Cristina Cereda

Effect of nitric oxide on lymphocytes from sporadic amyotrophic lateral sclerosis patients: toxic or protective role?

Increased incidence of FMO1 gene single nucleotide polymorphisms in sporadic amyotrophic lateral sclerosis.

TNF and sTNFR1/2 plasma levels in ALS patients.

Hydrogen peroxide-mediated induction of SOD1 gene transcription is independent from Nrf2 in a cellular model of neurodegeneration.

Long non-coding and coding RNAs characterization in Peripheral Blood Mononuclear Cells and Spinal Cord from Amyotrophic Lateral Sclerosis patients.

Lymphoblastoid cell lines as a model to understand amyotrophic lateral sclerosis disease mechanisms.

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene.

SOD1 in Amyotrophic Lateral Sclerosis: "Ambivalent" Behavior Connected to the Disease.

A motor neuron strategy to save time and energy in neurodegeneration: adaptive protein stoichiometry.

Pathological Proteins Are Transported by Extracellular Vesicles of Sporadic Amyotrophic Lateral Sclerosis Patients.

A Novel Nonsense Angiogenin Mutation is Associated With Alzheimer Disease.

A pilot study assessing T1-weighted muscle MRI in amyotrophic lateral sclerosis (ALS).

Long non coding RNAs and ALS: Still much to do.

From Neuronal Differentiation of iPSCs to 3D Neuro-Organoids: Modelling and Therapy of Neurodegenerative Diseases.

Curcumin and Novel Synthetic Analogs in Cell-Based Studies of Alzheimer's Disease.

Next Generation Molecular Diagnosis of Hereditary Spastic Paraplegias: An Italian Cross-Sectional Study.

A Novel Mutation in the Stalk Domain of Causes a Slowly Progressive Atypical Motor Syndrome.

Sine causa tetraparesis: A pilot study on its possible relationship with interferon signature analysis and Aicardi Goutières syndrome related genes analysis.

RNA-Seq profiling in peripheral blood mononuclear cells of amyotrophic lateral sclerosis patients and controls.

The spectrum of intermediate SCN8A-related epilepsy.

Leukocyte Derived Microvesicles as Disease Progression Biomarkers in Slow Progressing Amyotrophic Lateral Sclerosis Patients.

Nuclear Phospho-SOD1 Protects DNA from Oxidative Stress Damage in Amyotrophic Lateral Sclerosis.

Molecular Genetics and Interferon Signature in the Italian Aicardi Goutières Syndrome Cohort: Report of 12 New Cases and Literature Review.

Proteostasis and ALS: protocol for a phase II, randomised, double-blind, placebo-controlled, multicentre clinical trial for colchicine in ALS (Co-ALS).

Altered immune system in frailty: Genetics and diet may influence inflammation.

HuR interacts with lincBRN1a and lincBRN1b during neuronal stem cells differentiation.

Bioink Composition and Printing Parameters for 3D Modeling Neural Tissue.

Agenesis of the putamen and globus pallidus caused by recessive mutations in the homeobox gene GSX2.

Generation of three iPSC lines from fibroblasts of a patient with Aicardi Goutières Syndrome mutated in TREX1.

HSC70 expression is reduced in lymphomonocytes of sporadic ALS patients and contributes to TDP-43 accumulation.

Establishment of three iPSC lines from fibroblasts of a patient with Aicardi Goutières syndrome mutated in RNaseH2B.

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.

3D Printed Conductive Nanocellulose Scaffolds for the Differentiation of Human Neuroblastoma Cells.

MRI study of paraspinal muscles in patients with Amyotrophic Lateral Sclerosis (ALS).

Biomaterials in Neurodegenerative Disorders: A Promising Therapeutic Approach.