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acanthocytosis
acetylcholine
acoustic neurinoma, bilateral
adrenoleukodystrophy
advances in neurology
adverse drug reaction
albinism
alcohol intolerance
alcohol, neurologic complications with
algorithm
alpha-fetoprotein
alternating rapid movement
Alzheimer's disease
amantadine
aminoacidopathies
amyotrophic lateral sclerosis
anemia
antibodies to voltage-gated calcium channels
anticholinesterase
anticonvulsants
anticonvulsants, selection of
antioxidant
apraxia of eye movements
areflexia
Arnold Chiari malformation
arrhythmia, cardiac
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
ataxic-dystonia syndromes
ataxin
ataxin-2
atypical
auditory evoked brainstem potentials
autonomic dysfunction
Babinski sign
baclofen
bacterial infection
basal ganglia, degeneration
Bassen-Kornzweig syndrome
benign essential tremor
biologic markers
blindness
blood dyscrasias, neurologic findings with
bradykinesia
brain atrophy
brainstem, atrophy
brainstem, lesion of
CAG repeats
calcium channel dysfunction
carcinoembryonic antigen
carcinoma
carcinoma of lung
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataracts
celiac disease, adult
central core disease
cerebellar ataxia, autosomal recessive
cerebellar ataxia, children
cerebellar ataxia, children, differential diagnosis of
cerebellar ataxia, hereditary
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar vermis
cerebral cortical atrophy
cerebral glucose metabolism
cerebro hepato renal syndrome
cerebrovascular accident
Chediak-Higashi syndrome
cherry red spot-myoclonus syndrome
children
chloride channel dysfunction
choking
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 12
chromosome 14
chromosome 6
chromosome 9
cigarette smoking
cirrhosis
Clinical Pathologic Conference(C.P.C.)
clonus
clubfoot as related to neurologic disease
Cockayne's syndrome
cognition
Collier's sign
cone-rod dystrophy
congestive heart failure
consanguinity
controversies in neurology
conversion reaction
copper deficiency
cornea, abnormal
cranio-cervical junction
creatine phosphokinase(CPK)elevated
Cuba
cystic fibrosis, neurologic complications with
deafmute
deafness
deep tendon reflexes
degenerative diseases of CNS
delay in diagnosis
dementia
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
depression
dexterity, impaired
diabetes mellitus
diabetes mellitus, chemical
dilantin
diplopia
disability, neurological
distal muscle atrophy
DNA probes
down-beat nystagmus
down-beat nystagmus, primary position of gaze
drooling
drug induced neurologic disorders
dwarfism
dysarthria
dysdiadochokinesia
dysmetria
dysmorphic
dysphagia
dyspraxia
dystonia
echocardiogram
echocardiogram, LVH
electrocardiogram, abnormal
electrocardiogram, LVH
electroencephalogram, abnormalities of
electromyogram
electronystagmography
electronystagmography, abnormal
electroretinograph
endocardial fibrosis
enzyme, defect
epidemiology of neurology
episodic neurologic deficits
ethics in neurology
evoked potentials
excitotoxin
exome sequencing
eye movement, disorders of
falling
familial
familial hemiplegic migraine
family planning
fasciculation
fatigue
fever
finger nose finger test
foot numbness
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
fragile-X syndrome, carrier
frataxin
Friedreich's ataxia
Friedreich's ataxia, late onset
fundus, abnormality of
gait disorder
gangliosidosis GM2
gargoylism
gastrectomy, neurologic complications following
gaze palsy
gaze palsy, supranuclear
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glaucoma
globus pallidus, lesion of
glutamate dehydrogenase deficiency
glutamic acid
glycogen storage disease
growth retardation
Guillain Barre syndrome
Hallervorden Spatz disease
Hallgren's syndrome
hammertoes
handwriting
head injury
head nodding
hearing loss
heart block
heel-knee-shin test
hepatolenticular degeneration(Wilson's disease)
hexosaminidase-A and B
HLA
hot cross bun sign
huntingtin
Huntington's chorea
Hurler's syndrome
hydroxytryptophan L-5(L-5 HTP)
hyperreflexia
hypertonia
hypokalemic periodic paralysis
hyposmia
hypotonia
hypoxia
imbalance
imbalance, postural
immunodeficiency
immunosuppression
inclusion bodies
inclusion bodies, intracytopasmic
inclusion bodies, ubiquitin
incoordination
intellectual deficit
internuclear ophthalmoplegia
internuclear ophthalmoplegia, bilateral
intestinal lymphangiectasia
jaw jerk, abnormal
Kearns-Sayre syndrome
keratoconus
kyphoscoliosis, neurologic causes of
kyphosis
Lafora's disease
Laurence-Moon-Bardet-Biedl syndrome
L-dopa
lecithin
leg weakness, bilateral
Leigh's disease
leukemia
leukocyte peroxidase
leukodystrophy
leukoencephalopathy
life expectancy
lipid storage disorder of CNS
lipid storage myopathy
liver disease
low back pain
lymphoma
macular degeneration
malabsorption
malabsorption syndrome
malformation, CNS, congenital
malignant hyperpyrexia
malondialdehyde
Marinesco-Sjogren syndrome
memory, impairment of
mental retardation
MERRF syndrome
metabolic disorder, primary
Mexican
middle cerebellar peduncle
middle cerebellar peduncle, lesion
migraine
migraine, hemiplegic
mimics
mirror writing
misdiagnosis
mitochondrial disease
molecular genetics
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, FLAIR
MRI, negative
MRI, spinal cord
mucopolysaccharidoses
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
multiple system atrophy
muscle biopsy
muscle cramp
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, cardiovascular changes with
muscular dystrophy, Duchenne
myasthenic syndrome
myelogram
myelomalacia
myeloneuropathy
myelopathy
myoclonic jerks
myoclonus
myoclonus, epilepsy
myopathy
myopathy, mitochondrial
myopia
myotonia congenita
myotonia dystrophica
neoplasm, primary intracranial
neoplasm, primary of CNS
nerve conduction studies
neuritis
neurocutaneous disease
neuroendocrinology
neurologic disease
neurologic disease, diagnoses of
neurologic signs
neuronal ceroid-lipofuscinosis
neuronal migration disorder
neuronopathy
neuroophthalmology
neuropathology
neuropathy
neuropathy, amyloid
neuropathy, hereditary peripheral
neuropathy, peripheral
neurotoxin
neurotransmitter
neutropenia
nicotine
night blindness
numbness, extremity
nystagmus
nystagmus, primary position of gaze
nystagmus, upbeating-in primary position of gaze
nystagmus, vertical
obesity
ocular motility, disorders of
ocular myopathy
old age, neurology of
ophthalmoplegia
ophthalmoplegia, progressive external
optic atrophy
optic nerve
optic neuropathy
optical coherence tomography
orbit, tomograms of
orthostatic hypotension
pain
pain, management of chronic
palatal myoclonus
pancytopenia
paramyotonia congenita
paraparesis, familial spastic
Parkinson disease
Parkinson disease, familial
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
paroxysmal neurologic deficits
pathologic reflex
pathology
periodic paralysis
peroxisomal disease
pes cavus
photophobia
physostigmine
pigmentary retinopathy
polydactyly
polymerase chain reaction
polymyositis
polyneuropathy
pons, atrophy
pontocerebellar atrophy
posterior column disease
potassium channel antibodies
potassium channel dysfunction
prevention of neurologic disorders
progeria
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
proprioception, abnormal
pseudobulbar palsy
pseudoretinitis pigmentosa
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, neurologic problems
Purkinje cell
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract
pyramidal tract dysfunction
radiation hypersensitivity
Red flags
refractive errors
Refsum's disease
remission
remote effect of cancer on the nervous system
retina, abnormal
retinal degeneration
retinal lesion
retinitis pigmentosa
retinopathy
review article
risk factors
Romberg's sign
saccadic eye movements, abnormal
schizophrenia
scoliosis
seizure
seizure, paradoxical
seizure, treatment of
sensorineural hearing loss
sensory loss
Shy-Drager syndrome
sinemet
skew deviation
skew deviation, alternating
skin, biopsy
skin, lesions in neurologic disorders
sleep apnea
sleep pathology and physiology
sodium channel dysfunction
spastic ataxia
spasticity
sphingolipodoses
Spielmeyer Vogt syndrome
spinal cord, cervical
spinal cord, lesion of
spinal cord, neoplasm
spinal cord, neoplasm, intramedullary
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 10
spinocerebellar ataxia type 12
spinocerebellar ataxia type 14
spinocerebellar ataxia type 16
spinocerebellar ataxia type 17
spinocerebellar ataxia type 2
spinocerebellar ataxia type 28
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar ataxia type 5
spinocerebellar ataxia type 6
spinocerebellar ataxia type 7
spinocerebellar ataxia type 8
spinocerebellar degeneration
spinopontine atrophy, dominant
staggering
steatorrhea
striatonigral degeneration
syphilis, neurologic complications with
tandem gait, ataxic
tapetoretinal degeneration
telangiectases
thalamus
thyrotropin-releasing hormone
tinnitus
trazodone
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
trimethoprim-sulfamethoxazole
trinucleotide repeats
Unverricht-Lundborg disease
upgaze, paralysis of
Usher's syndrome
vertigo
vertigo, episodic
vestibulopathy
vibratory sensation
vibratory sensation, abnormal
visual acuity, decreased
visual evoked response
visual field defect
visual fields, constricted
visual loss
visual loss, progressive
visual loss, slow
vitamin deficiency
vitamin E
vitamin E deficiency
vitamin supplementation
Von Hippel Lindau
walking, difficulty with
wheelchair
white matter disease
wide based gait
workup
X-linked bulbospinal neuronopathy
Showing articles 850 to 900 of 1208 << Previous Next >>

The Spectrum of Cerebellar Infarctions
Neurol 41:973-979, Amarenco,P., 1991

Clinicopath Conf
Radiation Induced Cerebellar Astrocytoma, Case 23-1991, NEJM 324:1651-1659991., , 1991

Clinicopath Conf
Tertiary Neurosyphilis, Case 32-1991, NEJM 325:414-422991., , 1991

Microangiopathy of the Brain, Retina, and Ear:Improvement without Immunosuppressive Therapy
Stroke 22:933-937, Gordon,D.L.,et al, 1991

Cat Scratch Disease, Acute Encephalopathy & Other Neurologic Manifestations
Am J Dis Child 145:98-101, Carithers,H.A.&Margileth,A.M., 1991

Infarction in the Anterior Rostral Cerebellum (the Territory of the Lateral Branch of the Superior Cerebellar Artery)
Neurol 41:253-258, Amarenco,P.,et al, 1991

Central Nervous System Involvement in Von Hippel-Lindau Disease
Neurol 41:41-46, Filling-Katz,M.R.,et al, 1991

Lateral Medullary Infarction:Prognosis in an Unselected Series
Neurol 41:244-248, Norrving,B.&Cronqvist,S., 1991

Sensory Ataxic Hemiparesis in Thalamic Hemorrhage
Stroke 21:1749-1753, Dobato,J.L.,et al, 1990

Neurologic Manifestations of Giant Cell Arteritis
Am J Med 89:67-72, Reich,K.A.,et al, 1990

Capsular Hypesthetic Ataxic Hemiparesis
Stroke 21:24-33, Helgason,C.M.&Wilbur,A.C., 1990

Relative Increase of T Cells Expressing Gamma/Delta Rather than Alpha/Beta Receptor in Ataxia-Telangietasia
NEJM 322:73-76, 1241990., Carbonari,M.,et al, 1990

Extrapyramidal Involvement in Rett's Syndrome
Neurol 40:293-295, FitzGerald,P.M.,et al, 1990

Neuronal Intranuclear Inclusion Disease in a Child:Diagnosis by Rectal Biopsy
Ann Neurol 27:103-106, Goutieres,F.,et al, 1990

Antemortem Diagnosis of Diffuse Lewy Body Disease
Neurol 40:1523-1528, Crystal,H.A.,et al, 1990

The Marinesco-Sjogren Syndrome Examined by CT, MR, and 18F-2-Fluoro-2-Deoxy-D-Glucose & PET
Arch Neurol 47:1239-1242, Bromberg,M.B.,et al, 1990

Progressive Myoclonic Ataxia (The Ramsay Hunt Syndrome)
Arch Neurol 47:1121-1125, Marsden,C.D.,et al, 1990

Neurological Sequelae of Cerebral Malaria in Children
Lancet 336:1039-1043, Brewster,D.R.,et al, 1990

Geriatrics:Gait Disorders in the Elderly
NEJM 322:1441-1446, Sudarsky,L., 1990

'Rubral'Gait Ataxia
Neurol 40:1004-1005, Felice,K.J.,et al, 1990

Migraine Assoc with Focal Cerebral Edema, CSF Pleocytosis, & Prog Cerebellar Ataxia:MRI Documentation
Neurol 40:1284-1287, Goldstein,J.M.,et al, 1990

Progressive Rubella Panencephalitis
In Handbk of Clin Neurol, Vinken & Bruyn, Ed, N Holland Publ Co, 56:405-416, Wolinsky,J.S., 1990

Miller Fisher Syndrome Associated with Q Fever
JNNP 53:615-616, Diaz Ortuno,A.,et al, 1990

Neurological Deterioration in Young Adults with Phenylketonuria
Lancet 336:602-605, Thompson,A.J.,et al, 1990

Acute Triphenyltin Intoxication:A Case Report
JNNP 53:356-357, Wu,RM.,et al, 1990

Cerebral Cortex and Brainstem Involvement in Marinesco-Sjogren Syndrome
Ann Neurol 27:448-449, Katafuchi,Y.,et al, 1990

Movement Disorders in Alcoholism:A Review
Neurol 40:741-746, Neiman,J.,et al, 1990

Ataxic Sensory Neuropathy and Dorsal Root Ganglionitis Associated with Sjogren's Syndrome
Ann Neurol 27:304-315, Griffin,J.W.,et al, 1990

Clinicopath Conf
Familial Visceral Myopathy (Oculogastrointestinal Muscular Dystrophy) , Case 12-1990, NEJM 322:829-8, 1, 19, 1990

Clinicopath Conf
Sarcoidosis of CNS and Mediastinal Lymph Nodes, Case Record 6-1990, NEJM 322:388-397990., , 1990

Neuromuscular Involvement in Mild, Asymptomatic Primary Hyperparathyroidism
Am J Med 87:553-557, Turken,S.A., 1989

Opsoclonus-Myoclonus Syndrome:Correlation of Radiographic and Pathological Observations
Neuroradiology 31:250-252, Turchman,R.F.,et al, 1989

Cerebral Palsy Diplegia:Improvements for Walking
BMJ 299:1115-1116, Patrick,J., 1989

Variables Predicting Surgical Outcome in Symptomatic Hydrocephalus in the Elderly
Neurol 39:1601-1604, Graff-Radford,R.N.,et al, 1989

Symptomatic Congenital Hydrocephalus in the Elderly Simulating Normal Pressure Hydrocephalus
Neurol 39:1596-1600, Graff-Radford,N.R.&Godersky,J.C., 1989

Isolated Midbrain Lesion Resulting From Closed Head Injury:A Unique Presentation of Ataxia Hemiparesis
Neurol 39:452-453, Hershkowitz,N.,et al, 1989

Hypesthetic Ataxic Hemiparesis in a Thalamic Lacune
Stroke 20:819-821, Lee,N.,et al, 1989

Clinicopath Conf
Subacute Cerebellar Degeneration, Cystadenocarcinoma of Ovary, (with Paraneoplastic Syndrome) , Case, 34-1EJM 321:524-535,1989., 1989

Adrenoleukodystrophy
JAMA 262:1504-1506, Ladenson,P.W., 1989

Risk Factors for Recurrent Nonsyncopal Falls, A Prospective Study
JAMA 261:2663-2668, Nevitt,M.C.,et al, 1989

Prevention of Falls Among the Elderly
NEJM 320:1055-1059, Tinetti,M.E.&Speechley,M., 1989

Radiation-Induced Dementia in Patients Cured of Brain Metastases
Neurol 39:789-796, DeAngelis,L.M.,et al, 1989

Clinicopath Conf
HTLV-I Infection, with Adult T-Cell Lymphoma and Tropical Spastic Paraparesis, Case 36-2989, NEJM 32, :6675,1989., 1989

Human T-Lymphotropic Virus Type I-Associated Myelopathy Presenting as Spinocerebellar Syndrome
Ann Neurol 25:419-420, Iwasaki,Y.,et al, 1989

Guillain-Barre Syndrome Presenting as High-Altitude Cerebral Edema
NEJM 321:545, Shlim,D.R.&Cohen,M.T., 1989

Clinicopath Conf
Chronic Osteomyelitis of Spine, with Intervertebral Diskitis (T3-T4) & Epidural Abscess (Staph Aureu, ) , Cas9,NEJM 320:1610-1618,1989., 1989

Central Nervous System Manifestations of Lyme Disease
Arch Neurol 46:790-795, Pachner,A.R.,et al, 1989

Late Onset of Distinct Neurologic Syndromes in Galactosemic Siblings
Neurol 39:741-742, Friedman,J.H.,et al, 1989

Dopa Responsive Dystonia:A Treatable Condition Misdiagnosed as Cerebral Palsy
BMJ 298:1019-1020, Boyd,K.&Patterson,V., 1989

Hysterical Gait Disorders:60 Cases
Neurol 39:586-589, Keane,J.R., 1989



Showing articles 850 to 900 of 1208 << Previous Next >>