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The one-and-a-half syndrome: a distinctive clinical finding in a patient with multiple sclerosis.
- Published in:
- Neurological Sciences, 2023, v. 44, n. 9, p. 3331, doi. 10.1007/s10072-023-06805-w
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- Publication type:
- Article
Neurological manifestations in patients and disease carriers in an Italian family with osteosclerosis.
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- Neurological Sciences, 2023, v. 44, n. 4, p. 1393, doi. 10.1007/s10072-022-06541-7
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- Publication type:
- Article
Babylonian knowledge about temporal lobe epilepsy: distinguishing mesial from lateral forms.
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- 2022
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- Publication type:
- journal article
Late epileptic seizures following cerebral venous thrombosis: a systematic review and meta-analysis.
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- Neurological Sciences, 2022, v. 43, n. 9, p. 5229, doi. 10.1007/s10072-022-06148-y
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- Publication type:
- Article
Incidental evidence of hypointensity in brain grey nuclei on routine MR imaging: when to suspect a neurodegenerative disorder?
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- Neurological Sciences, 2022, v. 43, n. 1, p. 643, doi. 10.1007/s10072-021-05292-1
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- Publication type:
- Article
Guillain-Barré syndrome following BNT162b2 COVID-19 vaccine.
- Published in:
- 2021
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- Publication type:
- Letter
Opicapone-induced reversible myopathy in a patient with advanced Parkinson's disease and familial hyperCKemia.
- Published in:
- 2021
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- Publication type:
- Letter
Facemask headache: a new nosographic entity among healthcare providers in COVID-19 era.
- Published in:
- Neurological Sciences, 2021, v. 42, n. 4, p. 1267, doi. 10.1007/s10072-021-05075-8
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- Publication type:
- Article
The impact of sexual abuse on psychopathology of patients with psychogenic nonepileptic seizures.
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- Neurological Sciences, 2021, v. 42, n. 4, p. 1423, doi. 10.1007/s10072-020-04652-7
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- Publication type:
- Article
Perampanel as first add-on choice on the treatment of mesial temporal lobe epilepsy: an observational real-life study.
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- Neurological Sciences, 2021, v. 42, n. 4, p. 1389, doi. 10.1007/s10072-020-04636-7
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- Publication type:
- Article
Coverage of the requirements of first and second level stroke unit in Italy.
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- Neurological Sciences, 2021, v. 42, n. 3, p. 1073, doi. 10.1007/s10072-020-04616-x
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- Article
Hypertension, seizures, and epilepsy: a review on pathophysiology and management.
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- 2019
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- Publication type:
- journal article
Relationship between severity of migraine and vitamin D deficiency: a case-control study.
- Published in:
- 2018
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- Publication type:
- journal article
The mystery of unexplained traumatic sudden falls. A clinical case that adds a new feasible cause.
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- 2017
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- Publication type:
- Case Study
An SNP site in pri-miR-124, a brain expressed miRNA gene, no contribution to mesial temporal lobe epilepsy in an Italian sample.
- Published in:
- 2016
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- Publication type:
- journal article
A puzzling case without solution: isolated late-onset epileptic seizure.
- Published in:
- 2015
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- Publication type:
- Case Study
Reversible symmetrical external capsule hyperintensity as an early finding of autoimmune encephalitis.
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- 2014
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- Publication type:
- Case Study
Reversible symmetrical external capsule hyperintensity as an early finding of autoimmune encephalitis.
- Published in:
- 2014
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- Publication type:
- Letter
Septo-optic dysplasia plus bilateral perisylvian polymicrogyria: a case report.
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- 2013
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- Publication type:
- Letter
Migraine attack triggering a generalised seizure: is this a case of migralepsy or ictal epileptic headache?
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- 2012
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- Publication type:
- Letter
Association study between four polymorphisms in the HFE, TF and TFR genes and Parkinson's disease in Southern Italy.
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- Neurological Sciences, 2011, v. 32, n. 3, p. 525, doi. 10.1007/s10072-011-0504-9
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- Publication type:
- Article
Presenilin-2 gene mutation presenting as Lewy Body dementia?
- Published in:
- 2011
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- Publication type:
- Letter
Synovial sarcoma diagnosis on fine needle cytology sample confirmed by fluorescence in situ hybridisation.
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- Cytopathology, 2019, v. 30, n. 3, p. 314, doi. 10.1111/cyt.12651
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- Publication type:
- Article
Structural network alterations in focal and generalized epilepsy assessed in a worldwide ENIGMA study follow axes of epilepsy risk gene expression.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-31730-5
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- Publication type:
- Article
REM-Sleep Behavior Disorder in Patients With Essential Tremor: What Is Its Clinical Significance?
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- Frontiers in Neurology, 2019, p. N.PAG, doi. 10.3389/fneur.2019.00315
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- Publication type:
- Article
Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsy.
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- 2022
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- Publication type:
- journal article
Homozygous STXBP1 variant causes encephalopathy and gain-of-function in synaptic transmission.
- Published in:
- 2020
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- Publication type:
- journal article
Kufs disease due to mutation of CLN6: clinical, pathological and molecular genetic features.
- Published in:
- 2019
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- Publication type:
- journal article
PRRT2 controls neuronal excitability by negatively modulating Na+ channel 1.2/1.6 activity.
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- 2018
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- Publication type:
- journal article
DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy.
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- Epilepsia (Series 4), 2015, v. 56, n. 10, p. e168, doi. 10.1111/epi.13094
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- Publication type:
- Article
Letter: Beyond and within CA1 subfield in magnetic resonance imaging negative temporal lobe epilepsy.
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- Epilepsia (Series 4), 2015, v. 56, n. 9, p. 1471, doi. 10.1111/epi.13069
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- Publication type:
- Article
Why should we change the term psychogenic nonepileptic seizures?
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- Epilepsia (Series 4), 2015, v. 56, n. 7, p. 1178, doi. 10.1111/epi.13014
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- Publication type:
- Article
White matter abnormalities differentiate severe from benign temporal lobe epilepsy.
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- Epilepsia (Series 4), 2015, v. 56, n. 7, p. 1109, doi. 10.1111/epi.13027
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- Publication type:
- Article
No evidence of a role for cystatin B gene in juvenile myoclonic epilepsy.
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- Epilepsia (Series 4), 2015, v. 56, n. 4, p. e40, doi. 10.1111/epi.12944
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- Publication type:
- Article
Mild Lafora disease: Clinical, neurophysiologic, and genetic findings.
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- Epilepsia (Series 4), 2014, v. 55, n. 12, p. e129, doi. 10.1111/epi.12806
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- Publication type:
- Article
Thalamotemporal impairment in benign temporal lobe epilepsy: Same hypotheses?
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- Epilepsia (Series 4), 2014, v. 55, n. 6, p. 944, doi. 10.1111/epi.12636
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- Publication type:
- Article
Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations.
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- Epilepsia (Series 4), 2013, v. 54, n. 7, p. 1288, doi. 10.1111/epi.12194
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- Publication type:
- Article
Divergent effects of the T1174S SCN1A mutation associated with seizures and hemiplegic migraine.
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- Epilepsia (Series 4), 2013, v. 54, n. 5, p. 927, doi. 10.1111/epi.12123
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- Publication type:
- Article
Homozygous c.649dupC mutation in PRRT2 worsens the BFIS/PKD phenotype with mental retardation, episodic ataxia, and absences.
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- Epilepsia (Series 4), 2012, v. 53, n. 12, p. e196, doi. 10.1111/epi.12009
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- Publication type:
- Article
Neuroanatomic correlates of psychogenic nonepileptic seizures: A cortical thickness and VBM study.
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- Epilepsia (Series 4), 2012, v. 53, n. 2, p. 377, doi. 10.1111/j.1528-1167.2011.03347.x
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- Publication type:
- Article
Clinical and neurophysiologic features of progressive myoclonus epilepsy without renal failure caused by SCARB2 mutations.
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- Epilepsia (Series 4), 2011, v. 52, n. 12, p. 2356, doi. 10.1111/j.1528-1167.2011.03307.x
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- Publication type:
- Article
A functional polymorphism in the SCN1A gene does not influence antiepileptic drug responsiveness in Italian patients with focal epilepsy.
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- Epilepsia (Series 4), 2011, v. 52, n. 5, p. e40, doi. 10.1111/j.1528-1167.2011.03097.x
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- Publication type:
- Article
Neocortical thinning in 'benign' mesial temporal lobe epilepsy.
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- Epilepsia (Series 4), 2011, v. 52, n. 4, p. 712, doi. 10.1111/j.1528-1167.2011.03038.x
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- Publication type:
- Article
Voxel-based morphometry of sporadic epileptic patients with mesiotemporal sclerosis.
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- Epilepsia (Series 4), 2010, v. 51, n. 4, p. 506, doi. 10.1111/j.1528-1167.2009.02310.x
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- Publication type:
- Article
Characteristics of a large population of patients with refractory epilepsy attending tertiary referral centers in Italy.
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- Epilepsia (Series 4), 2010, v. 51, n. 5, p. 921, doi. 10.1111/j.1528-1167.2009.02512.x
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- Publication type:
- Article
Benign temporal lobe epilepsy.
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- Epilepsia (Series 4), 2010, v. 51, p. 45, doi. 10.1111/j.1528-1167.2009.02444.x
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- Publication type:
- Article
Eyelid fluttering, typical EEG pattern, and impaired intellectual function: A homogeneous epileptic condition among the patients presenting with eyelid myoclonia.
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- Epilepsia (Series 4), 2009, v. 50, n. 6, p. 1536, doi. 10.1111/j.1528-1167.2008.02002.x
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- Publication type:
- Article
Familial mesial temporal lobe epilepsies: Clinical and genetic features.
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- Epilepsia (Series 4), 2009, v. 50, p. 55, doi. 10.1111/j.1528-1167.2009.02123.x
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- Publication type:
- Article
Clinical spectrum of SCN1A mutations.
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- Epilepsia (Series 4), 2009, v. 50, p. 20, doi. 10.1111/j.1528-1167.2009.02115.x
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- Publication type:
- Article
Prognostic factors in patients with mesial temporal lobe epilepsy.
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- Epilepsia (Series 4), 2009, v. 50, p. 41, doi. 10.1111/j.1528-1167.2008.01969.x
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- Publication type:
- Article