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Differential
(Click to cross reference)
acquired immunodeficiency syndrome
activated protein C resistance
addiction, heroin
alcohol
algorithm
amphotericin B
anticardiolipin antibodies
anticoagulant, treatment
antiphospholipid antibodies
antithrombin III deficiency
aspirin
Behcet's syndrome
blood dyscrasias, neurologic findings with
bulbar palsy
carbenoxolone
cardiac arrest
cardiac arrest and resuscitation
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, delta sign, empty
CAT scan, venography
cerebral infarction
cerebral ischemia
cerebral venous infarction
cerebral venous thrombosis
cerebral venous thrombosis, deep
cerebral venous thrombosis, etiology
cerebral venous thrombosis, recurrent
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
chromosome 11
clofibrate
coagulopathy
compartment syndrome
complications
cost effectiveness
craniectomy, decompressive
creatine phosphokinase(CPK)elevated
D-dimer
dipyridamole
disseminated intravascular coagulation(DIC)
diuretic
drug induced neurologic disorders
dural sinus thrombosis
electrocardiogram, abnormal
electromyogram
embolism, platelet
endovascular therapy
enolase
enzyme, defect
enzyme, muscle disease
epidemiology of neurology
epsilon-aminocaproic acid(E.A.C.A.)
evidence-based research
exercise
exercise intolerance
exercise-related muscle strength increase
Factor V Leiden
false negative
familial
fatigue
fibrinolytic agents
fibrinolytic agents, intra-venous local infusion
floppy infant
gadolinium
gene
gene mutation
genetic neurologic disorders
genetic testing
glycogen storage disease
head injury
head injury, pediatric
headache
headache, persistent
headache, severe
hemiparesis
hemoglobin abnormality, neurologic complications of
human immunodeficiency virus type 1
hydrocephalus
hypercholesterolemia
hypokalemia
hypotonia, infants
hypoxic encephalopathy
iatrogenic neurologic disorders
incidence
infantile hemiplegia
interobserver agreement
intracranial hypertension, benign
intracranial pressure, increased
ipecac
ischemic exercise test
leukemia
leukemia, neurologic findings assoc.with
leukocytes
level of consciousness, decreased
lipid lowering agent
lipids
liquorice
lupus anticoagulant
McArdle's disease
McArdle's disease, adult onset
meningitis
middle cerebral artery territory infarction
middle cerebral artery, occlusion of
misdiagnosis
molecular genetics
mortality
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, false negative
MRI, negative
MRI, venography
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle cramp
muscle pain
muscle phosphofructokinase deficiency
muscle phosphorylase deficiency
muscle stiffness
muscle swelling
muscle tenderness
muscle weakness
muscle weakness, causes of
muscle weakness, proximal
myeloproliferative disorder
myoglobinuria
myopathy
myopathy, acute
myopathy, alcoholic
myopathy, drug-induced
myopathy, hypokalemic
myopathy, metabolic
myopathy, proximal
myopathy, steroid induced
nausea and vomiting
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination, focal
neuron specific enolase
nonsteroidal anti-inflammatory drug
oral contraceptives
oral contraceptives, cerbrovascular disease and
oral contraceptives, neurologic complications with
pain
pain, arm
paroxysmal nocturnal hemoglobinuria
PAS positive
perhexiline maleate
phosphorylase b kinase deficiency
pitfalls
plasminogen deficiency
platelet inhibiting drugs
polycythemia, primary
polymerase chain reaction
practice guidelines
pregnancy, neurologic complications in
prethrombotic state
primary thrombocythemia
prognosis
protein C deficiency
protein S deficiency
proximal muscle atrophy
pulmonary embolism
renal failure
respiratory failure
review article
RFLPs
rhabdomyolysis
risk factors
S-100 protein
second wind phenomena
seizure
sickle cell disease
steroid
straight sinus
sulfinpyrazone
superior sagittal sinus thrombosis
thrombocytopenia
thrombophlebitis
tissue plasminogen activator, intravenous
transient ischemic attack
transient ischemic attack, treatment of
treatment of neurologic disorder
triglycerides
urine, dark
vincristine neurotoxicity
weakness
weakness, generalized
workup
Showing articles 0 to 36 of 36

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

Spontaneous "Second Wind" and Glucose-Induced Second "Second Wind" in McArdle Disease
Arch Neurol 59:1395-1402, Haller,R.G.&Vissing,J., 2002

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

Acute Compartment Syndrome After Forearm Ischemic Work Test in a Patient with McArdle's Disease
Neurol 56:1779-1780, Lindner,A.,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

Diagnosis of McArdle's Disease by Molecular Genetic Analysis of Blood
Neurol 47:579-580, El-Schahawi,M.,et al, 1996

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

Clinical and Biochemical Features of 10 Adult Patients with Muscle Phosphorylase Kinase Deficiency
Neurol 44:461-466, Wilkinson,D.A.,et al, 1994

Molecular Genetic Heterogeneity of Myophosphorylase Deficiency (McArdle's Disease)
NEJM 329:241-245, Tsujino,S.,et al, 1993

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

McArdle's Disease with Late-Onset Symptoms:Case Report & Review of the Literature
JNNP 55:407-408, Felice,K.J.,et al, 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

McArdle's Disease:Biochemical and Molecular Genetic Studies
Ann Neurol 24:774-781, Servidei,S.,et al, 1988

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

Phosphorylase Deficiency
In Englel & Banker, Myology, McGraw-Hill Book Co, Ch 52, 1585-1601, DiMauro,S.&Bresolin,N., 1986

McArdle's Disease in the 1980s
NEJM 312:370-371, Layzer,R.B., 1985

Fatal Infantile Form of Muscle Phosphorylase Deficiency
Neurol 28:1124-1129, DiMauro,S.,et al, 1978

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

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



Showing articles 0 to 36 of 36