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Differential
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abdominal cramps
acid maltase deficiency
acid maltase deficiency, adult
acral sensory symptoms
acyl CoA dehydrogenase deficiency
adrenoleukodystrophy
adrenomyeloneuropathy
adverse drug reaction
agalsidase alfa
alpha glucosidase
aminoacidopathies
aminoacidurias
amniocentesis
angina pectoris
angiokeratoma
anhidrosis
anterior horn cell disease
anterior tibial muscle weakness
antiviral agents
Arnold Chiari malformation
arthropathy
arthropathy, neuropathic
arylsulfatase A
aspartate aminotransferase
aspiration
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, progressive
athetosis
atidarsagene autotemcel
attention deficit disorder with hyperactivity
attention span
autonomic dysfunction
axonal spheroid
Babinski sign
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basilar impression
behavioral disorder
blindness
blood dyscrasias, neurologic findings with
bone marrow biopsy
bone marrow transplantation
brain atrophy
brain biopsy
brain biopsy, complications of
brain biopsy, false negative
brain biopsy, indication
brainstem, infarction of
burning feet
burning feet, differential diagnosis of
burning hands
burning paresthesia
cardiomyopathy
carnitine deficiency
carnitine deficiency myopathy
CAT scan
CAT scan, abnormal
CAT scan, false negative
cataplexy
cataracts
cerebellar ataxia, children
cerebellar ataxia, children, differential diagnosis of
cerebellar infarction
cerebral cortical atrophy
cerebral ischemia
cerebrospinal fluid, gammaglobulin of
cerebrotendinous xanthomatosis
cerebrovascular accident
cerebrovascular accident, cryptogenic
cerebrovascular accident, familial occurrence
cerebrovascular accident, non atherosclerotic cause of
cerebrovascular accident, young adult
cerebrovascular disease
cerebrovascular disease, cardiovascular disease with
cherry red spot
cherry red spot-myoclonus syndrome
children
chorea
choreoathetosis
chromosomal abnormality
chronic graft versus host disease
Clinical Pathologic Conference(C.P.C.)
coagulopathy
cognition
coma
complications
compression fracture
congestive heart failure
consanguinity
contractures, joint
cornea, abnormal
cornea, opacification in infancy-causes of
cornea, opacity of
corneal dystrophy
corpus callosum
corpus callosum, hypoplastic
corpus callosum, lesion of
creatine phosphokinase(CPK)elevated
creatinine, elevated
cry, abnormal
cultured skin fibroblasts
cystinosis
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, childhood
dementia, diagnostic evaluation of
developmental disability
developmental milestones, loss of
developmental retardation
diarrhea
differential diagnosis
difficulty going down stairs
diplopia
distal muscle weakness
drooling
dropped head syndrome
dysarthria
dysmorphic
dysostosis multiplex
dysphagia
dystonia
dystonia, face
dystonia, focal
dystonic lipidosis
echocardiogram
efficacy
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
electron microscopy
enzyme treatment
enzyme, defect
enzyme, muscle disease
enzyme, serum
episodic disorders
episodic neurologic deficits
exercise
exercise intolerance
exercise-induced neurologic dysfunction
exome sequencing
eye movement, disorders of
Fabry's disease
facial appearance, abnormal
falling
familial
Farber's disease
fatigue
fever
fluctuate
foam cells
fracture, pathologic
Friedreich's ataxia
fucosidosis
gait disorder
galactosidase
gangliosidosis GM1
gangliosidosis GM2
gargoylism
Gaucher's disease
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
glucocerebrosidase
glycogen storage disease
glycoprotein
growth retardation
hand pain
head injury
hearing loss
heat intolerance
hemorrhagic diathesis
hepatic failure
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
hepatosplenomegaly
heralding manifestation
hexosaminidase-A
hexosaminidase-A and B
high arched feet
Hurler's syndrome
hydrocephalus
hyperreflexia
hypertonia
hypoglycemia
hypoglycemic coma
hypohidrosis
hypomyelination
hyporeflexia
hypotonia
hypotonia, infants
inattention
inborn errors of metabolism
inborn errors of metabolism, screening
inclusion bodies, intracytopasmic
incoordination
infection, recurrent
intellectual deficit
intellectual deterioration
intelligence quotient
intrathecal medication
Jakob-Creutzfeldt disease
jaundice
Jewish
klippel feil syndrome
Krabbe's disease
kyphoscoliosis, neurologic causes of
lactic acidemia
lactic dehydrogenase(LDH)
lead poisoning
learning disability, in children
leg weakness, bilateral
Leigh's disease
leukocyte enzyme abnormality
leukodystrophy
Lewy body disease, diffuse
life expectancy
limb-girdle weakness
lipid storage disorder of CNS
lipid storage myopathy
liver disease
lymphadenopathy
lysosomal storage disease
lysosomes, abnoral
macrocephaly
Marinesco-Sjogren syndrome
megalencephaly
memory, impairment of
meningitis, chronic
mental retardation
metabolic acidosis
metabolic disorder, primary
metabolic disorder, primary-screening tests
metachromatic leukodystrophy
metachromatic leukodystrophy, adult onset
metachromatic leukodystrophy, juvenile
metachromatic leukodystrophy, late-infantile
misdiagnosis
mitral valve prolapse
molecular genetics
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, hypointense signal foci on
MRS
mucopolysaccharidoses
multiple sclerosis
multiple sclerosis, differential diagnosis of
muscle biopsy
muscle cramp
muscle pain
muscle spasm
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscular dystrophy, Duchenne
myelopathy
myocardial infarction
myoclonus
myoglobinuria
myopathy
myopathy, metabolic
myopathy, proximal
myopathy, vacuolar
N-acetyl-L-aspartic acid
neck weakness
neonatal screening, genetic neurologic disorders
neoplasm, primary of CNS
neuraminidase deficiency
neuroaxonal dystrophy
neuroaxonal dystrophy, infantile
neurofibrillary degeneration
neurolipidosis IV
neurologic complications of, surgery
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic testing
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathic pain scale
neuropathology
neuropathy
neuropathy, demyelinating
neuropathy, painful
neuropathy, small-fiber
neuropathy, small-fiber, painful sensory
neurosis
next-generation sequencing
Niemann-Pick disease
ophthalmoplegia
optic atrophy
optokinetic nystagmus, abnormal
osteopetrosis
pain
pain, leg
pain, neuropathic
Parkinsonism syndrome
paroxysmal neurologic deficits
patient in waiting
pediatric neurology
peroxisomal disease
pes cavus
photophobia
polymerase chain reaction
polyneuropathy
Pompe's disease of glycogen storage
postpartum
precipitating factors
preclinical
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
prognosis
progressive neurologic disorder
propranolol
proteinuria
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychomotor retardation
psychosis
quadriparesis
quadriplegia
rectal biopsy
recurrent
remote effect of cancer on the nervous system
renal failure
respiratory failure
respiratory tract infection
retinal degeneration
retinopathy
retropulsion
review article
rhabdomyolysis
rigidity
safety
Salla disease
Sandhoff's disease
schizophrenia
scoliosis, neurologic association with
screening
sea-blue histiocytes
seizure
seizure, children
seizure, laughing as manifestation
sensorineural hearing loss
short stature
sick sinus syndrome
skin, biopsy
skin, lesions in neurologic disorders
slit lamp examination
small vessel disease
sodium valproate
sodium valproate, toxicity
spasticity
speech, delayed development of
sphingolipodoses
sphingomyelin
spinal cord, compression of
spinocerebellar degeneration
splenomegaly
startle reaction
stem cell transplantation
subdural hematoma
systemic illness
tandem gait, ataxic
Tay-Sachs disease
thalamus, lesion of
thalamus, lesion of-bilateral
thrombocytopenia
toe walking
tone, muscle, increased
tongue, enlarged
treatment of neurologic disorder
tremor
tremor, intention
tripping
type 1 muscle fiber
urea-cycle enzymopathies
urinary sulfatidase excretion
urine test for metabolic disorders
urine, dark
vasculopathy
ventricular enlargement
vertebral-basilar insufficiency
vertigo
vision, failure of in childhood
visual acuity, decreased
visual fields, constricted
visual loss
visual loss, transient
Von Hippel Lindau
walking, delayed
walking, difficulty with
weakness
weakness, chronic
weakness, fluctuating
weakness, generalized
weakness, progressive
weakness, proximal
white matter disease
wide based gait
Showing articles 200 to 250 of 335 << Previous Next >>

Pravastatin Therapy and The Risk of Stroke
NEJM 343:317-326, White,H.D. et al, 2000

Statins and the Risk of Dementia
Lancet 356:1627-1631, Jick,H.,et al, 2000

An Overview of Acute Stroke Therapy
Arch Int Med 160:3196-3206, Fisher,M. & Schaebitz,W., 2000

Autosomal Dominant Diffuse Leukoencephalopathy with Neuroaxonal Spheroids
Neurol 54:463-468, van der Knaap,M.S.,et al, 2000

Cholesterol and Strokes
BMJ 320:459-460, Oliver,M.F., 2000

HMG-CoA Reductase Inhibitors (Statins)
Neurol 54:790-795, Hess,D.C.,et al, 2000

Treating Nondementia Illnesses in Patients With Dementia
JAMA 283:3230-3235, Brauner,D.J. et al, 2000

Is Cholesterol a Risk Factor for Stroke? No
Arch Neurol 56:1521-1524, Landau,W.M., 1999

Is Cholesterol a Risk Factor for Stroke? Yes
Arch Neurol 56:1518-1520,1524, Demchuk,A.M.,et al, 1999

Prevention of a First Stroke,A Review of Guidelines and a Multidisciplinary Consensus Statement from the National Stroke Association
JAMA 281:1112-1120,1146, Gorelick,P.B.,et al, 1999

Infantile Neuroaxonal Dystrophy,Clinical Spectrum and Diagnostic Criteria
Neurol 52:1472-1478, Nardocci,N.,et al, 1999

Low-Density Lipoprotein Cholesterol and the Risk of Dementia with Stroke
JAMA 282:254-260, Moroney,J.T.,et al, 1999

Neuroprotective Properties of Statins in Cerebral Ischemia and Stroke
Stroke 30:1969-1973, Vaughan,C.J.&Delanty,N., 1999

Stroke Patterns of Internal Carotid Artery Dissection in 40 Patients
Stroke 29:2646-2648, Lucas,C.,et al, 1998

Effect of HMGcoA Reductase Inhibitors on Stroke, A Meta-Analysis of Controlled Trials
Ann Int Med 128:89-95, Bucher,H.C.,et al, 1998

Axonal Transection in the Lesions of Multiple Sclerosis
NEJM 338:278-285, 3231998., Trapp,B.D.,et al, 1998

Lovastatin for X-Linked Adrenoleukodystrophy
NEJM 339:702-703, Singh,I.,et al, 1998

HIV-Protease Inhibitors
NEJM 338:1281-1292, Flexner,C., 1998

Migrainous Visual Accompaniments are not Rare in Late Life:The Framingham Study
Stroke 29:1539-1543, Wijman,C.A.C.,et al, 1998

Vascular Effects of Statins in Stroke
Stroke 28:2315-2320, Delanty,N.&Vaughan,C.J., 1997

High-Density Lipoprotein Cholesterol & Risk of Ischemic Stroke Mortality:21-Yr FU of 8586 Men-Israeli Ischemic Heart Dis Study
Stroke 28:83-87, Tanne,D.,et al, 1997

Cumulative Effects of High Cholesterol Levels, High Blood Pressure, & Cigarette Smoking on Carotid Stenosis
NEJM 337:516-522, Wilson,P.W.F.,et al, 1997

Influence of Cholesterol on Survival After Stroke:Retrospective Study
BMJ 314:1584-1588, Dyker,A.G.,et al, 1997

Epidemiology of Stroke
JNNP 61:333-338, Khaw,K.T., 1996

Pravastatin Reduces Carotid Intima-Media Thickness Prog in an Asympt Hypercholesterolemic Pop, CAIUS Study
Am J Med 101:627-634, Mercuri,M.,et al, 1996

Low Total Serum Cholesterol and Intracerebral Hemorrhagic Stroke:Is the Assoc Confined to Elderly Men
Stroke 27:1993-1998, Iribarren,C.,et al, 1996

Reduction in Carotid Arterial Wall Thickness Using Lovastatin & Dietary Therapy
Ann Int Med 124:548-556, Hodis,H.N.,et al, 1996

Lipids and Stroke
Arch Neurol 53:303-308, Hachinski,V.,et al, 1996

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

Predictors of Stroke in Middle-Aged Patients with Non-Insulin-Dependent Diabetes
Stroke 27:63-68, Lehto,S.,et al, 1996

Primary Prevention of Stroke
NEJM 333:1392-1400, Bronner,L.L.,et al, 1995

Lipoprotein (a) & Asympt Carotid Art Disease:Evidence of a Prominent Role in the Evol of Advanced Carotid Plaques
Stroke 26:1582-1587, Willeit,J.,et al, 1995

Plasma Concentration of Lipoprotein (a) and the Risk of Future Stroke
JAMA 273:1269-1273, Ridker,P.M.,et al, 1995

Genotype-Phenotype Correlation in Adult-Onset Acid Maltase Deficiency
Ann Neurol 38:450-454, Wokke,J.H.J.,et al, 1995

Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
Medicine 74:131-135, Felice,K.J.,et al, 1995

Parkinsonism Unmasked by Lovastatin
Ann Neurol 37:685-686, Muller,T.,et al, 1995

Peripheral Neuropathy with Bezafibrate
BMJ 309:929, Ellis,C.J.,et al, 1994

Neuropathy Associated with Hyperlipidemia
Neurol 44:2185-2186, McManis,P.G.,et al, 1994

Failure of Aspirin Treatment After Stroke
Stroke 25:275-277, Bornstein,N.M.,et al, 1994

Dementia of Adult Polyglucosan Body Disease, Evidence of Cortical and Subcortical Dysfunction
Arch Neurol 51:90-94, Rifai,Z.,et al, 1994

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

HMG-CoA Reductase Inhibitor Therapy and Peripheral Neuropathy
Ann Int Med 120:970, Jacobs,M.B., 1994

Guillain-Barre Syndrome after Exogenous Gangliosides in Italy
BMJ 307:1463-1464, Landi,G.,et al, 1993

Serum Lipid Levels During Carbamazepine Medication
Arch Neurol 50:590-593, Isojarvi,J.I.T.,et al, 1993

One-Year Reduction and Longitudinal Analysis of Carotid Intima-Media Thickness Associated with Colestipol/Niacin Therapy
Stroke 24:1779-1783, Mack,W.J.,et al, 1993

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

Risk Factors for Cervical Atherosclerosis in patients with Transient Ischemic Attack or Minor Ischemic Stroke
Stroke 24:970-975, Palomaki,H.,et al, 1993

High Serum Lipoprotein (a) Levels Are an Independent Risk Factor for Cerebral Infarction
Stroke 24:965-969, Shintani,S.,et al, 1993

Cholesterol Reduction and the Risk for Stroke in Men, A Meta-Analysis of Randomized, Controlled Trials
Ann Int Med 119:136-145, Atkins,D.,et al, 1993

Polyglucosan Body Disease Simulating Amyotrophic Lateral Sclerosis
Neurol 43:785-790, McDonald,T.D.,et al, 1993



Showing articles 200 to 250 of 335 << Previous Next >>