Accuracy of the Clinical Diagnosis of Corticobasal Degeneration:A clinicopathologic Study
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Evaluation of Neurologic Function in Gulf War Veterans:A Blinded Case-Control Study
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Muscle-Eye-Brain Disease:A Neuropathological Study
Ann Neurol 41:173-180, Haltia,M.,et al, 1997
CT and MR Findings of Neuroacanthocytosis
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Myotonic Dystrophy, The Role of Large Triplet Repeat Length in the Develop of Mental Retardation
Arch Neurol 54:251-254, Spranger,M.,et al, 1997
Cognitive Function and Academic Performance in Neurofibromatosis 1:North
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Long-Term Cognitive Impairment Associated with Caudate Stroke
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Serial Neuropsychological Assess & Magnetic Resonance Imagingf Analysis in Multiple Sclerosis
Arch Neurol 54:1018-1025, Hohol,M.J.,et al, 1997
Prevalence and Severity of Cognitive Impairment with and without Dementia in an Elderly Population
Lancet 349:1793-1796, Graham,J.E.,et al, 1997
A 44-Month Clinical-Brain MRI Follow-Up in a Patient with B12 Deficiency
Neurol 49:878-881, Stojsavljevic,N.,et al, 1997
Human Immunodeficiency Virus Infection and Stroke in Young Patients
Arch Neurol 54:1150-1153, Qureshi,A.I.,et al, 1997
Primary Adhalinopathy (x-Sarcoglycanopathy) :Clin, Path & Genetic Correl in 20 Pts with Autosomal Recessive Muscular Dystrophy
Neurol 48:1227-1234, Eymard,B.,et al, 1997
Clinical Features of Perineuritis
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A Longitudinal Magnetic Resonance Imaging Study of Brain Changes in Adolescents with Anorexia Nervosa
Arch Pediatr Adolesc Med 151:793-797, Katzman,D.K.,et al, 1997
The X-Linked Infantile Spasms Syndrome (MIM 308350) Maps to Xp11. 4-Xpter in Two Pedigrees
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Bilirubin Metabolism and Kernicterus
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Coma From Long-Term Overingestion of Isoniazid
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Mutations in the Sarcoglycan Genes in Patients with Myopathy
NEJM 336:618-624, Duggan,D.J.,et al, 1997
The Muscular Dystrophies-Clarity or Chaos
NEJM 336 650-651, Dubowitz,V., 1997
Clinical Course of a Cohort in the Cuban Epidemic Optic and Peripheral Neuropathy
Neurol 48:19-22, Mojon,D.S.,et al, 1997
Wernicke's Encephalopathy:An Excitotoxicity Hypothesis
Metabolic Brain Disease 12:183-192, McEntee,W.J., 1997
Adult-Onset Krabbe's Disease in Siblings with Novel Mutations in the Galactocerebrosidase Gene
Ann Neurol 41:111-114, Bernardini,G.L.,et al, 1997
Adult-Onset Krabbe Disease with Mutation in the Galactocerebrosidase Gene, MRI of Corticospinal Tract Demyelin
Neurol 49:1392-1399, Satoh,J.-I.,et al, 1997
Bilat Periventricular Nodular Heterotopia with Mental Retard & Syndactyly in Boys:New X-Linked MR Synd
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A Simplified Six-Item Checklist for Screening for Fragile X Syndrome in the Pediatric Population
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Severe Hypoglycaemia and Cognitive Impairment in Diabetes
BMJ 313:767-768, Deary,I.J., 1996
Diagnostic Test for the Prader-Willi Syndrome by SNRPN Expression in Blood
Lancet 348:1068-1069, Wevrick,R.&Francke,U., 1996
Paraneoplastic Limbic Encephalitis in Hodgkin's Disease
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Diagnostic Guidelines in Central Nervous System Whipple's Disease
Ann Neurol 40:561-568, Louis,E.D.,et al, 1996
Whipple Disease Confined to the Central Nervous System in Childhood
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Unusual Clinical Presentations of Cortical-Basal Ganglionic Degeneration
Ann Neurol 40:893-900, Bergeron,C.,et al, 1996
Isolated Vitamin E Deficiency
Muscle & Nerve 19:1161-1165996., Jackson,C.E.,et al, 1996
Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
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Brief Report:Deficiency of a Dystrophin-Assoc Glycoprotein (Adhalin) in Pt with Muscular Dystrophy & Cardiomyopathy
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Progressive Ataxia, Focal Seizures, and Malabsorption Syndrome in a 41 Year Old Woman
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A Man with Weight Loss, Ataxia, and Confusion for 3 Months
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Reversibility of Cerebral Ventricular Enlargement in Anorexia Nervosa, Demonstrated by Quant MR
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Cognitive Dysfunction as the Major Presenting Feature of Becker's Muscular Dystrophy
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Clinical Heterogeneity of Adhalin Deficiency
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Wernicke's Encephalopathy After Vertical Banded Gastroplasty for Morbid Obesity
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Optic Neuropathy
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MRI of White Matter Changes in the Sjogren-Larsson Syndrome
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Cognitive Impairment & Mortality in a Cohort of Elderly People
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Reduced Response to Activated Protein C is Associated with Increased Risk for Cerebrovascular Disease
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Cerebral Venous Sinus Thrombosis Associated with Factor V Gene Mutation
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Carotid Artery Thrombus Associated with Severe Iron-Deficiency Anemia and Thrombocytosis
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Leukoencephalopathy Associated with Cobalamin Deficiency
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Effect of Malnutrition after Acute Stroke on Clinical Outcome
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Diagnosis of McArdle's Disease by Molecular Genetic Analysis of Blood
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