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Use and subjective experience of the impact of motor-assisted movement exercisers in people with amyotrophic lateral sclerosis: a multicenter observational study.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-13761-6
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- Publication type:
- Article
Routine Cerebrospinal Fluid (CSF) Parameters in Patients With Spinal Muscular Atrophy (SMA) Treated With Nusinersen.
- Published in:
- Frontiers in Neurology, 2019, v. 10, p. 1, doi. 10.3389/fneur.2019.01179
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- Publication type:
- Article
A novel CHCHD10 mutation implicates a Mia40‐dependent mitochondrial import deficit in ALS.
- Published in:
- EMBO Molecular Medicine, 2018, v. 10, n. 6, p. 1, doi. 10.15252/emmm.201708558
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- Publication type:
- Article
Poly- GP in cerebrospinal fluid links C9orf72-associated dipeptide repeat expression to the asymptomatic phase of ALS/ FTD.
- Published in:
- EMBO Molecular Medicine, 2017, v. 9, n. 7, p. 859, doi. 10.15252/emmm.201607486
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- Publication type:
- Article
Comparison of Sirtuin 3 Levels in ALS and Huntington's Disease--Differential Effects in Human Tissue Samples vs. Transgenic Mouse Models.
- Published in:
- Frontiers in Molecular Neuroscience, 2017, p. 1, doi. 10.3389/fnmol.2017.00156
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- Publication type:
- Article
Reply: Adult-onset distal spinal muscular atrophy: a new phenotype associated with KIF5A mutations.
- Published in:
- 2019
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- Publication type:
- Letter
Hot-spot KIF5A mutations cause familial ALS.
- Published in:
- 2018
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- Publication type:
- journal article
NEK1 mutations in familial amyotrophic lateral sclerosis.
- Published in:
- 2016
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- Publication type:
- Letter
Screening for CHCHD10 mutations in a large cohort of sporadic ALS patients: no evidence for pathogenicity of the p.P34S variant.
- Published in:
- 2016
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- Publication type:
- commentary
Serum microRNAs in patients with genetic amyotrophic lateral sclerosis and pre-manifest mutation carriers.
- Published in:
- 2014
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- Publication type:
- journal article
Increased cytotoxic potential of microglia from ALS‐transgenic mice.
- Published in:
- Glia, 2004, v. 48, n. 2, p. 179, doi. 10.1002/glia.20062
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- Publication type:
- Article
Clinical and patient‐reported outcomes and neurofilament response during tofersen treatment in SOD1‐related ALS—A multicenter observational study over 18 months.
- Published in:
- Muscle & Nerve, 2024, v. 70, n. 3, p. 333, doi. 10.1002/mus.28182
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- Publication type:
- Article
Neurofilament light‐chain response during therapy with antisense oligonucleotide tofersen in SOD1‐related ALS: Treatment experience in clinical practice.
- Published in:
- Muscle & Nerve, 2023, v. 67, n. 6, p. 515, doi. 10.1002/mus.27818
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- Publication type:
- Article
Targeting toxic proteins for turnover.
- Published in:
- Nature Medicine, 2005, v. 11, n. 10, p. 1052, doi. 10.1038/nm1005-1052
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- Publication type:
- Article
Clinical Trials in Spinal and Bulbar Muscular Atrophy-Past, Present, and Future.
- Published in:
- Journal of Molecular Neuroscience, 2016, v. 58, n. 3, p. 379, doi. 10.1007/s12031-015-0682-7
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- Publication type:
- Article
Towards a European Registry and Biorepository for Patients with Spinal and Bulbar Muscular Atrophy.
- Published in:
- Journal of Molecular Neuroscience, 2016, v. 58, n. 3, p. 394, doi. 10.1007/s12031-015-0704-5
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- Publication type:
- Article
Prodromal Huntington Disease as a Model for Functional Compensation of Early Neurodegeneration.
- Published in:
- PLoS ONE, 2014, v. 9, n. 12, p. 1, doi. 10.1371/journal.pone.0114569
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- Publication type:
- Article
Two-Point Magnitude MRI for Rapid Mapping of Brown Adipose Tissue and Its Application to the R6/2 Mouse Model of Huntington Disease.
- Published in:
- PLoS ONE, 2014, v. 9, n. 8, p. 1, doi. 10.1371/journal.pone.0105556
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- Publication type:
- Article
Incidence and Geographical Variation of Amyotrophic Lateral Sclerosis (ALS) in Southern Germany – Completeness of the ALS Registry Swabia.
- Published in:
- PLoS ONE, 2014, v. 9, n. 4, p. 1, doi. 10.1371/journal.pone.0093932
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- Publication type:
- Article
Neuropathology of Partial PGC-1α Deficiency Recapitulates Features of Mitochondrial Encephalopathies but Not of Neurodegenerative Diseases.
- Published in:
- Neurodegenerative Diseases, 2013, v. 12, n. 4, p. 177, doi. 10.1159/000346267
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- Publication type:
- Article
A single nucleotide polymorphism in the coding region of PGC-1α is a male-specific modifier of Huntington disease age-at-onset in a large European cohort.
- Published in:
- BMC Neurology, 2014, v. 14, n. 1, p. 1, doi. 10.1186/1471-2377-14-1
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- Publication type:
- Article
Huntington-Erkrankung.
- Published in:
- Medizinische Genetik, 2018, v. 30, n. 2, p. 246, doi. 10.1007/s11825-018-0190-6
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- Publication type:
- Article
A Remote Digital Monitoring Platform to Assess Cognitive and Motor Symptoms in Huntington Disease: Cross-sectional Validation Study.
- Published in:
- 2022
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- Publication type:
- journal article
Oxytocin in Huntington's disease and the spectrum of amyotrophic lateral sclerosis-frontotemporal dementia.
- Published in:
- Frontiers in Molecular Neuroscience, 2022, v. 15, p. 1, doi. 10.3389/fnmol.2022.984317
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- Publication type:
- Article
Correction to: Short-term safety results from compassionate use of risdiplam in patients with spinal muscular atrophy in Germany.
- Published in:
- Orphanet Journal of Rare Diseases, 2022, v. 17, n. 1, p. 1, doi. 10.1186/s13023-022-02548-7
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- Publication type:
- Article
Short-term safety results from compassionate use of risdiplam in patients with spinal muscular atrophy in Germany.
- Published in:
- 2022
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- Publication type:
- journal article
Human central neurocytoma cells show neuronal physiological properties in vitro.
- Published in:
- Acta Neuropathologica, 1996, v. 91, n. 2, p. 209, doi. 10.1007/s004010050416
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- Publication type:
- Article
Cardiac troponin T as a serum biomarker of respiratory impairment in amyotrophic lateral sclerosis.
- Published in:
- Annals of Clinical & Translational Neurology, 2024, v. 11, n. 8, p. 2063, doi. 10.1002/acn3.52126
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- Publication type:
- Article
Neurofilament levels as biomarkers in asymptomatic and symptomatic familial amyotrophic lateral sclerosis.
- Published in:
- 2016
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- Publication type:
- journal article
Mutual exacerbation of peroxisome proliferator-activated receptor γ coactivator 1α deregulation and α-synuclein oligomerization.
- Published in:
- Annals of Neurology, 2015, v. 77, n. 1, p. 15, doi. 10.1002/ana.24294
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- Publication type:
- Article
Mutual exacerbation of peroxisome proliferator-activated receptor γ coactivator 1α deregulation and α-synuclein oligomerization.
- Published in:
- 2015
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- Publication type:
- journal article
Serum irisin is upregulated in patients affected by amyotrophic lateral sclerosis and correlates with functional and metabolic status.
- Published in:
- Journal of Neurology, 2018, v. 265, n. 12, p. 3001, doi. 10.1007/s00415-018-9093-3
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- Publication type:
- Article
Telomere length as a modifier of age-at-onset in Huntington disease: a two-sample Mendelian randomization study.
- Published in:
- Journal of Neurology, 2018, v. 265, n. 9, p. 2149, doi. 10.1007/s00415-018-8972-y
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- Publication type:
- Article
The metabolic and endocrine characteristics in spinal and bulbar muscular atrophy.
- Published in:
- Journal of Neurology, 2018, v. 265, n. 5, p. 1026, doi. 10.1007/s00415-018-8790-2
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- Publication type:
- Article
Can lesions to the motor cortex induce amyotrophic lateral sclerosis?
- Published in:
- Journal of Neurology, 2014, v. 261, n. 2, p. 283, doi. 10.1007/s00415-013-7185-7
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- Publication type:
- Article
Teaching an old dog new tricks: serum troponin T as a biomarker in amyotrophic lateral sclerosis.
- Published in:
- Brain Communications, 2021, v. 3, n. 4, p. 1, doi. 10.1093/braincomms/fcab274
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- Publication type:
- Article
Full-length PGC-1α salvages the phenotype of a mouse model of human neuropathy through mitochondrial proliferation.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 25, p. 5096, doi. 10.1093/hmg/ddt359
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- Publication type:
- Article
PGC-1α is a male-specific disease modifier of human and experimental amyotrophic lateral sclerosis.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 17, p. 3477, doi. 10.1093/hmg/ddt202
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- Publication type:
- Article
A greatly extended PPARGC1A genomic locus encodes several new brain-specific isoforms and influences Huntington disease age of onset†.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 15, p. 3461
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- Publication type:
- Article
The concept and diagnostic criteria of primary lateral sclerosis.
- Published in:
- Acta Neurologica Scandinavica, 2017, v. 136, n. 3, p. 204, doi. 10.1111/ane.12713
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- Publication type:
- Article
Serum neurofilament light chain in distinct phenotypes of amyotrophic lateral sclerosis: A longitudinal, multicenter study.
- Published in:
- European Journal of Neurology, 2024, v. 31, n. 9, p. 1, doi. 10.1111/ene.16379
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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.
- Published in:
- European Journal of Neurology, 2023, v. 30, n. 6, p. 1600, doi. 10.1111/ene.15773
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- Publication type:
- Article
Proteomics in cerebrospinal fluid and spinal cord suggests UCHL1, MAP2 and GPNMB as biomarkers and underpins importance of transcriptional pathways in amyotrophic lateral sclerosis.
- Published in:
- Acta Neuropathologica, 2020, v. 139, n. 1, p. 119, doi. 10.1007/s00401-019-02093-x
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- Publication type:
- Article
Peripheral monocytes are functionally altered and invade the CNS in ALS patients.
- Published in:
- Acta Neuropathologica, 2016, v. 132, n. 3, p. 391, doi. 10.1007/s00401-016-1548-y
- By:
- Publication type:
- Article
User expectations and experiences of an assistive robotic arm in amyotrophic lateral sclerosis: a multicenter observational study.
- Published in:
- Neurological Research & Practice, 2024, v. 6, n. 1, p. 1, doi. 10.1186/s42466-024-00342-3
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- Publication type:
- Article
Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia.
- Published in:
- Nature Neuroscience, 2015, v. 18, n. 5, p. 631, doi. 10.1038/nn.4000
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- Publication type:
- Article
Endocannabinoids accumulate in spinal cord of SOD1<sup>G93A</sup> transgenic mice.
- Published in:
- Journal of Neurochemistry, 2004, v. 89, n. 6, p. 1555, doi. 10.1111/j.1471-4159.2004.02544.x
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- Publication type:
- Article
Creatine Kinase MB Isoenzyme Is a Complementary Biomarker in Amyotrophic Lateral Sclerosis.
- Published in:
- International Journal of Molecular Sciences, 2023, v. 24, n. 14, p. 11682, doi. 10.3390/ijms241411682
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- Publication type:
- Article
Frustration grows over EU grant application procedures.
- Published in:
- Nature, 2000, v. 404, n. 6779, p. 695, doi. 10.1038/35008229
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- Publication type:
- Article
German research agency stifles creativity.
- Published in:
- Nature, 2000, v. 404, n. 6775, p. 217, doi. 10.1038/35005249
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- Publication type:
- Article