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Differential
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abscess, intracerebral
abscess, intracranial
algorithm
amyloidosis
anemia
aneurysm
aneurysm, berry
aneurysm, intracranial
aneurysm, intracranial, familial
aneurysm, intracranial, screening for
angiography, cerebral
angiography, cerebral, false negative
antibiotic prophylaxis
antibiotics
arrhythmia, cardiac
arteriovenous malformation
arteriovenous malformation, cerebral
arteriovenous malformation, cerebral, spontaneous occlusion
arteriovenous malformation, multiple
arteriovenous malformation, pulmonary
asymptomatic
atrial myxoma
basal ganglia, lesion of
basal ganglia, lesion, bilateral
bleeding disorder
brain biopsy
brain biopsy, stereotaxic
bruit
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, abscess, cerebral
CAT scan, chest
CAT scan, ring sign
cavernous hemangioma
central nervous system, infection of
cerebral embolism
cerebral infarction
cerebral ischemia
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
chest x-ray, abnormal
children
chromosome 9
cirrhosis
Clinical Pathologic Conference(C.P.C.)
clubbing of fingers
coagulopathy
coin lesion on chest X-ray
complications
confusion
congestive heart failure
contraindications
controversies in neurology
C-reactive protein, elevated
cyanosis
dental procedure, neurologic complications with
developmental venous anomalies
diagnostic criteria
dizziness
doppler, transcranial
dyspnea
echocardiogram
echocardiogram, contrast
echocardiogram, transesophageal
Ehlers-Danlos syndrome
embolism, air
embolism, paradoxical
embolism, septic
empyema, epidural-spinal
encephalopathy
endocarditis, prophylaxis
endovascular therapy
epistaxis
epistaxis, recurrent
esophageal varices
ethics in neurology
Fabry's disease
familial
fever
fibrinolytic agents, contraindications
fibromuscular dysplasia
fistula, arterio-venous
fistula, arterio-venous, pulmonary
gait disorder
gastrointestinal bleeding
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic screening
genetic testing
headache
headache, sudden onset of
hematuria, gross
hematuria, microscopic
hemiparesis
hemiplegia
hemoglobin abnormality, neurologic complications of
hemoptysis
hemorrhagic diathesis
hepatic encephalopathy
hepatic failure
hepatomegaly
heralding manifestation
hereditary hemorrhagic telangiectasia(HHT)
homocystinuria
hyperbilirubinemia
hyperphosphatasia
hypoxia
intracerebral hemorrhage
intracerebral hemorrhage, young adult
intracranial hemorrhage
irritability
leukocytosis
liver disease
malformation, vascular
malformation, vascular, cerebral
malformation, vascular, familial
malformation, vascular, screening for
malformation, Vein of Galen
malformation, venous
meningitis
microsurgery
migraine
migraine, hemiplegic
misdiagnosis
mitral valve prolapse
molecular genetics
mortality
moyamoya
MRI
MRI, abnormal
MRI, angiography
MRI, contrast enhanced
MRI, diffusion weighted
MRI, false negative
MRI, high signal foci on
MRI, high signal intensity of basal ganglia
MRI, perfusion
MRI, T1 weighted high signal foci
neurocutaneous disease
neurofibromatosis 1
neurologic complications of, chronic pulmonary disease
neurologic disease, diagnoses of
neurologic disease, tempo
neurologic examination, focal
paraparesis
patient information and support
platelet inhibiting drugs
polycythemia, primary
polycythemia, secondary
portal caval shunt
pregnancy, neurologic complications in
prevention of neurologic disorders
prognosis
protein C deficiency
pseudoxanthoma elasticum
pulmonary disease
pulmonary hypertension
pulmonary nodules
radiation therapy, CNS treatment and complications with
radiation therapy, stereotactic
recurrent
review article
risk factors
screening
seizure
sickle cell disease
skin, lesions in neurologic disorders
spinal cord
spinal cord, lesion of
spinal cord, vascular malformation of
subarachnoid hemorrhage
telangiectases
telangiectases, retinal
thrombocytopenia
tissue plasminogen activator, intravenous
tongue, red papules
tranexamic acid
transient ischemic attack
treatment of neurologic disorder
tuberous sclerosis
twins
undiagnosed
vertigo
Von Hippel Lindau
workup
Showing articles 0 to 35 of 35

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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



Showing articles 0 to 35 of 35