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Therapeutic Advances in Neurological Disorders|February 14, 2022
Pharyngeal electrical stimulation in amyotrophic lateral sclerosis: a pilot studyChristine Herrmann, Falk Schradt, Beate Lindner-Pfleghar, et al.Neurology|October 21, 2021
Life Course of Physical Activity and Risk and Prognosis of Amyotrophic Lateral Sclerosis in a German ALS RegistryAngela Rosenbohm, Raphael Peter, Johannes Dorst, et al.European Journal of Neurology|September 28, 2022
Mutation-specific metabolic profiles in presymptomatic amyotrophic lateral sclerosisKailin Xia, Simon Witzel, Christina Witzel, et al.Journal of Neurology, Neurosurgery, and Psychiatry|January 13, 2022
Fat-rich versus carbohydrate-rich nutrition in ALS: a randomised controlled studyJohannes Dorst, Judith Doenz, Katharina Kandler, et al.Neuroscience Letters|October 27, 2009
Proteome analysis reveals candidate markers of disease progression in amyotrophic lateral sclerosis (ALS)Johannes Brettschneider, Vera Lehmensiek, Helga Mogel, et al.European Journal of Neurology|March 31, 2023
Lipids and amyotrophic lateral sclerosis: A two-sample Mendelian randomization studyKailin Xia, Veronika Klose, Josef Högel, et al.Journal of Neurology|May 13, 2023
Presymptomatic grey matter alterations in ALS kindreds: a computational neuroimaging study of asymptomatic C9orf72 and SOD1 mutation carriersPeter Bede, Dorothée Lulé, Hans-Peter Müller, et al.Frontiers in Neurology|May 22, 2023
CSF oligoclonal IgG bands are not associated with ALS progression and prognosisVeronika Klose, Sarah Jesse, Jan Lewerenz, et al.Neuroimage. Clinical|September 11, 2023
Structural and microstructural neuroimaging signature of C9orf72-associated ALS: A multiparametric MRI studyMaximilian Wiesenfarth, Hans-Jürgen Huppertz, Johannes Dorst, et al.Scientific Reports|January 9, 2025
Hypothalamic atrophy in primary lateral sclerosis, assessed by convolutional neural network-based automatic segmentationJan Kassubek, Francesco Roselli, Simon Witzel, et al.Pageof 59