Mucolipidosis Type IV; Characteristic MRI Findings
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Diagnosing Syncope
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Diagnosing Syncope, Part 2:Unexplained Syncope
Ann Int Med 127:76-86, Linzer,M.,et al, 1997
Chronic Inflammatory Demyelinating Polyradiculoneuropathy:Unusual Clinical Features and Therapeutic Responses
Neurol 46:1206-1212, Midroni,G.&Dyck,P.J., 1996
Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
Lancet 1458-1463, Barrett,T.G.,et al, 1995
Clinical Significance of Fetal Choroid Plexus Cysts
Lancet 346:724-729, Gupta,J.K.,et al, 1995
Charcot-Marie-Tooth Neuropathies:From Clinical Description to Molecular Genetics
Muscle & Nerve 18:267-275995., Ionasecu,V.V., 1995
Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995
Neurologic Manifestations of HIV Infection
Ann Int Med 121:769-785, Simpson,D.M.&Tagliati,M., 1994
Autonomic Involvement in Guillain-Barre Syndrome:A Review
Muscle & Nerve 17:1145-1155994., Zochodne,D.W., 1994
Methylmercury Poisoning:Long-Term Clinical, Radiological, Toxicological, and Pathological Studies of an Affected Family
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MR Findings in Seven Patients with Organic Mercury Poisoning (Minamata Disease)
AJNR 15:1575-1578, Korogi,Y.,et al, 1994
Salvage of Vision After Hypotension-Induced Ischemic Optic Neuropathy
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Acquired Ocular Visual Impairment in Children, 1960-1989
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Treatment of Convulsive Status Epilepticus
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Leber's Hereditary Optic Neuropathy as a Cause of Severe Visual Loss in Childhood
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Neuro-Ophthalmic Features of Carotid Cavernous Fistulas and Their Treatment by Endoarterial Balloon Embolisation
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Progressive Vison Loss, A Rare Manifestation of Familial Cavernous Angiomas
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MR Imaging of the Spinal Cord in 23 Subjects with ALD-AMN Complex
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Occurrence of MS-Like Illness in Women Who Have a Leber's Hereditary Optic Neuropathy Mitochondrial DNA Mutation
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Cockayne Syndrome: Review of 140 Cases
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A Clinical Study of Noonan Syndrome
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Thyroid-Associated Eye Disease:Clinical Management
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Syncope:1991
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Sarcoidosis of the Nervous System, A Clinical Approach
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Neurologic Aspects of Cobalamin Deficiency
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Hallervorden-Spatz Syndrome and Brain Iron Metabolism
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Infantile CNS Spongy Degeneration-14 Cases:Clinical Update
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Molecular Genetics of Duchenne and Becker Muscular Dystrophy
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Improved Molecular-Genetic Diagnosis of Leber's Hereditary Optic Neuropathy
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Current Management of Amaurosis Fugax
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Neurologic Manifestations of Giant Cell Arteritis
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The Rational Management of Idiopathic Intracranial Hypertension
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Subacute Combined Degeneration of the Spinal Cord
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Surgical Treatment of Progressive Visual Loss in Traumatic Optic Neuropathy, Report of Two Cases
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Follow-up and Diagnostic Reappraisal of 75 Patients with Leber's Congenital Amaurosis
Am J Ophthalmol 107:624-631, Lambert,S.R.,et al, 1989
Mitochondrial DNA and Genetic Disease
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Neurofibromatosis Type 1 (Recklinghausen's Disease) , Neurologic and Cognitive Assessment
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A Mitochondrial DNA Mutation as a Cause of Leber's Hereditary Optic Neuropathy
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MR Imaging of a Group I Case of Hallervorden-Spatz Disease
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Familial Oculoleptomeningeal Amyloidosis, Report of a New Family with Unusual Features
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Noninvasive Eval of Extracranial Carotid Arteries in Patients with Cerebrovascular Events & Atrial Fib
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Paraneoplastic Syndromes Involving the Eyes
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Computed Tomography and Magnetic Resonance Imaging in the Diagnosis of Inflammatory Disease of the Optic Nerve
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Ocular Complications of Tangier Disease
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Clinicopath. Conference
Malignant Lymphoma (B-Cell Type) , Brain (Right-Frontal-Lobe White Matter) , Case 22-1986, NEJM 314:, 498-150, 1986
The Posterior Cerebral Artery Syndrome
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Olivopontocerebellar Atrophy with Dementia, Blindness, & Chorea, Response to Baclofen
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Somatization Disorder, One of Medicine's Blind Spots
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