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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 400 to 450 of 822 << Previous Next >>

The Management of Acute Visual Failure
JNNP 56:234-240, Wray,S.H., 1993

TORCH Infections in the Newborn
Semin Neurol 13:106-115, Donley,D.K., 1993

Signs and Symptoms of Reflex Sympathetic Dystrophy:Prospective Study of 829 Patients
Lancet 342:1012-1016, Veldman,P.H.J.M.,et al, 1993

Molecular Genetics in Neurology
Ann Neurol 34:757-773, Martin,J.B., 1993

The Polymerase Chain Reaction:Application to Nervous System Disease
Ann Neurol 34:513-523, Darnell,R.B., 1993

Cyclosporine Increases Muscular Force Generation in Duchenne Muscular Dystrophy
Neurol 43:527-532, Sharma,K.R.,et al, 1993

Direct Diagnosis of Myotonic Dystrophy with a Disease-Specific DNA Marker
NEJM 328:471-475, Shelbourne,P.,et al, 1993

Brief Report:Reverse Mutation in Myotonic Dystrophy
NEJM 328:476-480, Brunner,H.G.,et al, 1993

Genetics and Physiology of the Myotonic Muscle Disorders
NEJM 328:482-489, Ptacek,L.J.,et al, 1993

Abnormal Expression of Dystrophin-Associated Proteins in Fukuyama-Type Congenital Muscular Dystrophy
Lancet 341:521-522, Matsumura,K.,et al, 1993

Transient Monocular Blindness Associated with Cocaine Abuse
Neurol 43:228-229, Libman,R.B.,et al, 1993

Fatal Rabies Associated with Extensive Demyelination
Arch Neurol 50:317-323, Nelson,D.A.&Berry,R.G., 1993

Diag of Occult Muscular Dystrophy:"Chance"Finding of Elevated Serum Aminotransferase Act
J Pediatr 122:254-256, Morse,R.P.&Rosman,N.P., 1993

Experience with Screening Newborns for Duchenne Muscular Dystrophy in Wales
BMJ 306:357-360, 3491993., Bradley,D.M.,et al, 1993

Duchenne Dystrophy:Randomized, Controlled Trial of Prednisone (18 months) & Azathioprine (12 months)
Neurol 43:520-527, Griggs,R.C.,et al, 1993

Mosaic Express of Dystrophin in Carriers of Becker's Muscular Dyst & X-Linked Synd of Myalgia & Cramps
NEJM 327:1100, Minetti,C.&Bonilla,E., 1992

Upper Gastrointestinal Tract Motility in Children with Progressive Muscular Dystrophy
J Pediatr 121:720-724, Staiano,A.,et al, 1992

Skeletal Muscle Toxoplasmosis in Patients with Acquired Immunodeficiency Syndrome:A Clinicopath Study
Ann Neurol 32:535-542, Gherardi,R.,et al, 1992

Head Injury in Very Young Children:Mech, Injury & Ophthal Findings in 100 Hosp Pts
Pediatrics 90:179-185, Duhaime,A.C.,et al, 1992

Central Nervous System Lesions in von Hippel-Lindau Syndrome
JNNP 55:898-901, Neumann,H.P.H.,et al, 1992

Tamoxifen Retinopathy:A Rare But Serious Complication
BMJ 304:495-496, Bentley,C.R.,et al, 1992

Clinicopath Conf
Emery-Dreifus Muscular Dystrophy, NEJM 327:548-5571992., , 1992

Glycogen Storage Disease Type III (Glucogen Debranching Enzyme Def) :Biochem Defects & Myopathy & Cardiomyopathy
Ann Int Med 116:896-900, Coleman,R.A.,et al, 1992

Lethal Cytomegalovirus Infection in Preterm Infants:Clinical, Radiological, and Neuropathological Findings
Ann Neurol 31:64-68, Perlman,J.M.&Argyle,C., 1992

ELISA Quantitation of Dystrophin for the Diagnosis of Duchenne and Becker Muscular Dystrophies
Neurol 42:570-576, Byers,T.J.,et al, 1992

The Heart in Myotonic Dystrophy
Editorial, Lancet 339:528-5291992., , 1992

Small Infarctions of Cochlear, Retinal, and Encephalic Tissue in Young Women
Stroke 23:903-907, Schwitter,J.,et al, 1992

Dystrophinopathy in Isolated Cases of Myopathy in Females
Neurol 42:967-975, Hoffman,E.P.,et al, 1992

Detection of Duchenne and Becker MD Carriers by Quant Multiplex Polymerase Chain Reaction
Neurol 42:1783-1790, Ioannou,P.,et al, 1992

Diagnosis of Duchenne & Becker Muscular Dystrophies by Polymerase Chain Reaction
Multicenter Study Group, JAMA 267:2609-26151992., , 1992

Oculomotor, Auditory, and Vestib ular Responses in Myotonic Dystrophy
Arch Neurol 49:954-960, Verhagen,W.I.M.,et al, 1992

Unstable DNA Sequence in Myotonic Dystrophy
Lancet 339:1125-1128, Harley,H.G.,et al, 1992

Phenotypic Expression of the Myotonic Dystrophy Gene in Monozygotic Twins
Neurol 42:1815-1817, Dubel,J.R.,et al, 1992

Familial Adult-Onset Muscular Dystrophy with Leukoencephalopathy
Ann Neurol 32:577-580, vanEngelen,B.G.M.,et al, 1992

Idiopathic Intracranial Hypertension:Report of Seven Cases
Am J Med 93:391-395, Jain,N.&Rosner,F., 1992

The Ocular Manifestations of Multiple Sclerosis 1, Abnormalities of the Afferent Visual System
JNNP 55:747-752, McDonald,W.I.&Barnes,D., 1992

The Use of Magnetic Resonance Imaging in Diagnosing Infantile Neuroaxonal Dystrophy
Neurol 43:110-113, Tanabe,Y.,et al, 1992

Fasioscapulohumeral and Scapuloperoneal Syndromes
In Handbook Clin Neurol 62:161-177, Munsat,T.L.&Serratrice,G., 1992

Serial MRI in Fukuyama Type Congenital Muscular Dystrophy
Neuroradiol 34:396-398, Aihara,M.,et al, 1992

Ventricular Late Potentials in Myotonic Dystrophy
Ann Int Med 115:607-613, Milner,M.R.,et al, 1991

Hearing Loss in Facioscapulohumeral Muscular Dystrophy
Neurol 41:1878-1881, Brouwer,O.F.,et al, 1991

Stroke-Like Syndrome, Mineralizing Microangiopathy, and Neuroaxonal Dyst with Intrathecal Methotrexate
Neurol 41:1847-1848, Phanthumchinda,K.,et al, 1991

Polymyositis, Dermatomyositis, and Inclusion-Body Myositis
NEJM 325:1487-1498, Dalakas,M.C., 1991

Long-Term Benefit from Prednisone Therapy in Duchenne Muscular Dystrophy
Neurol 41:1874-1877, Fenichel,G.M.,et al, 1991

Preretinal Bleeding Due to Pontine Hemorrhage
Neurol 41:1694, Keane,J.R., 1991

Ocular Manifestations of AIDS
JAMA 266:3019-3022, deSmet,M.D.&Nussenbatt,R.B., 1991

A Randomized, Controlled Trial of Foscarnet in the Treatment of Cytomegalovirus Retinitis in Pts with AIDS
Ann Int Med 115:665-673, Palestine,A.G.,et al, 1991

Central Retinal Artery Occlusion in Giant Cell Arteritis:Treatment with Nitroclycerin
Neurol 41:1698-1699, Charnes,M.E.&Liu,G.T., 1991

Effect of High Dose Steroid Bolus on Occlusion of Ocular Central Artery:Angiographic Study
BMJ 303:1445-1446, Hausmann,N.&Richard,G., 1991

Clinical & Laboratory Findings in the Oculocerebrorenal Syndrome of Lowe, with Special Ref to Growth & Renal Function
NEJM 324:1318-1325, Charnas,L.R.,et al, 1991



Showing articles 400 to 450 of 822 << Previous Next >>