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Differential
(Click to cross reference)
acquired immunodeficiency syndrome
activated protein C resistance
acute cerebellar ataxia
addiction, heroin
adrenoleukodystrophy
adverse drug reaction
alcohol
algorithm
amphotericin B
anosmia
anticardiolipin antibodies
anticoagulant, treatment
antiphospholipid antibodies
antithrombin III deficiency
arrhythmia, cardiac
aspirin
ataxia
ataxic gait
Bassen-Kornzweig syndrome
behavioral disorder
Behcet's syndrome
blood dyscrasias, neurologic findings with
carbenoxolone
cardiac arrest
cardiac arrest and resuscitation
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, delta sign, empty
CAT scan, venography
cataracts
cerebellar ataxia, children
cerebellar ataxia, children, differential diagnosis of
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
cerebrospinal fluid, elevated protein of
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
Charcot-Marie-Tooth
children
chloroquine
cholesterol
clofibrate
clubfoot as related to neurologic disease
coagulopathy
Cockayne's syndrome
complications
cost effectiveness
craniectomy, decompressive
cyanide poison
D-dimer
deafness
Dejerine-Sottas syndrome
dilantin
dipyridamole
disseminated intravascular coagulation(DIC)
diuretic
DNA probes
drug induced neurologic disorders
drug induced neurologic disorders in children
dural sinus thrombosis
dysmorphic
electrocardiogram, abnormal
electronystagmography
electroretinograph
embolism, platelet
endovascular therapy
enolase
enzyme, muscle disease
epidemiology of neurology
epsilon-aminocaproic acid(E.A.C.A.)
evidence-based research
facial nerve palsy
Factor V Leiden
false negative
familial
fibrinolytic agents
fibrinolytic agents, intra-venous local infusion
Fisher's syndrome
foot deformity
foot drop
fundus, abnormality of
gadolinium
gene mutation
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
Guillain Barre syndrome, variant forms of
Hallervorden Spatz disease
Hallgren's syndrome
Hartnup's disease
head injury
head injury, pediatric
headache
headache, persistent
headache, severe
hearing loss
hemiparesis
hemoglobin abnormality, neurologic complications of
hepatomegaly
human immunodeficiency virus type 1
hydrocephalus
hypercholesterolemia
hypoglycemia
hypokalemia
hypotonia
hypoxia
hypoxic encephalopathy
incidence
infantile hemiplegia
interobserver agreement
intracranial hypertension, benign
intracranial pressure, increased
ipecac
Kearns-Sayre syndrome
kyphoscoliosis, neurologic causes of
Laurence-Moon-Bardet-Biedl syndrome
leukemia
leukemia, neurologic findings assoc.with
level of consciousness, decreased
lipid lowering agent
lipids
liquorice
lupus anticoagulant
macular degeneration
meningitis
mental retardation
middle cerebral artery territory infarction
middle cerebral artery, occlusion of
mimics
misdiagnosis
mortality
motor neuron disease
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, false negative
MRI, negative
MRI, venography
mucopolysaccharidoses
muscle atrophy, progressive
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
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination, focal
neuron specific enolase
neuronal ceroid-lipofuscinosis
neuropathy
neuropathy, ataxic
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, onion bulb
night blindness
nonsteroidal anti-inflammatory drug
nystagmus
nystagmus, pendular
ophthalmoplegia
optic atrophy
optic nerve
optic neuropathy
oral contraceptives
oral contraceptives, cerbrovascular disease and
oral contraceptives, neurologic complications with
paroxysmal nocturnal hemoglobinuria
perhexiline maleate
peroneal muscle atrophy, causes of
peroxisomal disease
peroxisomes
pes cavus
phytanic acid
pigmentary retinopathy
pitfalls
plasminogen deficiency
platelet inhibiting drugs
poison, mercury
polycythemia, primary
polyneuropathy
practice guidelines
pregnancy, neurologic complications in
prethrombotic state
primary thrombocythemia
prognosis
protein C deficiency
protein S deficiency
psychomotor retardation
pulmonary embolism
pupil, abnormality in neurologic disorders
pupil, light reflex, abnormal
refractive errors
Refsum's disease
retinal degeneration
retinal lesion
retinitis pigmentosa
retinopathy
review article
rhabdomyolysis
risk factors
Roussy Levy syndrome
roving eye movements
S-100 protein
seizure
seizure, neonatal
sensorineural hearing loss
sensory loss
sickle cell disease
spinocerebellar degeneration
steroid
straight sinus
sudden death
sulfinpyrazone
superior sagittal sinus thrombosis
tapetoretinal degeneration
thrombocytopenia
thrombophlebitis
tissue plasminogen activator, intravenous
toxins, nervous system
transient ischemic attack
transient ischemic attack, treatment of
treatment of neurologic disorder
triglycerides
Usher's syndrome
vincristine neurotoxicity
viral infection, CNS
visual acuity, decreased
visual field defect
visual fields, constricted
visual loss
weakness
workup
Showing articles 0 to 35 of 35

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

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

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

Variants and Mimics of Guillain Barre Syndrome
The Neurologist 10:61-74, Levin,K.H., 2004

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

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

Refsum Disease
In Rowland's Merritt's Textbk of Neurology, Lea & Febiger, Phila, 8thEd, p. 509, Menkes,J.H., 1989

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

The Peroxisome:Nervous System Role of a Previously Underrated Organelle, The 1987 Robert Wartenberg Lecture
Neurol 38:1617-1627, Moser,H.W., 1988

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

Phytanic Acid Storage Disease:Hearing Maintained After 15 Years of Dietary Treatment
Neurol 33:237-240, Djupesland,G.,et al, 1983

Heredopathia Atactica Polyneuritiformis
Arch Neurol 38:605-606, Refsum,S., 1981

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

Tapetoretinal Degeneration in Childhood Presenting as a Disturbance of Behavior
BMJ 202, 1972 Jan., Harcourt,B.,et al, 1972

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

Lower Motor & Primary Sensory Neuron Diseases with Peroneal Muscular Atrophy
Arch Neurol 18:603, Dyck,P.,et al, 1968

Ataxia In Childhood
Dev Med Child Neurol 10:388-389, Wilson,J., 1968



Showing articles 0 to 35 of 35