Works matching AU Petri, Susanne
Results: 162
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
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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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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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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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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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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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
Glial fibrillary acidic protein in cerebrospinal fluid of patients with spinal muscular atrophy.
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- Annals of Clinical & Translational Neurology, 2022, v. 9, n. 9, p. 1437, doi. 10.1002/acn3.51645
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- Article
Validity and reliability of the German multidimensional fatigue inventory in spinal muscular atrophy.
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- Annals of Clinical & Translational Neurology, 2022, v. 9, n. 3, p. 351, doi. 10.1002/acn3.51520
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- Article
Serum creatine kinase and creatinine in adult spinal muscular atrophy under nusinersen treatment.
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- Annals of Clinical & Translational Neurology, 2021, v. 8, n. 5, p. 1049, doi. 10.1002/acn3.51340
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- Article
Spreading in ALS: The relative impact of upper and lower motor neuron involvement.
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- Annals of Clinical & Translational Neurology, 2020, v. 7, n. 7, p. 1181, doi. 10.1002/acn3.51098
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- Article
Serum neurofilament light chain in distinct phenotypes of amyotrophic lateral sclerosis: A longitudinal, multicenter study.
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- European Journal of Neurology, 2024, v. 31, n. 9, p. 1, doi. 10.1111/ene.16379
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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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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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- 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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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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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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Parthenolide regulates microglial and astrocyte function in primary cultures from ALS mice and has neuroprotective effects on primary motor neurons.
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- PLoS ONE, 2025, v. 20, n. 3, p. 1, doi. 10.1371/journal.pone.0319866
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Sporadic late-onset nemaline myopathy: clinico-pathological characteristics and review of 76 cases.
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- 2017
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- journal article
FiNuTyper: Design and validation of an automated deep learning‐based platform for simultaneous fiber and nucleus type analysis in human skeletal muscle.
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- Acta Physiologica, 2023, v. 239, n. 1, p. 1, doi. 10.1111/apha.13982
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Effect of High-Caloric Nutrition on Survival in Amyotrophic Lateral Sclerosis.
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- 2020
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- journal article
Correction: Clinical characterization of common pathogenic variants of SOD1-ALS in Germany.
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- 2025
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- Correction Notice
Narrative review of diagnosis, management and treatment of dysphagia and sialorrhea in amyotrophic lateral sclerosis.
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- Journal of Neurology, 2024, v. 271, n. 10, p. 6508, doi. 10.1007/s00415-024-12657-x
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Clinical characterization of common pathogenic variants of SOD1-ALS in Germany.
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- Journal of Neurology, 2024, v. 271, n. 10, p. 6667, doi. 10.1007/s00415-024-12564-1
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Correction to: Diagnostic value of neurofilaments in differentiating motor neuron disease from multifocal motor neuropathy.
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- 2024
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- Correction Notice
Non-motor symptoms in patients with amyotrophic lateral sclerosis: current state and future directions.
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- Journal of Neurology, 2024, v. 271, n. 7, p. 3953, doi. 10.1007/s00415-024-12455-5
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Diagnostic value of neurofilaments in differentiating motor neuron disease from multifocal motor neuropathy.
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- Journal of Neurology, 2024, v. 271, n. 7, p. 4441, doi. 10.1007/s00415-024-12355-8
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- Article
An observational cohort study on pulmonary function in adult patients with 5q-spinal muscular atrophy under nusinersen therapy.
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- Journal of Neurology, 2023, v. 270, n. 7, p. 3616, doi. 10.1007/s00415-023-11711-4
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A SUMO4 initiator codon variant in amyotrophic lateral sclerosis reduces SUMO4 expression and alters stress granule dynamics.
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- Journal of Neurology, 2022, v. 269, n. 9, p. 4863, doi. 10.1007/s00415-022-11126-7
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An observational cohort study on impact, dimensions and outcome of perceived fatigue in adult 5q-spinal muscular atrophy patients receiving nusinersen treatment.
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- Journal of Neurology, 2021, v. 268, n. 3, p. 950, doi. 10.1007/s00415-020-10227-5
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SPG7 mutations in amyotrophic lateral sclerosis: a genetic link to hereditary spastic paraplegia.
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- Journal of Neurology, 2020, v. 267, n. 9, p. 2732, doi. 10.1007/s00415-020-09861-w
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Treatment expectations and patient-reported outcomes of nusinersen therapy in adult spinal muscular atrophy.
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- Journal of Neurology, 2020, v. 267, n. 8, p. 2398, doi. 10.1007/s00415-020-09847-8
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- Article
Impact of comorbidities and co-medication on disease onset and progression in a large German ALS patient group.
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- Journal of Neurology, 2020, v. 267, n. 7, p. 2130, doi. 10.1007/s00415-020-09799-z
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- Article
Neurofilament light chain in serum of adolescent and adult SMA patients under treatment with nusinersen.
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- Journal of Neurology, 2020, v. 267, n. 1, p. 36, doi. 10.1007/s00415-019-09547-y
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- Article
Prognostic factors in ALS: a comparison between Germany and China.
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- Journal of Neurology, 2019, v. 266, n. 6, p. 1516, doi. 10.1007/s00415-019-09290-4
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- Article
Significance of CSF NfL and tau in ALS.
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- Journal of Neurology, 2018, v. 265, n. 11, p. 2633, doi. 10.1007/s00415-018-9043-0
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Therapeutic decisions in ALS patients: cross-cultural differences and clinical implications.
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- Journal of Neurology, 2018, v. 265, n. 7, p. 1600, doi. 10.1007/s00415-018-8861-4
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- Article
The metabolic and endocrine characteristics in spinal and bulbar muscular atrophy.
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- Journal of Neurology, 2018, v. 265, n. 5, p. 1026, doi. 10.1007/s00415-018-8790-2
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- Article
Clinical features and differential diagnosis of flail arm syndrome.
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- Journal of Neurology, 2016, v. 263, n. 2, p. 390, doi. 10.1007/s00415-015-7993-z
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Structural hallmarks of amyotrophic lateral sclerosis progression revealed by probabilistic fiber tractography.
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- Journal of Neurology, 2015, v. 262, n. 10, p. 2257, doi. 10.1007/s00415-015-7841-1
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Percutaneous endoscopic gastrostomy in amyotrophic lateral sclerosis: a prospective observational study.
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- Journal of Neurology, 2015, v. 262, n. 4, p. 849, doi. 10.1007/s00415-015-7646-2
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- Article
Central white matter degeneration in bulbar- and limb-onset amyotrophic lateral sclerosis.
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- Journal of Neurology, 2014, v. 261, n. 10, p. 1961, doi. 10.1007/s00415-014-7434-4
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Validation of the German version of the extended ALS functional rating scale as a patient-reported outcome measure.
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- Journal of Neurology, 2013, v. 260, n. 9, p. 2242, doi. 10.1007/s00415-013-6955-6
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Patterns of cortical activity differ in ALS patients with limb and/or bulbar involvement depending on motor tasks.
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- Journal of Neurology, 2011, v. 258, n. 5, p. 804, doi. 10.1007/s00415-010-5842-7
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