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Tourette Syndrome and Other Tic Disorders, Diagnosis, Pathophysiology, and Treatment
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Tourette's Syndrome:Current Concepts
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Transient Tic Disorder and the Spectrum of Tourette's Syndrome
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Tourette Syndrome
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A Rating Scale for Gilles de la Tourette's Syndrome:Description, Reliability, & Validity Data
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The Inheritance of Gilles De La Tourette's Syndrome & Associated Behaviors
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Gilles de la Tourette's Syndrome, A Review of Clinical, Research & Future Directions for Investigation
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Familial Tourette Syndrome
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Tics & Tourette's:A Continuum of Symptoms
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Purine Phosphoribosyltransferase in Gilles de la Tourette Syndrome
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Dentate Update: Imaging Features of Entities that Affect the Dentate Nucleus
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Brain Arteriovenous Malformation Multiplicity Predicts the Diagnosis of Hereditary Hemorrhagic Telangiectasia Quantitive Assessment
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Adrenoleukodystrophy
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Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL)
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A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
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Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients
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Multiple-System Atrophy is Genet Distinct from Ident Inherited Causes of Spinocerebellar Degen
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Clin Electrophy & Molec Correl in 13 Families with Hered Neurop with Liabil to Press Palsies & Chromosome 17p11. 2 Deletion
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Inherited Primary Peripheral Neuropathies
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Hematologic Disorders and Ischemic Stroke
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Clinicopathological Conference
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Sclerosteosis:Neurogenetic & Pathophysiologic Analysis of an American Kinship
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Systematic Genetic Assessment in Young Patients with Cryptogenic Stroke: The ES-EASY Project
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A 57-Year-Old Man With Chronic Gait Unsteadiness and Diminished Lower Extremity Sensation
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Rapidly Progressive Frontotemporal Dementia with Amytrophic Lateral Sclerosis in an Elderly Female
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Clinodactyly as a Key Finding in Distal Spinal Muscular Atrophy
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Unmasking Cerebrotendinous Xanthomatosis, Clinical Recognition of a Treatable Cause of Progressive Ataxia
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A 10-Year-Old Boy with Progressive Tremor, Insomnia and Autonomic Dysfunction
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Multivessel Cerebral Occlusion in Noonan Syndrome
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A 26-Year-Old Woman with Chronic Progressive Gait Dysfunction
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Genome Sequencing in the NICU and PICU is Here to Stay
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A 35-Year-Old Woman with Personality Change and Gait Impairment
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A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium
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Neonatal Seizures
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Multicenter Consensus Approach to Evaluation of Neonatal Hypotonia in the Genomic Era
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More Than a Little Unsteady
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Amyotrophic Lateral Sclerosis
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Spinal Muscular Atrophy
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The Phenotypic Continuum of ATP1A3-Related Disorders
Neurol 99:e1511-e1526, Vezyroglou,A., et al, 2022
A Middle-aged Woman with Severe Scoliosis and Encephalopathy
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Alzheimers Disease
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Imaging Patterns Characterizing Mitochondrial Leukodystrophies
AJNR 42:1334-1340, Roosendaal, S.D.,et al, 2021
Clinicopathologic Conference, Vascular Ehlers-Danlos Syndrome
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Duchenne Muscular Dystrophy
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