Phosphorylase Deficiency
In Englel & Banker, Myology, McGraw-Hill Book Co, Ch 52, 1585-1601, DiMauro,S.&Bresolin,N., 1986

Acid Maltase Deficiency
Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986

Benign Sexual Headach within a Family
Arch Neurol 43:1158-1160, Johns,D.R., 1986

Late-Life Migraine Accompaniments-Further Experience
Stroke 17:1033-1042, Fisher,C.M., 1986

Optic-Nerve Degeneration in Alzheimer's Disease
NEJM 315:485-487, Hinton,D.R.,et al, 1986

Gerstmann-Straussler-Scheinker Disease:Autopsy Study of a Familial Case
Ann Neurol 20:540-543, Vinters,H.V.,et al, 1986

Paradoxical Gas Embolism in a Scuba Diver with an Atrial Septal Defect
BMJ 293:1277, Wilmshurst,P.T.,et al, 1986

Identical Twins with Hereditary Hemorrhagic Telangiectasia Concordant for Cerebrovascular Arteriovenous Malformations
Am J Med 81:931-934, Lesser,B.A.,et al, 1986

The Inheritance of Gilles De La Tourette's Syndrome & Associated Behaviors
NEJM 315:993-997, Pauls,D.L.&Leckman,J.F., 1986

Arteriovenous Malformation Presenting as Hemidystonia
Neurol 36:1590-1593, Friedman,D.I.,et al, 1986

Familial Myoclonic Dementia Masquerading as Creutzfeldt-Jakob Disease
Ann Neurol 20:231-239, Little,B.W.,et al, 1986

Fatal Familial Insomnia & Dysautonomia with Selective Degeneration of Thalamic Nuclei
NEJM 315:997-1003, Lugaresi,E.,et al, 1986

Neuro-Ophthalmologic Findings in Vestibulocerebellar Ataxia
Arch Neurol 43:1050-1053, Farris,B.K.,et al, 1986

A Population-Based Study of Multiple Sclerosis in Twins
NEJM 315:1638-1642, Ebers,G.C.,et al, 1986

Hereditary Dystonia-Parkinsonism Syndrome of Juvenile Onset
Neurol 36:1424-1428, Nygaard,T.C.&Duvoisin,R.C., 1986

Parkinson's Disease
BMJ 293:379-382, Quinn,N.P.&Husain,F.A., 1986

Episodic Neurologic Dysfunction in Patients with Hodgkin's Disease
Arch Neurol 43:1227-1233, Feldman,E.&Posner,J.B., 1986

Transketolase Abnormality in Tolazamide-Induced Wernicke's Encephalopathy
Neurol 36:1508-1510, Mukherjee,A.B.,et al, 1986

Ornithine Transcarbamylase Deficiency-A Cause of Bizarre Behavior in a Man
NEJM 315:744-747, DiMagno,E.P.,et al, 1986

Lyme Disease Associated with Optic Neuropathy
Am J Med 81:143-145, Schechter,S.L., 1986

Adult-Onset Autosomal Dominant Limb-Girdle Muscular Dystrophy
Ann Neurol 20:240-248, Chutkow,J.G.,et al, 1986

Location of the Gene for X-Linked Spinal Muscular Atrophy
Neurol 36:1595-1598, Fischbeck,K.H.,et al, 1986

Infarcts of the Inferior Division of the Right Middle Cerebral Artery:Mirror Image of Wernicke's Aphasia
Neurol 36:1015-1020, Caplan,L.R.,et al, 1986

Embolic Complications in Paroxysmal Atrial Fibrillation
Stroke 17:622-626, Petersen,P.&Godtfredsen,J., 1986

Familial Hyperlipidemia in Stroke in the Young
Stroke 17:1142-1145, Bansal,B.C.,et al, 1986

Ultrasound Screening for Spina Bifida:Cranial & Cerebellar Signs
Lancet 2:72-74, Nicolaides,K.H.,et al, 1986

Multiple Sclerosis:Magnetic Resonance Imaging, Evoked Responses, & Spinal Fluid Electroporesis
Neurol 36:828-831, Farlow,M.R.,et al, 1986

Cardiac Manifestations of Complex Partial Seizures
Am J Med 80:195-202, Devinsky,O.,et al, 1986

Sudden Unexpected Death of Epileptic Patient Due to Cardiac Arrhythmia after Seizure
Arch Neurol 43:194-196, Dasheiff,R.M.&Dickinson,L.J., 1986

Paradoxical Cerebral Embolism:Eight Cases
Neurol 36:1356-1360, Biller,J.,et al, 1986

Clinically Silent Atrial Septal Defects with Evidence for Cerebral Embolization
Ann Int Med 105:695-697, Harvey,J.R.,et al, 1986

On Heredity, Twins, & Parkinson's Disease
Ann Neurol 19:409-411, Duvoisin,R.C., 1986

Parkinson's Disease in Monozygotic Twins
Ann Neurol 19:405-408, Jankovic,J.&Reches,A., 1986

Monozygotic Twins with Parkinson's Disease
Ann Neurol 19:402-405, Koller,W.,et al, 1986

Double-Blind Assessment of Potential Pergolide-Induced Cardiotoxicity
Neurol 36:993-995, Kurlan,R.,et al, 1986

Infantile Bilateral Striatal Necrosis, Clinicopathological Classification
Arch Neurol 43:677-680, Mito,T.,et al, 1986

Antecedents of Cerebral Palsy, Multivariate Analysis of Risk
NEJM 315:81-86, 124-1261986., Nelson,K.B.&Ellenberg,J.H., 1986

Clinicopath. Conference
Pick's Disease of Brain, with Frontal Lobar Atrophy, Degen of Basal Ganglia, Case 16-1986, NEJM 314:, 101-,1986., 1986

Electrocardiographic Accompaniments of Temporal Lobe Epileptic Seizures
Lancet 1:1051-1056, Blumhardt,L.D.,et al, 1986

Familial Association of Intracranial Aneurysms & Multiple Congenital Anomalies
Arch Neurol 43:30-33, Berg,H.W.M.,et al, 1986

Clinical Signs in the Wernicke-Korsakoff Complex:A Retrospective Analysis of 131 Cases Diagnosed at Necropsy
JNNP 49:341-345, Harper,C.G.,et al, 1986

Albert's Test:A Neglected Test of Perceptual Neglect
Lancet 1:430-432, Fullerton,K.J.,et al, 1986

Familial Amyloidosis with Cranial Neuropathy & Corneal Lattice Dystrophy
Neurol 36:432-435, Darras,B.T.,et al, 1986

Visual & Auditory Neurotoxicity in Patients Receiving Subcutaneous Deferoxamine Infusions
NEJM 314:869-873, Olivieri,N.F.,et al, 1986

Computed Tomography of Familial Pineoblastoma
J Comput Assist Tomogr 10:32-33, Peyster,R.G.,et al, 1986

Inherited Multiple Meningiomas:A Clinical, Pathological & Cytogenetic Study of an Affected Family
JNNP 49:362-368, Battersby,R.D.E.,et al, 1986

Silent Brain Lesions in Patients with Isolated Idiopathic Optic Neuritis
Arch Neurol 43:452-455, Jacobs,L.,et al, 1986

Isolated Idiopathic Optic Neuritis, Analysis of Free K-Light Chains in CSF & NMR
Arch Neurol 43:456-458, Rudick,R.A.,et al, 1986

The AIDS Dementia Complex:I. Clinical Features
Ann Neurol 19:517-524, Navia,B.A.,et al, 1986

Autosomal Dominant Osteosclerosis Associated with Familial Spinal Canal Stenosis
Neurol 36:687-692, Yasuda,Y.,et al, 1986