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acetazolamide
acetylcholine receptor antibody
Addison's disease
adrenergic blocker
advances in neurology
adverse drug reaction
agoraphobia
airway obstruction
alcohol
alcohol, neurologic complications with
alcoholism
Alexanders disease
Alexanders disease, adult onset
algorithm
alpha adrenergic blocker
alprazolam
alternating rapid movement
Alzheimer's disease
amenorrhea
aminoacidurias
ammonia
amygdala
amyloidosis
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, misdiagnosis
anatomy of
anemia
anemia, hemolytic
aneurysm, intracranial
ankle edema
ankle reflex, absent
ankle, swelling of
anorexia
anterocollis
anticholinergic drugs
anticonvulsants
anticonvulsants, untoward effects of
anxiety
aorta, atherosclerosis
aphonia
apraxia
areflexia
Arnold Chiari malformation
arotinolol
artane
arthritis
arylsulfatase A
ascites
aspartate aminotransferase
asterixis
astrogliopathy
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
ataxic-dystonia syndromes
athetosis
athetosis, causes of
attention deficit disorder with hyperactivity
atypical
auditory evoked brainstem potentials
auditory evoked potentials
autism
autonomic dysfunction
autosomal rcessive spastic ataxia of Charlevoix-Saguenay
axonal spheroid
Babinski sign
basal ganglia
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basilar artery occlusion
behavioral disorder
Behcet's syndrome
benign essential tremor
benign essential tremor, refractory
beta adrenergic blocker
biologic markers
blepharospasm
blinking, reduced
blood dyscrasias, neurologic findings with
bone marrow suppression
botulinum toxin
botulinum toxin, complications of
bradykinesia
brain atrophy
brain transplantation
brainstem, lesion of
Brueghel's syndrome
bulbar palsy
caffeine
CAG repeats
calcification, intracranial
calcium antagonist
camptocormia
carbon monoxide poisoning
carbonic anhydrase inhibitor
carcinoma
carcinoma of pancreas
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataracts
catatonia
caudate nucleus, lesion of
caudate nucleus, lesion of, bilateral
central nervous system, infection of
central pontine myelinolysis
cerebellar ataxia, autosomal recessive
cerebellar ataxia, children
cerebellar ataxia, children, differential diagnosis of
cerebellar ataxia, hereditary
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebellum, disease of
cerebral blood flow
cerebral cortex
cerebral cortical atrophy
cerebral infarction
cerebral infarction, hemorrhagic
cerebral palsy
cerebral venous thrombosis
cerebral venous thrombosis, deep
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
ceruloplasmin, serum
Charcot-Marie-Tooth
chelation therapy
cherry red spot
cherry red spot-myoclonus syndrome
children
China
cholelithiasis
chorea
chorea, causes of
choreoathetosis
chromosomal abnormality
chromosome 14
chromosome 3
chromosome 6
cingulate island sign
cirrhosis
cirrhosis, causes of childhood
claustrum
Clinical Pathologic Conference(C.P.C.)
clubbing of fingers
clubfoot as related to neurologic disease
coagulopathy
coat-hanger pain
cognition
cogwheel rigidty
Collier's sign
comorbidities
complicated migraine
complications
consanguinity
copper
copper metabolism, abnormal
cornea, abnormal
coronary artery bypass
corpus callosum, lesion of
corpus callosum, thinning
cough
Cushing's syndrome
cyst
cyst, parenchymal
deafness
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
delayed dentition
dementia
dementia, childhood
dementia, familial
depression
developmental milestones
developmental milestones, loss of
developmental retardation
dexterity, impaired
diabetic coma, diagnosis and treatment
diarrhea
diet
differential diagnosis
dilantin
disability, neurological
distal muscle atrophy
distal muscle weakness
diuretic
dizziness
DNA probes
DNA sequencing
dopa responsive dystonia
dopamine agonist
dopamine receptor, D2
drooling
drug induced neurologic disorders
dysarthria
dysdiadochokinesia
dyskinesia
dyskinesia, buccal lingual facial
dyskinesia, causes of
dyskinesia, drug induced
dysmetria
dysphagia
dysphonia
dyspnea
dyspraxia
dystonia
dystonia musculorum deformens
dystonia, cervical
dystonia, classification
dystonia, etiology of
dystonia, evaluation of
dystonia, face
dystonia, focal
dystonia, laryngeal
dystonia, post traumatic
dystonia, prevalence of
dystonia, symptomatic
dystonia, treatment of
DYT1 mutation
edema, pedal
efficacy
electroencephalogram, abnormalities of
electrolyte imbalance
electromyogram
electron microscopy
electronystagmography
emotional lability
encephalitis
encephalitis, Japanese
encephalitis, viral
encephalopathy
epidemiology of neurology
epistaxis
equinovarus
erectile dysfunction
esophageal varices
evoked potentials
excitotoxin
exome sequencing
extrapyramidal
eye movement, disorders of
Fabry's disease
facial appearance, abnormal
facial expression abnormality
Fahr disease
failed medical management
failure to thrive
falling
familial
familial hemiplegic migraine
fasciculation
fatal familial insomnia
fatigue
fine motor function, impaired
finger nose finger test
fingerprint bodies
flavivirus
flunarizine
foot deformity
foot drop
fracture, long bone
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
fragile-X syndrome, carrier
Friedreich's ataxia
frontal lobe, lesion of
frontal lobe, pathologic signs of
gabapentin
gait disorder
gait, festinating
gamma knife therapy
gaze fixation, distractable
gaze palsy
gaze palsy, supranuclear
gender
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
gests antagoniste
GFAP gene
Gilles de la Tourette syndrome
glabellar sign
glioma
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glucose tolerance test, abnormal
granular osmiphilic material
grimacing
gynecomastia
Hallervorden Spatz disease
hammertoes
handedness
handwriting
head injury
head nodding
headache
heavy metal intoxication
heel-knee-shin test
hemochromatosis
hemochromatosis, primary
hemorrhagic diathesis
hepatic encephalopathy
hepatic failure
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), late onset
hepatolenticular degeneration(Wilson's disease), presymptomatic
hepatolenticular degeneration(Wilson's disease), screening for
hepatolenticular degeneration, non-Wilsonian
hepatomegaly
hepatosplenomegaly
heralding manifestation
Huntington's chorea
hyperactivity
hyperadrenalism
hyperbilirubinemia
hyperglycemia
hyperparathyroidism
hyperreflexia
hyperthyroidism
hypoalbuminemia
hypochloremia
hypodontia
hypoglycemia
hypokalemia
hypometric saccades
hypomyelination
hyponatremia
hypoparathyroidism
hyporeflexia
hyposmia
hypotension, neurologic causes of
hypotension, systemic
hypothyroidism
hypotonia
hypoxic encephalopathy
iatrogenic neurologic disorders
imbalance
imbalance, postural
immunotherapy
impulsivity
inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with
inborn errors of metabolism
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, intranuclear
inclusion bodies, ubiquitin
incoordination
infertility
insomnia
intellectual deficit
intellectual deterioration
intelligence quotient
intracerebral hemorrhage
intrinsic hand muscles, wasting of
iron, brain
Jakob-Creutzfeldt disease
jaundice
jaw contractures
joint hypermobility
Kayser-Fleischer ring
kinesia paradoxica
kyphoscoliosis, neurologic causes of
lactic acidemia
laminectomy
laminectomy, lumbar
laterocollis
L-dopa
L-dopa, drug interactions with and side effects of
leg weakness, bilateral
Leigh's disease
lenticular nucleus, lesion of
lenticular nucleus, lesion of, bilateral
lethargy
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
leukoencephalopathy, hereditary diffuse
leukopenia
level of consciousness, decreased
Lewy body
Lewy body disease, diffuse
lightheaded
lipid storage disorder of CNS
liver biopsy
liver disease
liver function enzymes
liver transplantation
locus ceruleus, lesion of
lymphoma involving CNS
lysosomal storage disease
macrocephaly
marche a petits pas
Marinesco-Sjogren syndrome
masked facies
memory, impairment of
mental retardation
metabolic disorder, primary
metachromatic leukodystrophy
metachromatic leukodystrophy, juvenile
metoprolol
micrographia
midbrain
midbrain, atrophy
midbrain, lesion of
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
migraine, hemiplegic
mimics
mirror writing
misdiagnosis
mitochondrial disease
molecular genetics
mood change
mortality
movement disorder
movement disorder, drug induced
movement disorder, extrapyramidal
movement disorder, treatment of
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, face of giant panda sign on
MRI, false negative
MRI, high signal foci on
MRI, high signal intensity of basal ganglia
MRI, negative
MRI, paramagnetic effect
MRI, T1 weighted high signal foci
MRS
multiple sclerosis
multiple sclerosis, cognitive presenttion
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
multiple system atrophy
muscle biopsy
muscle cramp
muscle stiffness
myasthenia gravis
myelomalacia
myoclonic jerks
myoclonus
myoclonus, epilepsy
myoclonus, essential
myopia
mysoline
nadolol
nausea and vomiting
neck pain
negative
neoplasm, intracranial
neoplasm, primary of CNS
nerve biopsy
nerve conduction studies
neuroaxonal leukodystrophy
neuroendocrinology
neurofibromatosis 1
neurologic complications of, burns
neurologic complications of, surgery
neurologic disease
neurologic disease, diagnoses of
neurologic signs
neurologic symptoms
neuronal ceroid-lipofuscinosis
neuronopathy
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, peripheral
neuropathy, sensory
neuropsychiatry
neurotoxin
nigrostriatal pathway
nimodipine
nutritional deficiency
nystagmus
nystagmus, pendular
nystagmus, primary position of gaze
nystagmus, rotary
nystagmus, upbeating-in primary position of gaze
nystagmus, vertical
obsessive-compulsive disorder
ocular motility, disorders of
oculogyric crisis
old age, neurology of
opened mouth
optic atrophy
organ transplantation
orthostatic hypotension
osmotic demyelination syndrome
ovarian insufficiency
pain
pain, abdominal
pain, head
palatal myoclonus
palilalia
pallidotomy
pancreatitis
pancytopenia
panic attacks
paraparesis
paraparesis, spastic
parenteral alimentation
paresthesias
Parkinson disease
Parkinson disease, arteriosclerotic
Parkinson disease, atypical
Parkinson disease, benign tremulous
Parkinson disease, diagnosis
Parkinson disease, differential diagnosis of
Parkinson disease, drug induced
Parkinson disease, familial
Parkinson disease, fluctuations in
Parkinson disease, freezing phenomena in
Parkinson disease, L-dopa nonresponsive
Parkinson disease, misdiagnosis
Parkinson disease, pathogenesis of
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
Parkinson disease, young onset
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
paroxysmal neurologic deficits
PAS positive
PAS positive material in the brain
past pointing
patient information and support
Pelizaeus Merzbacher
penicillamine
pernicious anemia
personality change
pes cavus
phenobarbital
phenylketonuria
phenylketonuria, adult onset
pheochromocytoma
phlebotomy
poison, neurologic problems with
POLR3B
polyneuropathy
pons, lesion of
porphyria
positional head-hanging test
postoperative neurologic complications
postural abnormality
practice guidelines
pregnancy, neurologic complications in
prion disease
PRKN gene
prognosis
progressive neurologic disorder
progressive supranuclear palsy
propranolol
prothrombin time, prolonged
pruritus
pseudobulbar palsy
psychiatric disorder
psychiatric manifestations of brain tumors
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
psychosis, cause of
psychosocial aspects
pulmonary function tests
Purkinje cell
pursuit eye movements, abnormal
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract
pyramidal tract dysfunction
pyruvate metabolism, abnormality of
quadriparesis
quadriplegia
quality of life
radiation therapy, stereotactic
radiculopathy
raphe nuclei
reading disorder, acquired
reflex sympathetic dystrophy
rehabilitation for neurologic disorders
remote effect of cancer on the nervous system
renal failure
renal stones
respirations in CNS disease
respiratory failure
retinal degeneration
retinitis pigmentosa
retrocollis
retropulsion
reversible neurologic disorder
review article
RFLPs
rheumatoid arthritis
rickets
rigidity
risk factors
risus sardonicus
Rosenthal fibers
saccadic eye movements, abnormal
safety
salivation, excessive
schizophrenia
scoliosis
screening
sea-blue histiocytes
seizure
seizure, children
seizure, differential diagnosis of
seizure, psychomotor-temporal lobe
sensory tricks
serum alanine aminotransferase
shaking
short stature
shoulder, pain in
sinemet
single photon emission computed tomography
skin, biopsy
skin, darkening of
sleep pathology and physiology
slit lamp examination
smell
Smell Identification Test
SNCA duplication
somatosensory evoked potentials
spastic dysphonia
spasticity
speech disorder
speech disorder, childhood
speech disorder, non aphasic
speech, delayed development of
speech, loss of
speech, slowed
speech, soft
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 12
spinocerebellar ataxia type 28
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar degeneration
spinopontine atrophy, dominant
splenium of corpus callosum
splenomegaly
spongy degeneration of brain
stage-fright
staggering
stare
status epilepticus
steppage gait
stereotaxic surgery
stimulation, deep brain
stimulation, thalamic
storage disease of CNS
striatonigral degeneration
striatonigral degeneration, infantile
striatum, lesion of
striatum, lesion of, bilateral
stridor
striopallidodentate calcifications, familial idiopathic
stuttering
substantia nigra
subthalamic nucleus
subthalamic nucleus deep brain stimulation
suicide
sural nerve
symmetric brain lesions
syncope
syphilis, neurologic complications with
systemic illness
systemic lupus erythematosus
tandem gait, ataxic
tantrum
tardive dyskinesia
tardive dystonia
tauopathy
teeth, abnormal
teeth, number of in infants
testicular enlargement
tetrabenazine
tetrathiomolybdate
thalamic tumors
thalamic tumors, bilateral
thalamotomy
thalamotuberal artery
thalamus
thalamus, focused ultrasound ablation
thalamus, infarction of
thalamus, infarction, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
thiazide diuretic
thrombocytopenia
thrombus, mural
thymus and neuromuscular function
thyrotoxicosis
tic
titubation
toe walking
tongue, fasciculations of
tongue, protrusion of
tonic foot response
topiramate
torticollis
torticollis, post traumatic
transient neurologic deficit
trauma
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, classification
tremor, differential diagnosis of
tremor, intention
tremor, jaw
tremor, leg
tremor, orthostatic
tremor, physiologic
tremor, post traumatic
tremor, postural
tremor, psychogenic
tremor, resting
tremor, rubral
tremor, surgical treatment of
tremor, thalamic stimulation for suppression of
tremor, treatment of
tremor, voice
tremor, wing beating
tremor, writing
trientine dihydrochloride
trinucleotide repeats
twins
ultrasonography
ultrasonography, head
ultrasonography, high-intensity focused
uric acid, low
urine test for metabolic disorders
urine, dark
ventricular enlargement
vertigo
vertigo, migraine causing
vestibulopathy
vibratory sensation, abnormal
viral infection
visual acuity, decreased
visual evoked response
visual fields, constricted
visual loss
vitamin deficiency
vitamin E
vitamin E deficiency
voice, abnormality of
Von Hippel Lindau
walking frame
walking, difficulty with
weakness
weight loss
Wernicke's encephalopathy
wheelchair
white matter disease
wide based gait
work loss
workup
writers cramp
writing
X-linked bulbospinal neuronopathy
x-linked intellectual deficit
x-linked mental retardation
zinc
Showing articles 1750 to 1800 of 2512 << Previous Next >>

Olivopontocerebellar Atrophy:MR Diagnosis and Relationahip to Multisystem Atrophy
Radiology 174:693-696, Savoiardo,M.,et al, 1990

Idiopathic Cerebellar Ataxia of Late Onset:Natural History and MRI Morphology
JNNP 53:297-305, Klockgether,T.,et al, 1990

Neurofibromatosis Type I in Children
J Pediatr 116:845-853, Listernick,R.&Charrow,J., 1990

Neurofibromatosis 2 (Bilateral Acoustic Neurofibromatosis) An Update
Ann Int Med 113:39-52, Mulvihill,J.J.,et al, 1990

Central Nervous System Haemangioblastoma:A Clinical & Genetic Study of 52 Cases
JNNP 53:644-648, Boughey,A.M.,et al, 1990

Electroencephalography Laboratory Diagnosis of Prolonged QT Interval
Ann Neurol 28:387-390, Gospe,S.M.&Gabor,A.J., 1990

Superior Sagittal Sinus Thrombosis in a Patient with Protein S Deficiency
Stroke 21:633-636, Cros,D.,et al, 1990

Progress in Tuberous Sclerosis
Editorial, Lancet 336:598-5991990., , 1990

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

A Disorder of Azonal Development, Necrotizing Myopathy, Cardiomyopathy, and Cataracts:A New Familial Disease
Ann Neurol 27:193-199, Lyon,G.,et al, 1990

Joubert Syndrome:A Clinico-Radiological Study
Neuroradiology 31:502-506, Kendall,B.,et al, 1990

Diaphragmatic Flutter, the Moving Umbilicus Syndrome, and "Belly Dancers" Dyskinesia
Movement Disorders 5:15-22, Illiceto,G., et al, 1990

Cerebral Infarction in Hereditary Spherocytosis
Stroke 20:1755-1756, van Hilten,J.J.,et al, 1989

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

Life-Threatening Cranial Dystonia Following Trihexyphenidyl Withdrawal
Movement Disorders 4:349-353, Gimenez-Roldan,S.,et al, 1989

REcurrent Familial Brachial Plexus Palsies as the ONly Clinical Expression of'Tomaculous'Neuropathy
Eur Neurol 29:61-66, Martinelli,P.,et al, 1989

Follow-up and Diagnostic Reappraisal of 75 Patients with Leber's Congenital Amaurosis
Am J Ophthalmol 107:624-631, Lambert,S.R.,et al, 1989

Diphenhydramine-Induced Dystonia
Clin Pharmacy 8:471, Santora,J.,et al, 1989

Friedreich Ataxia
In Rowland, L. P. Merritt's Textbook of Neurology, 8th Ed, Lea & Febiger, Phila, Ch 13, p627, Rosenberg,R.N., 1989

DNA Restriction Fragment Length Polymorphisms in Diff Dx of Genetic Disease:Appl in Neuromusc Dis
Hum Genet 82:55-58, Defesche,J.C.,et al, 1989

Dyslexia
Editorial, Lancet 2:719-7201989., , 1989

MRI in Cockayne Syndrome Type 1
Neuroradiology 31:276-277, Boltshauser,E.,et al, 1989

Familial Patterns of Narcolepsy
lancet 2:1376-1379, Guilleminault,C.,et al, 1989

Tardive Oculogyric Crises
Neurol 39:1434-1437, FitzGerald,P.M.&Jankovic,J., 1989

Mitochondrial Myopathies:Clinical & Biochem Features of 30 Patients with Major Deletions of Muscle Mitochondrial DNA
Ann Neurol 26:699-708, Hold,I.J.,et al, 1989

Familial X-linked Myalgia and Cramps:A Nonprogressive Myopathy Associated with a Deletion in the Dystrophin Gene
Neurol 39:1277-1280, Gospe,S.M.,et al, 1989

Peripheral Neuropathy in Amyotrophic Chorea-Acanthocytosis
Ann Neurol 26:583-587, Vista,G.,et al, 1989

Gerstmann-Straussler-Scheinker Disease, I, Extending the Clinical Spectrum
Neurol 39:1446-1452, Farlow,M.R.,et al, 1989

Adult-Onset Adrenoleukodystrophy Manifesting as Dementia
Am J Med 87:481-483, Panegyres,P.K.,et al, 1989

Familial Idiopathic Striopallidodentate Calcifications
Neurol 39:381-385, Ellie,E.,et al, 1989

Criteria for Establishing the Validity of Genetic Recombination in Myotonic Dystrophy
Neurol 39:420-421, Griggs,R.C.,et al, 1989

Mitochondrial DNA and Genetic Disease
Editorial, Lancet 1:250-2511989., , 1989

Cardioembolic Stroke in Primary Oxalosis with Cardiac Involvement
DiPasquale. G. , et al, Stroke 20:1403-14069., , 1989

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

Mild Parkinsonism in Persons Exposed to 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine (MPTP)
Neurol 39:1483-1487, Tetrud,J.W.,et al, 1989

Tourette's Syndrome:Current Concepts
Neurol 39:1625-1630, Kurland,R., 1989

Demyelinating Diseases
In Rowlands Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8th Ed, p. 749, Sibley,W.A.,et al, 1989

Refsum Disease
In Rowland's Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8thEd, p. 509, Menkes,J.H., 1989

Magnetic Resonance Imaging in a Family with Hereditary Cerebral Arteriovenous Malformations
Arch Neurol 46:184-187, Allard,J.C.,et al, 1989

Molecular Genetics of Amyloid Neuropathy in Europe
Lancet 1:524-526, Holt,I.J.,et al, 1989

Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred
Medicine 68:1-29, Lamiell,J.M.,et al, 1989

Bilateral Opercular Polymicrogyria
Ann Neurol 25:90-92, Becker,P.S.,et al, 1989

Predictive Testing for Huntington's Disease, Progress and Problems
BMJ 298:404-405, 1989, Harper,P.S.&Morris,M.J., 1989

Chronic Myelopathies Associated with HTLV-I, A Clinical, Serologic, and Immunovirologic Study of 10 Patients in France
Arch Neurol 46:255-260, Gout,O.,et al, 1989

Predisposing Locus for Alzheimer's Disease on Chromosome 21
Lancet 1:352-355, Goate,A.M.,et al, 1989

Lithium Carbonate Intoxication, A Case Report and Review of the Literature
Arch Int Med 149:36-46, Simard,M.,et al, 1989

Episodic Confusion and Tremor Associated with Extrahepatic Portacaval Shunting in Cirrhotic Liver Disease
Neurol 39:403-405, Russell,D.M.,et al, 1989

Cyanide-Induced Parkinsonism:Clinical, MRI, and 6-Fluorodopa PET Studies
Neurol 39:142-144, Rosenberg,N.L.,et al, 1989

Endemic Fluorosis with Spinal Cord Compression, A Case Report and Review
Arch Int Med 149:697-700, Fisher,R.L.,et al, 1989

Multicenter Study of Autologous Adrenal Medullary Transplantation to Corpus Striatum in Pts with Advanced Parkinson's Dis
NEJM 320:337-341, Goetz,C.G.,et al, 1989



Showing articles 1750 to 1800 of 2512 << Previous Next >>