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Differential
(Click to cross reference)
abdominal cramps
abducens nerve paralysis
abscess, intracerebral
abscess, intracranial
abscess, perivalvular
acid maltase deficiency
acid maltase deficiency, adult
acral sensory symptoms
activated protein C resistance
acute disseminated encephalomyelitis
akinetic mute
alcohol
algorithm
alopecia
alpha galactosidase A deficiency
Alzheimer's disease
aminoacidopathies
ammonia
amnestic syndrome
amyloid
amyloid angiopathy, cerebral
amyloid angiopathy, cerebral, Dutch type
amyloid angiopathy, hereditary cystatin C
amyloidosis
amyloidosis, oculoleptomeningeal, familial
anatomy of
anemia
aneurysm
aneurysm, asymptomatic
aneurysm, berry
aneurysm, intracranial
aneurysm, intracranial, familial
aneurysm, intracranial, screening for
aneurysm, intracranial, treatment of
aneurysm, multiple intracranial
aneurysm, size
aneurysm, unruptured
angina pectoris
angiography, cerebral
angiography, posterior fossa
angioid streaks
anhidrosis
antibiotic prophylaxis
anticoagulant, contraindications
anticoagulant, treatment
antiphospholipid antibodies
antithrombin III deficiency
anxiety
aortic valve, bicuspid
aortic valve, lesion of
aphasia
apraxia
arachnodactyly
arm weakness
arrhythmia, cardiac
arterial dissection
arterial dissection, aorta
arterial dissection, carotid
arterial dissection, intracranial
arterial dissection, multiple
arterial dissection, recurrent
arterial dissection, renal artery
arterial dissection, ruptured
arterial dissection, vertebral
arteriopathy
arteriovenous malformation
arteriovenous malformation, cerebral
arteriovenous malformation, pulmonary
arteritis, temporal
arthralgia
aspirin
asymptomatic
ataxia
ataxia telangiectasia
ataxia, progressive
ataxic gait
atherosclerosis, premature
atrial appendage closure
atrial fibrillation
atrial fibrillation, surgical treatment
atrial fibrillation, treatment
atrial myxoma
atrioventricular block
attention deficit disorder with hyperactivity
autonomic dysfunction
Babinski sign
bacterial endocarditis, neurologic manifestations of
bacterial infection
bacterial infection, CNS
basal ganglia, calcification of
basal ganglia, infarction
basal ganglia, lesion of
basilar impression
behavioral disorder
benign essential tremor
Binswanger disease
bleeding disorder
blood dyscrasias, neurologic findings with
bradycardia
brain atrophy
brain biopsy
brain purpura
brain scan, abnormal
brainstem, dysfunction
brainstem, hypoplasia
brainstem, infarction of
brainstem, lesion of
brainstem, malformation
brainstem, neoplasms of
brainstem, vascular malformation of
brucellosis
brucellosis, nervous system involvement with
bruising
bruit
buphthalmos
burning paresthesia
cafe au lait spots
calcification, gyral
calcification, heart
calcification, intracranial
calcification, muscle
calcium oxalate crystals
calf hypertrophy
Canavan's disease
capillary blush
carcinoma
carcinoma of pancreas
cardiac surgery
cardiomegaly
cardiomyopathy
caries
carotid angiogram
carotid artery disease
carotid artery occlusion, bilateral
carotid artery occlusion, intracranial
CAT scan
CAT scan, abnormal
CAT scan, abscess, cerebral
CAT scan, angiography
CAT scan, chest
CAT scan, disappearing lesion on
CAT scan, emission
CAT scan, false negative
cataracts
catecholamine
cavernous hemangioma
central nervous system, infection of
cerebellar atrophy, primary
cerebellar hemorrhage
cerebellar infarction
cerebellar peduncle
cerebellum, neoplasms of
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 edema, vasogenic
cerebral embolism
cerebral embolism, cardiac origin
cerebral embolism, carotid origin
cerebral infarction
cerebral infarction, hemorrhagic
cerebral infarction, small, deep
cerebral infarction, subcortical
cerebral ischemia
cerebral palsy
cerebral palsy, risk factors
cerebral peduncle
cerebral vasculature, calcification
cerebral venous infarction
cerebral venous thrombosis
cerebral venous thrombosis, etiology
cerebritis
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, red cells in
cerebrotendinous xanthomatosis
cerebrovascular accident
cerebrovascular accident, bilateral
cerebrovascular accident, cardiac disease causing
cerebrovascular accident, cryptogenic
cerebrovascular accident, etiology
cerebrovascular accident, familial occurrence
cerebrovascular accident, genetic
cerebrovascular accident, infancy and childhood
cerebrovascular accident, intrauterine
cerebrovascular accident, location of
cerebrovascular accident, mimics
cerebrovascular accident, multiple
cerebrovascular accident, neonatal
cerebrovascular accident, non atherosclerotic cause of
cerebrovascular accident, nonvascular territory
cerebrovascular accident, prevention of
cerebrovascular accident, recurrent
cerebrovascular accident, women
cerebrovascular accident, work up for
cerebrovascular accident, young adult
cerebrovascular disease
cerebrovascular disease, cardiovascular disease with
cerebrovascular disease, risk factors in
cerebrovascular disease, surgical treatment of
Charcot-Marie-Tooth
chest x-ray, abnormal
children
cholestanol
cholesterol
chorea
chromosomal abnormality
chromosome 11
chromosome 12
chromosome 19
chromosome 4
chromosome 5
chromosome 9
chronic progressive external ophthalmoplegia
cigarette smoking
cirrhosis
Clinical Pathologic Conference(C.P.C.)
clubbing of fingers
coagulopathy
codfish vertebrae
cognition
coin lesion on chest X-ray
collagen vascular disease
collateral circulation
coma
complications
compression neuropathy
confusion
congenital heart disease
congenital malformation
congestive heart failure
consanguinity
constipation
contractures, joint
contraindications
controversies in neurology
cornea, abnormal
cornea, opacity of
corneal dystrophy
coronary artery disease
corpus callosum
corpus callosum, infarction of
corpus callosum, lesion of
cortical blindness
cortical blindness, transient
cost effectiveness
cough
coumarin
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
Creutzfeldt-Jakob disease, genetic
cultured skin fibroblasts
cyanosis
cystic infarction
cystinuria
D-dimer
deafness
deafness, bilateral progressive vs.unilateral acute
deafness, unilateral
deep gray nuclei
deficiency of ADA2
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, cerebrovascular disease causing
dementia, rapidly progressive
dementia, subcortical
dementia, thalamic
demyelinating disease
dental procedure, neurologic complications with
dentate nuclei
dentate nuclei, lesion of
depression
developmental abnormality of brain
developmental retardation
developmental venous anomalies
diagnostic criteria
diaphragmatic paralysis
diarrhea
differential diagnosis
dilated aortic root
diplopia
diplopia, transient
disability rating scale, neurological
dizziness
DNA probes
dopamine
dural sinus thrombosis
Durett hemorrhages
dysarthria
dysmorphic
dyspnea
dyspraxia
dystonia
dystonia musculorum deformens
ear, pain in
early draining vein
echocardiogram
echocardiogram, contrast
echocardiogram, transesophageal, false negative
echocardiogram, transthoracic
echocardiogram, transthoracic, false negative
ectatic basilar artery
edema, pedal
Ehlers-Danlos syndrome
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electroencephalogram, monitoring, continuous
electroencephalogram, pediatric patients
electromyogram
electron microscopy
embolism
embolism, air
embolism, paradoxical
embolism, septic
embolism, systemic
embolization, therapeutic
emergencies, ocular
Emery-Dreifuss muscular dystrophy
emotional lability
encephalitis
encephalitis, viral
encephalopathy
encephalopathy, metabolic
encephalopathy, neonatal
encephalopathy, progressive
endocarditis
endocarditis, acute bacterial
endocarditis, prophylaxis
endovascular therapy
entrapment neuropathy
enzyme, defect
epidemiology of neurology
epileptic encephalopathy
episodic neurologic deficits
epistaxis
epistaxis, recurrent
esophageal varices
exercise intolerance
eye movement, disorders of
Fabry's disease
facial anomalies
facial appearance, abnormal
facial expression abnormality
facial hypoplasia
facial nerve palsy
facial nerve palsy, bilateral
facial nevus
Factor V Leiden
factor V, deficiency
factor VII, deficiency
Fahr disease
falling
false negative
familial
familial hemiplegic migraine
familial mediterranean fever
fever
fibrillations
fibrinogen
fibrinolytic agents, contraindications
fibromuscular dysplasia
fingers, abnormal
fistula, arterio-venous
fistula, arterio-venous, carotid-cavernous
fistula, arterio-venous, pulmonary
fluorescein angiography
foot drop
fourth ventricle, enlargement of
frontal bossing
fundus, abnormality of
gadolinium
gait disorder
galactosidase
gamma amino butyric acid
gangliosidosis GM2
gastrointestinal bleeding
gastrointestinal perforation
gaze palsy
gaze palsy, congenital horizontal
gaze palsy, horizontal
gaze palsy, horizontal-bilateral
gender
gene
gene mutation
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
genu of corpus callosum
Gilles de la Tourette syndrome
glaucoma
glioma
glutaric acidemia
gram negative rod
granular osmiphilic material
granulomatosis with polyangiitis
granulomatous disease
gyrus, abnormal
headache
headache, positional
headache, sudden onset of
headache, throbbing
headache, thunderclap
headache, unilateral
hearing loss
hearing loss, bilateral
heart block
heart block, complete
heart murmur
heart valve surgery
hemangioblastoma
hemangioma, facial
hemangioma, internal organs
hemangioma, leptomeningeal
hemangioma, skin
hematuria, gross
hematuria, microscopic
hemianopia
hemianopia, homonymous
hemianopia, transient
hemiparesis
hemiparesis, transient
hemiplegia
hemiplegia, congenital
hemoglobin abnormality, neurologic complications of
hemoptysis
hemorrhage, intracranial, newborn
hemorrhage, putamenal
hemorrhage, thalamic
hemorrhagic diathesis
hemorrhoids
hemosiderosis of CNS, superficial
hepatic encephalopathy
hepatic encephalopathy, treatment of
hepatic failure
hepatomegaly
hepatosplenomegaly
heralding manifestation
hereditary hemorrhagic telangiectasia(HHT)
herpes simplex encephalitis
herpes simplex encephalitis, differential diagnosis of
heterotopia
HGPPS
Hispanics
homocystinuria
homovanillic acid
Horner's syndrome
HTRA1 gene
human genome
hydronephrosis
hypercalcemia
hypercholesterolemia
hypercoagulable state
hyperhomocysteinemia
hyperlipidemia
hyperpigmentation of skin
hypersomnia
hypertension
hypertension, cerebrovascular disease with
hypertrophic cardiomyopathy
hypogammaglobulinemia
hypogonadism
hypoxia
hypoxic encephalopathy
hypoxic-ischemic leukoencephalopathy
ileus, paralytic
imbalance
impulsivity
inborn errors of metabolism
incidental finding
incoordination
infantile hemiplegia
infection
insulin resistance
intellectual deficit
intellectual deterioration
internuclear ophthalmoplegia
interobserver agreement
intracerebral hemorrhage
intracerebral hemorrhage, familial
intracerebral hemorrhage, lobar
intracerebral hemorrhage, recurrent
intracerebral hemorrhage, small
intracerebral hemorrhage, work up
intracerebral hemorrhage, young adult
intracranial hemorrhage
intrauterine
intraventricular hemorrhage
iris, abnormal
iron, brain
Jakob-Creutzfeldt disease
joint hypermobility
klippel feil syndrome
Krabbe's disease
KRIT1 gene
kyphoscoliosis, neurologic causes of
lactate
lactic acidemia
lacunar infarction
L-dopa
left atrial appendage, percutaneous closure
Leigh's disease
lens, dislocation of
lens, ectopic
leukodystrophy
leukoencephalopathy
leukopenia
level of consciousness, decreased
lifestyle modification
linear lesion
lipid storage disorder of CNS
Lisch nodules
livedo reticularis
liver disease
long bone lesion
low back pain
lupus anticoagulant
lymphoma
lymphoma involving CNS
lymphomatoid granulomatosis
lysosomal storage disease
macrocephaly
magnetic susceptibility
malaise
malformation, CNS, congenital
malformation, vascular
malformation, vascular, cerebral
malformation, vascular, familial
malformation, vascular, screening for
malformation, Vein of Galen
mania
manic-depressive
maple syrup urine disease
Marfan syndrome
marihuana
medulla oblongata
medulla oblongata, lesion of
medulla oblongata, malformation
melanomatosis, primary malignant
MELAS syndrome
memory, impairment of
meningeal enhancement
meningitis, brucellosis
mental retardation
mental status, abnormal
metabolic disorder, primary
methylene tetrahydrofolate reductase
metronidazole
Mexican
microangiopathy, brain
microhemorrhage, intracerebral
microspherophakia
midbrain, lesion of
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
middle cerebral artery territory infarction
middle cerebral artery, occlusion of
migraine
migraine with aura
migraine, hemiplegic
mimics
misdiagnosis
mitochondrial disease
mitochondrial disease, pathogenesis
mitochondrial encephalomyopathy
mitral valve lesion
mitral valve prolapse
molecular genetics
monoamines
mononeuropathy multiplex
monoparesis
mortality
motor cortex
motor neuron disease
movement disorder
moyamoya
moyamoya, adult
MRI
MRI pattern
MRI, abnormal
MRI, angiography
MRI, black holes on
MRI, CAT scan compared to
MRI, complications with
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, false negative
MRI, gradient-echo
MRI, incidental finding
MRI, paramagnetic effect
MRI, serial
MRI, spinal cord
MRI, susceptibility weighted
MRI, T1 weighted high signal foci
MRS
multiple endocrine neoplasia
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, familial
multiple sclerosis, misdiagnosis
muscle atrophy, progressive
muscle biopsy
muscle hypertrophy
muscle weakness
muscle weakness, proximal
muscular dystrophy
myasthenia gravis, differential diagnosis
myasthenia gravis, misdiagnosis of
myelinolysis, extrapontine
myelopathy
myocardial abscess
myocardial infarction
myoclonic jerks
myoclonus
myoclonus, cortical
myoclonus, stimulus sensitive
myopathy
myopathy, metabolic
myopathy, mitochondrial
myopathy, vacuolar
myopia
nausea and vomiting
neck pain
negative
neonatal epilepsy syndromes
neonatal epileptic encephalopathy
neoplasm, primary of CNS
nephrocalcinosis
nerve conduction studies
nerve root enhancement
neurocutaneous disease
neuroendocrinology
neurofibroma
neurofibromatosis 1
neurologic complications of, chronic pulmonary disease
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neurologic symptoms
neurologic testing
neuromuscular disease, electrodiagnosis of
neurons
neuroophthalmology
neuropathology
neuropathy
neuropathy, hereditary peripheral
neuropathy, peripheral
neuropathy, vasculitic, systemic
neurosis
neurotransmitter
next-generation sequencing
norepinephrine
normal
Notch3 gene
nystagmus
nystagmus, dissociated
nystagmus, vertical
obesity
occipital lobe
occipital lobe, infarction
occipital lobe, lesion of
ocular motility, disorders of
operculum syndrome
operculum syndrome, bilateral
ophthalmic artery occlusion
ophthalmoplegia
ophthalmoplegia, progressive external
optic atrophy
optic nerve, lesion of
organ rupture
ornithine transcarbamylase deficiency
orthopnea
osteogenesis imperfecta
osteoporosis
otosclerosis
oxalosis, primary
pacemaker, cardiac-transvenous
pain
pain, back
pain, flank
pain, head
palpitations
papilledema
paralysis
paralysis, recurrent
paraparesis
paraparesis, spastic
Parkinson disease
Parkinson disease, arteriosclerotic
Parkinsonism syndrome
paroxysmal neurologic deficits
PAS positive
PAS positive material in the brain
patent foramen ovale
patient information and support
pectus carinatum
pectus excavatum
pericardial effusion
peri-procedural
peroxisomal disease
personality change
phenylketonuria
pheochromocytoma
platelet inhibiting drugs
pleocytosis of cerebrospinal fluid
pneumothorax
POLG1 gene
polycystic kidneys
polycythemia, primary
polycythemia, secondary
polymerase chain reaction
polymicrogyria
polyneuropathy
pons, hypoplasia
pons, lesion of
port wine nevus
portal caval shunt
positive sharp waves
posterior cerebral artery territory infarction
posterior leukoencephalopathy syndrome
pregnancy, neurologic complications in
premature infant
prenatal diagnosis by amniocentesis
prethrombotic state
prevention of neurologic disorders
prion disease
prognathism
prognosis
progressive neurologic disorder
protein C deficiency
protein S deficiency
proteinuria
proximal muscle atrophy
pruritus
pseudobulbar palsy
pseudoxanthoma elasticum
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
psychosis, acute
psychosocial aspects
psychotic behavior
ptosis
pulmonary disease
pulmonary embolism
pulmonary infiltrates
pyramidal tract dysfunction
pyramidal tract, uncrossed
quadriparesis
quadriplegia, transient
radiation therapy, stereotactic
ragged-red fibers
rapidly progressing neurologic illness
rash
real-time quaking-induced conversion
recurrent
Red flags
renal cell carcinoma
renal cyst
renal failure
renal infarct
renal stones
respiratory failure
retinal artery tortuosity
retinal hemangioma
retinal hemorrhages
retinal ischemia
retinal lesion
retinal microvascular disease
retinal tumor
retinal vasculitis
retinal vasculopathy
retinal vasculopathy with cerebral leukodystrophy
retinopathy
reversible neurologic disorder
review article
Riley-Day syndrome
risk factors
risk factors, modification
risk-benefit assessment
Romberg's sign
root lesion, nerve
safety
Sandhoff's disease
Saudi Arabia
Schilder's disease
sclerae, blue
scoliosis
scoliosis, neurologic association with
screening
seizure
seizure, children
seizure, complications following
seizure, diagnosis of
seizure, etiology of
seizure, focal
seizure, intractable
seizure, neonatal
seizure, treatment of
seizure, workup of
sensorineural hearing loss
short stature
sibling
sick sinus syndrome
sickle cell disease
skin, biopsy
skin, hyperextensible
skin, lesions in neurologic disorders
skin, thin
skull x-ray, abnormal
slit lamp examination
small vessel disease
Sneddon's syndrome
speech disorder
spinal cord
spinal cord, compression of
spinal cord, infarction of
spinal cord, lesion of
spinal cord, neoplasm
spinal cord, vascular malformation of
splenium of corpus callosum
splenomegaly
spondylolysis
spondylosis
spontaneous remission
staphylococcus aureus
stare
stereotaxic surgery
steroid therapy, CNS treatment and complications with
straight sinus
streptococcal infection
streptococcus viridans
strokelike episodes
Sturge-Weber syndrome
subarachnoid hemorrhage
subarachnoid hemorrhage, familial
subarachnoid hemorrhage, prognosis
subarachnoid hemorrhage, recurrent
subcortical U fibers
subdural hematoma
sudden death
superior sagittal sinus thrombosis
sweating
sweating, abnormality of
symmetric brain lesions
syncope
synkinesis
systemic illness
tandem gait, ataxic
tardive dyskinesia
Tay-Sachs disease
telangiectases
telangiectases, retinal
temporal lobe, lesion
temporal lobe, lesion, bilateral
term infant
thalamic tumors
thalamic tumors, bilateral
thalamus
thalamus, infarction of
thalamus, infarction, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
thiamine deficiency
thromboangiitis obliterans cerebri
thrombocytopenia
thrombophlebitis
thrombotic thrombocytopenia purpura
tic
tinnitus
tissue plasminogen activator, intravenous
toe walking
tongue, enlarged
tongue, weakness
top of the basilar syndrome
torticollis
transient global amnesia
transient ischemic attack
transient ischemic attack, recurrent
transient neurologic deficit
trauma
treatment of neurologic disorder
tuberous sclerosis
twins
undiagnosed
upgaze, paralysis of
urea-cycle enzymopathies
uremia
urinary catecholamines
urinary incontinence
uveitis
varicose veins
vasculitides
vasculopathy
vasospasm, cerebral
vertebral-basilar insufficiency
vertigo
Virchow-Robin spaces, dilated
visual acuity, decreased
visual field defect
visual loss
visual loss, progressive
visual loss, slow
visual loss, transient
vital capacity
vitreous opacities
Von Hippel Lindau
walking, difficulty with
Watchman device
weakness
weakness, acute
weakness, focal
weakness, progressive
web sites
weight loss
Wernicke's encephalopathy
white matter disease
white matter disease, location
white matter disease, subcortical
wide based gait
Williams syndrome
winging of scapula
workup
wound healing, poor
Showing articles 50 to 100 of 8878 << Previous Next >>

Hyperhomocysteinemia, Low Folate and Vitamin B12 Concentrations, and Methylene Tetrahydrofolate Reductase Mutation in Cerebral Venous Thrombosis
Stroke 35:1790-1794, Cantu,C.,et al, 2004

Familial Leptomeningeal Amyloidosis With a Transthyretin Variant Asp18Gly Representing Repeated Subarachnoid Haemorrhages With Superficial Siderosis
JNNP 75:1463-1466, Jin,K.,et al, 2004

CADASIL: Cerebral Autosomal Subcortical Infarcts and Leukoecephalopathy
, Chabriat, H., Joutel A., Vahedi, K., Tournier-Lasserve, &E., Bousser M.G., 2004

Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy (CADASIL)
Pract Neurology 4:50-55, Razvi,S.S.M. &Muir,K.W., 2004

Neurobrucellosis:Clinical and Neuroimaging Correlation
AJNR 25:395-401, Al-Sous,M.W.,et al, 2004

Can We Prevent Cerebral Palsy?
NEJM 349:1765-1769, Nelson,K.B., 2003

Repeated Screening for Intracranial Aneurysms in Familial Subarachnoid Hemorrhage
Stroke 34:2788-2791, Wermer,M.J.H.,et al, 2003

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

New Players in the Genetics of Stroke
NEJM 347:1711-1712, Tournier-Lasserve,E., 2002

Subarachnoid Hemorrhage
Stroke 33:1321-1326, Kissela,B.M.,et al, 2002

A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
The Neurologist 8:302-312, Thambisetty,M.,et al, 2002

Clinical Profile of Stroke in 900 Patients with Hypertrophic Cardiomyopathy
J Am Coll Cardiol 39:301-307, Maron,B.J.,et al, 2002

Hypertrophic Cardiomyopathy A Systematic Review
JAMA 287:1308-1320, Maron, B.J., 2002

Is Patent Foramen Ovale a Family Trait?
Stroke 32:1563-1566, Arquizan,C.,et al, 2001

Advances in the Genetics of Cerebrovascular Disease and Stroke
Neurol 56:997-1008, Hademenos,G.J.,et al, 2001

Impact of the Human Genome Projects and Identification of a Stroke Gene
Stroke 32:1239-1241, Alberts,M.J., 2001

Cerebrovascular Manifestations in 321 Cases of Hereditary Hemorrhagic Telangiectasia
Stroke 32:877-882, Maher,C.O.,et al, 2001

Recommendations for the Management of Patients with Unruptured Intracranial Aneurysms
Stroke 31:2742-2750, Bederson,J.B.,et al, 2000

Familial Occipital Calcifications, hemorrhagic Strokes, Leukoencephalopathy, Dementia, and External Carotid Dysplasia
Neurol 55:1661-1667, Iglesias,S.,et al, 2000

Risk of Subarachnoid Haemorrhage in First Degree Relatives of Patients with Subarachnoid Haemorrhage: Follow Up Study Based on National Registries in Denmark
BMJ 320:141-145, Gaist,D.,et al, 2000

Angiographic and Clinical Characteristics of Patients with Cerebral Arteriovenous Malformations Associated with Hereditary Hemorrhagic Telangiectasia
AJNR 21:1016-1020, Matsubara,S.,et al, 2000

Presence of Diarrhea and Absence of Tendon Xanthomas in Patients With Cerebrotendinous Xanthomatosis
Arch Neurol 57:520-524, Verrips,A.,et al, 2000

Inborn Errors of Metabolism as a Cause of Neurological Disease in Adults: An Approach to Investigation
JNNP 69: 5-12, Gray,R.G.F. et al, 2000

Familial Form of Intracranial Cavernous Angioma:MR Imaging Findings in 51 Families
Radiology 214:209-216, Brunereau,L.,et al, 2000

De Novo Mutation in the Notch3 Gene Causing CADASIL
Ann Neurol 47:388-391, Joutel,A.,et al, 2000

Distribution of Cranial MRI Abnormalities in Patients with Symptomatic and Subclinical CADASIL
BJR 73:256-265, Coulthard, A.,et al, 2000

Bicuspid Aortic Valve - A Silent Danger: Analysis of 50 Cases of Infective Endocarditis
Clin Inf Dis 30:336-341, Lamas, C.C. & Eykyn, S.J., 2000

Aneurysms in Relatives of Patients with Subarachnoid Hemorrhage,Frequency and Risk Factors
Neurol 53:982-988, Raaymakers,T.W.M.&the MARS Study Group, 1999

Risks and Benefits of Screening for Intracranial Aneurysms in First-Degree Relatives of Patients with Sporadic Subarachnoid Hemorrhage
NEJM 341:1344-1350, The Magnetic Resonance Angiography in Relatives of, 1999

Familial Subarachnoid Hemorrhage, Outcome Study
Stroke 30:1099-1102, Ronkainen,A.,et al, 1999

Prethrombotic Disorders in Children with Arterial Ischemic Stroke and Sinovenous Thrombosis
Arch Neurol 56:967-971, Bonduel,M.,et al, 1999

Adult-Onset MELAS Presenting as Herpes Encephalitis
Arch Neurol 56:241-243, Sharfstein,S.R.,et al, 1999

MR Angiography as a Screening Tool for Intracranial Aneurysms:Feasibility, Test Characteristics, and Interobserver Agreement
AJR 173:1469-1475, Raaymakers,T.W.M.,et al, 1999

Middle Cerebral Artery Main Stem Thrombosis in Two Siblings with Familial Thrombotic Thrombocytopenic Purpura
Neurol 50:1157-1160, Kelly,P.J.,et al, 1998

Clinicopath Conf,Syndrome of Mitochondrial Encephalopathy,Lactic Acidosis,and Stroke-Like Episodes (MELAS),Case 39-1998
NEJM 339:1914-1923, , 1998

Initial and Follow-up Screening for Aneurysms in Families with Familial Subarachnoid Hemorrhage
Neurol 51:1125-1130, Raaymakers,T.W.M.,et al, 1998

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

Sneddon's Syndrome:Neuro-Ophthalmologic Manifestations in a Possible Autosomal Recessive Pattern
Neurol 51:1185-1187, Rehany,U.,et al, 1998

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

Inherited Prothrombotic States and Ischaemic Stroke in Childhood
JNNP 65:508-511, Ganesan,V.,et al, 1998

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

Familial Intracranial Aneurysms
Lancet 349:380-384, Ronkainen,A.,et al, 1997

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

Cerebral Venous Thrombosis:Role of Activated Protein C Resistance and Factor V Gene Mutation
Stroke 27:1719-1720, Brey,R.L.&Coull,B.M., 1996

Adult-Onset MELAS
Stroke 27:1420-1423, Gilchrist,J.M.,et al, 1996

Cerebrovascular Complications of Fabry's Disease
Ann Neurol 40:8-17, Mitsias,P.&Levine,S.R., 1996

Stroke in Williams Syndrome
Stroke 27:143-146, Wollack,J.B.,et al, 1996

Intracranial Aneurysms:MR Angiographic Screening in 400 Asymptomatic Individuals with Increased Familial Risk
Radiology 195:35-40, Ronkainen,A.,et al, 1995

Outcome in Familial Subarachnoid Hemorrhage
Stroke 26:961-963, Bromberg,J.E.C.,et al, 1995

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



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