Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
abdominal tenderness
abducens nerve paralysis
abducens nerve paralysis, bilateral
aciduria
Addison's disease
adducted thumb
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
advances in neurology
adverse drug reaction
algorithm
allergic angiitis
alopecia
alpha-fetoprotein
amaurosis fugax
amniocentesis
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, misdiagnosis
ANA
anemia
anergy
anesthesia, general
aneurysm
angiotensin-converting enzyme
anorexia
antibiotics
anticonvulsants, hypersensitivity syndrome
anticonvulsants, untoward effects of
anti-myeloperoxidase
antineutrophil cytoplasmic autoantibodies
aortic valve, insufficiency
aphasia
arachnoiditis
arcuate scotoma, differential diagnosis of
areflexia
arrhythmia, cardiac
arsenic
arteritides
arthralgia
arthritis
ascending paralysis
aspartate aminotransferase
aspiration
aspirin
asthma
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, progressive
ataxic gait
atrial fibrillation
atrioventricular block
attention deficit disorder with hyperactivity
autism
autoimmune disease
autonomic dysfunction
Babinski sign
bacterial endocarditis, neurologic manifestations of
bacterial infection
BAL
Balint's syndrome
basal ganglia
basophilic stippling of red blood cells
Bassen-Kornzweig syndrome
Beau's lines
bitemporal visual field defect
blindness
blood cultures
bone marrow suppression
bone marrow transplantation
brain atrophy
brain biopsy
brainstem, infarction of
brainstem, lesion of
brainstem, neoplasms of
brainstem, tuberculoma of
bulbar palsy
BUN, elevated
burning feet
burning paresthesia
CAG repeats
calcification, intracranial
calcification, muscle
calf hypertrophy
carcinoma
carcinoma of lung
carcinoma of pancreas
cardiomegaly
cardiomyopathy
cardiovascular disease
carpo-pedal spasm
CAT scan
CAT scan, abnormal
CAT scan, chest
CAT scan, muscle
cataracts
cauda equina
cauda equina, lesion of
central nervous system, infection of
central nuclei, muscle
cerebellar ataxia, children
cerebellum, disease of
cerebellum, neoplasms of
cerebral edema
cerebral embolism
cerebral infarction
cerebral palsy
cerebro hepato renal syndrome
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, red cells in
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, multiple
cervical spine
cervical spine abnormality
chest pain
chest x-ray, abnormal
children
chills
cholelithiasis
chorea
chromosomal abnormality
chromosome 14
Churg-Strauss syndrome
Chvostek sign
Clinical Pathologic Conference(C.P.C.)
Cockayne's syndrome
Cogan's syndrome
cognition
collagen vascular disease
coma
complications
confusion
congenital myopathy
congestive heart failure
conjunctival injection
conjunctivitis
contractures, joint
coronavirus
corpus callosum, lesion of
corpus callosum, thinning
cortical infarction
cough
COVID-19
cranial nerve palsies
cranial neuropathy, multiple
craniopharyngioma
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
Cushing's syndrome
cyclophosphamide
Danon disease
D-dimer
deafness
deafness, bilateral
deafness, unilateral
degenerative diseases of CNS
delirium
dementia
dementia, childhood
demyelinating disease
depression
dermatitis
dermatomyositis
dermatomyositis, childhood
diabetes insipidus
diabetes mellitus
diabetes mellitus, neurologic manifestations of
diagnostic criteria
diarrhea
diet
differential diagnosis
difficulty climbing stairs
digits, abnormal
dilantin
dilantin, hypersensitivity to
diplopia
disseminated intravascular coagulation(DIC)
distal muscle atrophy
distal muscle weakness
diurnal variation
DNA probes
dopa responsive dystonia
drug induced neurologic disorders
dysarthria
dysarthria-clumsy hand syndrome
dysmetria
dysmorphic
dysphagia
dyspnea
dystonia
dystonia, etiology of
dystonia, painful
dystrophic calcification
dystrophin
ear, abnormal
echocardiogram
echocardiogram, transesophageal
echocardiogram, transthoracic, false negative
edema, pedal
edema, periorbital
ejection fraction
ejection fraction, abnormal
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electromyogram
electronystagmography
electroretinograph
embolism, septic
Emery-Dreifuss muscular dystrophy
encephalitis
encephalomyelitis
encephalopathy
endocarditis
endocarditis, acute bacterial
endocarditis, infectious
endophthalmitis
eosinophilia
eosinophilia-myalgia syndrome
eosinophilic fasciitis
epidemiology of neurology
epistaxis
equinovarus
erectile dysfunction
erythema multiforme
erythrocyte
exophthalmus
eye movement, disorders of
eye, pain in
face, numbness of
facial nerve palsy
facial nerve palsy, bilateral
facial weakness
falling
false positive VDRL
familial
fasciculation
fatigue
fatty acid, elevated plasma content
ferritin, elevated
fetus
fever
fingernails, abnormal
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
fragile-X syndrome, carrier
Friedreich's ataxia
fundus, abnormality of
gait disorder
gallium scan
gammaglobulin therapy, intravenous
gastroenteritis
gastrointestinal bleeding
gaze palsy
gaze palsy, horizontal
gaze palsy, supranuclear
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
Gowers maneuver
granuloma, eosinophilic
granulomatosis, allergic
granulomatous disease
granulomatous hypophysitis
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
gynecomastia
Hallervorden Spatz disease
hallucination
hallucination, auditory
hallucination, visual
hand weakness
Hand-Schuller-Christian disease
headache
headache, bifrontal
headache, positional
headache, progressive
headache, severe
hearing loss
heart block
heart murmur
heavy metal intoxication
heliotrope rash
hemangioblastoma
hematuria, microscopic
hemianopia, homonymous
hemiparesis
hemoglobinuria
hemophilus influenza
hepatitis
hepatomegaly
hepatosplenomegaly
histochemistry of muscle
hormone replacement
Huntington's chorea
hydrocephalus
hydrocephalus, congenital
hydrocephalus, fetal
hydrocephalus, intrauterine
hyperadrenalism
hyperamylasemia
hypercalcemia
hypereosinophilic syndrome(HES)
hyperesthesia
hypergammaglobulinemia
hyperinsulinism
hyperkalemia
hyperkeratosis
hyperparathyroidism
hypersensitivity reaction
hypersomnia
hypertension
hyperthyroidism
hypertrophic intracranial pachymeningitis
hypoglycorrhachia
hypogonadism
hypokalemic periodic paralysis
hypokinetic left ventricle
hyponatremia
hypoparathyroidism
hypopyon
hyporeflexia
hypothalamus
hypothalamus, disturbance of
iatrogenic neurologic disorders
imbalance
immunodeficiency
immunohistochemistry
immunosuppressive agents
impulsivity
inclusion body myositis
Indonesia
infection
intellectual deficit
interferonopathy
intestinal biopsy
intracerebral hemorrhage
intracranial pressure, increased
intrinsic hand muscles, wasting of
intubation
iritis
islet cell tumor
karyotyping
Kawasaki disease
Kearns-Sayre syndrome
keratitis
lacrimation
lactic dehydrogenase(LDH)
Laurence-Moon-Bardet-Biedl syndrome
L-dopa
leg spasms
leg spasms, painful
leg weakness, bilateral
Legionella pneumophilia
Legionnaires'disease
leptospirosis
leukocytosis
leukodystrophy
leukopenia
level of consciousness, decreased
life expectancy
livedo reticularis
liver disease
liver function enzymes
Lorenzo's oil
L-tryptophan
lymphadenitis
lymphadenopathy
lymphadenopathy, hilar
lymphocyte capping, diminished
lymphoid adenohypophysitis
lymphoma
lymphopenia
macular degeneration
malabsorption
malignant hyperpyrexia
masked facies
mastoiditis
mediastinum, mass of
medulla oblongata, lesion of
Mees lines
memory, impairment of
meningismus
meningitis
meningitis, aseptic
meningitis, basilar
meningitis, chronic
meningitis, recurrent
meningoencephalitis
meningomyelitis
mental retardation
mental retardation, familial
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
misdiagnosis
mitral valve lesion
mitral valve vegetation
molecular genetics
mononeuritis multiplex
mononeuropathy
mononeuropathy multiplex
mortality
mosquito
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, muscle
MRI, sulcal hyperintensity
mucopolysaccharidoses
multiple sclerosis, misdiagnosis
muscle biopsy
muscle cramp
muscle pain
muscle stiffness
muscle tenderness
muscle weakness
muscle weakness, causes of
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, classification
muscular dystrophy, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
muscular dystrophy, lymphocyte capping, diminished
muscular dystrophy, systemic membrane defect
myasthenia gravis
myasthenia gravis, receptor site in
myelitis, longitudinal
myelopathy
myocarditis
myoclonus
myoedema
myoglobinuria
myopathy
myopathy, centronuclear
myopathy, distal
myopathy, drug-induced
myopathy, hereditary
myopathy, inflammatory
myopathy, mitochondrial
myopathy, quadriceps
myopathy, vacuolar
myopia
myositis
myotonia dystrophica
myotonic discharges
myotubularin
myxedema coma
myxedema, neurologic manifestations of
nasal polyp
nasal septum, perforation of
nausea and vomiting
neck extension
neck pain
neoplasm, pituitary
neoplasm, primary intracranial
neoplasm, primary of CNS
neoplastic angioendotheliosis
nerve biopsy
nerve conduction studies
neuritis, heavy metals causing
neuroendocrinology
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic signs
neuromuscular disease, electrodiagnosis of
neuronal ceroid-lipofuscinosis
neuronal migration disorder
neuronopathy
neuropathology, brain
neuropathy
neuropathy, amyloid
neuropathy, hereditary peripheral
neuropathy, painful
neuropathy, peripheral
neuropathy, toxic
neuropathy, vasculitic, systemic
neurotoxic
night blindness
night sweats
nystagmus
obsessive-compulsive disorder
ocular myopathy
odynophagia
ophthalmoplegia
ophthalmoplegia, plus syndrome
ophthalmoplegia, total
optic atrophy
optic nerve
optic neuropathy
orange peel appearance of skin
otitis, neurologic complications with
pain
pain, abdominal
pain, flank
pain, foot
pain, leg
pain, testicular
pancreatitis
pancytopenia
papilledema
paranoia
paraparesis
paraparesis, spastic
parathyroid adenoma
paresthesias
paresthesias, feet
paresthesias, hands
Parkinsonism syndrome
parotitis
PAS positive
periarteritis nodosa
pericardial effusion
pericarditis
periodic paralysis
peripheral blood smear
peripheral blood smear, abnormal
peripheral nerve, lesion of
peroxisomal disease
pheochromocytoma
photophobia
pigmentary retinopathy
pituitary, enlargement
pituitary, lesion of
pleocytosis of cerebrospinal fluid
pleocytosis of cerebrospinal fluid, neutrophilic
pleural effusion
pleurisy
pneumonia
polycystic kidneys
polymerase chain reaction
polymerase chain reaction, false negative
polymyositis
polymyositis, eosinophilic
polyneuropathy
pons, lesion of
position sensation, abnormal
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
primary aldosteronism
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
proprioception, abnormal
proteinuria
prothrombin time, prolonged
proximal muscle atrophy
psychiatric problems in neurologic disorders
psychosis
ptosis
ptosis, bilateral
pulmonary edema
pulmonary infection
pulmonary infiltrates
pulmonary opacity
pyloric stenosis
quadriceps atrophy
quadriparesis
quadriplegia
radiculopathy
rash
rash, hand
Raynaud's phenomenon
recombinant DNA
refractive errors
Refsum's disease
renal cell carcinoma
renal cyst
renal failure
renal stones
respiratory distress syndrome, neurologic status with
respiratory failure
respiratory tract infection
reticulum cell sarcoma
retinal artery occlusion
retinal degeneration
retinal hemangioma
retinal lesion
retinal tumor
retinitis pigmentosa
retinopathy
reversible neurologic disorder
review article
RFLPs
rhabdomyolysis
rheumatoid arthritis
rheumatoid arthritis factor(R.A.factor)
rhinorrhea
rickettsial organism
rigid spine syndrome
rippling muscle disease
risk factors
Rocky Mountain spotted fever
sarcoidosis
sarcoidosis, CNS
scleroderma
scleroderma, neurologic involvement with
scoliosis
scotoma
sedimentation rate
sedimentation rate, elevated
seizure
seizure, familial
sella turcica, enlargement of
sensorineural hearing loss
serologic testing
serum alanine aminotransferase
serum sickness
severe acute respiratory syndrome
sinemet
sinusitis
skin, biopsy
skin, darkening of
skin, lesions in neurologic disorders
skin, tight
skull x-ray
skull x-ray, abnormal
sonophobia
southeast asia
Southern immunoblot test
spinal cord, lesion of
spinal cord, neoplasm
spinal muscular atrophy
spinocerebellar degeneration
spirochete infection
splenic infarcts
splenomegaly
splinter hemorrhages
standing difficulty
steroid
steroid therapy, CNS treatment and complications with
Stevens-Johnson syndrome
streptococcus pneumoniae
subarachnoid hemorrhage
subcutaneous edema
suprasellar lesion
sweating
sweating, abnormality of
swimming
systemic illness
systemic lupus erythematosus, drug induced
tachycardia
tandem gait, ataxic
tapetoretinal degeneration
telangiectases
telangiectases, periungual
testicular atrophy
testicular biopsy
testicular enlargement
tetany
third nerve palsy
thrombocytopenia
thrombocytosis
thyrotoxicosis
tick bite
tinnitus
toe walking
tongue, fasciculations of
tonsillar herniation of cerebellum
toxic encephalopathy
toxic oil syndrome
transient ischemic attack
travel, foreign
treatment of neurologic disorder
tremor
tremor, intention
tremor, postural
trigeminal neuropathy
trigeminal neuropathy, sensory
trinucleotide repeats
troponin T
Trousseau's sign
tuberculoma of CNS
tuberculosis
tuberculosis, miliary
tumor necrosis factor inhibitor
uncal herniation
uremia
urine test in toxic screen
Usher's syndrome
uveitis
vasculitides
Venereal Disease Research Laboratory test
vertigo
very long chain fatty acids
viral myopathy
vision, blurred
visual acuity, decreased, monocular
visual field defect
visual loss
visual loss, sudden-unilateral
vital capacity
Von Hippel Lindau
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weakness, proximal
web sites
weight loss
Western immunoblot test
wheelchair
Whipple's disease
white matter disease
xerostomia
X-linked bulbospinal neuronopathy
x-linked hydrocephalus
x-linked mental retardation
X-linked myopathy
x-linked myopathy with excessive autophagy
x-ray, cervical spine
 		Showing articles 1000 to 1050 of 1544 << Previous Next >>

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

Human Leptospirosis-A Review of 50 Cases
Infection 17:10-14, Lecour,H.,et al, 1989

Antecollis in Parkinsonism
Lancet 1:1320-1321, Jorens,P.G.,et al, 1989

Hypothyroidism
In Neurologic Clinics, W. B. Saunders Co, Phila, 7:492-493., Kaminski,H.J.&Ruff,R.L., 1989

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

Encephalotrigeminal Angiomatosis
In Rowland's Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8thEd, p. 582, Gold,A.P., 1989

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

Dietary Erucic Acid Therapy for X-Linked Adrenoleukodystrophy
Neurol 39:1415-1422, Rizzo,W.B.,et al, 1989

MRI Detects Cerebral Involvement in Neurologically Asymptomatic Patients with Adrenoleukodystrophy
Neurol 39:1619-1621, Aubourg,P.,et al, 1989

Clinicopath Conf
Diffuse Idiopathic Skeletal Hyperostosis, Case Record 43-1989, NEJM 321:1178-1187989., , 1989

Pleural and Retroperitoneal Fibrosis from Dihydroergotamine
NEJM 321:1760, Malaquin,F.,et al, 1989

HTLV-1 and Polymyositis in Jamaica
Lancet 2:1184-1187, Morgan,O.S.,et al, 1989

HTLV-1 Associated Myelopathy and Polymyositis in a US Native
Neurol 39:1572-1575, Evans,B.K.,et al, 1989

Thyrotoxic Periodic Paralysis
Arch Int Med 149:2597-2600, Kelley,D.E.,et al, 1989

Cerebral Erdheim-Chester Disease:Persistent Enhancement with Gd-DTPA on Mr Images
Radiology 172:791-792, Tien,R.D.,et al, 1989

Flaccid Quadriparesis Associated with Yersinia Enterocolitis-Induced Hypokalemia
Arch Int Med 149:1193-1194, Orman,R.A.&Lewis,J.B., 1989

Clinicopath Conf
Chronic Osteomyelitis of Spine, with Intervertebral Diskitis (T3-T4) & Epidural Abscess (Staph Aureu, ) , Cas9,NEJM 320:1610-1618,1989., 1989

Current Concepts in the Idiopathic Inflammatory Myopathies:Polymyositis, Dermatomyositis, and Related Disorders
Ann Int Med 111:143-157, Plotz,P.H.,et al, 1989

Duchenne Muscular Dystrophy:Patterns of Clinical Progression and Effects of Supportive Therapy
Neurol 39:475-481, Brooke,M.H.,et al, 1989

Genetic Abnormalities in Duchenne and Becker Dystrophies:Clinical Correlations
Neurol 39:461-465, 584-5851989., Medori,R.,et al, 1989

Molecular and Clinical Correlations of Deletions Leading to Duchenne and Becker Muscular Dystrophies
Neurol 39:465-474, 584-5851989., Baumbach,L.L.,et al, 1989

Mitochondrial Myopathies, Mechanisms Now Better Understood
BMJ 298:1127-1128, Schapira,A.H.V., 1989

Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome
NEJM 320:1293-1299, Moraes,C.T.,et al, 1989

Mitochondrial Encephalomyopathy with Associated Aminoacidopathy in a Male Sibship
J Pediatr 115:81-88, Sooth,F.A.,et al, 1989

Cardiac Transplantation in a Patient with Muscular Dystrophy and Cardiomyopathy
Arch Neurol 46:705-707, Donofrio,P.D.,et al, 1989

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

Pyomyositis in a Child with Acquired Immunodeficiency Syndrome
Am J Dis Child 143:779-781, Raphael,S.A.,et al, 1989

Nicotinic Acid-Associated Myopathy:A Report of Three Cases
Am J Med 86:481-483, Litin,S.C.&Snderson,C.G., 1989

Congenital Muscular Dystrophy
J Pediatr 115:214-221, Leyten,Q.H.,et al, 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

Brain Metastases from Undiagnosed Systemic Neoplasms
Arch Int Med 149:1076-1080, Merchut,M.P., 1989

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

Orbital Myositis and Giant Cell Myocarditis
Neurol 39:988-990, Klein,B.R.,et al, 1989

Dopa Responsive Dystonia:A Treatable Condition Misdiagnosed as Cerebral Palsy
BMJ 298:1019-1020, Boyd,K.&Patterson,V., 1989

Clinicopath Conf
Metastatic Adenocarcinoma Compatible with Breast Origin of Mastoid and Temporal Bone, Case Record 14, 189,NEJM 320:924-930,1989., 1989

Chronic Inflammatory Demyelinating Polyradiculoneuropathy, Clin Characteristics, Course, & Diag Criteria
Arch Neurol 46:878-884, Barohn,R.J.,et al, 1989

Intracranial Injury after Moderate Head Trauma in Children
J Pediatr 115:346-350, Rosenthal,B.W.&Bergman,I., 1989

Phenytoin-Induced Acute Respiratory Failure with Pulmonary Eosinophilia
Am J Med 87:93-94, Mahatma,M.,et al, 1989

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

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

Clinicopath Conf
Recurrent Hodgkin's Disease, with Intracranial and Orbital Involvement, Case Record 7-1989, NEJM 320, 4477,1989., 1989

Selective Criteria May Increase Lumbosacral Spine Roentgenogram Use in Acute-Low-Back Pain
Arch Int Med 149:47-50, 271989., Frazier,L.M.,et al, 1989

Short-Term Outcomes of Skull Fracture:A Population-Based Study of Survival and Neurologic Complications
Neurol 39:96-102, Wiederholt,W.C.,et al, 1989

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

Comatose Patients Smelling of Alcohol, All Need Measurements of Blood Alcohol Concentrations and Skull Radiography
BMJ 299:410, Quaghebeur,G.&Richards,P., 1989

Brain-Stem Tuberculoma, An Analysis of 11 Patients
Arch Neurol 46:529-535, Talamas,O.,et al, 1989

Adrenoleukodystrophy
JAMA 262:1504-1506, Ladenson,P.W., 1989

Diagnosis of Gerstmann-Straussler Syndrome in Familial Dementia with Prion Protein Gene Analysis
Lancet 2:15-17, Collinge,J.,et al, 1989

AIDS and the Nervous System
JAMA 261:2396-2399, Dalakas,M.,et al, 1989

Zidovudine-Associated Myopathy
Am J Med 86:814-818, Gertner,E.,et al, 1989



Showing articles 1000 to 1050 of 1544 << Previous Next >>