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Autoimmune Encephalopathy
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The Neurological Masquerade of Intravascular Lymphomatosis
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Neurologic IgG4-Related Disease
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Neurologic Presentation of Whipple Disease
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Neuroradiologic Aspects of Chester-Erdheim Disease
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A Hereditary Moyamoya Syndrome With Multisystemic Manifestations
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A 60-Year Old Man with Asymmetric Weakness and Persistent Fever
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Clinicopathologic Conference, Granulomatosis with Polyangiitis
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The Boston Criteria Version 2.0 for Cerebral Amylois Angiopathy:A Multicentre, Retrospective, MRI-Neuropathology Diagnostic Accuracy Study
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Clinicopathologic Conference, Systemic Primary Amyloidosis
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A 13-Year-Old Boy with Subacute-Onset Spastic Gait
JAMA Neurol 78:e1-e2, Xie, N.,et al, 2021
Vitamin B12 Deficiency in a 29-Year-Old Woman
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A 47-year-old Man with Rapidly Progressive Ataxia and Vitiligo
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A 22-Year-Old Man with Progressive Bilateral Visual Loss
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Sensory Ganglionopathy
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Central Nervous System Involvement in Erdheim-Chester Disease
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Fat Embolism Syndrome in Sickle Cell Disease
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Diagnosis and Management of the Antiphospholipid Syndrome
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Behcet Disease
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Diagnostic Challenges in a Young Patient with Hypereosinophilia
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Neuropsychiatric Involvement of Behcets Disease
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Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Whipple Disease
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Neurologic Complications Associated with Sjogrens Disease: Case Reports and Modern Pathogenic Dilemma
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A 62-Yeal-Old Man with Fluctuating Neurological Deficits and Skin Lesions
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Central Nervous System Involvement in Whipple Disease
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Mycoplasma Pneumoniae Infection: Neurologic Complications
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CNS-Immune Reconstitution Inflammatory Syndrome in the Setting of HIV Infection, Part 1: Overview and Discussion of Progressive Multifocal Leukoencephalopathy-Immune Reconstitution Inflammatory Syndrome and Cryptococcal-Immune Reconstitution Inflammatory Syndrome
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Primary Sjogren Syndrome
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Neurologic Manifestations of E Coli infection - induced Hemolytic-Uremic Syndrome in Adults
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Cerebral Sinus Thrombosis in Scleroderma
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Treatment of Severe Neurological Deficits with IgG Depletion through Immunoadsorption in Patients with Escherichia coli O104:H4-Associated Haemolytic Uraemic Syndrome: A Prospective Trial
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Clinical Characteristics of Pediatric-onset Neuro-Behcet Disease
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