Clinicopathologic Conference, Granulomatosis with Polyangiitis
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Updates on Sturge-Weber Syndrome
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Behcet Disease
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Neuropsychiatric Involvement of Behcets Disease
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Clinical Manifestations, Pathologic Features, and Diagnosis of Langerhans Cell Histiocytosis
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Cerebral Sinus Thrombosis in Scleroderma
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Diagnosis and Management of Cerebral Venous Thrombosis: A Statement for Healthcare Professionals From the American Heart Association/American Stroke Association
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Clinical Characteristics of Pediatric-onset Neuro-Behcet Disease
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Skin Lesion with a Fatal Neurologic Outcome (Degos'Disease)
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Neurologic Aspects of Inflammatory Bowel Disease
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Clinicopathological Conference
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Blue Rubber Bleb Nevus Syndrome with CNS Involvement & Thrombosis of a Vein of Galen Malformation
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Neurological Complications of Wegener's Granulomatosis
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A 60-Year Old Man with Asymmetric Weakness and Persistent Fever
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Clinicopathologic Conference, Encephalitis due to Behcets Disease
NEJM 387:925-933, Case 27-2022, 2022
The Boston Criteria Version 2.0 for Cerebral Amylois Angiopathy:A Multicentre, Retrospective, MRI-Neuropathology Diagnostic Accuracy Study
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Sweet Syndrome
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Clinicopathologic Conference, Systemic Primary Amyloidosis
NEJM 384:363-372, Case 3-2021, 2021
A 13-Year-Old Boy with Subacute-Onset Spastic Gait
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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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Central Nervous System Involvement in Erdheim-Chester Disease
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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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Progressive Neurological Impairment and an Enhancing Brainstem Lesion in a Middle-Aged Man
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Diagnosis and Management of the Antiphospholipid Syndrome
NEJM 378:2010-2021, Garcia, D. & Erkan, D., 2018
Diagnostic Challenges in a Young Patient with Hypereosinophilia
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A Young Woman with Blurred Vision and Distal Paresthesias
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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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The Myositis Autoantibody Phenotypes of the Juvenile Idiopathic Inflammatory Myopathies
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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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Gradient Echo T2*-weighted Magnetic Resonance Imaging Revealing Cerebral Microbleeds in a Patient with Microscopic Polyangiitis Complicated by Cerebrovascular Disease
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Beh�et Disease: Evolution of Clincal Manifestations
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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
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A Hereditary Moyamoya Syndrome With Multisystemic Manifestations
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Clinicopath Conf, Neuro-Behcets Disease
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Clinicopath Conf., Atypical Hemolytic-Uremic Syndrome
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Sarcoidosis
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Multiple Bilateral Non-Hemorrhagic Cerebral Infarctions Associated with Microscopic Polyangiitis
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Nervous system dysfunction in Henoch-Schonlein Syndrome: Systematic review of the Literature
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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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