Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
acquired immunodeficiency syndrome
activated protein C resistance
addiction, heroin
alcohol
algorithm
aminoacidurias
ammonia
amphotericin B
anatomy of
anorexia
anticardiolipin antibodies
anticoagulant, treatment
antiphospholipid antibodies
antithrombin III deficiency
Arnold Chiari malformation
aspirin
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, truncal
ataxic gait
Babinski sign
basal ganglia
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basilar artery occlusion
Behcet's syndrome
beriberi
beriberi, infantile
blood dyscrasias, neurologic findings with
brain atrophy
brainstem
brainstem, lesion of
bulimia
calcification, intracranial
Canavan's disease
carbenoxolone
carbon monoxide poisoning
cardiac arrest
cardiac arrest and resuscitation
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, contrast enhanced
CAT scan, delta sign, empty
CAT scan, false negative
CAT scan, venography
cataracts
caudate nucleus
caudate nucleus, lesion of
caudate nucleus, lesion of, bilateral
central nervous system, infection of
central pontine myelinolysis
cerebellar ataxia, children
cerebellar ataxia, children, differential diagnosis of
cerebellar atrophy, secondary
cerebellar lesion
cerebral cortex
cerebral infarction
cerebral ischemia
cerebral venous infarction
cerebral venous thrombosis
cerebral venous thrombosis, deep
cerebral venous thrombosis, etiology
cerebral venous thrombosis, recurrent
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, acute management of
cerebrovascular accident, cost of
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, mimics
cerebrovascular accident, nonvascular territory
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
chorea
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
clofibrate
coagulopathy
coenzyme Q10 deficiency
cognition
color vision, impaired
complications
cost effectiveness
craniectomy, decompressive
crying
cultured skin fibroblasts
cytochrome c oxidase
cytochrome c oxidase, deficiency
D-dimer
deafness
deafness, congenital
deep gray nuclei
degenerative diseases of CNS
dementia
dentate nuclei
dentate nuclei, lesion of
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes mellitus
differential diagnosis
dipyridamole
disseminated intravascular coagulation(DIC)
diuretic
dizziness
drug induced neurologic disorders
dural sinus thrombosis
dysarthria
dystonia
electrocardiogram, abnormal
electron microscopy
embolism, platelet
encephalitis
encephalitis, Japanese
encephalitis, viral
encephalopathy
encephalopathy, neonatal
endovascular therapy
enkephalins
enolase
enzyme, defect
enzyme, muscle disease
epidemiology of neurology
epsilon-aminocaproic acid(E.A.C.A.)
evidence-based research
eye movement, disorders of
Fabry's disease
Factor V Leiden
Fahr disease
failure to thrive
false negative
familial
fibrinolytic agents
fibrinolytic agents, intra-venous local infusion
flavivirus
fontanel, bulging
Friedreich's ataxia
gadolinium
gene
gene mutation
gene therapy
genetic counselling
genetic neurologic disorders
genetic testing
glioma
glutaric acidemia
gyrus, abnormal
head injury
head injury, pediatric
head lag
headache
headache, persistent
headache, severe
hearing loss
heart block
hemiparesis
hemoglobin abnormality, neurologic complications of
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
hiccoughs
histochemistry
histochemistry of muscle
human immunodeficiency virus type 1
hydrocephalus
hypercholesterolemia
hyperglycemia
hyperphagia
hyperreflexia
hypoglycemia
hypokalemia
hyponatremia
hypothermia
hypotonia
hypotonia, infants
hypoxic encephalopathy
iatrogenic neurologic disorders
inborn errors of metabolism
incidence
infant and newborn with distress, neurologic prognosis in
infant, evaluation of
infantile hemiplegia
intellectual deterioration
internuclear ophthalmoplegia
internuclear ophthalmoplegia, unilateral
interobserver agreement
intestinal pseudoobstruction
intracranial hypertension, benign
intracranial pressure, increased
intraventricular hemorrhage
ipecac
iron, brain
irritability
Jakob-Creutzfeldt disease
Kearns-Sayre syndrome
lactic acidemia
Leber's hereditary optic neuropathy
leg numbness
leg weakness, bilateral
Leigh's disease
Leigh's disease, adult variety
lenticular nucleus, lesion of
lenticular nucleus, lesion of, bilateral
lethargy
leukemia
leukemia, neurologic findings assoc.with
leukocyte enzyme abnormality
leukodystrophy
leukoencephalopathy
level of consciousness, decreased
lipid lowering agent
lipid storage disorder of CNS
lipids
liquorice
liver disease
lupus anticoagulant
magnetic susceptibility
maple syrup urine disease
Marinesco-Sjogren syndrome
MELAS syndrome
meningitis
mental retardation
MERRF syndrome
metabolic disorder, primary
metabolic disorder, primary-screening tests
metronidazole
microhemorrhage, intracerebral
midbrain, lesion of
middle cerebral artery territory infarction
middle cerebral artery, occlusion of
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
mitochondrial recessive ataxic syndrome
MNGIE syndrome
molecular genetics
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, complications with
MRI, contrast enhanced
MRI, diffusion weighted
MRI, false negative
MRI, negative
MRI, paramagnetic effect
MRI, serial
MRI, spinal cord
MRI, T1 weighted high signal foci
MRI, target sign
MRI, venography
MRS
multiple sclerosis
multiple sclerosis, differential diagnosis of
muscle biopsy
muscle pain
muscle swelling
muscle tenderness
muscle weakness
muscle weakness, causes of
myelitis, longitudinal
myelopathy
myeloproliferative disorder
myoclonic jerks
myoclonus
myoclonus, epilepsy
myoglobinuria
myopathy
myopathy, acute
myopathy, alcoholic
myopathy, drug-induced
myopathy, hypokalemic
myopathy, mitochondrial
myopathy, proximal
myopathy, steroid induced
nausea and vomiting
neoplasm, primary of CNS
neurofibromatosis 1
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neuron specific enolase
neuropathology
neuropathology, brain
neuropathy
neuropathy, ataxia, retinitis pigmentosa
neuropathy, peripheral
neurotoxin
nonsteroidal anti-inflammatory drug
nutritional deficiency
nystagmus
nystagmus, rotary
ophthalmoplegia
ophthalmoplegia, progressive external
optic atrophy
optic atrophy, hereditary
optic neuropathy
oral contraceptives
oral contraceptives, cerbrovascular disease and
oral contraceptives, neurologic complications with
osmotic demyelination syndrome
overlap syndrome
owl's eye sign of spinal cord
pancytopenia
paraparesis, spastic
Parkinson disease
paroxysmal nocturnal hemoglobinuria
perhexiline maleate
pes cavus
pigmentary retinopathy
pitfalls
plasminogen deficiency
platelet inhibiting drugs
POLG1 gene
polycythemia, primary
polyneuropathy
pons, lesion of
practice guidelines
pregnancy, neurologic complications in
prethrombotic state
primary thrombocythemia
prognosis
progressive infantile poliodystrophy
protein C deficiency
protein S deficiency
psychiatric problems in neurologic disorders
psychomotor retardation
ptosis
pulmonary embolism
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract dysfunction
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriparesis
ragged-red fibers
remote effect of cancer on the nervous system
respiratory failure
restless leg syndrome
retinopathy
review article
rhabdomyolysis
risk factors
Romberg's sign
S-100 protein
seizure
seizure, children
sensorineural hearing loss
sensory loss
short stature
sickle cell disease
spasticity
speech, loss of
spinal cord
spinal cord, lesion of
spinocerebellar degeneration
spongy degeneration of brain
status epilepticus
steroid
straight sinus
striatonigral degeneration
striatonigral degeneration, infantile
striatum, lesion of
striatum, lesion of, bilateral
strokelike episodes
substantia nigra
suck, poor
sulfinpyrazone
superior sagittal sinus thrombosis
symmetric brain lesions
term infant
thalamic tumors
thalamic tumors, bilateral
thalamus
thalamus, infarction of
thalamus, infarction, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
thiamine deficiency
thrombocytopenia
thrombophlebitis
tissue plasminogen activator, intravenous
titubation
tonic spasms
transient ischemic attack
transient ischemic attack, treatment of
treatment of neurologic disorder
tremor
tremor, intention
triglycerides
urine test for metabolic disorders
vincristine neurotoxicity
visual acuity, decreased
vitamin deficiency
Von Hippel Lindau
weakness
weakness, progressive
weight loss
Wernicke's encephalopathy
white matter disease
white matter disease, periventricular
wide based gait
workup
Showing articles 0 to 50 of 63 Next >>

Pediatric Leigh Syndrome
Ann Neurol 88:218-232, Alves, C.A.P.F.,et al, 2020

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

Pyruvate Dehydrogenase Deficiency (PDCD)
eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018

Dentate Update: Imaging Features of Entities that Affect the Dentate Nucleus
AJNR 38:1467-1474, Bond, K.M.,et al, 2017

Clinical, Genetic, and Radiological Features of Extrapyramidal Movement Disorders in Mitochondrial Disease
JAMA Neurol 73:668-674, Martikainen, M.H.,et al, 2016

Inherited Metabolic Diseases of the Nervous System, Subacute Necrotizing Encephalopathy (Leigh Disease)
Adams & Victors Principles of Neurology, Chp 37, pg 996, Ropper, A.H.,et al, 2014

Differential Diagnosis of Bilateral Abnormalities of the Basal Ganglia and Thalamus
RadioGraphics 31:5-30, Hegde,A.N.,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

The Use of Neuroimaging in the Diagnosis of Mitochondrial Disease
Dev Disabil Res Rev 16:129-135, Friedman, S.D.,et al, 2010

A 41-Year-Old Woman with Progressive Leg Weakness and Numbness, Dizziness, and Myalgia
Neurol 72:1262-1276, DiMauro,S.,et al, 2009

Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
JNNP 80:943-953, Rahman,S. &Hanna,M.G., 2009

Bilateral Thalamic Lesions
AJR 192:W53-W62, Smith,A.B.,et al, 2009

Clinicopath Conf., Leighs syndrome, Intraventricular Hemorrhage and Periventricular Leukomalacia
NEJM 359:1156-1166, Case 28-2008, 2008

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

The Incidence of Mitochondrial Encephalomyopathies in Childhood: Clinical Features and Morphological, Biochemical, and DNA Abnormalities
Ann Neurol 49:377-383, Darin,N.,et al, 2001

Leigh Syndrome: Serial MR Imaging and Clinical Follow-Up
AJNR 21:1502-1509, Arii,J. & Tanabe,Y., 2000

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

Leigh Syndrome:Clinical Features and Biochemical DNA Abnormalities
Ann Neurol 39:343-351, Rahman,S.,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

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

Prothrombotic States in Young People with Idiopathic Stroke:Prospective Study
Stroke 25:287-290, Baringarrementeria,F., 1994

The Mutations at nt 8993 of Mitochondrial DNA is a Common Cause of Leigh's Syndrome
Ann Neurol 34:827-834, Santorelli,F.M.,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

Molecular Genetic Characterization of an X-Linked Form of Leigh's Syndrome
Ann Neurol 33:652-655, Matthews,P.M.,et al, 1993

Protein S Deficiency in Middle-Aged Women with Stroke
Neurol 42:1029-1033, Green,D.,et al, 1992

Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992

Superior Sagittal Sinus Thrombosis in a Child with Protein S Deficiency
Neurol 42:2303-2305, Prats,J.M.,et al, 1992

Neurodegenerative Diseases of Childhood:MR and CT Evaluation
J Comput Assist Tomogr 15:210-222, Mirowitz,S.A.,et al, 1991

Superior Sagittal Sinus Thrombosis in a Patient with Protein S Deficiency
Stroke 21:633-636, Cros,D.,et al, 1990

MR Findings in Patients with Subacute Necrotizing Encephalomyelopathy (Leigh Syndrome)
AJR 154:1269-1274, Medina,L.,et al, 1990

Hematologic Disorders and Ischemic Stroke
Stroke 21:1111-1121, Hart,R.G.&Kanter,M.C., 1990

Leigh Disease:Value of CT in Presymptomatic Patients and Variability of the Lesions with Time
J Comput Assist Tomogr 13:207-210, Taccone,A.,et al, 1989

Leigh Disease (Subacute Necrotizing Encephalomyelopathy) :CT & MR in Five Cases
J Comput Assist Tomogr 12:40-44, Geyer,C.A.,et al, 1988

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

Progressive Dystonia with Bilateral Putaminal Hypodensities
Arch Neurol 44:1184-1187, Berkovic,S.F.,et al, 1987

Magnetic Resonance Imaging in Autopsy-Proved Adult Subacute Necrotizing Encephalomyelopathy (Leigh's Disease)
Arch Neurol 44:563-566, Kissel,J.T.,et al, 1987

Cytochrome c Oxidase Deficiency in Leigh Syndrome
Ann Neurol 22:498-506, DiMauro,S.,et al, 1987

Infantile Beriberi Presenting as Subacute Necrotizing Encephalomyelopathy
J Pediatr 110:888-892, Wyatt,D.T.,et al, 1987

Computerized Tomography in Subacute Necrotizing Encephalomyelopathy (Leigh Disease)
Ann Neurol 10:268-271, Schwartz,W.J.,et al, 1981

Hyper-Endorphin Syndrome in a Child With Necrotizing Encephalomyelopathy
NEJM 303:914-916, Brandt,N.J.,et al, 1980

Familial Subacute Necrotizing Encephalomyelopathy of the Adult Form (Adult Leigh Syndrome)
Ann Neurol 6:200-206, Kalimo,H.,et al, 1979



Showing articles 0 to 50 of 63 Next >>