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Differential
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abdominal muscle paralysis
acalculia
acetylcholine
acetylcholine in CNS
acid maltase deficiency
acid maltase deficiency, adult
acral sensory symptoms
acyl CoA dehydrogenase deficiency
adenosine deaminase deficiency
adrenoleukodystrophy
adrenomyeloneuropathy
adult polyglucosan body disease
advances in neurology
adverse drug reaction
agalsidase alfa
alexia
alexia with agraphia
alopecia
alpha galactosidase A deficiency
alpha glucosidase
alpha-fetoprotein
alveolar hypoventilation
Alzheimer's disease
aminoacidopathies
aminoacidurias
aminoacylase 1 deficiency
ammonia
amniocentesis
anal wink response
anemia
anemia, hemolytic
aneurysm
aneurysm, intracranial
aneurysm, multiple intracranial
angiokeratoma
angiotensin-converting enzyme
angiotensin-converting enzyme, inhibitors
animal exposure
ankle edema
anorexia nervosa
anosmia
anterior horn cell disease
anticoagulant, complications of
anticoagulant, treatment
anticoagulant, treatment in CVD
anticonvulsants
anticonvulsants, blood level determination of
anticonvulsants, compliance
anticonvulsants, hypersensitivity syndrome
anticonvulsants, teratogenicity of
anticonvulsants, untoward effects of
apixaban
apraxia
apraxia of eye movements
areflexia
aromatic amino acid decarboxylase deficiency
arrhythmia, cardiac
arsenic
arterial dissection, carotid
arteriopathy
arthralgia
arthritis
arthropathy
arthropathy, neuropathic
arylsulfatase A
ascending paralysis
ascites
aspartate aminotransferase
aspartocyclase
asymptomatic
ataxia
ataxia, cerebellar
ataxic gait
athetosis
atrial fibrillation
atrial fibrillation, nonvalvular
atrioventricular block
autism
autonomic dysfunction
Babinski sign
BAL
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basophilic stippling of red blood cells
behavioral disorder
biotin deficiency
biotinidase deficiency
blacks
bladder dysfunction
blindness
blood dyscrasias, neurologic findings with
bone age
bone marrow suppression
bone marrow transplantation
bradycardia
brain atrophy
brain biopsy
brain natriuretic peptide
brain purpura
brainstem
brainstem, infarction of
brainstem, lesion of
breast feeding
bulimia
bulimia nervosa
burning feet
burning feet, differential diagnosis of
burning hands
burning paresthesia
calcification, intracranial
calf hypertrophy
Canavan's disease
carbamazepine
carbamyl phosphate synthetase-I deficiency
carbidopa
carbonic anhydrase II deficiency
carcinoma
cardiac enzymes
cardiomegaly
cardiomyopathy
cardiovascular disease
carnitine deficiency myopathy
carotid angiogram
carotid artery occlusion, neck
CAT scan
CAT scan, abdomen
CAT scan, abnormal
CAT scan, angiography
CAT scan, dense artery sign
CAT scan, emission, abnormal
CAT scan, false negative
cataracts
cathartic
caudate nucleus, lesion of
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar hemorrhage
cerebellar infarction
cerebellar lesion
cerebellar vermis
cerebral artery, encasement
cerebral cortical atrophy
cerebral infarction
cerebral infarction, hemorrhagic
cerebral infarction, subcortical
cerebral ischemia
cerebral palsy
cerebral venous thrombosis
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, enzymes in
cerebrospinal fluid, glycine
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, protein of
cerebrospinal fluid, proteincytologic dissociation
cerebrotendinous xanthomatosis
cerebrovascular accident
cerebrovascular accident, cryptogenic
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, multiple
cerebrovascular accident, non atherosclerotic cause of
cerebrovascular accident, prevention of
cerebrovascular accident, recurrent
cerebrovascular accident, thrombolytic agents in treatment
cerebrovascular accident, young adult
cerebrovascular disease
cerebrovascular disease, cardiovascular disease with
ceruloplasmin, serum
chelation therapy
chemotherapy, CNS treatment and complications with
cherry red spot
cherry red spot-myoclonus syndrome
chest pain
children
chills
cholesterol
choline acetyltransferase
choline chloride
chorea
choreoathetosis
chromosomal abnormality
chromosome 20
chromosome 6
chronic graft versus host disease
cirrhosis
cirrhosis, infancy
Clinical Pathologic Conference(C.P.C.)
clofibrate
codfish vertebrae
coenzyme Q10 deficiency
cogwheel rigidty
color desaturation
coma
complications
compression fracture
conduction block
confusion
congenital birth defects
congenital malformation
congenital malformation, non CNS
congestive heart failure
conjunctivitis
consanguinity
contractures, joint
conus medullaris, lesion of
coprolalia
cornea, abnormal
cornea, opacification in infancy-causes of
cornea, opacity of
corneal dystrophy
coumarin
counselling
cranial nerve enlargement
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
creatinine, elevated
cry, abnormal
crying
cultured skin fibroblasts
cyst, bone
cystinuria
cytochrome c oxidase
cytochrome c oxidase, deficiency
D-dimer
deep gray nuclei
deficiency of ADA2
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, presenile
demyelinating disease
dentate nuclei
dentate nuclei, lesion of
depression
dermatitis
dermatomyositis
developmental milestones, loss of
developmental retardation
diabetes insipidus
diagnostic criteria
diaphragmatic paralysis
diarrhea
diet
difficulty climbing stairs
dilantin
dilantin, hypersensitivity to
disability, neurological
distal muscle atrophy
distal muscle weakness
dizziness
DNA probes
DNA sequencing
dopa responsive dystonia
dopamine
drooling
dropped head syndrome
drug interactions
dysarthria
dysdiadochokinesia
dyskinesia
dysmorphic
dysostosis multiplex
dysphagia
dyspnea
dyspraxia
dystonia
dystonia, children
dystonic reaction, acute
dystrophic calcification
dystrophin
eating disorder
echolalia
eculizumab
edema, pedal
edema, periorbital
efficacy
ejection fraction
ejection fraction, abnormal
ejection fraction, abnormal, transient
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electromyogram
electron microscopy
ELISA
emergencies, neurologic
emotional lability
encephalitis
encephalitis, viral
encephalopathy
encephalopathy, neonatal
encephalopathy, progressive
endarterectomy, carotid
enzyme treatment
enzyme, defect
enzyme, induction
enzyme, muscle disease
enzyme, serum
eosinophilia
epidemiology of neurology
erythema migrans
erythrocyte
esophageal varices
evoked potentials
exercise
exercise intolerance
eye movement, disorders of
eye movement, painful
Fabry's disease
facial anomalies
facial appearance, abnormal
facial expression abnormality
facial hypoplasia
facial nerve palsy
facial nerve palsy, bilateral
facial weakness
factor Xa inhibitor
failure to thrive
falling
familial
Farber's disease
fatigue
fatty acid, elevated plasma content
feeding disorder
fever
fibrillations
fibrinolytic agents
fine motor function, impaired
fingernails, abnormal
fingolimod
floppy infant
flow study, carotid artery
flu-like illness
folic acid
fornix, lesion of
fracture, pathologic
Fragile-X associated tremor/ataxia-syndrome
fragile-X syndrome
frontal bossing
frontal lobe, behavior with disease of
frontal lobe, lesion of
fucosidosis
fundus, abnormality of
gadolinium
gait disorder
galactocerebrosidase
galactorrhea
galactosemia
galactosidase
gangliosidosis GM1
gangliosidosis GM2
gangliosidosis GM2-AB variant
gastroenteritis
Gaucher's disease
gender
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic neurologic disorders
genetic screening
genetic testing
Gerstmann syndrome
Gilles de la Tourette syndrome
globoid cells
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glucocerebrosidase
glutamate dehydrogenase deficiency
glutaric acidemia
glutaric aciduria
glycine
glycogen debranching enzyme deficiency
glycogen storage disease
glycoprotein
Gowers maneuver
granulomatous disease
growth retardation
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
Hallervorden Spatz disease
Hallervorden Spatz disease, late onset
hallucination
hallucination, auditory
hallucination, visual
hand pain
hand weakness
hands, fisted
head lag
headache
headache, progressive
headache, severe
headache, thunderclap
headbanging
hearing loss
heart block
heart block, complete
heart murmur
heart rhythm
heart wall motion dysfunction
heavy metal intoxication
hematopoietic tissue, extramedullary
hematuria, microscopic
hemianopia
hemianopia, homonymous
hemochromatosis
hemoglobin abnormality, neurologic complications of
hemoglobinuria
hemolysis
hemorrhagic diathesis
hepatic encephalopathy
hepatic failure
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
hepatomegaly
hepatosplenomegaly
heralding manifestation
herniated disc, thoracic
herpes simplex encephalitis
herpes zoster
herpes zoster, disseminated
hexosaminidase-A
hexosaminidase-A and B
histochemistry
histochemistry of muscle
hoarseness
homocystinuria
Howell-Jolly bodies
Hurler's syndrome
hydrocephalus
hydrocephalus, normal pressure
hydroxytryptophan L-5(L-5 HTP)
hyperammonemic encephalopathy
hyperamylasemia
hyperbilirubinemia
hypercalcemia
hyperglycinemia
hyperhomocysteinemia
hyperkeratosis
hyperphosphatasia
hyperreflexia
hypersensitivity reaction
hypertension
hypertonia
hypoalbuminemia
hypogammaglobulinemia
hypoglycemia
hypokalemia
hypomyelination
hyponatremia
hyporeflexia
hypothalamus
hypothalamus, disturbance of
hypothermia
hypotonia
hypotonia, infants
iatrogenic neurologic disorders
ileus, paralytic
imbalance
immunosuppression
immunosuppressive agents
impotence
impulsivity
inborn errors of metabolism
inborn errors of metabolism, screening
inclusion bodies
inclusion bodies, intracytopasmic
inclusion body myositis
incontinence, fecal
infection
infection, recurrent
insulin resistance
intellectual deficit
intellectual deterioration
intelligence quotient
interferon beta 1-a
internal capsule
internuclear ophthalmoplegia
internuclear ophthalmoplegia, unilateral
intracerebral hemorrhage
intrauterine
iron, brain
iron, serum
irritability
ischemic exercise test
jaundice
Jewish
Kayser-Fleischer ring
Kearns-Sayre syndrome
Korsakoff's psychosis
Krabbe's disease
kyphoscoliosis, neurologic causes of
lactate
lactic dehydrogenase(LDH)
lacunar infarction
L-dopa
learning disability
learning disability, in children
Leber's hereditary optic neuropathy
left-right orientation
leg weakness, bilateral
Leigh's disease
Leigh's disease, adult variety
lens, dislocation of
lens, ectopic
Lesch-Nyhan syndrome
lethargy
leukocyte enzyme abnormality
leukodystrophy
leukoencephalopathy
leukopenia
level of consciousness, decreased
levonorgestrel
life expectancy
lipid lowering agent
lipid storage disorder of CNS
livedo reticularis
liver biopsy
liver disease
liver function enzymes
liver transplantation
low back pain
Lowe's syndrome
Lyme disease
lymphadenopathy
lymphoma
lymphoma involving CNS
lysosomal storage disease
lysosomes, abnoral
macrocephaly
malformation, CNS, congenital
Marcus Gunn pupil
marihuana
masked facies
McArdle's disease
meconium staining
Mees lines
melanomatosis, primary malignant
MELAS syndrome
memory, defect of recent
memory, impairment of
meningeal biopsy
meningeal enhancement
meningitis
mental retardation
mental status, abnormal
MERRF syndrome
mesial temporal lobe
metabolic acidosis
metabolic disorder, primary
metabolic disorder, primary-screening tests
metachromatic leukodystrophy
metachromatic leukodystrophy, adult onset
microcephaly
microspherophakia
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
monoclonal antibodies
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, demyelinating disease
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, eye of tiger sign
MRI, hypointense signal foci on
MRI, mass effect on
MRI, muscle
MRI, paramagnetic effect
MRI, vessel wall
MRI, vessel wall enhancement
MRS
mucopolysaccharidoses
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, relapsing
multiple sclerosis, treatment of
multiple system atrophy
muscle atrophy, progressive
muscle biopsy
muscle cramp
muscle hypertrophy
muscle pain
muscle phosphofructokinase deficiency
muscle phosphorylase deficiency
muscle spasm
muscle stiffness
muscle strength, testing
muscle tenderness
muscle wasting, diffuse
muscle weakness
muscle weakness, insidious onset of
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, central nervous system abnormality
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, carrier
muscular dystrophy, Duchenne, neonatal screening
muscular dystrophy, Duchenne, presymptomatic detection
myelomalacia
myeloneuropathy
myelopathy
myocardial infarction
myocarditis
myoclonic jerks
myoclonus
myoglobinuria
myopathy
myopathy, acute
myopathy, distal, vacuolar
myopathy, genetic
myopathy, metabolic
myopathy, mitochondrial
myopathy, necrotizing
myopathy, vacuolar
myopia
myositis
myotonic discharges
nausea and vomiting
neck pain
neck tenderness
neck weakness
neonatal screening, genetic neurologic disorders
neoplastic angioendotheliosis
nephritis
nerve biopsy
nerve conduction studies
neuraminidase deficiency
neuritis, heavy metals causing
neurocardiology
neurogenic bladder
neurologic complications of, surgery
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination
neurologic signs
neuromuscular disease, electrodiagnosis of
neuropathology
neuropathy
neuropathy, ataxia, retinitis pigmentosa
neuropathy, ischemic
neuropathy, painful
neuropathy, peripheral
neuropathy, sensory
neuropathy, toxic
neurotransmitter
Niemann-Pick disease
NMDA antagonists
nocturia
nystagmus
obstetric neurologic injuries
oculogyric crisis
old age, neurology of
opened mouth
ophthalmoplegia
ophthalmoplegia, progressive external
opisthotonus
opportunistic infection
optic atrophy
optic chiasm, enlarged
optic disc edema
optic nerve
optic nerve, enlarged
optic neuritis
optic neuropathy
oral contraceptives
orchitis
ornithine transcarbamylase deficiency
orthopnea
osteoporosis
pain
pain, abdominal
pain, back
pain, foot
pain, leg
palilalia
palpitations
pancreatitis
pancytopenia
PANK2 mutation
papilledema
paraparesis
paraparesis, spastic
paraspinal muscle
paraspinal muscle weakness
paresthesias
paresthesias, feet
paresthesias, hands
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
paroxysmal nocturnal hemoglobinuria
PAS positive
PAS positive material in the brain
patient information and support
pectus excavatum
pediatric neurology
penicillamine
pericardial effusion
pericarditis
peripheral blood smear
peripheral blood smear, abnormal
peroxisomal disease
peroxisomes
perseveration
personality change
phenobarbital
phenylketonuria
phosphorylase b kinase deficiency
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
pleural effusion
polyglucosan body
polyglucosan body disease
polymerase chain reaction
polymyositis
polyneuropathy
Pompe's disease of glycogen storage
porphyria
position sensation, abnormal
postpartum
postpartum coma
postural abnormality
practice guidelines
precipitating factors
pregnancy, anticonvulsants during
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
prognathism
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
prolactin, elevated
proprioception, abnormal
proteinuria
pseudomyotonia
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychomotor retardation
psychosis
putamen, lesion of
pyramidal tract
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
pyruvate-kinase deficiency anemia
quadriparesis
quadriplegia
quinidine
race
radiation therapy, CNS treatment and complications with
rash
rectal sphincter tone, decreased
recurrent
remote effect of cancer on the nervous system
renal failure
renal stones
renal tubular acidosis
respiratory failure
respiratory tract infection
retinal degeneration
retinopathy
reversible cerebral vasoconstrictive syndromes
reversible neurologic disorder
review article
Reye's syndrome
rhabdomyolysis
rigidity
risk factors
risk-benefit assessment
risus sardonicus
safety
Sandhoff's disease
Sanfilippo syndrome
sarcoidosis
sarcoidosis, CNS
schizophrenia
scoliosis
scoliosis, neurologic association with
screaming
screening
second wind phenomena
seizure
seizure, children
seizure, neonatal
seizure, pregnancy
seizure, psychomotor-temporal lobe
seizure, treatment of
seizure, treatment of, monotherapy
seizure, women
self-mutilation
semialdehyde dehydrogenase deficiency
sensory loss
serologic testing
serum alanine aminotransferase
short stature
sickle cell crisis
sickle cell disease
skin, biopsy
skin, lesions in neurologic disorders
slit lamp examination
slurred speech
small vessel disease
sodium valproate
sodium valproate, toxicity
somnolence
sore throat
spasticity
speech disorder
speech disorder, childhood
speech, delayed development of
sphingolipodoses
spina bifida
spinal cord
spinal cord, compression of
spinal cord, infarction of
spinal cord, lesion of
spinocerebellar ataxia type 1
spinocerebellar degeneration
spirochete infection
splenic-vein thrombosis
splenomegaly
spongy degeneration of brain
SPORTIF trial
startle reaction
stem cell rescue
stem cell transplantation
steroid
steroid therapy, CNS treatment and complications with
strabismus
striatum, lesion of
stuporous
stuttering
subarachnoid hemorrhage
subarachnoid hemorrhage, cerebral convexity
substantia nigra
suck, poor
sweating, abnormality of
symmetric brain lesions
systemic illness
Takotsubo cardiomyopathy
tandem gait, ataxic
target red cells
Tay-Sachs disease
temporal lobe, lesion
teratogenic drugs
teratoma, ovarian
term infant
testicular teratoma
tetrahydrobiopterin
thalamus, lesion of
thalamus, lesion of-bilateral
thiamine
thrombin inhibitor
thrombocytopenia
tick bite
tinnitus
tissue plasminogen activator, intravenous
tone, muscle, increased
tongue, enlarged
tongue, weakness
transketolase
treatment of neurologic disorder
tremor
tremor, intention
tremor, wing beating
tremor, writing
trientine dihydrochloride
tripping
troponin T
tyrosine
tyrosine hydroxylase deficiency
tyrosinemia
ultrasonography
ultrasonography, head, fetus-neonate
umbilical-cord blood transplantation
unconsciousness
urea
urea-cycle enzymopathies
uremia
urinary frequency
urinary incontinence
urinary urgency
urine test for metabolic disorders
urine test in toxic screen
urine, dark
uveitis
vasculitides
vasculopathy
vertebral-basilar insufficiency
vertigo
vertigo, episodic
viral infection
viral infection, CNS
visual acuity, decreased
visual acuity, decreased, monocular
visual field defect
visual loss
visual loss, slow-unilateral
vital capacity
vitamin deficiency
vitamin K
vitamin supplementation
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
Wernicke's encephalopathy
wheelchair
white matter disease
wide based gait
winging of scapula
writing
ximelagatran
zinc
Showing articles 1300 to 1350 of 3473 << Previous Next >>

Familial Dementia With Lewy Bodies
Arch Neurol 59:1622-1630, Tsuang,D.W.,et al, 2002

Familial Infantile Bilateral Striatal Necrosis
Neurol 59:983-989, Straussberg,R.,et al, 2002

Potentially Reversible Conditions in 1000 Consecutive Memory Clinic Patients
JNNP 73:390-394, Hejl,A.,et al, 2002

New Evidence for Stroke Prevention
JAMA 288:1388-1395, Straus,S.E.,et al, 2002

The PROGRESS Trial: Preventing Strokes by Lowering Blood Pressure in Patients With Cerebral Ischemia
Stroke 33:319-320, van Gijn,J., 2002

Mild Therapeutic Hypothermia to Improve the Neurologic Outcome After Cardiac Arrest
NEJM 346:549-556,612,546, The Hypothermia After Cardiac Arrest Study Group, 2002

Clinicopath Conf, Hyperviscosity Syndrome Due to IgG Multiple Myeloma
NEJM 346:603-610, Case 6-2002, 2002

Familial Amyotrophic Lateral Sclerosis
Muscle Nerve 25:135-159, Hand,C.K. &Rouleau,G.A., 2002

Cognitive Functioning of Long-term Heavy Cannabis Users Seeking Treatment
JAMA 287:1123-1131,1172, Solowij,N.,et al, 2002

Hearing Loss is a Common Feature of Symptomatic Children with Profound Biotinidase Deficiency
J Pediatr 140:242-246, Wolf,B.,et al, 2002

Stroke Prevention Therapy Beyond Antithrombotics: Unifying Mechanisms in Ischemic Stroke Pathogenesis and Implications for Therapy
Stroke 33:862-875, Gorelick,P.B., 2002

Clinical and Imaging Findings in Cryptogenic Stroke Patients With and Without Patent Foramen Ovale
Stroke 33:706-711, Lamy,C.,et al, 2002

Functional Deficits in Patients with Mild Cognitive Impairment
Neurol 58:758-764, Tabert,M.H.,et al, 2002

The Neurological Masquerade of Intravascular Lymphomatosis
Arch Neurol 59:439-443, Beristain,X.&Azzarelli,B., 2002

Spinocerebellar Ataxia Type 10 is Rare in Populations Other Than Mexicans
Neurol 58:983-984, Matsuura,T.,et al, 2002

Recent Developments in Neurology
BMJ 324:656-660, Wiebe,S.,&Nicolle,M.W., 2002

Lead Encephalopathy: CT and MR Findings
J Comput Assist Tomogr 26:479-481, Tuzun,M.,et al, 2002

Subarachnoid Hemorrhage
Stroke 33:1321-1326, Kissela,B.M.,et al, 2002

Familial Temporal Lobe Epilepsy with Febrile Seizures
Neurol 58:1429-1433, Depondt,C.,et al, 2002

Patients with Multiple Sclerosis and Risk of Type 1 Diabetes Mellitus in Sardinia,Italy: A Cohort Study
Lancet 359:1461-1465,1450, Marrosu,M.G.,et al, 2002

Mitochondrial Optic Neuropathies
JNNP 72:423-425, Sadun,A.A., 2002

Cholinergic Vesicular Transporters in Progressive Supranuclesar Palsy
Neurol 58:1013-1018,997, Suzuki,M.,et al, 2002

Use of Ramipril in Preventing Stroke: Double Blind Randomised Trial
BMJ 324:699-702,687, Bosch,J.,et al, 2002

Unexplained Sudden Amnesia
Arch Neurol 59:1310-1313, Fisher,C.M., 2002

Occurrence of Hemispheric and Retinal Ischemia in Atrial Fibrillation Compared with Carotid Stenosis
Stroke 33:1963-1968, Anderson,D.C.,et al, 2002

Giant-cell Arteritis
NEJM 347:272-278, Case 23-2002, 2002

Dermoid Inclusion Cysts and Early Spinal Cord Tethering After Fetal Surgery for Myelomeningocele
NEJM 347:256-259,230, Mazzola,C.A.,et al, 2002

Blood Pressure Control in Stroke Patients
Neurol 59:23-25, Messerli,F.H.,et al, 2002

Valproate Embryopathy in Three Sets of Siblings: Further Proof of Hereditary Susceptibility
Neurol 59:630-633, Malm,H.,et al, 2002

Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
NEJM 347:672-680, Case 27-2002, 2002

Goosebumps
Lancet 360:690, Cutts,J.,et al, 2002

Jaw Drop in Kennedy's Disease
Neurol 59:1471-1472, Sumner,C.J. &Fischbeck,K.H., 2002

Clinicopath Conf., Prolactinoma
NEJM 347:1604-1611, Case 35-2002, 2002

Prevalence of Atrial Fibrillation and Antithrombotic Prophylaxis in Emergency Department Patients
Stroke 33:2664-2669, Scott,P.A.,et al, 2002

Atrial Fibrillation, Stroke, and Acute Antithrombotic Therapy
Stroke 33;2722-2727, Hart,R.G.,et al, 2002

Effect of Radiotherapy and Other Treatment-Related Factors on Mid-Term to Long-Term Cognitive Sequelae in Low-Grade Gliomas: A Comparative Study
Lancet 360:1361-1368, Klein,M.,et al, 2002

Prospective Assessment of Risk Factors for Recurrent Stroke During Childhood--A 5-year Follow-up Study
Lancet 360:1540-1545,1526, Strater,R.,et al, 2002

Oral Anticoagulants vs Aspirin in Nonvalvular Atrial Fibrillation
JAMA 288:2441-2448, van Walraven,C.,et al, 2002

A Reversible Paralysis
Lancet 360:1160, Maury,E.,et al, 2002

New Players in the Genetics of Stroke
NEJM 347:1711-1712, Tournier-Lasserve,E., 2002

Benefit of Atrial Pacing in Sleep Apnea Syndrome
NEJM 346:404-412,390,444, Garrigue,S., et al, 2002

Expression of p53 and Prognosis in Children With Malignant Gliomas
NEJM 346:420-427, Pollack,I.F.,et al, 2002

Mutations in Each of the Five Subunits of Translation Initiation Factor eIF2B Can Cause Leukoencephalopathy with Vanishing White Matter
Ann Neurol 51:264-270, van der Knaap,M.S.,et al, 2002

Epilepsy Presenting as AD: Neuroimaging, Electroclinical Features, and Response to Treatment
Neurol 58:298-301, Hogh,P.,et al, 2002

Fragile X Premutation Carriers: Characteristic MR Imaging Findings of Adult Male Patients with Progressive Cerebellar and Cognitive Dysfunction.
AJNR 23:1757-1766, Brunberg,J.A.,et al, 2002

Delirium Resulting From Paraneoplastic Limbic Encephalitis Caused by Hodgkins Disease
Psychosomatics 43:498-501, Kung,S.,et al, 2002

Treatment of Women with Epilepsy
Seminars in Neurology 22:289-297, Pack.A.M.&Morrell,M.J., 2002

A Practical Approach to the Diagnosis and Management of MELAS: Case Report and Review
The Neurologist 8:302-312, Thambisetty,M.,et al, 2002

Hypertrophic Cardiomyopathy A Systematic Review
JAMA 287:1308-1320, Maron, B.J., 2002

Clinical Profile of Stroke in 900 Patients with Hypertrophic Cardiomyopathy
J Am Coll Cardiol 39:301-307, Maron,B.J.,et al, 2002



Showing articles 1300 to 1350 of 3473 << Previous Next >>