Nearly Fatal Muscle Carnitine Deficiency with Full Recovery after Replacement Therapy
Neurol 33:1629-1631, Prockop,L.D.,et al, 1983

Unrecognized Chronic Lithium Neurotoxic Reactions
JAMA 250:2029-2030, Lewis,D.A., 1983

Action Tremor as a Manifestation of Chylomicron Retention Disease
Ann Neurol 14:591, Gauther,S.,et al, 1983

Glutamate Dehydrogenase Deficiency in Patients with Olivopontocerebellar Atrophy
Neurol 33:1322-1326, Duvoisin,R.C.,et al, 1983

Treatment of Dystonia with Tetrahydrobiopterin
NEJM 308:157-158, LeWitt,P.A.,et al, 1983

"Lhermitte's Sign"as a Presenting Symptom of Subacute Combined Degeneration of the Cord
Ann Neurol 13:215, Sandyk,R.,et al, 1983

Vitamin E & Neurological Function
Lancet 1:225-228, Muller,D.P.R.,et al, 1983

Wernicke's Encephalopathy Induced by Tolazamide
NEJM 309:599-600, Kwee,I.L.,et al, 1983

Myeloneuropathy & Macrocytosis Associated with Nitrous Oxide Abuse
Arch Neurol 40:416-418, Bianco,G.,et al, 1983

Pyridoxine-Dependency Seizure:Report of a Rare Presentation
Ann Neurol 13:103-104, Krishnamoorthy,K.S., 1983

Ultrastructure & Electrodiagnosis of Peripheral Neuropathy in Cockayne's Syndrome
Neurol 33:1606-1609, Grunnet,M.L.,et al, 1983

Familial Spastic Paraplegia, Mental Retardation, & Precocious Puberty
Arch Neurol 40:809-810, Raphaelson,M.I.,et al, 1983

Primary Position Upbeating Nystagmus:A Variety of Central Positional Nystagmus
Brain 106:949-964, Fisher,A.,et al, 1983

Prenatal Diagnosis of Fragile X Chromosome
Lancet 1:99-100, Shapiro,L.R.,et al, 1982

Fragile X Chromosome & X-Linked Mental Retardation
CMA Journal 127:123-126, Larbrisseau,A.,et al, 1982

Nevoid Basal Cell Carcinoma Syndrome & Epilepsy
Ann Neurol 11:372-376, Murphy,M.J.,et al, 1982

The Child Who is Slow to Talk
BMJ 285:671-672, Robinson,R.J., 1982

Cockayne Syndrome
J Comput Assist Tomogr 6:1172-1174, Levinson,E.D.,et al, 1982

Generalized Paroxysmal Fast Activity:Electoencephalographic & Clinical Features
Ann Neurol 11:386-390, Brenner,R.P.,et al, 1982

Maternal Seizure Disorder, Outcome of Pregnancy, & Neurologic Abnormalities in the Children
Neurol 32:1247-1254, Nelson,K.B.,et al, 1982

Lhermitte's Sign in Multiple Sclerosis:A Clinical Survey & Review of the Literature
JNNP 45:308-312, Kanchandani,R.,et al, 1982

Spinocerebellar Degeneration Secondary to Chronic Intestinal Malabsorption:A Vitamin E Deficiency Syndrome
Ann Neurol 12:419-424, Harding,A.E.,et al, 1982

Hypomelanosis of Ito (incontinentia pigmenti achromians) :Macrocephaly & Gray Matter Heterotopias
Neurol 32:1013-1016, Ross,D.L.,et al, 1982

Release Of Adenylate Kinase Into CSF During Open-Heart Surgery & Its Relation To Postop. Intellectual Function
Lancet 1:1139-1142, Aberg,T.,et al, 1982

Brain Damage After Open-heart Surgery
Editorial, Lancet 1:1161-11631982., , 1982

Two Cases of Van Buchem's Disease
JNNP 45:913-918, Dixon,J.M.,et al, 1982

Wernicke-Korsakoff Encephalopathy after Gastric Plication
JAMA 247:2566-2567, Haid,R.W.,et al, 1982

Benign Intracranial Hypertension Induced by Deficiency of Vitamin A During Infancy
Neurol 32:1292-1295, Kasarskis,E.J.,et al, 1982

Wernicke's Encephalopathy Following"Hunger Strike"
Postgrad Med J 58:427-428, Pentland,B.,et al, 1982

Wernicke's Encephalopathy In Prolonged Fasting
Lancet 2:1108-1109, Devathasan,G.,et al, 1982

Anorexia Nervosa & Wernicke's Encephalopathy:An Underdiagnosed Association
Lancet 2:771-772, Handler,O.E.,et al, 1982

Impaired Biotin Status in Anticonvulsant Therapy
Ann Neurol 12:485-486, Krause,K-H.,et al, 1982

Colpocephaly, An Error of Morphogenesis
Arch Neurol 39:243-246, Garg,B.P., 1982

Santavuori Disease:Diagnosis by Leukocyte Ultrastructure
Neurol 32:1277-1281, Baumann,R.J.,et al, 1982

Fibrodysplasia Ossificans Progressiva, The Clinical Features & Natural Hx of 34 Pts
J Bone Joint Surg 64B:76-83, Connor,J.M.&Evans,D.A.P., 1982

Pellagra, Endocronology System, Vol. 4
The Ciba Collection of Medical Illustrations, p. 254-255981., Netter,F.H., 1981

Neurologic Disease & Nutrition
Res & Staff Physician August 1981, pp. 77-81., Dreyfus,P.M., 1981

Biotin-Responsive Carboxylase Deficiency Associated With Subnormal Plasma & Urinary Biotin
NEJM 304:817-820, Thoene,J.,et al, 1981

Biotin Deficiency:An Unusual Complication Of Parenteral Alimentation
NEJM 304:820-823, Mock,D.M.,et al, 1981

Biotin For Neurologic Disorders of Uremia
NEJM 304:764, Yatzidis,H.,et al, 1981

Septo-optic Dysplasia in an Infant of a Diabetic Mother
Arch Neurol 38:590-591, Donat,J.F.G., 1981

Penicillamine-Induced Neuropathy in Rheumatoid Arthritis
Ann Int Med 95:457-458, Pool,K.D.,et al, 1981

Progressive Infantile Poliodystrophy, Assoc. With Disturbed Pyruvate Oxidation in Muscle & Liver
Arch Neurol 38:767-772, Prick,M.J.J.,et al, 1981

Evoked Responses in Vitamin B12 Deficiency
Ann Neurol 9:407-409, Krumholz,A.,et al, 1981

Lhermitte's Sign in Cobalamin (Vitamin B12) Deficiency
JAMA 245:1059, Butler,W.M.,et al, 1981

Dystrophic Axons & Spinal Cord Demyelination in Cystic Fibrosis
Neurol 31:714-718, Cavalier,S.J.,et al, 1981

Lipid Storage Myopathy:Successful Treatment with Propranolol
BMJ 282:1997-1999, Martyn,C.,et al, 1981

A Progressive Neurologic Syndrome In Children With Chronic Liver Disease
NEJM 304:503-508, Rosenblum,J.L.,et al, 1981

Effects of Prophyl. Treat. of CNS on Intellect. Funct. of Children with Acute lymph. Leuk
Am J Med 71:47-52, Moss,H.A., 1981

Depression, Intellectual Impairment & Parkinson Disease
Neurol 31:645-650, Mayeux,R.,et al, 1981