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Differential
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abdominal distention
acanthocytosis
adrenoleukodystrophy
adverse drug reaction
alopecia
Alzheimer's disease
anisocoria
anosmia
antiretinal antibodies
aphasia
apraxia of eye movements
aqueduct of Sylvius, stenosis
aqueductal stenosis
areflexia
Argyll Robertson pupil
arrhythmia, cardiac
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxic gait
autoantibodies
Babinski sign
baclofen
basal ganglia
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
Bassen-Kornzweig syndrome
battered child syndrome
behavioral disorder
bladder dysfunction
blepharospasm
blindness
bradykinesia
brain atrophy
brain biopsy
brainstem, atrophy
brainstem, hypoplasia
bulbar palsy
cachexia
calcification, intracranial
calf hypertrophy
CAR syndrome
carcinoma
carcinoma of lung
cardiomyopathy
caries
carotid artery occlusion, neck
CAT scan
CAT scan, abnormal
CAT scan, false negative
cataracts
cataracts, congenital
central nervous system, infection of
cerebellar ataxia, children
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar hypoplasia
cerebellar lesion
cerebellar vermis
cerebral cortical atrophy
cerebral palsy
cerebro hepato renal syndrome
cerebrospinal fluid, elevated protein of
cerebrovascular accident
cerebrovascular accident, young adult
cherry red spot
cherry red spot-myoclonus syndrome
children
chorea
choreoathetosis
chorioretinitis
chromosomal abnormality
chromosome 17
chromosome 20
chronic progressive external ophthalmoplegia
cisterna magna, enlarged
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
Coats syndrome
Cockayne's syndrome
color vision
color vision, impaired
cone-rod dystrophy
congenital heart disease
congenital infection, CNS
conjunctival biopsy
consanguinity
contractures, joint
cornea, abnormal
cornea, opacity of
corpus callosum
corpus callosum, hypoplastic
cranial nerve palsies
craniopharyngioma
creatine phosphokinase(CPK)elevated
cry, weak
cryptorchidism
cyst
cyst, parenchymal
cyst, subcortical
cytochrome c oxidase
cytochrome c oxidase, deficiency
deafmute
deafness
deep gray nuclei
degenerative diseases of CNS
dementia
developmental abnormality of brain
developmental milestones, loss of
developmental retardation
diabetes insipidus
diabetes mellitus
diarrhea
differential diagnosis
diplegia, spastic cerebral
DNA probes
drug induced neurologic disorders
dwarfism
dysarthria
dysmetria
dysmorphic
dysphagia
dystonia
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electron microscopy
electronystagmography
electroretinograph
encephalocele
enzyme, defect
epidermal nevus syndrome
extraocular muscle lesion
eye injury
eye movement, disorders of
eyes, sunken
facial appearance, abnormal
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
falling
false negative
false negative VDRL
familial
fasciculation
fatty acid dehydrogenase deficiency
feeding disorder
fingerprint bodies
fluorescein angiography
fluorescent treponema antibody absorption(FTA-ABS)
foot deformity
fourth ventricle, enlargement of
Friedreich's ataxia
fundus, abnormality of
funduscopic exam
gait disorder
gargoylism
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gaze palsy
gaze palsy, supranuclear
gene
gene mutation
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
glare, light-induced
glaucoma
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
growth retardation
Hallervorden Spatz disease
Hallervorden Spatz disease, late onset
Hallgren's syndrome
hand flapping
headache
hearing loss
hearing loss, bilateral
hearing loss, congenital
hearing problems in children
heart block
hepatomegaly
heralding manifestation
Hurler's syndrome
hydrocephalus
hydrocephalus, congenital
hyperpigmentation of skin
hyperreflexia
hypocholesterolemia
hypogonadism
hypomagnesemia
hypoparathyroidism
hyposmia
hypotonia
imbalance
immunofluorescence
immunosuppressive agents
inborn errors of metabolism
inclusion bodies
inclusion bodies, intracytopasmic
incoordination
intellectual deficit
intellectual deterioration
internuclear ophthalmoplegia
intestinal pseudoobstruction
intrauterine infection, viral of CNS
iris, abnormal
iris, atrophy of
iron, brain
Joubert syndrome
Kearns-Sayre syndrome
keratoconus
kyphoscoliosis, neurologic causes of
kyphosis
lactic acidemia
Laurence-Moon-Bardet-Biedl syndrome
Leber's hereditary optic neuropathy
Leigh's disease
lens, dislocation of
lenticular nucleus, lesion of, bilateral
leukodystrophy
leukoencephalopathy
life expectancy
light-near dissociation, causes of
lissencephaly
lymphocyte fingerprint profiles
lysosomal storage disease
macular degeneration
malabsorption
malformation, CNS, congenital
malformation, vascular
malformation, vascular, cerebral
marche a petits pas
Marcus Gunn pupil
medial longitudinal fasciculus(MLF)
MELAS syndrome
memory, impairment of
mental retardation
MERRF syndrome
microcephaly
micropthalmia
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, eye of tiger sign
MRI, paramagnetic effect
MRI, serial
MRS
mucopolysaccharidoses
muscle atrophy, progressive
muscle biopsy
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, differential diagnosis of
muscular dystrophy, facioscapulohumeral
myelopathy
myoclonic jerks
myoclonus
myopathy
myopathy, mitochondrial
myopia
myotonia dystrophica
nausea and vomiting
neuraminidase deficiency
neuritis
neurocutaneous disease
neuroendocrinology
neurogenic vs.myopathic atrophy
neuroichthyosis
neurolipidosis IV
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic signs
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, ataxic
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, onion bulb
neuropathy, peripheral
neurosyphilis
nevus
night blindness
nystagmus
nystagmus, pendular
obesity
ocular myopathy
ophthalmoplegia
ophthalmoplegia, progressive external
optic atrophy
optic atrophy, hereditary
optic glioma
optic nerve
optic nerve, lesion of
optic nerve, neoplasm of
optic neuropathy
optic neuropathy, hereditary
optical coherence tomography
pain, abdominal
palilalia
pancytopenia
PANK2 mutation
paraparesis
paraparesis, spastic
Parkinson disease
Parkinsonism syndrome
PAS positive material in the brain
patent ductus arteriosus
peroxisomal disease
peroxisomes
pes cavus
photophobia
photosensitivity, eye
photosensitivity, skin
phytanic acid
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
polydactyly
polymyositis
polyneuropathy
Poretti-Boltshauser syndrome
postural abnormality
progeria
prognosis
progressive neurologic disorder
pseudohypertrophy
pseudoretinitis pigmentosa
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
ptosis
pupil
pupil, abnormality in neurologic disorders
pupil, light reflex, abnormal
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quadriplegia
ragged-red fibers
rash
refractive errors
Refsum's disease
remote effect of cancer on the nervous system
retina, abnormal
retinal arteriole attenuation
retinal degeneration
retinal detachment
retinal dysplasia
retinal lesion
retinitis pigmentosa
retinoblastoma
retinopathy
retropulsion
review article
RFLPs
rigidity
Romberg's sign
roving eye movements
rubella syndrome
schizophrenia
scotoma
scotoma, central
scotoma, paracentral-homonymous
sea-blue histiocytes
sedimentation rate, elevated
seizure
seizure, children
seizure, neonatal
sensorineural hearing loss
sensory loss
serologic test for syphilis
sheathing of retinal veins
short stature
Sjogren-Larsson syndrome
skin, biopsy
skin, lesions in neurologic disorders
skull x-ray, abnormal
spastic diplegia
spasticity
speech disorder
speech disorder, childhood
Spielmeyer Vogt syndrome
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 7
spinocerebellar degeneration
spongy degeneration of brain
steatorrhea
steroid
steroid therapy, CNS treatment and complications with
stooped posture
substantia nigra
sudden death
syphilis, diagnosis and treatment
syphilis, neurologic complications with
syphilis, ocular
systemic illness
tabes dorsalis
Tangier's disease
tapetoretinal degeneration
telangiectases
telangiectases, retinal
testicular atrophy
third nerve palsy
titubation
trauma
treatment of neurologic disorder
tremor
trinucleotide repeats
Usher's syndrome
uveitis
ventricular enlargement
viral infection, CNS
vision loss, sequential
vision, blurred
vision, failure of in childhood
visual acuity
visual acuity, decreased
visual acuity, decreased, monocular
visual evoked response
visual field defect
visual field defect, altitudinal
visual fields, constricted
visual impairment
visual loss
visual loss, progressive
visual loss, slow
visual loss, sudden
vitamin A
vitamin deficiency
vitamin E
vitamin E deficiency
vitamin K
vitritis
Walker-Warburg syndrome
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weaning from respirator, failure to
weight loss
white matter disease
wide based gait
Wolfram syndrome
workup
Showing articles 450 to 500 of 822 << Previous Next >>

Carotid Endarterectomy and Prevention of Cerebral Ischemia in Symptomatic Carotid Stenosis
JAMA 266:3289-3294, 33321991., Mayberg,M.R.,et al, 1991

Acute Cerebrovascular Episodes in Systemic Lupus Erythematosus
Quart J Med 293:739-750, Eustace,S.,et al, 1991

The Effect of Spine Fusion on Respiratory Function in Duchenne Muscular Dystrophy
Neurol 41:38-40, Miller,R.G.,et al, 1991

Myotonic Heart Disease:A Clinical Follow-Up
Neurol 41:259-262, Hawley,R.J.,et al, 1991

Response to Treatment with Antihistamines in a Family with Myotonia Congenita
Lancet 337:28-30, Hughes,E.F.&Wilson,J., 1991

Glucose-Induced Exertional Fatigue in Muscle Phosphofructokinase Deficiency
NEJM 324:364-369, 4111991., Haller,R.G.&Lewis,S.F., 1991

Prognosis and Prognostic Factors of Retinal Infarction:A Prospective Cohort Study
BMJ 302:499-504, Hankey,G.J.,et al, 1991

Cerebral Ischemic Events Associated with Endocarditis, Retinal Vascular Disease, & Lupus Anticoagulant
Am J Med 90:299-309, Pope,J.M.,et al, 1991

Clinicopath Conf
Pheochromocytoma of Adrenal Gland, Von Hippel-Lindau Disease, Case 16-1991, NEJM 324:1119-112791., , 1991

Recurrent Attacks of Amaurosis Fugax Treated with Calcium Channel Blocker
Ann Neurol 30:423-425, Winterkorn,J.M.S.&Teman,A.J., 1991

Transient Monocular Blindness Caused by Vasospasm
NEJM 325:870-873, Burger,S.K.,et al, 1991

MRC European Carotid Surgery Trial:Results for (70-99% ) or with Mild (0-29% ) Carotid Stenosis
European Carotid Surg Group, Lancet 337:1235-1243, 1255-1256991., , 1991

Microangiopathy of the Brain, Retina, and Ear:Improvement without Immunosuppressive Therapy
Stroke 22:933-937, Gordon,D.L.,et al, 1991

Prednisone in Duchenne Dystrophy, A Randomized, Controlled Trial Defining the Time Course & Dose Response
Arch Neurol 48:383-388, Griggs,R.C.,et al, 1991

Mononuclear Cell Analysis of Muscle Biopsies in Prednisone-Treated & Untreated Duchenne Muscular Dystrophy
Neurol 41:667-672, Kissel,J.T.,et al, 1991

A Comparison of Daily and Alternate-Day Prednisone Therapy in the Treatment of Duchenne Muscular Dystrophy
Arch Neurol 48:575-579, Fenichel,G.M.,et al, 1991

Prevalence and Incidence of Becker Muscular Dystrophy
Lancet 337:1022-1024, Bushby,K.M.D.,et al, 1991

The Frequency of Patients with Dystrophic Abnormalities in a Limb-Girdle Patient Population
Neurol 41:1491-1496, Arikawa,E.,et al, 1991

Autosomal Recessive Distal Dystrophy
Neurol 41:1365-1370, Barohn,R.J.,et al, 1991

Welander's Distal Myopathy:Clinical Neurophysiol & Muscle Biopsy Obser in Young & Middle Aged Adults with Early Symptoms
JNNP 54:494-498, Borg,K., 1991

Direct Diagnosis of Carriers of Duchenne & Becker Muscular Dystrophy by Amplification of Lymphocyte RNA
Roberts. R. G. , et al, Lancet 336:1523-1526., , 1990

Incidence of Impact Trauma with Cranial Injuries Ascribed to Shaking
Am J Dis Child 144:724-726, Alexander,R.,et al, 1990

Presymptomatic and Prenatal Diagnosis in Myotonic Dystrophy by Genetic Linkage Studies
Neurol 40:671-676, Speer,M.C.,et al, 1990

Location of Facioscapulohumeral Muscular Dystrophy Gene on Chromosome 4
Lancet 336:651-653, Wijmenga,C.,et al, 1990

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

Vision and Hearing During Deferoxamine Therapy
J Pediatr 117:326-330, Cohen,A.,et al, 1990

Night-Time Nasal Ventilation in Neuromuscular Disease
Lancet 335:579-582, Heckmatt,J.Z.,et al, 1990

Causalgia and Other Reflex Sympathetic Dystrophies
In the Management of Pain, Lea & Febiger, Phila, p. 220, Bonica,J.J., 1990

Perineal Reflex Sympathetic Dystrophy Treated with Bilateral Lumbar Sympathectomy
Ann Int Med 113:633-634, Olson,W.L., 1990

Echocardiographic Evaluation of Patients with Clinically Suspected Arterial Emboli
Lancet 336:1421-1424, Hofmann,T.,et al, 1990

Cerebral Malaria in Children
Lancet 336:1355-1360, Phillips,R.E.&Solomon,T., 1990

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

Dystrophin Analysis in Duchenne & Becker Muscular Dystrophy Carriers:Correl with Intracellular Calcium & Albumin
Ann Neurol 28:674-679, Morandi,L.,et al, 1990

Wyburn-Mason Syndrome
Neuroradiology 31:544-546, Patel,U.&Gupta,S.C., 1990

Spontaneous Visual Phenomena with Visual Loss:104 Patients with Lesions of Retinal and Neural Afferent Pathways
Neurol 40:444-447, Lepore,F.E., 1990

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

Clinicopath Conf
Malignant Angioendotheliomatosis, Am J Med 88:522-5281990., , 1990

Polyneuropathy, Ophthalmoplegia, Leukoencephalopathy, and Intestinal Pseudo-Obstruction:POLIP Syndrome
Ann Neurol 28:349-360, Simon,L.T.,et al, 1990

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

Migraine-Related Stroke in the Context of the International Headache Society Classification of Head Pain
Arch Neurol 47:458-462, Welch,K.M.A.&Levine,S.R., 1990

Attitudes of Mothers to Neonatal Screening for Duchenne Muscular Dystrophy
BMJ 300:1112, Smith,R.A.,et al, 1990

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

Transient Monocular Visual Loss Patterns and Associated Vascular Abnormalities
Stroke 21:34-39, Bruno,A.,et al, 1990

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

Clinicopath Conf
Familial Visceral Myopathy (Oculogastrointestinal Muscular Dystrophy) , Case 12-1990, NEJM 322:829-8, 1, 19, 1990

Neuromuscular Blockade
Lancet 335:382-384, , 1990

Adult Phosphorylase b Kinase Deficiency
Ann Neurol 28:529-538, Clemens,P.R.,et al, 1990

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

Nitroglycerin to Treat Acute Loss of Vision, Letter
NEJM 323:1428, Kuritzky,S., 1990

DNA Restriction Fragment Length Polymorphisms in Diff Dx of Genetic Disease:Appl in Neuromusc Dis
Hum Genet 82:55-58, Defesche,J.C.,et al, 1989



Showing articles 450 to 500 of 822 << Previous Next >>