebnisse der Patienten, die im Zeitraum von 1. Januar bis 31. Dezember 2006 in der Augenklinik W{\"u}rzburg mehrere intravitreale Injektionen mit Bevacizumab bei altersabh{\"a}ngiger Makuladegeneration mit subfovealer choroidaler Neovaskularisation erhalten hatten.},
  subject      = {altersabh{\"a}ngige Makuladegeneration},
  language  = {de}
}
@article{SchleicherArbetEngelsBaacketal.2019,
  author    = {Schleicher, Bernd and Arbet-Engels, Axel and Baack, Dominik and Balbo, Matteo and Biland, Adrian and Blank, Michael and Bretz, Thomas and Bruegge, Kai and Bulinski, Michael and Buss, Jens and Doerr, Manuel and Dorner, Daniela and Elsaesser, Dominik and Grischagin, Sergej and Hildebrand, Dorothee and Linhoff, Lena and Mannheim, Karl and Mueller, Sebastian Achim and Neise, Dominik and Neronov, Andrii and Noethe, Maximilian and Paravac, Aleksander and Rhode, Wolfgang and Schulz, Florian and Sedlaczek, Kevin and Shukla, Amit and Sliusar, Vitalii and Willert, Elan and Walter, Roland},
  title     = {Fractional Variability—A Tool to Study Blazar Variability},
  series = {Galaxies},
  volume    = {7},
  journal   = {Galaxies},
  number    = {2},
  issn      = {2075-4434},
  doi       = {10.3390/galaxies7020062},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-197348},
  year      = {2019},
  abstract  = {Active Galactic Nuclei emit radiation over the whole electromagnetic spectrum up to TeV energies. Blazars are one subtype with their jets pointing towards the observer. One of their typical features is extreme variability on timescales, from minutes to years. The fractional variability is an often used parameter for investigating the degree of variability of a light curve. Different detection methods and sensitivities of the instruments result in differently binned data and light curves with gaps. As they can influence the physics interpretation of the broadband variability, the effects of these differences on the fractional variability need to be studied. In this paper, we study the systematic effects of completeness in time coverage and the sampling rate. Using public data from instruments monitoring blazars in various energy ranges, we study the variability of the bright TeV blazars Mrk 421 and Mrk 501 over the electromagnetic spectrum, taking into account the systematic effects, and compare our findings with previous results. Especially in the TeV range, the fractional variability is higher than in previous studies, which can be explained by the much longer (seven years compared to few weeks) and more complete data sample.},
  language  = {en}
}
@article{TemmeAdamAhnenetal.2017,
  author    = {Temme, Fabian and Adam, Jan and Ahnen, Max L. and Baack, Dominik and Balbo, Matteo and Bergmann, Matthias and Biland, Adrian and Blank, Michael and Bretz, Thomas and Br{\"u}gge, Kai A. and Buss, Jens and Dmytriiev, Anton and Dorner, Daniela and Einecke, Sabrina and Hempfling, Christina and Hildebrand, Dorothee and Hughes, Gareth and Linhoff, Lena and Mannheim, Karl and M{\"u}ller, Sebastian and Neise, Dominik and Neronov, Andrii and N{\"o}the, Max and Paravac, Aleksander and Pauss, Felicitas and Rhode, Wolfgang and Shukla, Amit and Thaele, Julia and Walter, Roland},
  title     = {Long-Term monitoring of bright blazars in the multi-GeV to TeV range with FACT},
  series = {Galaxies},
  volume    = {5},
  journal   = {Galaxies},
  number    = {1},
  publisher = {MDPI},
  issn      = {2075-4434},
  doi       = {10.3390/galaxies5010018},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-198088},
  pages     = {18},
  year      = {2017},
  abstract  = {Blazars like Markarian 421 or Markarian 501 are active galactic nuclei (AGN), with their jets orientated towards the observer. They are among the brightest objects in the very high energy (VHE) gamma ray regime (>100 GeV). Their emitted gamma-ray fluxes are extremely variable, with changing activity levels on timescales between minutes, months, and even years. Several questions are part of the current research, such as the question of the emission regions or the engine of the AGN and the particle acceleration. A dedicated longterm monitoring program is necessary to investigate the properties of blazars in detail. A densely sampled and unbiased light curve allows for observation of both high and low states of the sources, and the combination with multi-wavelength observation could contribute to the answer of several questions mentioned above. FACT (First G-APD Cherenkov Telescope) is the first operational telescope using silicon photomultiplier (SiPM, also known as Geigermode—Avalanche Photo Diode, G-APD) as photon detectors. SiPM have a very homogenous and stable longterm performance, and allow operation even during full moon without any filter, leading to a maximal duty cycle for an Imaging Air Cherenkov Telescope (IACT). Hence, FACT is an ideal device for such a longterm monitoring of bright blazars. A small set of sources (e.g., Markarian 421, Markarian 501, 1ES 1959+650, and 1ES 2344+51.4) is currently being monitored. In this contribution, the FACT telescope and the concept of longterm monitoring of bright blazars will be introduced. The results of the monitoring program will be shown, and the advantages of densely sampled and unbiased light curves will be discussed.},
  language  = {en}
}
@article{GschmackMonoranuMaroufetal.2022,
  author    = {Gschmack, Eva and Monoranu, Camelia-Maria and Marouf, Hecham and Meyer, Sarah and Lessel, Lena and Idris, Raja and Berg, Daniela and Maetzler, Walter and Steigerwald, Frank and Volkmann, Jens and Gerlach, Manfred and Riederer, Peter and Koutsilieri, Eleni and Scheller, Carsten},
  title     = {Plasma autoantibodies to glial fibrillary acidic protein (GFAP) react with brain areas according to Braak staging of Parkinson's disease},
  series = {Journal of Neural Transmission},
  volume    = {129},
  journal   = {Journal of Neural Transmission},
  number    = {5-6},
  doi       = {10.1007/s00702-022-02495-4},
  url       = {http://nbn-resolving.de/urn:nbn:de:bvb:20-opus-325161},
  pages     = {545-555},
  year      = {2022},
  abstract  = {Idiopathic Parkinson's disease (PD) is characterized by a progredient degeneration of the brain, starting at deep subcortical areas such as the dorsal motor nucleus of the glossopharyngeal and vagal nerves (DM) (stage 1), followed by the coeruleus-subcoeruleus complex; (stage 2), the substantia nigra (SN) (stage 3), the anteromedial temporal mesocortex (MC) (stage 4), high-order sensory association areas and prefrontal fields (HC) (stage 5) and finally first-order sensory association areas, premotor areas, as well as primary sensory and motor field (FC) (stage 6). Autoimmunity might play a role in PD pathogenesis. Here we analyzed whether anti-brain autoantibodies differentially recognize different human brain areas and identified autoantigens that correlate with the above-described dissemination of PD pathology in the brain. Brain tissue was obtained from deceased individuals with no history of neurological or psychiatric disease and no neuropathological abnormalities. Tissue homogenates from different brain regions (DM, SN, MC, HC, FC) were subjected to SDS-PAGE and Western blot. Blots were incubated with plasma samples from 30 PD patients and 30 control subjects and stained with anti-IgG antibodies to detect anti-brain autoantibodies. Signals were quantified. Prominent autoantigens were identified by 2D-gel-coupled mass spectrometry sequencing. Anti-brain autoantibodies are frequent and occur both in healthy controls and individuals with PD. Glial fibrillary acidic protein (GFAP) was identified as a prominent autoantigen recognized in all plasma samples. GFAP immunoreactivity was highest in DM areas and lowest in FC areas with no significant differences in anti-GFAP autoantibody titers between healthy controls and individuals with PD. The anti-GFAP autoimmunoreactivity of different brain areas correlates with the dissemination of histopathological neurodegeneration in PD. We hypothesize that GFAP autoantibodies are physiological but might be involved as a cofactor in PD pathogenesis secondary to a leakage of the blood-brain barrier.},
  language  = {en}
}