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Differential
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abdominal cramps
abducens nerve paralysis
abscess, intracerebral
abscess, intracranial
abscess, perivalvular
acanthosis nigricans
acetazolamide
acetylcholinesterase
acetylcholinesterase deficiency
acid maltase deficiency
acid maltase deficiency, adult
acral sensory symptoms
activated protein C resistance
acute disseminated encephalomyelitis
adverse drug reaction
akinetic mute
alcohol
alcohol injection
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
ANA
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
angiography, spinal
angioid streaks
anhidrosis
anterior spinal artery
antibiotic prophylaxis
antibiotics
antibiotics, neurologic complications with
anticoagulant, contraindications
anticoagulant, treatment
antiphospholipid antibodies
antithrombin III deficiency
anxiety
aortic valve, bicuspid
aortic valve, lesion of
aphasia
apraxia
arachnodactyly
areflexia
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, multiple
arteriovenous malformation, pulmonary
arteritis, temporal
arthralgia
aspirin
asymptomatic
ataxia
ataxia telangiectasia
ataxic gait
atherosclerosis, premature
atlanto-axial subluxation
atrial appendage closure
atrial fibrillation
atrial fibrillation, surgical treatment
atrial fibrillation, treatment
atrial myxoma
atrioventricular block
attention deficit disorder with hyperactivity
autoimmune disease
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
benign sexual headache
beta adrenergic blocker
Binswanger disease
bleeding disorder
blind spot, enlarged
blood dyscrasias, neurologic findings with
blue rubber bleb nevus syndrome
botulism
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
Brown Sequard syndrome
brucellosis
brucellosis, nervous system involvement with
bruising
bruit
bulbar palsy, acute
buphthalmos
burning paresthesia
cafe au lait spots
calcification, gyral
calcification, heart
calcification, intracranial
calcification, muscle
calcium oxalate crystals
calf hypertrophy
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, emission
CAT scan, false negative
CAT scan, spine
cataracts
catecholamine
cavernous hemangioma
central nervous system, infection of
cerebellar hemangioma
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 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 vasculature, calcification
cerebral venous infarction
cerebral venous thrombosis
cerebral venous thrombosis, etiology
cerebritis
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, pressure increased
cerebrospinal fluid, red cells in
cerebrospinal fluid, xanthochromia of
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, 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
cervical spine injury, compression
chest x-ray, abnormal
chiasmal syndromes
children
cholestanol
cholesterol
chorea
chromosomal abnormality
chromosome 11
chromosome 12
chromosome 19
chromosome 4
chromosome 5
chromosome 7
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
congenital myasthenic syndromes
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
Cowden syndrome
cranial nerves
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
cyanosis
cyst
cyst, peritumoral
cyst, neoplastic cerebellum
cystic infarction
cystinuria
D-dimer
deafness
deafness, bilateral progressive vs.unilateral acute
deafness, unilateral
deep gray nuclei
deficiency of ADA2
delay in diagnosis
dementia
dementia, cerebrovascular disease causing
dementia, rapidly progressive
dementia, subcortical
dementia, thalamic
demyelinating disease
dental procedure, neurologic complications with
depression
developmental abnormality of brain
developmental retardation
developmental venous anomalies
diabetes mellitus
diagnostic criteria
diaphragmatic paralysis
diarrhea
differential diagnosis
dilated aortic root
diplopia
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
Ehlers-Danlos syndrome, classification
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
empty sella
encephalitis
encephalitis, viral
encephalopathy
encephalopathy, metabolic
encephalopathy, neonatal
encephalopathy, progressive
endarterectomy, carotid
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
familial
familial hemiplegic migraine
familial mediterranean fever
fatigue
fever
fibrillations
fibrinogen
fibrinolytic agents, contraindications
fibromuscular dysplasia
fingers, abnormal
fistula, arterio-venous
fistula, arterio-venous, carotid-cavernous
fistula, arterio-venous, dural
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
Gilles de la Tourette syndrome
glaucoma
glioma
gram negative rod
granular osmiphilic material
granulomatosis with polyangiitis
granulomatous disease
gyrus, abnormal
hamartoma
headache
headache, positional
headache, sudden onset of
headache, throbbing
headache, thunderclap
headache, treatment of
headache, unilateral
headache, vascular
hearing loss
hearing loss, bilateral
heart block
heart block, complete
heart murmur
heart valve surgery
hemangioblastoma
hemangioma
hemangioma, facial
hemangioma, internal organs
hemangioma, leptomeningeal
hemangioma, skin
hemangioma, vertebral
hematuria, gross
hematuria, microscopic
hemianopia
hemianopia, homonymous
hemianopia, transient
hemidystonia
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
hepatomegaly
hepatosplenomegaly
heralding manifestation
hereditary hemorrhagic telangiectasia(HHT)
herpes simplex encephalitis
herpes simplex encephalitis, differential diagnosis of
heterotopia
HGPPS
Hispanics
HLA
homocystinuria
homovanillic acid
Horner's syndrome
HTRA1 gene
human genome
hydronephrosis
hypercalcemia
hypercholesterolemia
hypercoagulable state
hyperglycemia
hyperhidrosis
hyperhomocysteinemia
hyperlipidemia
hypernephroma
hyperpigmentation of skin
hypersomnia
hypertension
hypertension, cerebrovascular disease with
hypertrophic cardiomyopathy
hypogammaglobulinemia
hypoglossal nerve paralysis
hypogonadism
hyporeflexia
hypoxia
hypoxic encephalopathy
hypoxic-ischemic leukoencephalopathy
iatrogenic neurologic disorders
ileus, paralytic
imbalance
immunology and the nervous system
inborn errors of metabolism
incidental finding
inclusion bodies
inclusion bodies, intranuclear
inclusion body myositis
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
intracranial hypertension, benign
intracranial hypertension, benign, differential diagnosis
intracranial hypertension, benign, pathogenesis of
intracranial pressure, increased
intrauterine
intraventricular hemorrhage
iris, abnormal
irritability
joint hypermobility
Krabbe's disease
KRIT1 gene
kyphoscoliosis, neurologic causes of
lactic acidemia
lacunar infarction
L-dopa
left atrial appendage, percutaneous closure
leg numbness
leg weakness, bilateral
lens, dislocation of
lens, ectopic
leukodystrophy
leukoencephalopathy
leukopenia
level of consciousness, decreased
Lewy body
Lewy body disease, diffuse
Lhermitte-Duclos disease
lifestyle modification
lipid storage disorder of CNS
Lisch nodules
livedo reticularis
liver disease
long bone lesion
low back pain
lumbar puncture
lupus anticoagulant
lymphoma
lymphoma involving CNS
lymphomatoid granulomatosis
lysosomal storage disease
macrocephaly
malaise
malformation, CNS, congenital
malformation, vascular
malformation, vascular, cerebral
malformation, vascular, familial
malformation, vascular, screening for
malformation, vascular, treatment of
malformation, Vein of Galen
mania
manic-depressive
Marfan syndrome
marihuana
medulla oblongata
medulla oblongata, lesion of
medulla oblongata, malformation
melanomatosis, primary malignant
MELAS syndrome
memory, impairment of
meningeal enhancement
meningioma
meningitis
meningitis, brucellosis
menses
mental retardation
mental status, abnormal
metabolic disorder, primary
Mexican
Mexico
microangiopathy, brain
microhemorrhage, intracerebral
microspherophakia
middle cerebral artery territory infarction
middle cerebral artery, occlusion of
migraine
migraine with aura
migraine, hemiplegic
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
mitral valve lesion
mitral valve prolapse
molecular genetics
monoamines
mononeuropathy multiplex
mortality
motor neuron disease
movement disorder
moyamoya
moyamoya, adult
MRI
MRI, abnormal
MRI, angiography
MRI, black holes on
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, false negative
MRI, gradient-echo
MRI, incidental finding
MRI, serial
MRI, spinal cord
MRI, spine
MRI, susceptibility weighted
multiple endocrine neoplasia
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, familial
multiple sclerosis, misdiagnosis
multiple system atrophy
muscle atrophy, progressive
muscle biopsy
muscle hypertrophy
muscle weakness
muscle weakness, proximal
muscular dystrophy
myasthenia gravis
myasthenia gravis, congenital
myasthenia gravis, differential diagnosis
myasthenia gravis, distal weakness
myasthenia gravis, etiology of
myasthenia gravis, familial incidence of
myasthenia gravis, infantile and juvenile
myasthenia gravis, limb-girdle
myasthenia gravis, misdiagnosis of
myasthenia gravis, neonatal
myasthenia gravis, neuromuscular junction in
myasthenia gravis, receptor site in
myasthenia gravis, treatment of
myasthenic syndrome
myelinolysis, extrapontine
myelitis, longitudinal
myelopathy
myelopathy, chronic progressive
myocardial abscess
myocardial infarction
myoclonus
myopathy
myopathy, inclusion body
myopathy, inclusion body, hereditary
myopathy, metabolic
myopathy, mitochondrial
myopathy, vacuolar
myopia
nausea and vomiting
neck pain
negative
neonatal epilepsy syndromes
neonatal epileptic encephalopathy
neoplasm, metastatic to CNS
neoplasm, primary of CNS
neoplasm, primary of CNS-surgical treatment of
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
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
optic atrophy
optic chiasm
optic nerve
optic nerve sheath fenestration
optic nerve, decompression of
optic nerve, lesion of
organ rupture
orgasm
ornithine transcarbamylase deficiency
orthopnea
osteogenesis imperfecta
osteoporosis
otosclerosis
oxalosis, primary
pacemaker, cardiac-transvenous
pain
pain, arm
pain, back
pain, flank
pain, head
pain, leg
palpitations
papilledema
paraparesis
paraparesis, spastic
paraplegia
Parkinson disease
Parkinson disease, arteriosclerotic
Parkinson disease, diagnosis
Parkinson disease, differential diagnosis of
Parkinson disease, drug induced
Parkinson disease, misdiagnosis
Parkinsonism multiple-system atrophy
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
phakomatoses
phenylketonuria
pheochromocytoma
platelet inhibiting drugs
pleocytosis of cerebrospinal fluid
pneumothorax
polycystic kidneys
polycythemia, primary
polycythemia, secondary
polymerase chain reaction
polymicrogyria
polymyositis
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
prognathism
prognosis
progressive neurologic disorder
progressive supranuclear palsy
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 hypertension
pulmonary infiltrates
pyramidal tract dysfunction
pyramidal tract, uncrossed
quadriparesis
quadriplegia
radiation therapy, CNS treatment and complications with
radiation therapy, stereotactic
ragged-red fibers
rash
recurrent
Red flags
renal cell carcinoma
renal cyst
renal failure
renal infarct
renal stones
research
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
rheumatoid arthritis
rheumatoid arthritis, neurologic complications of
Riley-Day syndrome
risk factors
risk factors, modification
risk-benefit assessment
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
sensory level
sexual intercourse
short stature
shunt procedure, lumboperitoneal
sibling
sick sinus syndrome
sickle cell disease
skin, biopsy
skin, darkening of
skin, hyperextensible
skin, lesions in neurologic disorders
skin, thin
skin, translucent
skull x-ray, abnormal
slit lamp examination
small vessel disease
Sneddon's syndrome
speech disorder
spinal cord
spinal cord, cervical
spinal cord, compression of
spinal cord, extramedullary cyst of
spinal cord, infarction of
spinal cord, injury of
spinal cord, ischemic lesion of
spinal cord, lesion of
spinal cord, neoplasm
spinal cord, vascular disorders Affecting
spinal cord, vascular malformation of
splenomegaly
spondylosis
spontaneous remission
staphylococcus aureus
stare
stent, venous sinus
stereotaxic surgery
steroid
steroid therapy, CNS treatment and complications with
straight sinus
streptococcal infection
streptococcus viridans
stridor
strokelike episodes
Sturge-Weber syndrome
subarachnoid hemorrhage
subarachnoid hemorrhage, familial
subarachnoid hemorrhage, prognosis
subarachnoid hemorrhage, recurrent
subdural hematoma
sudden death
superior sagittal sinus thrombosis
sweating
sweating, abnormality of
symmetric brain lesions
syncope
syringomyelia
systemic illness
systemic lupus erythematosus
systemic lupus erythematosus, neurologic complications with
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
thymoma
thyrotoxicosis
tinnitus
tissue plasminogen activator, intravenous
toe walking
tomaculous neuropathy
tongue, enlarged
tongue, weakness
top of the basilar syndrome
torticollis
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
venous hemangioma
vertebral-basilar insufficiency
vertigo
Virchow-Robin spaces, dilated
visual acuity, decreased
visual field defect
visual field testing
visual loss
visual loss, slow
visual loss, transient
vital capacity
vitreous opacities
Von Hippel Lindau
walking, difficulty with
Watchman device
weakness
weakness, progressive
weight loss
Wernicke's encephalopathy
wheelchair
white matter disease
white matter disease, location
white matter disease, subcortical
Williams syndrome
winging of scapula
workup
wound healing, poor
xerostomia
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Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
Neurol 100:766-783, Manini,A.,&Pantoni,L., 2023

Neonatal Seizures
NEJM 388:1692-1700, Ropper.A.H., 2023

Hereditary Hemorrhagic Telangiectasia, Clinical Presentations, and Management
Stroke 54:e512-e515, Silveira,L.,et al, 2023

Clinicopathologic Conference, Vascular Ehlers-Danlos Syndrome
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High Prevalence of Spinal Cord Cavernous Malformations in the Familial Cerebral Cavernous Malformations
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Smoking Causes Fatal Subarachnoid Hemorrhage
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Recurrent Cerebral Ischemia During Pregnancies
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A 14-Year-Old Girl with Headache, Seizures, and Confusion
Neurol 92:e161-e167, Xiao, L.,et al, 2019

Ehlers-Danlos Syndromes
BMJ 366:I4966, Ghali, N.,et al, 2019

Cranial Cavernous Malformations
Stroke 49:1029-1035, Stapleton, C.J. & Barker, F.G., 2018

Sudden-Onset Pulsatile Headache in a Previously Healthy Young Man
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Clinicopathologic Conference, Vascular Malformations in Liver, Stomach, Esophagus, and Lungs that are Consistent with Hereditary Hemorrhagic Telangiectasia, Complicated
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Neurological Management of Von Hippel-Lindau Disease
Neurologist 21:73-78, Hodgson, T.S.,et al, 2016

Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency
NEJM 375:1879-1890, Case 34-2016, 2016

A 44-Year-Old Man with Eye, Kidney, and Brain Dysfunction
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Mystery Case: A 21-Year-Old Man with Visual Loss Following Marijuana Use
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Corticosteroid-Induced Paraplegia - A Diagnostic Clue for Spinal Dural Arterial Venous Fistula
JAMA Neurol 72:833-834, Hocker, S., 2015

Percutaneous Left Atrial Appendage Closure:Technical Aspects and Prevention of Periprocedural Complications with the Watchman Device
Workd J Cardiol 26:65-75, Mobius-Winkler,S.,et al, 2015

Sturge-Weber Syndrome
UptoDate , Nov, Bodensteiner, J.B., 2014

Disturbances of Cerebrospinal Fluid, Including Hydrocephalus, Pseudotumor Cerebri, and Low-Pressure Syndromes, Pseudotumor Cerebri
Adams & Victors Principles of Neurology, Chp 30, pg 628, Ropper, A.H.,et al, 2014

Vertebral Artery Dissection in Patients with Autosomal Dominant Polycystic Kidney Disease
J Stroke Cerebrovasc Dis 23:441-443, Kuroki, T.,et al, 2014

Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
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Sturge-Weber Syndrome
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Cerebral Amyloid Angiopathy
eMedicine, Jan, Menon, R.S., 2012

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Stroke 43:2871-2876, Pescini, F.,et al, 2012

Screening Patients with a Family History of Subarachnoid Haemorrhage for Intracranial Aneurysms: Screening Uptake, Patient Characteristics and Outcome
JNNP 83:86-88, Miller, T.D.,et al, 2012

Brain Arteriovenous Malformation Multiplicity Predicts the Diagnosis of Hereditary Hemorrhagic Telangiectasia Quantitive Assessment
Stroke 43:72-78, Bharatha, A.,et al, 2012

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

An unusual cause of stroke and hypoxia
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Pediatric Moyamoya Disease: An Analysis of 410 Consecutive Cases
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A Hereditary Moyamoya Syndrome With Multisystemic Manifestations
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Update on the Natural History of Cavernous Malformations and Factors Predicting Aggressive Clinical Presentation
Neurosurg Focus 29:E7, Washington,C.W.,et al, 2010

Comparison of Clinical, Familial, and MRI Features of CADASIL and NOTCH3-Negative Patients
Neurol 74:57-63, Pantoni,L.,et al, 2010

Familial Versus Sporadic Cavernous Malformations: Differences in Developmental Venous Anomaly Association and Lesion Phenotype
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Familial Mediterranean Fever and Central Nervous System Involvement: A Case Series
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Optimal Screening Strategy for Familial Intracranial Aneurysms: A Cost-Effectiveness Analysis
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Clinicopath Conf, Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL)
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Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease
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Genomewide Association Studies of Stroke
NEJM 360:1718-1728, Ikram,M.A.,et al, 2009

Decoding Cryptogenic Cardioembolism
Ann Neurol 64:364-365, Meschia,J.F., 2008

Pulmonary Arteriovenous Malformations in Hereditary Hemorrhagic Telangiectasia: A Series of 126 Patients
Medicine 86:1-7, Cottin,V.,et al, 2007

Differential Diagnosis of Bilateral Thalamic Lesions
Clin Neuroradiol 17:3-22, Linn,J.,et al, 2007

Prevalence of Fabry Disease in Patients with Cryptogenic Stroke: A Prospective Study
Lancet 366:1794-1796,1754, Rolfs,A.,et al, 2006

Metabolic Disease and Stroke: MELAS
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Brain Magnetic Resonance Imaging in Patients with Cowden Syndrome
Medicine 84:129-136, Lok,C.,et al, 2005

Phaeochromocytoma
Lancet 366:665-675, Lenders,J.W.M.,et al, 2005

Migraine and Cerebral White Matter Lesions
The Neurologist 11:19-29, Gladstone,J.P. &Dodick,D.W., 2005

Psychosocial Impact of Screening for Intracranial Aneurysms in Relatives with Familial Subarachnoid Hemorrhage
Stroke 36:836-840, Wermer,M.J.H.,et al, 2005

Value of Gradient-Echo Magnetic REsonance Imaging in the Diagnosis of Familial Cerebral Cavernous Malformation
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