28 results on '"Cereda, Cristina"'
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2. Bone Marrow Mesenchymal Stem Cells Expanded Inside the Nichoid Micro-Scaffold: a Focus on Anti-Inflammatory Response
3. Inflammation and cell-to-cell communication, two related aspects in frailty
4. Glut1 deficiency syndrome throughout life: clinical phenotypes, intelligence, life achievements and quality of life in familial cases
5. Missense mutation in ATXN2 gene (c.2860C > T) in an amyotrophic lateral sclerosis patient with aggressive disease phenotype
6. Fast quantification of extracellular vesicles levels in early breast cancer patients by Single Molecule Detection Array (SiMoA)
7. A novel homozygous variant in JAM3 gene causing hemorrhagic destruction of the brain, subependymal calcification, and congenital cataracts (HDBSCC) with neonatal onset
8. Ruxolitinib in Aicardi-Goutières syndrome
9. Familial hemiplegic migraine type 2 due to a novel missense mutation in ATP1A2
10. Hydroxychloroquine modulates immunological pathways activated by RNA:DNA hybrids in Aicardi–Goutières syndrome patients carrying RNASEH2 mutations
11. cGAS-mediated induction of type I interferon due to inborn errors of histone pre-mRNA processing
12. Air pollution as a contributor to the inflammatory activity of multiple sclerosis
13. Reduced mitochondrial D-loop methylation levels in sporadic amyotrophic lateral sclerosis
14. BAG3 and BAG6 differentially affect the dynamics of stress granules by targeting distinct subsets of defective polypeptides released from ribosomes
15. RNA-Seq profiling in peripheral blood mononuclear cells of amyotrophic lateral sclerosis patients and controls
16. A pilot study assessing T1-weighted muscle MRI in amyotrophic lateral sclerosis (ALS)
17. Correction: The absence that makes the difference: choroidal abnormalities in Legius syndrome
18. Long non-coding and coding RNAs characterization in Peripheral Blood Mononuclear Cells and Spinal Cord from Amyotrophic Lateral Sclerosis patients
19. The absence that makes the difference: choroidal abnormalities in Legius syndrome
20. Erratum to: De novo exonic duplication of ATP1A2 in Italian patient with hemiplegic migraine: a case report
21. De novo exonic duplication of ATP1A2 in Italian patient with hemiplegic migraine: a case report
22. Analysis of amplicon-based NGS data from neurological disease gene panels: a new method for allele drop-out management
23. Transcriptional induction of the heat shock protein B8 mediates the clearance of misfolded proteins responsible for motor neuron diseases
24. Legius Syndrome: two novel mutations in the SPRED1 gene
25. Regulation of FMO and PON Detoxication Systems in ALS Human Tissues
26. Flavin-Containing Monooxygenase mRNA Levels are Up-Regulated in ALS Brain Areas in SOD1-Mutant Mice
27. Comparison of three methods for genotyping of prothrombotic polymorphisms
28. Paraneoplastic brainstem encephalitis in a patient with malignant fibrous histiocytoma and atypical anti-neuronal antibodies
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