Works matching AU Landwehrmeyer, G. Bernhard
Results: 73
Intact sensory-motor network structure and function in far from onset premanifest Huntington's disease.
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- Scientific Reports, 2017, p. 43841, doi. 10.1038/srep43841
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- Article
Huntington disease alters the actionable information in plasma extracellular vesicles.
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- Clinical & Translational Medicine, 2024, v. 14, n. 1, p. 1, doi. 10.1002/ctm2.1525
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- Article
Identification of Extreme Motor Phenotypes in Huntington’s Disease.
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- American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2017, v. 174, n. 3, p. 283, doi. 10.1002/ajmg.b.32514
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- Article
Expression of NMDA receptor subunit mRNAs in neurochemically identified projection and interneurons in the human striatum.
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- Journal of Comparative Neurology, 2000, v. 419, n. 4, p. 407, doi. 10.1002/(SICI)1096-9861(20000417)419:4<407::AID-CNE1>3.0.CO;2-I
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- Article
Localization of alternatively spliced NMDAR1 glutamate receptor isoforms in rat striatal neurons.
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- Journal of Comparative Neurology, 1999, v. 415, n. 2, p. 204, doi. 10.1002/(SICI)1096-9861(19991213)415:2<204::AID-CNE5>3.0.CO;2-V
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- Article
Localization of metabotropic glutamate receptor 7 mRNA and mGluR7a protein in the rat basal ganglia.
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- Journal of Comparative Neurology, 1999, v. 415, n. 2, p. 266, doi. 10.1002/(SICI)1096-9861(19991213)415:2<266::AID-CNE9>3.0.CO;2-7
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- Article
Expression of N-Methyl-D-Aspartate receptor subunit mRNAs in the human brain: Striatum and globus pallidus.
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- Journal of Comparative Neurology, 1998, v. 390, n. 1, p. 63, doi. 10.1002/(SICI)1096-9861(19980105)390:1<63::AID-CNE6>3.0.CO;2-O
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- Article
Expression of N-Methyl-D-Aspartate receptor subunit mRNA in the human brain: Mesencephalic dopaminergic neurons.
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- Journal of Comparative Neurology, 1998, v. 390, n. 1, p. 91, doi. 10.1002/(SICI)1096-9861(19980105)390:1<91::AID-CNE8>3.0.CO;2-L
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- Article
Expression of N-Methyl-D-Aspartate receptor subunit mRNAs in the human brain: Hippocampus and cortex.
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- Journal of Comparative Neurology, 1998, v. 390, n. 1, p. 75, doi. 10.1002/(SICI)1096-9861(19980105)390:1<75::AID-CNE7>3.0.CO;2-N
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- Article
Differential expression of mGluR5 metabotropic glutamate receptor mRNA by rat striatal neurons.
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- Journal of Comparative Neurology, 1995, v. 354, n. 2, p. 241, doi. 10.1002/cne.903540207
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- Article
Shifting focus from ideality to reality: a qualitative study on how quality of life is defined by premanifest and manifest Huntington's disease gene expansion carriers.
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- Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03461-x
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- Article
Development of an ELISA assay for the quantification of soluble huntingtin in human blood cells.
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- BMC Biochemistry, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2091-14-34
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- Article
Defining pediatric huntington disease: Time to abandon the term Juvenile Huntington Disease?
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- 2019
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- Letter
Validation of a prognostic index for Huntington's disease.
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- 2017
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- journal article
Krankheitsmodifizierende Therapieansätze bei der Huntington-Krankheit: Blicke zurück und Blicke voraus.
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- Der Nervenarzt, 2022, v. 93, n. 2, p. 179, doi. 10.1007/s00115-021-01224-8
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- Article
An exploratory double-blind, randomized clinical trial with selisistat, a SirT1 inhibitor, in patients with Huntington's disease.
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- British Journal of Clinical Pharmacology, 2015, v. 79, n. 3, p. 465, doi. 10.1111/bcp.12512
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- Article
Speech biomarkers in Huntington's disease: A cross‐sectional study in pre‐symptomatic, prodromal and early manifest stages.
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- European Journal of Neurology, 2023, v. 30, n. 5, p. 1262, doi. 10.1111/ene.15726
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- Article
Magnetic resonance perfusion imaging of resting-state cerebral blood flow in preclinical Huntington's disease.
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- Journal of Cerebral Blood Flow & Metabolism, 2011, v. 31, n. 9, p. 1908, doi. 10.1038/jcbfm.2011.60
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- Article
Establishing normative data for the evaluation of cognitive performance in Huntington's disease considering the impact of gender, age, language, and education.
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- Journal of Neurology, 2023, v. 270, n. 10, p. 4903, doi. 10.1007/s00415-023-11823-x
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- Article
Quality of life, health-related quality of life, and associated factors in Huntington's disease: a systematic review.
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- Journal of Neurology, 2023, v. 270, n. 5, p. 2416, doi. 10.1007/s00415-022-11551-8
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- Article
Risk factors of suicidal ideation in Huntington’s disease: literature review and data from Enroll-HD.
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- Journal of Neurology, 2018, v. 265, n. 11, p. 2548, doi. 10.1007/s00415-018-9013-6
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- Article
Summary of cerebrospinal fluid routine parameters in neurodegenerative diseases.
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- Journal of Neurology, 2011, v. 258, n. 6, p. 1034, doi. 10.1007/s00415-010-5876-x
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- Article
Huntington's disease age at motor onset is modified by the tandem hexamer repeat in TCERG1.
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- NPJ Genomic Medicine, 2022, v. 7, n. 1, p. 1, doi. 10.1038/s41525-022-00317-w
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- Article
SCA7 mouse models show selective stabilization of mutant ataxin-7 and similar cellular responses in different neuronal cell types.
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- Human Molecular Genetics, 2001, v. 10, n. 16, p. 1679, doi. 10.1093/hmg/10.16.1679
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- Article
Expanded polyglutamines induce neurodegeneration and trans-neuronal alterations in cerebellum and retina of SCA7 transgenic mice.
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- Human Molecular Genetics, 2000, v. 9, n. 17, p. 2491, doi. 10.1093/hmg/9.17.2491
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- Article
Thalamic Atrophy in Huntington's Disease Co-varies with Cognitive Performance: A Morphometric MRI Analysis.
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- Cerebral Cortex, 2005, v. 15, n. 6, p. 846, doi. 10.1093/cercor/bhh185
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- Article
How to Arrange Follow-Up Time-Intervals for Longitudinal Brain MRI Studies in Neurodegenerative Diseases.
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- Frontiers in Neuroscience, 2021, v. 15, p. 1, doi. 10.3389/fnins.2021.682812
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- Article
Body weight is a robust predictor of clinical progression in Huntington disease.
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- 2017
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- Publication type:
- journal article
Riluzole in Huntington's disease: a 3-year, randomized controlled study.
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- Annals of Neurology, 2007, v. 62, n. 3, p. 262, doi. 10.1002/ana.21181
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- Article
Low stability of huntington muscle Mitochondria against Ca2+ in R6/2 mice.
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- Annals of Neurology, 2006, v. 59, n. 2, p. 407
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- Article
Protein surveillance machinery in brains with spinocerebellar ataxia type 3: redistribution and differential recruitment of 26S proteasome subunits and chaperones to neuronal intranuclear inclusions.
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- 2002
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- Publication type:
- journal 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.
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- BMC Neurology, 2014, v. 14, n. 1, p. 1, doi. 10.1186/1471-2377-14-1
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- Article
Impact of the control for corrupted diffusion tensor imaging data in comparisons at the group level: an application in Huntington disease.
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- 2014
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- journal article
Medication Use in Early-HD Participants in TrackHD: an Investigation of its Effects on Clinical Performance.
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- PLoS Currents, 2016, p. 280, doi. 10.1371/currents.hd.8060298fac1801b01ccea6acc00f97cb
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- Article
Current Pharmacological Management in Juvenile Huntington's Disease.
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- PLoS Currents, 2012, p. 152, doi. 10.1371/currents.RRN1304
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- Article
Utilisation of Healthcare and Associated Services in Huntington's disease: a data mining study.
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- PLoS Currents, 2011, p. 671, doi. 10.1371/currents.RRN1206
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- Article
Stability effects on results of diffusion tensor imaging analysis by reduction of the number of gradient directions due to motion artifacts: an application to presymptomatic Huntington's disease.
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- PLoS Currents, 2011, p. 596, doi. 10.1371/currents.RRN1292
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- Article
NMDA receptor gene variations as modifiers in Huntington disease: a replication study.
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- PLoS Currents, 2011, p. 454, doi. 10.1371/currents.RRN1247
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- Article
Assessment of Motor Symptoms and Functional Impact in Prodromal and Early Huntington Disease.
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- PLoS Currents, 2011, p. 200, doi. 10.1371/currents.RRN1244
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- Article
Discrepancies in reporting the CAG repeat lengths for Huntington's disease.
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- European Journal of Human Genetics, 2012, v. 20, n. 1, p. 20, doi. 10.1038/ejhg.2011.136
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- Article
High-resolution respirometry of fine-needle muscle biopsies in pre-manifest Huntington’s disease expansion mutation carriers shows normal mitochondrial respiratory function.
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- PLoS ONE, 2017, v. 12, n. 4, p. 1, doi. 10.1371/journal.pone.0175248
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- Article
Fast-to-Slow Transition of Skeletal Muscle Contractile Function and Corresponding Changes in Myosin Heavy and Light Chain Formation in the R6/2 Mouse Model of Huntington’s Disease.
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- PLoS ONE, 2016, v. 11, n. 11, p. 1, doi. 10.1371/journal.pone.0166106
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- Article
Commentary: Acanthocytes identified in Huntington's disease.
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- Frontiers in Neuroscience, 2022, v. 16, p. 1, doi. 10.3389/fnins.2022.1049676
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- Article
Riluzole prolongs survival time and alters nuclear inclusion formation in a transgenic mouse model of Huntington's disease.
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- Movement Disorders, 2002, v. 17, n. 4, p. 748, doi. 10.1002/mds.10229
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- Article
Validation Study of a German Cognitive Battery for Huntington's Disease: Relationship Between Cognitive Performance, Functional Decline, and Disease Burden.
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- Archives of Clinical Neuropsychology, 2021, v. 36, n. 1, p. 74, doi. 10.1093/arclin/acaa038
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- Article
Catatonia: looking back and moving forward.
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- 2022
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- Publication type:
- journal article
Gabapentin-lactam, but not gabapentin, reduces protein aggregates and improves motor performance in a transgenic mouse model of Huntington’s disease.
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- Naunyn-Schmiedeberg's Archives of Pharmacology, 2004, v. 370, n. 2, p. 131, doi. 10.1007/s00210-004-0959-9
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- Article
A greatly extended PPARGC1A genomic locus encodes several new brain-specific isoforms and influences Huntington disease age of onset†.
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- Human Molecular Genetics, 2012, v. 21, n. 15, p. 3461
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- Article
Corrigendum: Combining Literature Review With a Ground Truth Approach for Diagnosing Huntington's Disease Phenocopy.
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- 2022
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- Correction Notice
Combining Literature Review With a Ground Truth Approach for Diagnosing Huntington's Disease Phenocopy.
- Published in:
- Frontiers in Neurology, 2022, v. 13, p. 1, doi. 10.3389/fneur.2022.817753
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- Publication type:
- Article