Intracranial Hypertension Associated with Poly-Cranio-Radicular-Neuropathies A Case Report and Review of the Literature
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Neuroimaging Features of Biotinidase Deficiency
AJNR 44:328-333, Biswas,A.,et al, 2023
Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD): Clinical Features and Diagnosis
UptoDate.com, March, Flanagan,E.P. & Tillema,J-M, 2023
Severe Hippocampal Atrophy in a Patient with Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy
JAMA Neurol 80:642-643, Bartels,F.,et al, 2023
Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD):Clinical Features and Diagnosis
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Neuromyelitis Optica Spectrum Disorder
NEJM 387:631-639, Wingerchuk, D.M. & Lucchinetti, C.F., 2022
Behcet Disease
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A Patient with a History of Encephalomyelitis and Recurrent Optic Neuritis
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A Young Man with Acute Encephalopathy Loss of Vision, and Upper Motor Neuron Signs
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Neuromyelitis Optica Spectrum Disorders
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Posterior Reversible Encephalopathy Syndrome with Spinal Cord Involvement
Neurol 83:2002-2006,1996, de Havenon, A.,et al, 2014
Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Sarcoidosis
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Cogan Syndrome An Analysis of Reported Neurological Manifestations
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Acute severe visual loss and a brainstem mass
Lancet 380:1790, Meleth, A.,et al, 2012
Current Concept of Neuromyelitis Optica (NMO) and NMO Spectrum Disorders
JNNP doi:10.1136/JNNP-2012-302310, Jacob, A.,et al, 2012
Neuromyelitis Optica in France: A Multicenter Study of 125 Patients
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NMO-IgG Predicts the Outcome of Recurrent Optic Neuritis
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Current Concepts in the Etiology and Treatment of Behcet Disease
Surv Ophthalmol 50:297-350, Evereklioglu,C., 2005
Behcet's Disease
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Mucolipidosis Type IV; Characteristic MRI Findings
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Chronic Inflammatory Demyelinating Polyradiculoneuropathy:Unusual Clinical Features and Therapeutic Responses
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Neurologic Aspects of Cobalamin Deficiency
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Acute Disseminated Encephalomyelitis, MRI Findings & the Distinction from Multiple Sclerosis
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Neurologic Disease in Biopsy-Proven Giant Cell (Temporal) Arteritis
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Familial Oculoleptomeningeal Amyloidosis, Report of a New Family with Unusual Features
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Hysterical Conversion Reactions Mimicking Neurological Disease
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Parainfectious Optic Neuritis
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Two Cases of Van Buchem's Disease
JNNP 45:913-918, Dixon,J.M.,et al, 1982
Neurologic Manifestations in Macroglobulinemia
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Behcet's Syndrome
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Acute Intermittent Porphyria
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