Neudle.com: malformation vascular familial

Differential
(Click to cross reference)

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

alpha galactosidase A deficiency

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, Dutch type

amyloid angiopathy, hereditary cystatin C

amyloidosis

amyloidosis, oculoleptomeningeal, familial

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

arterial dissection, aorta

arterial dissection, carotid

arterial dissection, cerebral

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

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

autism

autistic behavior

autoimmune disease

autonomic dysfunction

Babinski sign

bacterial endocarditis, neurologic manifestations of

bacterial infection

bacterial infection, CNS

basal ganglia, calcification of

basal ganglia, hemorrhage

basal ganglia, infarction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar impression

behavioral disorder

Behcet's syndrome

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

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

calcification, intracranial

calcification, muscle

calcium oxalate crystals

calf hypertrophy

capillary blush

carbon monoxide poisoning

carcinoma

carcinoma of pancreas

carotid artery disease

carotid artery occlusion, bilateral

carotid artery occlusion, intracranial

carotid artery stenosis, 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, isodense lesion with acute hemorrhage

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, deep

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

chromosomal abnormality

chronic progressive external ophthalmoplegia

cigarette smoking

cirrhosis

Clinical Pathologic Conference(C.P.C.)

coin lesion on chest X-ray

COL4A1 related disorder

collagen vascular disease

collateral circulation

compression neuropathy

confusion

congenital heart disease

congenital malformation

congenital myasthenic syndromes

congestive heart failure

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

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

cyanosis

cyst

cyst, peritumoral

cyst, neoplastic cerebellum

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

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

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

embolism, paradoxical

embolism, septic

embolism, systemic

embolization, therapeutic

emergencies, ocular

Emery-Dreifuss muscular dystrophy

emotional lability

empty sella

encephalitis

encephalitis, Japanese

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

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

familial

familial hemiplegic migraine

familial mediterranean fever

fibrinolytic agents, contraindications

fibromuscular dysplasia

fingers, abnormal

fistula, arterio-venous

fistula, arterio-venous, carotid-cavernous

fistula, arterio-venous, dural

fistula, arterio-venous, pulmonary

flavivirus

fluorescein angiography

foot drop

fourth ventricle, enlargement of

frontal bossing

frontal lobe, behavior with disease of

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

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

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

hemangioma, brainstem

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

hepatolenticular degeneration(Wilson's disease)

hepatomegaly

hepatosplenomegaly

heralding manifestation

hereditary hemorrhagic telangiectasia(HHT)

herpes simplex encephalitis

herpes simplex encephalitis, differential diagnosis of

hypercoagulable state

hyperpigmentation of skin

hypersomnia

hypertension

hypertension, cerebrovascular disease with

hypertrophic cardiomyopathy

hypocalcemia

hypogammaglobulinemia

hypoglossal nerve paralysis

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

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

Jakob-Creutzfeldt disease

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

level of consciousness, decreased

Lewy body

Lewy body disease, diffuse

Lhermitte-Duclos disease

lifestyle modification

lipid storage disorder of CNS

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

medulla oblongata, lesion of

medulla oblongata, malformation

megalencephaly

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

middle cerebral artery, stenosis of

mitochondrial disease

mitochondrial encephalomyopathy

mitral valve lesion

mitral valve prolapse

molecular genetics

monoamines

mononeuropathy multiplex

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, 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

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

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, vasculitic, systemic

neurosis

neurotoxin

neurotransmitter

next-generation sequencing

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

optic nerve sheath fenestration

optic nerve, decompression of

optic nerve, lesion of

organ rupture

orgasm

ornithine transcarbamylase deficiency

orthopnea

osmotic demyelination syndrome

osteogenesis imperfecta

osteoporosis

otosclerosis

oxalosis, primary

pacemaker, cardiac-transvenous

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

platelet inhibiting drugs

pleocytosis of cerebrospinal fluid

pneumothorax

poison, neurologic problems with

polycystic kidneys

polycythemia, primary

polycythemia, secondary

polymerase chain reaction

posterior cerebral artery territory infarction

posterior leukoencephalopathy syndrome

pregnancy, neurologic complications in

premature infant

prenatal diagnosis by amniocentesis

prethrombotic state

prevention of neurologic disorders

primary familial brain calcification

prognathism

prognosis

progressive neurologic disorder

progressive supranuclear palsy

protein C deficiency

protein S deficiency

proteinuria

proximal muscle atrophy

pruritus

pseudobulbar palsy

pseudohypoparathyroidism

pseudoxanthoma elasticum

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

PTEN hamartoma tumor syndrome

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

retinal artery tortuosity

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

scoliosis, neurologic association with

screening

seizure

seizure, children

seizure, complications following

seizure, diagnosis of

seizure, treatment of

seizure, workup of

sensorineural hearing loss

sensory level

sexual intercourse

short stature

shunt procedure, lumboperitoneal

skin, hyperextensible

skin, lesions in neurologic disorders

skin, thin

skin, translucent

skull x-ray, abnormal

slit lamp examination

small vessel disease

small vessel disease, cerebral

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

steroid therapy, CNS treatment and complications with

straight sinus

streptococcal infection

streptococcus viridans

striatonigral degeneration

stridor

striopallidodentate calcifications, familial idiopathic

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

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

urea-cycle enzymopathies

uremia

urinary catecholamines

vertebral-basilar insufficiency

vertigo

Virchow-Robin spaces, dilated

visual acuity, decreased

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

Showing articles 50 to 100 of 9559 << Previous Next >>

Metabolic Disease and Stroke: MELAS
emedicine.com, Mandava,P.,et al, 2006

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

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
Arch Neurol 62:653-658, Lehnhardt,F-G.,et al, 2005

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

Neurologic Features of Horizontal Gaze Palsy and Progressive Scoliosis with Mutations in ROBO3
Neurol 64:1196-1203, Bosley, T.M.,et al, 2005

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

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

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

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

Hereditary Neuropathy With Liability to Pressure Palsies Mimicking Hypoglossal Nerve Injuries
Neurol 61:1457-1458, Corwin,H.M. &Girardet,R.E., 2003

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

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

Prospective Follow-up of 33 Asymptomatic Patients with Familial Cerebral Cavernous Malformations
Neurol 57:1825-1828, Labauge,P.,et al, 2001

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

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

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

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

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

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

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

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

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

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

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

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

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

Hereditary Cerebral Cavernous Angiomas:Clinical and Genetic Features in 57 French Families
Lancet 352:1892-1897, Labauge,P.,et al, 1998

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

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

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

Showing articles 50 to 100 of 9559 << Previous Next >>