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Differential
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abducens nerve paralysis
abscess, intracerebral
abscess, intracranial
acetazolamide
acid maltase deficiency
acid maltase deficiency, adult
acral sensory symptoms
adverse drug reaction
alcohol
algorithm
alopecia
alpha galactosidase A deficiency
Alzheimer's disease
Alzheimer's disease, preclinical
amyloid angiopathy, cerebral
amyloid beta protein
amyloidosis
amyloidosis, oculoleptomeningeal, familial
anemia
aneurysm
aneurysm, asymptomatic
aneurysm, berry
aneurysm, intracranial
aneurysm, intracranial, detection
aneurysm, intracranial, familial
aneurysm, intracranial, natural history
aneurysm, intracranial, screening for
aneurysm, intracranial, treatment of
aneurysm, multiple intracranial
aneurysm, ruptured
aneurysm, size
aneurysm, unruptured
angiography, cerebral
angioid streaks
antibiotic prophylaxis
aortic valve, bicuspid
arachnodactyly
arrhythmia, cardiac
arterial dissection
arterial dissection, aorta
arterial dissection, carotid
arterial dissection, intracranial
arterial dissection, multiple
arterial dissection, ruptured
arterial dissection, vertebral
arteriopathy
arteriovenous malformation, cerebral
arteritis, temporal
asymptomatic
atrial myxoma
Babinski sign
behavioral disorder
biologic markers
blind spot, enlarged
blood dyscrasias, neurologic findings with
blue rubber bleb nevus syndrome
brainstem, infarction of
brainstem, neoplasms of
bruising
calcification, intracranial
calf hypertrophy
carcinoma
carcinoma of pancreas
cardiomegaly
cardiomyopathy
carotid artery occlusion, bilateral
CAT scan
CAT scan, abnormal
CAT scan, abscess, cerebral
CAT scan, angiography
CAT scan, emission
CAT scan, emission, abnormal
cavernous hemangioma
cerebellum, neoplasms of
cerebral atherosclerosis
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy
cerebral embolism
cerebral infarction
cerebral infarction, subcortical
cerebral ischemia
cerebral palsy
cerebral venous thrombosis
cerebritis
cerebrospinal fluid, biochemical markers of CNS disease
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, pressure increased
cerebrospinal fluid, red cells in
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, non atherosclerotic cause of
cerebrovascular accident, young adult
cerebrovascular disease
children
chromosomal abnormality
cigarette smoking
cirrhosis
clubbing of fingers
coagulopathy
cognition
coin lesion on chest X-ray
collagen vascular disease
confusion
congenital malformation
congenital malformation, non CNS
congestive heart failure
controversies in neurology
corpus callosum, lesion of
cost effectiveness
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
cultured skin fibroblasts
cyanosis
D-dimer
delay in diagnosis
dementia
dementia, rapidly progressive
diagnostic criteria
diaphragmatic paralysis
dilated aortic root
dizziness
dural sinus thrombosis
Ehlers-Danlos syndrome
Ehlers-Danlos syndrome, classification
electroencephalogram, abnormalities of
electromyogram
electron microscopy
embolism, air
embolism, paradoxical
embolism, septic
embolization, therapeutic
emotional lability
empty sella
encephalopathy, anoxic
encephalopathy, neonatal
endovascular therapy
enzyme, defect
epidemiology of neurology
epistaxis
esophageal varices
Fabry's disease
facial nerve palsy
factor VII, deficiency
familial
fibromuscular dysplasia
fingers, abnormal
fistula, arterio-venous
fistula, arterio-venous, carotid-cavernous
fistula, arterio-venous, pulmonary
fundus, abnormality of
gait disorder
gastrointestinal bleeding
gender
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
granulomatosis with polyangiitis
headache
headache, positional
headache, thunderclap
hearing loss
hemangioblastoma
hemangioma
hemangioma, internal organs
hemangioma, skin
hematuria, gross
hematuria, microscopic
hemianopia, homonymous
hemoglobin abnormality, neurologic complications of
hemoptysis
hemorrhage, putamenal
hemorrhage, thalamic
hemorrhagic diathesis
hemosiderosis of CNS, superficial
hepatic encephalopathy
hepatomegaly
hereditary hemorrhagic telangiectasia(HHT)
hippocampus
homocystinuria
Horner's syndrome
HTRA1 gene
hyperhidrosis
hyperhomocysteinemia
hyperpigmentation of skin
hypertension
hypoxia
hypoxia, newborn
hypoxic encephalopathy
iatrogenic neurologic disorders
intellectual deficit
interobserver agreement
intracerebral hemorrhage
intracerebral hemorrhage, familial
intracerebral hemorrhage, young adult
intracranial hemorrhage
intracranial hypertension, benign
intracranial hypertension, benign, differential diagnosis
intracranial hypertension, benign, pathogenesis of
intracranial pressure, increased
joint hypermobility
lacunar infarction
leukoencephalopathy
liver disease
lumbar puncture
malformation, vascular
malformation, vascular, cerebral
malformation, vascular, familial
malformation, vascular, screening for
malformation, Vein of Galen
Marfan syndrome
marihuana
MELAS syndrome
meningeal enhancement
menses
microhemorrhage, intracerebral
migraine
migraine, hemiplegic
misdiagnosis
mitral valve prolapse
molecular genetics
mononeuropathy multiplex
mortality
moyamoya
MRI
MRI, abnormal
MRI, angiography
MRI, contrast enhanced
MRI, diffusion weighted
muscle biopsy
muscle hypertrophy
muscle weakness
muscle weakness, proximal
myopathy
myopathy, metabolic
myopathy, vacuolar
nausea and vomiting
neoplasm, primary of CNS
neurocutaneous disease
neurofibromatosis 1
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neuropathy
neuropathy, vasculitic, systemic
next-generation sequencing
obesity
ophthalmoplegia
optic nerve sheath fenestration
optic nerve, decompression of
optic nerve, lesion of
orthopnea
osteogenesis imperfecta
pain, flank
papilledema
paraparesis
paraparesis, spastic
Parkinsonism syndrome
patient information and support
pheochromocytoma
pleocytosis of cerebrospinal fluid
polycystic kidneys
polycythemia, primary
polycythemia, secondary
portal caval shunt
preclinical
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
prognosis
protein C deficiency
pseudobulbar palsy
pseudoxanthoma elasticum
psychiatric problems in neurologic disorders
psychosocial aspects
radiation therapy, stereotactic
renal cell carcinoma
renal cyst
renal failure
respiratory failure
retinal hemangioma
retinal hemorrhages
retinal tumor
retinopathy
review article
risk factors
risk factors, modification
risk-benefit assessment
screening
seizure
short stature
shunt procedure, lumboperitoneal
sibling
sickle cell disease
skin, biopsy
skin, hyperextensible
skin, lesions in neurologic disorders
skin, thin
skin, translucent
skull x-ray, abnormal
small vessel disease
spinal cord
spinal cord, lesion of
spinal cord, neoplasm
spinal cord, vascular malformation of
spondylosis
stare
stent, venous sinus
subarachnoid hemorrhage
subarachnoid hemorrhage, familial
subarachnoid hemorrhage, prognosis
subarachnoid hemorrhage, recurrent
subdural hematoma
superior sagittal sinus thrombosis
systemic illness
telangiectases
telangiectases, retinal
thrombocytopenia
tongue, enlarged
tongue, weakness
transient ischemic attack
treatment of neurologic disorder
tuberous sclerosis
twins
vasculopathy
venous hemangioma
visual field defect
visual field testing
visual loss
visual loss, slow
vital capacity
Von Hippel Lindau
weakness, progressive
white matter disease
white matter disease, subcortical
wound healing, poor
Showing articles 0 to 50 of 9045 Next >>

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

Smoking Causes Fatal Subarachnoid Hemorrhage
Stroke 51:3018-3022, Rautalin, I.,et al, 2020

A 14-Year-Old Girl with Headache, Seizures, and Confusion
Neurol 92:e161-e167, Xiao, L.,et al, 2019

Ehlers-Danlos Syndromes
BMJ 366:I4966, Ghali, N.,et al, 2019

Mystery Case: A 21-Year-Old Man with Visual Loss Following Marijuana Use
Neurol 84:e165-e169, Whitlock, J.B.,et al, 2015

Disturbances of Cerebrospinal Fluid, Including Hydrocephalus, Pseudotumor Cerebri, and Low-Pressure Syndromes, Pseudotumor Cerebri
Adams & Victors Principles of Neurology, Chp 30, pg 628, Ropper, A.H.,et al, 2014

Vertebral Artery Dissection in Patients with Autosomal Dominant Polycystic Kidney Disease
J Stroke Cerebrovasc Dis 23:441-443, Kuroki, T.,et al, 2014

Screening Patients with a Family History of Subarachnoid Haemorrhage for Intracranial Aneurysms: Screening Uptake, Patient Characteristics and Outcome
JNNP 83:86-88, Miller, T.D.,et al, 2012

Treat Alzheimer Disease Before It Is Symptomatic
Arch Neurol 68:1237-1238, , 2011

Optimal Screening Strategy for Familial Intracranial Aneurysms: A Cost-Effectiveness Analysis
Neurol 74:1671-1679, Bor,A.S.E., et al, 2010

Screening for Intracranial Aneurysms in ADPKD: A More Accurate Risk Assignment Model Is Needed
BMJ 339:706-707, Ong,A., 2009

Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease
NEJM 360:1729-1739, Hara,K.,et al, 2009

Psychosocial Impact of Screening for Intracranial Aneurysms in Relatives with Familial Subarachnoid Hemorrhage
Stroke 36:836-840, Wermer,M.J.H.,et al, 2005

Familial Leptomeningeal Amyloidosis With a Transthyretin Variant Asp18Gly Representing Repeated Subarachnoid Haemorrhages With Superficial Siderosis
JNNP 75:1463-1466, Jin,K.,et al, 2004

Repeated Screening for Intracranial Aneurysms in Familial Subarachnoid Hemorrhage
Stroke 34:2788-2791, Wermer,M.J.H.,et al, 2003

Subarachnoid Hemorrhage
Stroke 33:1321-1326, Kissela,B.M.,et al, 2002

Advances in the Genetics of Cerebrovascular Disease and Stroke
Neurol 56:997-1008, Hademenos,G.J.,et al, 2001

Risk of Subarachnoid Haemorrhage in First Degree Relatives of Patients with Subarachnoid Haemorrhage: Follow Up Study Based on National Registries in Denmark
BMJ 320:141-145, Gaist,D.,et al, 2000

Recommendations for the Management of Patients with Unruptured Intracranial Aneurysms
Stroke 31:2742-2750, Bederson,J.B.,et al, 2000

MR Angiography as a Screening Tool for Intracranial Aneurysms:Feasibility, Test Characteristics, and Interobserver Agreement
AJR 173:1469-1475, Raaymakers,T.W.M.,et al, 1999

Familial Subarachnoid Hemorrhage, Outcome Study
Stroke 30:1099-1102, Ronkainen,A.,et al, 1999

MR Angiography and Surgery for Unruptured Familial Intracranial Aneurysms in Persons with a Family History of Cerebral Aneurysms
AJR 173:133-138, Brown,B.M.&Soldevilla,F., 1999

Aneurysms in Relatives of Patients with Subarachnoid Hemorrhage,Frequency and Risk Factors
Neurol 53:982-988, Raaymakers,T.W.M.&the MARS Study Group, 1999

Risks and Benefits of Screening for Intracranial Aneurysms in First-Degree Relatives of Patients with Sporadic Subarachnoid Hemorrhage
NEJM 341:1344-1350, The Magnetic Resonance Angiography in Relatives of, 1999

Should We Screen for Familial Intracranial Aneurysm?
Stroke 30:312-316, Crawley,F.,et al, 1999

Risk of Harboring an Unruptured Intracranial Aneurysm
Stroke 29:359-362, Ronkainen,A.,et al, 1998

Initial and Follow-up Screening for Aneurysms in Families with Familial Subarachnoid Hemorrhage
Neurol 51:1125-1130, Raaymakers,T.W.M.,et al, 1998

Familial Intracranial Aneurysms
Lancet 349:380-384, Ronkainen,A.,et al, 1997

Subarachnoid Hemorrhage and Family History:A Population-Based Case-Control Study
Arch Neurol 52:202-204, Wang,P.S.,et al, 1995

Intracranial Aneurysms:MR Angiographic Screening in 400 Asymptomatic Individuals with Increased Familial Risk
Radiology 195:35-40, Ronkainen,A.,et al, 1995

Outcome in Familial Subarachnoid Hemorrhage
Stroke 26:961-963, Bromberg,J.E.C.,et al, 1995

Predictors of Neonatal Encephalopathy in Full Term Infants
BMJ 331:598-602, Adamson,S.J.,et al, 1995

Familial Aorto-Cervicocephalic Arterial Dissections and Congenitally Bicuspid Aortic Valve
Stroke 26:1935-1940, Schievink,W.I.&Mokri,B., 1995

Familial Subarachnoid Hemorrhage:Distinctive Features and Patterns of Inheritance
Ann Neurol 38:929-934, Bromberg,J.E.C.,et al, 1995

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

Cerebrovascular Complications in Ehlers-Danlos Syndrome Type IV
Ann Neurol 38:960-964, North,K.N.,et al, 1995

On the Inheritance of Intracranial Aneurysms
Stroke 25:2028-2037, Schievnink,W.I.,et al, 1994

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

Neurovascular Manifestations of Heritable Connective Tissue Disorders:A Review
Stroke 25:889-903, Schievink,W.I.,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 Aneurysms, A Review
Stroke 23:1024-1030, terBerg,H.W.M.,et al, 1992

Intracranial Aneurysms in Autosom Dominant Polycystic Kidney Disease
NEJM 327:916-920, 9531992., Chapman,A.B.,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

Familial Association of Intracranial Aneurysms and Cervical Artery Dissections
Stroke 22:1426-1430, Schievink,W.I.,et al, 1991

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

Cerebrovascular Disease in Ehlers-Danlos Syndrome Type IV
Stroke 21:626-632, Schievink,W.I.,et al, 1990

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

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

Adult Polycystic Kidney Disease & Intracranial Aneurysms
BMJ 295:526, Saifuddin,A.&Dathan,J.R.E., 1987



Showing articles 0 to 50 of 9045 Next >>