Familial Porencephaly
Arch Neurol 40:567-569, Berg,R.A.,et al, 1983
Evoked Response Studies in Patients with Adreno-leukodystrophy & Heterozygous Relatives
Arch Neurol 40:356-359, Garg,B.P.,et al, 1983
Posttraumatic Syringomyelia with Paroxysmal Episodes of Unconsciousness
Arch Neurol 40:322-324, McComas,C.F.,et al, 1983
Torticollis in Three Children with Syringomyelia & Spinal Cord Tumor
Neurol 33:956-958, Kiwak,K.J.,et al, 1983
Huntington's Chorea:Neglected Opportunities for Preventive Medicine
Lancet 1:634-636, Martindale,B.,et al, 1983
Familial Paroxysmal Dystonic Choreoathetosis & Response to Alternate-Day Oxazepam Therapy
Ann Neurol 13:456-457, Kurlan,R.,et al, 1983
Family Studies in Tuberous Sclerosis
JAMA 249:1302-1304, Cassidy,S.B.,et al, 1983
Effect of a Single Oral Dose of Propranolol on Essential Tremor:A Double-Blind Controlled Study
Ann Neurol 13:165-177, Calzetti,S.,et al, 1983
Nadolol in Essential Tremor
Neurol 33:1076-1077, Koller,W.C., 1983
Phenobarbital & Propranolol in Essential Tremor:A Double-Blind Controlled Clinical Trial
Neurol 33:296-300, Baruzzi,A.,et al, 1983
Blepharospasm & Orofacial-Cervical Dystonia:Clinical & Pharmacological Findings in 100 Patients
Ann Neurol 13:402-411, Jankovic,J.,et al, 1983
Acetazolamide-Responsive Episodic Ataxia Syndrome
Neurol 33:1212-1214, Zasorin,N.L.,et al, 1983
A Family with Histologially Confirmed Alzheimer's Disease
Arch Neurol 40:203-208, Nee,L.E.,et al, 1983
Lipomembranous Polycystic Osteodysplasia (Brain, Bone, & Fat Disease)
Neurol 33:81-86, Bird,T.D.,et al, 1983
Hyperekplexia
Arch Neurol 40:246-248, Kurczysnki,T.W., 1983
Taste & Smell in Disease (First of Two Parts)
NEJM 308:1275-1279, Schiffman,S.S., 1983
The Malignant Hyperthermia Syndrome
NEJM 309:416-418, Nelson,T.E.,et al, 1983
Sclerosteosis:Neurogenetic & Pathophysiologic Analysis of an American Kinship
Neurol 33:267-277, Stein,S.A.,et al, 1983
Recombinant DNA & Neurologic Disease:The Coming of a New Age
Neurol 33:622-625, Rosenberg,R.N., 1983
Supranuclear Gaze Palsy in Familial Creutzfeldt-Jakob Disease
Arch Neurol 40:618-622, Bertoni,J.M.,et al, 1983
Livedo Reticularis & Cerebrovascular Lesions (Sneddon's Syndrome) , Clin, Radiolog & Path Features in Eight Cases
Brain 106:965-979, Rebollo,M.,et al, 1983
Familial Spastic Paraplegia, Mental Retardation, & Precocious Puberty
Arch Neurol 40:809-810, Raphaelson,M.I.,et al, 1983
Mucopolysaccaridosis IV (Morquio Syndrome) , in The Metabolic Basis of Inherited Disease
(Ed) 5th Ed. , McGraw-Hill, New York, p. 766, Stanbury,J.B., 1983
Fragile X Chromosome & X-Linked Mental Retardation
CMA Journal 127:123-126, Larbrisseau,A.,et al, 1982
Essential Myoclonus
In Movement Disorder, CD Marsden & S Fahn (Ed) , Butterworth, London, 1982, p 207., , 1982
Detection Of Adrenoleucodystrophy Carriers By Means Of Evoked Potentials
Lancet 2:852-853, Moloney,J.B.,et al, 1982
Where am I
BMJ 285:85-86, Godwin-Austen,R.B., 1982
Controlled Study of Metoprolol & Propranolol During Prolonged Administration in Patients with Essential Tremor
JNNP 45:893-897, Calzetti,S.,et al, 1982
Double-blind Controlled Study of Primidone in Essential Tremor:Preliminary Results
BMJ 285:608, Findley,L.J., 1982
Prevalence of Essential Tremor
Arch Neurol 39:750-751, Haerer,A.F.,et al, 1982
Genetics of Alzheimer's Disease
BMJ 284:1065-1066, Harris,R., 1982
Hypomelanosis of Ito (incontinentia pigmenti achromians) :Macrocephaly & Gray Matter Heterotopias
Neurol 32:1013-1016, Ross,D.L.,et al, 1982
Two Cases of Van Buchem's Disease
JNNP 45:913-918, Dixon,J.M.,et al, 1982
A Surgical Approach To The Treatment Of Fetal Hydrocephalus
NEJM 306:1320-1325, Clewell,W.H.,et al, 1982
Motor Spastic Paraplegia & Unilateral Infra-nuclear Facial Palsy Complicating Tetanus
BMJ 285:477-478, Jain,M.K.,et al, 1982
An Autosomal-dominant Dystrophy with Humeropelvic Distribution & Cardiomyopathy
Neurol 32:1399-1401, Fenichel,G.M.,et al, 1982
Distal Myopathy, Histochemical & Ultrastructural Studies
Arch Neurol 39:367-371, Kumamoto,T.,et al, 1982
Benign Familial Spinal Muscular Atrophy With Hypertrophy of the Calves
Arch Neurol 39:657-660, D'Alessandro,R.,et al, 1982
Exacerbation of Charcot-Marie-Tooth Disease in Pregnancy
Neurol 32:1311-1314, Pollock,M.,et al, 1982
Clinical & Electrophysiological Studies in Primary Lateral Sclerosis
Jr. , Arch Neurol 39:662-664982., Russo,L.S., 1982
Inborn Errors of Metabolism
Ann Neurol 11:221-232, Kolodny,E.H.,et al, 1982
The Neuropathology of Glycine Encephalopathy:Five Cases with Immunohistochemical & Ultrastructural Observations
Neurol 32:975-985, Agamanolis,D.P.,et al, 1982
Nevoid Basal Cell Carcinoma Syndrome & Epilepsy
Ann Neurol 11:372-376, Murphy,M.J.,et al, 1982
Cockayne Syndrome
J Comput Assist Tomogr 6:1172-1174, Levinson,E.D.,et al, 1982
Familial X-linked Addison Dise. as an Expression of Adrenoleukodystr. :C26 Fatty Acid in Cult. Skin Fibroblasts
Neurol 32:543-547, O'Neill,B.P.,et al, 1982
Periodic Meningitis & Familial Mediterranean Fever
Arch Int Med 142:378-379, Vilaseca,J.,et al, 1982
Narcolepsy-Cataplexy
Arch Neurol 39:164-168, Kales,A.,et al, 1982
The Genetics of Susceptibility to Multiple Sclerosis
Epidemiol Rev 4:45-65, Spielman,R.S.&Nathanson,N., 1982
Biochemical Genetics Of Neurologic Disease
NEJM 305:1181-1193, Rosenberg,R.N., 1981
Familial Hemiplegic Migraine:EEG & CT Scan Study of Two Cases
Ann Neurol 10:392-295, Gastaut,J.L.,et al, 1981