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Predicting type 2 diabetes based on polymorphisms from genome-wide association studies: a population-based study.
- Published in:
- 2008
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- Publication type:
- journal article
Neonatal infarction within basal cerebral vein territory.
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- 2001
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- Publication type:
- journal article
How idiopathic is idiopathic external hydrocephalus?
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- 1991
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- Publication type:
- journal article
The LRRK2 R1441C mutation is more frequent than G2019S in Parkinson's disease patients from Southern Italy.
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- Movement Disorders, 2011, v. 26, n. 9, p. 1732, doi. 10.1002/mds.23735
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- Article
Autosomal dominant restless legs syndrome maps to chromosome 20p13 (RLS-5) in a Dutch kindred.
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- Movement Disorders, 2010, v. 25, n. 11, p. 1715, doi. 10.1002/mds.23248
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- Article
Pseudo-orthostatic and resting leg tremor in a large spanish family with homozygous truncating parkin mutation.
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- Movement Disorders, 2009, v. 24, n. 1, p. 144, doi. 10.1002/mds.22349
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- Publication type:
- Article
A large Italian family with Gilles de la Tourette syndrome: Clinical study and analysis of the SLITRK1 gene.
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- Movement Disorders, 2007, v. 22, n. 15, p. 2229, doi. 10.1002/mds.21697
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- Article
High prevalence of LRRK2 mutations in familial and sporadic Parkinson's disease in Portugal.
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- 2007
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- Publication type:
- journal article
Spinocerebellar ataxia associated with a mutation in the fibroblast growth factor 14 gene (SCA27): A new phenotype.
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- Movement Disorders, 2006, v. 21, n. 3, p. 396, doi. 10.1002/mds.20708
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- Publication type:
- Article
Clinical features and neuroimaging of PARK7-linked parkinsonism.
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- 2003
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- Publication type:
- journal article
CYP2D6 polymorphism in Parkinson's disease: The Rotterdam study.
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- Movement Disorders, 2001, v. 16, n. 2, p. 290, doi. 10.1002/mds.1041
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- Publication type:
- Article
Novel imaging techniques to study postmortem human fetal anatomy: a systematic review on microfocus-CT and ultra-high-field MRI.
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- 2020
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- Publication type:
- journal article
Heritability of dietary food intake patterns.
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- Acta Diabetologica, 2013, v. 50, n. 5, p. 721, doi. 10.1007/s00592-012-0387-0
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- Publication type:
- Article
Ultra-high-field MRI of postmortem human fetal wrist joints: initial experience.
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- European Radiology Experimental, 2023, v. 7, n. 1, p. 1, doi. 10.1186/s41747-023-00341-0
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- Publication type:
- Article
Linkage analysis of adult height in a large pedigree from a Dutch genetically isolated population.
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- Human Genetics, 2009, v. 126, n. 3, p. 457, doi. 10.1007/s00439-009-0686-x
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- Publication type:
- Article
A new syndrome with noncompaction cardiomyopathy, bradycardia, pulmonary stenosis, atrial septal defect and heterotaxy with suggestive linkage to chromosome 6p.
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- Human Genetics, 2008, v. 122, n. 6, p. 595, doi. 10.1007/s00439-007-0436-x
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- Publication type:
- Article
Evidence for novel loci for late-onset Parkinson’s disease in a genetic isolate from the Netherlands.
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- Human Genetics, 2006, v. 119, n. 1/2, p. 51, doi. 10.1007/s00439-005-0108-7
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- Publication type:
- Article
Chasing genes in Alzheimer’s and Parkinson’s disease.
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- Human Genetics, 2004, v. 114, n. 5, p. 413, doi. 10.1007/s00439-004-1097-7
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- Publication type:
- Article
Timing of the absence of FMR1 expression in full mutation chorionic villi.
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- Human Genetics, 2002, v. 110, n. 6, p. 601, doi. 10.1007/s00439-002-0723-5
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- Article
A fragile X case with an amplification/deletion mosaic pattern.
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- Human Genetics, 2000, v. 106, n. 3, p. 366, doi. 10.1007/s004390000256
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- Publication type:
- Article
Complex multi-trait responses to multivariate environmental cues in a seasonal butterfly.
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- Evolutionary Ecology, 2020, v. 34, n. 5, p. 713, doi. 10.1007/s10682-020-10062-0
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- Publication type:
- Article
The contribution of participation in meaningful activities on mental health during the COVID-19 lockdown in the Spanish population.
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- Anales de Psicología, 2023, v. 39, n. 2, p. 176, doi. 10.6018/analesps.512291
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- Publication type:
- Article
Assessment of Aerodynamic Plates Subjected to Von Kármán Vortex Street for Enhancing the Wind Energy Generation in Blade-Less Devices.
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- Resources (2079-9276), 2023, v. 12, n. 8, p. 90, doi. 10.3390/resources12080090
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- Article
On the fate of seasonally plastic traits in a rainforest butterfly under relaxed selection.
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- Ecology & Evolution (20457758), 2014, v. 4, n. 13, p. 2654, doi. 10.1002/ece3.1114
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- Article
Association of HSP70 and its Co-Chaperones with Alzheimer's Disease.
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- Journal of Alzheimer's Disease, 2011, v. 25, n. 1, p. 93, doi. 10.3233/JAD-2011-101560
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- Publication type:
- Article
Association of HSP70 and its co-chaperones with Alzheimer's disease.
- Published in:
- 2011
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- Publication type:
- journal article
A Study of the SORL1 Gene in Alzheimer's Disease and Cognitive Function.
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- Journal of Alzheimer's Disease, 2009, v. 18, n. 1, p. 51, doi. 10.3233/JAD-2009-1137
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- Article
Does the definition of a novel environment affect the ability to detect cryptic genetic variation?
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- Journal of Evolutionary Biology, 2023, v. 36, n. 11, p. 1618, doi. 10.1111/jeb.14238
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- Publication type:
- Article
Predicting long-term neurocognitive outcome after pediatric intensive care unit admission for bronchiolitis—preliminary exploration of the potential of machine learning.
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- European Journal of Pediatrics, 2024, v. 183, n. 1, p. 471, doi. 10.1007/s00431-023-05307-3
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- Article
Complement Factor H Polymorphism, Complement Activators, and Risk of Age-Related Macular Degeneration.
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- JAMA: Journal of the American Medical Association, 2006, v. 296, n. 3, p. 301, doi. 10.1001/jama.296.3.301
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- Publication type:
- Article
Fetal echocardiography-based three-dimensional heart models: creating a web-based application as a new learning tool.
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- Cardiology in the Young, 2022, v. 32, p. S72
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- Publication type:
- Article
Fetal echocardiography-based three-dimensional heart models: creating a web-based application as a new learning tool.
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- Cardiology in the Young, 2022, v. 32, n. S2, p. S72, doi. 10.1017/S1047951122001950
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- Publication type:
- Article
The development of the human notochord.
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- PLoS ONE, 2018, v. 13, n. 10, p. 1, doi. 10.1371/journal.pone.0205752
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- Article
Unraveling the pathogenesis of Parkinson's disease -- the contribution of monogenic forms.
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- Cellular & Molecular Life Sciences, 2004, v. 61, n. 14, p. 1729
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- Article
Fragile X Mental Retardation Protein Regulates New Neuron Differentiation in the Adult Olfactory Bulb.
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- Journal of Neuroscience, 2011, v. 31, n. 6, p. 2205, doi. 10.1523/JNEUROSCI.5514-10.2011
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- Publication type:
- Article
A genome-wide search for genes involved in type 2 diabetes in a recently genetically isolated population from the Netherlands.
- Published in:
- 2003
- By:
- Publication type:
- journal article
A genome-wide search for linkage-disequilibrium with type 1 diabetes in a recent genetically isolated population from the Netherlands.
- Published in:
- 2002
- By:
- Publication type:
- journal article
A polymorphism in the gene for IGF-I: functional properties and risk for type 2 diabetes and myocardial infarction.
- Published in:
- 2001
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- Publication type:
- journal article
A Polymorphism in the Gene for IGF-I.
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- Diabetes, 2001, v. 50, n. 3, p. 637, doi. 10.2337/diabetes.50.3.637
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- Publication type:
- Article
CGG-repeat length and neuropathological and molecular correlates in a mouse model for fragile X-associated tremor/ataxia syndrome.
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- Journal of Neurochemistry, 2008, v. 107, n. 6, p. 1671, doi. 10.1111/j.1471-4159.2008.05747.x
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- Publication type:
- Article
Menopause impacts the relation of plasma adiponectin levels with the metabolic syndrome.
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- Journal of Internal Medicine, 2010, v. 267, n. 4, p. 402, doi. 10.1111/j.1365-2796.2009.02162.x
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- Publication type:
- Article
Broadening the phenotype of TARDBP mutations: the TARDBP Ala382Thr mutation and Parkinson's disease in Sardinia.
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- Neurogenetics, 2011, v. 12, n. 3, p. 203, doi. 10.1007/s10048-011-0288-3
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- Publication type:
- Article
Novel ATP13A2 ( PARK9) homozygous mutation in a family with marked phenotype variability.
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- Neurogenetics, 2011, v. 12, n. 1, p. 33, doi. 10.1007/s10048-010-0259-0
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- Publication type:
- Article
Tourette disorder spectrum maps to chromosome 14q31.1 in an Italian kindred.
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- Neurogenetics, 2010, v. 11, n. 4, p. 417, doi. 10.1007/s10048-010-0244-7
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- Publication type:
- Article
A novel 16p locus associated with BSCL2 hereditary motor neuronopathy: a genetic modifier?
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- Neurogenetics, 2009, v. 10, n. 4, p. 289, doi. 10.1007/s10048-009-0193-1
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- Publication type:
- Article
The LRRK2 Arg1628Pro variant is a risk factor for Parkinson’s disease in the Chinese population.
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- Neurogenetics, 2008, v. 9, n. 4, p. 271, doi. 10.1007/s10048-008-0140-6
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- Publication type:
- Article
The cholesteryl ester transfer protein (CETP) gene and the risk of Alzheimer’s disease.
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- Neurogenetics, 2007, v. 8, n. 3, p. 189, doi. 10.1007/s10048-007-0089-x
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- Publication type:
- Article
A three‐dimensional analysis of the development of cranial nerves in human embryos.
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- Clinical Anatomy, 2022, v. 35, n. 5, p. 666, doi. 10.1002/ca.23889
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- Publication type:
- Article
The triangular fibrocartilage complex in the human wrist: A scoping review toward uniform and clinically relevant terminology.
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- Clinical Anatomy, 2022, v. 35, n. 5, p. 626, doi. 10.1002/ca.23880
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- Publication type:
- Article
Characterizing the coalescence area of conjoined twins to elucidate congenital disorders in singletons.
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- Clinical Anatomy, 2021, v. 34, n. 6, p. 845, doi. 10.1002/ca.23725
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- Publication type:
- Article