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Differential
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anticonvulsants, discontinuation in seizure-free epileptics
apraxia
asymptomatic
ataxia
behavioral disorder
bone pain
calcification, intracranial
CAT scan
CAT scan, abnormal
CAT scan, false negative
cerebral cortical atrophy
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, young adult
chromosome 8
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
color vision, impaired
coma
degenerative diseases of CNS
dementia
dementia, presenile
dementia, rapidly progressive
depression
diplopia
electroencephalogram
electroencephalogram, abnormalities of
encephalopathy
encephalopathy, progressive
familial
familial adult myoclonic epilepsy
Gaucher's disease
Gaucher's disease, adult onset
gaze palsy, supranuclear
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
hallucination
hallucination, visual
headache
hearing loss
hepatosplenomegaly
inclusion bodies
inclusion bodies, intracytopasmic
intellectual deficit
intellectual deterioration
juvenile myoclonus epilepsy
lactic acidemia
Lafora body
Lafora's disease
Leigh's disease
Leigh's disease, adult variety
lethargy
MELAS syndrome
mental retardation
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
MRI, abnormal
muscle biopsy
muscle weakness
muscle weakness, proximal
myasthenia gravis, differential diagnosis
myasthenia gravis, misdiagnosis of
myoclonic jerks
myoclonus
myoclonus, epilepsy
negative
neuroendocrinology
neurologic disease, diagnoses of
neuroophthalmology
neuropathology
neuropathology, brain
neuropsychiatry
normal
ophthalmoplegia
optic atrophy
optic atrophy, hereditary
paraparesis, spastic
PAS positive
PAS positive material in the brain
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
psychiatric problems in neurologic disorders
psychosis
ptosis
ragged-red fibers
review article
seizure
seizure, children
seizure, diagnosis of
seizure, familial
seizure, intractable
seizure, prognosis in adults
seizure, teenager
seizure, treatment of
short stature
skin, biopsy
sodium valproate
sphingolipodoses
strokelike episodes
treatment of neurologic disorder
upgaze, paralysis of
weakness
Showing articles 500 to 550 of 5748 << Previous Next >>

Familial Idiopathic Striopallidodentate Calcifications
Neurol 39:381-385, Ellie,E.,et al, 1989

Agenesis of the Corpus Callosum and Gyral Malformations are Frequent Manifestations of Nonketotic Hyperglycinemia
Neurol 39:817-820, Dobyns,W.B., 1989

Busulphan and Phenytoin
Ann Int Med 111:1049-1050, Grigg,A.P.,et al, 1989

Nifedipine and Myoclonic Disorders
Nephron 51:281, Pedro-Botet,M.L.,et al, 1989

A Creutzfeldt-Jakob Like Syndrome Due to Lithium Toxicity
JNNP 51:120-123, Smith,S.J.M.&Kocen,R.S., 1988

Myoclonus During Combined Tricyclic Antidepressant and Lithium Treatment
J Clin Psychopharmacol 8:446-447, Devanand,D.P.,et al, 1988

A Single Seizure, Likely to Recur
BMJ 297:1422-1423, Reynolds,E.H., 1988

The Course Untreated Epilepsy
BMJ 297:948-950, Elwes,R.D.C.,et al, 1988

Brain Metabolism in Mitochondrial Encephalomyopathy:A PET Study
J Comput Assist Tomogr 12:854-857, DeVolder,A.,et al, 1988

Familial Alzheimer's Disease with Myoclonus and'Spongy Change'
Arch Neurol 45:1097-1100, Duffy,P.,et al, 1988

Discontinuing Antiepileptic Drugs
NEJM 319:871-872, Rosen,J.A., 1988

Outcome from Coma After Cardiopulmonary Resuscitation:Relation to Seizures & Myoclonus
Neurol 38:401-405, Krumholz,A.,et al, 1988

Cerebral Cavernous Malformations:Incidence and Familial Occurrence
NEJM 319:343-347, Rigamonti,D.,et al, 1988

Rett Syndrome:Natural History and Management
Pediatrics 82:1-10, Moeschler,J.B.,et al, 1988

Withdrawal of Anticonvulsant Drugs in Pts Free of Seizures for Two Years, A Prospective Study
NEJM 318:942-946, 982-9841988., Callaghan,N.,et al, 1988

The First Seizure in Adult Life, Value of Clinical Features, EEG & CT Scanning in Prediction of Seizure Recurrence
Lancet 1:721-726, Hopkins,A.,et al, 1988

Mutation in Cystatin C Gene Causes Hereditary Brain Hemorrhage
Lancet 2:603-604, Palsdottir,A.,et al, 1988

Familial Oculoleptomeningeal Amyloidosis, Report of a New Family with Unusual Features
Arch Neurol 45:1118-1122, Uitti,R.J.,et al, 1988

Chronic Progressive Spinobulbar Spasticity, A Rare Form of Primary Lateral Sclerosis
Arch Neurol 45:509-513, Gastaut,J.L.,et al, 1988

Rapidly Progressive Dementia Caused by Spongiform Encephalopathy
West J Med 148:313-319, Enos,B.E.&Vinters,H.V., 1988

Discontinuation of Antiepileptic Therapy:A Prospective Study in Children
JNNP 50:1579-1583, Bouma,P.A.D.,et al, 1987

Seizures:Common Causes & Treatment in the Elderly
Geriatrics 42:73-78, Mahler,M.E., 1987

Risk Factors for Generalized Tonic-Clonic Seizures:A Population-Based Case-Control Study in Rochester, Minnesota
Neurol 37:1315-1322, Rocca,W.A.,et al, 1987

Factors Prognostic of Unprovoked Seizures After Febrile Convulsions
NEJM 316:493-498, Annegers,J.F.,et al, 1987

Childhood Stroke Associated with Protein C or S Deficiency
J Pediatr 111:562-564, Israels,S.J.&Seshia,S.S., 1987

First Seizure Management-Reconsidered, Response I, II, & III, Controversies in Neurology
Fisher, R. S. , Dasheiff, R. , Arch Neurol 44:1189-1191, Fromm,G.H., 1987

CT in Ceroid Lipofuscinosis
Neurol 37:1025-1026, Dunn,D.W., 1987

Mendelian Etiologies of Stroke
Ann Neurol 22:175-192, Natowicz,M.&Kelley,R.I., 1987

Clinical Spectrum of Hereditary Hemorrhagic Telangiectasia (Osler-Wever-Rendu Disease)
Am J Med 82:989-997, Perry,W.H., 1987

MELAS Syndrome Involving a Mother & Two Children
Arch Neurol 44:971-973, Driscoll,P.F.,et al, 1987

Photic Cortical Reflex Myoclonus
Ann Neurol 22:252-257, Shibasaki,H.&Neshige,R., 1987

Incontinentia Pigmenti:Association with Anterior Horn Cell Degeneration
Neurol 37:446-450, Larsen,R.,et al, 1987

Computed Tomography in Adult-Onset Epileptic Seizures in a City Hospital Population
Epilepsia 28:519-522, Daras,M.,et al, 1987

Should People be Treated after a First Seizure
Arch Neurol 43:1287-1288, 12901986., Hauser,W.A., 1986

Seizure Recurrence After a First Unprovoked Seizure
Arch Neurol 43:1289-1290, Hart,R.G.&Easton,J.D., 1986

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

Medical Complications of Cocaine Abuse
NEJM 315:1495-1499, Cregler,L.L.&Mark,H., 1986

Clinicopath Conf
Tuberous Sclerosis, Case 41-1986, NEJM 315:1013-1022986., , 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

Seizures & Myoclonus in Patients with Alzheimer's Disease
Neurol 36:1226-1230, Hauser,W.A.,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

Chronic Demyelinating Peripheral Neuropathy in Cerebrotendinous Xanthomatosis
Ann Neurol 20:89-91, Argov,Z.,et al, 1986

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

Benign Versive or Circling Epilepsy with Bilateral 3-Cps Spike- & -Wave Discharges in Late Childhood
Ann Neurol 19:301-303, Gastaut,H.,et al, 1986

Etiology of Seizures in the Elderly
Epilepsia 27:458-463, Luhdorf,K.,et al, 1986

Epilepsy in the Elderly:Incidence, Social Function, & Disability
Epilepsia 27:135-141, Luhdorf,K.,et al, 1986

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

Drop Attacks:An Ominous Change in the Evolution of Partial Epilepsy
Neurol 35:1725-1720, Pazzaglia,P.,et al, 1985

Biotinidase Deficiency:Initial Clinical Features & Rapid Diagnosis
Ann Neurol 18:614-617, Wolf,B.,et al, 1985



Showing articles 500 to 550 of 5748 << Previous Next >>