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Differential
(Click to cross reference)
abducens nerve paralysis
abscess, intracerebral
abscess, intracranial
abscess, perivalvular
algorithm
alopecia
Alzheimer's disease
amyloid
amyloid angiopathy, cerebral
amyloid angiopathy, cerebral, Dutch type
amyloid angiopathy, hereditary cystatin C
amyloidosis
amyloidosis, oculoleptomeningeal, familial
anemia
aneurysm
aneurysm, berry
aneurysm, intracranial
aneurysm, intracranial, familial
aneurysm, intracranial, screening for
angiography, cerebral
angiography, posterior fossa
angioid streaks
antibiotic prophylaxis
anticoagulant, contraindications
aortic valve, bicuspid
aortic valve, lesion of
arrhythmia, cardiac
arteriopathy
arteriovenous malformation
arteriovenous malformation, cerebral
arteriovenous malformation, pulmonary
arteritis, temporal
asymptomatic
ataxia
ataxia telangiectasia
atrial appendage closure
atrial fibrillation
atrial fibrillation, surgical treatment
atrial fibrillation, treatment
atrial myxoma
bacterial endocarditis, neurologic manifestations of
basal ganglia, calcification of
basal ganglia, hemorrhage
basal ganglia, lesion, bilateral
basilar impression
blood dyscrasias, neurologic findings with
brain atrophy
brain biopsy
brain purpura
brain scan, abnormal
brainstem, infarction of
brainstem, neoplasms of
brainstem, vascular malformation of
calcification, intracranial
Canavan's disease
capillary blush
carcinoma
carcinoma of pancreas
cardiac surgery
cardiomyopathy
caries
carotid artery disease
carotid artery occlusion, bilateral
CAT scan
CAT scan, abnormal
CAT scan, abscess, cerebral
CAT scan, chest
CAT scan, isodense lesion with acute hemorrhage
cataracts
cavernous hemangioma
central nervous system, infection of
cerebellar atrophy, primary
cerebellar hemorrhage
cerebellum, neoplasms of
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy
cerebral embolism
cerebral infarction
cerebral infarction, hemorrhagic
cerebral infarction, subcortical
cerebral ischemia
cerebral peduncle
cerebral vasculature, calcification
cerebral venous thrombosis
cerebritis
cerebroretinal vasculopathy
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, cardiac disease causing
cerebrovascular accident, familial occurrence
cerebrovascular accident, genetic
cerebrovascular accident, infancy and childhood
cerebrovascular accident, neonatal
cerebrovascular accident, prevention of
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
cerebrovascular disease
chest x-ray, abnormal
children
chromosome 9
cirrhosis
clubbing of fingers
coagulopathy
cognition
coin lesion on chest X-ray
COL4A1 related disorder
collagen vascular disease
complications
compression fracture
compression neuropathy
congenital heart disease
congestive heart failure
contraindications
controversies in neurology
cornea, abnormal
cornea, opacity of
corneal dystrophy
corpus callosum, lesion of
cranial neuropathy
cranial neuropathy, multiple
cyanosis
deafness
deep gray nuclei
deficiency of ADA2
degenerative diseases of CNS
dementia
dementia, rapidly progressive
dental procedure, neurologic complications with
dentate nuclei
dentate nuclei, lesion of
developmental venous anomalies
diagnostic criteria
differential diagnosis
dizziness
DNA probes
Durett hemorrhages
dysmorphic
dyspnea
dystonia
early draining vein
echocardiogram
echocardiogram, contrast
echocardiogram, transesophageal, false negative
echocardiogram, transthoracic
echocardiogram, transthoracic, false negative
ectatic basilar artery
Ehlers-Danlos syndrome
electroencephalogram, abnormalities of
electroencephalogram, monitoring, continuous
embolism, air
embolism, paradoxical
embolism, septic
encephalopathy, neonatal
endocarditis
endocarditis, acute bacterial
endocarditis, prophylaxis
endovascular therapy
entrapment neuropathy
enzyme, defect
epidemiology of neurology
epileptic encephalopathy
epistaxis
esophageal varices
Fabry's disease
facial nerve palsy
Factor V Leiden
factor V, deficiency
factor VII, deficiency
Fahr disease
familial
fever
fibrinolytic agents, contraindications
fibromuscular dysplasia
fistula, arterio-venous
fistula, arterio-venous, pulmonary
fundus, abnormality of
gadolinium
gait disorder
gastrointestinal bleeding
gender
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic testing
glutaric acidemia
granulomatosis with polyangiitis
headache
headache, positional
hearing loss
heart murmur
heart valve surgery
hemangioblastoma
hemangioma, brainstem
hemangioma, internal organs
hematuria, gross
hematuria, microscopic
hemiparesis
hemoglobin abnormality, neurologic complications of
hemoptysis
hemorrhage, intracranial, newborn
hemorrhage, putamenal
hemorrhage, thalamic
hemorrhagic diathesis
hepatic encephalopathy
hepatomegaly
hepatosplenomegaly
heralding manifestation
hereditary hemorrhagic telangiectasia(HHT)
Hispanics
homocystinuria
Horner's syndrome
hypercoagulable state
hypertension
hypocalcemia
hypogammaglobulinemia
hypoparathyroidism
hypoxia
hypoxic-ischemic leukoencephalopathy
incidental finding
infantile hemiplegia
infection
intellectual deficit
intracerebral hemorrhage
intracerebral hemorrhage, familial
intracerebral hemorrhage, lobar
intracerebral hemorrhage, recurrent
intracerebral hemorrhage, small
intracerebral hemorrhage, work up
intracerebral hemorrhage, young adult
intracranial hemorrhage
intraventricular hemorrhage
iron, brain
kyphoscoliosis, neurologic causes of
lacunar infarction
left atrial appendage, percutaneous closure
Leigh's disease
leukoencephalopathy
livedo reticularis
liver disease
low back pain
magnetic susceptibility
malaise
malformation, vascular
malformation, vascular, cerebral
malformation, vascular, familial
malformation, vascular, screening for
malformation, Vein of Galen
maple syrup urine disease
memory, impairment of
mental status, abnormal
metabolic disorder, primary
metronidazole
Mexican
microhemorrhage, intracerebral
midbrain, lesion of
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
migraine, hemiplegic
misdiagnosis
mitral valve prolapse
molecular genetics
mononeuropathy multiplex
mortality
movement disorder
moyamoya
MRI
MRI pattern
MRI, abnormal
MRI, angiography
MRI, blooming effect
MRI, complications with
MRI, contrast enhanced
MRI, gradient-echo
MRI, incidental finding
MRI, paramagnetic effect
MRI, repeat
MRI, ring sign
MRI, susceptibility weighted
MRI, T1 weighted high signal foci
MRS
multiple sclerosis
myelopathy
myocardial abscess
neonatal epilepsy syndromes
neonatal epileptic encephalopathy
neoplasm, primary of CNS
neoplasm, primary of CNS-familial occurrence
neurocutaneous disease
neuroendocrinology
neurofibromatosis 1
neurologic complications of, chronic pulmonary disease
neurologic disease, diagnoses of
neurologic examination, focal
neuropathy
neuropathy, hereditary peripheral
neuropathy, vasculitic, systemic
next-generation sequencing
occipital lobe
ophthalmoplegia
optic nerve, lesion of
osteogenesis imperfecta
osteoporosis
otosclerosis
pain
pain, back
pain, flank
pain, head
papilledema
paraparesis
paraparesis, spastic
Parkinsonism syndrome
patient information and support
pectus carinatum
pericardial effusion
peri-procedural
pheochromocytoma
platelet inhibiting drugs
pleocytosis of cerebrospinal fluid
poison, neurologic problems with
polycystic kidneys
polycythemia, primary
polycythemia, secondary
polyneuropathy
pons, lesion of
portal caval shunt
premature infant
prevention of neurologic disorders
primary familial brain calcification
prognosis
progressive neurologic disorder
protein C deficiency
pseudobulbar palsy
pseudohypoparathyroidism
pseudotumor
pseudoxanthoma elasticum
psychiatric problems in neurologic disorders
psychosis
pulmonary disease
pulmonary embolism
radiation therapy, CNS treatment and complications with
radiation therapy, stereotactic
recurrent
renal cell carcinoma
renal cyst
retinal artery tortuosity
retinal hemangioma
retinal hemorrhages
retinal lesion
retinal microvascular disease
retinal tumor
retinopathy
review article
risk factors
risk factors, modification
root lesion, nerve
safety
sclerae, blue
scoliosis
screening
seizure
seizure, complications following
seizure, diagnosis of
seizure, etiology of
seizure, intractable
seizure, neonatal
seizure, treatment of
seizure, workup of
sensorineural hearing loss
short stature
sickle cell disease
skin, biopsy
skin, lesions in neurologic disorders
skull x-ray, abnormal
small vessel disease
small vessel disease, cerebral
spinal cord
spinal cord, compression of
spinal cord, lesion of
spinal cord, neoplasm
spinal cord, vascular malformation of
splenomegaly
spondylolysis
staphylococcus aureus
stereotaxic surgery
streptococcal infection
streptococcus viridans
striatonigral degeneration
striopallidodentate calcifications, familial idiopathic
subarachnoid hemorrhage
subcortical U fibers
subdural hematoma
sudden death
symmetric brain lesions
symptomatic
systemic illness
telangiectases
telangiectases, retinal
term infant
thalamus, lesion of-bilateral
thrombocytopenia
thrombophlebitis
tongue, enlarged
transient ischemic attack
treatment of neurologic disorder
tuberous sclerosis
twins
vasculitides
vasculopathy
vertebral-basilar insufficiency
Virchow-Robin spaces, dilated
visual loss
visual loss, slow
vitreous opacities
Von Hippel Lindau
Watchman device
white matter disease
white matter disease, subcortical
workup
Showing articles 0 to 50 of 7195 Next >>

Cavernous Maliformations of the Central Nervous System
NEJM 390:1022-1028, Smith,E.R., 2024

Vascular Malformations of the Central Nervous System
www.UptoDate.Com, March, Singer,R.J.,et al, 2024

A 50-YEar-Old Man with Intracerebral Hemorrhage and Tortuous Retinal Arterioles
Neurol 103:e209796, Bouchart,J.,et al, 2024

Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
Neurol 100:766-783, Manini,A.,&Pantoni,L., 2023

Neonatal Seizures
NEJM 388:1692-1700, Ropper.A.H., 2023

Basa Ganglia Calcifications (Fahrs Syndrome): Related Conditions and Clinical Features
Neurol Sci 40:2251-2263, Donzuso,G.,et al, 2019

Cranial Cavernous Malformations
Stroke 49:1029-1035, Stapleton, C.J. & Barker, F.G., 2018

Dentate Update: Imaging Features of Entities that Affect the Dentate Nucleus
AJNR 38:1467-1474, Bond, K.M.,et al, 2017

Characyeristic features and progression of abnormalities on MRI for CARASIL
Neurol 85:459-463, Sekine, Y., etal, 2015

Percutaneous Left Atrial Appendage Closure:Technical Aspects and Prevention of Periprocedural Complications with the Watchman Device
Workd J Cardiol 26:65-75, Mobius-Winkler,S.,et al, 2015

Cerebral Abnormalities in Adults with Ataxia-Telangiectasia
AJNR 35:119-123, Lin, D.D.M.,et al, 2014

Early-Onset Stroke and Vasculopathy Associated with Mutations in ADA2
NEJM 370:911-920, Zhou, Q.,et al, 2014

Cerebral Amyloid Angiopathy
eMedicine, Jan, Menon, R.S., 2012

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

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

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

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

Familial Occipital Calcifications, hemorrhagic Strokes, Leukoencephalopathy, Dementia, and External Carotid Dysplasia
Neurol 55:1661-1667, Iglesias,S.,et al, 2000

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

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

Cerebroretinal Vasculopathy Mimicking a Brain Tumor:A Case of a Rare Hereditary Syndrome
Neurol 53:629-631, Weil,S.,et al, 1999

Cerebrovascular Complications of Fabry's Disease
Ann Neurol 40:8-17, Mitsias,P.&Levine,S.R., 1996

Familial Cerebral Cavernous Angiomas:Clinical and Radiologic Studies
Neurol 45:492-497, Kattapong,V.J.,et al, 1995

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

Congential Deficienty of Factor VII in Subarachnoid Hemorrhage
Stroke 25:508-510, Papa,M.L.,et al, 1994

Neurological Involvement in Wegener's Granulomatosis:An Analysis of 324 Consecutive Pts at the Mayo Clin
Neurol 33:4-9, Nishino,H.,et al, 1993

Familial Intracranial Haemorrhage Due to Factor V Deficiency
JNNP 55:227-228, Wadia,R.S.,et al, 1992

Cerebral Haemorrhage and Berry Aneurysm:Evidence from a Family for a Pattern of Autosomal Dominant Inheritance
JNNP 54:838-840, Shinton,R.,et al, 1991

Intracranial Hemorrhage in Patients with Polycystic Kidney Disease
Stroke 21:291-294, Ryu,S.J., 1990

Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred
Medicine 68:1-29, Lamiell,J.M.,et al, 1989

Familial Oculoleptomeningeal Amyloidosis, Report of a New Family with Unusual Features
Arch Neurol 45:1118-1122, Uitti,R.J.,et al, 1988

Mutation in Cystatin C Gene Causes Hereditary Brain Hemorrhage
Lancet 2:603-604, Palsdottir,A.,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

Cerebral Amyloid Angiopathy, A Critical Review
Stroke 18:311-324, Vinters,H.V., 1987

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

Cerebral Haemorrhagic Infarction in Young Patients with Hereditary Protein C Deficiency
BMJ 290:350-352, Wintzen,A.R.,et al, 1985

Abnormal Metabolism of y-Trace Alkaline Microprotein
NEJM 311:1547-1549, Grubb,A.,et al, 1984

Familial Vascular Malformation or Chance Occurrence
Neurol 28:98, Barre,R.G.,et al, 1978

Pseudoxanthoma Elasticum:A Review of Neurological Complications
Ann Neurol 4:18, Iqbal,A.,et al, 1978

Familial Cavernous Angiomas
Arch Neurol 35:746-749, Bicknell,J.M.,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

Osteogenesis Imperfecta, in Heritable Disorders of Connective Tissue
(Ed) , 4th edition, The C. V. Mosby Company St. Louis, Chap. 8, pp. 390. , 1972, McKusick,V.A., 1972

Spectrum of Intracranial Hemorrhages in Cerebral Venous Thrombosis, A Pictorial Case Series and Review of Pathophysiology and Management
Neurologist 30:45-51, Jha,S.,et al, 2025

Stroke-Like Migraine Attacks After Radiation Therapy Syndrome
Neurol 104:e210203, Lubotzky,A.,t al, 2025

Clinicopathologic Conference, Posterior Reversible Encephalopathy Syndrome Due to Sickle Cell Disease
NEJM 392:268-276, Case 2-2025, 2025

A 32 Year-Old Woman with Recurrent Intracerebral Hemorrhages
Neurol 104:e213422, Hindsholm,M.F.,et al, 2025



Showing articles 0 to 50 of 7195 Next >>