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Paradigm shift in Parkinson's disease: using continuous telemonitoring to improve symptoms control. Results from a 2-years journey.
- Published in:
- Frontiers in Neurology, 2024, p. 1, doi. 10.3389/fneur.2024.1415970
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- Article
Results of a Web-Based Survey on 2565 Greek Migraine Patients in 2023: Demographic Data, Imposed Burden and Satisfaction to Acute and Prophylactic Treatments in the Era of New Treatment Options.
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- Journal of Clinical Medicine, 2024, v. 13, n. 10, p. 2768, doi. 10.3390/jcm13102768
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- Article
Motor and Non‐motor Outcomes of Deep Brain Stimulation across the Genetic Panorama of Parkinson's Disease: A Multi‐Scale Meta‐Analysis.
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- Movement Disorders Clinical Practice, 2024, v. 11, n. 5, p. 465, doi. 10.1002/mdc3.13994
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- Article
Sortilin Expression Levels and Peripheral Immunity: A Potential Biomarker for Segregation between Parkinson's Disease Patients and Healthy Controls.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 3, p. 1791, doi. 10.3390/ijms25031791
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- Article
Validity of the CALERA Research Sensor to Assess Body Core Temperature during Maximum Exercise in Patients with Heart Failure.
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- Sensors (14248220), 2024, v. 24, n. 3, p. 807, doi. 10.3390/s24030807
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- Article
Effects of OnabotulinumtoxinA on Allodynia and Interictal Burden of Patients with Chronic Migraine.
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- Toxins, 2024, v. 16, n. 2, p. 106, doi. 10.3390/toxins16020106
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- Article
Nine-Month Continuous Fremanezumab Prophylaxis on the Response to Triptans and Also on the Incidence of Triggers, Hypersensitivity and Prodromal Symptoms of Patients with High-Frequency Episodic Migraine.
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- Journal of Clinical Medicine, 2024, v. 13, n. 2, p. 386, doi. 10.3390/jcm13020386
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- Article
SARS‐CoV‐2 Associated Neurocognitive Disorder (SAND): Molecular validation of a pathogenetic hypothesis.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.077044
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- Publication type:
- Article
Single OnabotulinumtoxinA Session Add-On to Carbamazepine or Oxcarbazepine in Treatment-Refractory Trigeminal Neuralgia: A Case Series with 24-Week Follow Up.
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- Toxins, 2023, v. 15, n. 9, p. 539, doi. 10.3390/toxins15090539
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- Publication type:
- Article
Effects of Fremanezumab on Psychiatric Comorbidities in Difficult-to-Treat Patients with Chronic Migraine: Post Hoc Analysis of a Prospective, Multicenter, Real-World Greek Registry.
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- Journal of Clinical Medicine, 2023, v. 12, n. 13, p. 4526, doi. 10.3390/jcm12134526
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- Publication type:
- Article
Efficacy and safety of fremanezumab for migraine prophylaxis in patients with at least three previous preventive failures: Prospective, multicenter, real‐world data from a Greek registry.
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- European Journal of Neurology, 2023, v. 30, n. 5, p. 1435, doi. 10.1111/ene.15740
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- Publication type:
- Article
Predictors of Response to Fremanezumab in Migraine Patients with at Least Three Previous Preventive Failures: Post Hoc Analysis of a Prospective, Multicenter, Real-World Greek Registry.
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- Journal of Clinical Medicine, 2023, v. 12, n. 9, p. 3218, doi. 10.3390/jcm12093218
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- Article
Mediterranean diet is associated with a lower probability of prodromal Parkinson's disease and risk for Parkinson's disease/dementia with Lewy bodies: A longitudinal study.
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- European Journal of Neurology, 2023, v. 30, n. 4, p. 934, doi. 10.1111/ene.15698
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- Article
The Experience of a Tertiary Reference Hospital in the Study of Rare Neurological Diseases.
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- Medicina (1010660X), 2023, v. 59, n. 2, p. 266, doi. 10.3390/medicina59020266
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- Publication type:
- Article
Parkinson's Disease, It Takes Guts: The Correlation between Intestinal Microbiome and Cytokine Network with Neurodegeneration.
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- Biology (2079-7737), 2023, v. 12, n. 1, p. 93, doi. 10.3390/biology12010093
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- Publication type:
- Article
Peripheral Inflammatory Markers TNF-α and CCL2 Revisited: Association with Parkinson's Disease Severity.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 1, p. 264, doi. 10.3390/ijms24010264
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- Article
Cognitive impairment in COVID‐19 Survivors: Analysis and Extensions on Population Studies in Greece.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2022, v. 18, n. 7, p. 1, doi. 10.1002/alz.066877
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- Publication type:
- Article
OnabotulinumtoxinA Add-On to Monoclonal Anti-CGRP Antibodies in Treatment-Refractory Chronic Migraine.
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- Toxins, 2022, v. 14, n. 12, p. 847, doi. 10.3390/toxins14120847
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- Publication type:
- Article
Worldwide trends in mortality related to Parkinson's disease in the period of 1994-2019: Analysis of vital registration data from the WHO Mortality Database.
- Published in:
- Frontiers in Neurology, 2022, v. 13, p. 1, doi. 10.3389/fneur.2022.956440
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- Publication type:
- Article
Post-COVID-19 Parkinsonism and Parkinson's Disease Pathogenesis: The Exosomal Cargo Hypothesis.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 17, p. 9739, doi. 10.3390/ijms23179739
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- Article
CADASIL in Greece: Mutational spectrum and clinical characteristics based on a systematic review and pooled analysis of published cases.
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- European Journal of Neurology, 2022, v. 29, n. 3, p. 810, doi. 10.1111/ene.15180
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- Article
Novel Mutation of the Membrane Metallo-Endopeptidase Gene Related to Late-Onset Hereditary Polyneuropathy: Case Report and Review of the Literature.
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- Laboratory Medicine, 2022, v. 53, n. 2, p. 210, doi. 10.1093/labmed/lmab060
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- Article
Plasma Glutathione and Prodromal Parkinson's Disease Probability.
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- Movement Disorders, 2022, v. 37, n. 1, p. 200, doi. 10.1002/mds.28826
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- Publication type:
- Article
Association of the Polygenic Risk Score With the Probability of Prodromal Parkinson's Disease in Older Adults.
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- Frontiers in Molecular Neuroscience, 2021, p. 1, doi. 10.3389/fnmol.2021.739571
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- Article
Τhe Greek Variant in APP Gene: The Phenotypic Spectrum of APP Mutations.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 22, p. 12355, doi. 10.3390/ijms222212355
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- Article
Hereditary cerebral amyloid angiopathy mimicking CADASIL syndrome.
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- European Journal of Neurology, 2021, v. 28, n. 11, p. 3866, doi. 10.1111/ene.14981
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- Article
Factors associated with recurrent transient global amnesia: systematic review and pathophysiological insights.
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- Reviews in the Neurosciences, 2021, v. 32, n. 7, p. 751, doi. 10.1515/revneuro-2021-0009
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- Article
SORL1 mutation in a Greek family with Parkinson's disease and dementia.
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- Annals of Clinical & Translational Neurology, 2021, v. 8, n. 10, p. 1961, doi. 10.1002/acn3.51433
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- Article
Intergenic SNPs in Obstructive Sleep Apnea Syndrome: Revealing Metabolic, Oxidative Stress and Immune-Related Pathways.
- Published in:
- Diagnostics (2075-4418), 2021, v. 11, n. 10, p. 1753, doi. 10.3390/diagnostics11101753
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- Article
Clinically Silent Small Vessel Disease of the Brain in Patients with Obstructive Sleep Apnea Hypopnea Syndrome.
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- Diagnostics (2075-4418), 2021, v. 11, n. 9, p. 1673, doi. 10.3390/diagnostics11091673
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- Article
α-Synuclein (SNCA) A30G Mutation as a Cause of a Complex Phenotype Without Parkinsonism.
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- 2021
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- Publication type:
- letter
Frailty and Prodromal Parkinson's Disease: Results From the HELIAD Study.
- Published in:
- 2021
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- Publication type:
- journal article
A novel task-specific dystonia type: Hemifacial spasm in a photographer.
- Published in:
- 2021
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- Publication type:
- journal article
Identification of a novel de novo KMT2B variant in a Greek dystonia patient via exome sequencing genotype–phenotype correlations of all published cases.
- Published in:
- Molecular Biology Reports, 2021, v. 48, n. 1, p. 371, doi. 10.1007/s11033-020-06057-3
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- Article
Neurodegeneration and Inflammation—An Interesting Interplay in Parkinson's Disease.
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- International Journal of Molecular Sciences, 2020, v. 21, n. 22, p. 8421, doi. 10.3390/ijms21228421
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- Article
A Prospective Validation of the Updated Movement Disorders Society Research Criteria for Prodromal Parkinson's Disease.
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- Movement Disorders, 2020, v. 35, n. 10, p. 1802, doi. 10.1002/mds.28145
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- Publication type:
- Article
Association between Helicobacter pylori infection and Guillain‐Barré Syndrome: A meta‐analysis.
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- European Journal of Clinical Investigation, 2020, v. 50, n. 5, p. 1, doi. 10.1111/eci.13218
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- Publication type:
- Article
A novel homozygous SACS mutation identified by whole exome sequencing-genotype phenotype correlations of all published cases.
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- Journal of Molecular Neuroscience, 2020, v. 70, n. 1, p. 131, doi. 10.1007/s12031-019-01410-z
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- Publication type:
- Article
Motor function and the probability of prodromal Parkinson's disease in older adults.
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- 2019
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- Publication type:
- journal article
Mediterranean diet adherence is related to reduced probability of prodromal Parkinson's disease.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Genetic variations in the SULF1 gene alter the risk of cervical cancer and precancerous lesions.
- Published in:
- Oncology Letters, 2018, v. 16, n. 3, p. 3833, doi. 10.3892/ol.2018.9104
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- Publication type:
- Article
Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients.
- Published in:
- Human Genomics, 2017, v. 11, p. 1, doi. 10.1186/s40246-017-0126-2
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- Publication type:
- Article
Genotype-phenotype correlations and expansion of the molecular spectrum of AP4M1-related hereditary spastic paraplegia.
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- 2017
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- Publication type:
- journal article
Genetic and phenotypic characterization of complex hereditary spastic paraplegia.
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- 2016
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- Publication type:
- journal article
The clinical and genetic heterogeneity of paroxysmal dyskinesias.
- Published in:
- 2015
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- Publication type:
- journal article
Familial case of speech-induced tongue-protrusion dystonia.
- Published in:
- Movement Disorders, 2013, v. 28, n. 9, p. 1315, doi. 10.1002/mds.25372
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- Publication type:
- Article
The syndrome of deafness-dystonia: Clinical and genetic heterogeneity.
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- Movement Disorders, 2013, v. 28, n. 6, p. 795, doi. 10.1002/mds.25394
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- Publication type:
- Article
An Early Presentation of Neurosyphilis as Persistent Headache and Opthalmoplegia.
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- International Journal of Caring Sciences, 2013, v. 6, n. 2, p. 286
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- Publication type:
- Article
THAP1 mutations and dystonia phenotypes: Genotype phenotype correlations.
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- Movement Disorders, 2012, v. 27, n. 10, p. 1290, doi. 10.1002/mds.25146
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- Article
Identical twins with Leucine rich repeat kinase type 2 mutations discordant for Parkinson's disease.
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- Movement Disorders, 2012, v. 27, n. 10, p. 1323, doi. 10.1002/mds.24924
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- Publication type:
- Article