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acetazolamide
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
akinetic mute
alternating rapid movement
alternating rapid movement, impaired
amyotrophic lateral sclerosis
anorexia
areflexia
arm swing, reduced
arrhythmia, cardiac
aspiration
astrocytoma
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
ataxic hemiparesis
atrial fibrillation
attention deficit disorder with hyperactivity
attention span
Babinski sign
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
biologic markers
bone marrow transplantation
bradykinesia
brain atrophy
brainstem, infarction of
brainstem, lesion of
brainstem, neoplasms of
brainstem, syndrome
cardiomyopathy
CAT scan
CAT scan, abnormal
catalepsy
cataplexy
cerebellar ataxia, autosomal recessive
cerebellar ataxia, hereditary
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar hemorrhage
cerebellar infarction
cerebellum, disease of
cerebral cortex
cerebral cortical atrophy
cerebral embolism
cerebral embolism, cardiac origin
cerebral palsy
cerebral palsy, associated problems with
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrovascular accident
Charcot-Marie-Tooth
children
chorea
choreoathetosis
chromosomal abnormality
Clinical Pathologic Conference(C.P.C.)
cognition
congestive heart failure
consanguinity
corona radiata
cortical-basal ganglionic degeneration
cough
cranial neuropathy
cultured skin fibroblasts
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, presenile
dementia, rapidly progressive
depression
developmental milestones, loss of
dexterity, impaired
diabetes mellitus
diarrhea
diplopia
disease modifying agents
dizziness
down-beat nystagmus
down-beat nystagmus, primary position of gaze
drooling
dying
dysarthria
dysarthria-clumsy hand syndrome
dysdiadochokinesia
dysmetria
dysphagia
dyspraxia
dystonia
dystonia musculorum deformens
dystonia, cervical
electroencephalogram, abnormalities of
electromyogram
electrophoretic pattern, CSF
embolism
encephalitis
encephalopathy
epileptic encephalopathy
exome sequencing
eye movement, disorders of
failure to thrive
falling
familial
familial periodic ataxia
FARS2 deficiency
fatigue
fine motor function, impaired
finger nose finger test
finger numbness
foam cells
foot drop
Friedreich's ataxia
Friedreich's ataxia, late onset
gait disorder
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
Gerstmann-Straussler-Scheinker disease
glabellar sign
granular osmiphilic material
hammertoes
handwriting
head nodding
headache
hearing loss
heel-knee-shin test
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatosplenomegaly
heralding manifestation
hormone replacement
hydrocephalus
hyperreflexia
hypersomnia
hypertension
hypertonia
hypogonadism
hypogonadism, hypogonadotropic
hypometric saccades
hypotonia
iatrogenic neurologic disorders
imbalance
immunohistochemistry
inattention
incoordination
inferior olivary nucleus
insomnia
intellectual deficit
intellectual deterioration
intelligence quotient
internal capsule
introverted
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, variant
jaundice
Kayser-Fleischer ring
lacunar infarction
lacunar infarction, differential diagnosis of
lateropulsion
leg weakness, bilateral
leukodystrophy
leukoencephalopathy
lipid storage disorder of CNS
liver disease
Lorenzo's oil
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
lysosomal storage disease
medulla oblongata, neoplasm of
memory, defect of recent
memory, impairment of
meningitis, CSF cell count-normal
microcephaly
midbrain, atrophy
misdiagnosis
mitochondrial disease
molecular genetics
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion weighted
MRI, false negative
MRI, negative
MRI, spinal cord
MRI, spine
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
myelomalacia
myelopathy
myelopathy, chronic progressive
myoclonic jerks
myoclonus
nausea and vomiting
neoplasm, primary of CNS
neoplasm, primary of CNS-children
nerve conduction studies
neurofibrillary degeneration
neurofibromatosis 1
neurologic disease, diagnoses of
neurologic signs
neurologic symptoms
neuronal ceroid-lipofuscinosis
neuropathology
neuropathy
neuropathy, demyelinating
neuropathy, hereditary peripheral
neuropathy, sensory
next-generation sequencing
Niemann-Pick disease
numb clumsy hands syndrome
nystagmus
ocular motility, disorders of
olivary degeneration, hypertrophic
optic atrophy
ovarian dysgenesis
palatal myoclonus
paraparesis
paraparesis, familial spastic
paraparesis, spastic
Parkinson disease
Parkinsonism syndrome
Perrault syndrome
personality change
pes cavus
pons, infarction of
pontine hemorrhage
positional head-hanging test
prevention of neurologic disorders
prion disease
prion protein gene
prognosis
progressive ataxia and palatal tremor
progressive myoclonic epilepsy
progressive neurologic disorder
proprioception, abnormal
protein 14-3-3, cerebrospinal fluid
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, neurologic problems
psychosis
pure dysarthria
pure motor hemiplegia
pursuit eye movements, abnormal
pyramidal tract dysfunction
rapidly progressing neurologic illness
reading disorder, acquired
real-time quaking-induced conversion
release phenomena
retropulsion
review article
rigidity
risk factors
Romberg's sign
rubella encephalitis
rubella encephalitis, progressive
rubella virus
saccadic eye movements, abnormal
salivation, excessive
scoliosis
seizure
seizure, children
sensorimotor stroke
sensorineural hearing loss
sensory loss
serologic testing
serologic testing of cerebrospinal fluid
slit lamp examination
slurred speech
spastic ataxia
spastic diplegia
spasticity
speech disorder
speech disorder, non aphasic
spinal cord
spinal cord, lesion of
spinocerebellar ataxia
splenomegaly
spontaneous remission
square wave jerks
staggering
strokelike episodes
suck reflex
superior cerebellar artery infarction
superior cerebellar artery syndrome
symmetric brain lesions
tandem gait, ataxic
tau protein
tauopathy
thalamus, lesion of-bilateral
titubation
toe walking
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
trinucleotide repeats
upgaze, paralysis of
vertigo
vertigo, episodic
very long chain fatty acids
vestibulopathy
vibratory sensation, abnormal
viral infection, CNS
vision, blurred
vitamin E deficiency
voice, abnormality of
walking frame
walking, difficulty with
weakness
weakness, progressive
weight loss
white matter disease
wide based gait
workup
Showing articles 800 to 850 of 1088 << Previous Next >>

Clinicopath Conf
Cerebral Mucormycosis, Case 52-1990, NEJM 323:1823-1833990., , 1990

Misdiagnosis in Patients with Amyotrophic Lateral Sclerosis
Arch Int Med 150:2301-2305, Belsh,J.M.&Schiffman,P.L., 1990

Clinical Features and Associations of 560 Cases of Motor Neuron Disease
JNNP 53:1043-1045, Li,T.,et al, 1990

Clinical & PET Studies in the'Extrapyramidal Syndrome'of Dementia of the Alzheimer Type
Arch Neurol 47:1318-1323, Tyrrell,P.J.,et al, 1990

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

Encephalitis Caused by HIV:CT & MR Imaging Manifestations with Clinical and Path Correlation
Radiology 175:185-191, Chrysikopoulos,H.S.,et al, 1990

Ipsilateral Extinction in the Hemineglect Syndrome
Arch Neurol 47:802-804, Feinberg,T.E.,et al, 1990

Clinical Features of Proven Basilar Artery Occlusion
Stroke 21:1135-1142, Ferbert,A.,et al, 1990

Incidence of Impact Trauma with Cranial Injuries Ascribed to Shaking
Am J Dis Child 144:724-726, Alexander,R.,et al, 1990

Isopropyl Alcohol Intoxication
Arch Neurol 47:322-324, Rich,J.,et al, 1990

Distal Ulnar Neuropathy as a Cause of Finger Tremor:A Case Report
Neurol 40:153-154, Streib,E.W., 1990

Combined Resting-Postural Tremor of Lower Limbs:Another Essential Trem, or Variant
Neurol 40:1006, Rapoport,A.,et al, 1990

Cortical-Basal Ganglionic Degeneration
Neurol 40:1203-1212, Riley,D.E.,et al, 1990

Magnetic Resonance Imaging Findings In HIV Cognitive Impairment
Arch Neurol 47:643-645, Kieburtz,K.D.,et al, 1990

Long Latency Event-Related Potentials in Patients Infected with Human Immunodeficiency Virus
Ann Neurol 27:414-419, 4201990., Goodin,D.S.,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

Congenital Inflammatory Myopathy
Neurol 40:1111-1114, Shevell,M.,et al, 1990

Extensive Brain Calcif & Prog Dysarthris & Dysphagia Assoc with Chronic Hypoparathyroidism
Arch Neurol 47:1038-1039, Cheek,J.C.,et al, 1990

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

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

Early HIV-1 Infection and the AIDS Dementia Complex
Neurol 40:323-326, Sidtis,J.J.&Price,R.W., 1990

Post-Traumatic Midbrain Tremors
Neurol 40:62-66, Samie,M.R.,et al, 1990

The Movement Disorder of Reflex Sympathetic Dystrophy
Neurol 40:57-61, Schwartzman,R.J.&Kerrigan,J., 1990

Clinicopath Conf
Eosinophilic Fasciitis, Case Study 4-1990, NEJM 322:252-261, 93190., , 1990

Development of Diffuse Fasciitis with Eosinophilia During L-Tryptophan Treatment:Elevated Type I Collagen Gene
Ann Int Med 112:344-351, Varga,J.,et al, 1990

Perfusion Insufficiency in Limb-Shaking Transient Ischemic Attacks
Stroke 21:341-347, Tatemichi,T.K.,et al, 1990

Caudate Infarcts
Arch Neurol 47:133-143, Caplan,L.R.,et al, 1990

Stereotaxic Thalamotomy-Experiences from the Levodopa Era
JNNP 53:427-430, Wester,K.&Hauglie-Hanssen,E., 1990

Physical Features of Prader-Willi Syndrome in Neonates
Am J Dis Child 144:1251-1254, Aughton,D.J.&Cassidy,S.B., 1990

Pontine Supranuclear Facial Palsy
Stroke 21:1754-1757, Hopf,H.C.,et al, 1990

Multifocal Vacuolar Leucoencephalopathy:A Distinct HIV-Associated Lesion of the Brain
Neuropath Appl Neurobiol 16:437-443, Schmidbauer,M.,et al, 1990

Rigid Spine Syndrome and Rigid Spine Sign in Myopathies
J Child Neurol 4:273-282, Merlini,L.,et al, 1989

Tenosynovitis; Stenosing Tenovaginitis
Arthritis & Allied Conditions, A Textbook of Rheumatology, Lea & Febiger, Phila, p. 1379, in McCarty,D.J., 1989

Paroxysmal Cerebellar Ataxia
Aust NZ J Med 19:113-117, Feeney,G.F.&Boyle,R.S., 1989

Acute and Chronic Effects of Propranolol and Primidone in Essential Tremor
Neurol 39:1587-1588, Koller,W.C.&Vetere-Overfield,B., 1989

Metoclopramide-Induced Movement Disorders
Arch Int Med 149:2486-2492, Miller,L.G.&Jankovic,J., 1989

Cheiro-Oral Syndrome with Bilateral Oral Involvement:A Study of Pontine Lesions by High-Resolution MRI
JNNP 52:792-794, Matsumoto,S.,et al, 1989

Treatment of Cerebellar Tremors with Carbamazepine:A Controlled Trial with Long-Term Follow-Up
Neurol 39:1113-1115, Sechi,G.P.,et al, 1989

Eosinophilia-Myalgia Syndrome-New Mexico
JAMA 262:3116, Belvins,W.L.,et al, 1989

Declining Incidence of AIDS Dementia Complex after Introduction of Zidovudine Treatment
BMJ 299:819-821, Portegies,P.,et al, 1989

Neuropathology of HIV Infection in Haemophiliacs:Comparative Necropsy Study
BMJ 299:1312-1315, Esiri,M.M.,et al, 1989

Acute Fatal HIV Encephalitis with Negative Serologic Antibody and Antigen:Diagnosis by Polymerase Chain Reaction
NEJM 320:1494-1495, Varma,V.A.,et al, 1989

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

Computeritis, Who's Responsible When PCs Make Employees Sick?
Infoworld 11:51-54, Flynn,L., 1989

The Alien Hand Syndrome, Clinical and Postmortem Findings
Arch Neurol 46:456-459, Banks,G.,et al, 1989

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

Improved Diagnosis of Becker Muscular Dystrophy by Dystrophin Testing
Neurol 39:1011-1017, Hoffman,E.P.,et al, 1989

Inclusion Body Myositis, Observations in 40 Patients
Brain 112:727-747, Lotz,B.P.,et al, 1989

Congenital Muscular Dystrophy
J Pediatr 115:214-221, Leyten,Q.H.,et al, 1989

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



Showing articles 800 to 850 of 1088 << Previous Next >>