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Sturge-Weber Syndrome
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A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
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Clinical Characteristics, Risk Factors, and Outcomes of POEMS Syndrome
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Clinical and Neuroimaging Features in Gorlin-Goltz Syndrome
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Myelopathy in Behcets Disease: The Bagel Sign
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The Syndrome of Cutaneous Photosensitivity, Growth Failure, and Basal Ganglia Calcification
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Bannayan-Riley-Ruvalcaba Syndrome: MRI Neuroimaging Features in a Series of 7 Patients
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Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Lyme Disease (Erythema Chronicum Migrans; Borreliosis
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Inherited Metabolic Diseases of the Nervous System, Lipogranulomatosis (Farber Disease)
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Sturge-Weber Syndrome and Port-Wine Stains Caused by Somatic Mutation in GNAQ
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Herpes Zoster Ophthalmicus-Induced Oculomotor Nerve Palsy
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Clinicopath Conf, The POEMS Syndrome, with Demyelinating Neuropathy and Solitary Pharmacytoma of Bone
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Herpes Zoster Ophthalmicus-Related Oculomotor Palsy Accompanied by Hutchinson Sign
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Clinicopath Conf, Neuro-Behcets Disease
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Clinical and Mutational Spectrum of Neurofibromatosis Type 1-Like Syndrome
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Aicardi-Gouti�res Syndrome
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Neurologic Improvement After Peripheral Blood Stem Cell Transplantation in POEMS Syndrome
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Central Nervous System Involvement after Herpes Zoster Ophthalmicus
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Phenylketonuria
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Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
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New Developments in the Neurobiology of the Tuberous Sclerosis Complex
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Motor Involvement in Acute Herpes Zoster
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Skin Involvement in Amyotrophic Lateral Sclerosis
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Cockayne Syndrome: Review of 140 Cases
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A Clinical Study of Noonan Syndrome
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Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
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Clinical Follow-Up and Immunogenetic Studies of 32 Patients with Eosinophilia-Myalgia Syndrome
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Incontinentia Pigmenti:Association with Anterior Horn Cell Degeneration
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Tick-Bite Meningoradiculoneuritis:Clinical, Electrophysiologic, & Histolic Findings in 10 Cases
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Acute Arsenic Intoxication Presenting as Guillain-Barre-Like Syndrome:Donofrio
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Biotinidase Deficiency:Initial Clinical Features & Rapid Diagnosis
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Biotin-Responsive Carboxylase Deficiency Associated With Subnormal Plasma & Urinary Biotin
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Neurologic Abnormalities of Lyme Disease
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Neurologic Manifestations of Periarteritis Nodosa (1972)
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Angiokeratoma Corporis Diffusum
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