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acetylcholine
advances in neurology
akinetic mute
algorithm
alien hand syndrome
Alzheimer's disease
anomic aphasia
anticholinesterase
anticonvulsants
anticonvulsants, selection of
antineutrophil cytoplasmic autoantibodies
aphasia
aphasia, progressive, primary
aphasia, transcortical
aphasia, transcortical-motor
apolipoprotein E
apraxia
apraxia of eye movements
apraxia, constructional
apraxia, speech
areflexia
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxic gait
atypical
auditory evoked brainstem potentials
autonomic dysfunction
axonal degeneration
axonal injury
Babinski sign
baclofen
basal ganglia, degeneration
basal ganglia, lesion, bilateral
Bing-Neel syndrome
blindness
blinking, reduced
brachium pontis
bradykinesia
brain atrophy
brain biopsy
brainstem, atrophy
brainstem, lesion of
Broca's aphasia
burning paresthesia
CAG repeats
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, orbits
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar degeneration
cerebellar lesion
cerebellar vermis
cerebellum
cerebral cortical atrophy
chemosis
cherry red spot-myoclonus syndrome
children
chorea
choreoathetosis
chromosome 12
chromosome 14
chromosome 6
chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids
cigarette smoking
Clinical Pathologic Conference(C.P.C.)
cobalt toxicity
cognition
color vision, impaired
complications
controversies in neurology
corpus callosum
corpus callosum, atrophy of
cortical-basal ganglionic degeneration
cranial nerve enlargement
cranial nerve palsies
cranial nerve palsy, alternating
degenerative diseases of CNS
dementia
dementia, frontotemporal
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
depression
dexterity, impaired
diagnostic criteria
differential diagnosis
diplopia
donut sign
down-beat nystagmus, primary position of gaze
dysarthria
dyskinesia, buccal lingual facial
dysphagia
dyspnea
dyspraxia
dysthyroid ocularmyopathy
dysthyroidism
dystonia
dystonia, focal
edema, periorbital
ejection fraction, abnormal
enzyme, defect
ethics in neurology
evoked potentials
excitotoxin
exophthalmus
extraocular muscle enlargement
extraocular muscle lesion
eye movement, disorders of
eye movement, painful
eye, pain in
falling
familial
fragile-X syndrome
Friedreich's ataxia
frontal behavioral spatial syndrome
fundus, abnormality of
gadolinium
gait disorder
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene mutation
genetic counselling
genetic neurologic disorders
genetic screening
genetic testing
glabellar sign
glioma
globus pallidus, lesion of
glutamate dehydrogenase deficiency
glutamic acid
granulomatosis with polyangiitis
Graves ophthalmopathy
headache
headache, unilateral
hearing loss
hip arthroplasty
HLA
hot cross bun sign
huntingtin
Huntington's chorea
hydroxytryptophan L-5(L-5 HTP)
hyperreflexia
hyperthyroidism
hypothalamus
hypothalamus, lesion of
hypotonia
hypoxia
ibrutinib
IgG4, serum
IgG4-related disease
imbalance
imbalance, postural
immunotherapy
inattention
incidence
intellectual deficit
internuclear ophthalmoplegia
internuclear ophthalmoplegia, bilateral
intracranial pressure, increased
Jakob-Creutzfeldt disease
jaw pain
jocularity
Lafora's disease
language disorder in adults
lateral rectus palsy
L-dopa
leukodystrophy
levitation
life expectancy
lobar atrophy
lymphoma
lymphoma involving CNS
macroglobulinemia
macular degeneration
malignant optic glioma of adulthood
masked facies
maxillary nerves
memory, defect of recent
memory, impairment of
meningitis
mental retardation
MERRF syndrome
methotrexate
midbrain
midbrain, atrophy
mimics
misdiagnosis
molecular genetics
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion weighted
MRI, FLAIR
MRI, nodular enhancement
MRI, optic nerve
MRI, orbit
multiple system atrophy
muscle biopsy, extraocular
mutism
myelomalacia
myoclonic jerks
myoclonus
myoclonus, epilepsy
myoclonus, stimulus sensitive
myopathy, necrotizing
myopathy, steroid responsive
myositis
myositis, ocular
myotonia dystrophica
necrotizing vasculitis
neuroaxonal degeneration
neurofibromatosis 1
neurologic complications of, surgery
neurologic disease
neurologic disease, diagnoses of
neurologic disease, diagnoses of, clinical bedside
neurologic disease, tempo
neurologic signs
neurologic symptoms
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neurotoxic
neurotoxin
neurotransmitter
nystagmus
ocular motility, disorders of
ophthalmoplegia
ophthalmoplegia, painful
ophthalmoplegia, total
optic atrophy
optic canal
optic canal, enlargement of
optic chiasm, enlarged
optic chiasm, lesion of
optic disc edema
optic glioma
optic nerve sheath enhancement
optic nerve, enhancement
optic nerve, enlarged
optic nerve, lesion of
optic nerve, neoplasm of
optic neuropathy
optic neuropathy, bilateral
optic neuropathy, ischemic
optic neuropathy, ischemic, posterior
orbit
orbit, biopsy
orbit, fat
orbit, inflammation in
orbit, lesions of
orbit, mass
orbital apex
orthostatic hypotension
pain
palatal myoclonus
papilledema
paresthesias
paresthesias, feet
Parkinson disease
Parkinson disease, atypical
Parkinson disease, dementia with
Parkinson disease, differential diagnosis of
Parkinson disease, L-dopa nonresponsive
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
pathology
perineuritis
perineuritis, optic
perivascular enhancement
personality change
photophobia
photosensitivity, skin
physostigmine
Pick's disease
pleocytosis of cerebrospinal fluid
polymerase chain reaction
pons, atrophy
pons, lesion of
pontocerebellar atrophy
postoperative neurologic complications
postoperative visual loss
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
progressive supranuclear palsy
proptosis
proptosis, unilateral
proteinopathy
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychological testing
psychological testing, neurologic problems
ptosis
Purkinje cell
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract dysfunction
radiation therapy, CNS treatment and complications with
rapidly progressing neurologic illness
rash
release phenomena
retinal degeneration
retinitis pigmentosa
retro-orbital pain
review article
rigidity
rigidity, axial
risk factors
rituximab
saccadic eye movements
saccadic eye movements, abnormal
salivary gland enlargement
scotoma
seizure
seizure, paradoxical
seizure, treatment of
sella turcica, enlargement of
sensorineural hearing loss
sensory loss
sensory loss, cortical
Shy-Drager syndrome
sialadenitis
sinuses, diseases of
sinusitis
sleep apnea
sleep pathology and physiology
speech disorder
spinal cord, lesion of
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 2
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar ataxia type 6
spinocerebellar ataxia type 7
spinocerebellar degeneration
spinopontine atrophy, dominant
steroid therapy, CNS treatment and complications with
striatonigral degeneration
subthalamic nucleus
suck reflex
synucleinopathy
tau protein
tauopathy
tram-track sign
trazodone
treatment of neurologic disorder
tremor
tremor, intention
trinucleotide repeats
Unverricht-Lundborg disease
upgaze, paralysis of
vasculitides
vision, blurred
visual acuity, decreased
visual acuity, decreased, monocular
visual field defect
visual field defect, altitudinal
visual loss
visual loss, progressive
visuospatial disturbance
Waldenstrom's macroglobulinemia
weight loss
Wernicke's aphasia
white matter disease
X-linked bulbospinal neuronopathy
Showing articles 1650 to 1700 of 2361 << Previous Next >>

Sulfite Oxidase Deficiency:Clinical, Neuroradiologic, and Biochemical Features in Two New Patients
Neurol 39:252-257, Brown,G.K.,et al, 1989

Acute Profound Dystonia in Infants with Glutaric Acidemia
Pediatrics 83:228-234, Bergman,I.,et al, 1989

Cerebellar Degeneration in Neuroleptic Malignant Synd:Neuropath & Review of Lit Concerning Heat-Related Nervous Syst Injury
JNNP 52:387-391, Lee,S.,et al, 1989

Cerebellar Atrophy Following Acute Intoxication with Phenytoin
Neurol 39:432-433, Masur,H.,et al, 1989

Ethanol and the Nervous System
NEJM 321:442-454, Charness,M.E.,et al, 1989

Primary Progressive Cerebellar Ataxia
Neuroradiology 31:16-18, Bradac,G.B.,et al, 1989

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

Cerebrovascular Disease & Antiphospholipis Antibodies in SLE, Lupus-Like Dis, & Primary Antiphospholipid Synd
Am J Med 86:391-399, Asherson,R.A.,et al, 1989

MR Imaging in Progressive Suupranuclear Palsy and Shy-Drager Syndrome
J Comput Assist Tomogr 13:555-560, Savoiardo,M.,et al, 1989

Frontal Lobe Syndrome in a Patient with Bilateral Globus Pallidus Lesions
Arch Neurol 46:1024-1027, Strub,R.L., 1989

Magnetic Resonance Imaging of Spinal Cord Lesions in Multiple Sclerosis
JNNP 52:459-466, Honig,L.S.&Sheremata,W.A., 1989

Quantitation of Cerebral Atrophy in Preclinical and End-Stage Alzheimer's Disease
Ann Neurol 25:450-459, delaMonte,S.M., 1989

Intermittent Obstructive Hydrocephalus in the Arnold-Chiari Malformation
Ann Neurol 26:401-404, Vrabee,T.R.,et al, 1989

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

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

Occluded Fourth Ventricle After Multiple Shunt Revisions for Hydrocephalus
Pediatrics 83:981-985, Coker,S.B.&Anderson,C.L., 1989

Management Problems in Acute Hydrocephalus after Subarachnoid Hemorrhage
Stroke 20:747-753, Hasan,D.,et al, 1989

Acute Hydrocephalus After Subarachnoid Hemorrhage
Stroke 20:715-717, Heros,R.C., 1989

Factors Assoc with Hydrocephalus after Subarachnoid Hemorrhage
Arch Neurol 46:744-752, Graff-Redford,N.R.,et al, 1989

Tuberculous Meningitis in Children:Treatment with Isoniazid and Rifampicin for Twelve Months
J Pediatr 114:875-879, Visudhiphan,P.&Chiemchanya,S., 1989

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

Respiratory Muscle Weakness in Charcot-Marie-Tooth Disease, A Field Study
Arch Int med 149:1389-1391, Nathanson,B.N.,et al, 1989

Hereditary Motor & Sensory Neuropathy with Optic Atrophy, Ultrastructural and Morphometic Observations
Arch Neurol 46:973-977, Sommer,C.&Schroder,J.M., 1989

Compression Syndromes Due to Hypertrophic Nerve Roots in Hereditary Motor Sensory Neuropathy Type I
Neurol 39:1173-1177, Rosen,S.A.,et al, 1989

Rising Mortality From Motoneuron Disease in the USA, 1962-84
Lancet 1:710-712, Lilienfeld,D.E.,et al, 1989

Amyotrophic Lateral Sclerosis:Abnormalities of the Tongue on Magnetic Resonance Imaging
Ann Neurol 25:468-472, Cha,C.H.&Patten,B.M., 1989

A Mitochondrial DNA Mutation as a Cause of Leber's Hereditary Optic Neuropathy
NEJM 320:1300-1305, Singh,G.,et al, 1989

A Defect in Mitochondrial Electron-Transport Activity in Leber's Hereditary Optic Neuropathy
NEJM 320:1331-1333, Parker,W.D.,et al, 1989

Posthemorrhagic Hydrocephalus in High-Risk Preterm Infants:Natural History, Management, & Long-Term Outcome
J Pediatr 114:611-618, Dykes,F.D.,et al, 1989

Neurologic Complications in Long-Standing Nephropathic Cystinosis
Arch Neurol 46:543-548, Fink,J.K.,et al, 1989

Computed Tomography of the Brain in the Diagnosis of and Prognosis in Normal Pressure Hydrocephalus
Neuroradiology 31:160-165, Wikkelso,C.,et al, 1989

Clinical-Pathologic Correlation in Huntington's Disease:A Neuropsychological and Computed Tomography Study
Neurol 39:796-801, Bamford,K.A.,et al, 1989

Surgical Treatment of Progressive Visual Loss in Traumatic Optic Neuropathy, Report of Two Cases
J Neurosurg 70:799-801, Guy,J.,et al, 1989

Internuclear Ophthalmoplegia in Tuberculous Meningitis
Tubercle 70:61-64, Teoh,R.,et al, 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

Respiratory Complications and Their Management in Motor Neuron Disease
Brain 112:1155-1170, Howard,R.S.,et al, 1989

Congenital AIDS:Review of Neurological Problems
Child's Nerv Syst 5:9-11, Curles,R.G., 1989

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

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

MR of Deep Cerebral Venous Thrombosis
Can J Neurol Sci 16:417-421, Ashforth,R.A.,et al, 1989

Late Hypoglossal Nerve Palsy Following Fracture of Occipital Condyle
Surg Neurol 31:402-404, Orbay,T.,et al, 1989

Chronic Progressive Spinobulbar Spasticity, A Rare Form of Primary Lateral Sclerosis
Arch Neurol 45:509-513, Gastaut,J.L.,et al, 1988

Bilateral Optic Neuropathy and Osteolytic Sinusitis
JAMA 259:72-74, Newman,N.M.,et al, 1988

Sarcoidosis of the Anteroir Visual Pathway: Successes and Failures
JNNP 51:1473-1480, Gelwan,M.J., 1988

Facioscapulohumeral Muscular Dystrophy, in Neuromuscular Disease
Springer-Verlag, NY, p289988., Swash,M.&Schwartz,M.S., 1988

Mineralization of the Basal Ganglia Detected by CT in Hallervorden-Spatz Syndrome
Neurol 38:154-155, Tennison,M.B.,et al, 1988

Paraneoplastic Syndromes Involving the Eyes
In Walsh & Hoyt's Clin Neuro-ophthal, 4th ed, Williams & Wilkins, Vol 3, p 1735-1746, Miller,N.R., 1988

Amyotrophic Lateral Sclerosis Presenting with Sleep Hypopnea Syndrome
Chest 93:1309-1312, Carre,P.C.,et al, 1988

Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988

Emery-Dreifuss Muscular Dystrophy:Disease Spectrum and Differential Diagnosis
Neuropediatrics 19:62-71, Voit,T.,et al, 1988



Showing articles 1650 to 1700 of 2361 << Previous Next >>