37 results on '"Cereda, Cristina"'
Search Results
2. Long-term cytokine profile in multisystem inflammatory disease among children
3. Effective lowering of α-synuclein expression by targeting G-quadruplex structures within the SNCA gene
4. Towards genomic-Newborn Screening: Technical feasibility of Exome Sequencing starting from dried blood spots
5. Space research to explore novel biochemical insights on Earth
6. Identification of a novel pathway in sporadic Amyotrophic Lateral Sclerosis mediated by the long non-coding RNA ZEB1-AS1
7. Detection of SARS-CoV-2 genome and whole transcriptome sequencing in frontal cortex of COVID-19 patients
8. Raman spectroscopy reveals biochemical differences in plasma derived extracellular vesicles from sporadic Amyotrophic Lateral Sclerosis patients
9. Phenotypic spectrum of short-chain enoyl-Coa hydratase-1 (ECHS1) deficiency
10. Prevalence and prognostic value of Delirium as the initial presentation of COVID-19 in the elderly with dementia: An Italian retrospective study
11. Characterization of the molecular dysfunctions occurring in Aicardi-Goutières syndrome patients with mutations in ADAR1
12. Genome-wide Analyses Identify KIF5A as a Novel ALS Gene
13. Gene expression analysis in subcutaneous adipose tissue reveals a predominant influence of lncRNAs during growth
14. Sporadic and familial glut1ds Italian patients: A wide clinical variability
15. Production of an induced pluripotent stem cell line CSSi018-A (14192) from a patient with hypomyelinating leukodystrophy 7 (HLD7) carrying biallelic variants of POLR3A (c.1802 T > A; c.4072G > A)
16. Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study
17. Chromosome 9p21.3 genotype is associated with vascular dementia and Alzheimer's disease
18. Clinical and genetic features of a large cohort of Italian SPG4 patients from the D.A.I.S.Y. collaborative network
19. Time course of oxidant markers and antioxidant defenses in subgroups of amyotrophic lateral sclerosis patients
20. TNF and sTNFR1/2 plasma levels in ALS patients
21. C9orf72 repeat expansions are restricted to the ALS-FTD spectrum
22. Analysis of hnRNPA1, A2/B1, and A3 genes in patients with amyotrophic lateral sclerosis
23. C9ORF72 repeat expansion in a large Italian ALS cohort: evidence of a founder effect
24. Mutational analysis of VCP gene in familial amyotrophic lateral sclerosis
25. A novel peripherin gene ( PRPH) mutation identified in one sporadic amyotrophic lateral sclerosis patient
26. Lack of association of PON polymorphisms with sporadic ALS in an Italian population
27. RNA-seq dataset of subcutaneous adipose tissue: Transcriptional differences between obesity and healthy women
28. COVID-19 patients and Dementia: Frontal cortex transcriptomic data
29. Generation of three isogenic induced Pluripotent Stem Cell lines (iPSCs) from fibroblasts of a patient with Aicardi Goutières Syndrome carrying a c.2471G>A dominant mutation in IFIH1 gene
30. Establishment of three iPSC lines from fibroblasts of a patient with Aicardi Goutières syndrome mutated in RNaseH2B
31. Generation of three iPSC lines from fibroblasts of a patient with Aicardi Goutières Syndrome mutated in TREX1
32. INFLUENCE OF GENETIC POLYMORPHISMS ON CHANGE IN COGNITIVE DOMAINS, COGNITIVE IMPAIRMENT AND DEMENTIA: AGE EFFECT? RESULTS FROM A FOUR-YEAR LONGITUDINAL STUDY IN AN ELDERLY POPULATION (INVECE.AB)
33. SLOW AND FAST DECLINE DEMENTIA: CLINICAL, PATHOLOGICAL AND GENETIC CHARACTERIZATION OF TWO RELATED CASES
34. Severe familial ALS with a novel exon 4 mutation (L106F) in the SOD1 gene
35. Screening of the PFN1 gene in sporadic amyotrophic lateral sclerosis and in frontotemporal dementia
36. No association of DPP6 with amyotrophic lateral sclerosis in an Italian population
37. Potential therapeutic usefulness of hydrogen peroxide in conditions of brain ischemia
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