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Vitamin D Supplementation Modulates ICOS+ and ICOS- Regulatory T Cell in Siblings of Children With Type 1 Diabetes.
- Published in:
- 2020
- By:
- Publication type:
- journal article
HLA alleles modulate EBV viral load in multiple sclerosis.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Pediatric Onset of Generalized Dystonia, Cognitive Impairment, and Dysmorphic Features in a Patient Carrying Compound Heterozygous GNAL Mutations.
- Published in:
- Movement Disorders Clinical Practice, 2024, v. 11, n. 8, p. 1047, doi. 10.1002/mdc3.14124
- By:
- Publication type:
- Article
A case of early-onset Parkinson's disease in a patient with KBG syndrome.
- Published in:
- Neurological Sciences, 2023, v. 44, n. 12, p. 4537, doi. 10.1007/s10072-023-06988-2
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- Publication type:
- Article
Analysis of the GCG repeat length in NIPA1 gene in C9orf72-mediated ALS in a large Italian ALS cohort.
- Published in:
- 2019
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- Publication type:
- journal article
Familial clustering in Italian progressive-onset and bout-onset multiple sclerosis.
- Published in:
- Neurological Sciences, 2014, v. 35, n. 5, p. 789, doi. 10.1007/s10072-014-1650-7
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- Publication type:
- Article
DESIGN OF THE STUDY OF A RESEARCH PROJECT: THE CASE OF THE OPERATIONAL BEHAVIOR OF THE VETERINARY SECTOR COMPANIES.
- Published in:
- Revista de Comunicación de la SEECI, 2018, v. 22, n. 47, p. 107, doi. 10.15198/seeci.2018.0.107-124
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- Publication type:
- Article
A Scoping Review on Body Fluid Biomarkers for Prognosis and Disease Activity in Patients with Multiple Sclerosis.
- Published in:
- Journal of Personalized Medicine, 2022, v. 12, n. 9, p. N.PAG, doi. 10.3390/jpm12091430
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- Publication type:
- Article
Targeted Next-Generation Sequencing for the Identification of Genetic Predictors of Radiation-Induced Late Skin Toxicity in Breast Cancer Patients: A Preliminary Study.
- Published in:
- Journal of Personalized Medicine, 2021, v. 11, n. 10, p. 967, doi. 10.3390/jpm11100967
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- Publication type:
- Article
The Impact of Lifetime Alcohol and Cigarette Smoking Loads on Multiple Sclerosis Severity.
- Published in:
- Frontiers in Neurology, 2019, p. 1, doi. 10.3389/fneur.2019.00866
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- Publication type:
- Article
Genetic variants are major determinants of CSF antibody levels in multiple sclerosis.
- Published in:
- 2015
- By:
- Publication type:
- journal article
C9ORF72 Repeat Expansion Affects the Proteome of Primary Skin Fibroblasts in ALS.
- Published in:
- International Journal of Molecular Sciences, 2021, v. 22, n. 19, p. 10385, doi. 10.3390/ijms221910385
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- Publication type:
- Article
Etiological research in pediatric multiple sclerosis: A tool to assess environmental exposures (PEDiatric Italian Genetic and enviRonment ExposurE Questionnaire).
- Published in:
- Multiple Sclerosis Journal - Experimental, Translational & Clinical, 2021, p. 1, doi. 10.1177/20552173211059048
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- Publication type:
- Article
Etiological research in pediatric multiple sclerosis: A tool to assess environmental exposures (PEDiatric Italian Genetic and enviRonment ExposurE Questionnaire).
- Published in:
- Multiple Sclerosis Journal - Experimental, Translational & Clinical, 2021, v. 7, n. 4, p. 1, doi. 10.1177/20552173211059048
- By:
- Publication type:
- Article
Parkinsonism in SCA19/22: Dopamine Transporter Imaging in an Italian Family Harboring a Novel Mutation.
- Published in:
- 2024
- By:
- Publication type:
- Case Study
La inmigración hacia dentro: argumentos sobre la necesidad de la coordinación de las políticas de inmigración en un Estado multinivel.
- Published in:
- Politica y Sociedad, 2008, v. 45, n. 1, p. 11
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- Publication type:
- Article
Validation of an Algorithm to Detect Multiple Sclerosis Cases in Administrative Health Databases in Piedmont (Italy): An Application to the Estimate of Prevalence by Age and Urbanization Level.
- Published in:
- Neuroepidemiology, 2021, v. 55, n. 2, p. 119, doi. 10.1159/000513763
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- Publication type:
- Article
COVID-19 and Health Outcomes in People with Multiple Sclerosis: A Population-Based Study in Italy.
- Published in:
- Life (2075-1729), 2023, v. 13, n. 5, p. 1089, doi. 10.3390/life13051089
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- Publication type:
- Article
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis.
- Published in:
- Nature Genetics, 2013, v. 45, n. 11, p. 1353, doi. 10.1038/ng.2770
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- Publication type:
- Article
Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis.
- Published in:
- 2010
- By:
- Publication type:
- Letter
Corrigendum: Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus.
- Published in:
- 2008
- By:
- Publication type:
- Correction Notice
Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus.
- Published in:
- Nature Genetics, 2008, v. 40, n. 2, p. 211, doi. 10.1038/ng.79
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- Publication type:
- Article
Next Generation Sequencing of Pooled Samples: Guideline for Variants' Filtering.
- Published in:
- Scientific Reports, 2016, p. 33735, doi. 10.1038/srep33735
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- Publication type:
- Article
Inverse correlation of genetic risk score with age at onset in bout-onset and progressive-onset multiple sclerosis.
- Published in:
- Multiple Sclerosis Journal, 2015, v. 21, n. 11, p. 1463, doi. 10.1177/1352458514561910
- By:
- Publication type:
- Article
Multiple Polymorphisms Affect Expression and Function of the Neuropeptide S Receptor (NPSR1).
- Published in:
- PLoS ONE, 2011, v. 6, n. 12, p. 1, doi. 10.1371/journal.pone.0029523
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- Publication type:
- Article
Association of Systemic Lupus Erythematosus Clinical Features with European Population Genetic Substructure.
- Published in:
- PLoS ONE, 2011, v. 6, n. 12, p. 1, doi. 10.1371/journal.pone.0029033
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- Publication type:
- Article
Immunoproteasome LMP2 60HH Variant Alters MBP Epitope Generation and Reduces the Risk to Develop Multiple Sclerosis in Italian Female Population.
- Published in:
- PLoS ONE, 2010, v. 5, n. 2, p. 1, doi. 10.1371/journal.pone.0009287
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- Publication type:
- Article
Early onset frontotemporal dementia with psychiatric presentation due to the C9ORF72 hexanucleotide repeat expansion: a case report
- Published in:
- BMC Neurology, 2014, v. 14, n. 1, p. 228, doi. 10.1186/s12883-014-0228-6
- By:
- Publication type:
- Article
Early onset frontotemporal dementia with psychiatric presentation due to the C9ORF72 hexanucleotide repeat expansion: a case report.
- Published in:
- 2014
- By:
- Publication type:
- journal article
ATXN- 2 CAG repeat expansions are interrupted in ALS patients.
- Published in:
- Human Genetics, 2011, v. 130, n. 4, p. 575, doi. 10.1007/s00439-011-1000-2
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- Publication type:
- Article
A genome screen for multiple sclerosis in Sardinian multiplex families.
- Published in:
- European Journal of Human Genetics, 2001, v. 9, n. 8, p. 621, doi. 10.1038/sj.ejhg.5200680
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- Publication type:
- Article
Linkage analysis of multiple sclerosis with candidate region markers in Sardinian and Continental Italian families.
- Published in:
- European Journal of Human Genetics, 1999, v. 7, n. 3, p. 377, doi. 10.1038/sj.ejhg.5200301
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- Publication type:
- Article
Author Correction: Next Generation Sequencing of Pooled Samples: Guideline for Variants' Filtering.
- Published in:
- 2020
- By:
- Publication type:
- Correction Notice
No evidence for a role of rare CYP27B1 functional variations in multiple sclerosis.
- Published in:
- Annals of Neurology, 2013, v. 73, n. 3, p. 433, doi. 10.1002/ana.23834
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- Publication type:
- Article
Characterization of the p.L145F and p.S135N Mutations in SOD1: Impact on the Metabolism of Fibroblasts Derived from Amyotrophic Lateral Sclerosis Patients.
- Published in:
- Antioxidants, 2022, v. 11, n. 5, p. 815, doi. 10.3390/antiox11050815
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- Publication type:
- Article
A Census of Tandemly Repeated Polymorphic Loci in Genic Regions Through the Comparative Integration of Human Genome Assemblies.
- Published in:
- Frontiers in Genetics, 2018, p. 1, doi. 10.3389/fgene.2018.00155
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- Publication type:
- Article
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 25, p. 6746, doi. 10.1093/hmg/ddu392
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- Publication type:
- Article
A systemic sclerosis and systemic lupus erythematosus pan-meta-GWAS reveals new shared susceptibility loci.
- Published in:
- Human Molecular Genetics, 2013, v. 22, n. 19, p. 4021, doi. 10.1093/hmg/ddt248
- By:
- Publication type:
- Article
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 25, p. 1, doi. 10.1093/hmg/ddu392
- By:
- Publication type:
- Article
IL12B polymorphism and type 1 diabetes in the Italian population: a case-control study.
- Published in:
- 2002
- By:
- Publication type:
- journal article
Ultrastructural Characterization of Human Gingival Fibroblasts in 3D Culture.
- Published in:
- Cells (2073-4409), 2022, v. 11, n. 22, p. 3647, doi. 10.3390/cells11223647
- By:
- Publication type:
- Article
The Impact of Osteopontin Gene Variations on Multiple Sclerosis Development and Progression.
- Published in:
- Clinical & Developmental Immunology, 2012, p. 1, doi. 10.1155/2012/212893
- By:
- Publication type:
- Article
Identification of a new putative functional IL18 gene variant through an association study in systemic lupus erythematosus.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 19, p. 3739, doi. 10.1093/hmg/ddp301
- By:
- Publication type:
- Article
A loss-of-function variant of PTPN22 is associated with reduced risk of systemic lupus erythematosus.
- Published in:
- Human Molecular Genetics, 2009, v. 18, n. 3, p. 569
- By:
- Publication type:
- Article
Polymorphisms in the Dopaminergic Receptor D3 Gene Correlate with Disease Progression Rate in Relapsing–Remitting Multiple Sclerosis Patients.
- Published in:
- Genes, 2024, v. 15, n. 6, p. 736, doi. 10.3390/genes15060736
- By:
- Publication type:
- Article
Variability in Clinical Phenotype in TARDBP Mutations: Amyotrophic Lateral Sclerosis Case Description and Literature Review.
- Published in:
- Genes, 2023, v. 14, n. 11, p. 2039, doi. 10.3390/genes14112039
- By:
- Publication type:
- Article
Neuroinflammatory Pathways in the ALS-FTD Continuum: A Focus on Genetic Variants.
- Published in:
- Genes, 2023, v. 14, n. 8, p. 1658, doi. 10.3390/genes14081658
- By:
- Publication type:
- Article
Manifestaciones oculares de la COVID-19.
- Published in:
- MediSur, 2022, v. 20, n. 6, p. 1169
- By:
- Publication type:
- Article
Expanding the genetic spectrum of primary familial brain calcification due to SLC2OA2 mutations: a case series.
- Published in:
- Neurogenetics, 2021, v. 22, n. 1, p. 65, doi. 10.1007/s10048-021-00634-9
- By:
- Publication type:
- Article
Nonparametric linkage analysis of alcohol dependence with chromosome 1 and 7 markers.
- Published in:
- Genetic Epidemiology, 1999, v. 17, p. S127, doi. 10.1002/gepi.1370170722
- By:
- Publication type:
- Article