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Differential
(Click to cross reference)
acoustic nerve
adrenoleukodystrophy
adverse drug reaction
Alzheimer's disease
anemia
anemia, aplastic
anosmia
anticoagulant, complications of
antiretinal antibodies
apraxia of eye movements
arrhythmia, cardiac
arteritis, temporal
aspirin
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxic gait
autoantibodies
Babinski sign
basal ganglia, calcification of
basilar impression
Bassen-Kornzweig syndrome
battered child syndrome
behavioral disorder
blindness
blindness, sudden
bradycardia
brain atrophy
brain biopsy
brainstem, hypoplasia
brainstem, lesion of
calcification, intracranial
calcitonin
CAR syndrome
carcinoma
carcinoma of lung
carotid artery occlusion, neck
CAT scan
CAT scan, abnormal
CAT scan, false negative
cataracts
cerebellar ataxia, children
cerebellar lesion
cerebellar vermis
cerebral cortical atrophy
cerebro hepato renal syndrome
cerebrospinal fluid, elevated protein of
cerebrovascular accident
Charles Bonnet's syndrome
cherry red spot
cherry red spot-myoclonus syndrome
chest x-ray, abnormal
children
chorioretinitis
chromosomal abnormality
chromosome 17
Clinical Pathologic Conference(C.P.C.)
cluster, geographic
Cockayne's syndrome
color vision
color vision, impaired
complications
compression fracture
cornea, opacity of
corpus callosum
corpus callosum, hypoplastic
cranial nerve palsies
cranial neuropathy, multiple
craniopharyngioma
cyst
cyst, parenchymal
cyst, subcortical
cytochrome c oxidase
cytochrome c oxidase, deficiency
deafness
degenerative diseases of CNS
dementia
developmental abnormality of brain
developmental milestones, loss of
developmental retardation
diarrhea
differential diagnosis
diplopia
DNA probes
drug induced neurologic disorders
dysmorphic
dystonia
electroencephalogram, abnormalities of
electron microscopy
electronystagmography
electroretinograph
endophthlamitis
enzyme, defect
epidermal nevus syndrome
exophthalmus
eye injury
eye movement, disorders of
facial nerve palsy
falling
familial
fatty acid dehydrogenase deficiency
fingolimod
fluorescein angiography
fourth ventricle, enlargement of
fundus, abnormality of
gastrointestinal motility
gaze palsy
gaze palsy, supranuclear
gene
gene mutation
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
glare, light-induced
glaucoma
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
Hallervorden Spatz disease
Hallervorden Spatz disease, late onset
Hallgren's syndrome
hallucination
hallucination, visual
hallucination, visual, benign
hand flapping
head circumference
hearing loss
heart block
hemifacial spasm
hepatomegaly
hydrocephalus
hypomagnesemia
hypoparathyroidism
hypotonia
iatrogenic neurologic disorders
imbalance
immunomodulation
immunosuppression
immunosuppressive agents
inborn errors of metabolism
inclusion bodies, intracytopasmic
incoordination
intellectual deficit
intellectual deterioration
internuclear ophthalmoplegia
intestinal pseudoobstruction
Jehovah's witness
Joubert syndrome
Kearns-Sayre syndrome
Laurence-Moon-Bardet-Biedl syndrome
Leber's hereditary optic neuropathy
Leber's idiopathic stellate retinopathy
leukodystrophy
leukoencephalopathy
leukopenia
low back pain
lymphadenopathy, hilar
lymphocyte fingerprint profiles
lysosomal storage disease
macular degeneration
macular degeneration, senile
macular degeneration, senile disciform
macular edema
macular hemorrhage
macular star
macular wrinkling
maculopathy
malformation, CNS, congenital
malformation, vascular
malformation, vascular, cerebral
medial longitudinal fasciculus(MLF)
mental retardation
microcephaly
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, CAT scan compared to
MRS
mucopolysaccharidoses
multiple sclerosis
multiple sclerosis, treatment of
multiple sclerosis, tumefactive
muscle biopsy
myoclonic jerks
myoclonus
myopathy
myopathy, mitochondrial
myopia
nausea and vomiting
neuraminidase deficiency
neurocutaneous disease
neuroendocrinology
neuroichthyosis
neurolipidosis IV
neurologic disease, diagnoses of
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology
neuropathy
neuropathy, hereditary peripheral
neuropathy, peripheral
neuroretinitis
nevus
night blindness
nystagmus
nystagmus, pendular
old age, neurology of
ophthalmoplegia
ophthalmoplegia, progressive external
optic atrophy
optic atrophy, hereditary
optic atrophy, unilateral
optic disc edema
optic glioma
optic nerve
optic nerve, lesion of
optic nerve, neoplasm of
optic neuritis
optic neuropathy
optic neuropathy, hereditary
orbit, cellulitis of
Paget's disease
Paget's disease, psychosis in
Paget's disease, spinal cord problem in
pain
papilledema
papillitis
Parkinson disease
Parkinsonism syndrome
peroxisomal disease
peroxisomes
photocoagulation
photophobia
photosensitivity, eye
pigmentary retinopathy
platelet inhibiting drugs
polyneuropathy
Poretti-Boltshauser syndrome
prognosis
psychomotor retardation
ptosis
pupil, abnormality in neurologic disorders
pupil, light reflex, abnormal
quadriparesis
quadriplegia
radiculopathy
refractive errors
Refsum's disease
remote effect of cancer on the nervous system
respiratory tract infection
retina, abnormal
retinal arteriole attenuation
retinal artery occlusion
retinal degeneration
retinal detachment
retinal hemorrhages
retinal lesion
retinal vasculitis
retinitis pigmentosa
retinoblastoma
retinopathy
retropulsion
review article
RFLPs
root lesion, nerve
roving eye movements
sarcoidosis
scotoma
scotoma, central
scotoma, paracentral-homonymous
seizure
seizure, children
seizure, neonatal
sensorineural hearing loss
short stature
Sjogren-Larsson syndrome
skin, biopsy
skin, lesions in neurologic disorders
skull x-ray, abnormal
spastic diplegia
spinal cord, compression of
spinocerebellar ataxia type 1
spinocerebellar degeneration
spongy degeneration of brain
steroid
steroid therapy, CNS treatment and complications with
superior orbital fissure syndrome
tapetoretinal degeneration
third nerve palsy
titubation
trauma
treatment of neurologic disorder
tremor
trigeminal neuralgia
Usher's syndrome
uveitis
ventricular enlargement
vertebral-basilar insufficiency
viral infection
vision, blurred
vision, failure of in childhood
visual acuity
visual acuity, decreased
visual acuity, decreased, monocular
visual field defect
visual fields, constricted
visual impairment
visual loss
visual loss, slow
visual loss, sudden
white matter disease
wide based gait
Showing articles 0 to 37 of 37

Blurred Vision
BMJ 368:m569, Zhou, S.,et al, 2020

Early-Onset Head Titubation in a Child with Poretti-Boltshauser Syndrome
Neurol 88:1478-1479, Masson, R.,et al, 2017

Profound Anemia and Acute Blindness in a Jehovahs Witness
Lancet 382:998, Bretagnol, A.,et al, 2013

Fingolimod-Associated Macular Edema
Neurol 78:672-680, Jain,N. and Bhatti,M.T., 2012

Tumefactive Multiple Sclerosis Lesions under Fingolimod Treatment
Neurol 79:2000-2002,1942, Visser, F.,et al, 2012

"Retinal Diplopia" Associated with Macular Wrinkling
Neurol 63:925-927, Barton,J.J.S., 2004

Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
NEJM 347:672-680, Case 27-2002, 2002

Ocular Involvement in Sarcoidosis
Br J Ophthalmol 84:110-116, Rothova, A., 2000

Sjogren-Larsson Syndrome, Clinical and MRI/MRS Findings in FALDH-Deficient Patients
Neurol 52:1345-1352,1307, Van Domburg,P.H.M.F.,et al, 1999

Mucolipidosis Type IV; Characteristic MRI Findings
Neurol 51:565-569, Frei,K.P.,et al, 1998

Visual Hallucinations in Psychologically Normal People:Charles Bonnet's Syndrome
Lancet 347:794-797, Teunisse,R.J.,et al, 1996

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

Acquired Ocular Visual Impairment in Children, 1960-1989
Am J Dis Child 147:325-328, Robinson,G.C.&Jan,J.E., 1993

Joubert Syndrome:A Clinico-Radiological Study
Neuroradiology 31:502-506, Kendall,B.,et al, 1990

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

A Mitochondrial DNA Mutation as a Cause of Leber's Hereditary Optic Neuropathy
NEJM 320:1300-1305, Singh,G.,et al, 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

Macular Hemorrhage in the Aging Eye:The Effects of Anticoagulants
NEJM 318:1126-1127, Kingham,J.D.,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

Hallervorden-Spatz Syndrome:Clinical and Magnetic Resonance Imaging Correlations
Ann Neurol 24:692-694, Sethi,K.D.,et al, 1988

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

Paraneoplastic Syndromes Involving the Eyes
In Walsh & Hoyt's Clin Neuro-ophthal, 4th ed, Williams & Wilkins, Vol 3, p 1735-1746, Miller,N.R., 1988

Does Neuroretinitis Rule Out Multiple Sclerosis
CPT, et al, Arch Neurol 44:1045-1048987., Parmley,V.C., 1987

Optic-Nerve Degeneration in Alzheimer's Disease
NEJM 315:485-487, Hinton,D.R.,et al, 1986

Leber's Idiopathic Stellate Retinopathy
Am J Ophthalmol 93:96-101, Carroll,D.M.,et al, 1982

Santavuori Disease:Diagnosis by Leukocyte Ultrastructure
Neurol 32:1277-1281, Baumann,R.J.,et al, 1982

Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981

Peripheral Neuropathy in the Cherry-Red Spot-Myoclonus Syndrome (Sialidosis Type I)
Ann Neurol 7:450-456, Steinman,L.,et al, 1980

Neurologic Disturbances in Pagets Disease of Bone:Response to Calcitonin
Neurol 29:448-457, Chen,J.R.,et al, 1979

Basal Ganglia Calcification in Kearns-Sayre Syndrome
Arch Neurol 36:711-713, Robertson,W.C.Jr., 1979

Senile Disciform Macular Degeneration
Editioral, BMJ 1:1444-14451979., , 1979

Clinical Pathological Conference
Neuronal Veroid-lipfuscinosis, Juvenile Variant, (Batten's disease) , NEJM 299:189., , 1978

Neurological Involvement in the Epidermal Naevus Syndrome
JNNP 41:466, McAuley,D.L.,et al, 1978

Kearns-Sayre Syndrome with Hypoparathyroidism
Ann Neurol 3:513, Horwitz,S.J.,et al, 1978

Kearns-Sayre Syndrome & Hypoparathyroidism
Ann Neurol 3:455, Pellock,J.M.,et al, 1978

Juvenile Amaurotic Idiocy (Neuronal Ceroid Lipofuscinosis) & Lymphocyte Fingerprint Profiles
Ann Neurol 4:531-536, Baumann,R.J.,et al, 1978

Tapetoretinal Degeneration in Childhood Presenting as a Disturbance of Behavior
BMJ 202, 1972 Jan., Harcourt,B.,et al, 1972



Showing articles 0 to 37 of 37