Works by Kuhlenbäumer, Gregor
Results: 52
Determinants of Platelet-Leukocyte Aggregation and Platelet Activation in Stroke.
- Published in:
- Cerebrovascular Diseases, 2015, v. 39, n. 3/4, p. 176, doi. 10.1159/000375396
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- Publication type:
- Article
Febrile infection-related epilepsy syndrome (FIRES) is not caused by SCN1A, POLG, PCDH19 mutations or rare copy number variations.
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- Developmental Medicine & Child Neurology, 2012, v. 54, n. 12, p. 1144, doi. 10.1111/j.1469-8749.2012.04435.x
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- Article
No association between polymorphisms in the glutamate transporter SLC1A2 and Parkinson's disease.
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- Movement Disorders, 2013, v. 28, n. 9, p. 1305, doi. 10.1002/mds.25330
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- Publication type:
- Article
The role of SCARB2 as susceptibility factor in Parkinson's disease.
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- Movement Disorders, 2013, v. 28, n. 4, p. 538, doi. 10.1002/mds.25349
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- Publication type:
- Article
No association between NOD2 variants and Parkinson's disease.
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- Movement Disorders, 2012, v. 27, n. 9, p. 1191, doi. 10.1002/mds.25059
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- Publication type:
- Article
No evidence for differential methylation of α-synuclein in leukocyte DNA of Parkinson's disease patients.
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- Movement Disorders, 2012, v. 27, n. 4, p. 590, doi. 10.1002/mds.24907
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- Publication type:
- Article
LINGO1 polymorphisms are associated with essential tremor in Europeans.
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- Movement Disorders, 2010, v. 25, n. 6, p. 717, doi. 10.1002/mds.22887
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- Article
Painless legs and moving toes in a mother and her daughter.
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- Movement Disorders, 2003, v. 18, n. 6, p. 718, doi. 10.1002/mds.10435
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- Publication type:
- Article
Chlamydia pneumoniae infection and Alzheimer's disease: a connection to remember?
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- Medical Microbiology & Immunology, 2010, v. 199, n. 4, p. 283, doi. 10.1007/s00430-010-0162-1
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- Publication type:
- Article
MRI Features of Pontine Autosomal Dominant Microangiopathy and Leukoencephalopathy (PADMAL).
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- Journal of Neuroimaging, 2010, v. 20, n. 2, p. 134, doi. 10.1111/j.1552-6569.2008.00336.x
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- Publication type:
- Article
Novel septin 9 repeat motifs altered in neuralgic amyotrophy bind and bundle microtubules.
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- Journal of Cell Biology, 2013, v. 203, n. 6, p. 895, doi. 10.1083/jcb.201308068
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- Article
Novel genomic techniques open new avenues in the analysis of monogenic disorders.
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- Human Mutation, 2011, v. 32, n. 2, p. 144, doi. 10.1002/humu.21400
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- Article
Cerebrospinal Fluid Biomarkers in Cerebral Amyloid Angiopathy: New Data and Quantitative Meta-Analysis.
- Published in:
- Frontiers in Aging Neuroscience, 2022, v. 14, p. 1, doi. 10.3389/fnagi.2022.783996
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- Publication type:
- Article
Two-Stage Convolutional Neural Network for Classification of Movement Patterns in Tremor Patients.
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- Information (2078-2489), 2024, v. 15, n. 4, p. 231, doi. 10.3390/info15040231
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- Article
Validity and Prognostic Value of a Polygenic Risk Score for Parkinson's Disease.
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- Genes, 2021, v. 12, n. 12, p. 1859, doi. 10.3390/genes12121859
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- Publication type:
- Article
HLA and KIR genetic association and NK cells in anti-NMDAR encephalitis.
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- Frontiers in Immunology, 2024, p. 1, doi. 10.3389/fimmu.2024.1423149
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- Publication type:
- Article
Hereditary amyloidosis of the Finnish type in a German family: Clinical and electrophysiological presentation.
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- Muscle & Nerve, 2010, v. 41, n. 5, p. 679, doi. 10.1002/mus.21534
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- Article
Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke.
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- Annals of Neurology, 2008, v. 64, n. 4, p. 402, doi. 10.1002/ana.21480
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- Article
Aberrations of dermal connective tissue in patients with cervical artery dissection (sCAD).
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- Journal of Neurology, 2008, v. 255, n. 3, p. 340, doi. 10.1007/s00415-008-0585-4
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- Publication type:
- Article
Plasma homocysteine, MTHFR C677T, CBS 844ins68bp, and MTHFD1 G1958A polymorphisms in spontaneous cervical artery dissections.
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- Journal of Neurology, 2004, v. 251, n. 10, p. 1242, doi. 10.1007/s00415-004-0523-z
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- Publication type:
- Article
Neither collagen 8A1 nor 8A2 mutations play a major role in cervical artery dissection: A mutation analysis and linkage study.
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- Journal of Neurology, 2004, v. 251, n. 3, p. 357, doi. 10.1007/s00415-004-0335-1
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- Publication type:
- Article
Cervical artery dissection--clinical features, risk factors, therapy and outcome in 126 patients.
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- Journal of Neurology, 2003, v. 250, n. 10, p. 1179, doi. 10.1007/s00415-003-0174-5
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- Publication type:
- Article
Clinical features and molecular genetics of hereditary peripheral neuropathies.
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- Journal of Neurology, 2002, v. 249, n. 12, p. 1629, doi. 10.1007/s00415-002-0946-3
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- Publication type:
- Article
Hereditary Neuralgic Amyotrophy (HNA) is genetically heterogeneous.
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- Journal of Neurology, 2001, v. 248, n. 10, p. 861
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- Publication type:
- Article
Family and literature analysis demonstrates phenotypic effect of two variants in the calpain-3 gene.
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- Neurogenetics, 2023, v. 24, n. 4, p. 273, doi. 10.1007/s10048-023-00728-6
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- Publication type:
- Article
Evidence for pathogenicity of variant ATM Val1729Leu in a family with ataxia telangiectasia.
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- Neurogenetics, 2021, v. 22, n. 2, p. 143, doi. 10.1007/s10048-021-00639-4
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- Publication type:
- Article
Archimedes Spiral Ratings: Determinants and Population‐Based Limits of Normal.
- Published in:
- Movement Disorders Clinical Practice, 2024, v. 11, n. 10, p. 1257, doi. 10.1002/mdc3.14201
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- Publication type:
- Article
Genetic TPH2 variants and the susceptibility for migraine: association of a TPH2 haplotype with migraine without aura.
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- Journal of Neural Transmission, 2010, v. 117, n. 11, p. 1253, doi. 10.1007/s00702-010-0468-6
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- Publication type:
- Article
Functional gene variants of the serotonin-synthesizing enzyme tryptophan hydroxylase 2 in migraine.
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- Journal of Neural Transmission, 2009, v. 116, n. 7, p. 815, doi. 10.1007/s00702-009-0236-7
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- Publication type:
- Article
Association of the functional V158M catechol-O-methyl-transferase polymorphism with panic disorder in women.
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- International Journal of Neuropsychopharmacology, 2004, v. 7, n. 2, p. 183, doi. 10.1017/s146114570400416x
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- Publication type:
- Article
Real-time classification of movement patterns of tremor patients.
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- Biomedical Engineering / Biomedizinische Technik, 2022, v. 67, n. 2, p. 119, doi. 10.1515/bmt-2021-0140
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- Article
Characterizing mixed location hemorrhages/microbleeds with CSF markers.
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- International Journal of Stroke, 2023, v. 18, n. 6, p. 728, doi. 10.1177/17474930231152124
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- Publication type:
- Article
Decreased Cerebrospinal Fluid Amyloid Beta 38, 40, 42, and 43 Levels in Sporadic and Hereditary Cerebral Amyloid Angiopathy.
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- Annals of Neurology, 2023, v. 94, n. 1, p. 205, doi. 10.1002/ana.26671
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- Publication type:
- Article
Long-Lived Individuals Show a Lower Burden of Variants Predisposing to Age-Related Diseases and a Higher Polygenic Longevity Score.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 18, p. N.PAG, doi. 10.3390/ijms231810949
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- Article
Electroencephalography based delirium screening in acute supratentorial stroke.
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- BMC Neurology, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12883-024-03942-3
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- Publication type:
- Article
K-variant BCHE and pesticide exposure: Gene-environment interactions in a case–control study of Parkinson’s disease in Egypt.
- Published in:
- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-35003-4
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- Article
Genetic refinement of the hereditary neuralgic amyotrophy (HNA) locus at chromosome 17q25.
- Published in:
- European Journal of Human Genetics, 1999, v. 7, n. 8, p. 920, doi. 10.1038/sj.ejhg.5200384
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- Publication type:
- Article
Mutations in SEPT9 cause hereditary neuralgic amyotrophy.
- Published in:
- Nature Genetics, 2005, v. 37, n. 10, p. 1044, doi. 10.1038/ng1649
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- Article
Candidate variants in TUB are associated with familial tremor.
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- PLoS Genetics, 2020, v. 16, n. 9, p. 1, doi. 10.1371/journal.pgen.1009010
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- Publication type:
- Article
Pontine autosomal dominant microangiopathy with leukoencephalopathy: Col4A1 gene variants in the original family and sporadic stroke.
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- Journal of Neurology, 2023, v. 270, n. 5, p. 2631, doi. 10.1007/s00415-023-11590-9
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- Article
Clinical and radiological differences between patients with probable cerebral amyloid angiopathy and mixed cerebral microbleeds.
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- Journal of Neurology, 2020, v. 267, n. 12, p. 3602, doi. 10.1007/s00415-020-10038-8
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- Publication type:
- Article
Autosomal dominant epilepsy with auditory features: a new LGI1 family including a phenocopy with cortical dysplasia.
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- Journal of Neurology, 2016, v. 263, n. 1, p. 11, doi. 10.1007/s00415-015-7921-2
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- Publication type:
- Article
Arterial elongation ('redundancy') is not a feature of spontaneous cervical artery dissection.
- Published in:
- Journal of Neurology, 2011, v. 258, n. 2, p. 250, doi. 10.1007/s00415-010-5737-7
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- Publication type:
- Article
Validation of the QUEST for German-speaking countries.
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- International Journal of Neuroscience, 2016, v. 126, n. 2, p. 127, doi. 10.3109/00207454.2015.1077241
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- Article
Large‐Scale Screening: Phenotypic and Mutational Spectrum in Isolated and Combined Dystonia Genes.
- Published in:
- Movement Disorders, 2024, v. 39, n. 3, p. 526, doi. 10.1002/mds.29693
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- Publication type:
- Article
Early- and late-onset essential tremor patients represent clinically distinct subgroups.
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- 2016
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- Publication type:
- journal article
Alpha synuclein and crystallin expression in human lens in Parkinson's disease.
- Published in:
- 2016
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- Publication type:
- journal article
Mutations in HTRA2 are not a common cause of familial classic ET.
- Published in:
- Movement Disorders, 2015, v. 30, n. 8, p. 1149, doi. 10.1002/mds.26252
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- Publication type:
- Article
The impact of rare variants in FUS in essential tremor.
- Published in:
- Movement Disorders, 2015, v. 30, n. 5, p. 721, doi. 10.1002/mds.26145
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- Publication type:
- Article
Aβ38 and Aβ43 do not differentiate between Alzheimer's disease and cerebral amyloid angiopathy.
- Published in:
- Annals of Clinical & Translational Neurology, 2024, v. 11, n. 3, p. 806, doi. 10.1002/acn3.51987
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- Publication type:
- Article