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Differential
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abdominal distention
abdominal protrusion
abducens nerve paralysis
addiction, heroin
addiction, heroin-neurologic complications with
Addison's disease
adolescent medicine
adverse drug reaction
airway obstruction
akinetic mute
algorithm
alpha-fetoprotein
alpha-synuclein
Alzheimer's disease
amyloid angiopathy, cerebral
amyloidosis
amyotrophic lateral sclerosis
anatomy of
anemia
angiography, cerebral
anti Tr antibodies
anticoagulant, treatment
anticonvulsants
anticonvulsants, untoward effects of
antiphospholipid antibodies
anxiety
apraxia
apraxia of eye movements
aqueduct of Sylvius, stenosis
aqueductal stenosis
areflexia
Argyll Robertson pupil
arteritic anterior ischemic optic neuropathy
arteritis, temporal
arthralgia
arthritis
ascites
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, truncal
ataxic gait
atypical
autoantibodies
autoimmune cerebellar ataxia
autoimmune disease
autonomic cardiovascular reflexes
autonomic dysfunction
autonomic dysfunction, acute
autonomic dysfunction, evaluation of
autonomic nervous system
autonomic neuropathy
autonomic neuropathy, idiopathic
B 12 deficiency
B12
basal ganglia, lesion of
basal ganglia, lesion, bilateral
Behcet's syndrome
benign essential tremor
biologic markers
bladder dysfunction
blinking
blinking, reduced
bone biopsy
bone pain
bone scanning
botulism
bradykinesia
bradykinesia, facial
BRAF protooncogene
brain atrophy
brain biopsy
brain purpura
brainstem, atrophy
brainstem, lesion of
cachexia
calcification, intracranial
carcinoembryonic antigen
carcinoma
cardiac surgery, neurologic complications with
cardiomyopathy
carotid artery occlusion, intracranial
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, venography
cauda equina, lesion of
celiac disease, adult
celiac disease, childhood
central nervous system, infection of
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 lesion
cerebellar vermis
cerebellum, disease of
cerebral arteries
cerebral cortical atrophy
cerebral edema, vasogenic
cerebral venous infarction
cerebral venous thrombosis
cerebral venous thrombosis, deep
cerebral venous thrombosis, etiology
cerebral venous thrombosis, recurrent
cerebrospinal fluid, elevated protein of
cerebrovascular accident
cerebrovascular accident, acute management of
cerebrovascular accident, prevention of
cerebrovascular accident, prognosis in
cerebrovascular accident, recurrent
cerebrovascular accident, thrombolytic agents in treatment
cerebrovascular accident, young adult
children
chorea
choreoathetosis
choroidopathy
chromosomal abnormality
chromosome 11
cigarette smoking
Clinical Pathologic Conference(C.P.C.)
clonidine
clubbing of fingers
cognition
cogwheel rigidty
cold hands sign
collateral circulation
complications
confusion
conjunctivitis
consanguinity
constipation
contractures, joint
controversies in neurology
corpus callosum, lesion of
cortical-basal ganglionic degeneration
cotton-wool spots
cough
CPAP
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
craniectomy, decompressive
creatine phosphokinase(CPK)elevated
critical care unit
cryopyrin-associated periodic syndrome
cytokines
D-dimer
deafness
deep gray nuclei
degenerative diseases of CNS
dementia
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, reversible
dementia, thalamic
dementia, treatment of
demyelinating disease
depression
dermatitis herpetiformis
developmental retardation
diabetes insipidus
diabetes mellitus
diarrhea
differential diagnosis
difficulty climbing stairs
distal muscle weakness
dopamine receptor
dopamine receptor, D2
down-beat nystagmus
drooling
dural sinus thrombosis
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dysphasia
dystonia
dystonia, face
edema, pedal
edema, periorbital
electroencephalogram, abnormalities of
electromyogram
emergencies, ocular
emotional lability
empty sella
encephalitis
encephalitis, autoimmune
encephalitis, focal
encephalomalacia
encephalopathy
endovascular therapy
enzyme, defect
epidemiology of neurology
episodic disorders
Erdheim-Chester disease
erectile dysfunction
erythema migrans
evidence-based research
extraocular muscle lesion
extrapyramidal movement disorder, progressive
eye movement, disorders of
facial appearance, abnormal
facial expression abnormality
facial weakness
Factor V Leiden
falling
false negative
false positive
familial
fatal familial insomnia
fatigue
fever
fever, recurrent
fibrinolytic agents
fibrinolytic agents, intra-venous local infusion
fine motor function, impaired
fingers, abnormal
fluorescein angiography
foot drop
foot drop, bilateral
foot numbness
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
fragile-X syndrome, carrier
frontal bossing
gadolinium
gait disorder
gait, spastic
gait, waddling
gammaglobulin therapy, intravenous
ganglionitis
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastrointestinal perforation
gastroparesis
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic linkage
genetic neurologic disorders
genetic testing
genital ulcerations
giant cell arteritis
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glutamate dehydrogenase deficiency
gluten ataxia
gluten sensitivity
gluten-free diet
grasp reflex
growth hormone
growth retardation
Guillain Barre syndrome, differential diagnosis of
hallucination
hallucination, visual
head circumference
head injury
headache
headache, intermittent
headache, severe
hearing loss
hemiparesis
hepatitis
heralding manifestation
histiocytosis
HLA
Horner's syndrome
Horner's syndrome, childhood
hot cross bun sign
Huntington's chorea
hydrocephalus
hyperreflexia
hypertension
hypertrophic intracranial pachymeningitis
hypogonadism
hypophonia
hyporeflexia
hypotension, systemic
hypotonia
iatrogenic neurologic disorders
IgG4-related disease
imbalance
imbalance, postural
immunodeficiency
immunologic disease
immunosuppression
impotence
incidence
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
incontinence, fecal
infraorbital nerve
intellectual deficit
intellectual deterioration
intestinal pseudoobstruction
intracerebral hemorrhage
intracranial hypertension, benign
intracranial pressure, increased
intrathecal medication
iridocyclitis
iritis
Jakob-Creutzfeldt disease
keratoconjunctivitis
lacrimal gland enlargement
L-dopa
leg numbness
leg weakness, bilateral
lenticular nucleus, lesion of
lenticular nucleus, lesion of, bilateral
lethargy
leukemia
leukocytosis
leukodystrophy
leukoencephalopathy
level of consciousness, decreased
Lewy body
Lewy body disease, diffuse
lid
life expectancy
limbic encephalitis
long bone lesion
Lyme disease
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
malabsorption
malignant papulosis
marche a petits pas
masked facies
memory, impairment of
meningeal biopsy
meningeal enhancement
meningitis
meningitis, aseptic
meningitis, chronic
mental retardation
mental status, abnormal
methylmalonic aciduria
microcephaly
microinfarcts
midbrain
midbrain, atrophy
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
mimics
Mini Mental Status Examination
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
monoclonal gammopathy
mononeuritis multiplex
morning glory sign
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
moyamoya
moyamoya, adult
MRI
MRI, abnormal
MRI, ADC maps
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, functional
MRI, gradient-echo
MRI, hypointense signal foci on
MRI, mass effect on
MRI, spinal cord
MRI, venography
MRI, volumetry
MRS
multiple organ failure
multiple sclerosis
multiple system atrophy
muscle biopsy
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
myasthenic syndrome
myelopathy
myelopathy, necrotizing
myoclonic jerks
myoclonus
myoclonus, stimulus sensitive
myopathy
myopathy, inclusion body
myopathy, inclusion body with Paget's disease
nausea and vomiting
neurocutaneous disease
neuroendocrinology
neurologic complications of, surgery
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neuromyelitis optica (Devic's disease)
neuronopathy, sensory
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, amyloid
neuropathy, peripheral
nicotine
non-arteritic antererior ischemic optic neuropathy
nutritional deficiency
nystagmus
ocular motility, disorders of
old age, neurology of
Onufrowicz nucleus
ophthalmoplegia
ophthalmoplegia, painful
ophthalmoplegia, total
optic atrophy
optic atrophy, bilateral
optic disc cup
optic disc edema
optic disc ischemia
optic nerve
optic nerve, blood supply of
optic nerve, infarction of
optic neuritis
optic neuropathy
optic neuropathy, bilateral
optic neuropathy, ischemic
optic neuropathy, ischemic, anterior
optic neuropathy, ischemic, posterior
oral contraceptives
oral contraceptives, cerbrovascular disease and
oral ulcerations
orbit, fat
orbit, inflammation in
orbit, lesions of
orbit, pseudotumor of
orbit, tomograms of
orthostatic hypotension
orthostatic hypotension, idiopathic
osteoporosis
Paget's disease
pain, abdominal
pancreatitis
papilledema
paraparesis, spastic
parasympathetic nervous system
paresthesias
paresthesias, hands
Parkinson disease
Parkinson disease, arteriosclerotic
Parkinson disease, atypical
Parkinson disease, dementia with
Parkinson disease, diagnosis
Parkinson disease, differential diagnosis of
Parkinson disease, drug induced
Parkinson disease, L-dopa nonresponsive
Parkinson disease, misdiagnosis
Parkinson disease, rapid progression
Parkinson disease, treatment of
Parkinson disease, tremor, absence of
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
pars planitis
pathology
pitfalls
plasmacytoma
pleocytosis of cerebrospinal fluid
POEMS syndrome
polymerase chain reaction
polyneuropathy
polyneuropathy, critically ill
pons, atrophy
postoperative neurologic complications
postural abnormality
practice guidelines
pregnancy, neurologic complications in
prethrombotic state
prevention of neurologic disorders
prion disease
procainamide
progeria
prognosis
progressive neurologic disorder
progressive supranuclear palsy
proptosis
protein C deficiency
protein S deficiency
proteinopathy
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
psychosis, acute
ptosis
puberty
puberty, delayed
pupil
pupil, abnormality in neurologic disorders
pure autonomic failure
purple glove syndrome
purple hands
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract dysfunction
radiation hypersensitivity
ragged-red fibers
rapidly progressing neurologic illness
rash
recurrent
red eye
remote effect of cancer on the nervous system
renal failure
respirations in CNS disease
respirator
respiratory failure
respiratory tract infection
retina, abnormal
retinal hemorrhages
retinal ischemia
retinal lesion
retinal vasculitis
retinal vasculopathy
retinal vasculopathy with cerebral leukodystrophy
retinopathy
retroperitoneal mass
reversible neurologic disorder
review article
RFC1 gene
rigidity
rigidity, axial
Riley-Day syndrome
risk factors
Romberg's sign
scleritis
sclerosis, bone
sedimentation rate, elevated
seizure
sensorineural hearing loss
sensory loss
sensory loss, leg
septicemia
serologic testing
sexual behavior, disorder of
sexual dysfunction in neurologic disease
short stature
Shy-Drager syndrome
sicca syndrome
sinemet
single photon emission computed tomography
skin, biopsy
skin, lesions in neurologic disorders
skull bone, thickening
spinal cord, injury of
spinal cord, injury, sexual dysfunction in
spinal cord, lesion of
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 2
spinocerebellar ataxia type 7
spinocerebellar ataxia type 8
spinocerebellar degeneration
spirochete infection
stare
stem cell transplantation
steppage gait
steroid therapy, CNS treatment and complications with
striatonigral degeneration
stridor
subdural effusion
subdural hygroma
sudden death
superior sagittal sinus thrombosis
sympathetic nervous system
synucleinopathy
systemic illness
systemic lupus erythematosus
systemic lupus erythematosus, neurologic complications with
systemic lupus erythematosus, neuro-opthal.complications with
tandem gait, ataxic
tau protein
tauopathy
telangiectases
tendonitis
thalamus, lesion of
third nerve palsy
tissue plasminogen activator, intravenous
Tolosa Hunt syndrome
tongue, ulcer
tracheostomy
treatment of neurologic disorder
tremor
tremor, cerebellar
trigeminal nerve, hypertrophy
trigeminal neuralgia
trinucleotide repeats
trochlear nerve palsy
upgaze
upgaze, paralysis of
urinary incontinence
uveitis
vascular endothelial growth factor
vasculitides
vasculopathy
vegetarianism
Vemurafenib
vestibular areflexia
vibratory sensation, abnormal
visual acuity, decreased, monocular
visual field defect
visual field defect, altitudinal
visual loss
visual loss, progressive
visual loss, slow
visual loss, sudden-unilateral
vitamin deficiency
vitiligo
walking, difficulty with
walking, difficulty with in dark
Wallerian degeneration
weakness
weakness, generalized
weakness, progressive
weaning from respirator, failure to
weight loss
wheelchair
Whipple's disease
white matter disease
wide based gait
word-finding difficulty
workup
writing
xanthelasma
xerostomia
Showing articles 1050 to 1100 of 2408 << Previous Next >>

Chronic Neutrophilic Meningitis Caused by Candida Albicans
Neurologia 13:362-366, del Pozo, M.M.,et al, 1998

Candidal Meningitis in HIV-Infected Patients: Analysis of 14 Cases
Clin Inf Dis 25:473-476, Casado, J.L.,et al, 1997

ALS & Severe Cervical Spondylotic Myelopathy in Pt with a Posterior Fossa Archnoid Cyst:Diag Dilemma
South Medical J 80:1580-1583, Lee,S.K.&Kelly,D.L., 1997

Adult-Onset Neimann-Pick Type C Disease, Clinical, Biochemical and Genetic Study
Arch Neurol 54:1536-1541, Lossos,A.,et al, 1997

Complete Ophthalmoplegia After Zoster Ophthalmicus
J Neuro-Ophthalmol 17:262-265, Chang-Godinich,A.,et al, 1997

Small-Vessel Vasculitis
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Cerebral & Cerebellar Atrophy on Serial MRI in an Initially Symptom Free Subject at Risk of Familial Prion Disease
BMJ 315:856-857, Fox,N.C.,et al, 1997

Frontotemporal Degeneration, Pick Disease, and Corticobasal Degeneration
Arch Neurol 54:1425-1427, 14291997., Neary,D., 1997

Frontotemporal Dementia, Pick Disease, and Corticobasal Degeneration
Arch Neurol 54:1427-1429, Kertesz,A., 1997

Clinical Course of a Cohort in the Cuban Epidemic Optic and Peripheral Neuropathy
Neurol 48:19-22, Mojon,D.S.,et al, 1997

Prognosis in Familial ALS:Progr & Surv in Pts with glu100gly & ala4val Mutations in Cu, Zn Superoxide Dismutase
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Atrophy of Cerebellum & Brainstem in Dentatorubral Pallidoluysian Atrophy, CAG Repeat Size on MRI Findings
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Cordarone (Amiodarone)
Product Insert, Wyeth-Ayerst Laboratories, June 1997., , 1997

Multifocal Motor Neuropathy Presenting as Ophthalmoplegia
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Clinical Features of Perineuritis
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Anticedents of Cerebral Palsy in a Multicenter Trial of Indomethacin for Intraventricular Hemorrhage
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Postoperative Cerebral Edema Occurring in Children with Slit Ventricles
Pediatrics 99:625-630, Eldredge,E.,et al, 1997

Preliminary Results of Linear Accelerator Radiosurgery for Acoustic Schwannomas
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Ischemic Lesion Volumes in Acute Stroke by Diffusion-Weighted MRI Correlate with Clinical Outcome
Ann Neurol 42:164-170, Lovblad,K-O.,et al, 1997

Clinical Characteristics of Patients with Motor Disability Due to Conversion Disorder:A Prospective Study
JNNP 63:83-88, Binzer,M.,et al, 1997

Etiology and Early Prognosis of Newly Diagnosed Partial Seizures in Adults
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Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
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Clinical and Molecular Features of Spinocerebellar Ataxia Type 6
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Clinicopath Conf
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Gene Locus for Autosomal Recessive Distal Myopathy with Rimmed Vacuoles Maps to Chromosome 9
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ALS Standard of Care Consensus
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Effect of Noninvasive Positive-Pressure Ventilation on Survival in Amyotrophic Lateral Sclerosis
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Practice Advisory on the Trtm of ALS with Riluzole
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Motor Neuron Syndromes in Cancer Patients
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Familial Nature and Continuing Morbidity of the Amyotrophic Lateral Sclerosis-Parkinsonism Dementia Complex of Guam
Neurol 49:400-409, McGeer,P.L.,et al, 1997

Spinobulbar Muscular Atrophy Can Mimic ALS:The Importance of Genetic Testing in Male Patients with Atypical ALS
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Lymphoproliferative Disorders and Motor Neuron Disease:An Update
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Hepatoerythropoietic Porphyria:Neuroimaging Findings
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Optic Atrophy and Cerebral Infarcts Caused by Methanol Intoxication:MRI
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Clinicopath Conf
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Paraneoplastic Cerebellar Degeneration
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CIDP:Clinical Features & Responses to Trtm in 67 Consecutive Pts with/without a Monoclonal Gammopathy
Neurol 48:321-328, Gorson,K.G.,et al, 1997

Volumetric MRI Analysis Comparing Subjects Having Attention-Deficit Hyperactivity Disorder with Normal Controls
Neurol 48:589-601, Filipek,P.A.,et al, 1997

Neuroanatomy in Rett Syndrome:Cerebral Cortex and Posterior Fossa
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Longitudinal Change in Basal Ganglia Volume in Patients with Huntington's Disease
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Medial Temporal Lobe Volumetrics in Traumatic Brain Injury
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Correlation of MRI and Neuropathology in AIDS
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Dentate Nuclei Invol in AIDS Pts with CNS Cryptococcosis:Imaging Findings with Path Correl
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High Signal Intensity on T1 Weighted MRI of Anterolateral Column of Spinal Cord of Amyotrophic lateral Sclerosis
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CT and MR Findings of Neuroacanthocytosis
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What Are the Obstacles for an Accurate Clinical Diagnosis of Pick's Disease
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X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
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Cysticercosis, Clinical Classification Based on Imaging Studies
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Paramedian Pontine Infarction
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CAG Repeat Number Governs the Development Rate of Pathology in Huntington's Disease
Ann Neurol 41:689-692, Penney,J.B.,et al, 1997



Showing articles 1050 to 1100 of 2408 << Previous Next >>