Found: 15
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Candidate gene analysis of semaphorins in patients with Alzheimer's disease.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Phenotypic Heterogeneity of the GRN Asp22fs Mutation in a Large Italian Kindred.
- Published in:
- 2011
- By:
- Publication type:
- Journal Article
Cerebrospinal fluid biomarkers in progranulin mutations carriers.
- Published in:
- 2011
- By:
- Publication type:
- Journal Article
Role of OLR1 and Its Regulating hsa-miR369-3p in Alzheimer's Disease: Genetics and Expression Analysis.
- Published in:
- 2011
- By:
- Publication type:
- Journal Article
A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia.
- Published in:
- 2011
- By:
- Publication type:
- journal article
BAG1 is a Protective Factor for Sporadic Frontotemporal Lobar Degeneration but not for Alzheimer's Disease.
- Published in:
- 2011
- By:
- Publication type:
- Journal Article
DCUN1D1 is a risk factor for frontotemporal lobar degeneration.
- Published in:
- European Journal of Neurology, 2009, v. 16, n. 7, p. 870, doi. 10.1111/j.1468-1331.2009.02611.x
- By:
- Publication type:
- Article
The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degeneration.
- Published in:
- European Journal of Neurology, 2009, v. 16, n. 1, p. 37, doi. 10.1111/j.1468-1331.2008.02335.x
- By:
- Publication type:
- Article
Novel exon 1 progranulin gene variant in Alzheimer’s disease.
- Published in:
- European Journal of Neurology, 2008, v. 15, n. 10, p. 1111, doi. 10.1111/j.1468-1331.2008.02266.x
- By:
- Publication type:
- Article
Neuronal nitric oxide synthase C276T polymorphism increases the risk for frontotemporal lobar degeneration.
- Published in:
- European Journal of Neurology, 2008, v. 15, n. 1, p. 77, doi. 10.1111/j.1468-1331.2007.02007.x
- By:
- Publication type:
- Article
P-699 - Selective DNA methylation of BDNF promoter in bipolar disorder: differences among patients vs controls and potential influence of pharmacological treatments
- Published in:
- 2012
- By:
- Publication type:
- Abstract
Repetitive element hypermethylation in multiple sclerosis patients.
- Published in:
- BMC Immunology, 2016, v. 17, p. 1, doi. 10.1186/s12863-016-0395-0
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- Publication type:
- Article
Repetitive element hypermethylation in multiple sclerosis patients.
- Published in:
- BMC Genetics, 2016, v. 17, p. 1, doi. 10.1186/s12863-016-0395-0
- By:
- Publication type:
- Article
Bone involvement in adult patients affected with Ehlers-Danlos syndrome.
- Published in:
- Osteoporosis International, 2016, v. 27, n. 8, p. 2525, doi. 10.1007/s00198-016-3562-2
- By:
- Publication type:
- Article
MDC/CCL22 intrathecal levels in patients with multiple sclerosis.
- Published in:
- Multiple Sclerosis (13524585), 2008, v. 14, n. 4, p. 547, doi. 10.1177/1352458507084268
- By:
- Publication type:
- Article