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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 1600 to 1650 of 5752 << Previous Next >>

Neuropathy in Parkinson Disease
Neurol 77:1947-1950, e132, Rajabally, Y.A. and Martey, J., 2011

Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome)
UpToDate, Feb, Shovlin, C., 2011

Evidence-based guideline update: Treatment of Essential Tremor
Neurol 77:1752-1755, Zesiewicz, T.A.,et al, 2011

MR Imaging of Vogt-Koyanagi-Harada Syndrome with Leptomeningeal Enhancement
AJNR 32:E169-E171, Lohman, B.D.,et al, 2011

A Strange Case of Waitress Headache
Lancet 378:1824, Libera, D.D.,et al, 2011

Family Paralysis
Lancet 377:352, Sung,C.-C.,et al, 2011

Rhombencephalitis A Series of 97 Patients
Medicine 90:256-261, Moragas, M.,et al, 2011

Clinicopathologic conference, Neurologic form of immune reconstitution inflammatory syndrome (neuro-IRIS), without evidence of concurrent opportunistic infection
NEJM 362:2343-2352, Case 18-2011, 2011

Neurological disturbances caused by intravascular lymphomatosis
Brain Nerve 63:443-449, Mizutani, T., 2011

Contemporary management and recent advances in paediatric hydrocephalus
BMJ 343:d4191, Kandasamy, J.,et al, 2011

Longitudinal Assessment of Oxaliplatin-Induced Neuropathy
Neurol 77:980-986, Burakgazi, A.Z.,et al, 2011

Opsoclonus and Multiple Cranial Neuropathy as a Manifestation of Neuroborreliosis
Neurol 77:1013-1014, Sabien Van Erp, W.,et al, 2011

High-Resolution MR Neurography of Diffuse Peripheral Nerve Lesions
AJNR 32:1365-72, Thawait, S.K.,et al, 2011

Clinical Reasoning: A 34-year-old man with recurrent limb weakness
Neurol 77:e68-e72, Karam, C.,et al, 2011

A Middle-Aged Woman with Nausea, Weight Loss, and Orthostatic Hypotension
Neurol 77:489-495, Singer, W.,et al, 2011

Treatment of Severe Neurological Deficits with IgG Depletion through Immunoadsorption in Patients with Escherichia coli O104:H4-Associated Haemolytic Uraemic Syndrome: A Prospective Trial
Lancet 378:1166-1173,1120, Greinacher, A.,et al, 2011

Evidence-Based Guideline Update: Plasmapheresis in Neurologic Disorders: Report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology
Neurol 76:294-300, Cortese,I.,et al, 2011

Genes Associated With Adult Cerebral Venous Thrombosis
Stroke 42:913-918, Marjot,T.,et al, 2011

Diagnosis and Management of Cerebral Venous Thrombosis: A Statement for Healthcare Professionals From the American Heart Association/American Stroke Association
Stroke 42:1158-1192, Saposnik,G.,et al, 2011

Evidence-based guideline: Treatment of painful diabetic neuropathy
Neurol 76:1758-1765, Bril,V., et al, 2011

Clinicopathologic Conference, Sjogrens syndrome with dorsal-root ganglionitis
NEJM 364:1856-1865, Case 14-2011, 2011

An unusual cause of stroke and hypoxia
BMJ 342:c7200, Bell, S.L. & Eveson, D.J., 2011

Decompressive Craniectomy in Diffuse Traumatic Brain Injury
NJM 364:1493-1502, Cooper, D.J.,et al, 2011

Skin biopsy is useful for the antemortem diagnosis of neuronal intranuclear inclusion disease
Neurol 76:1372-1376, Sone, J.,et al, 2011

Redefining the Guillain-Barre Spectrum in Children: Neuroimaging Findings of Cranial Nerve Involvement
AJNR 32:639-42, Zuccoli, G.,et al, 2011

Deep Brain Stimulation
JAMA 305:732, Pluta,R.,et al, 2011

Pediatric Sciatic Neuropathies: A 30-year Prospective Study
Neurol 76:976-979, Srinivasan,J.,et al, 2011

Recognizing Guillain-Barr� Syndrome in Preschool Children
Neurol 76:807-810, Roodbol,J.,et al, 2011

Rituximab in Patients With Chronic Inflammatory Demyelinating Polyradiculoneuropathy: A Report of 13 Cases and Review of the Literature
JNNP 82:306-308, Benedetti,L.,et al, 2011

Spectrum of Paraneoplastic Disease Associated With Lymphoma
Neurol 76:705-710, Briani,C.,et al, 2011

Acute Brachial Diplegia Due to Lyme Disease
The Neurologist 17:24-27, Gorson,K.C.,et al, 2011

Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
NEJM 364:1062-1074, Case 8-2011, 2011

Epstein-Barr Virus Infections of the Nervous System
www.medlink.com, Nov, Amlie-Lefond,C., 2011

Sjogren Syndrome
emedicine.medscape.com,Oct, Miller,A.V., 2011

Internal Carotid Artery Dissection Heralded by an Oculomotor Nerve Palsy
Neurologist 17:333-337, Nizam, A.,et al, 2011

Ipsilateral Stroke in a Patient with Horizontal Gaze Palsy with Progressive Scoliosis and a Subcortical Infarct
Stroke 42:e1-e3, Ng, A.S.L.,et al, 2011

Lower Lip Numbness in a Patient with Colorectal Cancer
BMJ Case Reports doi:10.1136/BCR.01.2011.3682, Amin,A.,et al, 2011

Clincopath Conference, Endogenous Endophthalmitis Due to Aspergillus Niger
NEJM 363:1749-1758, Case 33-2010, 2010

Evidence for Acute Neurotoxicity After Chemotherapy
Ann Neurol 68:806-815, Petzold,A.,et al, 2010

Association Between Familial Atrial Fibrillation and Risk of New-Onset Atrial Fibrillation
JAMA 304:2263-2269, Lubitz,S.A.,et al, 2010

Vitamin B12-Responsive Severe Leukoencephalopathy and Autonomic Dysfunction in a Patient With "Normal" Serum B12 Levels
JNNP 81:1369-1371, Graber,J.J.,et al, 2010

Update on the Natural History of Cavernous Malformations and Factors Predicting Aggressive Clinical Presentation
Neurosurg Focus 29:E7, Washington,C.W.,et al, 2010

Pediatric Moyamoya Disease: An Analysis of 410 Consecutive Cases
Ann Neurol 68:92-101, Kim,S.-K., et al, 2010

A 64-Year-Old Man With Painful, Unilateral External Opthalmoplegia
Neurol 75:e35-e39, Bhatti,M.T., 2010

Pain in Guillain-Barre Syndrome: A Long-Term Follow-Up Study
Neurol 75:1439-1447, Ruts,L.,et al, 2010

Prediction of Respiratory Insufficiency in Guillain-Barr� Syndrome
Arch Neurol 67:781-787, Walgaard,C.,et al, 2010

Low Energy Diet and Intracranial Pressure in Women With Idiopathic Intracranial Hypertension: Prospective Cohort Study
BMJ 341:138,109, Sinclair,A.J., et al, 2010

Redefining Dysferlinopathy Phenotypes Based on Clinical Findings and Muscle Imaging Studies
Neurol 75:316-323,298, Paradas,C., et al, 2010

Infectious and Non-Infectious Neurologic Complications in Heart Transplant Recipients
Medicine 89:166-175, Mu�oz,P., et al, 2010

Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
Brain 133:655-670, Leen,W.G., et al, 2010



Showing articles 1600 to 1650 of 5752 << Previous Next >>