448 results on '"Cereda, Cristina"'
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2. Long-term cytokine profile in multisystem inflammatory disease among children
3. Cell environment shapes TDP-43 function with implications in neuronal and muscle disease
4. Towards genomic-Newborn Screening: Technical feasibility of Exome Sequencing starting from dried blood spots
5. ALDOC- and ENO2- driven glucose metabolism sustains 3D tumor spheroids growth regardless of nutrient environmental conditions: a multi-omics analysis
6. Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
7. Identification of a novel pathway in sporadic Amyotrophic Lateral Sclerosis mediated by the long non-coding RNA ZEB1-AS1
8. 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)
9. Inflammation and cell-to-cell communication, two related aspects in frailty
10. Glut1 deficiency syndrome throughout life: clinical phenotypes, intelligence, life achievements and quality of life in familial cases
11. Functional analysis and transcriptome profile of meninges and skin fibroblasts from human‐aged donors.
12. BAG3 and BAG6 differentially affect the dynamics of stress granules by targeting distinct subsets of defective polypeptides released from ribosomes
13. Genome-wide Analyses Identify KIF5A as a Novel ALS Gene.
14. Activated Human Adipose Tissue Transplantation Promotes Sensorimotor Recovery after Acute Spinal Cord Contusion in Rats
15. Prevalence and prognostic value of Delirium as the initial presentation of COVID-19 in the elderly with dementia: An Italian retrospective study
16. Study of lncRNAs in Pediatric Neurological Diseases: Methods, Analysis of the State-of-Art and Possible Therapeutic Implications
17. Hydroxychloroquine modulates immunological pathways activated by RNA:DNA hybrids in Aicardi–Goutières syndrome patients carrying RNASEH2 mutations
18. Familial hemiplegic migraine type 2 due to a novel missense mutation in ATP1A2
19. 3D photopolymerized microstructured scaffolds influence nuclear deformation, nucleo/cytoskeletal protein organization, and gene regulation in mesenchymal stem cells
20. Characterization of the molecular dysfunctions occurring in Aicardi-Goutières syndrome patients with mutations in ADAR1
21. Genome-wide Analyses Identify KIF5A as a Novel ALS Gene
22. Air pollution as a contributor to the inflammatory activity of multiple sclerosis
23. Gene expression analysis in subcutaneous adipose tissue reveals a predominant influence of lncRNAs during growth
24. Redox Imbalance in Neurological Disorders in Adults and Children
25. Subcutaneous Adipose Tissue Transcriptome Highlights Specific Expression Profiles in Severe Pediatric Obesity: A Pilot Study
26. Reduced mitochondrial D-loop methylation levels in sporadic amyotrophic lateral sclerosis
27. Menkes disease complicated by concurrent ACY1 deficiency: A case report
28. De novo exonic duplication of ATP1A2 in Italian patient with hemiplegic migraine: a case report
29. The absence that makes the difference: choroidal abnormalities in Legius syndrome
30. Sine causa tetraparesis: A pilot study on its possible relationship with interferon signature analysis and Aicardi Goutières syndrome related genes analysis
31. Sporadic and familial glut1ds Italian patients: A wide clinical variability
32. Characterization of Mitochondrial Alterations in Aicardi–Goutières Patients Mutated in RNASEH2A and RNASEH2B Genes
33. The Effect of Healthy Lifestyle Strategies on the Management of Insulin Resistance in Children and Adolescents with Obesity: A Narrative Review
34. Molecular Genetics of GLUT1DS Italian Pediatric Cohort: 10 Novel Disease-Related Variants and Structural Analysis
35. Bisdemethoxycurcumin (BDC)-Loaded H-Ferritin-Nanocages Mediate the Regulation of Inflammation in Alzheimer’s Disease Patients
36. Benefits of Physical Exercise as Approach to Prevention and Reversion of Non-Alcoholic Fatty Liver Disease in Children and Adolescents with Obesity
37. Differential Neuropathology, Genetics, and Transcriptomics in Two Kindred Cases with Alzheimer’s Disease and Lewy Body Dementia
38. Cell environment shapes TDP-43 function with implications in neuronal and muscle disease
39. Editorial: Epigenetics of Neurodevelopmental, Neuromuscular and Neurodegenerative Disorders
40. Use of Physical Activity and Exercise to Reduce Inflammation in Children and Adolescents with Obesity
41. The Mitogenome Relationships and Phylogeography of Barn Swallows (Hirundo rustica)
42. Patients’ Stem Cells Differentiation in a 3D Environment as a Promising Experimental Tool for the Study of Amyotrophic Lateral Sclerosis
43. SNCA-AS1 in aging and Parkinson’s disease
44. Lysosomes Dysfunction Causes Mitophagy Impairment in PBMCs of Sporadic ALS Patients
45. Additional file 3 of Glut1 deficiency syndrome throughout life: clinical phenotypes, intelligence, life achievements and quality of life in familial cases
46. Additional file 1 of Glut1 deficiency syndrome throughout life: clinical phenotypes, intelligence, life achievements and quality of life in familial cases
47. An over-oxidized form of superoxide dismutase found in sporadic amyotrophic lateral sclerosis with bulbar onset shares a toxic mechanism with mutant SOD1
48. Clinical-Genetic Features Influencing Disability in Spastic Paraplegia Type 4
49. Extracellular Vesicles Derived From Plasma of Patients With Neurodegenerative Disease Have Common Transcriptomic Profiling
50. Neurodegenerative Disease-Associated TDP-43 Fragments Are Extracellularly Secreted with CASA Complex Proteins
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