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Differential
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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 300 to 350 of 5680 << Previous Next >>

Neurologic Manifestations in Primary Sjogren Syndrome: A Study of 82 Patients
Medicine 83:280-291, Delalande,S.,et al, 2004

Clinical and Molecular Findings in Patients with Giant Axonal Neuropathy (GAN)
Neurol 62:13-16, Bruno,C.,et al, 2004

Charcot-Marie-Tooth Disease:Extensive Cranial Nerve Involvement on CT and MR Imaging
AJNR 25:494-497, Aho,T.R.,et al, 2004

Progressive Binasal Hemianopia
Lancet 363:1606, Pringle,E.,et al, 2004

Idiopathic Hypertrophic Pachymeningitis
Neurol 62:686-694, Kupersmith,M.J.,et al, 2004

Role of Magnetic Resonance Imaging Within Diagnostic Criteria for Multiple Sclerosis
Ann Neurol 56:273-278, Miller,D.H.,et al, 2004

Recent Developments in Thyroid Eye Disease
BMJ 329:385-390, Cawood,T.,et al, 2004

Neurologic Impairment 10 Years After Optic Neuritis
Arch Neurol 61:1386-1389, Optic Neuritis Study Group, 2004

The Natural History of Recurrent Optic Neuritis
Arch Neurol 61:1401-1405, Pirko,I.,et al, 2004

Long-Term Brain Magnetic Resonance Imaging Changes After Optic Neuritis in Patients Without Clinically Definite Multiple Sclerosis
Arch Neurol 61:1538-1541, Optic Neuritis Study Group, 2004

Plasma Exchange for Severe Optic Neuritis
Neurol 63:1081-1083, Ruprecht,K.,et al, 2004

Impact of Presymptomatic Genetic Testing for Hereditary Ataxia and Neuromuscular Disorders
Arch Neurol 61:875-880, Smith,C.O.,et al, 2004

The Occurence of Guillain-Barre Syndrome Within Families
Neurol 63:1747-1750, Geleijns,K.,et al, 2004

The CNS Phenotype of X-Linked Charcot-Marie-Tooth Disease
Neurol 61:1475-1478, Taylor,R.A.,et al, 2003

Telemedicine in Emergency Evaluation of Acute Stroke
Stroke 34:2842-2846, Handschu,R.,et al, 2003

Hereditary Neuropathy With Liability to Pressure Palsies Mimicking Hypoglossal Nerve Injuries
Neurol 61:1457-1458, Corwin,H.M. &Girardet,R.E., 2003

Spinal Cord MRI in Clinically Isolated Optic Neuritis
JNNP 74:1577-1580, Dalton,C.M.,et al, 2003

Hypoglossal Neuropathy in Hereditary Neuropathy with Liability to Pressure Palsy
Neurol 61:1154-1155, Winter,W.C. &Juel,V.C., 2003

Bilateral Anterior Toxic Optic Neuropathy and the Use of Infliximab
BMJ 326:579, ten Tusscher,M.P.M.,et al, 2003

Mitochondrial Respiratory-Chain Diseases
NEJM 348:2656-2668, DiMauro,S. &Schon,E.A., 2003

High- and Low-Risk Profiles for the Development of Multiple Sclerosis Within 10 Years After Optic Neuritis
Arch Ophthalmol 121:944-949, Optic Neuritis Study Group, 2003

CMT with Pyramidal Features
Neurol 60:696-699, Vucic,S.,et al, 2003

Posterior Ischemic Optic Neuropathy After Hemodialysis
Ophthalmol 110:1216-1218, Buono,L.M.,et al, 2003

Two Unusual Cases of Visual Loss Following Severe Non-Surgical Blood Loss
Eye 16:185-189, Michaelides,M.,et al, 2002

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

Indications and Usefulness of Nerve Biopsy
Arch Neurol 59:1532-1535, Said,G., 2002

Clinicopath Conf., Prolactinoma
NEJM 347:1604-1611, Case 35-2002, 2002

Two Patients With Unusual Forms of Varicella-Zoster Virus Vasculopathy
NEJM 347:1500-1503, Gilden,D.H.,et al, 2002

A Blinding Combination
Lancet 360:1220, Matthews,B.N.,et al, 2002

Thrombolysis in Stroke Beyond Three Hours: Targeting Patients With Diffusion and Perfusion MRI
Ann Neurol 51:11-13,28, Warach,S., 2002

Management of Acute Optic Neuritis
Lancet 360:1953-1962, Hickman,S.J.,et al, 2002

The Tolosa-Hunt Syndrome
JNNP 71:577-582, Kline,L.B. &Hoyt,W.F., 2001

Pachymeningitis and optic neuritis in Rheumatoid Arthritis: Successful Treatment with Cyclophosphamide
Clin Rheumatol 20:136-139, Yucel,A.E.,et al, 2001

Optic Neuropathy in Children With Lyme Disease
Pediatrics 108:477-481, Rothermel,H.,et al, 2001

Clinical Spectrum of Posterior Ischemic Optic Neuropathy
Am J Ophthalmol 132:743-750, Sadda,S.R.,et al, 2001

Clinical Spectrum of Chronic Acquired Demyelinating Polyneuropathies
Muscle & Nerve 24:311-324, Saperstein,D.S.,et al, 2001

A Blind Panic
Lancet 357:1262, Ayuk,J.,et al, 2001

Disability and Quality of Life in Charcot-Marie-Tooth Disease Type 1
JNNP 70:548-550, Pfeiffer,G.,et al, 2001

Acute Vocal Cord Paralysis in Hereditary Neuropathy With Liability to Pressure Palsies
Neurol 56:1415, Okhoshi,N.,et al, 2001

Visual Loss in Cysticercosis: Analysis of 23 Patients
Neurol 57:545-548, Chang,G.Y. &Keane,J.R., 2001

Craniofacial and Cutaneous Findings Expand the Phenotype of Hereditary Neuralgic Amyotrophy
Neurol 57:1963-1968, Jeannet,P.,et al, 2001

Recessive Ataxia With Ocular Apraxia
Arch Neurol 58:201-205,173, Barbot,C.,et al, 2001

Clinicopath Conf,Invasive Fungal Sinusitis & Osteomyelitis Due to Mucormycosis
NEJM 344:286-293, Case 3-2001, 2001

Neuro-Ophthalmic Manifestations of Sarcoidosis. Clincal Spectrum, Evaluation and Management
J Neuroophthalmol 21:132-137, Frohman,L.P,et al, 2001

Visual Manifestations of Giant Cell Arteritis
Medicine 79:283-292, Gonzalez-Gay,M.A.,et al, 2000

MR Imaging of the Cauda Equina in Hereditary Motor Sensory Neuropathies: Correlations with Sural Nerve Biopsy
AJNR 21:1793-1798,1779, Cellerini,M.,et al, 2000

Optic Neuritis in Multiple Sclerosis: An Update
The Neurologist 6:205-213, Chan,J.W., 2000

Practice Paramenter: The Role of Corticosteroids in the Management of Acute Monosymptomatic Optic Neuritis
Neurol 54:2039-2044, Kaufman,D.I.,et al, 2000

Interaction Between HLA-DR2 and Abnormal Brain MRI in Optic neuritis and Early MS
Neurol 54:1859-1861, Hauser,S.L.,et al, 2000

Evolution of Sporadic Olivopontocerebellar Atrophy Into Multiple System Atrophy
Neurol 55:527-532, Gilman,S. et al, 2000



Showing articles 300 to 350 of 5680 << Previous Next >>