Neudle.com: "Weber's syndrome"

Differential
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abscess, intracerebral

abscess, intracranial

acoustic neurinoma

acquired immunodeficiency syndrome

activated protein C resistance

addiction, heroin

adverse drug reaction

alcohol

alcoholic polyneuropathy

algorithm

amphotericin B

amyloidosis

amyotrophic lateral sclerosis

anemia

aneurysm

aneurysm, berry

aneurysm, cavernous sinus

aneurysm, internal carotid artery

aneurysm, intracranial

aneurysm, intracranial, familial

aneurysm, intracranial, screening for

angiography, cerebral

angiography, cerebral, false negative

ankylosing spondylitis

antibiotic prophylaxis

antibiotics

anticardiolipin antibodies

anticoagulant, treatment

antiphospholipid antibodies

antithrombin III deficiency

apomorphine

arrhythmia, cardiac

arteriovenous malformation

arteriovenous malformation, cerebral

arteriovenous malformation, cerebral, spontaneous occlusion

arteriovenous malformation, multiple

arteriovenous malformation, pulmonary

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Behcet's syndrome

bleeding disorder

blood dyscrasias, neurologic findings with

brain atrophy

brain biopsy

brain biopsy, stereotaxic

brainstem, infarction of

brainstem, lesion of

brainstem, syndrome

Brown Sequard syndrome

bruit

buphthalmos

calcification, gyral

calcification, intracranial

carbenoxolone

cardiac arrest

cardiac arrest and resuscitation

CAT scan, abscess, cerebral

CAT scan, brain scan compared to

CAT scan, brain tumors

CAT scan, cerebrovascular disease

CAT scan, chest

CAT scan, delta sign, empty

CAT scan, dementia

CAT scan, demyelinating disease

CAT scan, emission

CAT scan, metrizamide

CAT scan, ring sign

CAT scan, spinal cord

CAT scan, venography

cavernous hemangioma

central nervous system, infection of

cerebellum, neoplasms of

cerebral angiomatosis

cerebral embolism

cerebral infarction

cerebral ischemia

cerebral venous infarction

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebral venous thrombosis, etiology

cerebral venous thrombosis, recurrent

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, cost of

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, multiple

cerebrovascular accident, prevention of

cerebrovascular accident, recurrent

cerebrovascular accident, thrombolytic agents in treatment

cerebrovascular accident, women

cerebrovascular accident, work up for

cerebrovascular accident, young adult

cerebrovascular disease, risk factors in

cerebrovascular disease, treatment of

chemotherapy, CNS treatment and complications with

chest x-ray, abnormal

choroid plexus, abnormality of

choroid plexus, prominence of

chromosome 9

cirrhosis

Clinical Pathologic Conference(C.P.C.)

coin lesion on chest X-ray

complications

confusion

congestive heart failure

conjugate gaze, forced

conjunctival vessel tortuosity

contraindications

controversies in neurology

cortical dysplasia, focal

cost effectiveness

craniectomy, decompressive

craniopharyngioma

C-reactive protein, elevated

demyelinating disease

dental procedure, neurologic complications with

developmental retardation

developmental venous anomalies

diagnostic criteria

dipyridamole

disability, neurological

disseminated intravascular coagulation(DIC)

diuretic

dizziness

doppler, transcranial

drug induced neurologic disorders

dural sinus thrombosis

dyspnea

echocardiogram

echocardiogram, contrast

echocardiogram, transesophageal

Ehlers-Danlos syndrome

electrocardiogram, abnormal

electroencephalogram, abnormalities of

embolism, air

embolism, paradoxical

embolism, platelet

embolism, septic

empyema, epidural-spinal

encephalitis, focal

encephalitis, Rasmussen's

encephalopathy

endocarditis, prophylaxis

endocarditis, subacute bacterial

endovascular therapy

enolase

enzyme, muscle disease

eosinophilia

epidemiology of neurology

epistaxis

epistaxis, recurrent

epsilon-aminocaproic acid(E.A.C.A.)

esophageal varices

ethics in neurology

evidence-based research

fibrinolytic agents, contraindications

fibrinolytic agents, intra-venous local infusion

fibromuscular dysplasia

fistula, arterio-venous

fistula, arterio-venous, pulmonary

Foville syndrome

fundus, abnormality of

gadolinium

gait disorder

gastrointestinal bleeding

gene

gene mutation

genetic counselling

genetic neurologic disorders

head injury, pediatric

headache

headache, persistent

headache, severe

headache, sudden onset of

hearing loss

hearing loss, sudden, unilateral

hemangioma

hemangioma, facial

hemangioma, leptomeningeal

hemangioma, skin

hematuria, gross

hematuria, microscopic

hemoglobin abnormality, neurologic complications of

hemoptysis

hemorrhagic diathesis

hepatic encephalopathy

hepatic failure

hepatomegaly

heralding manifestation

hereditary hemorrhagic telangiectasia(HHT)

Hodgkin's disease, neurologic involvement with

homocystinuria

human immunodeficiency virus type 1

hydrocephalus

hyperbilirubinemia

hypercholesterolemia

hypereosinophilic syndrome(HES)

hyperphosphatasia

hypokalemia

hypoxia

hypoxic encephalopathy

intellectual deterioration

interobserver agreement

intracerebral hemorrhage

intracerebral hemorrhage, young adult

intracranial hemorrhage

intracranial hypertension, benign

intracranial pressure, increased

leukemia, neurologic findings assoc.with

leukocytosis

level of consciousness, decreased

lymphoma involving CNS

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

malformation, vascular, familial

malformation, vascular, screening for

malformation, Vein of Galen

malformation, venous

megalencephaly

meningeal enhancement

middle cerebral artery territory infarction

middle cerebral artery, occlusion of

migraine

migraine, hemiplegic

Millard Gubler syndrome

misdiagnosis

mitral valve prolapse

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, false negative

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, indications for

MRI, negative

MRI, perfusion

MRI, T1 weighted high signal foci

muscle weakness, causes of

myeloproliferative disorder

myopathy, drug-induced

myopathy, hypokalemic

myopathy, proximal

myopathy, steroid induced

myositis

nausea and vomiting

neoplasm, metastatic to CNS

neoplasm, metastatic to CNS, hemorrhagic

neoplasm, primary intracerebral

neoplasm, primary of CNS

neurocutaneous disease

neuroendocrinology

neurofibromatosis 1

neurologic complications of, chronic pulmonary disease

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic examination, focal

neurologic signs

neuron specific enolase

nevus

nonsteroidal anti-inflammatory drug

occipital lobe, lesion of

optic nerve

optic nerve, lesion of

oral contraceptives

oral contraceptives, cerbrovascular disease and

oral contraceptives, neurologic complications with

orbit

paraparesis

parasitic infection, CNS

Parkinson disease

Parkinson disease, treatment of

paroxysmal nocturnal hemoglobinuria

patient information and support

perhexiline maleate

phakomatoses

pitfalls

plasminogen deficiency

platelet inhibiting drugs

poliomyelitis

polycythemia, primary

polycythemia, secondary

port wine nevus

portal caval shunt

posterior fossa, differential diagnosis of lesions of

posterior inferior cerebellar artery syndrome

practice guidelines

pregnancy, neurologic complications in

prethrombotic state

prevention of neurologic disorders

primary thrombocythemia

prognosis

progressive neurologic disorder

protein C deficiency

protein S deficiency

pseudoxanthoma elasticum

psychomotor retardation

ptosis, unilateral

pulmonary disease

pulmonary embolism

pulmonary hypertension

pulmonary nodules

radiation therapy, CNS treatment and complications with

radiation therapy, stereotactic

Raymond-Castan syndrome

recurrent

review article

rhabdomyolysis

Rinne tuning fork test

seizure, intractable, treatment of

seizure, neonatal

seizure, surgical treatment of

seizure, treatment of

sensorineural hearing loss

sickle cell disease

skin, lesions in neurologic disorders

skull x-ray

skull x-ray, abnormal

spinal cord

spinal cord, lesion of

spinal cord, vascular malformation of

spontaneous remission

status epilepticus

steroid

steroid therapy, CNS treatment and complications with

straight sinus

strokelike episodes

Sturge-Weber syndrome

subarachnoid hemorrhage

subdural hematoma

sulfinpyrazone

superior sagittal sinus thrombosis

syringomyelia

systemic illness

systemic lupus erythematosus

tabes dorsalis

telangiectases

telangiectases, retinal

third nerve palsy

thrombocytopenia

thrombophlebitis

tissue plasminogen activator, intravenous

tongue, red papules

toxoplasmosis, acquired

toxoplasmosis, CNS

tranexamic acid

transient ischemic attack

transient ischemic attack, treatment of

transient neurologic deficit

treatment of neurologic disorder

vagus nerve stimulation

vascular malformation, children, intracranial

vasculopathy

vertigo

vincristine neurotoxicity

visual field defect

Von Hippel Lindau

Weber test

Weber-Christian's disease

Weber's syndrome

workup

Showing articles 0 to 50 of 87 Next >>

Brain Abscess and Stroke in Children and Adults with Hereditary Hemorrhagic Telangiectasia
Neurol 100:e2324-e2330, White,A.J.,et al, 2023

Drug Resistant Epilepsy in a 61-Year-Old Man with Abnormal MRI Brain Findings and Management with Vagal Nerve Stimulator
Neurol 100:1111-1116, Mankad,J.P. & Lavingia,J.R., 2023

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

Sturge-Weber Syndrome
www.UptoDate.com,Dec, Patterson,M.C., 2022

Updates on Sturge-Weber Syndrome
Stroke 53:3769-3779, Yeom,S.E.&Comi,A.M., 2022

Ocular Findings in the Sturge-Weber Syndrome
NEJM 385:e68, Sherman, S.V., 2021

Recurrent Cerebral Ischemia During Pregnancies
Neurol 95:e2453-e2457, Bulwa, Z.,et al, 2020

A Teenager with Persistent Headache
Neurol 92:e1526-e1531, Hu, Y.,et al, 2019

Recurrent Epistaxis in an Adolescent
BMJ 367:I5393, McLaren, O. & Ronan, N., 2019

Clinicopathologic Conference, Vascular Malformations in Liver, Stomach, Esophagus, and Lungs that are Consistent with Hereditary Hemorrhagic Telangiectasia, Complicated
NEJM 376:972-980, Case 7-2017, 2017

Basal Ganglia T1 Hyperintensity in Hereditary Hemorrhagic Telangiectasia
AJNR 38:1929-1933, Parvinian, A.,et al, 2017

Neurovascular Manifestations of Hereditary Hemorrhagic Telangiectasia: A Consecutive Series of 376 Patients during 15 Years
AJNR 37:1479-1486, Brinjikji, W.,et al, 2016

Complications and Mortality in Hereditary Hemorrhagic Telangiectasia
Neurol 84:1886-1893, Donaldson, J.W.,et al, 2015

Red Papules on the Tongue of a Patient with Hemiparesis
JAMA 312:741-742, Chiu, H.Y. & Lin, S.J., 2014

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

Sturge-Weber Syndrome
MedLink Neurology, July, Comi, A.M., 2013

Sturge-Weber Syndrome and Port-Wine Stains Caused by Somatic Mutation in GNAQ
NEJM 368:1971-1979, Shirley, M.,et al, 2013

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

Diagnosis and Management of Cerebral Venous Thrombosis: A Statement for Healthcare Professionals From the American Heart Association/American Stroke Association
Stroke 42:1158-1192, Saposnik,G.,et al, 2011

An unusual cause of stroke and hypoxia
BMJ 342:c7200, Bell, S.L. & Eveson, D.J., 2011

Presentation, Diagnosis, Pathophysiology, and Treatment of the Neurological Features of Sturge-Weber Syndrome
The Neurologist 17:179-184, Comi, A.M., 2011

Pulmonary AVMs, including hereditary hemorrhagic telangiectasia: Diagnosis and Treatment
UpTo Date, August, Gossage, J.R., 2010

Clinicopath Conf., Brain Abscess, Pulmonary Arteriovenous Malformation Due to Hereditary Hemorrhagic Telangiectasia
NEJM 362:1326-1333, Case 10-2010, 2010

Sturge-Weber Syndrome Presenting in a 58-Year-Old Woman With Seizures
Neurol 75:352, Traub,R.,et al, 2010

Idiopathic Sudden Sensorineural Hearing Loss
NEJM 359:833-840, Rauch,S.D., 2008

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

Amorphine-induced eosinophilic panniculitis and hypereosinophilia in Parkinson disease
Neurol 64:392-393, Pot, C., et al, 2005

Protein S Deficiency in HIV Associated Ischaemic Stroke:An Epiphenomenon of HIV Infection
JNNP 76:1455-1456,1331, Mochan,A.,et al, 2005

Radiosurgery for Cerebral Arteriovenous Malformations in Hereditary Hemorrhagic Telangiectasia
Neurol 63:367-369, Maarouf,M.,et al, 2004

Should Asymptomatic Patients with Hereditary Haemorrhagic Telangiectasia (HHT) be Screened for Cerebral Vascular Malformations? Data from 22 061 years of HHT Patient Life
JNNP 74:743-748, Easey,A.J.,et al, 2003

Tranexamic Acid in Hereditary Hemorrhagic Telangiectasia
NEJM 346:457, Sabra,C.,et al, 2002

Spontaneous Regression of Cerebral Arteriovenous Malformation in Hereditary Hemorrhagic Telangiectasia
AJNR 23:1049-1050, Cloft,H.J., 2002

Outcomes of 32 Hemispherectomies for Sturge-Weber Worldwide
Neurol 59:1735-1738, Kossoff,E.H.,et al, 2002

Use of Specialized Coagulation Testing in the Evaluation of Patients with Acute Ischemic Stroke
Neurol 56:624-627, Bushnell,C.,et al, 2001

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

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

Pulmonary Arteriovenous Malformations
Neurol 55:959-964, Moussouttas,M.,et al, 2000

Sturge-Weber Syndrome
Neurol 55:1472-1479, Arzimanoglou,A.A.,et al, 2000

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

Risk of Cerebral Sinus Thrombosis in Oral Contraceptive Users Who Are Carriers of Hered Prothrombotic Cond
BMJ 316:589-592, deBruijn,S.F.T.M.,et al, 1998

MR of Hereditary Hemorrhagic Telangiectasia:Prevalence and Spectrum of Cerebrovascular Malformations
AJNR 19:477-484, Fulbright,R.K.,et al, 1998

Neurology and the Blood:Haematological Abnormalities in Ischaemic Stroke
JNNP 64:150-159, Markus,H.S.&Hambley,H., 1998

Serum S-100 and Neuron-Specific Enolase for Prediction of Regaining Consciousness After Global Cerebral Ischemia
Stroke 29:2363-2366, Martens,P.,et al, 1998

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

Human Immunodeficiency Virus Infection and Stroke in Young Patients
Arch Neurol 54:1150-1153, Qureshi,A.I.,et al, 1997

Why Would You Remove Half a Brain? Outcome of 58 Children after Hemispherectomy-Johns Hopkins 1968-96
Pediatrics 100:163-171, Vining,E.P.G.,et al, 1997

Exceptional Multiplicity of Cerebral AVMs Assoc with Hereditary Hemorrhagic Telangiectasia (Osler-Weber-Rendu Syndrome)
AJNR 17:1733-1742, Putman,C.M.,et al, 1996

Cerebral Venous Thrombosis in Adults:A Study of 40 Cases From Saudi Arabia
Stroke 26:1193-1195, Daif,A.,et al, 1995

Showing articles 0 to 50 of 87 Next >>