Found: 18
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The Closure of Patent Foramen Ovale in Preventing Subsequent Neurological Events: A Bayesian Network Meta-Analysis to Identify the Best Device.
- Published in:
- Cerebrovascular Diseases, 2020, v. 49, n. 2, p. 124, doi. 10.1159/000507317
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- Article
Exploring by whole exome sequencing patients with initial diagnosis of Rubinstein-Taybi syndrome: the interconnections of epigenetic machinery disorders.
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- Human Genetics, 2019, v. 138, n. 3, p. 257, doi. 10.1007/s00439-019-01985-y
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- Article
A survey of the European Reference Network EpiCARE on clinical practice for selected rare epilepsies.
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- Epilepsia Open, 2021, v. 6, n. 1, p. 160, doi. 10.1002/epi4.12459
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- Article
Results From an Italian Expanded Access Program on Cannabidiol Treatment in Highly Refractory Dravet Syndrome and Lennox–Gastaut Syndrome.
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- Frontiers in Neurology, 2021, v. 11, p. 1, doi. 10.3389/fneur.2021.673135
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- Article
Uncommon intravascular lithotripsy for the treatment of subclavian steal syndrome: a case presenting with concomitant acute coronary syndrome and transient ischaemic attack.
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- 2022
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- Publication type:
- Case Study
Acute revascularization treatments for ischemic stroke in the Stroke Units of Triveneto, northeast Italy: time to treatment and functional outcomes.
- Published in:
- Journal of Thrombosis & Thrombolysis, 2021, v. 51, n. 1, p. 159, doi. 10.1007/s11239-020-02142-3
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- Article
Efficacy and Safety of Pulse Intravenous Methylprednisolone in Pediatric Epileptic Encephalopathies: Timing and Networks Consideration.
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- Journal of Clinical Medicine, 2024, v. 13, n. 9, p. 2497, doi. 10.3390/jcm13092497
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- Article
Correction to: Current territorial organization for access to revascularization therapies for acute ischemic stroke in the Veneto region (Italy) from 2017 to 2021.
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- Neurological Sciences, 2023, v. 44, n. 10, p. 3769, doi. 10.1007/s10072-023-06890-x
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- Article
Current territorial organization for access to revascularization therapies for acute ischemic stroke in the Veneto region (Italy) from 2017 to 2021.
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- Neurological Sciences, 2023, v. 44, n. 6, p. 2033, doi. 10.1007/s10072-023-06662-7
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- Article
Network meta-analysis on patent foramen ovale: is a stroke or atrial fibrillation worse?
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- Neurological Sciences, 2021, v. 42, n. 1, p. 101, doi. 10.1007/s10072-020-04922-4
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- Article
Efficacy of erenumab 70 mg in chronic migraine: Vicenza experience.
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- Neurological Sciences, 2020, v. 41, p. 479, doi. 10.1007/s10072-020-04665-2
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- Publication type:
- Article
A Male Child with Infantile Epilepsy due to a Mosaic Missense Variant of PCDH19.
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- Molecular Syndromology, 2024, v. 15, n. 2, p. 114, doi. 10.1159/000535144
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- Publication type:
- Article
Comparing cortical auditory processing in children with typical and atypical benign epilepsy with centrotemporal spikes: Electrophysiologic evidence of the role of non-rapid eye movement sleep abnormalities.
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- Epilepsia (Series 4), 2015, v. 56, n. 5, p. 726, doi. 10.1111/epi.12959
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- Article
Electroclinical presentation and genotype-phenotype relationships in patients with Unverricht-Lundborg disease carrying compound heterozygous CSTB point and indel mutations.
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- Epilepsia (Series 4), 2012, v. 53, n. 12, p. 2120, doi. 10.1111/j.1528-1167.2012.03718.x
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- Article
The Spectrum of Idiopathic Rolandic Epilepsy Syndromes and Idiopathic Occipital Epilepsies: From the Benign to the Disabling.
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- Epilepsia (Series 4), 2006, v. 47, p. 62, doi. 10.1111/j.1528-1167.2006.00693.x
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- Publication type:
- Article
Neuropsychological Findings: Myoclonic Astatic Epilepsy (MAE) and Lennox-Gastaut Syndrome (LGS).
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- Epilepsia (Series 4), 2006, v. 47, p. 56, doi. 10.1111/j.1528-1167.2006.00691.x
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- Publication type:
- Article
The use of cation exchange matrix separation coupled with ICP-MS to directly determine platinum group element (PGE) and other trace element emissions from passenger cars equipped with diesel particulate filters (DPF).
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- Analytical & Bioanalytical Chemistry, 2011, v. 399, n. 8, p. 2731, doi. 10.1007/s00216-010-4596-5
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- Article
Glucose transporter type 1 deficiency syndrome: Developmental delay and early-onset ataxia in a novel mutation of the SLC2A1 gene.
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- Journal of Pediatric Neurosciences, 2018, v. 13, n. 4, p. 496, doi. 10.4103/JPN.JPN_169_17
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- Article