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Updates on Sturge-Weber Syndrome
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Central Nervous System Involvement in Erdheim-Chester Disease
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Behcet Disease
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Neuropsychiatric Involvement of Behcets Disease
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Central Nervous System Involvement in Whipple Disease
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The Neurological Masquerade of Intravascular Lymphomatosis
Arch Neurol 59:439-443, Beristain,X.&Azzarelli,B., 2002
Neurologic Presentation of Whipple Disease
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Clinicopathologic Conference, Encephalitis due to Behcets Disease
NEJM 387:925-933, Case 27-2022, 2022
Clinicopathologic Conference, Granulomatosis with Polyangiitis
NEJM 387:1022-1032, Case 28-2022, 2022
The Boston Criteria Version 2.0 for Cerebral Amylois Angiopathy:A Multicentre, Retrospective, MRI-Neuropathology Diagnostic Accuracy Study
Lancet Neurol 21:714-725, Charidimou,A.,et al, 2022
Clinicopathologic Conference, Systemic Primary Amyloidosis
NEJM 384:363-372, Case 3-2021, 2021
Sensory Ganglionopathy
NEJM 383:1657-1662, Amato, A.A. & Ropper, A.H., 2020
Fat Embolism Syndrome in Sickle Cell Disease
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Neurologic IgG4-Related Disease
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Ehlers-Danlos Syndromes
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Diagnosis and Management of the Antiphospholipid Syndrome
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Diagnostic Challenges in a Young Patient with Hypereosinophilia
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Clinical Manifestations, Pathologic Features, and Diagnosis of Langerhans Cell Histiocytosis
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A 62-Yeal-Old Man with Fluctuating Neurological Deficits and Skin Lesions
JAMA Neurol 70:120-124, Konikkara, J.,et al, 2013
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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Neurologic Manifestations of E Coli infection - induced Hemolytic-Uremic Syndrome in Adults
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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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Autoimmune Encephalopathy
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Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
Brain 134:3326-3332, Garone, C.,et al, 2011
Periarteritis Nodosa
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Clinicopath Conf, Neuro-Behcets Disease
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Pituitary and Stalk Lesions (Infundibulo-Hypophysitis) Associated with Immunoglobulin G4-related Systemic Disease: an Emerging Clinical Entity
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Whipples Disease
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Clinical Spectrum of Chronic Acquired Demyelinating Polyneuropathies
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Diagnosis and Treatment of Intravascular Lymphomatosis
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Dystonia and Chorea in Acquired Systemic Disorders
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Small-Vessel Vasculitis
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A 60-Year Old Man with Asymmetric Weakness and Persistent Fever
Neurol 100:530-536, Zheng,Y.,et al, 2023
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 22-Year-Old Man with Progressive Bilateral Visual Loss
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Progressive Neurological Impairment and an Enhancing Brainstem Lesion in a Middle-Aged Man
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A Young Woman with Blurred Vision and Distal Paresthesias
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Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Whipple Disease
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Primary Sjogren Syndrome
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Gradient Echo T2*-weighted Magnetic Resonance Imaging Revealing Cerebral Microbleeds in a Patient with Microscopic Polyangiitis Complicated by Cerebrovascular Disease
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Cerebral Sinus Thrombosis in Scleroderma
Acta Med Iran 50:288-291, Fard, M.P. & Magham, S.K., 2012
Clinical Characteristics of Pediatric-onset Neuro-Behcet Disease
Neurol 77:1900-1905, Uludiz, D.,et al, 2011
A Hereditary Moyamoya Syndrome With Multisystemic Manifestations
Neurol 75:259-264, Herv�,D., et al, 2010
Cogan Syndrome
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Clinicopath Conf., Atypical Hemolytic-Uremic Syndrome
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Sarcoidosis
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