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abducens nerve paralysis
abiotrophy
aciduria
adolescent medicine
adrenoleukodystrophy
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
advances in neurology
adverse drug reaction
alcohol intolerance
alopecia
alternating hemiplegia
alternating hemiplegia of childhood
alternating rapid movement
ammonia
amyloid
amyloid angiopathy, cerebral
amyloidosis
amyloidosis, oculoleptomeningeal, familial
anemia
anosmia
anti MAG antibodies
apnea
apnea, primary central
apraxia
areflexia
arrhythmia, cardiac
arteritis, temporal
arthralgia
arylsulfatase A
arylsulfatase B
aspartocyclase
asymptomatic
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, truncal
ataxic gait
ATP1A3 gene
auditory evoked brainstem potentials
Babinski sign
basal ganglia
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
Bassen-Kornzweig syndrome
battered child syndrome
behavioral disorder
Behr's optic atrophy
biotin deficiency
biotinidase deficiency
bitemporal visual field defect
blindness
blindness, sudden
bone density
bone density, increased
bone marrow transplantation
brain biopsy
brainstem
brainstem, atrophy
brainstem, lesion of
bulbar palsy
bulbar palsy, childhood
bulbar palsy, progressive
cachexia
CAG repeats
calcification, intracranial
Canavan's disease
cardiomyopathy
caries
CAT scan
CAT scan, abnormal
CAT scan, false negative
cataracts
cerebellar ataxia, children
cerebellar atrophy, primary
cerebral cortical atrophy
cerebral edema
cerebral edema, vasogenic
cerebritis
cerebro hepato renal syndrome
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, protein of
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, young adult
Charcot-Marie-Tooth
cherry red spot
children
choking
chorea
choreoathetosis
chromosomal abnormality
chromosome 19
chronic progressive external ophthalmoplegia
cisternogram, radionuclide
Clinical Pathologic Conference(C.P.C.)
clonus
clubbing of fingers
clubfoot as related to neurologic disease
Cockayne's syndrome
coenzyme Q10 deficiency
color vision
color vision, impaired
coma
compression neuropathy
cone-rod dystrophy
confusion
conjunctivitis
consanguinity
contractures, joint
cornea, abnormal
cornea, opacity of
corpus callosum
corpus callosum, hypoplastic
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
craniopharyngioma
cry, weak
crying
cryopyrin-associated periodic syndrome
cryptorchidism
cultured skin fibroblasts
deafness
degenerative diseases of CNS
dementia
dementia, childhood
dementia, thalamic
demyelinating disease
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes insipidus
diabetes mellitus
diabetes mellitus, neurologic manifestations of
diabetes mellitus, ocular complications in
diabetic cranialneuropathies
diagnostic criteria
diplegia, brachial
diplopia
dissociated sensory loss
DNA probes
drug induced neurologic disorders
dwarfism
dysarthria
dyschromatopsia
dysmetria
dysmorphic
dysphagia
dyspraxia
dystonia
ear, abnormal
electroencephalogram, abnormalities of
electromyogram
electron microscopy
electronystagmography
electroretinograph
emergencies, ocular
empty sella
encephalopathy
encephalopathy, neonatal
encephalopathy, progressive
enophthalmous
entrapment neuropathy
enzyme, defect
episodic disorders
equinovarus
evoked potentials
exome sequencing
eye injury
eye movement, disorders of
eye, pain in
eyes, sunken
facial appearance, abnormal
facial nerve palsy
facial nerve palsy, bilateral
failure to thrive
falling
false negative
familial
fatigue
feeding disorder
fever
fever, recurrent
finger nose finger test
flaccid paralysis
flow study, carotid artery
fluorescein angiography
Friedreich's ataxia
frontal bossing
frontal lobe, pathologic signs of
fundus, abnormality of
funduscopic exam
gait disorder
gait, spastic
galactocerebrosidase
gangliosidosis GM2
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
globoid cells
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
granulomatosis with polyangiitis
growth retardation
Hallervorden Spatz disease
handwriting
head circumference
head lag
headache
hearing loss
hearing problems in children
heart block
heel-knee-shin test
hemiparesis
hemiplegia
hemophagocytic lymphohistiocytosis, cerebromeningeal
hemophagocytosis
hepatomegaly
hepatosplenomegaly
hexosaminidase-A
hiccoughs
hirsutism
HLA
Horner's syndrome
hydrocephalus
hydrocephalus, normal pressure
hydrocephalus, normal pressure in children
hydrocephalus, viral induced
hyperostosis
hyperostosis corticalis generalisata familiaris
hyperreflexia
hypertriglyceridemia
hypertrophic intracranial pachymeningitis
hypofibrinogenemia
hypogonadism
hypomyelination
hypotonia
hypotonia, infants
imbalance
immunofluorescence
immunologic disease
impulsivity
inborn errors of metabolism
inclusion bodies
infantile bilateral striatal necrosis
intellectual deficit
intellectual deterioration
intestinal pseudoobstruction
intracerebral hemorrhage
intracerebral hemorrhage, familial
intracranial hypertension, benign
intracranial pressure, increased
intrauterine
iritis
iron, brain
irritability
Jewish
Kearns-Sayre syndrome
Krabbe's disease
kyphoscoliosis, neurologic causes of
kyphosis
lactic acidemia
Laurence-Moon-Bardet-Biedl syndrome
Leber's hereditary optic neuropathy
Leigh's disease
Leigh's disease, adult variety
lenticular nucleus, lesion of, bilateral
leukocyte enzyme abnormality
leukocytosis
leukodystrophy
light-near dissociation, causes of
lymphadenopathy
lysosomal storage disease
lysosomes, abnoral
macrocephaly
macular degeneration
Marcus Gunn pupil
MELAS syndrome
memory, impairment of
meningioma
meningismus
meningitis, aseptic
meningitis, carcinomatous
meningitis, chronic
mental retardation
MERRF syndrome
metabolic acidosis
metabolic disorder, primary
metachromatic leukodystrophy
metachromatic leukodystrophy, juvenile
methylmalonic aciduria
microcephaly
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
mononeuropathy multiplex
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
movement disorder, hyperkinetic
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, optic nerve
MRI, spinal cord
mucopolysaccharidoses
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, familial
muscle atrophy, progressive
muscle biopsy
muscle weakness
muscle weakness, proximal
myasthenia gravis, differential diagnosis
myasthenia gravis, misdiagnosis of
myelitis
myelitis, longitudinal
myelitis, transverse
myelomalacia
myelopathy
myoclonic jerks
myoclonus
myoclonus, epilepsy
myopathy
myopathy, mitochondrial
myopia
nausea and vomiting
negative
nerve biopsy
nerve conduction studies
neuroaxonal dystrophy
neuroendocrinology
neurolipidosis IV
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination
neurologic signs
neuromyelitis optica (Devic's disease)
neuromyelitis optica spectrum disorder
neuromyelitis optica, IgG
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, ataxia, retinitis pigmentosa
neuropathy, demyelinating
neuropathy, hereditary peripheral
neuropathy, peripheral
neuropathy, vasculitic, systemic
neutropenia
night blindness
normal
nutritional deficiency
nystagmus
nystagmus, monocular
nystagmus, rotary
nystagmus, upbeating-in primary position of gaze
nystagmus, vertical
obesity
ophthalmoplegia
ophthalmoplegia, progressive external
opisthotonus
optic ataxia
optic atrophy
optic atrophy, bilateral
optic atrophy, hereditary
optic chiasm
optic chiasm, enlarged
optic chiasm, lesion of
optic disc cup
optic disc edema
optic foramina
optic foramina, abnormal
optic glioma
optic nerve
optic nerve, compression of
optic nerve, enhancement
optic nerve, enlarged
optic nerve, lesion of
optic nerve, neoplasm of
optic neuritis
optic neuritis, bilateral
optic neuritis, treatment of
optic neuropathy
optic neuropathy, bilateral
optic neuropathy, hereditary
optic neuropathy, ischemic
optic neuropathy, nutritional
optic neuropathy, toxic
optic tract, lesion of
optical coherence tomography
osteopetrosis
owl's eye sign of spinal cord
palatal myoclonus
pancytopenia
papilledema
paraparesis
paraparesis, familial spastic
paraparesis, spastic
paraplegia
Parkinson disease
Parkinson disease, dystonia with
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
PAS positive material in the brain
Pelizaeus Merzbacher
peroxisomal disease
personality change
pes cavus
photosensitivity, skin
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
polyneuropathy
polyneuropathy, familial
posterior leukoencephalopathy syndrome
precipitating factors
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
pretectal syndrome
prisoners of war, neurologic complications in
prognathism
prognosis
progressive neurologic disorder
propionic aciduria
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychological testing, neurologic problems
psychomotor retardation
psychosis
ptosis
pupil, abnormality in neurologic disorders
pupil, light reflex, abnormal
Purkinje cell
pyramidal tract
pyramidal tract dysfunction
pyruvate metabolism, abnormality of
quadriparesis
quadriplegia
ragged-red fibers
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
rash
recurrent
red eye
red free light
red free light, fundus exam with
refractive errors
Refsum's disease
release phenomena
renal failure
respiratory failure
retina, abnormal
retinal degeneration
retinal detachment
retinal ischemia
retinal lesion
retinal nerve fiber layer
retinal vasculitis
retinal vasculopathy
retinal vasculopathy with cerebral leukodystrophy
retinitis pigmentosa
retinoblastoma
retinopathy
review article
RFLPs
rigidity
Romberg's sign
sclerosteosis
scoliosis
scotoma
scotoma, central
screening
sea-blue histiocytes
sedimentation rate, elevated
seizure
seizure, children
seizure, neonatal
sensorineural hearing loss
sensory loss
short stature
skin, biopsy
skin, lesions in neurologic disorders
skull bone, thickening
skull x-ray, abnormal
spastic diplegia
spasticity
speech disorder
speech disorder, childhood
speech, loss of
spinal cord
spinal cord, compression of
spinal cord, lesion of
spinal cord, pathologic exam of
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 7
spinocerebellar degeneration
spinopontine atrophy, dominant
splenomegaly
spongy degeneration of brain
startle myoclonus
startle reaction
status epilepticus
stem cell transplantation
steroid therapy, CNS treatment and complications with
stooped posture
striatonigral degeneration
striatonigral degeneration, infantile
striatum, lesion of
striatum, lesion of, bilateral
strokelike episodes
subarachnoid hemorrhage
subcortical U fibers
substantia nigra
sudden death
sural nerve
symmetric brain lesions
syndactyly
systemic illness
Tangier's disease
tapetoretinal degeneration
Tay-Sachs disease
thalamus, lesion of
thrombocytopenia
titubation
tongue, enlarged
tonic spasms
trauma
treatment of neurologic disorder
tremor
tremor, intention
trigeminal nerve, lesion of
trigeminal neuropathy
trinucleotide repeats
umbilical-cord blood transplantation
upgaze, paralysis of
urea-cycle enzymopathies
urinary incontinence
urine test for metabolic disorders
Usher's syndrome
uveitis
vestibular function, tests of
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 impairment
visual loss
visual loss, progressive
visual loss, slow
visual loss, sudden
vitamin deficiency
vitreous opacities
walking, difficulty with
war
water channel antibodies
weakness
weight loss
wheelchair
white matter disease
white matter disease, subcortical
Wolfram syndrome
Showing articles 450 to 500 of 5705 << Previous Next >>

Anterior Ischemic Optic Neuropathy in Churg-Strauss Syndrome
Neurol 44:2200-2202, Kattah,J.C.,et al, 1994

Visual Morbidity in Giant Cell Arteritis:Clinical Characteristics and Prognosis for Vision
Ophthalmology 101:1779-1785, Liu,G.T.,et al, 1994

A Sproadic Form of Hereditary Neuropathy with Liability to Pressure Palsies:Clin, Electrodiag & Molecular Genetic Findings
Neurol 44:753-755, Reisecker,F.,et al, 1994

Mitochondrial DNA mutations in an Outbreak of Optic Neuropathy in Cuba
Neurol 44:843-845, Hirano,M.,et al, 1994

Orbital and Optic Pathway Sarcoidosis:MR Findings
AJNR 15:775-783, Carmody,R.F.,et al, 1994

Visual Loss from Idiopathic Intracranial Pachymeningitis
Neurol 44:694-698, Lam,B.L.,et al, 1994

Mitochondrial Neurogastrointestinal Encephalomyopathy (MMGIE) :Clin Biochem & Genetic Features of Auto Recess Mitochond Disorder
Neurol 44:721-727, Hirano,M.,et al, 1994

Methylmercury Poisoning:Long-Term Clinical, Radiological, Toxicological, and Pathological Studies of an Affected Family
Ann Neurol 35:680-688, Davis,L.E.,et al, 1994

Primary Brain Tumors:Review of Etiology Diagnosis and Treatment
Am Fam Physician 49:787-797, Newton,H.B., 1994

Clin & Path Features of an Autosomal Dominant, Adult-Onset Leukodystrophy Simul Chronic Progressive MS
Arch Neurol 51:757-766, Schwankhaus,J.D.,et al, 1994

DNA Analysis in Finnish Patients with Hereditary Neuropathy with Liability to Pressure Palsies (HNPP)
JNNP 57:1260-1262, Silander,K.,et al, 1994

Hered Neuralgic Amyotrophy & Hered Neuropathy with Liability to Pressure Palsies:Distinct Clin, Electrophy & Genetic Entities
Neurol 44:2250-2252, Gouider,R.,et al, 1994

Hereditary Neuralgic Amyotrophy & Hereditary Neuropathy with Liability to Pressure Palsies:Distinct Genetic Dis
Neurol 44:2253-2257, Chance,P.F.,et al, 1994

Epidemic Neuropathy in Cuba:A Plea to End the United States Economic Embargo on a Humanitarian Basis
Neurol 44:1784-1786, Roman,G.C., 1994

Liver Transplantation as a Treatment for Familial Amyloidotic Polyneuropathy
Ann Int Med 120:133-134, Skinner,M.,et al, 1994

Neuro-Ophthalmological Presentation of Non-Invasive Aspergillus Sinus Disease in the Non-Immunocompromised Host
JNNP 57:234-237, Brown,P.,et al, 1994

Cerebrotendinous Xanthomatosis:Molecular Diagnosis Enables Presymptomatic Detection of a Treatable Disease
Neurol 44:288-290, Meiner,V.,et al, 1994

Cerebral Involvement in McLeod Syndrome
Neurol 44:117-120, Danek,A.,et al, 1994

Clinical Genetics in Neurological Disease
JNNP 57:7-15, MacMillan,J.C.&Harper,P.S., 1994

Gliomas of the Anterior Visual Pathway
Surv Ophthalmol 38:427-452, Dutton, J., 1994

Brain Magnetic Resonance Imaging in Acute Optic Neuritis, Experience of the Optic Neuritis Study Group
Arch Neurol 50:841-846, Beck,R.W.,et al, 1993

Side Effects of Glucocorticoid Treatment, Experience of the Optic Neuritis Treatment Trial
JAMA 269:2110-2112, Chrousos,G.A.,et al, 1993

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

Anterior Ischemic Optic Neuropathy is Not Associated with Carotid Artery Atherosclerosis
Stroke 24:539-542, Fry,C.L.,et al, 1993

Hereditary Motor-Sensory Neuropathy (Charcot-Marie-Tooth Disease) with Nerve Deafness:A New Variant
J Pediatr 123:431-434, Hamiel,O.P.,et al, 1993

Charcot-Marie-Tooth Disease Type 1A:Association with a Spontaneous Point Mutation in the PMP22 Gene
NEJM 329:96-101, Roa,B.B.,et al, 1993

Werner's Syndrome Associated with Spastic Paraparesis and Peripheral Neuropathy
Neurol 43:1252-1254, Umehara,F.,et al, 1993

Optic Neuritis and HIV-1 Infection
JNNP 56:705-707, Sweeney,B.J.,et al, 1993

Cranial Pachymeningitis of Unknown Origin:A Study of Seven Cases
Neurol 43:1329-1334, Masson,C.,et al, 1993

Guillain-Barre Syndrome (GBS) with Bilateral Optic Neuritis and Central White Matter Disease
Neurol 43:842-843, Nadkarni,M.&Lisak,R.P., 1993

Visual Failure and Optic Atrophy Associated with Chlorambucil Therapy
BMJ 306:109, Yiannakis,P.H.&Larner,A.J., 1993

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

Acute Bacterial Meningitis in Adults, A Review of 493 Episodes
NEJM 328:21-28, Durand,M.L.,et al, 1993

Reduction in Incidence of Optic Nerve Disease with Annual Ivermectin to Control Onchocerciasis
Lancet 341:130-134, 153-1541993., Abiose,A.,et al, 1993

Devic's Neuromyelitis Optica:A Clinicopathological Study of 8 Patients
Ann Neurol 34:162-168, Mandler,R.N.,et al, 1993

Erythromelalgia:Association with Hereditary Sensory Neuropathy and Response to Amitriptyline
Neurol 43:621-622, Herskovitz,S.,et al, 1993

Clinicopath Conf
B-Cell Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma with Infilt of Orbital Muscle, Case 4, 193,NEJM 328:266-275,1993., 1993

Inherited Primary Peripheral Neuropathies
JAMA 270:2326, 23301993., Lupski,J.R.,et al, 1993

Cranial Nerve Palsies in Spontaneous Carotid Artery Dissection
JNNP 56:1191-1199, Sturzenegger,M.&Huber,P., 1993

The Effect of Corticosteroids for Acute Optic Neuritis on the Subsequent Development of Multiple Sclerosis
NEJM 329:1764-1769, 1808-18101993., Beck,R.W.,et al, 1993

Progressive Vison Loss, A Rare Manifestation of Familial Cavernous Angiomas
Arch Neurol 49:170-173, Malik,S.,et al, 1992

Frequent Involvement of the Optic Radiation in Patients with Acute Isolated Optic Neuritis
Neurol 42:77-79, Hornabrook,R.S.L.,et al, 1992

Risk Factors for the Neurologic Complications Associated with Aortic Aneurysms
Arch Neurol 49:284-285, Lynch,D.R.,et al, 1992

Fatal Familial Insomnia, A Prion Disease with a Mutation at Codon 178 of the Prion Protein Gene
NEJM 326:444-449, Medori,R.,et al, 1992

Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
Neurol 42:312-319, Manetto,V.,et al, 1992

Relapsing and Remitting Human Immunodeficiency Virus-Associated Leukoencephalomyelopathy
Ann Neurol 31:34-38, Berger,J.R.,et al, 1992

Brain MRI and Electrophysiologic Abnormalities in Preclinical and Clinical Adrenomyeloneuropathy
Neurol 42:85-91, Aubourg,P.,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

Intra-arterial Cisplatin-Associated Optic and Otic Toxicity
Arch Neurol 49:83-86, Maiese,K.,et al, 1992

A Randomized, Controlled Trial of Corticosteroids in the Treatment of Acute Optic Neuritis
NEJM 326:581-588, 6341992., Beck,R.W.,et al, 1992



Showing articles 450 to 500 of 5705 << Previous Next >>