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acral sensory symptoms
Adies pupil
adolescent medicine
advances in neurology
algorithm
allodynia
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, diagnosis of
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, etiology of
amyotrophic lateral sclerosis, prognosis
amyotrophic lateral sclerosis, treatment of
anemia
angiostrongylus cantonensis
areflexia
arm weakness
arrhythmia, cardiac
arsenic
ascending paralysis
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxic gait
autonomic dysfunction
B 12 deficiency
B12
Babinski sign
BAL
basophilic stippling of red blood cells
BiPAP
bone marrow suppression
bradykinesia
bulbar palsy
bulbar palsy, progressive
burning feet
burning feet, differential diagnosis of
burning hands
burning paresthesia
camptocormia
cardiomegaly
cardiomyopathy
carpal tunnel syndrome
cauda equina, lesion of
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, culture of
cerebrospinal fluid, culture of, viral
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, eosinophilia of
cerebrovascular accident, incidence of
Charcot-Marie-Tooth
children
chromosomal abnormality
chromosome 9
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
cognition
compression neuropathy
concentration, impaired
confusion
congestive heart failure
consanguinity
crying, pathologic
cyst
deep tendon reflexes
degenerative diseases of CNS
delay in diagnosis
dementia
denervation of muscle
denervation potentials
dermatitis
dexterity, impaired
diabetes mellitus
diabetes mellitus, chemical
diabetes mellitus, neurologic manifestations of
diagnostic criteria
diarrhea
differential diagnosis
disability, neurological
disorientation
distal muscle weakness
dopa responsive dystonia
drooling
dying
dysarthria
dyskinesia
dysmorphic
dysphagia
dyspnea
dystonia
edema, pedal
efficacy
electrocardiogram, abnormal
electroencephalogram, inflammatory disease
electromyogram
emotional lability
encephalitis
encephalitis, viral
encephalopathy
endemic area
enterovirus
enterovirus infection of CNS
eosinophilia
epidemiology of neurology
episodic disorders
erythrocyte
Fabry's disease
familial
fasciculation
fatigue
fever
fingernails, abnormal
flaccid paralysis
foot drop
foot drop, bilateral
foot drop, differential diagnoses of
foot numbness
foot, weakness
frataxin
Friedreich's ataxia
gait disorder
gammaglobulin therapy, intravenous
ganglion
gastroenteritis
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
geographic location
glucose tolerance test, abnormal
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
hammertoes
hand pain
hand weakness
headache
headache, progressive
hearing loss
heat intolerance
heavy metal intoxication
helminthic infection of CNS
hemiparesis
hemoglobinuria
hepatitis
heralding manifestation
herniated disc
herniated disc, lumbar
herpes simplex encephalitis
herpes simplex encephalitis, diagnosis of
herpes simplex virus
herpes virus infection
herpes, genital
Hispanics
hospice
hyperamylasemia
hyperkeratosis
hyperreflexia
hypersegmented polys
hypoglycorrhachia
idiopathic polyneuropathy
imbalance
inclusion bodies, intranuclear
incontinence, fecal
intellectual deficit
intrinsic hand muscles, wasting of
jaw jerk, abnormal
laughing, pathologic
L-dopa
leg atrophy
leg numbness
leg weakness, bilateral
leg weakness, unilateral
leukopenia
life expectancy
liver disease
liver function enzymes
lumbosacral plexopathy
lumbosacral plexus, lesion of
lysosomal storage disease
malaise
masked facies
Mees lines
memory, impairment of
meningismus
meningitis
meningitis, aseptic
meningitis, children
meningitis, CSF findings in
meningitis, eosinophilic
meningitis, rapid diagnosis
meningitis, viral etiology in
mental retardation
mental status, abnormal
Mills syndrome
mimics
misdiagnosis
molecular genetics
mononeuritis multiplex
mononeuropathy
mononeuropathy chronic inflammatory demyelinating
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, lumbosacral plexus
MRI, muscle
MRI, peripheral nerve
MRI, spinal cord
multiple sclerosis
muscle atrophy, progressive
muscle cramp
muscle pain
muscle wasting, diffuse
muscle weakness
myelin protein zero gene
myelitis
myelopathy
nausea and vomiting
neck weakness
nerve biopsy
nerve conduction studies
nerve conduction studies, motor
nerve enlargement
nerve root hypertrophy
nerve root, lumbar, lesion of
neuritis, heavy metals causing
neurologic disease, diagnoses of
neurologic examination
neurologic symptoms
neuromuscular disease, electrodiagnosis of
neuronal intranuclear inclusion disease
neuropathology
neuropathy
neuropathy, diabetic
neuropathy, etiologies of
neuropathy, hereditary peripheral
neuropathy, idiopathic
neuropathy, motor
neuropathy, motor, multifocal
neuropathy, multifocal
neuropathy, painful
neuropathy, peripheral
neuropathy, peripheral, treatment
neuropathy, sensory
neuropathy, small-fiber
neuropathy, small-fiber, painful sensory
neuropathy, toxic
neuropathy, work up for
neuroprotective agents
night blindness
numbness, extremity
optic neuropathy
orthostatic hypotension
pain
pain, management of chronic
pain, neuropathic
palliative care
pancreatitis
pancytopenia
paralysis, acute
paralysis, acute areflexic
paraparesis, spastic
parasitic infection
parasitic infection, CNS
paresthesias
paresthesias, feet
paresthesias, hands
Parkinson disease, dystonia with
Parkinson disease, juvenile
Parkinsonism syndrome
periarteritis nodosa
pericardial effusion
peripheral blood smear
peripheral blood smear, abnormal
peripheral nerve, lesion of
pernicious anemia
peroneal nerve
peroneal nerve palsy
peroneal nerve, lesion of
pes cavus
pleocytosis of cerebrospinal fluid
pleural effusion
poliomyelitis-like illness
polymerase chain reaction
polyneuropathy
position sensation, abnormal
precipitating factors
PRKN gene
prognosis
progressive neurologic disorder
proprioception, abnormal
pseudobulbar palsy
psychosis
pupil
pupil, dilated and fixed, bilateral
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quadriplegia
radiculopathy
raw fish ingestion
Red flags
respirator
respiratory failure
reversible neurologic disorder
review article
riluzole
risk factors
sciatic neuropathy
scoliosis
screening
sedimentation rate, elevated
seizure
sensory loss
sensory loss, cutaneous
sensory polyneuropathy
sensory polyneuropathy, cryptogenic
sensory testing, quantitative
sinemet
skin, biopsy
skin, lesions in neurologic disorders
sleep
sleep pathology and physiology
snail
spasticity
spinal cord, lesion of
steroid therapy, CNS treatment and complications with
sushi
sweating, abnormality of
tachycardia
thrombocytopenia
Tinel's sign
tonic foot response
travel history
travel, foreign
treatment of neurologic disorder
tremor
tremor, postural
trinucleotide repeats
tripping
ulnar nerve
ulnar nerve, compression of
uremia
urinary incontinence
urine test in toxic screen
varicella zoster virus
vibratory sensation, abnormal
viral infection
viral infection, CNS
viral isolation
visual impairment
visual loss
vitamin deficiency
weakness
weakness, progressive
weight loss
wheelchair
workup
Showing articles 1200 to 1250 of 1801 << Previous Next >>

Investigation of Variant Creutzfeldt-Jakob Disease and Other Human Prion Diseases with Tonsil Biopsy Samples
Lancet 353:183-189,163, Hill,A.F.,et al, 1999

Diagnostic Criteria for Parkinson Disease
Arch Neurol 56:33-39, Gelb,D.J.,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

Problems in the Management of Attention-Deficit-Hyperactivity Disorder
NEJM 340:40-46, Zametkin,A.J.&Ernst,M., 1999

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

Diagnosis and Treatment of Ischemic Stroke
Am J Med 106:211-221, Alberts,M.J., 1999

Clinical and Neuroradiological Features of Intracranial Vertebrobasilar Artery Dissection
Stroke 30:1083-1090, Hosoya,T.,et al, 1999

Diagnosis, Management, and Treatment of Alzheimer Disease, A Guide for the Internist
Arch Int Med 159:789-798, Richards,S.S.&Hendrie,H.C., 1999

Neurologic Manifestations of AIDS in Older Adults
Infect Dis Clin Practice 8:179-185, Finelli,P.F.,et al, 1999

Fibromyalgia Syndrome a Decade Later
Arch Int Med 159:777-785, Goldenberg,D.L., 1999

Physician Assistants in Neurology Practice
Neurol 52:1513, Taft,J.M.&Hooker,R.S., 1999

Proton Magnetic Resonance Spectroscopy Pattern of Progressive Multifocal Leukoencephalopathy in AIDS
JNNP 66:520-523, Iranzo,A.,et al, 1999

Abnormal Diffusion-Weighted Magnetic Resonance Images in Creutzfeldt-Jakob Disease
Arch Neurol 56:577-583, Bahn,M.M.,&Parchi,P., 1999

Cat-Scratch Disease Encephalopathy:A Cause of Status Epilepticus in School-Aged Children
J Pediatrics 134:635-638, Armengol,C.E.&Hendley,J.O., 1999

Phenotypic Variability in Rippling Muscle Disease
Neurol 52:1453-1459, Vorgerd,M.,et al, 1999

Fatal Enterovirus 71 Encephalomyelitis
J Pediatrics 133:796-798, Lum,L.C.S.,et al, 1998

Use of the Polymerase Chain Reaction in the Diagnosis of Herpes Simplex Encephalitis:A Decision Analysis Model
Am J Med 105:287-295, Tebas,P.,et al, 1998

The Muscular Dystrophies
BMJ 317:991-995, Emery,A.E.H., 1998

Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
NEJM 339:1994-2004, Johnson,R.T. & Gibbs,Jr.,C.J., 1998

Rapid Diagnosis of Varicella Zoster Virus Infection in Acute Facial Palsy
Neurol 51:1202-1205, Murakami,S.,et al, 1998

Dystonia and Chorea in Acquired Systemic Disorders
JNNP 65:436-445, Janavs,J.L.&Aminoff,M.J., 1998

PCR-Based Strategy for Dx of Hered Neuropathy with Liability to Pressure Palsies & Charcot-Marie-Tooth Dis Type 1A
Neurol 50:760-763, Young,P.,et al, 1998

Dyslexia
NEJM 338:307-312, Shaywitz,S.E., 1998

MR Angiography in Internal Carotid Artery Dissection:Improvement of Diagnosis by Selective Demonstration of the Intramural Haematoma
Neuroradiology 40:704-709, Kirsch,E.,et al, 1998

A 69-Year-Old Man with Chronic Dizziness
JAMA 280:2111-2118, Drachman,D. A., 1998

Clinical Approach to Inherited Peroxisomal Disorders: A Series of 27 Patients
Ann Neurol 44:720-730,713, Baumgartner,M.R.,et al, 1998

Detection of a Varient Protein in Hair:New Diagnostic Method in Portuguese Type Familial Amyloid Polyneuropathy
BMJ 316:1500-1501, Ando,Y.,et al, 1998

Patients with Features Similar to Huntington's Disease, Without CAG Expansion in Huntingtin
Neurol 51:215-220, Rosenblatt,A.,et al, 1998

Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
Pediatrics 102:98-100, Cabana,M.D.,et al, 1998

Tardive Dyskinesia:Diagnosis, Pathogenesis, and Management
The Neurologist 4:180-187, Trugman,J.M., 1998

Tourette Syndrome:Update and Review of the Literature
The Neurologist 4:188-195, Feigin,A.&Clarke,H., 1998

Preclinical Prediction of Alzheimer's Disease Using SPECT
Neurol 50:1563-1571, Johnson,K.A.,et al, 1998

Longitudinal Study of CSF Levels of Tau, A beta 1-40, and A beta 1-42 (43) in Alzheimer's Disease
Ann Neurol 44:17-26, 61998., Kanai,M.,et al, 1998

MR Sialography in Patients with Sjogren Syndrome
AJNR 19:1199-1203, Tonami,H.,et al, 1998

Clinicopath Conf
Subacute Sclerosing Panencephalitis, Case 15-1998, NEJM 338:1448-1456998., , 1998

Diagnostic Utility of the Polymerase Chain Reaction in 2 Cases of Suspected Whipple Disease
Arch Int Med 158:801-803, Tasken,K.,et al, 1998

Evaluation and Management of Intracranial Mass Lesions in AIDS
Rpt of Quality Stnds Subcomm of the AAN, Neurol 50:21-261998., , 1998

Diagnosis of Cytomegalovirus Encephalitis in Pts with AIDS by Cytomegalovirus Genomes in Cells of Cerebrospinal Fluid
Neurol 50:693-697, Wildemann,B.,et al, 1998

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

Utility of the Apolipoprotein E Genotype in the Diagnosis of Alzheimer's Disease
NEJM 338:506-511, Mayeux,R.,et al, 1998

A Clinical Role for 99mTC-HMPAO SPECT in the Investigation of Dementia
JNNP 64:306-313, Talbot,P.R.,et al, 1998

Diagnostic Aspects of Narcolepsy
Neurol 50:S2-S7, Aldrich,M.S., 1998

Presentation of Narcolepsy After 40
Neurol 50:459-465, Rye,D.B.,et al, 1998

SPECT in the Identif of New Variant Creutzfeldt-Jakob Disease:Case Reports
BMJ 316:593-594, 5631998., deSilva,R.,et al, 1998

The Role of 99m-Tc HMPAO SPECT in the Diagnosis of Creutzfeldt-Jacob Disease
AJNR 19:454-455, Miller,D.A.,et al, 1998

Detection of 14-3-3 Protein in Cerebrospinal Fluid Supports Dx of Creutzfeldt-Jakob Disease
Ann Neurol 43:32-40, Zerr,I.,et al, 1998

Diagnosis of Creutzfeldt-Jakob Disease by Measurement of S100 Protein in Serum:Case-Control Study
BMJ 316:577-581, 5631998., Otto,M.,et al, 1998

Cytologically Negative Carcinomatous Meningitis:Usefulness of CSF Biochemical Markers
Neurol 50:1173-1175, Chamberlain,M.C., 1998

Cervical Rib and Median Sternotomy-Related Brachial Plexopathies, A Reassessment
Neurol 50:1407-1413, Levin,K.H.,et al, 1998

Small-Fiber Sensory Neuropathies:Clinical Course and Neuropathology of Idiopathic Cases
Ann Neurol 44:47-59, Holland,N.R.,et al, 1998



Showing articles 1200 to 1250 of 1801 << Previous Next >>