Coma From Long-Term Overingestion of Isoniazid
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Delirium and a Subclavian Abscess
Lancet 350:1294, Yamasaki,K.,et al, 1997
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
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Drugs and Myasthenia Gravis, An Update
Arch Int Med 157:399-408, Wittbrodt,E.T., 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
Neurol 49:1042-1047, Dobyns,W.B.,et al, 1997
Association of Tuberous Sclerosis of Temporal Lobes with Autism and Atypical Autism
Lancet 349:392-395, Bolton,P.F.&Griffiths,P.D., 1997
Accuracy of the Clinical Diagnosis of Corticobasal Degeneration:A clinicopathologic Study
Neurol 48:119-125, Litvan,I.,et al, 1997
Evaluation of Neurologic Function in Gulf War Veterans:A Blinded Case-Control Study
JAMA 227:223-230, 2591997., Haley,R.W.,et al, 1997
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
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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
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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
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Primary Adhalinopathy (x-Sarcoglycanopathy) :Clin, Path & Genetic Correl in 20 Pts with Autosomal Recessive Muscular Dystrophy
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Clinical Features of Perineuritis
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A Longitudinal Magnetic Resonance Imaging Study of Brain Changes in Adolescents with Anorexia Nervosa
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The X-Linked Infantile Spasms Syndrome (MIM 308350) Maps to Xp11. 4-Xpter in Two Pedigrees
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Diagnostic Guidelines in Central Nervous System Whipple's Disease
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Whipple Disease Confined to the Central Nervous System in Childhood
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Unusual Clinical Presentations of Cortical-Basal Ganglionic Degeneration
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Isolated Vitamin E Deficiency
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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
NEJM 334:362-366, Fadic,R.,et al, 1996
Progressive Ataxia, Focal Seizures, and Malabsorption Syndrome in a 41 Year Old Woman
JNNP 60:225-230, Mumford,C.J.,et al, 1996
A Man with Weight Loss, Ataxia, and Confusion for 3 Months
Lancet 347:448, Beversdorf,D.,et al, 1996
Reversibility of Cerebral Ventricular Enlargement in Anorexia Nervosa, Demonstrated by Quant MR
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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
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Prenatal Magnesium Sulfate Expos/Risk for CP or MR Among Very Low-Birth-Weight Child Aged 3-5 Yrs
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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
BMJ 312:434, Seehra,H.,et al, 1996
Optic Neuropathy
Neurol 46:315-322, Newman,N.J., 1996
MRI of White Matter Changes in the Sjogren-Larsson Syndrome
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Clinicopath Conf
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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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