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Differential
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absence
acrocyanosis
agitation
Aicardi-Goutieres syndrome
akathisia
alcohol
alcohol intolerance
alcohol, neurologic complications with
Alexanders disease
Alexanders disease, adult onset
alternating rapid movement
alternating rapid movement, impaired
Alzheimer's disease
Alzheimer's disease, early onset
Alzheimer's disease, familial
amyloid angiopathy, cerebral
animal exposure
anticonvulsants
anticonvulsants, discontinuation in seizure-free epileptics
anticonvulsants, effectiveness
anticonvulsants, selection of
anxiety
aphasia
aphasia, progressive
apolipoprotein E
APP gene
apraxia
areflexia
arm weakness
asymptomatic
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, truncal
ataxic gait
atypical
autonomic dysfunction
axonal spheroid
Babinski sign
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
benign essential tremor
beta adrenergic blocker
biologic markers
blindness
bone pain
bovine spongiform encephalopathy
brain atrophy
brain biopsy
brainstem, atrophy
brainstem, lesion of
CAG repeats
calcification, intracranial
CAT scan
CAT scan, abnormal
CAT scan, false negative
cerebellar ataxia, children
cerebellar atrophy, primary
cerebellar degeneration
cerebellar lesion
cerebellar plaques, amyloid
cerebral cortex
cerebral cortical atrophy
cerebral vasculature
cerebrospinal fluid, abnormal
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, protein of
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, young adult
ceruloplasmin, serum
cherry red spot
cherry red spot-myoclonus syndrome
chewing movements
chilbran skin lesions
children
choking
chorea
chorea, familial
chorea, treatment of
choreoathetosis
choreoathetosis, paroxysmal
chromosomal abnormality
chromosome 12
chromosome 2
chromosome 7
chromosome 8
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
clonazepam
clonus
cognition
cognition, slowed
cogwheel rigidty
color vision, impaired
coma
confabulation
consanguinity
copper metabolism, abnormal
Creutzfeldt-Jakob disease, genetic
crying, pathologic
deafness
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, differential diagnosis of
dementia, familial
dementia, presenile
dementia, rapidly progressive
dementia, thalamic
dementia, transmissible
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
depression
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes insipidus
diabetes mellitus
diagnostic criteria
differential diagnosis
difficulty climbing stairs
diplopia
disability, neurological
distal muscle atrophy
distal muscle weakness
dizziness
Dravet syndrome
drooling
dropped head syndrome
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dyssynergia cerebellaris myoclonica
dystonia
dystonia, children
dystonia, face
dystonia, treatment of
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
electroencephalogram, video monitoring with
encephalopathy
encephalopathy, neonatal
encephalopathy, progressive
enzyme, defect
epidemiology of neurology
epileptic encephalopathy
epsilon sarcoglycan gene
exome sequencing
eye movement, disorders of
failure to thrive
falling
familial
familial adult myoclonic epilepsy
fasciculation
fatal familial insomnia
fatigue
feeding disorder
fever
finger nose finger test
fingerprint bodies
fundus, abnormality of
gait disorder
gangliosidosis GM2
Gaucher's disease
Gaucher's disease, adult onset
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
globus pallidus, lesion of
granular osmiphilic material
growth hormone
growth retardation
Hallervorden Spatz disease
hallucination
hallucination, visual
handwriting
head lag
head nodding
headache
hearing loss
heel-knee-shin test
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
hepatosplenomegaly
heralding manifestation
hexosaminidase-A
HLA
hyperekplexia
hyperhidrosis
hyperpyrexia, CNS disorder causing
hyperreflexia
hypertension
hyperthermia
hypertonia
hypertonia, congential
hypomyelination
hypothermia
hypotonia
iatrogenic neurologic disorders
imbalance
inattention
inborn errors of metabolism
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, intracytopasmic
insight, loss
insomnia
intellectual deficit
intellectual deterioration
interferon alpha
intrauterine
irritability
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, variant
Jewish
juvenile myoclonus epilepsy
Kayser-Fleischer ring
lactic acidemia
Lafora body
Lafora's disease
Leigh's disease
Leigh's disease, adult variety
lethargy
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
life expectancy
linear lesion
lipid storage disorder of CNS
liver biopsy
liver disease
lysosomal storage disease
macular degeneration
MELAS syndrome
memory, defect of recent
memory, impairment of
mental retardation
MERRF syndrome
microcephaly
miglustat
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
monoparesis
mortality
motor cortex
movement disorder
movement disorder, paroxysmal
movement disorder, treatment of
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, FLAIR
MRI, hypointense signal foci on
MRI, negative
MRI, punctate pattern
MRI, susceptibility weighted
multiple sclerosis, misdiagnosis
muscle biopsy
muscle spasm
muscle stiffness
muscle weakness
muscle weakness, proximal
mutism
myasthenia gravis, differential diagnosis
myasthenia gravis, misdiagnosis of
myelination of nervous system
myoclonic dystonia
myoclonic jerks
myoclonus
myoclonus, action
myoclonus, cortical
myoclonus, epilepsy
myoclonus, essential
myoclonus, sleep
myoclonus, stimulus sensitive
myopathy, mitochondrial
mysoline
negative
neuraminidase deficiency
neuroaxonal dystrophy
neuroaxonal dystrophy, infantile
neuroaxonal dystrophy, juvenile
neuroendocrinology
neurologic disease, diagnoses of
neurologic signs
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, peripheral
neuropsychiatry
next-generation sequencing
Niemann-Pick disease
normal
nystagmus
nystagmus, rotary
ophthalmoplegia
optic atrophy
optic atrophy, hereditary
palatal myoclonus
paraparesis
paraparesis, spastic
paratonia
Parkinson disease
Parkinsonism syndrome
paroxysmal dystonic choreoathetosis
paroxysmal kinesigenic dyskinesia
paroxysmal neurologic deficits
PAS positive
PAS positive material in the brain
pediatric neurology
penicillamine
pituitary, hormones of
pleocytosis of cerebrospinal fluid
polymerase chain reaction
polyneuropathy
pontocerebellar atrophy
prenatal
prion disease
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
progressive pallidum atrophy
propranolol
protein 14-3-3, cerebrospinal fluid
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
ptosis
Purkinje cell
pyramidal tract dysfunction
pyruvate metabolism, abnormality of
quadriparesis
ragged-red fibers
rapidly progressing neurologic illness
real-time quaking-induced conversion
respiratory failure
retinal degeneration
review article
rigidity
Romberg's sign
Rosenthal fibers
SCN1A gene
screening
seizure
seizure, children
seizure, diagnosis of
seizure, drug resistance
seizure, familial
seizure, febrile
seizure, intractable
seizure, laughing as manifestation
seizure, neonatal
seizure, paradoxical
seizure, photosensitive
seizure, prognosis in adults
seizure, stimulus sensitive
seizure, teenager
seizure, tonic-clonic
seizure, treatment of
sensorineural hearing loss
short stature
skin, biopsy
skin, lesions in neurologic disorders
sleep pathology and physiology
sodium channel dysfunction
sodium valproate
spastic dysphonia
spasticity
speech disorder
speech disorder, childhood
speech, loss of
sphingolipodoses
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 16
spinocerebellar ataxia type 7
spinopontine atrophy, dominant
spongy degeneration of brain
startle myoclonus
startle reaction
status epilepticus
stereotypy
storage disease of CNS
striatonigral degeneration
striatonigral degeneration, infantile
strokelike episodes
stuporous
stuttering
systemic illness
tachycardia
tandem gait, ataxic
Tay-Sachs disease
thalamus, atrophy of
thalamus, lesion of
thalamus, lesion of-bilateral
titubation
tone, muscle, increased
topiramate
treatment of neurologic disorder
tremor
tremor, intention
tremor, jaw
tremor, leg
tremor, treatment of
trichopoliodystrophy
trinucleotide repeats
Unverricht-Lundborg disease
upgaze, paralysis of
visual acuity, decreased
visual loss
visuospatial disturbance
walking frame
walking, difficulty with
weakness
weakness, acute
weakness, focal
weight loss
wheelchair
white matter disease
whole genome sequencing
wide based gait
Wolfram syndrome
workup
Showing articles 1200 to 1250 of 2026 << Previous Next >>

Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy
Neurol 41:823-828, Olney,R.K.,et al, 1991

The Phenotype of the X-Linked Dystonia-Parkinsonism Syndrome, An Assessment of 42 Cases in the Philippines
Medicine 70:179-187, Lee,J.V.,et al, 1991

Preclinical Detection of Parkinson's Disease
Neurology Suppl 2, 41:5-921991., Koller,W.C.&Langston,J.W., 1991

MR of Progressive Neurodegenerative Change in Treated Menkes'Kinky Hair Disease
Neuroradiology 33:181-182, Johnsen,D.E.,et al, 1991

Globoid Cell Leukodystrophy:A Family with Both Late-Infantile and Adult Type
Neurol 41:1382-1384, Verdru,P.,et al, 1991

Clinical & Laboratory Findings in the Oculocerebrorenal Syndrome of Lowe, with Special Ref to Growth & Renal Function
NEJM 324:1318-1325, Charnas,L.R.,et al, 1991

Use of CT, MRI, & Localized 1H MR Spectroscopy in Canavan's Disease:A Case Report
Ann Neurol 30:106-110, Marks,H.G.,et al, 1991

Benign Familial Neonatal Convulsions:Evidence for Clinical and Genetic Heterogeneity
Ann Neurol 29:469-473, Ryan,S.G.,et al, 1991

Epileptic Palatal Myoclonus
Neurol 41:1305-1306, Tatum,W.O.,et al, 1991

Hallervorden-Spatz Syndrome and Brain Iron Metabolism
Arch Neurol 48:1285-1293, Swaiman,K.F., 1991

Chronic Cardiomyopathy and WEakness or Acute Coma in Children with a Defect in Carnitine Uptake
Ann Neurol 30:709-716, Stanley,C.A.,et al, 1991

Erythromelalgia:Review of Clinical Characteristics and Pathophysiology
Am J Med 91:416-422, Jurzrock,R.&Cohen,P.R., 1991

The Spongiform Encephalopathies, Editorial
JNNP 54:761-763, Will,R.G., 1991

More Bad Luck for the X Chromosome:Thalassaemia/Mental Retardation
Lancet 338:1562-1563, , 1991

Clinical Genetics and Genetic Counseling in Alzheimer Disease
Ann Int Med 115:601-606, Breitner,J.C.S., 1991

Discordance and Concordance of Dementia of the Alzheimer Type (DAT) in Monozygotic Twins
Neurol 41:1549-1553, Rapoport,S.I.,et al, 1991

Familial Spinal Neurofibromatosis:Clinical and DNA Linkage Analysis
Neurol 41:1923-1927, Pulst,S.M.,et al, 1991

Truncal Asterixis Associated with Ceftazidine, A Third-Generation Cephalosporin
Neurol 41:2008, Hillsley,R.E.&Massey,E.W., 1991

Ear Click in Palatal Tremor:Its Origin and Treatment with Botulinum Toxin
Neurol 41:1677-1679, Deuschl,G.,et al, 1991

Prenatal Origin of Hemiparetic Cerebral Palsy:How Often and Why?
Pediatrics 88:1059-1062, Nelson,K.B., 1991

Monozygotic Twins with Seizures, Shared Characteristics
Arch Neurol 48:1041-1045, Segal,R.A.,et al, 1991

Creutzfeldt-Jakob Disease and Other Transmissible Spongiform Encephalopathies
Ed, F. O. Bastian, Mosby Year Book, St. Louis 9:153, Maertens,P.&Quindlen,E.A., 1991

Cumulative Risks of Developing Extrapyramidal Signs, Psychosis, or Myoclonus in the Course of Alzheimer's Disease
Arch Neurol 48:1141-1143, Chen,J.,et al, 1991

Hashimoto's Encephalopathy:A Steroid-Responsive Disorder Associated with High Anti-Thyroid Antibody Titers-Report of 5 Cases
Neurol 41:228-233, Shaw,P.J.,et al, 1991

Dopa-Responsive Dystonia:Long-Term Treatment Response and Prognosis
Neurol 41:174-181, Nygaard,T.G.,et al, 1991

Nystagmus of Pelizaeus-Merzbacher Disease
Arch Neurol 48:87-91, Trobe,J.D.,et al, 1991

Tourette Syndrome and Other Tic Disorders, Diagnosis, Pathophysiology, and Treatment
Medicine 70:15-32, Singer,H.S.&Walkup,J.T., 1991

A Genetic Study of Idiopathic Focal Dystonias
Ann Neurol 29:320-324, Waddy,H.M.,et al, 1991

Long-Term Suppression of Tremor by Chronic Stimulation of the Ventral Intermediate Thalamic Nucleus
Lancet 337:403-406, Benabid,A.L.,et al, 1991

Multistate Outbreak of Poisonings Associated with Illicit Use of Gamma Hydroxy Butyrate
JAMA 265:447-448, , 1991

HTLV-I-Associated Myelopathy Associated with Blood Transfusion in the US:Epidemiologic & Molecular Evidence
Neurol 41:192-197, Kaplan,J.E.,et al, 1991

Syphilitic Meningomyelitis
Neurol 41:325-326, Strom,T.&Schneck,S.A., 1991

Myelopathic Neurosarcoidosis:Diagnostic Value of Enhanced MRI
Neurol 41:150-151, Sauter,M.K.,et al, 1991

Clinicopathological Observations in Essential Tremor:Report of Six Cases
Neurol 41:1422-1424, Rajput,A.H.,et al, 1991

Relation Between Nicotine Intake and Alzheimer's Disease
BMJ 302:1491-1494, VanDuijn,C.M.&Holman,A., 1991

HTLV-I-Associated Myelopathy/Tropical Spastic Paraparesis in the United States
Neurol 41:1355-1357, Janssen,R.S.,et al, 1991

HTLV-I-Associated Myelopathy Endemic in Texas-Born Residents and Isolation of Virus from CSF Cells
Neurol 41:831-836, McKendall,R.R.,et al, 1991

Mutation of the Prion Protein in Libyan Jews with Creutzfeldt-Jakob Disease
NEJM 324:1091-1097, Hsiao,K.,et al, 1991

The First Report of Cluster Headache in Identical Twins
Neurol 41:761, Couturier,E.G.M.,et al, 1991

Acetazolamide-Responsive Vestibulocerebellar Syndrome:Clinical & Oculographic Features
Neurol 41:429-433, Baloh,R.W.&Winder,A., 1991

Corticosteroid-Responsive Dominantly Inherited Neuropathy in Childhood
Neurol 41:437-439, Bird,S.J.&Sladky,J.T., 1991

Lisch Nodules in Neurofibromatosis Type I
NEJM 324:1264-1266, 1283-12851991., Lubs,M-L.E.,et al, 1991

Clinicopath Conf
Pheochromocytoma of Adrenal Gland, Von Hippel-Lindau Disease, Case 16-1991, NEJM 324:1119-112791., , 1991

VonHippel-Lindau Disease
Editorial, Lancet 337:10651991., , 1991

Clinicopath Conf
Cerebral Amyloid Angiopathy, Case 27-1991, NEJM 325:42-54991., , 1991

Homocystinuria Due to 5, 10-Methylenetetrahydrofolate Reductase Deficiency Revealed by Stroke in Adult Siblings
Neurol 41:1313-1315, Visy,J.M.,et al, 1991

Diagnostic Tests for Choreoacanthocytosis
Neurol 41:1000-1006, Feinberg,T.E.,et al, 1991

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

Conjugal Multiple Sclerosis:A Clinical and Laboratory Study
Neurol 41:1320-1321, Finelli,P.F., 1991

Classification and Treatment of Tremor
JAMA 266:1115-1117, Hallett,M., 1991



Showing articles 1200 to 1250 of 2026 << Previous Next >>