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Differential
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abducens nerve paralysis
acetazolamide
adenosine deaminase deficiency
adverse drug reaction
Africa
agenesis of corpus callosum
albinism
alcohol
alcohol, neurologic complications with
alpha-fetoprotein
alternating hemiplegia
alternating hemiplegia of childhood
anemia
anosmia
anterior spinal artery
aphasia
apnea
apnea, primary central
apraxia of eye movements
areflexia
Arnold Chiari malformation
arthralgia
ascites
aspartocyclase
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
ataxia, progressive
ataxia, truncal
ataxic gait
athetosis
atlanto-axial subluxation
ATP1A3 gene
autonomic dysfunction
autosomal rcessive spastic ataxia of Charlevoix-Saguenay
Babinski sign
bacterial infection
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
benign essential tremor
blindness
bone marrow biopsy
brain biopsy
brainstem, atrophy
brainstem, dysfunction
brainstem, hypoplasia
brainstem, lesion of
brainstem, malformation
brainstem, neoplasms of
Brown-Vialetto-Van Laere syndrome
CAG repeats
Canavan's disease
carcinoma
cardiomyopathy
carotid angiogram
case studies
cassava
CAT scan
CAT scan, abnormal
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar hypoplasia
cerebellar peduncle
cerebellar vermis
cerebellum, disease of
cerebellum, neoplasms of
cerebral edema
cerebrospinal fluid
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, young adult
channelopathy
Chediak-Higashi syndrome
cherry red spot
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 19
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
Collier's sign
coma
coma, episodic
complicated migraine
congenital malformation
congenital ocular motor apraxia
consanguinity
contractures, joint
conus medullaris, lesion of
corneal dystrophy
cough
cranial nerve palsies
cranial nerves
cranial neuropathy
cranial neuropathy, multiple
cranio-cervical junction
cultured skin fibroblasts
cyanide poison
deafness
deafness, bilateral progressive vs.unilateral acute
deafness, unilateral
degenerative diseases of CNS
dementia
dementia, familial
dementia, frontotemporal
dementia, presenile
demyelinating disease
developmental abnormality of brain
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes insipidus
diabetes mellitus
diabetes mellitus, chemical
diabetes mellitus, neurologic manifestations of
diabetes mellitus, ocular complications in
diabetic cranialneuropathies
diagnostic criteria
differential diagnosis
diplopia
disconnection syndrome
down-beat nystagmus
down-beat nystagmus, primary position of gaze
drought
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dyspnea
dyspraxia
dystonia
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
electronystagmography
electroretinograph
encephalopathy
enzyme, defect
epidemiology of neurology
episodic disorders
episodic neurologic deficits
evoked potentials
exercise
eye movement, disorders of
Fabry's disease
face, numbness of
facial nerve palsy
facial nerve palsy, bilateral
failure to thrive
falling
familial
familial hemiplegic migraine
familial periodic ataxia
fasciculation
feeding disorder
fever
finger nose finger test
flunarizine
foam cells
foot drop
foot numbness
fourth ventricle, enlargement of
Friedreich's ataxia
frontotemporal dementia, behavioral variant
fundus, abnormality of
gadolinium
gait disorder
gait, spastic
gaze palsy
gaze palsy, congenital horizontal
gaze palsy, horizontal
gaze palsy, horizontal-bilateral
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
Gerstmann-Straussler-Scheinker disease
granulomatosis with polyangiitis
granulomatous disease
hammertoes
hand deformity
head circumference
head lag
head nodding
headache
hearing loss
hemangioblastoma
hemianopia
hemiparesis
hemiplegia
hemophagocytic lymphohistiocytosis, cerebromeningeal
hemophagocytosis
hepatomegaly
hepatosplenomegaly
HGPPS
Horner's syndrome
hyperreflexia
hypertension
hyperthyroidism
hypertriglyceridemia
hypofibrinogenemia
hypomyelination
hyporeflexia
hypotonia
imbalance
immunologic disease
immunosuppression
impulsivity
inborn errors of metabolism
inclusion bodies, intracytopasmic
incoordination
infantile bilateral striatal necrosis
infection, recurrent
intellectual deficit
internuclear ophthalmoplegia
internuclear ophthalmoplegia, bilateral
intracranial pressure, increased
iritis
irritability
Jakob-Creutzfeldt disease
jaundice
Jewish
Joubert syndrome
karyotyping
konzo
kyphoscoliosis, neurologic causes of
kyphosis
lactic acidemia
Leber's congenital amaurosis
Leigh's disease
leukocyte peroxidase
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
leukopenia
light-near dissociation, causes of
lipid storage disorder of CNS
livedo reticularis
lymphadenopathy
lymphoma involving CNS
lymphomatoid granulomatosis
macrocephaly
malformation, CNS, congenital
medulla oblongata
medulla oblongata, lesion of
medulla oblongata, malformation
memory, impairment of
meningismus
meningitis, carcinomatous
microcephaly
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
migraine, hemiplegic
misdiagnosis
mitochondrial disease
molecular genetics
movement disorder
movement disorder, extrapyramidal
movement disorder, hyperkinetic
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, spinal cord
multiple sclerosis, differential diagnosis of
multiple system atrophy
myasthenia gravis
myasthenia gravis, familial incidence of
myasthenia gravis, nystagmus in
myasthenia gravis, ocular
myasthenia gravis, sensory loss with
myelopathy
myoclonic jerks
myoclonus
myoclonus, epilepsy
myokymia
nausea and vomiting
neoplasm, primary of CNS
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic signs
neuromyotonia
neuronopathy
neuronopathy, sensory
neuroophthalmology
neuropathology
neuropathy
neuropathy, demyelinating
neuropathy, peripheral
neurotoxin
neutropenia
next-generation sequencing
Niemann-Pick disease
nystagmus
nystagmus, dissociated
nystagmus, gaze-evoked
nystagmus, gaze-paretic
nystagmus, hereditary
nystagmus, monocular
nystagmus, pendular
nystagmus, periodic
nystagmus, primary position of gaze
nystagmus, rotary
nystagmus, upbeating-in primary position of gaze
nystagmus, vertical
ocular motility, disorders of
ophthalmic artery occlusion
ophthalmoplegia
opisthotonus
optic ataxia
optic atrophy
optic disc cup
optical coherence tomography
optokinetic nystagmus, abnormal
oscillopsia
palatal myoclonus
pancytopenia
papilledema
paranoia
paraparesis
paraparesis, spastic
paraplegia
Parkinson disease
Parkinson disease, dystonia with
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
Pelizaeus Merzbacher
personality change
pes cavus
photophobia
pleocytosis of cerebrospinal fluid
POLG1 gene
pons, hypoplasia
precipitating factors
pregnancy, neurologic complications in
pretectal syndrome
primary episodic ataxia
prion disease
prognosis
progressive neurologic disorder
pseudointernuclear ophthalmoplegia
psychiatric problems in neurologic disorders
psychological testing, neurologic problems
psychomotor retardation
psychosis
ptosis
pulmonary infiltrates
pupil, abnormality in neurologic disorders
pupil, light reflex, abnormal
Purkinje cell
pursuit eye movements, abnormal
pyramidal tract dysfunction
pyramidal tract, uncrossed
pyruvate metabolism, abnormality of
quadriparesis
quadriplegia
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
rash
recurrent
release phenomena
renal tubular acidosis
respiratory failure
retinal degeneration
review article
RFC1 gene
rheumatoid arthritis
rheumatoid arthritis, neurologic complications of
riboflavin transporter deficiency
rigidity
Romberg's sign
scoliosis
scoliosis, neurologic association with
seizure
seizure, children
sensorineural hearing loss
sensory loss
sensory loss, leg
skin, lesions in neurologic disorders
slurred speech
Sneddon's syndrome
spastic ataxia
spastic diplegia
spasticity
speech, loss of
spinal cord, ischemic lesion of
spinal cord, neoplasm
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar ataxia type 6
spinocerebellar degeneration
spinopontine atrophy, dominant
splenomegaly
spongy degeneration of brain
status epilepticus
steroid therapy, CNS treatment and complications with
stress, emotional
striatonigral degeneration
striatonigral degeneration, infantile
striatum, lesion of
striatum, lesion of, bilateral
subcortical U fibers
syphilis, neurologic complications with
tandem gait, ataxic
telangiectases
tensilon test
thalamus, lesion of
thalamus, lesion of-bilateral
thrombocytopenia
thyrotoxicosis
tinnitus
titubation
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
trinucleotide repeats
uremia
urinary incontinence
uveitis
vertigo
vertigo, episodic
vertigo, treatment of
vestibular areflexia
vestibulopathy
vision, failure of in childhood
visual acuity, decreased
visual evoked response
Von Hippel Lindau
walking, difficulty with
walking, difficulty with in dark
weakness
weakness, generalized
weakness, progressive
weight loss
wheelchair
white matter disease
wide based gait
Wolfram syndrome
wrist drop
Showing articles 1250 to 1300 of 2207 << Previous Next >>

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

Genetic Predisposition to Iatrogenic Creutzfeldt-Jakob Disease
Lancet 337:1441-1442, Collinge,J.,et al, 1991

Autosomal Recessive Distal Dystrophy
Neurol 41:1365-1370, Barohn,R.J.,et al, 1991

Welander's Distal Myopathy:Clinical Neurophysiol & Muscle Biopsy Obser in Young & Middle Aged Adults with Early Symptoms
JNNP 54:494-498, Borg,K., 1991

Parental Sex Effect in Familial Amyotrophic Lateral Sclerosis
Neurol 41:1292-1294, Leone,M., 1991

Linkage of a Gene Causing Familial ALS to Chromosome 21 & Evidence of Genetic-Locus Heterogeneity
NEJM 324:1381-1384, 1430-14321991., Siddique,T.,et al, 1991

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

Brain Tumors
NEJM 324:1471-1476, 1555-15641991., Black,P.McL., 1991

Non-Neoplastic Pineal Cysts
Neurol 41:1034-1040, Fetell,M.R.,et al, 1991

Central Nervous System Germinomas, A Review
Arch Neurol 48:652-657, Horowitz,M.B.&Hall,W.A., 1991

Mental Retardation in Turner Syndrome
J Pediatr 118:415-417, VanDyke,D.L.,et al, 1991

Cesarean Section Before Onset of Labor & Motor Function in Infants with Meningomyelocele Diag Antenatally
NEJM 324:662-666, 6901991., Luthy,D.S.,et al, 1991

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

Essential Tremor:Clinical Correlates in 350 Patients
Neurol 41:234-238, Lou,J.&Jankovic,J., 1991

The Effect of Flunarizine on Essential Tremor
Neurol 41:311-312, Biary,N.,et al, 1991

Acquired Pendular Nystagmus in Toluene Addiction
Neurol 41:282-285, Maas,E.F.,et al, 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

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

Mid-Brain Pathology of Wilson's Disease:MRI Analysis of Three Cases
JNNP 54:624-626, Hitoshi,S.,et al, 1991

Predictive Testing for Wilson's Disease Using Tightly Linked and Flanking DNA Markers
Neurol 41:992-999, Farrer,L.A.,et al, 1991

Presynaptic Parkinsonism in Olivopontocerebellar Atrophy:Clinical, pathological, and Neurochemical Evidence
Ann Neurol 30:425-428, Pascual,J.,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

Botulinum Toxin Treatment of Tremors
Neurol 41:1185-1188, Jankovic,J.&Schwartz,K., 1991

Cervical Dystonia:Clinical Findings and Associated Movement Disorders
Neurol 41:1088-1091, Jankovic,J.,et al, 1991

Lateral Medullary Infarction:Prognosis in an Unselected Series
Neurol 41:244-248, Norrving,B.&Cronqvist,S., 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

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

Genetice of Cerebrovascular Disease
Stroke 22:276-280, Alberts,M.J., 1991

Detection of Tuberous Sclerosis in Parents by Magnetic Resonance Imaging
Neurol 41:262-265, Roach,E.S.,et al, 1991

Neurological and Neuropsychiatric Spectrum of Wilson's Disease:A Prospective Study of 45 Cases
J Neurol 238:281-287, Oder,W.,et al, 1991

Wilson's Disease with Neurological Impairment but no Kayser-Fleischer Rings
Lancet 337:1426, Willeit,J.&Kiechl,S.G., 1991

Wilson's Disease
In Oxford Textbook of Clin Hepatology, Oxford Univ Press, Vol 2, Ch 20. 1, p. 947, Sternlieb,I.&Scheinberg,I.H., 1991

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

Dissociated Vertical Nystagmus and Internuclear Ophthalmoplegia from a Midbrain Infarction
Arch Neurol 48:1304-1305, Marshall,R.S.,et al, 1991

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

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



Showing articles 1250 to 1300 of 2207 << Previous Next >>