Differential Diagnosis of Bilateral Abnormalities of the Basal Ganglia and Thalamus
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Essential Tremor Cured by Infarction Adjacent to the Thalamus
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Catecholamines & Neurologic Diseases
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Systematic Genetic Assessment in Young Patients with Cryptogenic Stroke: The ES-EASY Project
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Multivessel Cerebral Occlusion in Noonan Syndrome
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A 50-YEar-Old Man with Intracerebral Hemorrhage and Tortuous Retinal Arterioles
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RNF213 Polymorphisms in Intracranial Artery Dissection
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Neurologic Manifestations of Hyperthyroidism and Graves Disease
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Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
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Neonatal Seizures
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Hereditary Hemorrhagic Telangiectasia, Clinical Presentations, and Management
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Clinicopathologic Conference, Vascular Ehlers-Danlos Syndrome
NEJM 385:1317-1325, Case 30-2021, 2021
Symptomatic Isolated Tongue Tremor of Cortical Origin Due to Stroke
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Recurrent Cerebral Ischemia During Pregnancies
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Acute Cortical Lesions in MELAS Syndrome: Anatomic Distribution, Symmetry, and Evolution
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A 14-Year-Old Girl with Headache, Seizures, and Confusion
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Sudden-Onset Pulsatile Headache in a Previously Healthy Young Man
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Holmes Tremor
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A 44-Year-Old Man with Eye, Kidney, and Brain Dysfunction
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Spontaneous Limb Withdrawal Heralding Hyperacute Stroke or Stroke Worsening
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Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency
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Holmes Tremor
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Mystery Case: A 21-Year-Old Man with Visual Loss Following Marijuana Use
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Percutaneous Left Atrial Appendage Closure:Technical Aspects and Prevention of Periprocedural Complications with the Watchman Device
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Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
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Disorders of the Nervous System Caused by Drugs, Toxins, and Chemical Agents, Cocaine
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Vertebral Artery Dissection in Patients with Autosomal Dominant Polycystic Kidney Disease
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The Cerebral Autosomal-Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) Scale
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An unusual cause of stroke and hypoxia
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Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome)
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Comparison of Clinical, Familial, and MRI Features of CADASIL and NOTCH3-Negative Patients
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Familial Mediterranean Fever and Central Nervous System Involvement: A Case Series
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Clinicopath Conf, Intravascular Large-B-Cell Lympoma
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A Hereditary Moyamoya Syndrome With Multisystemic Manifestations
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Pediatric Moyamoya Disease: An Analysis of 410 Consecutive Cases
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Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease
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Genomewide Association Studies of Stroke
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Clinicopath Conf, Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL)
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Bilateral Thalamic Lesions
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Decoding Cryptogenic Cardioembolism
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Pulmonary Arteriovenous Malformations in Hereditary Hemorrhagic Telangiectasia: A Series of 126 Patients
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Differential Diagnosis of Bilateral Thalamic Lesions
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Prevalence of Fabry Disease in Patients with Cryptogenic Stroke: A Prospective Study
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Metabolic Disease and Stroke: MELAS
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Migraine and Cerebral White Matter Lesions
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Phaeochromocytoma
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Neurologic Features of Horizontal Gaze Palsy and Progressive Scoliosis with Mutations in ROBO3
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Neurobrucellosis:Clinical and Neuroimaging Correlation
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Post-Stroke Movement Disorders; Report of 56 Patients
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