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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 1200 to 1250 of 1786 << Previous Next >>

CT Characteristics of Orbital Pseudotumors and Other Orbital Inflammatory Processes
J Comput Assist Tomogr 13:40-47, Flanders,A.E.,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

Neurosyphilis Presenting with Raeder's Syndrome
Ann Neurol 25:418, Watanabe,K.,et al, 1989

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

Opsoclonus in Organophosphate Poisoning
Arch Neurol 46:704-705, Pullicino,P.&Aquilina,J., 1989

Bilateral Loss of Vision in Bright Light
Stroke 20:554-558, Weibers,D.O.,et al, 1989

Oculomotor Palsy with Cyclic Spasms
Neurol 39:1263-1264, Friedman,D.I.,et al, 1989

Neurologic Eye Signs Following Motorcycle Accidents
Arch Neurol 46:761-762, Keane,J.R., 1989

Neuroaxonal Dystrophy Due to Lysosomal a-N-Acetylgalactosaminidase Deficiency
NEJM 320:1735-1740, Schindler,D.,et al, 1989

Painful Horner Syndrome Associated with Occlusion of the Extracranial Internal Carotid Artery:MR Imaging
J Comput Assist Tomogr 13:918-920, Stern,M.J.,et al, 1989

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

Predictive Value of Carotid Bruit for Carotid Atherosclerosis
Arch Neurol 46:418-422, Ingall,T.J.,et al, 1989

Caze Distractibility in Wilson's Disease
Ann Neurol 25:415-417, Lennox,G.&Jones,R., 1989

Vestibular Testing in Comatose Patients
Arch Neurol 46:561-563, Buettner,U.W.&Zee,D.S., 1989

Aseptic Meningitis Complicating Adult Kawasaki Disease:Case Report and Review of the Literature
Am J Med 87:106-110, McIlroy,M.A.,et al, 1989

Ocular Pseudomyasthenia or Ocular Myasthenia'Plus':A Warning to Clinicians
Neurol 39:1150-1154, Moorthy,G.,et al, 1989

Non-Migranous Headaches, Classification and Management
BMJ 299:70-72, Clouch,C., 1989

Amaurosis Fugax and Ocular Infarction in Adolescents and Young Adults
Ann Neurol 26:69-77, Tippin,J.,et al, 1989

Neurosyphilis in Acquired Immunodeficiency Syndrome
Arch Neurol 46:895-898, Katz,D.A.&Berger,J.R., 1989

Lyme Disease
NEJM 321:586-596, Steere,A.C., 1989

Transient Ocular Motor Paresis Associated with Acute Internal Carotid Artery Occlusion
Ann Neurol 25:286-290, Wilson,W.B.,et al, 1989

Phenobarbital Rheumatism in Patients with Brain Tumor
Ann Neurol 25:92-94, Taylor,L.P.&Posner,J.B., 1989

Tardive Oculogyric Crises
Neurol 39:1434-1437, FitzGerald,P.M.&Jankovic,J., 1989

Painful Oculomotor Nerve Palsy Due to Dural-Cavernous Sinus Shunt
Arch Neurol 46:1252-1255, Hawke,S.H.,et al, 1989

Vertical and Horizontal Epileptic Gaze Deviation and Nystagmus
Neurol 39:1391-1393, Kaplan,P.W.&Lesser,R.P., 1989

Chiasmal Apoplexy:Haemorrhage from a Cavernous Malformation in the Optic Chiasm
JNNP 52:1095-1099, Regli,L.,et al, 1989

Clinicopathological Correlation in a Case of Painful Ophthalmoplegia:Tolosa-Hunt Syndrome
JNNP 52:1290-1293, Goadsby,P.J.&Lance,J.W., 1989

Divisional Oculomotor Nerve Paresis Caused by Intrinsic Brainstem Disease
Ann Neurol 26:714-718, Ksiazek,S.M.,et al, 1989

Pseudo One-and-a-half Syndrome with Ocular Myasthenia
Neurol 39:1553, Davis,T.L.&Lavin,P.J.M., 1989

Cancer-Associated Retinopathy (Car Syndrome) with Antibodies Reacting with Retinal, Optic-Nerve, and Cancer Cells
NEJM 321:1589-1594, 1607-16081989., Thirkill,C.E.,et al, 1989

Brain Stem Type Neuro-Behcet's Syndrome
Neuroradiology 31:258-262, Kataoka,S.,et al, 1989

Clinicopath Conf
Dengue Fever, Case 40-1989, NEJM 321:957-965989., , 1989

Mitochondrial Myopathies:Clinical & Biochem Features of 30 Patients with Major Deletions of Muscle Mitochondrial DNA
Ann Neurol 26:699-708, Hold,I.J.,et al, 1989

Myasthenia Gravis
In Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8th Ed, 697, Penn,A.S.&Rowland,L.P., 1989

Internuclear Ophthalmoplegia in Tuberculous Meningitis
Tubercle 70:61-64, Teoh,R.,et al, 1989

Oculogyric Crisis after Metoclopramide Therapy
Optometry and Vision Science 66:179-180, Edward,M.,et al, 1989

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

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

Computed Tomographic Features of Nonthyroid Extraocular Muscle Enlargement
Ophthalmol 96:1038-1047, Patrinely,J.R.,et al, 1989

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

Serum Antibodies to GM1 Ganglioside in Amytrophic Lateral Sclerosis
Neurol 38:1457-1461, Pestronk,A.,et al, 1988

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

The Peroxisome:Nervous System Role of a Previously Underrated Organelle, The 1987 Robert Wartenberg Lecture
Neurol 38:1617-1627, Moser,H.W., 1988

Anderson-Fabray Disease, A Commonly Missed Diagnosis
BMJ 297:872-873, Morgan,S.H.&Crawfurd,M., 1988

Pituitary Apoplexy
BMJ 297:1526-1527, Lewin,I.G.,et al, 1988

Nontraumatic Frontal Lobe Hemorrhages:Clinical-computed Tomographic Correlations
Neuroradiology 30:500-505, Weisberg,L.A.&Stazio,A., 1988

Dystonia and Tremor Induced by Peripheral Trauma:Predisposing Factors
JNNP 51:1512-1519, Jankovic,J.&VanDer Linden,C., 1988

Reflex Sympathetic Dystrophy in Children:Treatment with Transcutaneous Electric Nerve Stimulation
Pediatrics 82:728-732, Kesler,R.W.,et al, 1988



Showing articles 1200 to 1250 of 1786 << Previous Next >>