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Methods in Molecular Biology (Clifton, N.J.)|May 1, 2017
SILAC-Based Comparative Proteomic Analysis of Lysosomes from Mammalian Cells Using LC-MS/MSMelanie Thelen, Dominic Winter, Thomas Braulke, et al.
American Journal of Human Genetics|January 1, 1995
Multiple mutations are responsible for the high frequency of metachromatic leukodystrophy in a small geographic areaU Heinisch, J Zlotogora, S Kafert, et al.
Psychological Medicine|September 29, 2025
Ethical issues with psychedelic-assisted treatments in psychiatry: A systematic scoping reviewChiara Caporuscio, Christopher Poppe, Astrid Gieselmann, et al.
Fortschritte Der Neurologie-Psychiatrie|February 21, 2019
[Advance research directives in the context of dementia research: Ethical reflections on the disclosure requirement]Astrid Gieselmann, Matthé Scholten, Jakov Gather, et al.
Human Genetics|October 1, 1993
Simultaneous detection of the two most frequent metachromatic leukodystrophy mutationsJ Berger, B Molzer, V Gieselmann, et al.
Journal of Behavior Therapy and Experimental Psychiatry|December 30, 2019
Nightmare distress revisited: Cognitive appraisal of nightmares according to Lazarus' transactional model of stressAnnika Gieselmann, Nina Elberich, Jonas Mathes, et al.
Psychotherapy and Psychosomatics|June 26, 2017
The Effects of an Internet-Based Imagery Rehearsal Intervention: A Randomized Controlled TrialAnnika Gieselmann, Max Böckermann, Marjolijn Sorbi, et al.
Behavior Therapy|February 24, 2021
Communication Formats and Their Impact on Patient Perception and Working Mechanisms: A Mixed-Methods Study of Chat-Based vs. Face-to-Face Psychotherapy for InsomniaAnnika Gieselmann, Carmen Podleschka, Alexander Rozental, et al.
Human Genetics|February 1, 1995
A missense mutation P136L in the arylsulfatase A gene causes instability and loss of activity of the mutant enzymeS Kafert, U Heinisch, J Zlotogora, et al.
The Biochemical Journal|February 14, 2018
Identification of progesterone receptor membrane component-1 as an interaction partner and possible regulator of fatty acid 2-hydroxylaseRobert Hardt, Dominic Winter, Volkmar Gieselmann, et al.
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