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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 100 to 150 of 5680 << Previous Next >>

Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023

Neuroimaging Features of Biotinidase Deficiency
AJNR 44:328-333, Biswas,A.,et al, 2023

A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium
Neurol 100:631-637, Zeng,T.f.,et al, 2023

Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
Neurol 100:766-783, Manini,A.,&Pantoni,L., 2023

Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD): Clinical Features and Diagnosis
UptoDate.com, March, Flanagan,E.P. & Tillema,J-M, 2023

A 25-Year-Old Woman With Eye Swelling and HEadache
Neurol 100:879-883, Hehir,A.,et al, 2023

Posterior Reversible Encephalopathy Syndrome
NEJM 388:2171-2178, Geocadin,R.G., 2023

Management of Possible Multiple Sclerosis
NEJM 388:2195-2190, , 2023

Clinicopathologic Conference, Systemic Immunoglobulin Light-Chain (AL) Amyloidosis
NEJM 389:166-175, Case 21-2023, 2023

Woman With Acute Bilateral Ophthalmoplegia
Neurol 101:140-144, Giacobbe,Alket al, 2023

Progressive Cranial Neuropathy
JAMA Neurol 80:1375-1376, Buchberger,D.S.,et al, 2023

Cases with IgG4-related Ophthalmic Disease with Mass Lesions Surrounding the Optic Nerve
Am J Ophthalmol 25:101324, Hamaoka, S.,t al, 2022

Neuromyelitis Optica Spectrum Disorder
NEJM 387:631-639, Wingerchuk, D.M. & Lucchinetti, C.F., 2022

A 48-Year-Old Woman with 6 Months of Vivid Visual Hallucinations
Neurol 99:166-171, Kizza, J.,et al, 2022

Neurobrucellosis:The Great Mimicker
Rev Soc Bras Med Trop 55:e0567-e2012, Soares,C.N.,et al, 2022

Vision Loss in Giant Cell Arteritis
Pract Neurol 22:138-140, Donaldson, L. & Margolin, E., 2022

Transocular Sonography in Acute Arterial Occlusions of the Eye in Elderly Patients
PlusOne doi.org/10.1371/journal.pone.0247072, Czihal, M.,et al, 2021

A 79-Year-Old Woman with Subacute Bilateral Visual Loss
Neurol 97:e1159-e1165, Rossi, S.,et al, 2021

Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
NEJM 385:165-175, Case 20-2021, 2021

Chorioretinopathy After Corticosteroid Treatment for Optic Neuritis
Neurol 96:e305-e306, Ling, J. and Micieli, J.A., 2021

Cranial Nerve Disorders Associated with Immune Checkpoint Inhibitors
Neurol 96:e866-e875, Vogrig, A.,et al, 2021

Clinicopathologic Conference, Lympohplasmic Lymphoma of the CNS (Bing-Neel Syndrome)
NEJM 384:745-753, Case 6-2021, 2021

Clinical and Neuroimaging Findings in MOGAD-MRI and OCT
Clin Exp Immunol 206:266-281, Bartels,F.,et al, 2021

Giant Cell Arteritis:Its Ophthalmic Manifestations
Indian J Ophthalmol 69:227-235, Hayreh, S.S., 2021

The Tolosa-Hunt Syndrome
NJJP 71:577-582, Kline,L.B. & Hoyt,W.F., 2021

Immunoglobulin G4-Related Orbital Disease with Bilateral Optic Perineuritis and Maxillary Nerves Involvement:A Case Report
Ophthalmol Ther 9:1089-1099, Hung,C-H., 2020

An 11-year-old girl with focal seizures, fevers, and unilateral, enhancing cortical lesions
Neurol 95:e3153-e3159, Russ, J.B.,et al, 2020

A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
Neurol 94:e1213-e1218, Lima, J.E.E.,et al, 2020

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

A 53-year-old Woman with Lower Extremity Paresthesias
Neurol 94:1105-1108, Dehbashi, S.,et al, 2020

Clinical Characteristics, Risk Factors, and Outcomes of POEMS Syndrome
Neurol 95:e268-e279, Keddie, S.,et al, 2020

Complex Ataxia
Neurol 95:136-141, Abkur, T.,et al, 2020

COVID-19 Presenting with Ophthalmoparesis from Cranial Nerve Palsy
Neurol 95:221-223, Dinkin, M.,et al, 2020

A Woman with Monocular Vision Loss
Neurol 95:e1105-e1109, Danish, H.,et al, 2020

Looking Beyond the Usual
Delhi J Ophthal doi:7869/djo.555, Shakrawal, J.,et al, 2020

GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy
Ann Neurol 86:962-968,809, Okubo, M.,et al, 2019

Strokelike Episodes in a Patient with Chronic Gait Abnormalities
JAMA Neurol 76:621-622, Santoro, J.D. & Chitnis, T., 2019

A 58-year-old Man with Hand Tremor and Episodes of Neck Pain
Neurol 93:557-561, Urso, D.,et al, 2019

Optic Nerve Enhancement and Restricted Diffusion in Postoperative Visual Loss
Neuro-Ophthalmol 43:337-339, Finelli, P.F., 2019

A 14-Year-Old Girl with Headache, Seizures, and Confusion
Neurol 92:e161-e167, Xiao, L.,et al, 2019

Global Orbital Infarction Syndrome after a Carotid Artery Dissection
JAMA Neurol 76:111-112, Larrosa Campo, D.,et al, 2019

A 15-year-old Boy with Bilateral Wrist Pain in the Setting of Weight Loss
Neurol 92:486-492, Lau, K.H.V.,et al, 2019

An Unusual Fundus Finding in a Teenage Girl
JAMA Neurol 75:1566-1567, Filho, F.M.R.,et al, 2018

Clinicopathologic Conference, Granulomatosis with Polyangiitis
NEJM 379:2452-2461, Case 39-2018, 2018

Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect
Front Neurol doi:10.3389/fneur.2018.0069, Gagliardi, D.,et al, 2018

Seizures and Encephalitis in Myelin Oligodendrocyte Glycoprotein IgG Disease vs Aquaporin 4 IgG Disease
JAMA Neurol 75:65-71, Hamid, S.H.M.,et al, 2018

Optic Nerve Head Edema Among Patients Presenting to the Emergency Department
Neurol 90:e373-e379, Sachdeva, V.,et al, 2018

Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
Neurol 90:e625-e631, Set, K.K.,et al, 2018

A 60-year-old man with arm weakness and numbness
Neurol 90:190-196, Foster, L.A.,et al, 2018

Clinical Reasoning: A Teenager with Left Arm Weakness
Neurol 90:e907-e910, Al-Ghamdi, F.,et al, 2018



Showing articles 100 to 150 of 5680 << Previous Next >>