Works matching AU Petri, Susanne
Results: 161
Correction: Clinical characterization of common pathogenic variants of SOD1-ALS in Germany.
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- 2025
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- Publication type:
- Correction Notice
Provision, cough efficacy and treatment satisfaction of mechanical insufflation-exsufflation in a large multicenter cohort of patients with amyotrophic lateral sclerosis.
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- Scientific Reports, 2025, v. 15, n. 1, p. 1, doi. 10.1038/s41598-025-91692-8
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- Article
Preserved expression of fibroblast growth factor (FGF)-2 and FGF receptor 1 in brain and spinal cord of amyotrophic lateral sclerosis patients.
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- Histochemistry & Cell Biology, 2009, v. 131, n. 4, p. 509, doi. 10.1007/s00418-008-0549-x
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- Article
Smartphone-Based Assessment of Mobility and Manual Dexterity in Adult People with Spinal Muscular Atrophy.
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- Journal of Neuromuscular Diseases, 2024, v. 11, n. 5, p. 1049, doi. 10.3233/JND-240004
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- Article
Health-Related Quality of Life in Spinal Muscular Atrophy Patients and Their Caregivers—A Prospective, Cross-Sectional, Multi-Center Analysis.
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- Brain Sciences (2076-3425), 2023, v. 13, n. 1, p. 110, doi. 10.3390/brainsci13010110
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- Article
Nusinersen Wearing-Off in Adult 5q-Spinal Muscular Atrophy Patients.
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- Brain Sciences (2076-3425), 2021, v. 11, n. 3, p. 367, doi. 10.3390/brainsci11030367
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- Article
Cerebrospinal Fluid Parameters in Antisense Oligonucleotide-Treated Adult 5q-Spinal Muscular Atrophy Patients.
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- Brain Sciences (2076-3425), 2021, v. 11, n. 3, p. 296, doi. 10.3390/brainsci11030296
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- Article
Clinically Applicable Quantitative Magnetic Resonance Morphologic Measurements of Grey Matter Changes in the Human Brain.
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- Brain Sciences (2076-3425), 2021, v. 11, n. 1, p. 55, doi. 10.3390/brainsci11010055
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- Article
Cognitive Performance of Patients with Adult 5q-Spinal Muscular Atrophy and with Amyotrophic Lateral Sclerosis.
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- Brain Sciences (2076-3425), 2021, v. 11, n. 1, p. 8, doi. 10.3390/brainsci11010008
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- Article
Isoform‐selective as opposed to complete depletion of fibroblast growth factor 2 (FGF‐2) has no major impact on survival and gene expression in SOD1<sup>G93A</sup> amyotrophic lateral sclerosis mice.
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- European Journal of Neuroscience, 2019, v. 50, n. 6, p. 3028, doi. 10.1111/ejn.14405
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- Article
Expression of the axon-guidance protein receptor Neuropilin 1 is increased in the spinal cord and decreased in muscle of a mouse model of amyotrophic lateral sclerosis.
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- European Journal of Neuroscience, 2019, v. 49, n. 11, p. 1529, doi. 10.1111/ejn.14326
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- Article
Working Memory Network Changes in ALS: An fMRI Study.
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- Frontiers in Neuroscience, 2016, p. 1, doi. 10.3389/fnins.2016.00158
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- Article
Clinical and patient‐reported outcomes and neurofilament response during tofersen treatment in SOD1‐related ALS—A multicenter observational study over 18 months.
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- Muscle & Nerve, 2024, v. 70, n. 3, p. 333, doi. 10.1002/mus.28182
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- Article
Metabolic syndrome is common in adults with 5q‐spinal muscular atrophy and impacts quality of life and fatigue.
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- Muscle & Nerve, 2024, v. 70, n. 2, p. 257, doi. 10.1002/mus.28183
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- Article
Neural mitochondrial Ca<sup>2+</sup> capacity impairment precedes the onset of motor symptoms in G93A Cu/Zn-superoxide dismutase mutant mice.
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- Journal of Neurochemistry, 2006, v. 96, n. 5, p. 1349, doi. 10.1111/j.1471-4159.2006.03619.x
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- Article
Integrative role of cPLA<sub>2</sub> with COX-2 and the effect of non-steriodal anti-inflammatory drugs in a transgenic mouse model of amyotrophic lateral sclerosis.
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- Journal of Neurochemistry, 2005, v. 93, n. 2, p. 403, doi. 10.1111/j.1471-4159.2005.03024.x
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- Article
Functional Characterization of the Murine Serotonin Transporter Gene Promoter in Serotonergic Raphe Neurons.
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- Journal of Neurochemistry, 1998, v. 70, n. 3, p. 932, doi. 10.1046/j.1471-4159.1998.70030932.x
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- Article
Allelic Variation of Human Serotonin Transporter Gene Expression.
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- Journal of Neurochemistry, 1996, v. 66, n. 6, p. 2621, doi. 10.1046/j.1471-4159.1996.66062621.x
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- Article
Memory deficits in amyotrophic lateral sclerosis are not exclusively caused by executive dysfunction: a comparative neuropsychological study of amnestic mild cognitive impairment.
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- BMC Neuroscience, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1471-2202-15-83
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- Article
Memory deficits in amyotrophic lateral sclerosis are not exclusively caused by executive dysfunction: a comparative neuropsychological study of amnestic mild cognitive impairment.
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- 2014
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- Publication type:
- journal article
Diagnostic support for selected neuromuscular diseases using answer-pattern recognition and data mining techniques: a proof of concept multicenter prospective trial.
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- 2016
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- Publication type:
- journal article
Missing Medical Data in Neurological Emergency Care Compromise Patient Safety and Healthcare Resources.
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- Journal of Clinical Medicine, 2024, v. 13, n. 21, p. 6344, doi. 10.3390/jcm13216344
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- Article
Towards the Validation of Executive Functioning Assessments: A Clinical Study.
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- Journal of Clinical Medicine, 2022, v. 11, n. 23, p. 7138, doi. 10.3390/jcm11237138
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- Article
Pain-Related Coping Behavior in ALS: The Interplay between Maladaptive Coping, the Patient's Affective State and Pain.
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- Journal of Clinical Medicine, 2022, v. 11, n. 4, p. N.PAG, doi. 10.3390/jcm11040944
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- Article
A Multi-Center Cohort Study on Characteristics of Pain, Its Impact and Pharmacotherapeutic Management in Patients with ALS.
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- Journal of Clinical Medicine, 2021, v. 10, n. 19, p. 4552, doi. 10.3390/jcm10194552
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- Article
A Computational Study of Executive Dysfunction in Amyotrophic Lateral Sclerosis.
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- Journal of Clinical Medicine, 2020, v. 9, n. 8, p. 2605, doi. 10.3390/jcm9082605
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- Article
Safety and Effectiveness of Long-term Intravenous Administration of Edaravone for Treatment of Patients With Amyotrophic Lateral Sclerosis.
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- JAMA Neurology, 2022, v. 79, n. 2, p. 121, doi. 10.1001/jamaneurol.2021.4893
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- Article
Speech therapy and communication device: Impact on quality of life and mood in patients with amyotrophic lateral sclerosis.
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- Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2013, v. 14, n. 1, p. 20, doi. 10.3109/17482968.2012.692382
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- Article
The upper cervical spinal cord in ALS assessed by cross-sectional and longitudinal 3T MRI.
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- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-58687-z
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- Article
Transcriptome-wide Profiling of Cerebral Cavernous Malformations Patients Reveal Important Long noncoding RNA molecular signatures.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-54845-0
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- Article
Plekhg5 controls the unconventional secretion of Sod1 by presynaptic secretory autophagy.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-52875-5
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- Article
Emotional Lability at Disease Onset Is an Independent Prognostic Factor of Faster Disease Progression in Amyotrophic Lateral Sclerosis.
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- Aging & Disease, 2020, v. 11, n. 5, p. 1021, doi. 10.14336/AD.2019.1120
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- Article
Influence of Environment and Lifestyle on Incidence and Progress of Amyotrophic Lateral Sclerosis in A German ALS Population.
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- Aging & Disease, 2019, v. 10, n. 2, p. 205, doi. 10.14336/AD.2018.0327
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- Article
Analysis of the therapeutic potential of different administration routes and frequencies of human mesenchymal stromal cells in the SOD1<sup>G93A</sup> mouse model of amyotrophic lateral sclerosis.
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- Journal of Tissue Engineering & Regenerative Medicine, 2019, v. 13, n. 4, p. 649, doi. 10.1002/term.2846
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- Article
Intraspinal administration of human spinal cord-derived neural progenitor cells in the G93A-SOD1 mouse model of ALS delays symptom progression, prolongs survival and increases expression of endogenous neurotrophic factors.
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- Journal of Tissue Engineering & Regenerative Medicine, 2017, v. 11, n. 3, p. 751, doi. 10.1002/term.1972
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- Publication type:
- Article
European Academy of Neurology (EAN) guideline on the management of amyotrophic lateral sclerosis in collaboration with European Reference Network for Neuromuscular Diseases (ERNEURO‐NMD).
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- European Journal of Neurology, 2024, v. 31, n. 6, p. 1, doi. 10.1111/ene.16264
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- Article
In‐depth analysis of data from the RAS‐ALS study reveals new insights in rasagiline treatment for amyotrophic lateral sclerosis.
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- European Journal of Neurology, 2024, v. 31, n. 4, p. 1, doi. 10.1111/ene.16204
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- Publication type:
- Article
Performance of serum neurofilament light chain in a wide spectrum of clinical courses of amyotrophic lateral sclerosis—a cross‐sectional multicenter study.
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- European Journal of Neurology, 2023, v. 30, n. 6, p. 1600, doi. 10.1111/ene.15773
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- Article
Brain activity is contingent on neuropsychological function in a functional magnetic resonance imaging study of verbal working memory in amyotrophic lateral sclerosis.
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- European Journal of Neurology, 2021, v. 28, n. 9, p. 3051, doi. 10.1111/ene.14957
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- Publication type:
- Article
Treatment expectations and perception of therapy in adult patients with spinal muscular atrophy receiving nusinersen.
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- European Journal of Neurology, 2021, v. 28, n. 8, p. 2582, doi. 10.1111/ene.14902
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- Publication type:
- Article
EFNS guidelines on the Clinical Management of Amyotrophic Lateral Sclerosis (MALS) - revised report of an EFNS task force.
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- European Journal of Neurology, 2012, v. 19, n. 3, p. 360, doi. 10.1111/j.1468-1331.2011.03501.x
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- Article
Heterozygous DHTKD1 Variants in Two European Cohorts of Amyotrophic Lateral Sclerosis Patients.
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- Genes, 2022, v. 13, n. 1, p. 84, doi. 10.3390/genes13010084
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- Article
Botulinum Toxin as Preventive Treatment for Migraine: A Randomized Double-Blind Study.
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- European Neurology, 2009, v. 62, n. 4, p. 204, doi. 10.1159/000228987
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- Article
Small peptide CSF fingerprint of amyotrophic lateral sclerosis.
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- PLoS ONE, 2024, v. 19, n. 4, p. 1, doi. 10.1371/journal.pone.0302280
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- Article
Human GABA<sub>A</sub> receptors on dopaminergic neurons in the pars compacta of the substantia nigra.
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- Journal of Comparative Neurology, 2002, v. 452, n. 4, p. 360, doi. 10.1002/cne.10379
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- Article
Shared prognostic information in amyotrophic lateral sclerosis – systematic assessment of the patients' perception of neurofilament light chain and the ALS functional rating scale.
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- Neurological Research & Practice, 2025, v. 7, n. 1, p. 1, doi. 10.1186/s42466-024-00363-y
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- Article
User expectations and experiences of an assistive robotic arm in amyotrophic lateral sclerosis: a multicenter observational study.
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- Neurological Research & Practice, 2024, v. 6, n. 1, p. 1, doi. 10.1186/s42466-024-00342-3
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- Article
Patients' and caregivers' perception of multidimensional and palliative care in amyotrophic lateral sclerosis – protocol of a German multicentre study.
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- Neurological Research & Practice, 2024, v. 6, n. 1, p. 1, doi. 10.1186/s42466-024-00328-1
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- Article
Guideline "Motor neuron diseases" of the German Society of Neurology (Deutsche Gesellschaft für Neurologie).
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- Neurological Research & Practice, 2023, v. 5, n. 1, p. 1, doi. 10.1186/s42466-023-00251-x
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- Article
ALSFRS-R-SE: an adapted, annotated, and self-explanatory version of the revised amyotrophic lateral sclerosis functional rating scale.
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- Neurological Research & Practice, 2022, v. 4, n. 1, p. 1, doi. 10.1186/s42466-022-00224-6
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- Publication type:
- Article