Clinicopath Conf, The POEMS Syndrome, with Demyelinating Neuropathy and Solitary Pharmacytoma of Bone
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Acute Arsenic Intoxication Presenting as Guillain-Barre-Like Syndrome:Donofrio
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Neurological Manifestations in Xeroderma Pigmentosum
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Ross Syndrome & Skin Changes
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Recurrent Aseptic Meningitis in an Elderly Male, Unusual Prodromal Manifestation of SLE
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Behcets Syndrome
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Magnetic Resonance Imaging Features of Encephalitis of Scrub Typhus
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A 40-Year-Old Woman Presenting with Encepatholopathy and Paraparesis
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Rare Cause of Hemiparesis and Ataxia in a 36-Year-Old Man
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Updates on Sturge-Weber Syndrome
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Brain and Skin Involvement in Erdheim-Chester Disease
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Ocular Findings in the Sturge-Weber Syndrome
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Multiple Facial Ulcers Following a Stroke
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Central Nervous System Involvement in Erdheim-Chester Disease
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Clinical Characteristics and Treatment Outcomes for Patients Infected with Mycobacterium haemophilum
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A 30-year-old man with acute paraplegia and left foot gangrene
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A 56-year-old woman with acute vertigo and diplopia
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Behcet Disease
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Neuropsychiatric Involvement of Behcets Disease
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Sturge-Weber Syndrome and Port-Wine Stains Caused by Somatic Mutation in GNAQ
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Sjogren Syndrome: Neurologic Complications
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Clinicopath Conf, Neuro-Behcets Disease
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Brain Magnetic Resonance Imaging in Patients with Cowden Syndrome
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CSF and MRI Findings in Patients with Acute Herpes Zoster
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Cerebrovascular Complications of Fabry's Disease
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CNS Mycosis Fungoides:CT and MR Findings
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Fucosidosis Revisited:A Review of 77 Patients
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Wyburn-Mason Syndrome
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Incontinentia Pigmenti:Association with Anterior Horn Cell Degeneration
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Central Nervous System Involvement in Blue-Rubber-Bleb-Nevus Syndrome
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Clinicopathological Conference
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Central Nervous System Infections Associated with Hereditary Hemorrhagic Telangiectasia
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Nevoid Basal Cell Carcinoma Syndrome & Epilepsy
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Spontaneous Cervical Epidural Hemorrhage, Anterior Cord Syndrome, & Familial Vascular Malformation
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Behcet's Syndrome
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Blue Rubber Bleb Nevus Syndrome with CNS Involvement & Thrombosis of a Vein of Galen Malformation
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Neurological Manifestations of Hereditary Hemorrhagic Telangiectasia (Rendu-Osler-Weber Disease)
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Lymphomatoid Granulomatosis
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