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Development and resistance of a biofilm in a planar fracture during biostimulation, starvation, and varying flow conditions.
- Published in:
- Journal of Environmental Engineering & Science, 2007, v. 6, n. 4, p. 377, doi. 10.1139/S06-056
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- Publication type:
- Article
Penetrance estimate of LRRK2 p.G2019S mutation in individuals of non-Ashkenazi Jewish ancestry.
- Published in:
- 2017
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- Publication type:
- journal article
A new F-box protein 7 gene mutation causing typical Parkinson's disease.
- Published in:
- Movement Disorders, 2015, v. 30, n. 8, p. 1130, doi. 10.1002/mds.26266
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- Publication type:
- Article
Alpha-synuclein repeat variants and survival in Parkinson's disease.
- Published in:
- Movement Disorders, 2014, v. 29, n. 8, p. 1053, doi. 10.1002/mds.25841
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- Publication type:
- Article
The normal parkin sequence.
- Published in:
- Movement Disorders, 2012, v. 27, n. 3, p. 463, doi. 10.1002/mds.24050
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- Publication type:
- Article
Are parkin patients particularly suited for deep-brain stimulation?
- Published in:
- Movement Disorders, 2008, v. 23, n. 5, p. 740, doi. 10.1002/mds.21903
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- Publication type:
- Article
Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin gene.
- Published in:
- 2007
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- Publication type:
- journal article
Subthalamic nucleus stimulation is efficacious in patients with Parkinsonism and LRRK2 mutations.
- Published in:
- 2007
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- Publication type:
- journal article
Synaptojanin 1 Mutation in Parkinson's Disease Brings Further Insight into the Neuropathological Mechanisms.
- Published in:
- BioMed Research International, 2014, v. 2014, p. 1, doi. 10.1155/2014/289728
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- Publication type:
- Article
Mutation Analysis of Consanguineous Moroccan Patients with Parkinson's Disease Combining Microarray and Gene Panel.
- Published in:
- Frontiers in Neurology, 2017, p. 1, doi. 10.3389/fneur.2017.00567
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- Publication type:
- Article
Genetics of NIDDM in France.
- Published in:
- Diabetes, 1997, v. 46, n. 6, p. 1062, doi. 10.2337/diab.46.6.1062
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- Publication type:
- Article
Linkage analyses of the MODY3 locus on chromosome 12q with late-onset NIDDM.
- Published in:
- 1995
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- Publication type:
- journal article
Linkage analysis and molecular scanning of glucokinase gene in NIDDM families.
- Published in:
- 1993
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- Publication type:
- journal article
Case report of Lewy body disease mimicking Creutzfeldt-Jakob disease in a 44-year-old man.
- Published in:
- 2016
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- Publication type:
- journal article
Lack of evidence for association of UQCRC1 with autosomal dominant Parkinson's disease in Caucasian families.
- Published in:
- 2021
- By:
- Publication type:
- Letter
Segregation Analysis of Restless Legs Syndrome: Possible Evidence for a Major Gene in a Family Study Using Blinded Diagnoses.
- Published in:
- Human Heredity, 2006, v. 62, n. 3, p. 157, doi. 10.1159/000096443
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- Publication type:
- Article
Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 3, p. 615
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- Publication type:
- Article
Large-scale screening of the Gaucher's disease-related glucocerebrosidase gene in Europeans with Parkinson's disease.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 1, p. 202, doi. 10.1093/hmg/ddq454
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- Publication type:
- Article
Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 10, p. 1998
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- Publication type:
- Article
Parkinson's disease: from monogenic forms to genetic susceptibility factors.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. R1, p. R48, doi. 10.1093/hmg/ddp012
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- Publication type:
- Article
Significant linkage to spondyloarthropathy on 9q31–34.
- Published in:
- Human Molecular Genetics, 2004, v. 13, n. 15, p. 1641, doi. 10.1093/hmg/ddh179
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- Publication type:
- Article
A machine learning approach for gene prioritization in Parkinson's disease.
- Published in:
- Brain: A Journal of Neurology, 2024, v. 147, n. 3, p. 743, doi. 10.1093/brain/awae043
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- Publication type:
- Article
Association between the LRP1B and APOE loci in the development of Parkinson's disease dementia.
- Published in:
- Brain: A Journal of Neurology, 2023, v. 146, n. 5, p. 1873, doi. 10.1093/brain/awac414
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- Publication type:
- Article
Mitochondrial haplogroups and cognitive progression in Parkinson's disease.
- Published in:
- 2023
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- Publication type:
- journal article
Differences in Survival across Monogenic Forms of Parkinson's Disease.
- Published in:
- Annals of Neurology, 2023, v. 94, n. 1, p. 123, doi. 10.1002/ana.26636
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- Publication type:
- Article
Characterization of Recessive Parkinson Disease in a Large Multicenter Study.
- Published in:
- 2020
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- Publication type:
- journal article
A Novel Nonsense Mutation in DNAJC6 Expands the Phenotype of Autosomal-Recessive Juvenile-Onset Parkinson's Disease.
- Published in:
- 2016
- By:
- Publication type:
- commentary
G51D [alpha]-synuclein mutation causes a novel Parkinsonian-pyramidal syndrome.
- Published in:
- 2013
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- Publication type:
- Journal Article
G51D α-synuclein mutation causes a novel Parkinsonian-pyramidal syndrome.
- Published in:
- Annals of Neurology, 2013, v. 73, n. 4, p. 459, doi. 10.1002/ana.23894
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- Publication type:
- Article
A Multitracer Dopaminergic PET Study of Young-Onset Parkinsonian Patients With and Without Parkin Gene Mutations.
- Published in:
- Journal of Nuclear Medicine, 2009, v. 50, n. 8, p. 1244, doi. 10.2967/jnumed.109.063529
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- Publication type:
- Article
Biological effects of the PINK1 c.1366C>T mutation: implications in Parkinson disease pathogenesis.
- Published in:
- Neurogenetics, 2007, v. 8, n. 2, p. 103, doi. 10.1007/s10048-006-0072-y
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- Publication type:
- Article
Segregation of ATP10B variants in families with autosomal recessive parkinsonism.
- Published in:
- Acta Neuropathologica, 2020, v. 140, n. 5, p. 783, doi. 10.1007/s00401-020-02219-6
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- Publication type:
- Article
Detection of ATXN2 Expansions in an Exome Dataset: An Underdiagnosed Cause of Parkinsonism.
- Published in:
- Movement Disorders Clinical Practice, 2023, v. 10, n. 4, p. 664, doi. 10.1002/mdc3.13699
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- Publication type:
- Article
Genetic and Phenotypic Basis of Autosomal Dominant Parkinson's Disease in a Large Multi-Center Cohort.
- Published in:
- Frontiers in Neurology, 2020, v. 11, p. 1, doi. 10.3389/fneur.2020.00682
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- Publication type:
- Article
Exome Sequencing Reveals Signal Transduction Genes Involved in Impulse Control Disorders in Parkinson's Disease.
- Published in:
- Frontiers in Neurology, 2020, v. 11, p. 1, doi. 10.3389/fneur.2020.00641
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- Publication type:
- Article
Special Issue "Parkinson's Disease: Genetics and Pathogenesis".
- Published in:
- Genes, 2023, v. 14, n. 3, p. 737, doi. 10.3390/genes14030737
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- Publication type:
- Article
Does the Expression and Epigenetics of Genes Involved in Monogenic Forms of Parkinson's Disease Influence Sporadic Forms?
- Published in:
- Genes, 2022, v. 13, n. 3, p. 479, doi. 10.3390/genes13030479
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- Publication type:
- Article
Clustering of Crohn's disease within affected sibships.
- Published in:
- European Journal of Human Genetics, 2003, v. 11, n. 2, p. 179
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- Publication type:
- Article
Frequency of the LRRK2 G2019S Mutation in Siblings with Parkinson’s Disease.
- Published in:
- Neurodegenerative Diseases, 2007, v. 4, n. 2/3, p. 195, doi. 10.1159/000101844
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- Publication type:
- Article
De novo mutations in HCN1 cause early infantile epileptic encephalopathy.
- Published in:
- Nature Genetics, 2014, v. 46, n. 6, p. 640, doi. 10.1038/ng.2952
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- Publication type:
- Article
PARKIN Inactivation Links Parkinson's Disease to Melanoma.
- Published in:
- 2016
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- Publication type:
- journal article
From Genes to Proteins in Mendelian Parkinson's Disease: An Overview.
- Published in:
- Anatomical Record: Advances in Integrative Anatomy & Evolutionary Biology, 2009, v. 292, n. 12, p. 1893, doi. 10.1002/ar.20968
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- Publication type:
- Article
Beyond the usual suspects: approaching sleep in elderly people.
- Published in:
- 2007
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- Publication type:
- editorial
Beyond the Usual Suspects: Approaching Sleep in Elderly People.
- Published in:
- Journals of Gerontology Series A: Biological Sciences & Medical Sciences, 2007, v. 62, n. 1, p. 53, doi. 10.1093/gerona/62.1.53
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- Publication type:
- Article
PLA2G6‐associated late‐onset parkinsonism in a Sudanese family.
- Published in:
- Annals of Clinical & Translational Neurology, 2023, v. 10, n. 6, p. 983, doi. 10.1002/acn3.51781
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- Publication type:
- Article
Fine-Mapping, Gene Expression and Splicing Analysis of the Disease Associated <i>LRRK2</i> Locus.
- Published in:
- PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0070724
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- Publication type:
- Article
A Deleterious Mutation in DNAJC6 Encoding the Neuronal-Specific Clathrin-Uncoating Co-Chaperone Auxilin, Is Associated with Juvenile Parkinsonism.
- Published in:
- PLoS ONE, 2012, v. 7, n. 5, p. 1, doi. 10.1371/journal.pone.0036458
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- Publication type:
- Article
CARD15 mutations in Blau syndrome.
- Published in:
- Nature Genetics, 2001, v. 29, n. 1, p. 19, doi. 10.1038/ng720
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- Publication type:
- Article
LRRK2 G2019S Parkinson's disease with more benign phenotype than idiopathic.
- Published in:
- Acta Neurologica Scandinavica, 2018, v. 138, n. 5, p. 425, doi. 10.1111/ane.12996
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- Publication type:
- Article
Electroencephalographic hypersynchrony in a child with night terrors.
- Published in:
- Sleep & Breathing, 2013, v. 17, n. 2, p. 465, doi. 10.1007/s11325-012-0730-2
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- Publication type:
- Article