Works matching IS 23301619 AND DT 2021 AND VI 8 AND IP 3
Results: 34
Sex Differences in Huntington's Disease: Evaluating the Enroll‐HD Database.
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 420, doi. 10.1002/mdc3.13178
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Driving with Tic Disorders: An International Survey of Lived Experiences.
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 412, doi. 10.1002/mdc3.13177
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β‐Blocker–Induced Tremor.
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 449, doi. 10.1002/mdc3.13176
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It Is Time to Define Huntington's Disease Onset more Clearly.
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 493, doi. 10.1002/mdc3.13174
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Clinical and Imaging Profile of Patients with Palatal Tremor.
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 435, doi. 10.1002/mdc3.13173
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Are Antibody Panels Under‐Utilized in Movement Disorders Diagnosis? No.
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 347, doi. 10.1002/mdc3.13172
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Are Antibody Panels Under‐Utilized in Movement Disorders Diagnosis? Yes.
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 341, doi. 10.1002/mdc3.13171
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A Self‐Reported Clinical Tool Predicts Falls in People with Parkinson's Disease.
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 427, doi. 10.1002/mdc3.13170
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Foot‐Hand Synkinesis in Corticobasal Syndrome: Single Clinical Feature with Distinct Molecular Imaging Biomarkers.
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 491, doi. 10.1002/mdc3.13169
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Might it Be Possible to Assess Rigidity in PD Patients Remotely?
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 489, doi. 10.1002/mdc3.13167
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Neuronuclear and Neuromelanin‐Sensitive Imaging for Acquired Hepatocerebral Degeneration with Parkinsonism.
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 464, doi. 10.1002/mdc3.13166
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Challenges in Clinicogenetic Correlations: One Gene – Many Phenotypes.
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 299, doi. 10.1002/mdc3.13165
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Diagonistic Dyspraxia and Apraxia in NMDA Encephalitis: A Rare Etiology.
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 474, doi. 10.1002/mdc3.13164
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Challenges in Clinicogenetic Correlations: One Phenotype – Many Genes.
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 311, doi. 10.1002/mdc3.13163
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Reckless Generosity, Parkinson's Disease and Dopamine: A Case Series and Literature Review.
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 469, doi. 10.1002/mdc3.13156
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Bullous Pemphigoid Associated with Multiple System Atrophy: Case Series.
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 445, doi. 10.1002/mdc3.13160
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Persistence of Facio‐Skeletal Myorhythmia During Sleep in anti‐IgLON5 Disease.
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 460, doi. 10.1002/mdc3.13159
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Laboratory‐Supported Multiple System Atrophy beyond Autonomic Function Testing and Imaging: A Systematic Review by the MoDiMSA Study Group.
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 322, doi. 10.1002/mdc3.13158
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Severe Acute Respiratory Syndrome Coronavirus 2, Olfactory Mucosa, and the Entrance in the Central Nervous System: Expanding the Evidence?
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 350, doi. 10.1002/mdc3.13157
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Reappearance of Symptoms after GPi‐DBS Discontinuation in Cervical Dystonia.
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 406, doi. 10.1002/mdc3.13162
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Striatal Atrophy and Hypometabolism in Drug‐Resistant Non‐Ketotic Hyperglycemic Chorea‐Ballism.
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 486, doi. 10.1002/mdc3.13155
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Advanced Therapies for the Management of Dopamine Dysregulation Syndrome in Parkinson's Disease.
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 400, doi. 10.1002/mdc3.13154
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Intraventricular Baclofen Following Deep Brain Stimulation in a Child with Refractory Status Dystonicus.
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 456, doi. 10.1002/mdc3.13153
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Anti‐NMDA Receptor Encephalitis Associated with Coats‐Like Retinal Telangiectasia.
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 483, doi. 10.1002/mdc3.13152
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Neuropsychiatric Symptoms Are Associated with Dementia in Parkinson's Disease but Not Predictive of it.
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 390, doi. 10.1002/mdc3.13151
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Exploring Interrater Disagreement on Essential Tremor Using a Standardized Tremor Elements Assessment.
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 371, doi. 10.1002/mdc3.13150
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Brainstem Reflexes in Idiopathic Cervical Dystonia: Does Medullary Dysfunction Play a Role?
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 377, doi. 10.1002/mdc3.13149
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Disease Onset in Huntington's Disease: When Is the Conversion?
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 352, doi. 10.1002/mdc3.13148
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Multidimensional Apathy: The Utility of the Dimensional Apathy Scale in Huntington's Disease.
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 361, doi. 10.1002/mdc3.13147
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Fracture Risk Assessment in Atypical Parkinsonian Syndromes.
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 385, doi. 10.1002/mdc3.13146
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Brain Calcification in a Young Adult with Abnormal Copper Metabolism.
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 476, doi. 10.1002/mdc3.13145
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Novel Mutation in the TSFM Gene Causes an Early‐Onset Complex Chorea without Basal Ganglia Lesions.
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 453, doi. 10.1002/mdc3.13144
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Dystonia and Hereditary Motor Sensory Neuropathy 6B Due to SLC25A46 Gene Mutations.
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- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 480, doi. 10.1002/mdc3.13139
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- Article
Issue Information.
- Published in:
- Movement Disorders Clinical Practice, 2021, v. 8, n. 3, p. 293, doi. 10.1002/mdc3.12979
- Publication type:
- Article