Neudle.com: Weber s syndrome

Differential
(Click to cross reference)

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 50 to 87 of 87 << Previous

The Crossed Paralyses
Arch Neurol 52:635-638, Silverman,I.E.,et al, 1995

Hereditary Hemorrhagic Telangiectasia
NEJM 333:918-924, Guttmacher,A.E.,et al, 1995

Transcranial Doppler Ultrason & TEE in Invest Pulm AVM in Pts with Hereditary Hemorrhagic Telangiectasis with Stroke
Stroke 26:1941-1944, Yeung,M.,et al, 1995

Screening Family Members of Patients with Hereditary Hemorrhagic Telangiectasia
Am J Med 99:519-524, Haitjema,T.,et al, 1995

Prothrombotic States in Young People with Idiopathic Stroke:Prospective Study
Stroke 25:287-290, Baringarrementeria,F., 1994

Ischemic Stroke Due to Deficiency of Coagulation Inhibitors, Report of 10 Young Adults
Stroke 24:19-25, Martinez,H.R.,et al, 1993

Free Protein S Deficiency in Acute Ischemic Stroke, A Case-Control Study
Stroke 24:224-227, Mayer,S.A.,et al, 1993

An Unusual Cause of Cerebral Venous Thrombosis in a Four-Year-Old Child
Stroke 24:603-605, Rich,C.,et al, 1993

Diagnosis of Sturge-Weber Syndrome:Comparison of the Efficacy of CT & MR Imaging in 14 Cases
AJR 158:867-871, Marti-Bonmati,L.,et al, 1992

Protein S Deficiency in Middle-Aged Women with Stroke
Neurol 42:1029-1033, Green,D.,et al, 1992

Superior Sagittal Sinus Thrombosis in a Child with Protein S Deficiency
Neurol 42:2303-2305, Prats,J.M.,et al, 1992

Location of Port-Wine Stains and the Likelihood of Ophthalmic and/or CNS Complications
Pediatrics 87:323-327, Tallman,B.,et al, 1991

Superior Sagittal Sinus Thrombosis in a Patient with Protein S Deficiency
Stroke 21:633-636, Cros,D.,et al, 1990

Hematologic Disorders and Ischemic Stroke
Stroke 21:1111-1121, Hart,R.G.&Kanter,M.C., 1990

Encephalotrigeminal Angiomatosis
In Rowland's Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8thEd, p. 582, Gold,A.P., 1989

Epilepsy with Bilateral Occipital Calcifications:A Benign Onset with Progressive Severity
Neurol 38:913-920, Gobbi,G.,et al, 1988

Brain Abscess:Association with Pulmonary Arteriovenous Fistula and Hereditary Hemorrhagic Telangiectasia:3 Cases
Am J Med 85:718-720, Gelfand,M.S.,et al, 1988

Portosystemic Encephalopathy in Hereditary Hemorrhagic Telangiectasia
Am J Med 85:858-860, Fagel,W.J.,et al, 1988

Childhood Stroke Associated with Protein C or S Deficiency
J Pediatr 111:562-564, Israels,S.J.&Seshia,S.S., 1987

Mendelian Etiologies of Stroke
Ann Neurol 22:175-192, Natowicz,M.&Kelley,R.I., 1987

Clinical Spectrum of Hereditary Hemorrhagic Telangiectasia (Osler-Wever-Rendu Disease)
Am J Med 82:989-997, Perry,W.H., 1987

Sturge-Weber-Dimitri Disease without Facial Nevus
Neurol 37:1063-1064, Taly,A.B.,et al, 1987

Identical Twins with Hereditary Hemorrhagic Telangiectasia Concordant for Cerebrovascular Arteriovenous Malformations
Am J Med 81:931-934, Lesser,B.A.,et al, 1986

Central Nervous System Infections Associated with Hereditary Hemorrhagic Telangiectasia
Am J Med 77:86-92, Press,O.L.W.,et al, 1984

Multifocal Interstitial Myositis Associated With Localized Lipoatrophy
Arch Neurol 39:722-724, Palliyath,S.,et al, 1982

Craniopharyngioma with Midbrain Involvement
Arch Neurol 36:319-320, Waga,S.,et al, 1979

Drug-Induced Myopathies In Man
Lancet 2:562-566, Lane,R.J.M.,et al, 1978

Medical Implications of Computed Tomography ("Cat scanning")
NEJM 298:255, Abrams,H.L.,et al, 1978

Neurological Manifestations of Hereditary Hemorrhagic Telangiectasia (Rendu-Osler-Weber Disease)
Ann Neurol 4:130-144, Roman,G.,et al, 1978

Neurologic Aspects of Hereditary Hemorrhagic Telangiectasia
Arch Neurol 34:101, Adams,H.P.,et al, 1977

Clofibrate-Induced Muscle Damage with Myoglobinuria & Cardiomyopathy
NEJM 296:942, Smals,A.G.H., 1977

Brain Stem Toxoplasmosis Complicating Hodgkin's Disease
Arch Neurol 34:636, Slavick,H.E.,et al, 1977

SLE Presenting as Panniculitis (Lupus Profundus)
Ann Int Med 82:376, Diaz-Jouanen,E.,et al, 1975

Platelet-Inhibiting Drugs in the Prevention of Clinical Thrombotic Disease
NEJM 293:174, Genton,E.,et al, 1975

The Treatment of Cerebrovascular Disease with Clofibrate
VA Cooperative Study Group, Stroke 4:6841973., , 1973

Muscular Syndrome after Clofibrate
NEJM 286:1110, Katsilambros,N., 1972

Clofibrate for the Treatment of Occlusive CVD-Correspondence
NEJM 287:671, Hirsch,S.,et al, 1972

Clinical Cases-Dx:Functional Approach to Neuroanatomy pp 477-490 Earl Lawrence House
McGraw Hill 1967., , 1967

Showing articles 50 to 87 of 87 << Previous