Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
abdominal distention
acid maltase deficiency
acid maltase deficiency, adult
acromegaly
acute intermittant porphyria
advances in neurology
adverse drug reaction
alcohol, neurologic complications with
alcoholic polyneuropathy
alcoholism
amyloid
amyloidosis
anesthesia, general
aneurysm
aneurysm, thoracic aortic
anterior horn cell disease
anticonvulsants
antineurofascin antibodies
aortic wall, thickened
aortitis
areflexia
arrhythmia, cardiac
arterial dissection, aorta
arterial dissection, wall thickness
arteritis, temporal
asymptomatic
ataxia
ataxic gait
autism
autoantibodies
autoimmune disease
autonomic dysfunction
Babinski sign
bacterial infection
blindness
botulinum toxin
brachial neuritis, acute
bruxism
bulging of biceps
calf hypertrophy
carbamazepine
carcinoma
cardiomegaly
cardiomyopathy
cardiovascular disease
CAT scan
CAT scan, abnormal
CAT scan, angiography
CAT scan, emission, abnormal
CAT scan, metrizamide
CAT scan, muscle
CAT scan, myelogram with
cataracts
cauda equina
cauda equina, enhancement
cauda equina, lesion of
cavernous sinus
cavernous sinus, lesion of
central nervous system, infection of
cerebellar lesion
cerebral ischemia
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, proteincytologic dissociation
cerebrovascular accident
cerebrovascular disease, cardiovascular disease with
cerebrovascular disease, risk factors in
Charcot-Marie-Tooth
chemosis
chewing movements
chewing, impaired
children
chromosomal abnormality
chromosome 17
claudication, intermittent of cauda equina
Clinical Pathologic Conference(C.P.C.)
CLOVES syndrome
clubfoot as related to neurologic disease
complications
confusion
congenital malformation
congenital myopathy
congestive heart failure
contactin associated protein like 1 antibodies
contractures, joint
coronary artery disease
corticotropin level
corticotropin-releasing factor
cortisol, elevated
cranial nerve enlargement
cranial nerves
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
cry, abnormal
crying
Cushing's syndrome
cysticercosis
cysticercosis, cerebral
cysticercosis, disseminated
cysticercosis, intraventricular
cysticercosis, miliary
deafness
deep gray nuclei
Dejerine-Sottas syndrome
delay in diagnosis
denervation of muscle
dentate nuclei
dentate nuclei, lesion of
developmental milestones, loss of
developmental retardation
diabetes mellitus
diagnostic criteria
diamond on quadriceps
diaphragmatic paralysis
differential diagnosis
difficulty climbing stairs
dilantin
diplopia
distal muscle atrophy
distal muscle weakness
donut sign
dysferlinopathy
dysphonia
dysplasia of C.N.S.
dyspnea
dysthyroid ocularmyopathy
dystonia
dystonia, post traumatic
dystrophin
dystrophin associated proteins
echocardiogram
echocardiogram, LVH
edema, periorbital
electrocardiogram, abnormal
electrocardiogram, LVH
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
electron microscopy
encephalopathy
encephalopathy, progressive
entrapment neuropathy
enzyme, defect
eosinophilic fasciitis
epidermal nevus syndrome
exercise
exophthalmus
extraocular muscle enlargement
facial hair, excessive
facial pain
facial pain, atypical
facial weakness
facial weakness, bilateral
failed medical management
falling
familial
fatigue
feeding disorder
fever
fine motor function, impaired
fistula, arterio-venous, carotid-cavernous
fistula, arterio-venous, dural
foot deformity
foot drop
gadolinium
gait disorder
gait, waddling
gammaglobulin therapy, intravenous
gammaglobulin therapy, intravenous, refractory
gender
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
giant cell arteritis
globoid cells
Gowers maneuver
Graves ophthalmopathy
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
halo sign
hammertoes
hand deformity
hand weakness
hands, fisted
head injury
head lag
headache
headache, bilateral
headache, temporal
hearing loss
heart murmur
hemiatrophy, congenital
hemidiaphragm, paralysis of
hemihypertrophy, congenital
hemihypertrophy, facial
hemimegalencephaly
hemiparesis
hepatomegaly
hereditary myopathy with early respiratory failure
heterotopia
high arched feet
hirsutism
histochemistry
hoarseness
hypercalcemia
hyperreflexia
hypertension
hyperthyroidism
hypertonia
hypokalemia
hypomelanosis of Ito
hypopigmentation of skin
hyporeflexia
hypothyroidism
idiopathic
IgG4, serum
IgG4-related disease
inability to sit up
infantile spasm
intellectual deficit
intrinsic hand muscles, wasting of
irritability
Isaacs syndrome
Kobberling-Dunnigan syndrome
Krabbe's disease
Kugelberg-Welander syndrome
kyphoscoliosis, neurologic causes of
lacrimal gland enlargement
laminectomy, cervical
laminectomy, lumbar
learning disability
learning disability, in children
left ventricular dilatation
leg atrophy
leg numbness
leg swelling
leg weakness, unilateral
leukemia
leukocyte enzyme abnormality
leukocytosis
leukodystrophy
life expectancy
limb hypertrophy
limb-girdle weakness
lipodystrophy
liver function enzymes
lordosis
lumbosacral plexopathy
lymphoma
lymphopenia
macrocephaly
malformation, CNS, congenital
malformation, vascular
malformation, vascular, cerebral
malignant hyperpyrexia
masseter muscle hypertrophy
maxillary nerves
meconium staining
meningioma
mental retardation
mental status, abnormal
metabolic alkalosis
mexiletine
mimics
misdiagnosis
molecular genetics
monoclonal gammopathy
mononeuritis multiplex
mononeuropathy
mononeuropathy chronic inflammatory demyelinating
mortality
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, angiography
MRI, contrast enhanced
MRI, cranial nerves
MRI, hypointense signal foci on
MRI, lumbosacral plexus
MRI, muscle
MRI, optic nerve
MRI, orbit
MRI, peripheral nerve
MRI, spinal cord
MRI, spine
MRI, vessel wall
MRI, vessel wall enhancement
MRS
mucormycosis
multimodal neuroimaging
multiple myeloma
muscle atrophy, focal
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle hypertrophy
muscle hypertrophy, congenital
muscle pain
muscle stiffness
muscle swelling
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, Becker, carrier
muscular dystrophy, cardiovascular changes with
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, dystrophin normal
muscular dystrophy, facioscapulohumeral
muscular dystrophy, female occurrence of
muscular dystrophy, limb-girdle
muscular dystrophy, pattern of muscle involvement
myelogram
myelopathy
myeloradiculopathy
myocardial infarction
myoedema
myoglobinuria
myokymia
myopathy
myopathy, amyloid
myopathy, focal
myopathy, hereditary
myopathy, metabolic
myopathy, monomelic
myopathy, quadriceps
myopathy, vacuolar
myositis, ocular
myostatin
myotonia
myotonia congenita
nausea and vomiting
neoplasm, hormone producing, ectopic
neoplasm, metastatic to muscle
neoplasm, metastatic to orbit
neoplasm, peripheral nerve
nephrotic syndrome
nerve biopsy
nerve conduction studies
nerve enlargement
nerve hypertrophy
nerve injury
nerve root enhancement
nerve root hypertrophy
neuritis
neuritis, causes of
neuritis, heavy metals causing
neurocutaneous disease
neuroendocrinology
neurofibroma
neurofibromatosis 1
neurofibromin
neurologic disease, diagnoses of
neurologic examination
neurologic history
neurologic signs
neuromyotonia
neuroophthalmology
neuropathology
neuropathy
neuropathy, amyloid
neuropathy, ataxic
neuropathy, autoimmune
neuropathy, demyelinating
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, medication induced
neuropathy, onion bulb
neuropathy, peripheral
night blindness
night sweats
node of Ranvier
nodopathy, autoimmune
nonresponsive
ophthalmic artery
opisthotonus
optic atrophy
optic chiasm, enlarged
optic nerve
optic nerve sheath enhancement
optic nerve, compression of
optic nerve, enlarged
optic nerve, lesion of
optic neuropathy
optic neuropathy, bilateral
orbit, cellulitis of
orbit, inflammation in
orbit, lesions of
orbit, mass
orbit, meningioma of
orbit, neoplasms of
orbit, pseudotumor of
orthopnea
pain, leg
palpitations
paraparesis
paresthesias
paresthesias, feet
paresthesias, lower extremity
PAS positive material in the brain
pathology
percussion induced muscle contraction
perineuritis
perineuritis, optic
peripheral nerve, lesion of
peroxisomal disease
pes cavus
phakomatoses
phytanic acid
plasma cell dyscrasia
polyneuropathy
polyneuropathy, chronic idiopathic
polyneuropathy, chronic inflammatory demyelinating
polyneuropathy, chronic relapsing
polyneuropathy, familial
post polio syndrome
postural abnormality
prenatal diagnosis by amniocentesis
prognosis
progressive neurologic disorder
proptosis
proximal muscle atrophy
pseudohypertrophy
pseudomyotonia
ptosis
pulmonary embolism
pupil, tonic
pyramidal tract
quadriplegia
radiculopathy
Refsum's disease
respiratory failure
retinitis pigmentosa
review article
rhabdomyolysis
rhabdomyosarcoma
rhabdomyosarcoma of orbit
rigidity
rippling muscle disease
risk factors
root lesion, nerve
sarcoglycan
sarcoglycanopathy
sarcoidosis
scalp tenderness
sciatic neuropathy
scoliosis
screening
seizure
sensorineural hearing loss
sensory loss
shoulder, elevation
sinuses, diseases of
sinusitis
skin, lesions in neurologic disorders
somnolence
spasticity
speech disorder, childhood
speech, delayed development of
spinal accessory nerve
spinal cord, compression of
spinal cord, neoplasm
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, intermediate form
spinal stenosis
spinal stenosis, familial
startle reaction
steppage gait
steroid
steroid therapy, CNS treatment and complications with
subarachnoid hemorrhage
subcutaneous nodules
sudden death
superior ophthalmic vein
survival motor neuron gene
symmetric brain lesions
syncope
syringomyelia
systemic illness
telangiectases, retinal
temporal artery
temporalis muscle enhancement
temporalis muscle hypertrophy
temporalis muscle swelling
thalamus, lesion of-bilateral
thirst
thyrotoxicosis
tinnitus
titinopathy
toe walking
tongue, enlarged
tongue, weakness
tonic spasms
tram-track sign
transient ischemic attack
trauma
treatment of neurologic disorder
tremor
trigeminal nerve
trigeminal nerve, abnormality of
trigeminal nerve, hypertrophy
trigeminal nerve, lesion of
trigeminal neuralgia
tripping
ultrasonography, nerve
urinary frequency
urine, dark
vasculitis, large vessel
vertebral artery wall thickness
vision, blurred
visual acuity, decreased
visual fields, constricted
visual loss
vital capacity
weakness
weakness, generalized
weakness, progressive
weakness, proximal
web sites
weightlifting
wheelchair
white matter disease
winging of scapula
workup
x-ray, spine
Showing articles 2100 to 2150 of 3218 << Previous Next >>

Left Ventricular Thrombosis and Stroke Following Myocardial Infarction
Editorial, Lancet 335:759-7601990., , 1990

The Effect of Warfarin on Mortality and Reinfarction after Myocardial Infarction
NEJM 323:148-152, Smith,P.,et al, 1990

Clinical Study of 227 Patients with Lacunar Infarcts
Stroke 21:842-847, Arboix,A.,et al, 1990

Acute Disseminated Encephalomyelitis, MRI Findings & the Distinction from Multiple Sclerosis
Brain 113:291-302, Kesselring,J.,et al, 1990

Botulinum Toxin Treatment of Cranial-Cervical Dystonia, Spasmodic Dystonia, Focal Dystonias & Hemifacial Spasm
JNNP 53:633-639, Jankovic,J.,et al, 1990

Assessment:The Clinical Usefulness of Botulinum Toxin-A in Treating Neurologic Disorders
Subcommittee Report, Neurol 40:1332-13361990., , 1990

Cortical-Basal Ganglionic Degeneration
Neurol 40:1203-1212, Riley,D.E.,et al, 1990

Neurological Findings in Alzheimer's Disease and Normal Aging
Arch Neurol 47:625-627, Glasko,D.,et al, 1990

Facial Myokymia in Syringobulbia
Arch Neurol 47:472-474, Riaz,G.,et al, 1990

Autoantibodies to Gaba-Ergic Neurons & Pancreatic Beta Cells in Stiff-Man Syndrome
NEJM 322:1555-1560, Solimena,M.,et al, 1990

Ganciclovir in the Treatment of Progressive AIDS-Related Polyradiculopathy
Neurol 40:569-574, Miller,R.G.,et al, 1990

Mitochondrial Myopathy Caused by Long-Term Ziduvudine Therapy
NEJM 322:1098-1105, Dalakas,M.C.,et al, 1990

The Spectrum of Neurologic Disease Associated with Anti-GM1 Antibodies
Neurol 40:1067-1072, Sadiq,S.A.,et al, 1990

Acceleration-Induced Loss of Consciousness, A Review of 500 Episodes
Arch Neurol 47:764-776, Whinnery,J.E.&Whinnery,A.M., 1990

Clinicopath Conf
Acute Febrile Neutrophilic Dermatosis (Sweet's Syndrome) , Case 30-1990, NEJM 323:254-2630., , 1990

Progressive Rubella Panencephalitis
In Handbk of Clin Neurol, Vinken & Bruyn, Ed, N Holland Publ Co, 56:405-416, Wolinsky,J.S., 1990

Electrodiagnostic Abnormalities in 113 Consecutive Patients with Guillain-Barre Syndrome
Arch Neurol 47:881-887, Ropper,A.H.,et al, 1990

Capsaicin for the Treatment of Pain in Guillain-Barre Syndrome
Ann Neurol 28:199, Morgenlander,J.C.,et al, 1990

Blood Pressure Fluctuations in the Dysautonomia of Guillain-Barre Syndrome
Arch Neurol 47:706-708, Ropper,A.H.&Wijdicks,E.F.M., 1990

The Role of Plasmapheresis in Childhood Guillain-Barre Syndrome
Ann Neurol 28:65-69, Epstein,M.A.&Sladky,J.T., 1990

Molecular Genetics of Duchenne and Becker Muscular Dystrophy
J Pediatr 117:1-15, Darras,B.T., 1990

Unusual Cause of'Piriformis Muscle Syndrome'
Arch Neurol 47:1144-1146, Papadopoulos,S.M.,et al, 1990

Mandibular Nerve:MR vs. CT about 10 Proved Unusual Tumors
Neuroradiology 32:492-496, Marsot-Dupuch,K.,et al, 1990

Physical Features of Prader-Willi Syndrome in Neonates
Am J Dis Child 144:1251-1254, Aughton,D.J.&Cassidy,S.B., 1990

The Marinesco-Sjogren Syndrome Examined by CT, MR, and 18F-2-Fluoro-2-Deoxy-D-Glucose & PET
Arch Neurol 47:1239-1242, Bromberg,M.B.,et al, 1990

Infantile CNS Spongy Degeneration-14 Cases:Clinical Update
Neurol 40:1876-1882, Gascon,G.G.,et al, 1990

Progressive Myoclonic Ataxia (The Ramsay Hunt Syndrome)
Arch Neurol 47:1121-1125, Marsden,C.D.,et al, 1990

Eosinophilia-Myalgia Syndrome (L-Tryptophan-Associated Neuromyopathy)
Neurol 40:1793-1796, Turi,G.K.,et al, 1990

Quadriceps Myopathy:Forme Fruste of Becker Muscular Dystrophy
Ann Neurol 28:634-639, Sunohara,N.,et al, 1990

Neurosarcoidosis:Signs, Course and Treatment in 35 Confirmed Cases
Medicine 69:261-276, Chapelon,C.,et al, 1990

Clinicopath Conf
Hodgkin's Disease and Guillain Barre Syndrome, Case Record 39-1990, NEJM 323:895-908990., , 1990

Myopathy with Human Immunodeficiency Virus Type I (HIV-1) Infection:HIV-1 or Zidovudine?
Ann Int Med 113:492-493, Till,M.&MacDonell,K., 1990

Human Immunodeficiency Virus Assoc Myopathy:Immunocytochemical Ident of an HIV Antigen (gp41) in Muscle Macrophages
Ann Neurol 28:579-582, Chad,D.A.,et al, 1990

Anti-GM1 IgM Antibodies in Motor Neuron Disease and Neuropathy
Neurol 40:1747-1750, Nobile-Orazio,E.,et al, 1990

Magnetic Resonance Imaging of Radiation Optic Neuropathy
Am J Ophthalmol 110:389-394, Zimmerman,C.F.,et al, 1990

L-Tryptophan-Induced Eosinophila-Myalgia Syndrome and Myopathy
Neurol 40:1629-1630, Sagman,D.L.&Melamed,J.C., 1990

New Muscle Power Test in Neuromuscular Disease
Am J Dis Child 144:1083-1087, Tirosh,E.,et al, 1990

Coincidence of Myoclonus and Multiple Sclerosis:Dramatic Response to Clonazepam
Neurol 40:1633-1634, Smith,C.R.&Scheinberg,L., 1990

Phenotypic Heterogeneity of Spinal Muscular Atrophy Mapping to Chromosome 5q11. 2-12. 3 (SMA5q)
Neurol 40:1831-1836, Munsat,T.L.,et al, 1990

What Causes Motoneuron Disease?
Editorial, Lancet 336:1033-10351990., , 1990

Misdiagnosis in Patients with Amyotrophic Lateral Sclerosis
Arch Int Med 150:2301-2305, Belsh,J.M.&Schiffman,P.L., 1990

Aggravation of Myasthenia Gravis by Erythromycin
Ann Neurol 28:577-579, May,E.F.&Calvert,P.C., 1990

Clinical Features and Associations of 560 Cases of Motor Neuron Disease
JNNP 53:1043-1045, Li,T.,et al, 1990

Selective Involvement of the Pyramidal Tract on Magnetic Resonance Imaging in Primary Lateral Sclerosis
Neurol 40:1799-1800, Marti-Fabregas,J.&Pujol,J., 1990

X-Linked Spinal Muscular Atrophy (Kennedy's Syndrome) A Kindred with Hypobetalipoproteinemia
Arch Neurol 47:1117-1120, Warner,C.L.,et al, 1990

Treatment of Spasticity with Botulinum Toxin:A Double-Blind Study
Ann Neurol 28:512-515, Snow,B.J.,et al, 1990

Graves Orbitopathy:Correlation of CT and Clinical Findings
Radiology 177:675-682, Nugent,R.A.,et al, 1990

Hunter Disease (Mucopolysaccharidosis Type II) in a Karyotypically Normal Girl
Clin genet 37:355-362, Clarke,J.T.,et al, 1990

Skeletal Muscle Pathology in AIDS:An Autopsy Study
Muscle & Nerve, 13:508-51590., Wrzolek,M.A.,et al, 1990

Hypoxic-Ischemic Damage of the Basal Ganglia
Mov Disord 5:219-224, Hawker, K. & Lang, A.E., 1990



Showing articles 2100 to 2150 of 3218 << Previous Next >>