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
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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
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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
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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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
AJNR 17:1589-1591, Duprez,T.P.J.,et al, 1996
Unusual Clinical Presentations of Cortical-Basal Ganglionic Degeneration
Ann Neurol 40:893-900, Bergeron,C.,et al, 1996
Isolated Vitamin E Deficiency
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Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996
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
J Pediatr 128:296-301, Golden,N.H.,et al, 1996
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
Ann Neurol 39:196-202, Morandi,L.,et al, 1996
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
Neuroradiology 37:576-577, Hussain,M.Z.&Aihara,M., 1996
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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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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Congenital Muscular Dystrophy:Clinical & Pathologic Study of 50 Pts with Classical (Occidental) Merosin-Positive Form
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Congenital Muscular Dystrophy Syndromes Distinguished by Alkaline and Acid Phosphatase, Merosin, & Dystrophin Staining
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The Relation of Transient Hypothyroxinemia in Preterm Infants to Neurologic Development at Two Years of Age
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Ethylene Oxide Neurotoxicity:A Cluster of 12 Nurses with Peripheral and Central Nervous System Toxicity
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Maternal Phenylketonuria:Magnetic Resonance Imaging of the Brain in Offspring
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Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
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Niemann-Pick Disease Type C from Bench to Bedside
JAMA 276:561-564, Schiffmann,R., 1996
Intellectual Impairment in Children Exposed to Polychlorinated Biphenyls in Utero
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