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Differential
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airway obstruction
Alzheimer's disease
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
analgesic
anxiety
aqueduct of Sylvius, stenosis
aqueductal stenosis
asymptomatic
ataxia
atrioventricular block
basal ganglia, calcification of
behavioral disorder
benzodiazepine
blindness
bradycardia
brain atrophy
bruit, supraclavicular
C0ORF72
calcification, intracranial
cardiomegaly
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, false negative
cataracts
cataracts, congenital
cerebellar hypoplasia
cerebral cortex
cerebral cortical atrophy
cerebral embolism
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, young adult
cervical spine injury
cervical spondylosis
chronic progressive external ophthalmoplegia
claudication, extremity
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
cognition
coma
concussion
contractures, joint
controversies in neurology
cornea, opacity of
corpus callosum
corpus callosum, thinning
cortical muscular atrophy
cost
cost effectiveness
creatine phosphokinase(CPK)elevated
degenerative diseases of CNS
dementia
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
developmental disability
developmental milestones
developmental retardation
diabetes mellitus
diplopia
dying
dyspnea
dyspraxia
dystonia
electromyogram
Emery-Dreifuss muscular dystrophy
encephalocele
encephalopathy
encephalopathy, progressive
ethics in neurology
euthanasia
evidence-based research
evoked potentials
exercise intolerance
exercise-induced vascular symptoms
facial weakness, bilateral
familial
fasciculation
fetal movements, reduced
fetus
fibrillations
floppy infant
foot drop
frontal lobe, atrophy
frontotemporal dementia, behavioral variant
gait disorder
gene
gene mutation
genetic counselling
genetic neurologic disorders
glioma
gray matter
head injury
headache
hearing loss
heart block
heart block, complete
heart murmur
hemiplegia
heralding manifestation
herpes simplex encephalitis
herpes simplex encephalitis, diagnosis of
high arched feet
histochemistry
histochemistry of muscle
hospice
hunger
hydrocephalus
hydrocephalus, congenital
hypotonia
hypotonia, infants
intestinal pseudoobstruction
intrinsic hand muscles, wasting of
Kearns-Sayre syndrome
lactic acidemia
Leber's hereditary optic neuropathy
leg weakness, bilateral
Leigh's disease
leukodystrophy
life sustaining treatment
lissencephaly
lobar atrophy
locked-in syndrome
malformation, CNS, congenital
medical-legal aspects of neurology
MELAS syndrome
mental retardation
merosin
MERRF syndrome
micrognathia
micropthalmia
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
monomelic amyotrophy
morphine
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, FLAIR
MRI, functional
MRI, gradient-echo
MRI, susceptibility weighted
MRS
multiple sclerosis
multiple sclerosis, diagnosis of
muscle atrophy, focal
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, central nervous system abnormality
muscular dystrophy, congenital
muscular dystrophy, congenital, Fukuyama type
myasthenia gravis
myasthenia gravis, differential diagnosis
myasthenia gravis, misdiagnosis of
myelopathy
myoclonus
myopathy
myopathy, mitochondrial
myotonia
myotonia congenita
myotonia dystrophica
negative
neoplasm, intracranial
neoplasm, primary intracerebral
neoplasm, primary intracranial
neoplasm, primary of CNS
neuroendocrinology
neurologic complications of, systemic cancer
neurologic consultation
neurologic disease
neurologic disease, diagnoses of
neurologic symptoms
neuroophthalmology
neuropathology, brain
neuropathy
normal
ophthalmoplegia
optic atrophy
optic neuropathy
oxygen therapy
pacemaker, cardiac-transvenous
palliative care
pancytopenia
parietal lobe, lesion of
parietal lobe, syndromes of
Parkinson disease
Parkinsonism syndrome
personality change
physician assisted suicide
pigmentary retinopathy
polyneuropathy
positive sharp waves
practice guidelines
prognosis
progranulin
proximal muscle atrophy
psychiatric problems in neurologic disorders
psychomotor retardation
ptosis
pyramidal tract
quality of life
ragged-red fibers
release phenomena
respiratory failure
retinal detachment
retinal dysplasia
retinopathy
review article
right to die
sedation
seizure
sensorineural hearing loss
short stature
somatosensory evoked potentials
somatosensory evoked potentials, dermatomal
spinal cord, compression of
spinal cord, injury of
sternocleidomastoid muscle
strokelike episodes
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subclavian artery stenosis
suck, poor
sudden death
symmetric brain lesions
teleconsulting
telemedicine
teleneurology
telestroke
temporal lobe, atrophy
temporalis muscle wasting
term infant
thoracic outlet syndromes
toe walking
tongue, fasciculations of
treatment of neurologic disorder
trinucleotide repeats
ultrasonography
upgaze, paralysis of
valium
Walker-Warburg syndrome
walking, difficulty with
weakness
weakness, congenital
weakness, progressive
weight loss
white matter disease
white matter disease, periventricular
winging of scapula
Showing articles 500 to 550 of 9191 << Previous Next >>

Dementia as the Most Common Presentation of Cortical-Basal Ganglionic Degeneration
Neurol 53:1969-1974, Grimes,D.A.,et al, 1999

Serial Magnetic Resonance Imaging of Cerebral Atrophy in Preclinical Alzheimer's Disease
Lancet 353:2125, Fox,N.C.,et al, 1999

Hypertensive Brainstem Encephalopathy:Three Cases Presenting with Severe Brainstem Edema
Neurol 53:652-654, Chang,G.Y.&Keane,J.R., 1999

Safety and Factors Related to Survival After Percutaneous Endoscopic Gastrostomy in ALS
Neurol 53:1123-1125, Chio,A.,et al, 1999

Pathologic Heterogeneity in Clinically Diagnosed Corticobasal Degeneration
Neurol 53:795-800, Boeve,B.F.,et al, 1999

Molecular Basis of the Neurodegenerative Disorders
NEJM 340:1970-1980, Martin,J.B., 1999

Computed Tomography and Magnetic Resonance Imaging in Mild to Moderate Head Injury:Early and late Imaging Related to Outcome
Ann Neurol 46:70-78, van der Naalt,J.,et al, 1999

Adult-Onset Nemaline Myopathy:Another Cause of Dropped Head
Muscle & Nerve 22:1146-1150, Lomen-Hoerth,C.,et al, 1999

HTLV-I-Associated Myelopathy:Acute Progression and Atypical MR Findings
AJNR 20:1417-1421, Shakudo,M.,et al, 1999

Beneficial Effect of Siphoning in Treatment of Adult Hydrocephalus
Arch Neurol 56:1224-1229,1199, Bergsneider,M.,et al, 1999

An Algorithm for ALS Diagnosis and Management
Neurol 53:S58-S62, Swash,M., 1999

Fetal Surgery for Myelomeningocele, Promise, Progress, and Problems
JAMA 282:1873-1874,1819,1826, Simpson,J.L., 1999

Quantitative MRI in Patients with Clinically Isolated Syndromes Suggestive of Demyelination
Neurol 52:599-606, Sailer,M.,et al, 1999

Magnetic Resonance Imaging-Based Volumetry Differentiates Idiopathic Parkinson's Syndrome from Multiple System Atrophy and Progressive Supranuclear Palsy
Ann Neurol 45:65-74, Schulz,J.B.,et al, 1999

Primary and Transitional Progressive MS,A Clinical and MRI Cross-Sectional Study
Neurol 52:839-845, Stevenson,V.L.,et al, 1999

Clinicopath Conf,Wegener's Granulomatosis with Pachymeningeal Granulomatous Inflammation, Case 9-1999
NEJM 340:945-953, , 1999

Quantitative MRI in CADASIL, Correlation with Disability and Cognitive Performance
Neurol 52:1361-1367, Dichgans,M.,et al, 1999

Rapidly Progressive Dementia
Lancet 353:1150, Bornke,C.,et al, 1999

Clinicopath Conf:Multisystem Neurodegenerative Disease with Dementia Pugilistica
NEJM 340:1269-1277, Case 12-1999, 1999

MR Imaging of Acute Coccidioidal Meningitis
AJNR 20:509-514, Erly,W.K.,et al, 1999

Medial Temporal Lobe Atrophy on MRI in Dementia with Lewy Bodies
Neurol 52:1153-1158, Barber,R.,et al, 1999

Atypical Form of Amyotrophic Lateral Sclerosis
JNNP 66:581-585, Sasaki,S.&Iwata,M., 1999

Practice Parameter:The Care of the Patient with Amyotrophic Lateral Sclerosis (An Evidence-Based Review), Report of the Quality Standards Subcommittee of the AAN
Neurol 52:1311-1323, Miller,R.G.,et al, 1999

Infantile Neuroaxonal Dystrophy,Clinical Spectrum and Diagnostic Criteria
Neurol 52:1472-1478, Nardocci,N.,et al, 1999

Brain Structure and Neurocognitive and Behavioural Function in Adolescents Who Were Born Very Preterm
Lancet 353:1653-1657, Stewart,A.L.,et al, 1999

A Prospecitve Study of Preferences and Actual Treatment Choices in ALS
Neurol 53:278-283,248, Albert,S.M.,et al, 1999

A Longitudinal Study of Brain Atrophy in Relapsing Multiple Sclerosis
Neurol 53:139-148, Simon,J.H.,et al, 1999

MR Findings of Werdnig-Hoffmann Disease in Two Infants
AJNR 19:550-552, Hsu,C.,et al, 1998

MR of Extraocular Muscles in Chronic Progressive External Ophthalmoplegia
AJNR 19:95-99, Carlow,T.J.,et al, 1998

Estimation of Brainstem Neuronal Loss in ALS with in Vivo Proton Magnetic Resonance Spectroscopy
Neurol 50:72-77, Cwik,V.A.,et al, 1998

Risk of Amyotrophic Lateral Sclerosis & History of Physical Activity, A Population Study
Arch Neurol 55:201-206, Longstreth,W.T.,et al, 1998

Toward Earlier Diagnosis of Amyotrophic Lateral Sclerosis, Revised Criteria
Neurol 50:768-772, Ross,M.A.,et al, 1998

Hirayama Disease:MR Diagnosis
AJNR 19:365-368, Chen,C.,et al, 1998

Natural History & Survival of 14 Pts with Corticobasal Degeneration Confirmed as Postmortem Exam
JNNP 64:184-189, Wenning,G.K.,et al, 1998

Relationship Between Balance & Abnormalities in Cerebral MRI in Older Adults
Arch Neurol 55:73-79, Tell,G.S.,et al, 1998

Response to External Ventricular Drainage in Spont Intracerebral Hemorr with Hydrocephalus
Neurol 50:519-523, Adams,R.E.&Diringer,M.N., 1998

Retinocochleocerebral Vasculopathy
Medicine 77:12-40, Petty,G.W.,et al, 1998

Susac Syndrome
Medicine 77:3-11, Papo,T.,et al, 1998

Isolated Weakness of the Fingers in Cortical Infarction
Neurol 50:823-824, Lee,P.,et al, 1998

Thrombolysis-Related Intracranial Hemorrhage, Analysis of 224 Cases from GUSTO-1 Trial with Clin Correl
Stroke 29:563-569, Gebel,J.M.,et al, 1998

Dipsticks and Convulsions
Lancet 352:1824, Koch,H., 1998

Olfactory Dysfunction in Guamanian ALS,Parkinsonism,and Dementia
Neurol 51:1672-1677, Ahlskog,J.E.,et al, 1998

Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998
NEJM 339:1914-1923, , 1998

Attitudes of Patients with Amyotrophic Lateral Sclerosis and Their Care Givers Toward Assisted Suicide
NEJM 339:967-973,987, Ganzini,L.,et al, 1998

Clinical,Radiological,Neurophysiological,and Neuropathological Characteristics of Gluten Ataxia
Lancet 352:1582-1585, Hadjivassiliou,M.,et al, 1998

Predicting Neurologic Deterioration in Patients with Cerebellar Hematomas
Neurol 511:1364-1369, St. Louis,E.K.,et al, 1998

Surgical Treatment of Epilepsy in Tuberous Sclerosis,Strategies and Results in 18 Patients
Neurol 51:1263-1269, Guerreiro,M.M.,et al, 1998

Acute Obstructive Hydrocephalus complicating Bacterial Meningitis in Childhood
BMJ 316:1887-1889, Mactier,H.,et al, 1998

A Man Who Lost Weight and His Sight
Lancet 351:1174-1175, Moschos,M.&Droutsas,D., 1998

An Analysis of Extended Survival in Patients with Amyotrophic Lateral Sclerosis Treated with Riluzole
Arch Neurol 55:526-528, Riviere,M.,et al, 1998



Showing articles 500 to 550 of 9191 << Previous Next >>