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Reply: Infections and Stiff‐Person Spectrum Disorders.
- Published in:
- Movement Disorders Clinical Practice, 2024, v. 11, n. 5, p. 592, doi. 10.1002/mdc3.14002
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- Publication type:
- Article
Glycine Receptor Antibody‐Associated Progressive Encephalomyelitis with Rigidity and Myoclonus (PERM) During SARS‐CoV‐2 Infection: a Video‐Case Report.
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- Movement Disorders Clinical Practice, 2023, v. 10, n. 5, p. 824, doi. 10.1002/mdc3.13712
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- Publication type:
- Article
Movement Disorders Associated with GABA<sub>A</sub> Receptor Encephalitis: A Video Case Report.
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- Movement Disorders Clinical Practice, 2020, v. 7, n. 6, p. 681, doi. 10.1002/mdc3.12987
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- Publication type:
- Article
Nonmotor Symptoms in Dopa-Responsive Dystonia.
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- Movement Disorders Clinical Practice, 2015, v. 2, n. 4, p. 347, doi. 10.1002/mdc3.12211
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- Publication type:
- Article
Bibrachial amyotrophy as a rare manifestation of intraspinal fluid collection: a case report and systematic review.
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- Neurological Sciences, 2024, v. 45, n. 5, p. 2279, doi. 10.1007/s10072-023-07170-4
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- Publication type:
- Article
Cannabinoids for painful dystonia in corticobasal syndrome: a report of three patients.
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- Neurological Sciences, 2023, v. 44, n. 8, p. 2957, doi. 10.1007/s10072-023-06804-x
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- Publication type:
- Article
Clinical characteristics of a large cohort of patients with narcolepsy candidate for pitolisant: a cross-sectional study from the Italian PASS Wakix® Cohort.
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- 2022
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- Publication type:
- journal article
GABAA receptor and anti-titin antibody encephalitis in a patient with thymoma.
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- Neurological Sciences, 2022, v. 43, n. 9, p. 5633, doi. 10.1007/s10072-022-06186-6
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- Publication type:
- Article
Multiple sclerosis in patients with hereditary spastic paraplegia: a case report and systematic review.
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- Neurological Sciences, 2022, v. 43, n. 9, p. 5501, doi. 10.1007/s10072-022-06145-1
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- Publication type:
- Article
Benefit and danger from immunotherapy in myasthenia gravis.
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- Neurological Sciences, 2021, v. 42, n. 4, p. 1367, doi. 10.1007/s10072-021-05077-6
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- Publication type:
- Article
Exacerbation of myasthenia gravis after amoxicillin therapy: a case series.
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- Neurological Sciences, 2020, v. 41, n. 8, p. 2255, doi. 10.1007/s10072-020-04387-5
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- Publication type:
- Article
Effects on cognition of 20-day anodal transcranial direct current stimulation over the left dorsolateral prefrontal cortex in patients affected by mild cognitive impairment: a case-control study.
- Published in:
- 2019
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- Publication type:
- journal article
Italian recommendations for the diagnosis and treatment of myasthenia gravis.
- Published in:
- 2019
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- Publication type:
- journal article
Italian recommendations for diagnosis and management of congenital myasthenic syndromes.
- Published in:
- 2019
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- Publication type:
- journal article
Human figure drawing distinguishes Alzheimer's patients: a cognitive screening test study.
- Published in:
- Neurological Sciences, 2018, v. 39, n. 5, p. 851, doi. 10.1007/s10072-018-3288-3
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- Publication type:
- Article
Heterogeneity in ALSFRS-R decline and survival: a population-based study in Italy.
- Published in:
- 2015
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- Publication type:
- journal article
Quality of life in patients with craniocervical dystonia: Italian validation of the "Cervical Dystonia Impact Profile (CDIP-58)" and the "Craniocervical Dystonia Questionnaire (CDQ-24)".
- Published in:
- 2014
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- Publication type:
- journal article
Quality of life in patients with craniocervical dystonia: Italian validation of the 'Cervical Dystonia Impact Profile (CDIP-58)' and the 'Craniocervical Dystonia Questionnaire (CDQ-24)'.
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- Neurological Sciences, 2014, v. 35, n. 7, p. 1053, doi. 10.1007/s10072-014-1642-7
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- Publication type:
- Article
Somatic and autonomic small fiber neuropathy induced by bortezomib therapy: an immunofluorescence study.
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- 2011
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- Publication type:
- Letter
Idiopathic central sleep apnoea syndrome treated with zolpidem.
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- Neurological Sciences, 2008, v. 29, n. 5, p. 355, doi. 10.1007/s10072-008-0995-1
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- Publication type:
- Article
Broadening the Spectrum of Adulthood X-Linked Adrenoleukodystrophy: A Report of Two Atypical Cases.
- Published in:
- 2019
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- Publication type:
- Case Study
Plasma and CSF Neurofilament Light Chain in Amyotrophic Lateral Sclerosis: A Cross-Sectional and Longitudinal Study.
- Published in:
- Frontiers in Aging Neuroscience, 2021, v. 13, p. 1, doi. 10.3389/fnagi.2021.753242
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- Publication type:
- Article
Homozygous NOTCH3 null mutation and impaired NOTCH3 signaling in recessive early-onset arteriopathy and cavitating leukoencephalopathy.
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- EMBO Molecular Medicine, 2015, v. 7, n. 6, p. 848, doi. 10.15252/emmm.201404399
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- Publication type:
- Article
The empowerment of translational research: lessons from laminopathies.
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- 2012
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- Publication type:
- Letter
The empowerment of translational research: lessons from laminopathies.
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- Orphanet Journal of Rare Diseases, 2012, v. 7, n. 1, p. 37, doi. 10.1186/1750-1172-7-37
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- Publication type:
- Article
Phosphorylated α-synuclein in skin Schwann cells: a new biomarker for multiple system atrophy.
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- Brain: A Journal of Neurology, 2023, v. 146, n. 3, p. 1065, doi. 10.1093/brain/awac124
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- Publication type:
- Article
Behaviour and neuropathology in mice injected with human contactin-associated protein 2 antibodies.
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- 2019
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- Publication type:
- journal article
DGUOK recessive mutations in patients with CPEO, mitochondrial myopathy, parkinsonism and mtDNA deletions.
- Published in:
- 2018
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- Publication type:
- Letter
The spectrum of REM sleep-related episodes in children with type 1 narcolepsy.
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- Brain: A Journal of Neurology, 2017, v. 140, n. 6, p. 1669, doi. 10.1093/brain/awx096
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- Publication type:
- Article
The spectrum of REM sleep-related episodes in children with type 1 narcolepsy.
- Published in:
- 2017
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- Publication type:
- journal article
Reply: Both mitochondrial DNA and mitonuclear gene mutations cause hearing loss through cochlear dysfunction.
- Published in:
- 2016
- By:
- Publication type:
- Letter
ALDH18A1 gene mutations cause dominant spastic paraplegia SPG9: loss of function effect and plausibility of a dominant negative mechanism.
- Published in:
- 2016
- By:
- Publication type:
- Letter
OPA1-related auditory neuropathy: site of lesion and outcome of cochlear implantation.
- Published in:
- 2015
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- Publication type:
- journal article
Multimodal evaluation of the melanopsin retinal ganglion cells system in relation to circadian rhythms in Alzheimer's disease and aging.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2021, v. 17, p. 1, doi. 10.1002/alz.052286
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- Publication type:
- Article
A novel pedigree with familial cortical myoclonic tremor and epilepsy ( FCMTE): Clinical characterization, refinement of the FCMTE2 locus, and confirmation of a founder haplotype.
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- Epilepsia (Series 4), 2013, v. 54, n. 7, p. 1298, doi. 10.1111/epi.12216
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- Publication type:
- Article
Autosomal Dominant Early-onset Cortical Myoclonus, Photic-induced Myoclonus, and Epilepsy in a Large Pedigree.
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- Epilepsia (Series 4), 2006, v. 47, n. 10, p. 1643, doi. 10.1111/j.1528-1167.2006.00636.x
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- Publication type:
- Article
Iodine-123 Metaiodobenzylguanidine Scintigraphy and Iodine-123 Ioflupane Single Photon Emission Computed Tomography in Lewy Body Diseases: Complementary or Alternative Techniques?
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- Journal of Neuroimaging, 2014, v. 24, n. 2, p. 149, doi. 10.1111/j.1552-6569.2012.00774.x
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- Publication type:
- Article
Diagnostic and Prognostic Value of Conventional Brain MRI in the Clinical Work-Up of Patients with Amyotrophic Lateral Sclerosis.
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- Journal of Clinical Medicine, 2020, v. 9, n. 8, p. 2538, doi. 10.3390/jcm9082538
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- Publication type:
- Article
Progressive Ataxia and Palatal Tremor Is Not Associated with IgLON5 Antibodies: Results From Two Cases.
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- 2024
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- Publication type:
- Case Study
Insight into Elderly ALS Patients in the Emilia Romagna Region: Epidemiological and Clinical Features of Late-Onset ALS in a Prospective, Population-Based Study.
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- Life (2075-1729), 2023, v. 13, n. 4, p. 942, doi. 10.3390/life13040942
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- Publication type:
- Article
Reviewing the Clinical Implications of Treating Narcolepsy as an Autoimmune Disorder.
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- Nature & Science of Sleep, 2021, v. 13, p. 557, doi. 10.2147/NSS.S275931
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- Publication type:
- Article
Neurological Manifestations of Long COVID: A Single-Center One-Year Experience.
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- Neuropsychiatric Disease & Treatment, 2023, v. 19, p. 311, doi. 10.2147/NDT.S387501
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- Publication type:
- Article
Pain in Fabry Disease: Practical Recommendations for Diagnosis and Treatment.
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- CNS Neuroscience & Therapeutics, 2016, v. 22, n. 7, p. 568, doi. 10.1111/cns.12542
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- Publication type:
- Article
Pseudomyotonia in Romagnola cattle caused by novel ATP2A1 mutations.
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- BMC Veterinary Research, 2012, v. 8, n. 1, p. 186, doi. 10.1186/1746-6148-8-186
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- Publication type:
- Article
Motor unit number estimation via MScanFit MUNE in spinal muscular atrophy.
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- Muscle & Nerve, 2024, v. 70, n. 1, p. 71, doi. 10.1002/mus.28091
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- Publication type:
- Article
Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber’s hereditary optic neuropathy.
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- PLoS Genetics, 2018, v. 14, n. 2, p. 1, doi. 10.1371/journal.pgen.1007210
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- Publication type:
- Article
Cognitive Rehabilitation and Transcranial Direct Current Stimulation in a Patient with Posterior Cortical Atrophy: An fMRI Study.
- Published in:
- 2018
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- Publication type:
- Case Study
Pain Related Channels Are Differentially Expressed in Neuronal and Non-Neuronal Cells of Glabrous Skin of Fabry Knockout Male Mice.
- Published in:
- PLoS ONE, 2014, v. 9, n. 10, p. 1, doi. 10.1371/journal.pone.0108641
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- Publication type:
- Article
A Novel Null Homozygous Mutation Confirms<i>CACNA2D2</i> as a Gene Mutated in Epileptic Encephalopathy.
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- PLoS ONE, 2013, v. 8, n. 12, p. 1, doi. 10.1371/journal.pone.0082154
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- Publication type:
- Article
Rare Primary Mitochondrial DNA Mutations and Probable Synergistic Variants in Leber's Hereditary Optic Neuropathy.
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- PLoS ONE, 2012, v. 7, n. 8, p. 1, doi. 10.1371/journal.pone.0042242
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- Publication type:
- Article