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Differential
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abdominal distention
abducens nerve paralysis, bilateral
abiotrophy
acanthocytosis
advances in neurology
agammaglobulinemia
akinesia of eyelid function
ANA
apraxia of eyelid opening
aqueduct of Sylvius, stenosis
aqueductal stenosis
areflexia
arrhythmia, cardiac
asymptomatic
ataxia
ataxia, cerebellar
ataxia, progressive
atrial fibrillation
audiogram
auditory evoked brainstem potentials
basal ganglia, calcification of
Bassen-Kornzweig syndrome
blepharospasm
blindness
botulism
brainstem, lesion of
brainstem, tuberculoma of
cachexia
calcification, intracranial
carcinoma
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, false negative
cataracts
cataracts, congenital
cause of death
celiac disease, childhood
central core disease
cerebellar ataxia, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar hypoplasia
cerebral cortical atrophy
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, young adult
Charcot's sign
chemosis
children
chromosomal abnormality
chromosome 14
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
Cockayne's syndrome
cogwheel rigidty
collagen vascular disease
coma
congenital myopathy
conjunctival injection
consanguinity
contractures, joint
cornea, abnormal
cornea, opacity of
corneal dystrophy
cranial neuropathy, multiple
creatine phosphokinase isoenzyme elevation
creatine phosphokinase MB isoenzyme elevation
creatine phosphokinase(CPK)elevated
cricopharyngeal bar
cytochrome c oxidase
cytochrome c oxidase, deficiency
deafmute
deafness
dementia
dermatomyositis
diabetes mellitus
diarrhea
digitalis intoxication
diplopia
distal muscle weakness
dwarfism
dysarthria
dysphagia
dyspraxia
dysthyroid ocularmyopathy
dystonia
dystrophin
edema, periorbital
electroencephalogram, abnormalities of
electromyogram
electronystagmography
electronystagmography, abnormal
electroretinograph
encephalocele
encephalopathy
encephalopathy, progressive
enzyme, muscle disease
epidemiology of neurology
evoked potentials
exercise intolerance
extraocular muscle atrophy
extraocular muscle enlargement
extraocular muscle lesion
extrapyramidal movement disorder, progressive
eye closure
eye movement, disorders of
eye, pain in
face, numbness of
facial nerve palsy
facial nerve palsy, bilateral
facial nerve, lesion of
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
familial
fasciculation
fatigue
fever
fibrillations
Fisher C.M.
fistula, arterio-venous, carotid-cavernous
Friedreich's ataxia
gait disorder
gargoylism
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gaze palsy
gaze palsy, horizontal
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
glabellar sign
glaucoma
Graves ophthalmopathy
Hallgren's syndrome
headache
hearing loss
heart block
heart murmur
hemianopia, homonymous
hepatic failure
hepatomegaly
heralding manifestation
hippus
Hispanics
histochemistry of muscle
Hurler's syndrome
hydrocephalus
hydrocephalus, congenital
hyperthyroidism
hypoglycorrhachia
hypogonadism
hypotonia
imbalance
immunohistochemistry
immunologic disease
immunosuppressive agents
inclusion bodies, intracytopasmic
inclusion bodies, intranuclear
intestinal pseudoobstruction
jaw jerk, abnormal
joint hypermobility
Kearns-Sayre syndrome
keratoconus
lactic acidemia
Laurence-Moon-Bardet-Biedl syndrome
L-dopa
Leber's hereditary optic neuropathy
Leigh's disease
leukodystrophy
leukoencephalopathy
lid closure, weakness of
lissencephaly
malformation, CNS, congenital
masked facies
medial rectus palsy
medulla oblongata, lesion of
MELAS syndrome
Melkersson's syndrome
meningitis
meningitis, TB
mental retardation
MERRF syndrome
methotrexate
micropthalmia
migraine
misdiagnosis
mitochondrial disease
mitochondrial disease, pathogenesis
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
mortality
movement disorder
MRI
MRI, abnormal
mucopolysaccharidoses
muscle atrophy, progressive
muscle biopsy
muscle biopsy, extraocular
muscle pain
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, central nervous system abnormality
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, congenital, Fukuyama type
muscular dystrophy, congenital, Ullrich
muscular dystrophy, differential diagnosis of
muscular dystrophy, Duchenne
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, differential diagnosis
myasthenia gravis, distal weakness
myasthenia gravis, limb-girdle
myasthenia gravis, misdiagnosis of
myasthenia gravis, ocular
myasthenia gravis, seronegative
myasthenic syndrome
myelopathy
myoclonus
myopathy
myopathy, centronuclear
myopathy, distal
myopathy, mitochondrial
myopathy, steroid induced
myopia
myositis
myositis, ocular
myotonia dystrophica
nausea and vomiting
neck weakness
negative
nemaline rod myopathy
neuritis
neuroendocrinology
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic signs
neurologic symptoms
neuromuscular blockade
neuromuscular junction, abnormality of
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, peripheral
normal
nystagmus
nystagmus, vertical
obesity
obicularis oculi, weakness of
occipital lobe, lesion of
ocular motility, disorders of
ocular myopathy
ocular myopathy, differential diagnosis
oculopharyngeal muscular dystrophy
oculovestibular reflex
one and a half syndrome
ophthalmoplegia
ophthalmoplegia, painful
ophthalmoplegia, plus syndrome
ophthalmoplegia, progressive external
optic atrophy
optic disc edema
optic neuritis
optic neuropathy
orbicularis oculi muscle
orbit
orbit, lesions of
pain, abdominal
pancytopenia
paraparesis
paraparesis, spastic
Parkinsonism syndrome
photophobia
photophobia, central
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
POLG1 gene
polydactyly
polymerase chain reaction
polymyositis
polyneuropathy
pons, lesion of
prognosis
progressive infantile poliodystrophy
progressive neurologic disorder
progressive supranuclear palsy
proptosis
proptosis, bilateral
proptosis, unilateral
prostigmine
pseudobulbar palsy
pseudomyasthenia
pseudoretinitis pigmentosa
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
ptosis
ptosis, bilateral
ptosis, familial
pulmonary infiltrates
pupil, abnormality in neurologic disorders
pupil, dilated and fixed, bilateral
pupil, dilated and fixed, unilateral
ragged-red fibers
rash
Raynaud's phenomenon
retina, abnormal
retinal degeneration
retinal detachment
retinal dysplasia
retinal lesion
retinitis pigmentosa
retinopathy
retropulsion
review article
rigidity
saccadic eye movements
saccadic eye movements, abnormal
schizophrenia
scintillations
scleroderma
scleroderma, neurologic involvement with
screening
sedimentation rate
seizure
sensorineural hearing loss
seronegative
short stature
skin, tight
Southern immunoblot test
spasticity
Spielmeyer Vogt syndrome
standing difficulty
Stephens syndrome
steroid therapy, CNS treatment and complications with
strokelike episodes
symmetric brain lesions
systemic illness
tongue, fasciculations of
treatment of neurologic disorder
trinucleotide repeats
tuberculoma of CNS
tuberculosis
tuberculosis, miliary
upgaze, paralysis of
Usher's syndrome
visceral neuropathy
visual field defect
visual fields, constricted
visual loss
Walker-Warburg syndrome
weakness
weakness, fatiguable
weakness, generalized
weakness, progressive
weakness, proximal
weaning from respirator, failure to
web sites
weight loss
wheelchair
white matter disease
wide based gait
xanthopsia
Showing articles 1150 to 1200 of 1786 << Previous Next >>

Incomplete Unilateral Ophthalmoplegia as the Presenting Manifestation of Waldenstrom's Macroglobulinemia
Neurol 40:1801-1802, Lossos,A.,et al, 1990

Causalgia and Other Reflex Sympathetic Dystrophies
In the Management of Pain, Lea & Febiger, Phila, p. 220, Bonica,J.J., 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

Mapping of Acute (Type 1) Spinal Muscular Atrophy to Chromosome 5q12-q14
Lancet 336:271-273, Melki,J.,et al, 1990

Spinal Muscular Atrophies
Editorial, Lancet 336:280-2811990., , 1990

Polyclonal IgM Anti-GM1 Ganglioside Antibody in Patients with Motor Neuron Disease and Variants
Ann Neurol 27:558-563, Salazar-Grueso,E.F.,et al, 1990

Immunologic Reactivity Against Borrelia Burgdorfi in Patients with Motor Neuron Disease
Arch Neurol 47:586-594, Halperin,J.J.,et al, 1990

2-Amino-3- (methylamino) -Propanoic Acid (BMAA) in Cycad Flour:An Unlikely Cause of ALS & Parkinsonism-Dementia of Guam
Neurol 40:767-772, Duncan,M.W.,et al, 1990

Anderson-Fabry Disease
Editorial, Lancet 336:24-251990., , 1990

Neurologic Sequelae of Domoic Acid Intoxication Due to the Ingestion of Contaminated Mussels
NEJM 322:1781-1787, Teitelbaum,J.S.,et al, 1990

Paralytic Shellfish Poisoning:A Case Report and Serial Electrophysiologic Observations
Neurol 40:1310-1312, Long,R.R.,et al, 1990

A Clinical Triad to Diagnose Paraneoplastic Retinopathy
Ann Neurol 28:162-167, Jacobson,D.M.,et al, 1990

Diabetic 3rd Nerve Palsy:Evidence for a Mesencephalic Lesion
Neurol 40:1041-1045, Hopf,H.C.&Gutmann,L., 1990

Non-Invasive Radiological Investigation for Oculomotor Palsy
JNNP 53:549-553, Teasdale,E.,et al, 1990

Isolated Pupil-Sparing Third-Nerve Palsy as the Presenting Sign of Multiple Sclerosis
Arch Neurol 47:817-818, Newman,N.J.&Lessell,S., 1990

Vertical Ocular Motor Apraxia
Neurol 40:712-713, Ebner,R.,et al, 1990

The Characteristics and Mechanisms of Visual Disturbance Associated with Anticonvulsant Therapy
Neurol 40:791-796, Remler,B.F.,et al, 1990

A Familial Syndrome of Dystonia, Blepharospasm, and Pigmentary Retinopathy
Neurol 40:1359-1363, Coppeto,J.R.&Lessel,S., 1990

Ipsiversive Eye Deviation and Epileptic Nystagmus
Neurol 40:662-665, Tusa,R.J.,et al, 1990

Hemiplegia in Posterior Cerebral Artery Occlusion
Neurol 40:1496-1499, Hommel,M.,et al, 1990

How Frequently Does Classic Amyotrophic Lateral Sclerosis Develop in Survivors of Poliomyelitis
Neurol 40:172-174, Armon,C.,et al, 1990

Amyotrophic Lateral Sclerosis:A Case-Control Study Following Detection of a Cluster in a Small Wisconsin Community
Arch Neurol 47:38-41, Sienko,D.G.,et al, 1990

Oculo-Facial-Skeletal Myorhythmia in Whipple Disease:Treatment with Ceftriazone
Ann Int Med 112:467-469, Adler,C.H.&Galetta,S.L., 1990

Perineural Spread of Cutaneous Head and Neck Cancer
Arch Neurol 47:73-77, Clouston,P.D.,et al, 1990

Isolated Inferior Oblique Paresis from Brainstem Infarction
Arch Neurol 47:235-237, Castro,O.,et al, 1990

Permanent Cerebral Diplopia in a Migraineur
Neurol 40:1138-1139, Sinoff,S.E.&Rosenberg,M., 1990

Miller Fisher Syndrome Associated with Q Fever
JNNP 53:615-616, Diaz Ortuno,A.,et al, 1990

Extrapyramidal Involvement in Rett's Syndrome
Neurol 40:293-295, FitzGerald,P.M.,et al, 1990

MR Imaging of Tolosa-Hunt Syndrome
AJR 154:167-170, Yousem,D.M.,et al, 1990

Use of Immunosuppressive Agents in the Treatment of Severe Ocular and Vascular Manifestations of Cogan's Syndrome
Am J Med 88:296-301, Allen,N.B.,et al, 1990

Abnormality in the Cavernous Sinus in Three Patients with Tolosa-Hunt Syndrome:MRI and CT Findings
JNNP 53:231-234, Goto,Y.,et al, 1990

Orbital Pseudotumor Secondary to Giant Cell Arteritis:An Unreported Condition
BMJ 300:784, Laidlaw,D.A.H.,et al, 1990

Abnormalities of Horizontal Gaze, Clinical, Oculographic and Magnetic Resonance Imaging Findings, II Gaze Palsy and INO
JNNP 53:200-207, Bronstein,A.M.,et al, 1990

Warning Leak in Subarachnoid Haemorrhage
BMJ 301:190-191, Ostergaard,J.R., 1990

Neurologic Manifestations of Giant Cell Arteritis
Am J Med 89:67-72, Reich,K.A.,et al, 1990

Putaminal Hemorrhage:Clinical-Computed Tomographic Correlations
Neuroradiology 32:200-206, Weisberg,L.A.,et al, 1990

Apoplectic Headache and Oculomotor Nerve Palsy:An Unusual Presentation of Multiple Sclerosis
Neurol 40:1465-1466, Galer,B.S.,et al, 1990

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

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

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

The Movement Disorder of Reflex Sympathetic Dystrophy
Neurol 40:57-61, Schwartzman,R.J.&Kerrigan,J., 1990

Clinical Uses of Intravenous Immunoglobulins
Ann Int Med 112:278-292, Berkman,S.A.,et al, 1990

Unilateral Cavernous Angioma of the Thalamus Disclosed by Transitional Disorders in the Upward Gaze
Minerva Medica 81:731-733, Lazzarino,L.G.,et al, 1990

Cat-Scratch Disease Presenting as the Oculoglandular Syndrome of Parinaud:Two Cases
Postgrad Med J 66:467-468, Jawad,A.S.M.&Amen,A.A.A., 1990

Ptosis as the Sole Manifestation of Compression of the Oculomotor Nerve by an Aneurysm of the Posterior Communicating Artery
J Clin Neuroophthalmol 10:59-61, Good,E.F., 1990

Ocular and Periocular Pain
Otolaryn Clin North Am 22:1173-1203, Rosenblatt,M.A.&Sakol,P.J., 1989

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

Multifocal Fibrosclerosis with Hypertrophic Intracranial Pachymeningitis
Neurol 39:1345-1349, Berger,J.R.,et al, 1989



Showing articles 1150 to 1200 of 1786 << Previous Next >>