Found: 40
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Restless Legs Syndrome: Known Knowns and Known Unknowns.
- Published in:
- Brain Sciences (2076-3425), 2022, v. 12, n. 1, p. 118, doi. 10.3390/brainsci12010118
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- Publication type:
- Article
Gross Motor Function in Pediatric Onset TUBB4A -Related Leukodystrophy: GMFM-88 Performance and Validation of GMFC-MLD in TUBB4A.
- Published in:
- Journal of Child Neurology, 2023, v. 38, n. 8/9, p. 498, doi. 10.1177/08830738231188159
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- Publication type:
- Article
Pathophysiology of Motor Dysfunction in Parkinson’s Disease as the Rationale for Drug Treatment and Rehabilitation.
- Published in:
- Parkinson's Disease (20420080), 2016, p. 1, doi. 10.1155/2016/9832839
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- Publication type:
- Article
The Italian Consensus Conference on Pain in Neurorehabilitation: rationale and methodology.
- Published in:
- 2016
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- Publication type:
- Conference Paper
RFC1 expansions are a common cause of idiopathic sensory neuropathy.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Reply: Pentameric repeat expansions: cortical myoclonus or cortical tremor? and Cortical tremor: a tantalizing conundrum between cortex and cerebellum.
- Published in:
- 2020
- By:
- Publication type:
- letter
Unravelling the enigma of cortical tremor and other forms of cortical myoclonus.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Tongue Protrusion and Feeding Dystonia Can Develop in PPP2R2B‐Related Spinocerebellar Ataxia.
- Published in:
- Movement Disorders Clinical Practice, 2024, v. 11, n. 5, p. 578, doi. 10.1002/mdc3.14014
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- Publication type:
- Article
Neuropsychiatric Presentation of Anti‐DPPX Progressive Encephalomyelitis with Rigidity and Myoclonus.
- Published in:
- Movement Disorders Clinical Practice, 2024, v. 11, n. 1, p. 97, doi. 10.1002/mdc3.13928
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- Publication type:
- Article
A Reflection on Motor Overflow, Mirror Phenomena, Synkinesia and Entrainment.
- Published in:
- Movement Disorders Clinical Practice, 2023, v. 10, n. 9, p. 1243, doi. 10.1002/mdc3.13798
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- Publication type:
- Article
Parkinsonism Following SARS‐CoV‐2 Infection Unmasks a Genetic Twist.
- Published in:
- Movement Disorders Clinical Practice, 2023, v. 10, n. 7, p. 1146, doi. 10.1002/mdc3.13785
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- Publication type:
- Article
Presynaptic Hemiparkinsonism Following Cerebral Toxoplasmosis: Case Report and Literature Review.
- Published in:
- Movement Disorders Clinical Practice, 2023, v. 10, n. 2, p. 285, doi. 10.1002/mdc3.13631
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- Publication type:
- Article
Cranial Dystonia as an Isolated Presentation of DJ‐1 Disease: Case Report and Literature Review.
- Published in:
- Movement Disorders Clinical Practice, 2023, v. 10, n. 2, p. 313, doi. 10.1002/mdc3.13591
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- Publication type:
- Article
Childhood-Onset Choreo-Dystonia Due to a Recurrent Novel Homozygous Nonsense HPCA Variant: Case Series and Literature Review.
- Published in:
- Movement Disorders Clinical Practice, 2023, v. 10, n. 1, p. 101, doi. 10.1002/mdc3.13529
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- Publication type:
- Article
Abnormal DaTscan in GM1‐Gangliosidosis Type III Manifesting with Dystonia‐Parkinsonism.
- Published in:
- Movement Disorders Clinical Practice, 2022, v. 9, n. 6, p. 825, doi. 10.1002/mdc3.13512
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- Publication type:
- Article
Breakthrough News in Adenoviral Vector‐Mediated AADC Gene Therapy: Lessons from the Success in AADC Deficiency and Possible Future Applications.
- Published in:
- Movement Disorders Clinical Practice, 2022, v. 9, n. 6, p. 737, doi. 10.1002/mdc3.13503
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- Publication type:
- Article
PRKRAP1 and Other Pseudogenes in Movement Disorders: The Troublemakers in Genetic Analyses Are More Than Genomic Fossils.
- Published in:
- Movement Disorders Clinical Practice, 2022, v. 9, n. 5, p. 698, doi. 10.1002/mdc3.13499
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- Publication type:
- Article
Biallelic Loss‐of‐Function NDUFA12 Variants Cause a Wide Phenotypic Spectrum from Leigh/Leigh‐Like Syndrome to Isolated Optic Atrophy.
- Published in:
- Movement Disorders Clinical Practice, 2022, v. 9, n. 2, p. 218, doi. 10.1002/mdc3.13398
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- Publication type:
- Article
Heterozygous EIF2AK2 Variant Causes Adolescence‐Onset Generalized Dystonia Partially Responsive to DBS.
- Published in:
- Movement Disorders Clinical Practice, 2022, v. 9, n. 2, p. 268, doi. 10.1002/mdc3.13371
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- Publication type:
- Article
Movement Disorders and Liver Disease.
- Published in:
- Movement Disorders Clinical Practice, 2021, v. 8, n. 6, p. 828, doi. 10.1002/mdc3.13238
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- Publication type:
- Article
Throat‐Clearing Vocalizations in Primary Brain Calcification Syndromes.
- Published in:
- Movement Disorders Clinical Practice, 2021, v. 8, n. 4, p. 627, doi. 10.1002/mdc3.13175
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- Publication type:
- Article
Challenges in Clinicogenetic Correlations: One Gene – Many Phenotypes.
- Published in:
- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 299, doi. 10.1002/mdc3.13165
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- Publication type:
- Article
Late‐Onset Chorea in JAK2‐Associated Essential Thrombocythemia.
- Published in:
- Movement Disorders Clinical Practice, 2021, v. 8, n. 1, p. 145, doi. 10.1002/mdc3.13105
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- Publication type:
- Article
Toward an Early Real‐Time Quaking‐Induced Conversion–Based Diagnostic Biomarker for Lewy Body–Related Synucleinopathies.
- Published in:
- Movement Disorders Clinical Practice, 2020, v. 7, n. 7, p. 780, doi. 10.1002/mdc3.13050
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- Publication type:
- Article
Psychiatric Manifestations of ATP13A2 Mutations.
- Published in:
- Movement Disorders Clinical Practice, 2020, v. 7, n. 7, p. 838, doi. 10.1002/mdc3.13034
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- Publication type:
- Article
The Need to Tic.
- Published in:
- Movement Disorders Clinical Practice, 2020, v. 7, n. 7, p. 863, doi. 10.1002/mdc3.13023
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- Publication type:
- Article
Ciliary Dysfunction: The Hairy Explanation of Normal Pressure Hydrocephalus?
- Published in:
- Movement Disorders Clinical Practice, 2020, v. 7, n. 1, p. 30, doi. 10.1002/mdc3.12880
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- Publication type:
- Article
Twelve‐year Follow‐up of A Large Italian Family with Atypical Phenotypes of DYT1‐dystonia.
- Published in:
- Movement Disorders Clinical Practice, 2019, v. 6, n. 2, p. 166, doi. 10.1002/mdc3.12712
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- Publication type:
- Article
Long-Term Response of Neuropathic Pain to Intravenous Immunoglobulin in Relapsing Diabetic Lumbosacral Radiculoplexus Neuropathy. A Case Report.
- Published in:
- Pain Practice, 2014, v. 14, n. 2, p. E85, doi. 10.1111/papr.12133
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- Publication type:
- Article
The Association between Serum Cytokines and Damage to Large and Small Nerve Fibers in Diabetic Peripheral Neuropathy.
- Published in:
- Journal of Diabetes Research, 2015, v. 2015, p. 1, doi. 10.1155/2015/547834
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- Publication type:
- Article
Voxel-based morphometry and task functional magnetic resonance imaging in essential tremor: evidence for a disrupted brain network.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41598-020-69514-w
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- Publication type:
- Article
Effect of 5% Lidocaine Medicated Plaster on Pain Intensity and Paroxysms in Classical Trigeminal Neuralgia.
- Published in:
- Annals of Pharmacotherapy, 2014, v. 48, n. 11, p. 1521, doi. 10.1177/1060028014544166
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- Publication type:
- Article
Detection and Characterization of a De Novo Alu Retrotransposition Event Causing NKX2‐1‐Related Disorder.
- Published in:
- Movement Disorders, 2023, v. 38, n. 2, p. 347, doi. 10.1002/mds.29280
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- Publication type:
- Article
Digging into the Unknowns of the Human Genome Sequence: The T2T‐CHM13 Reference Assembly Release.
- Published in:
- Movement Disorders, 2022, v. 37, n. 11, p. 2192, doi. 10.1002/mds.29235
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- Publication type:
- Article
Reply to: Juvenile PLA2G6‐parkinsonism due to Indian 'Asian' p.R741Q mutation, and response to STN DBS.
- Published in:
- Movement Disorders, 2022, v. 37, n. 3, p. 658, doi. 10.1002/mds.28955
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- Publication type:
- Article
Dissecting the Phenotype and Genotype of PLA2G6-Related Parkinsonism.
- Published in:
- 2022
- By:
- Publication type:
- journal article
X‐Linked Parkinsonism: Phenotypic and Genetic Heterogeneity.
- Published in:
- Movement Disorders, 2021, v. 36, n. 7, p. 1511, doi. 10.1002/mds.28565
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- Publication type:
- Article
Childhood‐Onset Chorea Caused by a Recurrent De Novo DRD2 Variant.
- Published in:
- Movement Disorders, 2021, v. 36, n. 6, p. 1472, doi. 10.1002/mds.28634
- By:
- Publication type:
- Article
Childhood-Onset Chorea Caused by a Recurrent De Novo DRD2 Variant.
- Published in:
- 2021
- By:
- Publication type:
- letter
A 58‐year‐old man with B‐cell chronic lymphocytic leukemia and multiple strokes.
- Published in:
- Brain Pathology, 2021, v. 31, n. 6, p. 1, doi. 10.1111/bpa.13004
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- Publication type:
- Article