Thalamic Haemorrhage
Brain 119:1873-1886, Chung,C-S.,et al, 1996
Acute Demyelinating Polyneuropathy with Arsenic Ingestion
Muscle & Nerve 19:1611-1613996., Greenberg,S.A., 1996
Reversible Empty Sella in Idiopathic Intracranial Hypertension:An Indicator of Successful Therapy
AJNR 17:1953-1956, Zagardo,M.T.,et al, 1996
Management Protocol for an Enhancing Cerebral Lesion in HIV Infection
Conn Medicine 60:649-651, Finelli,P.F., 1996
Confirmation of Linkage of Oculopharyngeal Muscular Dystrophy to Chromosome 14q11. 2-q13
Ann Neurol 40:801-804, Stajich,J.M.,et al, 1996
Diagnostic Test for the Prader-Willi Syndrome by SNRPN Expression in Blood
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An Emotional 13-Year Old Girl
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A Gene for Parkinson's Disease
BMJ 313:1278, Hawkes,C., 1996
Clinical Genetic Analysis of Parkinson's Disease in the Contursi Kindred
Ann Neurol 40:767-775, Golbe,L.I.,et al, 1996
Genetic Factors in Alzheimer's Disease:A Review of Recent Advances
Ann Neurol 40:829-840, Levy-Lahad,E.&Bird,T.D., 1996
Elevated Risk of Alzheimer's Disease Among Workers with Likely Electromagnetic Field Exposure
Neurol 47:1477-1481, Sobel,E.,et al, 1996
Electromagnetic Field Exposure May Cause Increased Production of Amyloid Beta & Eventually lead to Alzheimer's Disease
Neurol 47:1594-1600, Sobel,E.&Davanipour,Z., 1996
Consensus Guidelines for Clin & Path Dx of Dementia with Lewy Bodies (DLB) :Report of DLB Intl Workshop
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Unusual Clinical Presentations of Cortical-Basal Ganglionic Degeneration
Ann Neurol 40:893-900, Bergeron,C.,et al, 1996
Age on Onset, Sex, & Cardiomyopathy as Predictors of Disability and Survival in Friedreich's Disease
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Clinicopath Conf
Distinguishing Acute Disseminated Encephalomyelitis from Multiple Sclerosis, BMJ 313:802-8041996., , 1996
Diagnosis of Patients Presenting to a Huntington Disease (HD) Clinic without a Family History of HD
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Cerebral Venous Thrombosis:Role of Activated Protein C Resistance and Factor V Gene Mutation
Stroke 27:1719-1720, Brey,R.L.&Coull,B.M., 1996
Restless Legs Syndrome:Clinicoetiologic Correlates
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Practice Parameter:Genetic Testing Alert
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The Effect on Memory of Chronic Prednisone Treatment in Patients with Systemic Disease
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Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
Medicine 75:233-250, Murakami,T.,et al, 1996
Stimulus-Evoked Sinus Arrest in Severe Guillain-Barre Syndrome:A Case Report
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The Role of Lab Investig in the Dx & Management of Pts with Suspected Herpes Simplex Encephalitis:A Consensus Rpt
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Clinicopath Conf
Granulomatous Encephalitis, Secondary to Schistosoma Mansoni Infection, Case 39-1996, NEJM 335:1906-, 91496., 1996
A Simplified Six-Item Checklist for Screening for Fragile X Syndrome in the Pediatric Population
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Acute Low Back Pain:A New Paradigm for Management
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Acute Phenytoin Toxicity Followed by Seizure Breakthrough From a Ticlopidine-Phenytoin Interaction
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Visual Hallucinations Associated with Parkinson Disease
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Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
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Paraneoplastic Limbic Encephalitis in Hodgkin's Disease
Can J Neurol Sci 23:138-140, Deodhare,S.,et al, 1996
Machado Joseph Disease Maps to Same Region of Chromosome 14 as Spinocerebellar Ataxia Type 3 Locus
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Benign Episodic Unilateral Mydriasis
Ophthalmol 102:1623-1627, Jacobson,D.M., 1995
Magnetic Resonance Imaging of the Brain in Nonarteritic Ischemic Optic Neuropathy
J Neuro-Ophthalmol 15:158-160, Arnold,A.C.,et al, 1995
Epidemic Optic Neuropathy in Cuba-Clinical Characterization and Risk FActors
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Multifocal Demyelinating Motor Neuropathy:Pathologic Evidence of Inflammatory Demyelinasting Polyradiculoneuropathy
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Clin Electrophy & Molec Correl in 13 Families with Hered Neurop with Liabil to Press Palsies & Chromosome 17p11. 2 Deletion
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Folate Levels and Neural Tube Defects:Implications for Prevention
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Canavan Disease:From Spongy Degeneration to Molecular Analysis
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Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia
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Anticonvulsant Hypersensitivity Syndrome
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Hereditary Hemorrhagic Telangiectasia
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Screening Family Members of Patients with Hereditary Hemorrhagic Telangiectasia
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Adult-Onset Spinocerebellar Dysfunction Caused by a Mutation in the Gene for the a-Tocopherol-Transfer Protein
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Digitalis-Induced Visual Disturbances with Therapeutic Serum Digitalis Concentrations
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Optic Neuropathy, Headache, & Diplopia with MRI Suggestive of Cerebral Arteritis in Relapsing Polychondritis
J Neuro-Ophthalmol 15:171-175, Massry,G.G.,et al, 1995
Cerebrovascular Complications in Ehlers-Danlos Syndrome Type IV
Ann Neurol 38:960-964, North,K.N.,et al, 1995
Familial Acephalgic Migraine
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Acute Bacterial meningitis
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