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Neonatal infarction within basal cerebral vein territory.
- Published in:
- 2001
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- Publication type:
- journal article
How idiopathic is idiopathic external hydrocephalus?
- Published in:
- 1991
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- Publication type:
- journal article
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
Understanding fragile X syndrome: insights from animal models.
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- Cytogenetic & Genome Research, 2003, v. 100, n. 1-4, p. 111, doi. 10.1159/000072845
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- Publication type:
- Article
The X chromosome and fragile X mental retardation.
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- Cytogenetic & Genome Research, 2002, v. 99, n. 1-4, p. 257, doi. 10.1159/000071602
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- Publication type:
- Article
Oxygen-dependence of chromosomal aberrations in Fanconi's anaemia.
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- Nature, 1981, v. 290, n. 5802, p. 142, doi. 10.1038/290142a0
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- Publication type:
- Article
Heritabilities, proportions of heritabilities explained by GWAS findings, and implications of cross-phenotype effects on PR interval.
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- Human Genetics, 2015, v. 134, n. 11/12, p. 1211, doi. 10.1007/s00439-015-1595-9
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- Publication type:
- Article
Common DNA variants predict tall stature in Europeans.
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- Human Genetics, 2014, v. 133, n. 5, p. 587, doi. 10.1007/s00439-013-1394-0
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- Publication type:
- Article
Linkage analysis for plasma amyloid beta levels in persons with hypertension implicates Aβ-40 levels to presenilin 2.
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- Human Genetics, 2012, v. 131, n. 12, p. 1869, doi. 10.1007/s00439-012-1210-2
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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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- Publication type:
- 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
Adolescents' perceptions of communication with parents relative to specific aspects of...
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- Journal of Adolescence, 1998, v. 21, n. 3, p. 305, doi. 10.1006/jado.1998.0155
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- Publication type:
- Article
Cross-cultural adaptation and psychometric properties of the engagement in meaningful activities survey.
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- British Journal of Occupational Therapy, 2023, v. 86, n. 11, p. 755, doi. 10.1177/03080226231187827
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- Publication type:
- Article
25‐1: Invited Paper: Technical Roadmap to Realize Reflective Full‐Color Video Displays for Street Furniture.
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- SID Symposium Digest of Technical Papers, 2024, v. 55, n. 1, p. 310, doi. 10.1002/sdtp.17517
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- Publication type:
- Article
46‐4: Invited Paper: Digital Out Of Home Displays That Run Forever On Solar Energy.
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- SID Symposium Digest of Technical Papers, 2023, v. 54, n. 1, p. 673, doi. 10.1002/sdtp.16648
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- Publication type:
- Article
The underpinning of meaningful activities by brain correlates: a systematic review .
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- Frontiers in Psychology, 2023, p. 1, doi. 10.3389/fpsyg.2023.1136754
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- Publication type:
- Article
Genetic Variation in Candidate Genes Like the HMGA2 Gene in the Extremely Tall.
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- Hormone Research in Paediatrics, 2011, v. 76, n. 5, p. 307, doi. 10.1159/000330764
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- Publication type:
- Article
Human tissue-engineered bone produced in clinically relevant amounts using a semi-automated perfusion bioreactor system: a preliminary study.
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- Journal of Tissue Engineering & Regenerative Medicine, 2010, v. 4, n. 1, p. 12, doi. 10.1002/term.197
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- Publication type:
- Article
Survival in Elderly Persons with Down Syndrome.
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- Journal of the American Geriatrics Society, 2008, v. 56, n. 12, p. 2311, doi. 10.1111/j.1532-5415.2008.01999.x
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- Publication type:
- Article
A Reduced Number of Metabotropic Glutamate Subtype 5 Receptors Are Associated with Constitutive Homer Proteins in a Mouse Model of Fragile X Syndrome.
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- Journal of Neuroscience, 2005, v. 25, n. 39, p. 8908, doi. 10.1523/JNEUROSCI.0932-05.2005
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- Publication type:
- Article
Homozygous PINK1 C-terminus mutation causing early-onset parkinsonism.
- Published in:
- 2004
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- Publication type:
- Journal Article
Homozygous PINK1 C‐terminus mutation causing early‐onset parkinsonism.
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- Annals of Neurology, 2004, v. 56, n. 3, p. 427
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- Publication type:
- Article
Localization of autosomal recessive early-onset parkinsonism to chromosome 1p36 (PARK7) in an independent dataset.
- Published in:
- 2002
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- Publication type:
- journal article
PARK6-linked parkinsonism occurs in several European families.
- Published in:
- 2002
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- Publication type:
- journal article
Hereditary frontotemporal dementia is linked to chromosome 17q21-q22: A genetic and clinicopathological study of three dutch families.
- Published in:
- Annals of Neurology, 1997, v. 41, n. 2, p. 150, doi. 10.1002/ana.410410205
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- Publication type:
- Article
Linking DJ-1 to neurodegeneration offers novel insights for understanding the pathogenesis of Parkinson’s disease.
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- Journal of Molecular Medicine, 2004, v. 82, n. 3, p. 163, doi. 10.1007/s00109-003-0512-1
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- Publication type:
- Article
Cross-Cultural Adaptation and Psychometric Evaluation of the Dutch Version of the Work Rehabilitation Questionnaire (WORQ-VL).
- Published in:
- Journal of Occupational Rehabilitation, 2019, v. 29, n. 3, p. 514, doi. 10.1007/s10926-018-9812-8
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- Publication type:
- Article
Ultra-wide field imaging to assess the optic nerve and retina in Boston type I and II keratoprosthesis patients.
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- Eye & Vision, 2022, v. 9, n. 1, p. 1, doi. 10.1186/s40662-022-00289-z
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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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- Publication type:
- Article
Predictability of cerebral palsy and its characteristics through neonatal cranial ultrasound in a high-risk NICU population.
- Published in:
- 2010
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- Publication type:
- journal article
Influence of gestational age on nosologic CP characteristics in a high-risk population.
- Published in:
- 2010
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- Publication type:
- journal article
Influence of gestational age on the type of brain injury and neuromotor outcome in high-risk neonates.
- Published in:
- 2008
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- Publication type:
- journal article
Warsaw Breakage Syndrome associated DDX11 helicase resolves G-quadruplex structures to support sister chromatid cohesion.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. N.PAG, doi. 10.1038/s41467-020-18066-8
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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
CGG repeat in the FMR1 gene: size matters.
- Published in:
- Clinical Genetics, 2011, v. 80, n. 3, p. 214, doi. 10.1111/j.1399-0004.2011.01723.x
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- Publication type:
- Article
Exceptional good cognitive and phenotypic profile in a male carrying a mosaic mutation in the FMR1 gene.
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- Clinical Genetics, 2007, v. 72, n. 2, p. 138, doi. 10.1111/j.1399-0004.2007.00829.x
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- Publication type:
- Article
Studying the genetics of Hirschsprung's disease: unraveling an oligogenic disorder.
- Published in:
- Clinical Genetics, 2005, v. 67, n. 1, p. 6, doi. 10.1111/j.1399-0004.2004.00319.x
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- Publication type:
- Article
The fragile X gene and its function.
- Published in:
- Clinical Genetics, 2001, v. 60, n. 6, p. 399, doi. 10.1034/j.1399-0004.2001.600601.x
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- Publication type:
- Article
On the many faces of Leber hereditary optic neuropathy.
- Published in:
- Clinical Genetics, 1997, v. 51, n. 6, p. 388, doi. 10.1111/j.1399-0004.1997.tb02496.x
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- Publication type:
- 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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- Publication type:
- Article
Familial clustering and genetic risk for dementia in a genetically isolated Dutch population.
- Published in:
- Brain: A Journal of Neurology, 2004, v. 127, n. 7, p. 1641, doi. 10.1093/brain/awh179
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- Publication type:
- Article
FAAP100 is essential for activation of the Fanconi anemia-associated DNA damage response pathway.
- Published in:
- EMBO Journal, 2007, v. 26, n. 8, p. 2104, doi. 10.1038/sj.emboj.7601666
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- Publication type:
- Article
Loss of FMR1 hypermethylation in somatic cell heterokaryons.
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- FASEB Journal, 2004, v. 18, n. 15, p. 1964, doi. 10.1096/fj.04-2499fje
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- Publication type:
- Article
Lack of association of two common polymorphisms on 9p21 with risk of coronary heart disease and myocardial infarction; results from a prospective cohort study.
- Published in:
- 2008
- By:
- Publication type:
- Journal Article
Regulatory and sequence evolution in response to selection for improved associative learning ability in Nasonia vitripennis.
- Published in:
- BMC Genomics, 2018, v. 19, n. 1, p. 1, doi. 10.1186/s12864-018-5310-9
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- Publication type:
- Article