Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Andreas, Johnen"'
Autor:
Jonathan Repple, Svea Haessner, Andreas Johnen, Nils C. Landmeyer, Andreas Schulte-Mecklenbeck, Marc Pawlitzki, Heinz Wiendl, Gerd Meyer zu Hörste
Publikováno v:
BMC Neurology, Vol 21, Iss 1, Pp 1-6 (2021)
Abstract Background The mu-opioid agonist methadone is administered orally and used in opioid detoxification and in the treatment of moderate-to-severe pain. Acute oral methadone–use and –abuse have been associated with inflammatory and toxic cen
Externí odkaz:
https://doaj.org/article/b7beb7ca41314ec481450cd510efb910
Autor:
Carsten Kirkeby, Klas Rydhmer, Samantha M. Cook, Alfred Strand, Martin T. Torrance, Jennifer L. Swain, Jord Prangsma, Andreas Johnen, Mikkel Jensen, Mikkel Brydegaard, Kaare Græsbøll
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-8 (2021)
Abstract Worldwide, farmers use insecticides to prevent crop damage caused by insect pests, while they also rely on insect pollinators to enhance crop yield and other insect as natural enemies of pests. In order to target pesticides to pests only, fa
Externí odkaz:
https://doaj.org/article/2e1c22a8f9124d7e81390cef1dddfb73
Autor:
Nils C. Landmeyer, Inga Dzionsko, Laura Brockhoff, Heinz Wiendl, Gregor Domes, Jens Bölte, Julia Krämer, Sven G. Meuth, Andreas Johnen
Publikováno v:
Frontiers in Neurology, Vol 11 (2020)
Background: Cognitive impairment (CI) is an early and frequent symptom of multiple sclerosis (MS). Likewise, affective symptoms (e.g., depression and anxiety) and alterations in the processing of emotional stimuli have been frequently reported. Thus,
Externí odkaz:
https://doaj.org/article/3fa8119b51af4db7bac398470aea51a6
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-10 (2018)
Abstract Background Niemann-Pick disease type C (NP-C) is a rare, progressive neurodegenerative disease caused by mutations in the NPC1 or the NPC2 gene. Neurocognitive deficits are common in NP-C, particularly in patients with the adolescent/adult-o
Externí odkaz:
https://doaj.org/article/801966a5d7174563a8308ab0edb66d4c
Publikováno v:
Alzheimer’s & Dementia: Diagnosis, Assessment & Disease Monitoring, Vol 10, Iss 1, Pp 363-371 (2018)
Abstract Introduction Apraxia is common in neurodegenerative dementias but underrepresented in clinical workup for differential diagnoses. Methods Praxis‐profiles were assessed with the Dementia Apraxia Test in 93 patients with early stages of biol
Externí odkaz:
https://doaj.org/article/fe0f1838dd324feaa22efb8b42c3af2a
Publikováno v:
Alzheimer’s Research & Therapy, Vol 9, Iss 1, Pp 1-12 (2017)
Abstract Background Neuropsychological testing is considered crucial for differential diagnosis of Alzheimer’s disease (AD) and behavioural variant frontotemporal dementia (bvFTD). In-depth neuropsychological assessment revealed specific dysfunctio
Externí odkaz:
https://doaj.org/article/8a5aeb9d0b0d46269707104e9bf80e7b
Autor:
Andreas Johnen, Maxime Bertoux
Publikováno v:
Frontiers in Neurology, Vol 10 (2019)
Behavioral variant frontotemporal dementia (bvFTD) is the second leading cognitive disorder caused by neurodegeneration in patients under 65 years of age. Characterized by frontal, insular, and/or temporal brain atrophy, patients present with heterog
Externí odkaz:
https://doaj.org/article/30537e56cf0d4cac87f3cf0eed407894
Autor:
Anna Semenkova, Olivier Piguet, Andreas Johnen, Matthias L. Schroeter, Jannis Godulla, Christoph Linnemann, Markus Mühlhauser, Thomas Sauer, Markus Baumgartner, Sarah Anderl-Straub, Markus Otto, Ansgar Felbecker, Reto W. Kressig, Manfred Berres, Marc Sollberger
Publikováno v:
Journal of Neurology
Background and objectives Early-stage behavioural variant frontotemporal dementia (bvFTD) is often misdiagnosed, highlighting the need for new diagnostic instruments. Based on the revised diagnostic criteria for bvFTD, we developed the Behavioural Dy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::209706f2a52664ef98abe3b5e4df8d43
https://doi.org/10.1007/s00415-023-11666-6
https://doi.org/10.1007/s00415-023-11666-6
Autor:
Daniela Renftle, Sara Becker, Kathrin Brockmann, Thomas Gasser, Katja Michaelis, Susanne Solbrig, Patricia Sulzer, Andreas Johnen, Inga Liepelt-Scarfone
Publikováno v:
Dementia and geriatric cognitive disorders 51(3), 271-278 (2022). doi:10.1159/000525618
Introduction: Ideomotor apraxia, a disorder of skilled movements affecting limbs and/or face, can be seen in patients with Parkinson’s disease (PD), yet tests of apraxia in PD are rare. The aim of this project was to evaluate the psychometric prope
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eae28084a3373ffa706a8d1c0bee8f12
https://doi.org/10.1159/000525618
https://doi.org/10.1159/000525618
Autor:
Christoph Mueller, Saskia Elben, Gregory S. Day, Pedro Alves, Julien Hebert, David F. Tang-Wai, Olga Holtmann, Raffaele Iorio, Daniela Perani, Maarten J. Titulaer, Niels Hansen, Thorsten Bartsch, Andreas Johnen, Zsolt Illes, Leah Borm, Alice G. Willison, Heinz Wiendl, Sven G. Meuth, Stjepana Kovac, Jens Bölte, Nico Melzer
Publikováno v:
Clinical Neurology and Neurosurgery. 224
Objectives: It is assumed that autoimmune limbic encephalitis (ALE) demonstrates distinct neuropsychological manifestations with differential responses to immunotherapy according to which associated autoantibody (AAB), if any, is identified. Towards
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d14a47bee99e028d8f73f7c8cd719155
http://www.scopus.com/inward/record.url?scp=85144360277&partnerID=8YFLogxK
http://www.scopus.com/inward/record.url?scp=85144360277&partnerID=8YFLogxK