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Differential
(Click to cross reference)
adverse drug reaction
agitation
anticholinergic drugs
anxiety
aortic valve, stenosis
arrhythmia, cardiac
autonomic cardiovascular reflexes
carotid sinus syndrome
confusion
conversion reaction
echocardiogram
electrocardiogram, abnormal
hallucination
Holter monitoring
hydrocephalus
hypertrophic cardiomyopathy
iatrogenic neurologic disorders
idiopathic hypertrophic subaortic stenosis
intracardiac electrophysiologic testing
intracranial pressure, increased
mortality
myocardial infarction
myocardial infarction, acute
old age, neurology of
orthostatic hypotension
pacemaker, cardiac-transvenous
Parkinson disease
prognosis
psychiatric disorder
psychosis
pupil, dilated and fixed, unilateral
pupil, dilated, unilateral
review article
scopolamine
Stokes-Adams syndrome
sudden death
syncope
syncope, differential diagnosis of
transdermal medication
transderm-V
transient ischemic attack
treatment of neurologic disorder
upright-tilt test
vertebral-basilar insufficiency
Showing articles 0 to 32 of 32

Transderm-induced Psychosis in Parkinson's Disease
Neurol 53:433-434, Minagar,A.,et al, 1999

Syncope:Current Diagnostic Evaluation and Management
Ann Int Med 112:850-863, Manolis,A.S.,et al, 1990

Transderm Pupil & Confusion in a 10-Year-Old
Ann Neurol 13:583, Johnson,S.F.,et al, 1983

Scopalamine Psychosis Revisited
Ann Neurol 13:582, Cairncross,J.G., 1983

Cycloplegia From Transdermal Scopolamine
NEJM 306:174, Chiaramonte,J.S., 1982

Anisocoria From Scopolamine Patches
JAMA 248:353-354, McCrary,J.A.,et al, 1982

Genes Associated With Adult Cerebral Venous Thrombosis
Stroke 42:913-918, Marjot,T.,et al, 2011

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

Artery of Percheron Infarction: Imaging Patterns and Clinical Spectrum
AJNR 31:1283-1289, Lazarro,N.A., et al, 2010

Inverted V Sign in Subacute Combined Degeneration of Spinal Cord
Neurol 72:e3, Kumar,A.&Singh,A.K., 2009

Investigating Suspected Cerebral Venous Thrombosis
BMJ 334:794-795, Smit,R. &Hourihan,M.D., 2007

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

Acute Compartment Syndrome After Forearm Ischemic Work Test in a Patient with McArdle's Disease
Neurol 56:1779-1780, Lindner,A.,et al, 2001

Factor V Leiden and Antiphospholipid Antibodies Are Significant Risk Factors for Ischemic Stroke in Children
Stroke 31:1283-1288, Kenet,G.,et al, 2000

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

High Risk of Cerebral-Vein Thromb in Carriers of Prothrombin-Gene Mutation & Users of Oral Contracept
NEJM 338:1793-1797, 18401998., Martinelli,I.,et al, 1998

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

Factor V Leiden Mutation is a Risk Factor for Cerebral Venous Thrombosis,A Case-Control Study of 55 Patients
Stroke 29:2507-2510, Ludemann,P.,et al, 1998

Factor V Leiden Mutation in a Case with Ischemic Stroke: Which Relationship?
Angiology 49:79-82, Orlandi, G.,et al, 1998

Reduced Response to Activated Protein C is Associated with Increased Risk for Cerebrovascular Disease
Ann Int Med 125:265-269, van der Bom,J.G.,et al, 1996

Cerebral Venous Sinus Thrombosis Associated with Factor V Gene Mutation
JNNP 61:204-205, Kimber,T.,et al, 1996

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

Cerebral Venous Thrombosis:Role of Activated Protein C Resistance and Factor V Gene Mutation
Stroke 27:1719-1720, Brey,R.L.&Coull,B.M., 1996

Ischemic Stroke in Young Pts with Activated Protein C Resistance:Rpt of Three Cases Belonging to Three Different Kindreds
Stroke 26:885-890, Simioni,P.,et al, 1995

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

McArdle's Disease with Late-Onset Symptoms:Case Report & Review of the Literature
JNNP 55:407-408, Felice,K.J.,et al, 1992

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

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

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



Showing articles 0 to 32 of 32