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Differential
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abdominal distention
abulia
aciduria
acrocyanosis
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
adult polyglucosan body disease
adult-onset leukodystrophy, with neuroaxonal spheroids
advances in neurology
affect, inappropriate
Aicardi-Goutieres syndrome
akinetic mute
Alexanders disease
Alexanders disease, adult onset
algorithm
alopecia
aminoacidurias
ammonia
angiitis
angiitis, granulomatous of CNS
angiitis, isolated of CNS
anti MAG antibodies
anxiety
aphasia
apraxia
areflexia
arteriopathy
arthralgia
arylsulfatase A
aspartocyclase
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, paroxysmal
ataxia, progressive
ataxia, sensory
ataxic gait
attention deficit disorder with hyperactivity
atypical
auditory evoked brainstem potentials
autonomic dysfunction
axonal degeneration
axonal spheroid
Babinski sign
bacterial infection
bacterial infection, CNS
basal ganglia
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, infarction
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
Binswanger disease
biologic markers
bladder dysfunction
blindness
body odor
bone marrow transplantation
bradykinesia
bradyphrenia
brain atrophy
brain biopsy
brainstem, atrophy
brainstem, lesion of
brucellosis
brucellosis, nervous system involvement with
bulbar palsy
cachexia
CAG repeats
calcification, intracranial
calcification, intracranial, rim
calcifications, intracranial, punctate
Canavan's disease
caries
CAT scan
CAT scan, abnormal
CAT scan, contrast enhanced
CAT scan, demyelinating disease
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, isodense lesion with acute hemorrhage
CAT scan, serial
cataracts
cataracts, congenital
central nervous system, infection of
cerebellar ataxia, autosomal recessive
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebral atherosclerosis
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortex
cerebral cortical atrophy
cerebral infarction
cerebral infarction, small, deep
cerebral infarction, subcortical
cerebral ischemia
cerebral peduncle
cerebral vasculature
cerebral vasculature, calcification
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, protein of
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, genetic
cerebrovascular accident, location of
cerebrovascular accident, multiple
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
cerebrovascular disease
Charcot-Marie-Tooth
chilbran skin lesions
children
choreoathetosis
chromosomal abnormality
chromosome 12
chromosome 17
chromosome 19
chromosome 3
Clinical Pathologic Conference(C.P.C.)
Cockayne's syndrome
cognition
complications
compression fracture
compression neuropathy
confusion
conjunctivitis
consanguinity
contractures, joint
corpus callosum
corpus callosum, infarction of
corpus callosum, lesion of
corpus callosum, thinning
cortical blindness
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
cry, weak
crying, pathologic
cryopyrin-associated periodic syndrome
cryptorchidism
cultured skin fibroblasts
cyst
cyst, parenchymal
cystic infarction
DARS
deafness
decerebrate posture
deep gray nuclei
degenerative diseases of CNS
Dejerine-Sottas syndrome
delayed dentition
dementia
dementia, cerebrovascular disease causing
dementia, childhood
dementia, familial
dementia, frontal lobe type
dementia, presenile
dementia, rapidly progressive
dementia, subcortical
demyelinating disease
dentate nuclei
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
depression
developmental milestones, loss of
developmental retardation
diagnostic criteria
diarrhea
diet
differential diagnosis
diplopia
diplopia, transient
DNA probes
dysarthria
dysarthria-clumsy hand syndrome
dyscalculia
dysdiadochokinesia
dysmetria
dysphagia
dyspraxia
dystonia
dystonia, children
dystroglycanopathies
eczema
electromyogram
electron microscopy
emotional lability
encephalopathy
enzyme, defect
enzyme, muscle disease
epicanthal folds
episodic disorders
episodic neurologic deficits
evoked potentials
exome sequencing
extraocular muscle lesion
eye movement, disorders of
eye, pain in
eyes, sunken
Fabry's disease
facial appearance, abnormal
Fahr disease
failure to thrive
falling
familial
fatigue
fatty acid dehydrogenase deficiency
feeding disorder
fever
fever, recurrent
flow study, carotid artery
foot deformity
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
fragile-X syndrome, carrier
Friedreich's ataxia
frontal bossing
frontal lobe, anatomy and physiology
frontal lobe, lesion of
frontal lobe, pathologic signs of
gadolinium
gait disorder
gait, spastic
galactocerebrosidase
gastrointestinal disease, neurologic complications
gastrointestinal motility
gastroparesis
gender
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
genu of corpus callosum
globus pallidus, lesion of, bilateral
glycogen storage disease
glycosyltransferase
gram negative rod
granular osmiphilic material
grasp reflex
growth retardation
gyrus, abnormal
handwriting
head circumference
head lag
headache
hearing loss
hemiparesis
hemiparesis, transient
hemophagocytic lymphohistiocytosis
hemophagocytic lymphohistiocytosis, cerebromeningeal
hepatolenticular degeneration(Wilson's disease)
heralding manifestation
hiccoughs
hormone replacement
HTRA1 gene
human immunodeficiency virus type 1
human T-lymphotropic virus type I(HTLV-I)
hyperactivity
hyperpigmentation of skin
hyperpyrexia, CNS disorder causing
hyperreflexia
hypertrophic intracranial pachymeningitis
hypocalcemia
hypodontia
hypogonadism
hypomyelination
hypoparathyroidism
hyporeflexia
hypotension, systemic
hypothermia
hypotonia
hypotonia, infants
imbalance
immunodeficiency
impulsivity
inattention
inborn errors of metabolism
inborn errors of metabolism, screening
inclusion bodies
inclusion bodies, intracytopasmic
inclusion bodies, intranuclear
inclusion bodies, ubiquitin
incontinentia pigmenti
incoordination
intellectual deficit
intellectual deterioration
intelligence quotient
interferon alpha
intestinal pseudoobstruction
intracerebral hemorrhage
intrauterine
intrinsic hand muscles, wasting of
irritability
Jewish
Kearns-Sayre syndrome
Krabbe's disease
lactate
lacunar infarction
laughing
laughing, pathologic
leg weakness, bilateral
Leigh's disease
lenticular nucleus, lesion of
lenticular nucleus, lesion of, bilateral
leukocyte enzyme abnormality
leukodystrophy
leukodystrophy, pigmented orthochromatic
leukoencephalopathy
leukoencephalopathy with calcification and cysts
leukoencephalopathy, adult onset, sporadic
leukoencephalopathy, differential diagnosis
leukoencephalopathy, hereditary diffuse
life expectancy
Lorenzo's oil
low back pain
lysosomes, abnoral
macrocephaly
mania
manic-depressive
maple syrup urine disease
Marinesco-Sjogren syndrome
MELAS syndrome
memory, defect of recent
memory, impairment of
meningeal enhancement
meningitis, aseptic
meningitis, brucellosis
mental retardation
metabolic acidosis
metachromatic leukodystrophy
metachromatic leukodystrophy, adult onset
metachromatic leukodystrophy, juvenile
methylmalonic aciduria
microangiopathy, brain
microcephaly
microdontia
microhemorrhage, intracerebral
midbrain, lesion of
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
migraine with aura
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
monoparesis
mortality
motor neuron disease
mousy odor
movement disorder
MRI
MRI pattern
MRI, abnormal
MRI, black holes on
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, diffusion tensor
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, false negative
MRI, FLAIR
MRI, gradient-echo
MRI, high signal foci on
MRI, negative
MRI, ring sign
MRI, serial
MRI, spinal cord
MRI, susceptibility weighted
MRI, target sign
MRS
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, familial
multiple sclerosis, misdiagnosis
multiple system atrophy
muscle biopsy
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, classification
muscular dystrophy, congenital
muscular dystrophy, differential diagnosis of
myelination of nervous system
myelitis, longitudinal
myelitis, transverse
myelomalacia
myeloneuropathy
myelopathy
myelopathy, chronic progressive
myoclonus
myopathy
myopia
myotonia
nausea and vomiting
nerve biopsy
nerve conduction studies
nerve root enhancement
neuroaxonal dystrophy
neuroaxonal leukodystrophy
neurocutaneous disease
neuroendocrinology
neurogenic bladder
neuroichthyosis
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic examination
neuromuscular disease, electrodiagnosis of
neuromyelitis optica (Devic's disease)
neuromyelitis optica spectrum disorder
neuromyelitis optica, IgG
neuronal intranuclear inclusion disease
neuropathology
neuropathology, brain
neuropathy
neuropathy, demyelinating
neuropathy, hereditary peripheral
neuropathy, peripheral
neuropathy, sensory
next-generation sequencing
NOTCH2NLC
Notch3 gene
nystagmus
nystagmus, rotary
oculodentodigital dysplasia
old age, neurology of
ophthalmoplegia
optic ataxia
optic atrophy
optic atrophy, bilateral
optic neuritis
optic neuritis, bilateral
optic neuropathy
overlap syndrome
owl's eye sign of spinal cord
pain
pain, abdominal
pain, back
pain, foot
palatal myoclonus
palmoplantar keratoderma
paralysis
paralysis, recurrent
paraparesis
paraparesis, familial spastic
paraparesis, spastic
paraparesis, spastic, tropical
Parkinson disease
Parkinson disease, arteriosclerotic
Parkinsonism syndrome
PAS positive
PAS positive material in the brain
Pelizaeus Merzbacher
peroxisomal disease
personality change
pes cavus
phenylketonuria
photosensitivity, skin
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
poison, neurologic problems with
POLR3B
polyglucosan body
polyglucosan body disease
polymerase chain reaction
polyneuropathy
pons, lesion of
posterior fossa, lesion of
posterior leukoencephalopathy syndrome
pregnancy, neurologic complications in
prenatal
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
primary familial brain calcification
prognosis
progressive neurologic disorder
propionic aciduria
proximal myotonic myopathy
pseudobulbar palsy
pseudohypoparathyroidism
pseudoxanthoma elasticum
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychological testing, neurologic problems
psychomotor retardation
psychosis
psychotic behavior
ptosis
pupil, dilated, bilateral
pupil, dilated, episodic
putamen, lesion of, bilateral
pyramidal
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quadriplegia
quadriplegia, transient
radiculopathy
ragged-red fibers
rash
recurrent
red eye
Red flags
release phenomena
retina, abnormal
retinal degeneration
retinal lesion
retinopathy
retrovirus
reversible neurologic disorder
review article
RFLPs
rigidity
Rosenthal fibers
saccadic eye movements, abnormal
sarpropterin
Saudi Arabia
Schilder's disease
schizophrenia
screening
seizure
seizure, drug resistance
self-mutilation
sensorineural hearing loss
sensory loss
short stature
Sjogren-Larsson syndrome
skin, biopsy
skin, darkening of
skin, lesions in neurologic disorders
skull bone, thickening
small vessel disease
small vessel disease, cerebral
somatosensory evoked potentials
spastic diplegia
spasticity
speech disorder, childhood
spinal cord, lesion of
spinocerebellar ataxia
splenium of corpus callosum
spondylolysis
spondylosis
spongy degeneration of brain
spontaneous remission
staggering
startle reaction
stem cell transplantation
steroid therapy, CNS treatment and complications with
stooped posture
striatum, lesion of
striopallidodentate calcifications, familial idiopathic
strokelike episodes
subarachnoid hemorrhage
subcortical U fibers
subdural hematoma
substantia nigra
succinate dehydrogenase deficiency
sural nerve
symmetric brain lesions
syndactyly
systemic illness
tandem gait, ataxic
teeth, abnormal
teeth, number of in infants
temporal lobe, lesion, bilateral
testicular biopsy
thalamus, lesion of
thalamus, lesion of-bilateral
titubation
tomaculous neuropathy
tongue, biting
transient ischemic attack
transient neurologic deficit
treatment of neurologic disorder
treatment resistant
tremor
tremor, cerebellar
tremor, intention
trichopoliodystrophy
trinucleotide repeats
umbilical-cord blood transplantation
unconsciousness
unconsciousness, transient
urea-cycle enzymopathies
urinary incontinence
urine test for metabolic disorders
vanishing white matter
vasculitides
vasculopathy
very long chain fatty acids
vibratory sensation, abnormal
visceral neuropathy
vision loss, sequential
visual acuity, decreased
visual loss
visual loss, progressive
visual loss, slow
visual loss, sudden
vitamin E deficiency
walking, difficulty with
water channel antibodies
weakness
weakness, generalized
weakness, progressive
weaning from respirator, failure to
wheelchair
white matter disease
white matter disease, location
white matter disease, pattern
white matter disease, subcortical
white matter disease, unilateral
workup
writing
X-linked neuropathy
Showing articles 400 to 450 of 2939 << Previous Next >>

Treatment-Induced Leukoencephalopathy in Primary CNS Lymphoma,A Clinical and Autopsy Study
Neurol 62:451-456, Lai,R.,et al, 2004

Reversible Leukoencephalopathy Associated with Cerebral Amyloid Angiopathy
Neurol 62:494-497, Oh,U.,et al, 2004

Migraine as a Risk Factor for Subclinical Brain Lesions
JAMA 291:427-434, Kruit,M.C.,et al, 2004

MRI Findings in Susac's Syndrome
Neurol 61:1783-1787, Susac,J.O.,et al, 2003

Leukoencephalopathy with Vanishing White Matter: An Adult Onset Case
Neurol 61:1818-1819, Biancheri,R.,et al, 2003

Acute Carbon Monoxide Poisoning: Diffusion MR Imaging Findings
AJNR 24;1475-1477, Sener,R.N., 2003

A Longitudinal Study of Gait and Balance Dysfunction in Normal Older People
Arch Neurol 60:835-839, Baloh,R.W.,et al, 2003

Subcortical White Matter Infarcts, Comparison of Superficial Perforating Artery and Internal Border-Zone Infarcts Using Diffusion-Weighted Magnetc Resonance Imaging
Stroke 34:2630-2635, Lee,P.H.,et al, 2003

Acute Marchiafava-Bignami Disease: MR Findigns in Two Patients
AJNR 24:1955-1957, Arbelaez,A.,et al, 2003

Dirty-Appearing White Matter in Multiple Sclerosis: Volumetric MR Imaging and Magnetization Transfer Ratio Histogram Analysis
AJNR 24:1935-1940,1929, Ge,Y.,et al, 2003

Symmetric Deep Cerebellar Lesions After Smoking Heroin
Arch Neurol 60:1605-1606, Ropper,A.H. &Blair,R., 2003

Hereditary Infantile Hemiparesis, Retinal Arteriolar Tortuosity, and Leukoencephalopathy
Neurol 60:57-63,8, Vahedi,K.,et al, 2003

"CADASIL Coma"" An Underdiagnosed Acute Encephalopathy
JNNP 74:249-252, Schon,F.,et al, 2003

Rasmussen's Encephalitis
Neurol 60:422-425, Granata,T.,et al, 2003

Acute Hemorrhagic Leukoencephalitis vs ADEM: FLAIR MRI and Neuropathology Findings
Neurol 60:721-722, Kuperan,S.,et al, 2003

Diffusion-Weighted MR Findings in Isolated Angilitis of the Central Nervous System (IACNS)
Acta Neurol Scand 108:346-351, Lee, S.-Y.,et al, 2003

Silent Infarcts Demonstrated by Diffusion-Weighted MRI in CADASIL
Eur Neurol 49: 178-180, Moon,S.Y.,et al, 2003

Conventional and Diffusion-Weighted MRI in the Evaluation of Methanol Poisoning
Acta Radiologica 44:691-695, Server, A.,et al, 2003

Angiotropic Large Cell Lymphoma with Imaging Characteristics of CNS Vasculitis
AJNR 23:239-242, Song,D.K.,et al, 2002

Clinicopath Conf., Acute Disseminated Encephalomyelitis
NEJM 347:1433-1440, Case 34-2002, 2002

Incidental Findings on Pediatric MR Images of the Brain
AJNR 23:1674-1677, Kim,B.S.,et al, 2002

Adult Onset Glutaric Aciduria Type I Presenting with a Leukoencephalopathy
Neurol 59:1802-1804, Bahr,O.,et al, 2002

A Case Suspected of Acute Gas Poisoning by Carbon Monoxide (CO), Presenting with Progressive Diffuse Leukoencephalopathy Associated with Marked Brain Edema
No To Shinkei 54:493-497, Akaiwa,Y.,et al, 2002

Diffusion-Weighted MR Imaging Findings in Carbon Monoxide Poisoning
Neuroradiology 44:109-113, Teksam,M.,et al, 2002

White Matter Hyperintensities and Neuropsychological Outcome Following Carbon Monoxide Poisoning
Neurol 58:1525-1532, Parkinson,R.B.,et al, 2002

Gluten Sensitivity as a Neurological Illness
JNNP 72:560-563, Hadjivassiliou,M.,et al, 2002

Cerebral White Matter Lesions, Retinopathy, and Incidenc Clinical Stroke
JAMA 288:67-74, Wong,T.Y.,et al, 2002

Cranial MR Findings in Chronic Toluene Abuse by Inhalation
AJNR 23:1173-1179,1072, Aydin, K.,et al, 2002

Normalization of T2 Signal Abnormalities in Hemispheric White Matter with Liver Transplant
Neurol 59:335-341, Rovira,A.,et al, 2002

Radiotherapy-induced Cerebral Abnormalities in Patients with Low-grade Glioma
Neurol 59:121-123,8, Postma,T.J.,et al, 2002

Lesions of the Corpus Callosum: MR Imaging and Differential Considerations in Adults and Children
AJR 179:251-257, Bourekas,E.C.,et al, 2002

Subcortical Lacunar Lesions:An MR Imaging Finding in Patients with Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
Radiology 224:791-796, van den Boom, R., et al, 2002

Out of Africa, Trypanosomiasis
NEJM 347:749-753, Sahlas,D.J.,et al, 2002

Neurological Presentation of Fabry's Disease in a 52 Year Old Man
JNNP 73:340-342, Mohanraj,R.,et al, 2002

Familial Dementia With Lewy Bodies
Arch Neurol 59:1622-1630, Tsuang,D.W.,et al, 2002

Metachromatic Leukodystrophy:Diffusion MR Imaging Findings
AJNR 23:1424-1426, Sener,R.N., 2002

The Neurological Masquerade of Intravascular Lymphomatosis
Arch Neurol 59:439-443, Beristain,X.&Azzarelli,B., 2002

Mutations in Each of the Five Subunits of Translation Initiation Factor eIF2B Can Cause Leukoencephalopathy with Vanishing White Matter
Ann Neurol 51:264-270, van der Knaap,M.S.,et al, 2002

Homocysteine, Silent Brain Infarcts, and White Matter Lesions: The Rotterdam Scan Study
Ann Neurol 51:285-289,279, Vermeer,S.E.,et al, 2002

Subacute Sclerosing Panencephalitis Clinical and Magnetic Resonance Imaging Evaluation of 36 Patients
J Child Neurol 17:25-29, Ozturk, A.,et al, 2002

Subacute Sclerosing Panencephalitis
Postgrad Med J 78:63-70, Garg, R.K.,et al, 2002

Toxic Leukoencephalopathy
NEJM 345:425-432, Filley,C.M. &Kleinschmidt-DeMasters,B.K., 2001

Acute Disseminated Encephalomyelitis as Manifestation of Primary HIV Infection
Neurol 57:1493-1496, Narciso,P.,et al, 2001

Alexander Disease: Diagnosis with MR Imaging
AJNR 22:541-552, van der Knaap,M.S.,et al, 2001

Neuronal Damage in the Interval From of CO Poisoning Determined by Serial Diffusion Weighted Magnetic Resonance Imaging Plus H-magnetic Resonance Spectroscopy
JNNP 71:250-253, Murata,T.,et al, 2001

Brain Magnetic Resonance Imaging in 23 Patients with Mucopolysaccharidoses and the Effect of Bone Marrow Transplantation
Ann Neurol 50:79-92, Seto,T.,et al, 2001

Transient MR Signal Changes in Patients with Generalized Tonic-Clonic Seizure or Status Eiplepticus: Periictal Diffusion-weighted Imaging
AJNR 22:1149-1160, Kim,J.,et al, 2001

Cerebral Amyloid Angiopathy Presenting as Nonhemorrhagic Diffuse Encephalopathy: Neuropathologic and Neuroradiologic Manifestations in One Case
AJNR 22:1072-1076, Caulo,M.,et al, 2001

MR Imaging in Comatose Survivors of Cardiac Resuscitation
AJNR 22:1561-1565, Wijdicks,E.F.M.,et al, 2001

MRI Hyperintensities of the Temporal Lobe and External Capsule in Patients with CADASIL
Neurol 56:628-634, O'Sullivan,M.,et al, 2001



Showing articles 400 to 450 of 2939 << Previous Next >>