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Differential
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acute disseminated encephalomyelitis
adrenoleukodystrophy
Alexanders disease
algorithm
amyloid angiopathy, cerebral
aneurysm, intracranial, familial
angiitis, granulomatous of CNS
angiitis, isolated of CNS
angiography, cerebral
anticoagulant, complications of
anxiety
aphasia
arrhythmia, cardiac
arteriopathy
asymptomatic
ataxia
atrial myxoma
atypical
B 12 deficiency
bacterial endocarditis, neurologic manifestations of
basal ganglia
basal ganglia, infarction
basal ganglia, lesion of
behavioral disorder
Behcet's syndrome
Binswanger disease
brain atrophy
brain biopsy
brain volume
brainstem, lesion of
calcification, intracranial
Canavan's disease
carbon monoxide poisoning
carotid artery stenosis
CAT scan
CAT scan, abnormal
central nervous system, infection of
central pontine myelinolysis
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortical atrophy
cerebral infarction
cerebral infarction, small, deep
cerebral infarction, subcortical
cerebral ischemia
cerebral venous thrombosis
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, genetic
cerebrovascular accident, location of
cerebrovascular accident, multiple
cerebrovascular accident, non atherosclerotic cause of
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
cerebrovascular disease
chemotherapy, CNS treatment and complications with
children
chromosomal abnormality
chromosome 19
cigarette smoking
Clinical Pathologic Conference(C.P.C.)
cocaine
cognition
coma
complications
confusion
confusional state, acute
corpus callosum
corpus callosum, infarction of
corpus callosum, lesion of
cortical blindness
cystic infarction
cytomegalovirus infection
deep gray nuclei
dementia
dementia, cerebrovascular disease causing
dementia, rapidly progressive
dementia, subcortical
demyelinating disease
depression
differential diagnosis
digital subtraction angiography
disability rating scale, neurological
dysarthria
electrocardiogram, abnormal
electroencephalogram, pediatric patients
electron microscopy
electroretinograph
emotional lability
encephalitis, human immunodeficiency virus type 1
encephalitis, viral
encephalopathy
encephalopathy, acute
endocarditis
endocarditis, infectious
external capsule
Fabry's disease
falling
false negative
familial
familial hemiplegic migraine
fever
gait disorder
gaze palsy, supranuclear
gene
gene mutation
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
gliomatosis cerebri
granular osmiphilic material
hallucination
head injury
headache
hearing loss
hemiparesis
heralding manifestation
herpes simplex encephalitis
human immunodeficiency virus type 1
hypertension
hypertensive encephalopathy
imbalance
intellectual deficit
internal carotid artery
intracerebral hemorrhage
intracerebral hemorrhage, lobar
intracerebral hemorrhage, recurrent
intracerebral hemorrhage, small
judgement, impaired
Krabbe's disease
lacunar infarction
L-dopa
leuko-araiosis
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
limbic encephalitis
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
mania
manic-depressive
MELAS syndrome
memory, impairment of
mesial temporal lobe
mesial temporal sclerosis
metachromatic leukodystrophy
microangiopathy, brain
microhemorrhage, intracerebral
middle cerebral artery territory infarction
middle cerebral artery, stenosis of
migraine
migraine with aura
migraine, hemiplegic
mimics
misdiagnosis
mitochondrial disease
movement disorder
moyamoya
MRI
MRI, abnormal
MRI, angiography
MRI, black holes on
MRI, diffusion tensor
MRI, diffusion weighted
MRI, gradient-echo
MRI, serial
MRI, volumetry
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, familial
multiple sclerosis, misdiagnosis
myocardial infarction
myoclonus
neoplasm, primary of CNS
neoplastic angioendotheliosis
neurologic disease, diagnoses of
neuropathology
neuropathy
next-generation sequencing
Notch3 gene
Notch3 gene, false negative
old age, neurology of
Parkinson disease
Parkinson disease, arteriosclerotic
Parkinson disease, L-dopa nonresponsive
Parkinsonism syndrome
PAS positive
PAS positive material in the brain
Pelizaeus Merzbacher
personality change
phenylketonuria
posterior leukoencephalopathy syndrome
postpartum
pregnancy, neurologic complications in
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
pseudobulbar palsy
pseudoxanthoma elasticum
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychosis
psychotic behavior
quadriparesis
radiation therapy, CNS treatment and complications with
Red flags
retina, abnormal
retinal lesion
retinopathy
reversible cerebral vasoconstrictive syndromes
reversible neurologic disorder
review article
risk factors
sarcoidosis
sarcoidosis, CNS
schizophrenia
screening
seizure
sickle cell disease
Sjogren's syndrome
Sjogren's syndrome, neurologic manifestations of
skin, biopsy
small vessel disease
small vessel disease, cerebral
spinal cord, infarction of
subarachnoid hemorrhage
subcortical U fibers
symmetric brain lesions
syncope
systemic lupus erythematosus
systemic lupus erythematosus, neurologic complications with
temporal lobe, lesion
temporal lobe, lesion, bilateral
thrombotic thrombocytopenia purpura
transient ischemic attack
transient ischemic attack, recurrent
treatment of neurologic disorder
treatment resistant
unconsciousness
urinary incontinence
vasculitides
vasculopathy
vertebral artery stenosis
vertigo
visual evoked response
walking, difficulty with
wheelchair
Whipple's disease
white matter disease
white matter disease, location
white matter disease, subcortical
white matter disease, unilateral
workup
Showing articles 50 to 63 of 63 << Previous

Quantitative MRI in CADASIL, Correlation with Disability and Cognitive Performance
Neurol 52:1361-1367, Dichgans,M.,et al, 1999

Cerebrospinal Fluid Findings in CADASIL
Neurol 53:233, Dichgans,M.,et al, 1999

Patterns of MRI Lesions in Cadasil
Neurol 51:452-457, Chabriat,H.,et al, 1998

Acute Leukoencephalopathies:Differential Diagnosis and Investigation
The Neurologist 4:148-166, Weinshenker,B.G.,et al, 1998

CADASIL in a North American Family:Clinical, Pathological, and Radiologic Findings
Neurol 51:844-849, Desmond,D.W.,et al, 1998

The Phenotypic Spectrum of CADASIL:Clinical Findings in 102 Cases,
Ann Neurol 44:731-739,715, Dichgans,M.,et al, 1998

Subcotical Arteriosclerotic Encephalopathy (Binswangers Disease)
, Ghika,J. &Bogousslavsky, J., 1998

Unusual Clinical Features and Early Brain MRI Lesions in a Family with Cerebral Autosomal Dominant Arteriopathy
Neurol 48:1200-1203, Malandrini,A.,et al, 1997

Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients
Lancet 350:1511-1515, 14901997., Joutel,A.,et al, 1997

Autosomal Dominant Migraine with MRI White-Matter Abnormalities Mapping to the CADASIL Locus
Neurol 45:1086-1091, Chabriat,H.,et al, 1995

Familial Hemiplegic Migraine and Autosomal Dominant Arteriopathy with Leukoencephalopathy (CADASIL)
Ann Neurol 38:817-824, Hutchinson,M.,et al, 1995

Clinical Spectrum of CADASIL:A Study of 7 Families
Lancet 346:934-939, Chabriat,H.,et al, 1995

New Phenotype of the Cerebral Autosomal Dominant Arteriopathy Mapped to Chromosome 19:Migraine as the Prominent Clinical Feature
JNNP 59:579-585, Verin,M.,et al, 1995

Progress in the Genetics of Cerebrovascular Disease Inherited Subcortical Arteriopathies
Stroke 25:1696-1698, Bowler,J.V.&Hachinski,V., 1994



Showing articles 50 to 63 of 63 << Previous