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Differential
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aciduria
adverse drug reaction
algorithm
ataxia
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune disease
basal ganglia, lesion of
basal ganglia, lesion, bilateral
caudate nucleus, lesion of, bilateral
central nervous system, infection of
cerebral palsy
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, lactic acid concentration
children
chromosomal abnormality
chromosome 1
delay in diagnosis
developmental retardation
diet
differential diagnosis
dopa responsive dystonia
drug induced neurologic disorders
dyskinesia
dystonia
dystonia, children
encephalitis, autoimmune
familial
gene
gene mutation
genetic counselling
genetic neurologic disorders
GLUT1
GLUT1 deficiency syndrome
hypoglycemia
hypoglycorrhachia
hypoglycorrhachia, causes of
hypotonia
inborn errors of metabolism
iron, brain
islet cell tumor
ketogenic diet
lactate
lenticular nucleus, lesion of, bilateral
lumbar puncture
mental retardation
metabolic disorder, primary
microcephaly
mimics
molecular genetics
movement disorder
MRI, abnormal
MRI, paramagnetic effect
neurologic disease, diagnoses of
neurotomy
next-generation sequencing
paroxysmal exertion-induced dyskinesia
review article
seizure
seizure, children
seizure, familial
seizure, neonatal
seizure, petit mal
spasticity
striatal encephalitis
symmetric brain lesions
treatment of neurologic disorder
walking, difficulty with
workup
Showing articles 1000 to 1050 of 1246 << Previous Next >>

Neurological Complications of Thyrotoxicosis in the Elderly
Ann Neurol 15:608, Florin,T., 1984

Limbic Encephalopathy as a Nonmetastatic Complication of Oat Cell Lung Cancer
Am J Med 75:518-520, Brennan,L.V.,et al, 1983

Downbeat Nystagmus
Arch Neurol 40:754-755, Coppeto,J.R.,et al, 1983

Pyridoxine Deficiency & Peripheral Neuropathy Associated with Long-Term Phenelzine Therapy
Am J Med 75:887-888, Heller,C.A.,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

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

Serum Folate Concentra. During Pregnancy in Women with Epilepsy:Relation to Antiepileptic Drug Concentrations
BMJ 287:577-579, Hiilesmaa,V.K.,et al, 1983

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

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

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

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

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

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



Showing articles 1000 to 1050 of 1246 << Previous Next >>