Lista de obras - Cristoforo Comi - Dominio Público Uruguay

A nationwide retrospective analysis on the effect of immune therapies in patients with chronic inflammatory demyelinating polyradiculoneuropathy

artículo científico publicado en 2009

A patient with autoimmune limb-girdle myasthenia, and a brief review of this treatable condition

artículo científico publicado en 2017

Abnormal response to glutamate of T lymphocytes from multiple sclerosis patients.

artículo científico publicado en 2003

Advances in neuroimmunology: from bench to bedside.

artículo científico publicado en 2014

Beta2-Adrenoceptor Agonists in Parkinson's Disease and Other Synucleinopathies

artículo científico publicado en 2019

CD4+ T-Cell Transcription Factors in Idiopathic REM Sleep Behavior Disorder and Parkinson's Disease

artículo científico publicado en 2020

Candidate gene analysis of SPARCL1 gene in patients with multiple sclerosis

artículo científico publicado en 2007

Cerebrospinal fluid biomarkers in Progranulin mutations carriers

artículo científico publicado en 2011

Chronic obstructive pulmonary disease may complicate Alzheimer's disease: a comorbidity problem

artículo científico publicado en 2018

Combined use of Kappa Free Light Chain Index and Isoelectrofocusing of Cerebro-Spinal Fluid in Diagnosing Multiple Sclerosis: Performances and Costs.

artículo científico publicado en 2017

Complex pattern of convulsive syncope in glossopharyngeal neuralgia: video/EEG report and short review.

artículo científico publicado en 2011

Current understanding on the role of standard and immunoproteasomes in inflammatory/immunological pathways of multiple sclerosis

scientific article published on 02 January 2014

Cutaneous silent period in human immunodeficiency virus-related peripheral neuropathy.

artículo científico publicado en 2004

Decreased function of Fas and variations of the perforin gene in adult patients with primary immune thrombocytopenia.

artículo científico publicado en 2016

Defective Fas-mediated T-cell apoptosis predicts acute onset CIDP

artículo científico publicado en 2009

Defective T cell Fas function in patients with multiple sclerosis

scientific article published on 01 October 2000

Defining the epsilon-sarcoglycan (SGCE) gene phenotypic signature in myoclonus-dystonia: a reappraisal of genetic testing criteria

artículo científico publicado en 2013

Discovery and verification of panels of T-lymphocyte proteins as biomarkers of Parkinson's disease

artículo científico publicado en 2012

Dopaminergic Receptors on CD4+ T Naive and Memory Lymphocytes Correlate with Motor Impairment in Patients with Parkinson's Disease.

artículo científico publicado en 2016

E-selectin A561C and G98T polymorphisms influence susceptibility and course of multiple sclerosis

artículo científico publicado en 2005

Effectiveness of intensive inpatient rehabilitation treatment on disease progression in parkinsonian patients: a randomized controlled trial with 1-year follow-up.

artículo científico publicado en 2011

Evidence of Pre-Synaptic Dopaminergic Deficit in a Patient with a Novel Progranulin Mutation Presenting with Atypical Parkinsonism†

scientific article published on 01 January 2014

Exploiting PLGA-Based Biocompatible Nanoparticles for Next-Generation Tolerogenic Vaccines against Autoimmune Disease ⬇️

journal article from 'International Journal of Molecular Sciences' published in 2019

Expression and genetic analysis of miRNAs involved in CD4+ cell activation in patients with multiple sclerosis

artículo científico publicado en 2011

Extracellular proteasome-osteopontin circuit regulates cell migration with implications in multiple sclerosis

artículo científico publicado en 2017

Fas-mediated T-cell apoptosis in chronic inflammatory demyelinating polyneuropathy

artículo científico publicado en 2011

Fas-mediated T-cell apoptosis is impaired in patients with chronic inflammatory demyelinating polyneuropathy

artículo científico publicado en 2006

GSK3β genetic variability in patients with Multiple Sclerosis

artículo científico publicado en 2011

Gender-specific influence of the chromosome 16 chemokine gene cluster on the susceptibility to Multiple Sclerosis

artículo científico publicado en 2007

Growth Arrest Specific 6 Concentration is Increased in the Cerebrospinal Fluid of Patients with Alzheimer's Disease.

artículo científico publicado en 2017

ICOS cooperates with CD28, IL-2, and IFN-gamma and modulates activation of human naïve CD4+ T cells

artículo científico publicado en 2006

ICOS gene haplotypes correlate with IL10 secretion and multiple sclerosis evolution

article

Impaired visual inhibition in migraine with aura.

artículo científico publicado en 2014

Insights into the protective role of immunity in neurodegenerative disease

artículo científico publicado en 2017

Intensive rehabilitation treatment in early Parkinson's disease: a randomized pilot study with a 2-year follow-up

artículo científico publicado en 2014

Levodopa-induced belly dancer's dyskinesias in Parkinson's disease: Report of one case

artículo científico publicado en 2010

LncRNAs expression profile in peripheral blood mononuclear cells from multiple sclerosis patients

scientific article published on 27 August 2018

Longitudinal Assessment of Transorbital Sonography, Visual Acuity, and Biomarkers for Inflammation and Axonal Injury in Optic Neuritis

artículo científico publicado en 2017

MDC/CCL22 intrathecal levels in patients with multiple sclerosis.

artículo científico publicado en 2008

MOG-antibody demyelinating diseases: a case of post-partum severe rhombencephalitis and transverse myelitis.

artículo científico publicado en 2018

MRI imaging and clinical features of sciatic nerve injection injury

artículo científico publicado en 2015

Osteopontin Bridging Innate and Adaptive Immunity in Autoimmune Diseases.

artículo científico publicado en 2016

Osteopontin gene haplotypes correlate with multiple sclerosis development and progression

scientific article published on 25 April 2005

Osteopontin is increased in the cerebrospinal fluid of patients with Alzheimer's disease and its levels correlate with cognitive decline.

artículo científico publicado en 2010

P-selectin glycoprotein ligand-1 variable number of tandem repeats (VNTR) polymorphism in patients with multiple sclerosis

artículo científico publicado en 2005

Parkinson's disease patients have a complex phenotypic and functional Th1 bias: cross-sectional studies of CD4+ Th1/Th2/T17 and Treg in drug-naïve and drug-treated patients.

artículo científico publicado en 2018

Peripheral nervous system involvement in Parkinson's disease: evidence and controversies

artículo científico publicado en 2014

Peripheral neuropathy as marker of severe Parkinson's disease phenotype.

artículo científico publicado en 2017

Polymorphisms of Dopamine Receptor Genes and Risk of L-Dopa-Induced Dyskinesia in Parkinson's Disease

artículo científico publicado en 2017

Polymorphisms of dopamine receptor genes and risk of visual hallucinations in Parkinson's patients

artículo científico publicado en 2016

Predicting cognitive decline in Parkinson's disease: can we ask the genes?

artículo científico publicado en 2014

Prevalence and burden of dysautonomia in advanced Parkinson's disease

artículo científico publicado en 2017

Prevalence and features of peripheral neuropathy in Parkinson's disease patients under different therapeutic regimens.

artículo científico publicado en 2013

Progranulin plasma levels as potential biomarker for the identification of GRN deletion carriers. A case with atypical onset as clinical amnestic Mild Cognitive Impairment converted to Alzheimer's disease

artículo científico publicado en 2009

Real life evaluation of safinamide effectiveness in Parkinson's disease

artículo científico publicado en 2018

Rehabilitation improves dyskinesias in Parkinsonian patients: a pilot study comparing two different rehabilitative treatments

artículo científico publicado en 2012

Revisiting the molecular mechanism of neurological manifestations in antiphospholipid syndrome: beyond vascular damage

artículo científico publicado en 2014

Rituximab in patients with chronic inflammatory demyelinating polyradiculoneuropathy: a report of 13 cases and review of the literature.

artículo científico publicado en 2010

Role of Anti-Osteopontin Antibodies in Multiple Sclerosis and Experimental Autoimmune Encephalomyelitis.

artículo científico publicado en 2017

Signals of apoptotic pathways in several types of meningioma.

artículo científico publicado en 2010

Spontaneous intracranial hypotension presenting as a reversible dorsal midbrain syndrome

artículo científico publicado en 2008

Subcutaneous inverse vaccination with PLGA particles loaded with a MOG peptide and IL-10 decreases the severity of experimental autoimmune encephalomyelitis

artículo científico publicado en 2014

TAM Receptor Pathways at the Crossroads of Neuroinflammation and Neurodegeneration

artículo científico publicado en 2019

The -346T polymorphism of the SH2D1A gene is a risk factor for development of autoimmunity/lymphoproliferation in males with defective Fas function.

artículo científico publicado en 2012

The impact of osteopontin gene variations on multiple sclerosis development and progression

artículo científico publicado en 2012

The measuring of substantia nigra hyperechogenicity in an Italian cohort of Parkinson disease patients: a case/control study (NOBIS Study).

artículo científico publicado en 2017

The role of T cell apoptosis in nervous system autoimmunity.

artículo científico

The role of osteopontin in neurodegenerative diseases.

artículo científico publicado en 2011

Thrombin Cleavage of Osteopontin Modulates Its Activities in Human Cells In Vitro and Mouse Experimental Autoimmune Encephalomyelitis In Vivo.

artículo científico publicado en 2016

Transorbital Sonography and Visual Outcome for the Diagnosis and Monitoring of Optic Neuritis

artículo científico publicado en 2016

Transorbital Sonography in Acute Optic Neuritis: A Case-Control Study

artículo científico publicado en 2014

Treatment of chronic inflammatory demyelinating polyneuropathy: from molecular bases to practical considerations.

artículo científico publicado en 2014

Untangling Extracellular Proteasome-Osteopontin Circuit Dynamics in Multiple Sclerosis

artículo científico publicado en 2019

Variations of the perforin gene in patients with chronic inflammatory demyelinating polyradiculoneuropathy

scientific article published on 30 October 2014

Variations of the perforin gene in patients with multiple sclerosis

article

Lista de obras de Cristoforo Comi

A nationwide retrospective analysis on the effect of immune therapies in patients with chronic inflammatory demyelinating polyradiculoneuropathy

A patient with autoimmune limb-girdle myasthenia, and a brief review of this treatable condition

Abnormal response to glutamate of T lymphocytes from multiple sclerosis patients.

Advances in neuroimmunology: from bench to bedside.

Beta2-Adrenoceptor Agonists in Parkinson's Disease and Other Synucleinopathies

CD4+ T-Cell Transcription Factors in Idiopathic REM Sleep Behavior Disorder and Parkinson's Disease

Candidate gene analysis of SPARCL1 gene in patients with multiple sclerosis

Cerebrospinal fluid biomarkers in Progranulin mutations carriers

Chronic obstructive pulmonary disease may complicate Alzheimer's disease: a comorbidity problem

Combined use of Kappa Free Light Chain Index and Isoelectrofocusing of Cerebro-Spinal Fluid in Diagnosing Multiple Sclerosis: Performances and Costs.

Complex pattern of convulsive syncope in glossopharyngeal neuralgia: video/EEG report and short review.

Current understanding on the role of standard and immunoproteasomes in inflammatory/immunological pathways of multiple sclerosis

Cutaneous silent period in human immunodeficiency virus-related peripheral neuropathy.

Decreased function of Fas and variations of the perforin gene in adult patients with primary immune thrombocytopenia.

Defective Fas-mediated T-cell apoptosis predicts acute onset CIDP

Defective T cell Fas function in patients with multiple sclerosis

Defining the epsilon-sarcoglycan (SGCE) gene phenotypic signature in myoclonus-dystonia: a reappraisal of genetic testing criteria

Discovery and verification of panels of T-lymphocyte proteins as biomarkers of Parkinson's disease

Dopaminergic Receptors on CD4+ T Naive and Memory Lymphocytes Correlate with Motor Impairment in Patients with Parkinson's Disease.

E-selectin A561C and G98T polymorphisms influence susceptibility and course of multiple sclerosis

Effectiveness of intensive inpatient rehabilitation treatment on disease progression in parkinsonian patients: a randomized controlled trial with 1-year follow-up.

Evidence of Pre-Synaptic Dopaminergic Deficit in a Patient with a Novel Progranulin Mutation Presenting with Atypical Parkinsonism†

Exploiting PLGA-Based Biocompatible Nanoparticles for Next-Generation Tolerogenic Vaccines against Autoimmune Disease ⬇️

Expression and genetic analysis of miRNAs involved in CD4+ cell activation in patients with multiple sclerosis

Extracellular proteasome-osteopontin circuit regulates cell migration with implications in multiple sclerosis

Fas-mediated T-cell apoptosis in chronic inflammatory demyelinating polyneuropathy

Fas-mediated T-cell apoptosis is impaired in patients with chronic inflammatory demyelinating polyneuropathy

GSK3β genetic variability in patients with Multiple Sclerosis

Gender-specific influence of the chromosome 16 chemokine gene cluster on the susceptibility to Multiple Sclerosis

Growth Arrest Specific 6 Concentration is Increased in the Cerebrospinal Fluid of Patients with Alzheimer's Disease.

ICOS cooperates with CD28, IL-2, and IFN-gamma and modulates activation of human naïve CD4+ T cells

ICOS gene haplotypes correlate with IL10 secretion and multiple sclerosis evolution

Impaired visual inhibition in migraine with aura.

Insights into the protective role of immunity in neurodegenerative disease

Intensive rehabilitation treatment in early Parkinson's disease: a randomized pilot study with a 2-year follow-up

Levodopa-induced belly dancer's dyskinesias in Parkinson's disease: Report of one case

LncRNAs expression profile in peripheral blood mononuclear cells from multiple sclerosis patients

Longitudinal Assessment of Transorbital Sonography, Visual Acuity, and Biomarkers for Inflammation and Axonal Injury in Optic Neuritis

MDC/CCL22 intrathecal levels in patients with multiple sclerosis.

MOG-antibody demyelinating diseases: a case of post-partum severe rhombencephalitis and transverse myelitis.

MRI imaging and clinical features of sciatic nerve injection injury

Osteopontin Bridging Innate and Adaptive Immunity in Autoimmune Diseases.

Osteopontin gene haplotypes correlate with multiple sclerosis development and progression

Osteopontin is increased in the cerebrospinal fluid of patients with Alzheimer's disease and its levels correlate with cognitive decline.

P-selectin glycoprotein ligand-1 variable number of tandem repeats (VNTR) polymorphism in patients with multiple sclerosis

Parkinson's disease patients have a complex phenotypic and functional Th1 bias: cross-sectional studies of CD4+ Th1/Th2/T17 and Treg in drug-naïve and drug-treated patients.

Peripheral nervous system involvement in Parkinson's disease: evidence and controversies

Peripheral neuropathy as marker of severe Parkinson's disease phenotype.

Polymorphisms of Dopamine Receptor Genes and Risk of L-Dopa-Induced Dyskinesia in Parkinson's Disease

Polymorphisms of dopamine receptor genes and risk of visual hallucinations in Parkinson's patients

Predicting cognitive decline in Parkinson's disease: can we ask the genes?

Prevalence and burden of dysautonomia in advanced Parkinson's disease

Prevalence and features of peripheral neuropathy in Parkinson's disease patients under different therapeutic regimens.

Progranulin plasma levels as potential biomarker for the identification of GRN deletion carriers. A case with atypical onset as clinical amnestic Mild Cognitive Impairment converted to Alzheimer's disease

Real life evaluation of safinamide effectiveness in Parkinson's disease

Rehabilitation improves dyskinesias in Parkinsonian patients: a pilot study comparing two different rehabilitative treatments

Revisiting the molecular mechanism of neurological manifestations in antiphospholipid syndrome: beyond vascular damage

Rituximab in patients with chronic inflammatory demyelinating polyradiculoneuropathy: a report of 13 cases and review of the literature.

Role of Anti-Osteopontin Antibodies in Multiple Sclerosis and Experimental Autoimmune Encephalomyelitis.

Signals of apoptotic pathways in several types of meningioma.

Spontaneous intracranial hypotension presenting as a reversible dorsal midbrain syndrome

Subcutaneous inverse vaccination with PLGA particles loaded with a MOG peptide and IL-10 decreases the severity of experimental autoimmune encephalomyelitis

TAM Receptor Pathways at the Crossroads of Neuroinflammation and Neurodegeneration

The -346T polymorphism of the SH2D1A gene is a risk factor for development of autoimmunity/lymphoproliferation in males with defective Fas function.

The impact of osteopontin gene variations on multiple sclerosis development and progression

The measuring of substantia nigra hyperechogenicity in an Italian cohort of Parkinson disease patients: a case/control study (NOBIS Study).

The role of T cell apoptosis in nervous system autoimmunity.

The role of osteopontin in neurodegenerative diseases.

Thrombin Cleavage of Osteopontin Modulates Its Activities in Human Cells In Vitro and Mouse Experimental Autoimmune Encephalomyelitis In Vivo.

Transorbital Sonography and Visual Outcome for the Diagnosis and Monitoring of Optic Neuritis

Transorbital Sonography in Acute Optic Neuritis: A Case-Control Study

Treatment of chronic inflammatory demyelinating polyneuropathy: from molecular bases to practical considerations.

Untangling Extracellular Proteasome-Osteopontin Circuit Dynamics in Multiple Sclerosis

Variations of the perforin gene in patients with chronic inflammatory demyelinating polyradiculoneuropathy

Variations of the perforin gene in patients with multiple sclerosis