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abscess, intracerebral
abscess, intracranial
acoustic neurinoma
adverse drug reaction
alcoholic polyneuropathy
algorithm
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
apomorphine
arrhythmia, cardiac
arteriovenous malformation
arteriovenous malformation, cerebral
arteriovenous malformation, cerebral, spontaneous occlusion
arteriovenous malformation, multiple
arteriovenous malformation, pulmonary
aspirin
asymptomatic
atrial myxoma
audiogram
basal ganglia, lesion of
basal ganglia, lesion, bilateral
bleeding disorder
brain atrophy
brain biopsy
brain biopsy, stereotaxic
brainstem, infarction of
brainstem, lesion of
brainstem, syndrome
Brown Sequard syndrome
bruit
buphthalmos
calcification, gyral
calcification, intracranial
cardiomyopathy
case studies
CAT scan
CAT scan, abnormal
CAT scan, abscess, cerebral
CAT scan, brain scan compared to
CAT scan, brain tumors
CAT scan, cerebrovascular disease
CAT scan, chest
CAT scan, dementia
CAT scan, demyelinating disease
CAT scan, emission
CAT scan, metrizamide
CAT scan, ring sign
CAT scan, spinal cord
cavernous hemangioma
central nervous system, infection of
cerebellum, neoplasms of
cerebral angiomatosis
cerebral embolism
cerebral infarction
cerebral ischemia
cerebral venous infarction
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, multiple
cerebrovascular accident, prevention of
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
chemotherapy, CNS treatment and complications with
chest x-ray, abnormal
children
chorea, Sydenham's
choroid plexus
choroid plexus, abnormality of
choroid plexus, prominence of
chromosome 9
cirrhosis
Clinical Pathologic Conference(C.P.C.)
clubbing of fingers
coagulopathy
Cobb syndrome
cognition
coin lesion on chest X-ray
complications
confusion
congestive heart failure
conjugate gaze, forced
conjunctival vessel tortuosity
contraindications
controversies in neurology
cortical dysplasia, focal
craniopharyngioma
C-reactive protein, elevated
crossed paralysis
cyanosis
deafness, sudden
demyelinating disease
dental procedure, neurologic complications with
developmental retardation
developmental venous anomalies
diagnostic criteria
disability, neurological
dizziness
doppler, transcranial
dyspnea
echocardiogram
echocardiogram, contrast
echocardiogram, transesophageal
Ehlers-Danlos syndrome
electroencephalogram, abnormalities of
embolism, air
embolism, paradoxical
embolism, septic
empyema, epidural-spinal
encephalitis, focal
encephalitis, Rasmussen's
encephalopathy
endocarditis, prophylaxis
endocarditis, subacute bacterial
endovascular therapy
eosinophilia
epistaxis
epistaxis, recurrent
esophageal varices
ethics in neurology
exophthalmus
Fabry's disease
facial nevus
familial
fever
fibrinolytic agents, contraindications
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
genetic screening
genetic testing
glaucoma
GNAQ gene
gyrus, abnormal
headache
headache, sudden onset of
hearing loss
hearing loss, sudden, unilateral
hemangioma
hemangioma, facial
hemangioma, leptomeningeal
hemangioma, skin
hematuria, gross
hematuria, microscopic
hemiatrophy
hemiparesis
hemiplegia
hemispherectomy
hemoglobin abnormality, neurologic complications of
hemoptysis
hemorrhagic diathesis
hepatic encephalopathy
hepatic failure
hepatomegaly
heralding manifestation
hereditary hemorrhagic telangiectasia(HHT)
herniated disc
herpes zoster
heterochromia iridis
Hodgkin's disease
Hodgkin's disease, neurologic involvement with
homocystinuria
hydrocephalus
hyperbilirubinemia
hypereosinophilic syndrome(HES)
hyperphosphatasia
hypoxia
immunosuppression
intellectual deficit
intellectual deterioration
intracerebral hemorrhage
intracerebral hemorrhage, young adult
intracranial hemorrhage
irritability
Jackson's syndrome
leukocytosis
lipodystrophy
liver disease
lobar atrophy
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
meningitis
mental retardation
microsurgery
midbrain, lesion of
migraine
migraine, hemiplegic
Millard Gubler syndrome
misdiagnosis
mitral valve prolapse
molecular genetics
mortality
moyamoya
MRI
MRI, abnormal
MRI, angiography
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, perfusion
MRI, T1 weighted high signal foci
myositis
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
nevus
occipital lobe, lesion of
optic nerve
optic nerve, lesion of
orbit
paraparesis
parasitic infection, CNS
Parkinson disease
Parkinson disease, treatment of
patient information and support
phakomatoses
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
pregnancy, neurologic complications in
prevention of neurologic disorders
prognosis
progressive neurologic disorder
protein C deficiency
pseudoxanthoma elasticum
psychomotor retardation
ptosis, unilateral
pulmonary disease
pulmonary hypertension
pulmonary nodules
radiation therapy, CNS treatment and complications with
radiation therapy, stereotactic
Raymond-Castan syndrome
recurrent
review article
Rinne tuning fork test
risk factors
screening
seizure
seizure, children
seizure, focal
seizure, intractable
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
strokelike episodes
Sturge-Weber syndrome
subarachnoid hemorrhage
subdural hematoma
syringomyelia
systemic illness
systemic lupus erythematosus
tabes dorsalis
telangiectases
telangiectases, retinal
third nerve palsy
thrombocytopenia
tissue plasminogen activator, intravenous
tongue, red papules
toxoplasmosis, acquired
toxoplasmosis, CNS
tranexamic acid
transient ischemic attack
transient neurologic deficit
treatment of neurologic disorder
tuberous sclerosis
twins
undiagnosed
vagus nerve stimulation
vascular malformation, children, intracranial
vasculopathy
vertigo
visual field defect
Von Hippel Lindau
Weber test
Weber-Christian's disease
Weber's syndrome
workup
Showing articles 0 to 50 of 61 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

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

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

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

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

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

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

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

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

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

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

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

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



Showing articles 0 to 50 of 61 Next >>