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Differential
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acanthocytosis
acquired immunodeficiency syndrome
activated protein C resistance
addiction, heroin
adrenoleukodystrophy
adverse drug reaction
alcohol
algorithm
amniocentesis
amphotericin B
anticardiolipin antibodies
anticoagulant, treatment
antiphospholipid antibodies
antithrombin III deficiency
aspirin
ataxia, cerebellar
basal ganglia, calcification of
basal ganglia, lesion, bilateral
Bassen-Kornzweig syndrome
Behcet's syndrome
blindness
blood dyscrasias, neurologic findings with
brain atrophy
brainstem, atrophy
cachexia
calcification, gyral
calcification, intracranial
carbenoxolone
cardiac arrest
cardiac arrest and resuscitation
cardiomyopathy
caries
CAT scan
CAT scan, abnormal
CAT scan, delta sign, empty
CAT scan, venography
cataracts
cerebellar atrophy, secondary
cerebellar degeneration
cerebral infarction
cerebral ischemia
cerebral venous infarction
cerebral venous thrombosis
cerebral venous thrombosis, deep
cerebral venous thrombosis, etiology
cerebral venous thrombosis, recurrent
cerebro hepato renal syndrome
cerebrovascular accident
cerebrovascular accident, acute management of
cerebrovascular accident, cost of
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
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
children
chloroquine
cholesterol
chromosomal abnormality
cisterna magna, enlarged
cisternogram, radionuclide
clofibrate
coagulopathy
Cockayne's syndrome
complications
consanguinity
contractures, joint
cornea, abnormal
cornea, opacity of
corpus callosotomy
cost effectiveness
craniectomy, decompressive
cry, weak
cryptorchidism
D-dimer
deafmute
deafness
dentate nuclei, lesion of
dermatitis
developmental retardation
dipyridamole
disseminated intravascular coagulation(DIC)
diuretic
DNA probes
drug induced neurologic disorders
dural sinus thrombosis
dwarfism
dysmorphic
ear, abnormal
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electron microscopy
electronystagmography
electroretinograph
embolism, platelet
endovascular therapy
enolase
enophthalmous
enzyme, muscle disease
epidemiology of neurology
epsilon-aminocaproic acid(E.A.C.A.)
evidence-based research
eyes, sunken
facial appearance, abnormal
Factor V Leiden
false negative
familial
feeding disorder
fibrinolytic agents
fibrinolytic agents, intra-venous local infusion
Friedreich's ataxia
fundus, abnormality of
gadolinium
gargoylism
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
glaucoma
growth retardation
Hallervorden Spatz disease
Hallgren's syndrome
head injury
head injury, pediatric
headache
headache, persistent
headache, severe
hearing loss
heart block
hemiparesis
hemoglobin abnormality, neurologic complications of
human immunodeficiency virus type 1
Hurler's syndrome
hydrocephalus
hydrocephalus, normal pressure
hydrocephalus, normal pressure in children
hypercholesterolemia
hyperpigmentation of skin
hypogonadism
hypokalemia
hypomyelination
hypoxic encephalopathy
incidence
infantile hemiplegia
interobserver agreement
intracranial hypertension, benign
intracranial pressure, increased
ipecac
Kearns-Sayre syndrome
keratoconus
Laurence-Moon-Bardet-Biedl syndrome
leukemia
leukemia, neurologic findings assoc.with
leukodystrophy
leukoencephalopathy
level of consciousness, decreased
lipid lowering agent
lipids
liquorice
lupus anticoagulant
macular degeneration
malformation, CNS, congenital
meningitis
mental retardation
microcephaly
middle cerebral artery territory infarction
middle cerebral artery, occlusion of
misdiagnosis
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, false negative
MRI, negative
MRI, venography
MRS
mucopolysaccharidoses
muscle pain
muscle swelling
muscle tenderness
muscle weakness
muscle weakness, causes of
myeloproliferative disorder
myoglobinuria
myopathy
myopathy, acute
myopathy, alcoholic
myopathy, drug-induced
myopathy, hypokalemic
myopathy, mitochondrial
myopathy, proximal
myopathy, steroid induced
myopia
nausea and vomiting
nerve biopsy
neuritis
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination, focal
neuron specific enolase
neuronal ceroid-lipofuscinosis
neuropathology, brain
neuropathy
neuropathy, hereditary peripheral
neuropathy, peripheral
night blindness
nonsteroidal anti-inflammatory drug
obesity
ocular myopathy
optic atrophy
optic nerve
optic neuropathy
oral contraceptives
oral contraceptives, cerbrovascular disease and
oral contraceptives, neurologic complications with
paroxysmal nocturnal hemoglobinuria
perhexiline maleate
peroxisomal disease
photosensitivity, skin
pigmentary retinopathy
pitfalls
plasminogen deficiency
platelet inhibiting drugs
polycythemia, primary
polydactyly
practice guidelines
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
prethrombotic state
primary thrombocythemia
progeria
prognathism
prognosis
protein C deficiency
protein S deficiency
pseudoretinitis pigmentosa
psychiatric disorder
psychomotor retardation
pulmonary embolism
pupil, abnormality in neurologic disorders
putamen, lesion of
putamen, lesion of, bilateral
rash
refractive errors
Refsum's disease
retinal degeneration
retinal lesion
retinitis pigmentosa
retinopathy
review article
rhabdomyolysis
risk factors
S-100 protein
schizophrenia
seizure
sensorineural hearing loss
short stature
sickle cell disease
skin, lesions in neurologic disorders
skull x-ray, bony defect on
Spielmeyer Vogt syndrome
spinocerebellar degeneration
steroid
stooped posture
straight sinus
sulfinpyrazone
superior sagittal sinus thrombosis
tapetoretinal degeneration
thrombocytopenia
thrombophlebitis
tissue plasminogen activator, intravenous
transient ischemic attack
transient ischemic attack, treatment of
treatment of neurologic disorder
triglycerides
Usher's syndrome
vincristine neurotoxicity
visual field defect
visual fields, constricted
visual loss
white matter disease
workup
Showing articles 0 to 37 of 37

A Teenager with Persistent Headache
Neurol 92:e1526-e1531, Hu, Y.,et al, 2019

The Syndrome of Cutaneous Photosensitivity, Growth Failure, and Basal Ganglia Calcification
Neurol 87:e56-e57, Saini, A.G.,et al, 2016

Diagnosis and Management of Cerebral Venous Thrombosis: A Statement for Healthcare Professionals From the American Heart Association/American Stroke Association
Stroke 42:1158-1192, Saposnik,G.,et al, 2011

Neuroimaging in Cockayne Syndrome
AJNR 31:1623-1630, Koob,M.,et al, 2010

Protein S Deficiency in HIV Associated Ischaemic Stroke:An Epiphenomenon of HIV Infection
JNNP 76:1455-1456,1331, Mochan,A.,et al, 2005

Use of Specialized Coagulation Testing in the Evaluation of Patients with Acute Ischemic Stroke
Neurol 56:624-627, Bushnell,C.,et al, 2001

Prethrombotic Disorders in Children with Arterial Ischemic Stroke and Sinovenous Thrombosis
Arch Neurol 56:967-971, Bonduel,M.,et al, 1999

Risk of Cerebral Sinus Thrombosis in Oral Contraceptive Users Who Are Carriers of Hered Prothrombotic Cond
BMJ 316:589-592, deBruijn,S.F.T.M.,et al, 1998

Neurology and the Blood:Haematological Abnormalities in Ischaemic Stroke
JNNP 64:150-159, Markus,H.S.&Hambley,H., 1998

Serum S-100 and Neuron-Specific Enolase for Prediction of Regaining Consciousness After Global Cerebral Ischemia
Stroke 29:2363-2366, Martens,P.,et al, 1998

Inherited Prothrombotic States and Ischaemic Stroke in Childhood
JNNP 65:508-511, Ganesan,V.,et al, 1998

Human Immunodeficiency Virus Infection and Stroke in Young Patients
Arch Neurol 54:1150-1153, Qureshi,A.I.,et al, 1997

Cerebral Venous Thrombosis in Adults:A Study of 40 Cases From Saudi Arabia
Stroke 26:1193-1195, Daif,A.,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

Cockayne Syndrome: Review of 140 Cases
Am J Med Genet 42:68-84, Nance,M.A. &Berry,S.A., 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

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

MRI in Cockayne Syndrome Type 1
Neuroradiology 31:276-277, Boltshauser,E.,et al, 1989

Retinitis Pigmentosa
Surv Ophthalmol 33:137-177, Pagon,R.A., 1988

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

Prenatal Diagnosis of Cockayne's Syndrome
Lancet 1:486-488, Lehmann,A.R.,et al, 1985

Ultrastructure & Electrodiagnosis of Peripheral Neuropathy in Cockayne's Syndrome
Neurol 33:1606-1609, Grunnet,M.L.,et al, 1983

Cockayne Syndrome
J Comput Assist Tomogr 6:1172-1174, Levinson,E.D.,et al, 1982

Cockayne Syndrome:Unusual Neuropathological Findings & Review of the Literature
Ann Neurol 6:340-348, 1979, Soffer,D.,et al, 1979

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

Normal Pressure Hydrocephalus, Recog & Relation to Neuro Abnormalities in Cockayne's Sydrome
Arch Neurol 35:337, Brumback,R.A.,et al, 1978

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

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

Genetic Counseling in Retinitis Pigmentosa
MCV Quart 8:283, Noah,V., 1972

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



Showing articles 0 to 37 of 37