Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
abdominal muscle paralysis
acetylcholine
acetylcholine in CNS
acid maltase deficiency
acid maltase deficiency, adult
aciduria
acral sensory symptoms
acyl CoA dehydrogenase deficiency
adenosine deaminase deficiency
adrenoleukodystrophy
adrenomyeloneuropathy
advances in neurology
adverse drug reaction
agalsidase alfa
agranulocytosis
alopecia
alpha galactosidase A deficiency
alpha glucosidase
Alzheimer's disease
amenorrhea
aminoacidopathies
aminoacidurias
aminoacylase 1 deficiency
ammonia
amniocentesis
ANA
anasarca
anemia
anemia, hemolytic
anesthesia, general
aneurysm
angina pectoris
angiography, cerebral, negative
angiography, neurologic complications with
angiokeratoma
angiotensin-converting enzyme
animal exposure
ankle edema
anorexia
anorexia nervosa
anterior horn cell disease
anticholinergic drugs
anticoagulant, complications of
anticonvulsants
anticonvulsants, hypersensitivity syndrome
anticonvulsants, untoward effects of
antiphospholipid antibodies
anxiety
apraxia
apraxia of eye movements
areflexia
aromatic amino acid decarboxylase deficiency
arrhythmia, cardiac
arsenic
arteritides
arthralgia
arthritis
arthropathy
arthropathy, neuropathic
arylsulfatase A
ascending paralysis
ascites
aspartate aminotransferase
aspartocyclase
asymptomatic
ataxia
ataxia, cerebellar
atherosclerosis, generalized
athetosis
autism
autonomic dysfunction
B12
B12, elevated
Babinski sign
bacterial infection
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
blindness
blood dyscrasias, neurologic findings with
bone marrow infarction
bone marrow necrosis
bone marrow suppression
bone marrow transplantation
brain atrophy
brain biopsy
brain biopsy, false negative
brain purpura
brainstem
brainstem, infarction of
brainstem, lesion of
breast feeding
BUN, elevated
burning feet
burning feet, differential diagnosis of
burning hands
burning paresthesia
cachexia
calcification, intracranial
calf hypertrophy
Canavan's disease
cancer, cerebrovascular accident complicating patients with
carbamazepine
carbamazepine, toxicity
carbamyl phosphate synthetase-I deficiency
carbidopa
carbonic anhydrase II deficiency
carcinoma
carcinoma of lung
cardiac catheterization, neurologic complications
cardiac surgery, neurologic complications with
cardiomegaly
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, chest
CAT scan, false negative
cataracts
caudate nucleus, lesion of
CD4 counts
central nervous system, infection of
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar hemorrhage
cerebellar infarction
cerebellar lesion
cerebellar vermis
cerebral cortical atrophy
cerebral embolism
cerebral embolism, cardiac origin
cerebral embolism, multiple
cerebral infarction
cerebral infarction, hemorrhagic
cerebral infarction, subcortical
cerebral ischemia
cerebral palsy
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, glycine
cerebrospinal fluid, protein of
cerebrospinal fluid, proteincytologic dissociation
cerebrospinal fluid, xanthochromia of
cerebrotendinous xanthomatosis
cerebrovascular accident
cerebrovascular accident, bilateral
cerebrovascular accident, cryptogenic
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, multiple
cerebrovascular accident, non atherosclerotic cause of
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
cerebrovascular disease
cerebrovascular disease, rapidly progressive
ceruloplasmin, serum
chemotherapy, CNS treatment and complications with
cherry red spot
cherry red spot-myoclonus syndrome
chest pain
chest x-ray, abnormal
children
cholesterol
choline acetyltransferase
choline chloride
chorea
choreoathetosis
chromosomal abnormality
chromosome 20
chromosome 6
cirrhosis
cirrhosis, infancy
Clinical Pathologic Conference(C.P.C.)
coagulopathy
codfish vertebrae
coenzyme Q10 deficiency
coinfection
coma
compliance
compression fracture
confusion
congestive heart failure
conjunctivitis
consanguinity
contractures, joint
cooling therapy
cop 1
copper metabolism, abnormal
coprolalia
cornea, opacification in infancy-causes of
cornea, opacity of
corneal dystrophy
coronary artery bypass
corpus callosum, infarction of
cortical blindness
cough
cranial nerve enlargement
cranial nerve palsies
crawl regression
C-reactive protein, elevated
creatine phosphokinase isoenzyme elevation
creatine phosphokinase(CPK)elevated
creatinine, elevated
cry, abnormal
crying
cultured skin fibroblasts
cyclophosphamide
cystinuria
cystoisospora belli
cytochrome c oxidase
cytochrome c oxidase, deficiency
D-dimer
decerebrate posture
decision analysis
deep gray nuclei
deficiency of ADA2
degenerative diseases of CNS
dehydration
dementia
dementia, presenile
demyelinating disease
dentate nuclei
dentate nuclei, lesion of
depression
dermatitis
developmental milestones, loss of
developmental retardation
diaphragmatic paralysis
diarrhea
diet
disorientation
disseminated intravascular coagulation(DIC)
distal muscle atrophy
distal muscle weakness
dopa responsive dystonia
dopamine
doxycycline
drooling
dropped head syndrome
drowsiness
dysarthria
dysdiadochokinesia
dysmorphic
dysostosis multiplex
dysphagia
dyspnea
dyspraxia
dystonia
dystonia, children
dystonic reaction, acute
ecchymoses
echocardiogram
echolalia
edema, facial
edema, pedal
edema, periorbital
efficacy
ehrlichiosis
ejection fraction
ejection fraction, abnormal
electrocardiogram, abnormal
electromyogram
electron microscopy
embolism
embolism, atheromatous
embolism, cholesterol
embolism, fat
embolism, retinal
emergencies, medical
emergencies, neurologic
encephalomyelitis
encephalopathy
encephalopathy, acute
encephalopathy, neonatal
encephalopathy, progressive
endemic area
endocarditis
endocarditis, marantic
enteritis
enzyme treatment
enzyme, defect
enzyme, muscle disease
enzyme, serum
eosinophilia
epidemiology of neurology
epistaxis
Epstein-Barr virus
Epstein-Barr virus, negative
erythrocyte
erythroderma
esophageal varices
exercise
exercise intolerance
eye movement, disorders of
Fabry's disease
facial anomalies
facial appearance, abnormal
facial expression abnormality
facial hypoplasia
facial weakness
failure to thrive
familial
Farber's disease
fatigue
fatty acid, elevated plasma content
feeding disorder
femoral artery catheterization
ferritin, elevated
fever
fibrin split products
fingernails, abnormal
floppy infant
flow study, carotid artery
flu-like illness
fornix, lesion of
fracture, pathologic
frontal bossing
frontal lobe, behavior with disease of
frontal lobe, lesion of
fucosidosis
fundus, abnormality of
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, prenatal
genetic neurologic disorders
genetic screening
genetic testing
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
growth retardation
Guillain Barre syndrome
Guillain Barre syndrome, differential diagnosis of
Hallervorden Spatz disease
Hallervorden Spatz disease, late onset
hallucination
hallucination, auditory
hamster
hand pain
hand weakness
hands, fisted
head lag
headache
headache, progressive
headache, severe
headache, thunderclap
headbanging
hearing loss
heart murmur
heatstroke
heavy metal intoxication
hematopoietic tissue, extramedullary
hematuria, microscopic
hemianopia, homonymous
hemiplegia
hemoglobin abnormality, neurologic complications of
hemoglobinuria
hemolytic-uremic syndrome
hepatic encephalopathy
hepatic failure
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
hepatolenticular degeneration(Wilson's disease), screening for
hepatomegaly
hepatosplenomegaly
heralding manifestation
herniated disc, thoracic
heterophile antibody test
hexosaminidase-A
hexosaminidase-A and B
histochemistry
histochemistry of muscle
homocystinuria
homosexual
human granulocytic anaplasmosis
human immunodeficiency virus type 1
human immunodeficiency virus type 1, acute infection
Hurler's syndrome
hydrocephalus
hydrocephalus, normal pressure
hydroxytryptophan L-5(L-5 HTP)
hyperammonemic encephalopathy
hyperamylasemia
hyperbilirubinemia
hyperglycinemia
hyperhomocysteinemia
hyperkalemia
hyperkeratosis
hyperreflexia
hypersensitivity reaction
hypertension
hyperthermia
hypertonia
hypoalbuminemia
hypogammaglobulinemia
hypoglycemia
hypoglycorrhachia
hypokalemia
hypokalemic paralysis
hypomyelination
hyponatremia
hyporeflexia
hypothermia
hypotonia
hypotonia, infants
iatrogenic neurologic disorders
ileus, paralytic
imbalance
immunosuppression
immunosuppressive agents
inborn errors of metabolism
inborn errors of metabolism, screening
inclusion bodies, intracytopasmic
incoordination
infection
infection, recurrent
infectious mononucleosis
insulin resistance
intellectual deficit
intellectual deterioration
intelligence quotient
interferon
interferon antibodies
interferon beta 1-a
interferon beta 1-b
internal capsule
internuclear ophthalmoplegia
internuclear ophthalmoplegia, unilateral
intracerebral hemorrhage
intrauterine
iron, brain
irritability
ischemic exercise test
jaundice
jaw pain
Jewish
Kayser-Fleischer ring
Kearns-Sayre syndrome
Korsakoff's psychosis
Krabbe's disease
kyphoscoliosis, neurologic causes of
lactate
lactic dehydrogenase(LDH)
lacunar infarction
lamotrigine
L-dopa
Leber's hereditary optic neuropathy
leg weakness, bilateral
Legionella pneumophilia
Legionnaires'disease
Leigh's disease
Leigh's disease, adult variety
lens, dislocation of
lens, ectopic
Lesch-Nyhan syndrome
lethargy
leukemia
leukemia, neurologic findings assoc.with
leukocyte enzyme abnormality
leukocytosis
leukodystrophy
leukopenia
life expectancy
lipid storage disorder of CNS
livedo reticularis
liver disease
liver function enzymes
liver transplantation
lymph node biopsy
lymphadenopathy
lymphadenopathy, axillary
lymphadenopathy, cervical
lymphadenopathy, paraaortic
lymphocytic choriomeningitis
lymphocytosis
lymphoma
lymphoma involving CNS
lymphopenia
lysosomal storage disease
lysosomes, abnoral
macrocephaly
malaise
malignant hyperpyrexia
marihuana
Massachusetts
McArdle's disease
meconium staining
Mees lines
melanomatosis, primary malignant
MELAS syndrome
memory, defect of recent
meningitis
meningitis, aseptic
meningitis, plasma cell
menses
menses, irregular
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
microangiopathic hemolytic anemia
microhemorrhage, intracerebral
microspherophakia
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
mitoxantrone
mitral valve vegetation
MNGIE syndrome
molecular genetics
mortality
motor neuron disease
movement disorder
movement disorder, drug induced
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, demyelinating disease
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, eye of tiger sign
MRI, false negative
MRI, gradient-echo
MRI, hypointense signal foci on
MRI, negative
MRI, paramagnetic effect
MRI, spine
MRI, susceptibility weighted
MRI, vessel wall
MRI, vessel wall enhancement
MRS
mucopolysaccharidoses
multiple sclerosis
multiple sclerosis, children
multiple sclerosis, differential diagnosis of
multiple sclerosis, early onset
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 wasting, diffuse
muscle weakness
muscle weakness, insidious onset of
muscle weakness, proximal
muscular dystrophy, Duchenne
muscular dystrophy, Duchenne, neonatal screening
mycoplasma
mycoplasma pneumoniae
myelopathy
myocardial injury
myoclonic jerks
myoclonus
myocytolysis
myoglobinuria
myopathy
myopathy, distal, vacuolar
myopathy, metabolic
myopathy, mitochondrial
myopathy, necrotizing
myopathy, vacuolar
myopia
myositis
nausea and vomiting
neck pain
neck weakness
neonatal screening, genetic neurologic disorders
neoplastic angioendotheliosis
nerve biopsy
nerve conduction studies
neuraminidase deficiency
neuritis, heavy metals causing
neuroleptic
neuroleptic malignant syndrome
neurologic complications
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination
neurologic signs
neuromuscular disease, electrodiagnosis of
neuropathology
neuropathy
neuropathy, ataxia, retinitis pigmentosa
neuropathy, painful
neuropathy, peripheral
neuropathy, toxic
neurotransmitter
neutropenia
nonsteroidal anti-inflammatory drug
nystagmus
obesity
oculogyric crisis
odynophagia
ophthalmoplegia
ophthalmoplegia, progressive external
opisthotonus
opportunistic infection
optic atrophy
optic chiasm, enlarged
optic nerve
optic nerve, enlarged
optic neuritis
organ donor
organ transplantation
ornithine transcarbamylase deficiency
orthopnea
osteoporosis
pain
pain, abdominal
pain, head
pain, leg
pain, thigh
palilalia
pancreatitis
pancytopenia
PANK2 mutation
paraparesis, spastic
paraspinal muscle
paraspinal muscle weakness
paresthesias, feet
paresthesias, hands
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
PAS positive
PAS positive material in the brain
pathology
patient information and support
pectus excavatum
pediatric neurology
penicillamine
periarteritis nodosa
pericardial effusion
peripheral blood smear
peripheral blood smear, abnormal
peroxisomal disease
peroxisomes
personality change
petechiae
phenylketonuria
phosphorylase b kinase deficiency
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
pleural effusion
pneumonia
polymerase chain reaction
polyneuropathy
Pompe's disease of glycogen storage
porphyria
position sensation, abnormal
postpartum
postpartum coma
postural abnormality
precipitating factors
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
prognathism
prognosis
progressive neurologic disorder
prolactin, elevated
proprioception, abnormal
proteinuria
protozoan infection
pseudomyotonia
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychomotor retardation
psychosis
pulmonary function tests
pulmonary infiltrates
putamen, lesion of
pyramidal tract
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
pyruvate-kinase deficiency anemia
quadriparesis
quadriplegia
rash
recurrent
renal biopsy
renal failure
renal failure, acute
renal stones
renal transplantation
renal tubular acidosis
respiratory failure
respiratory tract infection
retinal degeneration
retinal hemorrhages
retinopathy
reversible cerebral vasoconstrictive syndromes
reversible neurologic disorder
review article
Reye's syndrome
rhabdomyolysis
rickettsial organism
rigidity
risk factors
rodents
Roth spots
salivation, excessive
Sandhoff's disease
Sanfilippo syndrome
scalp swelling
scalp tenderness
schizophrenia
scoliosis
scoliosis, neurologic association with
screaming
screening
second wind phenomena
sedimentation rate
sedimentation rate, elevated
seizure
seizure, children
seizure, drug-induced
seizure, elderly
seizure, neonatal
seizure, psychomotor-temporal lobe
self-mutilation
semialdehyde dehydrogenase deficiency
serologic testing
serositis
serum alanine aminotransferase
serum glutamic oxaloacetic transaminase
short stature
sickle cell disease
skew deviation
skin, biopsy
skin, lesions in neurologic disorders
slit lamp examination
small vessel disease
sodium valproate
sodium valproate, toxicity
somnolence
sore throat
spasticity
speech disorder
speech disorder, childhood
sphingolipodoses
spinal cord
spinal cord, compression of
spinal cord, lesion of
spinocerebellar ataxia type 1
spinocerebellar degeneration
splenomegaly
splinter hemorrhages
spongy degeneration of brain
startle reaction
stem cell transplantation
steroid
steroid therapy, CNS treatment and complications with
stiff joints
strabismus
striatum, lesion of
stuporous
stuttering
subarachnoid hemorrhage
subarachnoid hemorrhage, cerebral convexity
subcutaneous nodules
substantia nigra
suck, poor
superior cerebellar artery infarction
sweating
sweating, abnormality of
symmetric brain lesions
systemic illness
systemic juvenile idiopathic arthritis
Tay-Sachs disease
temporal lobe, lesion
term infant
tetrahydrobiopterin
thalamus, lesion of
thalamus, lesion of-bilateral
thiamine
thrombocytopenia
thrombocytosis
tick bite
tinnitus
tone, muscle, increased
tongue, enlarged
tongue, weakness
tranquilizers, neurologic complications with
transketolase
transluminal angioplasty, coronary artery
treatment of neurologic disorder
tremor
trientine dihydrochloride
tyrosine
tyrosine hydroxylase deficiency
tyrosinemia
umbilical-cord blood transplantation
unconsciousness
urea
urea-cycle enzymopathies
uremia
urinary casts
urinary incontinence
urinary tract infection
urine test for metabolic disorders
urine test in toxic screen
urine, dark
urticaria
vasculitides
vasculopathy
vertebral infarction
vertebral-basilar insufficiency
vertigo
vertigo, episodic
viral infection
viral infection, CNS
vision, blurred
visual acuity, decreased
visual loss
vital capacity
vitamin deficiency
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
weakness, proximal
weight loss
Wernicke's encephalopathy
wheelchair
white matter disease
winging of scapula
writing
zinc
Showing articles 450 to 500 of 6302 << Previous Next >>

Evidence-based Guideline: Antiepileptic Drug Selection for People with HIV/AIDS
Neurol 78:139-145, Birbeck,G.L.,et al, 2012

Clinical Reasoning: A 33-year-old Woman with Severe Postpartum Occipital Headaches
Neurol 78:366-369, Maalouf,N. and Harik,S.I., 2012

Complications and Outcome of Infective Endocarditis
UpToDate January, Spelman, D. & Sexton, D., 2012

Fatal Cryptococcal Meningitis in a Patient with Chronic Lymphocytic Leukemia
Mediterr J Hematol Infect Dis doi 10.4084/MJHID.2012,039, Dizdar,O.S.,et al, 2012

Primary Central Nervous System T-Cell Lymphoma of the Brain
Open Neurosurg J 4:62-65, Behbahami, M. & Lyons, M., 2011

Epidemiology, Pathogenesis, Clinical Manifestations and Diagnosis of Waldenstrom Macroglobulinemia
UptoDate, May, Rajkumar, S.V., 2011

Patient with Unilateral White Matter Involvement Does Not Have Krabbe Disease
Arch Neurol 68:1345, Van der Knaap, M.S. and Wenger, D.A., 2011

Epidemic Profile of Shiga-Toxin-Producing Escherichia coli O104:H4 Outbreak in Germany
NEJM 365:1771-1780, Frank, C.,et al, 2011

Unilateral White Matter Involvement in Krabbe Disease
Arch Neurol 68:130-131, Lemmens,R.,et al, 2011

Cerebral Amyloid Angiopathy Related Inflammation: Three Case Reports and a Review
JNNP 82:20-26, Chung,K.K.,et al, 2011

Diagnosis of intravascular lymphoma: usefulness of random skin biopsies
Brain Neurol 63:451-458, Nakano, N.M., 2011

Neurological disturbances caused by intravascular lymphomatosis
Brain Nerve 63:443-449, Mizutani, T., 2011

Progressive Multifocal Leukoencephalopathy in Transplant Recipients
Ann Neurol 70:305-322, Mateen, F.J.,et al, 2011

Clinicopathologic conference, Neurologic form of immune reconstitution inflammatory syndrome (neuro-IRIS), without evidence of concurrent opportunistic infection
NEJM 362:2343-2352, Case 18-2011, 2011

Spontaneous Regression of an Intracerebral Lymphoma (ghost tumor) in a Liver-Engrafted Patient
The Neurologist 17:218-221, Korner, S.,et al, 2011

Central Nervous System Lymphoma: Characteristic Findings on Traditional and Advanced Imaging
AJNR 32:984-992, Haldorsen, I.S.,et al, 2011

Screening for tumours in paraneoplastic syndromes: report of an EFNS Task Force
Eur J Neurol 18:19-27, Titulaer, M.J.,et al, 2011

Random skin biopsy and bone marrow biopsy for diagnosis of intravascular large B cell lymphoma
Ann Hematol 90:417-421, Matsue, K.,et al, 2011

Acute Hyperammonemic Encephalopathy in Adults: Imaging Findings
AJNR 32:413-418, U-King-Im,J.M.,et al, 2010

Treatment and Prognosis of Primary Central Nervous System Lymphoma
Up to Date Sept 2010, Hochberg,F.H.,et al, 2010

Clinical Presentation, Pathologic Features, and Diagnosis of Primary Central Nervous System Lymphoma
Up to Date Sept 2010, Hochberg,F.H.,et al, 2010

Clincopath Conference, Endogenous Endophthalmitis Due to Aspergillus Niger
NEJM 363:1749-1758, Case 33-2010, 2010

Imaging Manifestations of Progressive Multifocal Leukoencephalopathy
Clinical Radiol 65:431-439, Shah,R.,et al, 2010

Acute Hepatic Encephalopathy: Diffusion-Weighted and Fluid-Attenuated Inversion Recovery Findings, and Correlation With Plasma Ammonia Level and Clinical Outcome
AJNR 31:1471-1479, McKinney,A.M.,et al, 2010

Progressive Multifocal Leukoencephalopathy in Individuals with Minimal or Occult Immunosuppression
JNNP 81:247-254, Gheuens,S., et al, 2010

Diagnosis and Management of the Antiphospholipid Syndrome
BMJ 340:1125-1132, Cohen,D., et al, 2010

Neuropsychological Dysfunction and Neuroimaging Abnormalities in Neurologically Intact Adults With Sickle Cell Anemia
JAMA 303:1823-1831, Vichinsky,E.P., et al, 2010

Spinal Cord Sarcoidosis: Clinical and Laboratory Profile and Outcome of 31 Patients in a Case-Control Study
Medicine 89:133-140, Cohen-Aubart,F.,et al, 2010

Neurosacrcoidosis: Presentations and Management
Neurologist 16:2-15, Terushkin,V.,et al, 2010

Positron Emission Tomography-Computed Tomography in Paraneoplastic Neurologic Disorders: Systematic Analysis and Review
Arch Neurol 67:322-329, McKeon,A.,et al, 2010

FDG-PET a Pivotal Imaging Modality for Diagnosis of Stroke-Onset Intravascular Lymphoma
Arch Neurol 67:366-367, Yamada,S.,et al, 2010

AIDS - Related Lymphomas: Primary CNS Lymphoma
UpToDate, April, Doweiko, J.P., 2010

Primary Brain T-Cell Lymphoma of the Lymphoblastic Type Presenting as Altered Mental Status
Acta Neurochir 152:163-168, Clark, A.,et al, 2010

Subacute sclerosing panencephalitis: An Update
Dev Med Child Neurol 52:901-907, Guitierrez, J.,et al, 2010

Pathophysiology of Thrombotic Thrombocytopenic Purpura
Int J Hematol 91:1-30, Tsai, H.M., 2010

Primary Central Nervous System Post-Transplantation Lymphoproliferative Disorder
CANCER 16:863-870, Cavaliere, R.,et al, 2010

Assessment of Potential Drug Interactions in Patients with Epilepsy: Impact of Age and Sex
Neurol 72:419-425, Gidal,B.E.,et al, 2009

Primary Central Nervous System Lymphoma with Cortical Laminar Hemorrhage
J Neurol Sci 287:281-284, Kimura, N.,et al, 2009

Aicardi-Gouti�res Syndrome
Br Med Bull 89:183-201, Orcesi, S.,et al, 2009

Plasmablastic Lymphoma: CNS Involvement, Coexistence of Other Malignancies, Possible Viral Etiology, and Dismal Outcome
Ann Hematol 88:351-358, Ustun, C.,et al, 2009

Reversible Extralimbic Paraneoplastic Encephalopathies with Large Abnormalities on Magnetic Resonance Images
Arch Neurol 66:268-271, McKeon,A.,et al, 2009

Aicardi-Gouti�res Syndrome: Neuroradiologic Findings and Follow-up
AJNR 30:1971-1976, Uggetti,C.,et al, 2009

Opportunistic Infections and Other Risks with Newer Multiple Sclerosis Therapies
Ann Neurol 65:367-377, Berger,J.R. &Houff,S., 2009

Clinicopath Conf, Acute HIV-1 Infection
NEJM 360:1540-1548, Case 11-2009, 2009

A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
Neurol 72:1607-1613, Lossos,A.,et al, 2009

Differential Diagnosis of Postpartum Headaches
Rev Mex Anest 32:Suppl1 S16-S23, MacArthur,A., 2009

Strokes at Time of Disease Diagnosis in a Series of 287 Patients with Biopsy-Proven Giant Cell Arteritis
Medicine 88:227-235, Gonzalez-Gay,M.A.,et al, 2009

Clinicopath Conf., Atypical Hemolytic-Uremic Syndrome
NEJM 361:389-400, Case 23-2009, 2009

Brain Lesions Are Most Often Reversible in Acute Thrombotic Thrombocytopenic Purpura
Neurol 73:66-70, Burrus,T.M.,et al, 2009

Lyme Neuroborreliosis: Manifestations of a Rapidly Emerging Zoonosis
AJNR 30:1079-1087, Hildenbrand,P.,et al, 2009



Showing articles 450 to 500 of 6302 << Previous Next >>