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Case-Control study of the extended tau gene haplotype in Parkinson's disease.
- Published in:
- 2001
- By:
- Publication type:
- journal article
Assessment of oesophageal position by direct visualization with luminal contrast compared with segmentation from pre-acquired computed tomography scan-implications for ablation strategy.
- Published in:
- 2014
- By:
- Publication type:
- journal article
Assessment of oesophageal position by direct visualization with luminal contrast compared with segmentation from pre-acquired computed tomography scan—implications for ablation strategy.
- Published in:
- EP: Europace, 2014, v. 16, n. 9, p. 1304, doi. 10.1093/europace/euu062
- By:
- Publication type:
- Article
The Gordon Research Seminar & Conference on Parkinson's disease: state of the Science 200 years after James Parkinson's essay on the Shaking Palsy.
- Published in:
- NPJ Parkinson's Disease, 2017, v. 3, n. 1, p. N.PAG, doi. 10.1038/s41531-017-0028-y
- By:
- Publication type:
- Article
Change in Epigenome-Wide DNA Methylation Over 9 Years and Subsequent Mortality: Results From the InCHIANTI Study.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Corrigendum to: 'Mini-Max' knotless acetabular labrum repair: repair construct rationale and allocation in a consecutive case series with minimum 1-year clinical outcomes.
- Published in:
- 2022
- By:
- Publication type:
- Correction Notice
'Mini-Max' knotless acetabular labrum repair: repair construct rationale and allocation in a consecutive case series with minimum 1-year clinical outcomes.
- Published in:
- Journal of Hip Preservation Surgery, 2021, v. 8, n. 3, p. 261, doi. 10.1093/jhps/hnab061
- By:
- Publication type:
- Article
Analysis of repeated leukocyte DNA methylation assessments reveals persistent epigenetic alterations after an incident myocardial infarction.
- Published in:
- Clinical Epigenetics, 2018, v. 10, n. 1, p. N.PAG, doi. 10.1186/s13148-018-0588-7
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- Publication type:
- Article
Meniscus Suture Repair.
- Published in:
- American Journal of Sports Medicine, 2015, v. 43, n. 9, p. 2222, doi. 10.1177/0363546515591260
- By:
- Publication type:
- Article
Homozygosity mapping reveals founder SEC23B- Y462C mutations in Indian congenital dyserythropoietic anemia type II.
- Published in:
- Clinical Genetics, 2015, v. 88, n. 2, p. 195, doi. 10.1111/cge.12527
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- Publication type:
- Article
Exome sequencing in Parkinson's disease.
- Published in:
- Clinical Genetics, 2011, v. 80, n. 2, p. 104, doi. 10.1111/j.1399-0004.2011.01722.x
- By:
- Publication type:
- Article
Mutations in EIF4G1 are not a common cause of Parkinson's disease.
- Published in:
- European Journal of Neurology, 2013, v. 20, n. 4, p. e59, doi. 10.1111/ene.12051
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- Publication type:
- Article
Exome sequencing: an efficient diagnostic tool for complex neurodegenerative disorders.
- Published in:
- European Journal of Neurology, 2013, v. 20, n. 3, p. 486, doi. 10.1111/j.1468-1331.2012.03883.x
- By:
- Publication type:
- Article
Screening for LRRK2 mutations in patients with Parkinson’s disease in Russia: identification of a novel LRRK2 variant.
- Published in:
- European Journal of Neurology, 2008, v. 15, n. 7, p. 692, doi. 10.1111/j.1468-1331.2008.02149.x
- By:
- Publication type:
- Article
Screening for SNCA and LRRK2 mutations in Greek sporadic and autosomal dominant Parkinson's disease: identification of two novel LRRK2 variants.
- Published in:
- European Journal of Neurology, 2007, v. 14, n. 1, p. 7, doi. 10.1111/j.1468-1331.2006.01551.x
- By:
- Publication type:
- Article
Answer to last month's radiology case and image: emergency decompressive craniotomy with banked skull flap in subcutaneous pocket.
- Published in:
- 2006
- By:
- Publication type:
- journal article
Genome-wide contribution of common short-tandem repeats to Parkinson's disease genetic risk.
- Published in:
- 2023
- By:
- Publication type:
- journal article
Heterozygous PRKN mutations are common but do not increase the risk of Parkinson's disease.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Clinical, pathological and functional characterization of riboflavin-responsive neuropathy.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Assessing the lack of diversity in genetics research across neurodegenerative diseases: A systematic review of the GWAS Catalog and literature.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, n. 8, p. 5740, doi. 10.1002/alz.13873
- By:
- Publication type:
- Article
A cross‐sectional study of α‐synuclein seed amplification assay in Alzheimer's disease neuroimaging initiative: Prevalence and associations with Alzheimer's disease biomarkers and cognitive function.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, n. 8, p. 5114, doi. 10.1002/alz.13858
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- Publication type:
- Article
Numbering fingers.
- Published in:
- Canadian Medical Association Journal, 1983, v. 128, n. 4, p. 372
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- Publication type:
- Article
Genetic risk factors in Parkinson’s disease.
- Published in:
- Cell & Tissue Research, 2018, v. 373, n. 1, p. 9, doi. 10.1007/s00441-018-2817-y
- By:
- Publication type:
- Article
FTO genotype and aging: pleiotropic longitudinal effects on adiposity, brain function, impulsivity and diet.
- Published in:
- Molecular Psychiatry, 2015, v. 20, n. 1, p. 140, doi. 10.1038/mp.2014.49
- By:
- Publication type:
- Article
Inhibition of HERG potassium channels by the antimalarial agent halofantrine.
- Published in:
- British Journal of Pharmacology, 2000, v. 130, n. 8, p. 1967, doi. 10.1038/sj.bjp.0703470
- By:
- Publication type:
- Article
Inhibition of the human ether-a-go-go-related gene (HERG) potassium channel by cisapride: affinity for open and inactivated states.
- Published in:
- 1999
- By:
- Publication type:
- journal article
Blockade by N-3 polyunsaturated fatty acid of the Kv4.3 current stably expressed in Chinese hamster ovary cells.
- Published in:
- British Journal of Pharmacology, 1999, v. 127, n. 4, p. 941, doi. 10.1038/sj.bjp.0702638
- By:
- Publication type:
- Article
Inhibition of HERG channels stably expressed in a mammalian cell line by the antianginal agent perhexiline maleate.
- Published in:
- British Journal of Pharmacology, 1999, v. 127, n. 1, p. 243, doi. 10.1038/sj.bjp.0702502
- By:
- Publication type:
- Article
Resolving the polymorphism-in-probe problem is critical for correct interpretation of expression QTL studies.
- Published in:
- Nucleic Acids Research, 2013, v. 41, n. 7, p. e88, doi. 10.1093/nar/gkt069
- By:
- Publication type:
- Article
Clinical and genetic analyses of familial and sporadic frontotemporal dementia patients in Southern Italy.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, n. 8, p. 858, doi. 10.1016/j.jalz.2017.01.011
- By:
- Publication type:
- Article
A candidate gene study of genetic risk for dementia and mild cognitive impairment (MCI) in women aged >65 years: Results from the women's health initiative memory study (WHIMS).
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2014, v. 10, p. P787, doi. 10.1016/j.jalz.2014.05.1525
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- Publication type:
- Article
Erratum: Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11.
- Published in:
- 2008
- By:
- Publication type:
- Correction Notice
Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11.
- Published in:
- Nature Genetics, 2007, v. 39, n. 12, p. 1434, doi. 10.1038/ng.2007.43
- By:
- Publication type:
- Article
Comparing Spatial Maps of Human Population-Genetic Variation Using Procrustes Analysis.
- Published in:
- Statistical Applications in Genetics & Molecular Biology, 2010, v. 9, n. 1, p. 1, doi. 10.2202/1544-6115.1493
- By:
- Publication type:
- Article
Intra-operative neurophysiological mapping to identify distorted functional anatomy of the 4th ventricle in a 5-month-old infant.
- Published in:
- 2022
- By:
- Publication type:
- Case Study
Imputation of Variants from the 1000 Genomes Project Modestly Improves Known Associations and Can Identify Low-frequency Variant - Phenotype Associations Undetected by HapMap Based Imputation
- Published in:
- PLoS ONE, 2013, v. 8, n. 5, p. 1, doi. 10.1371/journal.pone.0064343
- By:
- Publication type:
- Article
Genome Wide Assessment of Young Onset Parkinson's Disease from Finland.
- Published in:
- 2012
- By:
- Publication type:
- Case Study
Cooperative Genome-Wide Analysis Shows Increased Homozygosity in Early Onset Parkinson's Disease.
- Published in:
- PLoS ONE, 2012, v. 7, n. 3, p. 1, doi. 10.1371/journal.pone.0028787
- By:
- Publication type:
- Article
Genotype-phenotype correlations and expansion of the molecular spectrum of AP4M1-related hereditary spastic paraplegia.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Effect of cell-seeded hydroxyapatite scaffolds on rabbit radius bone regeneration.
- Published in:
- Journal of Biomedical Materials Research, Part A, 2014, v. 102, n. 5, p. 1458, doi. 10.1002/jbm.a.34834
- By:
- Publication type:
- Article
SLC25A46 Mutations Associated with Autosomal Recessive Cerebellar Ataxia in North African Families.
- Published in:
- Neurodegenerative Diseases, 2017, v. 17, n. 4/5, p. 208, doi. 10.1159/000464445
- By:
- Publication type:
- Article
Using DNA Methylation to Understand Biological Consequences of Genetic Variability.
- Published in:
- Neurodegenerative Diseases, 2012, v. 9, n. 2, p. 53, doi. 10.1159/000333097
- By:
- Publication type:
- Article
Comprehensive Screening of a North American Parkinson’s Disease Cohort for LRRK2 Mutation.
- Published in:
- Neurodegenerative Diseases, 2007, v. 4, n. 5, p. 386, doi. 10.1159/000105160
- By:
- Publication type:
- Article
Association of Tau Haplotype-Tagging Polymorphisms with Parkinson’s Disease in Diverse Ethnic Parkinson’s Disease Cohorts.
- Published in:
- Neurodegenerative Diseases, 2006, v. 3, n. 6, p. 327, doi. 10.1159/000097301
- By:
- Publication type:
- Article
A common genetic factor for Parkinson disease in ethnic Chinese population in Taiwan.
- Published in:
- BMC Neurology, 2006, v. 6, p. 47, doi. 10.1186/1471-2377-6-47
- By:
- Publication type:
- Article
Lack of evidence for a genetic association between FGF20 and Parkinson's disease in Finnish and Greek patients.
- Published in:
- BMC Neurology, 2005, v. 5, p. 1, doi. 10.1186/1471-2377-5-11
- By:
- Publication type:
- Article
Catheter ablation for ventricular tachycardia Lim et al. Ventricular tachycardia ablation.
- Published in:
- Internal Medicine Journal, 2010, v. 40, n. 10, p. 673, doi. 10.1111/j.1445-5994.2010.02202.x
- By:
- Publication type:
- Article
Left Ventricular Outflow Tract Ventricular Tachycardia Originating from the Noncoronary Cusp: Electrocardiographic and Electrophysiological Characterization and Radiofrequency Ablation.
- Published in:
- Journal of Cardiovascular Electrophysiology, 2009, v. 20, n. 11, p. 1287, doi. 10.1111/j.1540-8167.2009.01471.x
- By:
- Publication type:
- Article
Clinical and Neuropathological Correlates of Apolipoprotein E Genotype in Dementia with Lewy Bodies.
- Published in:
- Dementia & Geriatric Cognitive Disorders, 2002, v. 14, n. 4, p. 167, doi. 10.1159/000066022
- By:
- Publication type:
- Article
Childhood Brain Tumors: A Review of Strategies to Translate CNS Drug Delivery to Clinical Trials.
- Published in:
- Cancers, 2023, v. 15, n. 3, p. 857, doi. 10.3390/cancers15030857
- By:
- Publication type:
- Article