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anticholinergic drugs

arylsulfatase A

ataxia, cerebellar

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behavioral disorder

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Brueghel's syndrome

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cardiac arrest and resuscitation

CAT scan, abnormal

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, muscle

caudate nucleus, atrophy

cerebellar degeneration

cerebral cortical atrophy

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrovascular accident

cerebrovascular accident, infancy and childhood

chorea, Sydenham's

choreoathetosis

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

collapsin response mediator protein 5 IgG

conversion reaction

creatine phosphokinase(CPK)elevated

degenerative diseases of CNS

delay in diagnosis

dementia, presenile

developmental milestones, loss of

developmental retardation

diagnostic criteria

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disease modifying agents

dopa responsive dystonia

dopamine agonist

dopamine depleting agents

DPPX, antibodies

DPPX, antibodies, encephalitis

drug induced neurologic disorders

dyskinesia, buccal lingual facial

dyskinesia, drug induced

dystonia musculorum deformens

dystonia, classification

dystonia, delayed onset

dystonia, drug induced

dystonia, etiology of

dystonia, evaluation of

dystonia, focal

dystonia, treatment of

dystonia, truncal

dystonic reaction, acute

electroencephalogram, abnormalities of

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, paraneoplastic

encephalopathy, neonatal

encephalopathy, post anoxic

executive dysfunction

exome sequencing

eye movement, disorders of

facial nerve palsy

forceps delivery

gamma amino butyric acid receptor antibody

gammaglobulin therapy, intravenous

gaze palsy, supranuclear

gaze palsy, vertical

genetic counselling

genetic neurologic disorders

genetic testing

gests antagoniste

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

GLUT1 deficiency syndrome

glutamic acid decarboxylase, antibody

glycine receptor antibodies

Hallervorden Spatz disease

Hallervorden Spatz disease, late onset

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

Hodgkin's disease

Huntington's chorea

Huntington's disease, children

hypoglycorrhachia

hypotonia, infants

hypoxia, newborn

hypoxic encephalopathy

iatrogenic neurologic disorders

imbalance, postural

immunologic disease

inborn errors of metabolism

inclusion bodies, intranuclear

infantile hemiplegia

intellectual deficit

intellectual deterioration

internal cerebral vein

islet cell tumor

L-dopa, delayed treatment in Parkinsonism

L-dopa, drug interactions with and side effects of

left handedness

Leigh's disease

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

leucine rich glioma inactivated 1 antibodies

life expectancy

limbic encephalitis

lipid storage disorder of CNS

lumbar puncture

lysosomal storage disease

memory, impairment of

meningitis, carcinomatous

mental retardation

mental status, abnormal

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, adult onset

migraine, children

mitochondrial disease

monoclonal antibodies

movement disorder

movement disorder, delayed onset

movement disorder, drug induced

movement disorder, extrapyramidal

movement disorder, extrapyramidal-treatment of

movement disorder, hyperkinetic

movement disorder, treatment of

MRI, CAT scan compared to

MRI, eye of tiger sign

MRI, paramagnetic effect

muscle weakness

muscular dystrophy

myasthenia gravis

myopathy, metabolic

neuroleptic, atypical

neurologic disease, diagnoses of

neurologic signs

neuronal intranuclear inclusion disease

Niemann-Pick disease

nitroproprionic acid

NMDA antagonists

nystagmus, monocular

obsessive-compulsive disorder

oculogyric crisis

old age, neurology of

ophelia syndrome

paraspinal muscle

paraspinal muscle weakness

Parkinson disease

Parkinson disease, drug induced

Parkinson disease, dystonia with

Parkinson disease, fluctuations in

Parkinson disease, freezing phenomena in

Parkinson disease, juvenile

Parkinson disease, L-dopa nonresponsive

Parkinson disease, mode of onset

Parkinson disease, on-off phenomena in

Parkinson disease, prognosis of

Parkinson disease, rapid onset

Parkinson disease, treatment of

Parkinson disease, unilateral

Parkinson disease, young onset

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection

phenothiazine, dyskinesia associated with

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

postural abnormality

potassium channel antibodies

practice guidelines

precipitating factors

prevention of neurologic disorders

progressive neurologic disorder

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

psychotic behavior

putamen, lesion of

putamen, lesion of, bilateral

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quality of life

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

remote effect of cancer on the nervous system

reserpine treatment in movement disorder

retinal degeneration

retinitis pigmentosa

salivation, excessive

seizure, adult onset

seizure, children

seizure, laughing as manifestation

seizure, neonatal

seizure, unknown origin

sensorineural hearing loss

serologic testing

serologic testing, false negative

sleep pathology and physiology

speech disorder

status epilepticus

stem cell transplantation

steroid therapy, CNS treatment and complications with

stimulation, deep brain

stooped posture

streptococcal infection

streptococcus pyogens

striatal encephalitis

striatum, lesion of

sugarcane, mildewed

swallow evaluation

tardive akathisia

tardive dyskinesia

tardive dyskinesia, treatment of

tardive dystonia

tardive pain syndrome

tetrahydrobiopterin

thalamus, infarction of

thalamus, lesion of-bilateral

tonic foot response

torticollis, benign paroxysmal

torticollis, familial

torticollis, infants and children

toxic encephalopathy

toxins, nervous system

treatment of neurologic disorder

tremor, postural

tremor, resting

tremor, thalamic

tricyclic antidepressant

trinucleotide repeats

urinary sulfatidase excretion

walking, difficulty with

weakness, progressive

white matter disease

whole genome sequencing

wide based gait

Showing articles 1700 to 1750 of 1853 << Previous Next >>

Phencyclidine:The New American Street Drug
Editorial, BMJ 281:1511-15121980., , 1980

Dystonic Foot Response of Parkinsonism
Arch Neurol 37:132-136, Nausieda,P.A.,et al, 1980

Acute Cerebellar Ataxia Associated With Epstein-Barr Virus Infection
JAMA 243:148-149, Cleary,T.G.,et al, 1980

Mycoplasma Antibody in Guillain-Barre Syndrome & Other Neurological Disorders
Ann Neurol 7:108-112, Goldschmidt,B.,et al, 1980

Transient Global Amnesia
Ann Neurol 7:281-285, Shuping,J.R.,et al, 1980

Transient Global Amnesia Due to Glioma in the Dominant Hemisphere
Neurol 30:88-90, Shuping,J.R.,et al, 1980

Musical Performance During Transient Global Amnesia
Neurol 30:80-82, Byer,J.A., 1980

Delayed Stroke Following Carotid Occlusion
Neurol 30:84-88, Finklesten,S.,et al, 1980

Neonatal Polycythemia Causing Multiple Cerebral Infarcts
Arch Neurol 37:109-110, Amit,M.,et al, 1980

L-Dopa in Children with Progressive Neurological Disorders
Ann Neurol 7:93, Bugiani,O.,et al, 1980

Benign Familial Neonatal Seizures
E. , Arch Neurol 37:47-48980., Pettit,R., 1980

Facial Dyskinesia From Overdose Of An Anti-histamine
NEJM 303:107, Barone,D.A.,et al, 1980

Demonstration of CSF Gamma-globulin Banding in Presenile Dementia
Neurol 30:882-884, Williams,A.,et al, 1980

Decreased Computerized Tomography Numbers in Patients With Presenile Dementia
Arch Neurol 37:401-409, Naeser,M.A.,et al, 1980

Presenile Alzheimer Disease:Amyloid Plaques in the Cerebellum
Neurol 30:820-825, Pro,J.D.,et al, 1980

Febrile Seizures:Long-term Management of Children with Fever-associated Seizures
Editorial, BMJ 281:277-2791980., , 1980

Valproic Acid Therapy in Childhood Epilepsy
JAMA 244:785-788, Coulter,D.L.,et al, 1980

Paroxysmal Symptoms as the First Manifestations of Multiple Sclerosis
JNNP 43:296-304, Twomey,J.A.,et al, 1980

Neurologic Manifestations in Macroglobulinemia
In Vinken PJ, Bruyn GW, Eds, Handbook of Clin Neurol, Vol 39, North-Holland Publ Co, p. 189, Abramsky,O., 1980

Icepick-like Pain
Neurol 30:203-205, Raskin,N.H.&Schwartz,R.K., 1980

Alternating Hemiplegia in Infants:Report of Five Cases
Dev Med Child Neurol 22:784-791, Krageloh,I.&Aicardi,J., 1980

Paroxysmal Choreoathetosis Associated with Thyrotoxicosis
Ann Neurol 6:453-454, Fischblek,K.H.,et al, 1979

Meige's Disease, A Clinical Form of Facial Convulsion, Bilateral & Medial
Arch Neurol 36:635-637, Tolosa,E.S.,et al, 1979

Meige Disease:Striatal Dopaminergic Preponderance
Neurol 29:1126-1130, Tolosa,E.S.,et al, 1979

Drug Therapy, Bromocriptine
NEJM 301:873-878, Parkes,D., 1979

Phenobarbital Dosage for Control of Neonatal Seizures
Neurol 29:1445-1449, Lockman,L.A.,et al, 1979

Computed Tomography & Childhood Seizure Disorders
Neurol 29:1084-1088, Yang,P.J.,et al, 1979

Transient Global Amnesia:Clinical & Electroencephalographic Findings in 10 Cases
Neurol 29:869-872, Rowan,A.J.,et al, 1979

Presenile Dementia With Motor Neuron Disease in Japan, A New Entity
Arch Neurol 36:592-593, Mitsuyama,Y.,et al, 1979

Sexual Intercourse & Transient Global Amnesia
NEJM 300:864, Mayeux,R., 1979

Diagnosis & Treatment of Migraine in Children
Neurol 29:506-510, Prensky,A.L.,et al, 1979

Familial Psychosis & Diverse Neurologic Abnormalities in Adult-Onset Gaucher's Disease
Arch Neurol 36:95-99, Neil,J.F.,et al, 1979

Neurologic Disturbances in Pagets Disease of Bone:Response to Calcitonin
Neurol 29:448-457, Chen,J.R.,et al, 1979

Blepharospasm:Successful Treatment with Clonazepam
Ann Neurol 5:401-402, Merikangas,J.R.,et al, 1979

Early-Morning Dystonia-A Late Side Effect of Long-Term Levodopa Therapy
Arch Neurol 36:308-310, Melamed,E., 1979

Neurological Manifestations of Fabry Disease in Female Carriers
Ann Neurol 4:537-540, Bird,T.D.,et al, 1978

Adult Onset Nemaline Myopathy
Neurol 28:1306-1309, Brownell,A.K.W.,et al, 1978

Presenile Dementia with Lewy Bodies & Neurofibrillary Tangles
Arch Neurol 35:818-822, Forno,L.S.,et al, 1978

Oral Contraceptives & Stroke in Young Women:A Clinicopathologic Correlation
Neurol 28:1216-1219, Irey,N.S.,et al, 1978

Late Adult-onset Metachromatic Leukodystrophy
Arch Neurol 35:475, Bosch,E.P., 1978

Huntington Disease Associated with Alzheimer Disease
Ann Neurol 3:545, McIntosh,G.C.,et al, 1978

Juvenile Huntington Chorea:Clinical, Ultrastructural, & Biochemical Studies
Neurol 28:23, Goebel,H.H.,et al, 1978

Diagnosis of Treatable Wilson's Disease
NEJM 298:1347, Cartwright,G.E., 1978

Aggravation of Tardive Dyskinesia by Phenytoin
NEJM 298:457, DeVeaugh-Geiss,J., 1978

Autosomal Dominant System Degeneration in Portugese Families of the Azores Islands
Neurol 28:703, Coutinho,P.,et al, 1978

Clinical Aspects of Spasmodic Dysphonia
JNNP 41:361, Aminoff,M.J.,et al, 1978

Hemifacial Spasm
Arch Neurol 35:481, Maroon,J.C., 1978

Hemifacial Spasm Due to Aneurysmal Compression of the Facial Nerve
Arch Neurol 35:545, Maroon,J.C.,et al, 1978

Gaze-evoked Blepharoclonus
Ann Neurol 3:243, Keane,J.R., 1978

Onset & End-of-dose Levodopa-induced Dyskinesias
Arch Neurol 35:261, Lhermitte,F.,et al, 1978

Showing articles 1700 to 1750 of 1853 << Previous Next >>