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Differential
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abdominal cramps
abdominal reflex, absent
acute disseminated encephalomyelitis
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
ageusia
akinetic mute
alcohol
Alexanders disease
Alexanders disease, adult onset
aminoacidopathies
aminoacidurias
amnestic syndrome
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, prognosis
anatomy of
angiitis
angiitis, granulomatous of CNS
angiitis, isolated of CNS
angina pectoris
anhidrosis
anosmia
anti MAG antibodies
antispasticity drugs
aphasia
arteriopathy
asterixis
asymptomatic
ataxia
ataxia, cerebellar
ataxic gait
attention deficit disorder with hyperactivity
autonomic dysfunction
Babinski sign
baclofen
basal ganglia, infarction
basal ganglia, lesion of
behavioral disorder
benign essential tremor
beta adrenergic blocker
bladder dysfunction
blink reflex
bone marrow transplantation
brain biopsy
brainstem
brainstem, infarction of
brainstem, lesion of
burning paresthesia
calcification, intracranial
Canavan's disease
CAT scan
CAT scan, abnormal
CAT scan, demyelinating disease
CAT scan, serial
catecholamine
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortical atrophy
cerebral infarction
cerebral infarction, small, deep
cerebral infarction, subcortical
cerebral ischemia
cerebral palsy
cerebral venous infarction
cerebral venous thrombosis
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, cell count
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, immunoglobulins of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, protein of
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, multiple
cerebrovascular accident, nonvascular territory
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
cerebrovascular disease, cardiovascular disease with
Charcot-Marie-Tooth
children
chromosomal abnormality
Clinical Pathologic Conference(C.P.C.)
cognition
congenital malformation
congestive heart failure
corneal dystrophy
cortical blindness
cortical blindness, transient
crying, pathologic
cyst, porencephalic
cystinuria
deep gray nuclei
degenerative diseases of CNS
dementia
dementia, cerebrovascular disease causing
dementia, presenile
dementia, subcortical
dementia, thalamic
demyelinating disease
dentate nuclei
dentate nuclei, lesion of
depression
diabetes mellitus
diagnostic criteria
diarrhea
differential diagnosis
dilantin
diplopia
disability, neurological
dopamine
drug induced neurologic disorders
dysarthria
dysarthria-clumsy hand syndrome
dysdiadochokinesia
dysphagia
dystonia
dystonia musculorum deformens
echocardiogram
echolalia
electrical sensation
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electron microscopy
ELISA
emotional lability
encephalitis
encephalitis, viral
encephalomalacia
encephalopathy
encephalopathy, metabolic
enzyme, defect
evoked potentials
exercise intolerance
eye, pain in
Fabry's disease
facial nerve palsy
facial weakness
facial weakness, bilateral
Fahr disease
familial
fatigue
fever
flexor spasm
gadolinium
gait disorder
gamma amino butyric acid
gamma amino butyric acid-mimetic drug
gamma knife therapy
gangliosidosis GM2
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
Gilles de la Tourette syndrome
glioma
glutaric acidemia
granular osmiphilic material
haloperidol
head injury
head nodding
headache
hearing loss
hearing loss, bilateral
heavy metal intoxication
hemianopia
hemianopia, transient
hemiparesis
hemiparesis, transient
hemiplegia
hepatic encephalopathy
hepatic encephalopathy, treatment of
hepatolenticular degeneration(Wilson's disease)
hiccoughs
HLA
holoprosencephaly
homovanillic acid
hormone replacement
human immunodeficiency virus type 1
human T-lymphotropic virus type I(HTLV-I)
hydrocephalus
hyperreflexia
hypersomnia
hypertension
hyperthyroidism
hypoxic encephalopathy
iatrogenic neurologic disorders
imbalance
incoordination
intellectual deficit
intellectual deterioration
interferon
interferon beta 1-a
interferon beta 1-b
intrathecal antispasticity drugs
iron, brain
Japan
Krabbe's disease
lactic acidemia
lacunar infarction
laughing, pathologic
L-dopa
Leber's hereditary optic neuropathy
Leigh's disease
Leigh's disease, adult variety
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
level of consciousness, decreased
Lhermitte's sign
lipid storage disorder of CNS
liver disease
Lorenzo's oil
low birth weight
magnetic susceptibility
malformation, CNS, congenital
maple syrup urine disease
MELAS syndrome
mental retardation
metabolic disorder, primary
metachromatic leukodystrophy
metronidazole
microhemorrhage, intracerebral
migraine
misdiagnosis
mitochondrial disease
monoamines
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, complications with
MRI, contrast enhanced
MRI, demyelinating disease
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, negative
MRI, paramagnetic effect
MRI, serial
MRI, spinal cord
MRI, T1 weighted high signal foci
MRI, volumetry
multiple sclerosis
multiple sclerosis, asymptomatic
multiple sclerosis, chronic progressive
multiple sclerosis, clinical patterns
multiple sclerosis, conjugal
multiple sclerosis, diagnosis of
multiple sclerosis, differential diagnosis of
multiple sclerosis, etiology of
multiple sclerosis, familial
multiple sclerosis, linoleic acid in
multiple sclerosis, misdiagnosis
multiple sclerosis, parental transmission
multiple sclerosis, pathogenesis
multiple sclerosis, prognosis
multiple sclerosis, risk factors for
multiple sclerosis, spinal form
multiple sclerosis, treatment of
muscle biopsy
myelin basic protein gene
myelinolysis, extrapontine
myelitis
myelitis, longitudinal
myelitis, transverse
myelomalacia
myelopathy
myelopathy, chronic progressive
myocardial infarction
myoclonus
mysoline
nausea and vomiting
neurochemistry
neurogenic bladder
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neuromyelitis optica (Devic's disease)
neuromyelitis optica spectrum disorder
neuromyelitis optica, IgG
neuropathology
neuropathy
neuropathy, peripheral
neurotransmitter
norepinephrine
Notch3 gene
nystagmus
obsessive-compulsive disorder
occipital lobe, infarction
occipital lobe, lesion of
old age, neurology of
optic atrophy
optic atrophy, bilateral
optic atrophy, hereditary
optic nerve, hypoplasia of
optic neuritis
optic neuritis, bilateral
optic neuropathy
optic neuropathy, bilateral
optic neuropathy, hereditary
palatal myoclonus
palilalia
paraparesis
paraparesis, spastic
paraparesis, spastic, tropical
paraplegia
paratrigeminal syndrome
paresthesias
Parkinson disease
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
PAS positive
PAS positive material in the brain
Pelizaeus Merzbacher
periventricular leukomalacia
phenylketonuria
phenylketonuria, adult onset
pimozide
pleocytosis of cerebrospinal fluid
poison, neurologic problems with
polymerase chain reaction
pons, lesion of
posterior cerebral artery territory infarction
posterior leukoencephalopathy syndrome
premature infant
prevention of neurologic disorders
primary lateral sclerosis
prognosis
propranolol
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
pyramidal tract dysfunction
quadriparesis
quadriplegia
quality of life
radiation therapy, stereotactic
ragged-red fibers
Red flags
regional enteritis
renal stones
retrovirus
reversible neurologic disorder
review article
rigidity
Riley-Day syndrome
risk factors
Rosenthal fibers
Sandhoff's disease
Schilder's disease
scotoma
scotoma, central
seizure
seizure, children
seizure, neonatal
sensorineural hearing loss
sick sinus syndrome
skin, biopsy
skin, lesions in neurologic disorders
smell
spasticity
spasticity, treatment of
speech disorder
speech, loss of
spinal cord
spinal cord, injury of
spinal cord, injury, management of
spinal cord, lesion of
spontaneous remission
steroid therapy, CNS treatment and complications with
stimulation, deep brain
symmetric brain lesions
systemic lupus erythematosus
tardive dyskinesia
taste
Tay-Sachs disease
temporal lobe, lesion, bilateral
thalamic tumors
thalamic tumors, bilateral
thalamotomy
thalamus
thalamus, infarction of
thalamus, infarction, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
thiamine deficiency
thyrotoxicosis
tic
tinnitus
tongue, impaired movements of
top of the basilar syndrome
torticollis
transient ischemic attack
transient ischemic attack, recurrent
transient neurologic deficit
trauma
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, classification
tremor, differential diagnosis of
tremor, intention
tremor, jaw
tremor, leg
tremor, rubral
tremor, surgical treatment of
tremor, thalamic stimulation for suppression of
tremor, treatment of
twins
ulcerative colitis
uremia
urinary frequency
urinary incontinence
urinary urgency
vasculitides
vasculopathy
vasospasm, cerebral
vertigo
vertigo, episodic
very long chain fatty acids
viral infection
viral infection, CNS
vision loss, sequential
visual acuity, decreased
visual evoked response
visual loss
visual loss, progressive
visual loss, sudden
visual loss, transient
walking, difficulty with
water channel antibodies
weakness
Wernicke's encephalopathy
white matter disease
workup
Showing articles 3050 to 3100 of 5493 << Previous Next >>

Heritability of Carotid Artery Atherosclerotic Lesions
Stroke 36:5-8, Moskau,S.,et al, 2005

The Risk of Hemorrhage After Radiosurgery for Cerebral Arteriovenous Malformations
NEJM 352:146-153, Maruyama,K.,et al, 2005

Use of Levetiracetam to Treat Tics in Chidlren and Adolescents With Tourette Syndrome
Movement Disorders 20:714-718, Awaad,Y.,et al, 2005

Progressive Myoclonic Epilepsies: A Review of Genetic and Therapeutic Aspects
Lancet Neurol 4:239-248, Shahwan, A., et al, 2005

Neurologic Features of Horizontal Gaze Palsy and Progressive Scoliosis with Mutations in ROBO3
Neurol 64:1196-1203, Bosley, T.M.,et al, 2005

Multiple Actinomycosis Brain Abscesses
Presse Med 33:318-320, Liotier,J.,et al, 2004

CADASIL: Cerebral Autosomal Subcortical Infarcts and Leukoecephalopathy
, Chabriat, H., Joutel A., Vahedi, K., Tournier-Lasserve, &E., Bousser M.G., 2004

The Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcal Infection (PANDAS) Subgroup: Separating Fact From Fiction
Pediatrics 113:907-911, Swedo,S.,et al, 2004

The Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcal Infection (PANDAS) Etiology for Tics and Obsessive-Compulsive Symptoms: Hypothesis or Entity? Practical Considerations for the Clinician
Pediatrics 113:883-886, Kurlan,R. &Kaplan,E., 2004

Clinical Correlations of Mutations in the SCN1A Gene: From Febrile Seizures to Severe Myoclonic Epilepsy in Infancy
Pediatr Neurol 30:236-243, Ceulemans,B.P.G.M.,et al, 2004

Natural History of Nonketotic Hyperglycinemia in 65 Patients
Neurol 63:1847-1853, Hoover-Fong,J.E.,et al, 2004

The Occurence of Guillain-Barre Syndrome Within Families
Neurol 63:1747-1750, Geleijns,K.,et al, 2004

Practice Parameter: Recurrent Stroke with Patent Foramen Ovale and Atrial Septal Aneurysm
Neurol 62:1042-1050, Messe,S.R.,et al, 2004

White Matter Lesions, Congition, and Recurrent Hemorrhage in Lobar Intracerebral Hemorrhage
Neurol 63:1606-1612, Smith,E.E.,et al, 2004

An Unusual Cause of Visual Loss: Involvement of Bilateral Geniculate Bodies
AJNR 25:1544-1548, Lefebvre,P.R.,et al, 2004

PROTECT A Coordinated Stroke Treatment Program to Prevent Recurrent Thromboembolic Events
Neurol 63:1217-1222, Ovbiagele,B.,et al, 2004

Multiple Acute Cerebral Infarcts on Diffusion-Weighted Imaging and Risk of Recurrent Stroke
Neurol 63:1317-1319, Wen,H.M.,et al, 2004

Multiple Myeloma Invasion of the Central Nervous System
Arch Neurol 61:1423-1429, Schluterman,K.O.,et al, 2004

Peripheral Neuropathy
Lancet 363:2151-2161, England,J.D. &Asbury,A.K., 2004

Acute Korsakoff Syndrome Following Mammillothalamic Tract Infarction
AJNR 25:964-968,906, Yoneoka,Y.,et al, 2004

Hereditary Spastic Paraplegia
Arch Neurol 61:849-855,830, Orlacchio,A.,et al, 2004

Impact of Presymptomatic Genetic Testing for Hereditary Ataxia and Neuromuscular Disorders
Arch Neurol 61:875-880, Smith,C.O.,et al, 2004

Acute Bilateral Inferior Cerebellar Infarction in a Patient With Neurosyphillis
Arch Neurol 61:953-956, Umashankar,G.,et al, 2004

Most Cases of Dementia with Hippocampal Sclerosis May Represent Frontotemporal Dementia
Neurol 63:538-542, Hatanpaa,K.J.,et al, 2004

The Parkinsonian Phenotype of Spinocerebellar Ataxia Type 2
Arch Neurol 61:35-38, Lu,C.,et al, 2004

Lowering Homocysteine in Patients with Ischemic Stroke to Prevent Recurrent Stroke, Myocardial Infarction, and Death
JAMA 291:565-575,621, Toole,J.F.,et al, 2004

Antiphospholipid Antibodies and Subsequent Thrombo-occlusive Events in Patients with Ischemic Stroke
JAMA 291:576-584, The APASS Investigators, 2004

Brain Metastases
The Neurologist 10:31-46, Klos,K.J.&O'Neill,B.P., 2004

Imaging Cerebral Atrophy:Normal Ageing to Alzheimer's Disease
Lancet 363:392-394, Fox,N.C.&Schott,J.M., 2004

Patent Foramen Ovale and Recurrent Stroke: Closure is the Best Option: No
Stroke 35:804-805,806, Tong,D.C. &Becker,K.J., 2004

Patent Foramen Ovale and Recurrent Stroke: Closure is the Best Option: Yes
Stroke 35:803-804,806, Furlan,A.J., 2004

Early Risk of Recurrence by Subtype of Ischemic Stroke in Population-Based Incidence Studies
Neurol 62:569-573, Lovett,J.K.,et al, 2004

Ropinirole in Gilles de la Tourette Syndrome
Neurol 62:1626-1627, Anea,M.H.,et al, 2004

Efficacy and Tolerability of the New Antiepleptic Drugs II: Treatment of Refractory Epilepsy
Neurol 62:1261-1273, French,J.A.,et al, 2004

Fibromuscular Dysplasia
NEJM 350:1862-1871, Slovut,D.P. &Olin,J.W., 2004

Developmental Dyslexia
Lancet 363:1451-60, Demonet,J-F.,et al, 2004

Charcot-Marie-Tooth Disease:Extensive Cranial Nerve Involvement on CT and MR Imaging
AJNR 25:494-497, Aho,T.R.,et al, 2004

Neurobrucellosis:Clinical and Neuroimaging Correlation
AJNR 25:395-401, Al-Sous,M.W.,et al, 2004

West Nile Virus Infection in the United States
Arch Neurol 61:1190-1195, Tyler,K.L., 2004

The Neurological Complications of Bariatric Surgery
Arch Neurol 61:1185-1189, Berger,J.R., 2004

Seizure Outcomes After Stereotactic Radiosurgery for Cerebral Arteriovenous Malformations
Neurol 63:683-687, Schauble,B.,et al, 2004

Neurological Sequelae in Twins Born After Assisted Conception: Controlled National Cohort Study
BMJ 329:311-314, Pinborg,A.,et al, 2004

Poststroke Neurological Improvement Within 7 Days Is Associated with Subsequent Deterioration
Stroke 35:2165, Aslanyan,S.,et al, 2004

Age As a Determinant of Adverse Events in Medically Treated Cryptogenic Stroke Patients with Patent Foramen Ovale
Stroke 35:2145, Homma,S.,et al, 2004

Does Transcatheter Closure of Patent Foramen Ovale Really "Shut the Door?"
Stroek 35:2140, Anzola,G.P.,et al, 2004

Pathogenetic Mechanisms of Parkin in Parkinson's Disease
Lancet 364:722-724, Hattori,N. &Mizuno,Y., 2004

Clinicopath Conf, Multiple-System Atrophy
NEJM 351:912-921, Case 27-2004, 2004

Whole Brain Radiation Therapy With or Without Stereotactic Radiosurgery Boost for Patients with One to Three Brain Metastases: Phase III Results of the RTOG 9508 Randomised Trial
Lancet 363:1665-1672, Andrews,D.W.,et al, 2004

Recurrent Acroparaesthesia During Febrile Infections
Lancet 363:1698, Bodamer,O.A.,et al, 2004

Hemorrhage Burden Predicts Recurrent Intracerebral Hemorrhage After Lobar Hemorrhage
Stroke 35:1415-1420, Greenberg,S.M.,et al, 2004



Showing articles 3050 to 3100 of 5493 << Previous Next >>