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Differential
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abducens nerve paralysis
acetazolamide
acromegaly
adverse drug reaction
alcohol
Alexanders disease
Alexanders disease, adult onset
algorithm
alternating hemiplegia
alternating hemiplegia of childhood
amaurosis fugax
aminoacidopathies
aminoacidurias
amyloid angiopathy, cerebral
anemia
aneurysm
angiography, cerebral, beaded vessels
angiography, cerebral
angiography, cerebral, negative
angiography, vertebral artery
anorexia
anti IgLON5
antibodies to voltage-gated calcium channels
anxiety
aphasia
apnea
areflexia
arteritides
arteritis, temporal
arthralgia
astrogliopathy
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
ataxia, truncal
ataxic gait
ATP1A3 gene
autoantibodies
autoimmune disease
autonomic dysfunction
behavioral disorder
blindness
brain biopsy
brainstem, infarction of
brainstem, lesion of
bulbar palsy
calcium antagonist
calcium channel dysfunction
carbamazepine
CAT scan
CAT scan, abnormal
CAT scan, angiography
cataracts
central core disease
central retinal artery occlusion
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar degeneration
cerebellar lesion
cerebellar vermis
cerebral infarction
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, young adult
channelopathy
Charcot-Marie-Tooth
chemotherapy, CNS treatment and complications with
children
chills
chloride channel dysfunction
chorea
chromosomal abnormality
chromosome 19
ciguatera poisoning
Clinical Pathologic Conference(C.P.C.)
cognition
collagen vascular disease
coma
coma, episodic
complications
confusion
conversion reaction
cornea, abnormal
cough
deafness
deafness, unilateral
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
delirium
dementia
dementia, rapidly progressive
dentate nuclei, lesion of
depression
developmental retardation
diabetes insipidus
diagnostic criteria
differential diagnosis
digital subtraction angiography
diplopia
diurnal variation
down-beat nystagmus
down-beat nystagmus, primary position of gaze
drug induced neurologic disorders
dysarthria
dysphagia
dystonia
dystonia, psychogenic
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
encephalitis
encephalitis, autoimmune
encephalopathy
encephalopathy, acute
episodic disorders
episodic neurologic deficits
episodic unconsciousness
epistaxis
exercise
exercise intolerance
eye movement, disorders of
face, numbness of
facial nerve palsy
facial weakness
faciobrachial dystonic seizure
failure to thrive
falling
familial
familial hemiplegic migraine
familial periodic ataxia
fasciculation
fatigue
fever
fine motor function, impaired
Friedreich's ataxia
fundus, abnormality of
gait disorder
gene
gene mutation
genetic neurologic disorders
genetic testing
GFAP gene
glaucoma
globus pallidus, lesion of, bilateral
Guillain Barre syndrome
gynecomastia
hallucination
hallucination, visual
head turning
head turning, neurologic complications with
headache
headache, bifrontal
headache, elderly
headache, occipital
headache, recurrent
headache, severe
hearing loss
hemianopia
hemianopia, homonymous
hemimyoclonic jerks
hemiparesis
hemiplegia
hepatomegaly
hoarseness
hypercalcemia
hyperparathyroidism
hyperreflexia
hypersomnia
hypertension
hyperthyroidism
hypokalemia
hypokalemic periodic paralysis
hyponatremia
hypophonia
hypotonia
iatrogenic neurologic disorders
imbalance
immunotherapy
inborn errors of metabolism
incoordination
infection
intellectual deficit
intracerebral hemorrhage
iritis
jaw claudication
lactic acidemia
lateropulsion
leg numbness
leg weakness, bilateral
lethargy
leucine rich glioma inactivated 1 antibodies
leukemia
leukodystrophy
leukoencephalopathy
limbic encephalitis
lysosomal storage disease
macrocephaly
malignant hyperpyrexia
maple syrup urine disease
mastoiditis
memory, defect of recent
memory, impairment of
meningeal enhancement
meningitis
meningitis, aseptic
meningitis, carcinomatous
meningitis, elderly
mental status, abnormal
metabolic disorder, primary
methotrexate
microcephaly
microhemorrhage, intracerebral
migraine
migraine, hemiplegic
misdiagnosis
molecular genetics
mononeuropathy
mononeuropathy multiplex
monoparesis
mortality
motor dysfunction
motor neuron disease
motor neuron disease, misdiagnosis
movement disorder
movement disorder, hyperkinetic
movement disorder, psychogenic
MRI
MRI, abnormal
MRI, angiography
MRI, diffusion weighted
MRI, negative
MRI, spine
multimodal neuroimaging
multiple sclerosis
multiple sclerosis, pain in
multiple sclerosis, paroxysmal symptoms in
muscle biopsy
muscle cramp
muscle pain
muscle weakness
muscle weakness, proximal
myasthenic syndrome
myoclonic jerks
myoclonus
myokymia
myotonia
myotonia congenita
nasal septum, perforation of
nausea and vomiting
negative
neuroendocrinology
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neurologic examination, focal
neurologic signs
neurologic symptoms
neurologic symptoms, unexplained
neurologic testing
neuromyotonia
neuroophthalmology
neuropathy
neuropathy, hereditary peripheral
neuropathy, peripheral
neuropathy, vasculitic, systemic
neurotoxic
neurotoxicity, acute
night sweats
nystagmus
nystagmus, gaze-paretic
nystagmus, hereditary
nystagmus, intermittent
nystagmus, monocular
nystagmus, periodic
nystagmus, vertical
old age, neurology of
ophthalmoplegia
optic ataxia
optic atrophy
optic neuritis
optic neuropathy, ischemic
oscillopsia
otitis, neurologic complications with
pain
pain, abdominal
pain, leg
pain, testicular
palatal myoclonus
palinopsia
papilledema
paralysis
paralysis, acute areflexic
paramyotonia congenita
paraparesis
paresthesias
Parkinson disease, dystonia with
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
paroxysmal tonic upgaze
pathology
periarteritis nodosa
periodic paralysis
periodic paralysis, thyrotoxic
peroxisomal disease
personality disorder
pleocytosis of cerebrospinal fluid
polyneuropathy
polyuria
posterior leukoencephalopathy syndrome
potassium
potassium channel antibodies
potassium channel dysfunction
precipitating factors
pregnancy, neurologic complications in
primary episodic ataxia
prognosis
progressive neurologic disorder
psychiatric disorder
psychiatric problems in neurologic disorders
psychosis
psychosis, acute
ptosis
pulmonary infiltrates
pupil, abnormality in neurologic disorders
pupil, tonic
quadriplegia
quadriplegia, transient
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
rash
recurrent
REM sleep behavior disorder
retinal artery occlusion
retinopathy
reversible cerebral vasoconstrictive syndromes
review article
rheumatoid arthritis
rheumatoid arthritis factor(R.A.factor)
rhinorrhea
scleritis
scotoma
sedimentation rate, elevated
seizure
seizure, differential diagnosis of
seizure, focal
sensorineural hearing loss
sinusitis
skin, lesions in neurologic disorders
sleep pathology and physiology
sodium channel dysfunction
sore throat
spinal cord, compression of
spinal stenosis
spinal stenosis, cervical canal
spinocerebellar ataxia
spinocerebellar ataxia type 6
status epilepticus
steroid therapy, CNS treatment and complications with
stress, emotional
strokelike episodes
subarachnoid hemorrhage, cerebral convexity
symmetric brain lesions
syncope
tachycardia
tandem gait, ataxic
temporal lobe, lesion, bilateral
testicular biopsy
third nerve palsy
thirst
thyrotoxicosis
tinnitus
tonic spasms
toxic encephalopathy
transient ischemic attack
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, psychogenic
trigeminal neuralgia
trigeminal neuropathy
trigeminal neuropathy, sensory
trinucleotide repeats
unconsciousness
unconsciousness, episodic
unconsciousness, transient
upgaze
upgaze, sustained
urea-cycle enzymopathies
uremia
vaccination, neurologic complications with
vasculopathy
vasospasm, cerebral
vertebral artery
vertebral artery disease
vertebral artery occlusion
vertebral artery stenosis
vertebral-basilar insufficiency
vertigo
vertigo, episodic
Virchow-Robin spaces, dilated
vision, blurred
visual field defect
visual loss
vitamin E deficiency
vocalizations
walking, difficulty with
weakness
weakness, acute
weakness, episodic
weakness, generalized
weight loss
white matter disease
wide based gait
Showing articles 550 to 600 of 1608 << Previous Next >>

Metabolic Disease and Stroke: MELAS
emedicine.com, Mandava,P.,et al, 2006

Transient Hemiageusia in Cerebrovascular Lateral Pontine Lesions
JNNP 77:680-683, Landis,B.N.,et al, 2006

Stroke Among Patients with Dizziness, Vertigo and Imbalance in the Emergency Department, A Population-Based Study
Stroke 37:2484-2487, Kerber,K.A.,et al, 2006

Clinicopath Conf., Degoss Disease
NEJM 355:2575-2584, Case 38-2006, 2006

The Clinical and Genetic Spectrum of Spinocerebellar Ataxia 14
Neurol 64:1258-1260, Chen,D-H.,et al, 2005

Autonomic Dysfunction in Machado-Joseph Disease
Arch Neurol 62:630-636, Yeh,T-H.,et al, 2005

Cerebellar Ataxia and Central Nervous System Whipple Disease
Arch Neurol 62:618-620, Matthews,B.R.,et al, 2005

Leukoencephalopathy with Ataxia, Hypodontia, and Hypomyelination
Neurol 64:1461-1464, Wolf,N.I.,et al, 2005

Does This Patient Have Myasthenia Gravis?
JAMA 293:1906-1914, Scherer,K.,et al, 2005

Autoantibodies to Folate Receptors in the Cerebral Folate Deficiency Syndrome
NEJM 352:1985-1991, Ramaekers,V.T.,et al, 2005

Acute Intermittent Porphyria Presenting as a Diffuse Encephalopathy
Ann Neurol 67:581-584, Maramattom,B.V.,et al, 2005

Vertebrobasilar Disease
NEJM 352:2618-2626, Savitz,S.I.&Caplan,L.R., 2005

Systemic Mastocytosis: A Potential Neurologic Emergency
Neurol 65:332-333, Boncoraglio,G.B.,et al, 2005

Initial Diagnoses Given to Persons with the Fragile X Associated Tremor/Ataxia Syndrome (FXTAS)
Neurol 65:299-301, Hall,D.A.,et al, 2005

Hyperglycemic Hemianopia: A Reversible Complication of Non-Ketotic Hyperglycemia
Neurol 65:616-619, Lavin,P.J.M., 2005

Clinicopath Conf, Prion Disease (Sporadic Creutzfeldt-Jakob Disease)
NEJM 353:1042-1050, Case 27-2005, 2005

West Nile Virus Presenting as Opsoclonus-myoclonus Cerebellar Ataxia
Neurol 64: 1095-1096, Khosla,J.S., et al, 2005

Delayed Neurotoxicity in Primary Central Nervous System Lymphoma
Arch Neurol 62:1595-1600, Omuro,A.M.P.,et al, 2005

Autoantibodies in Postinfectious Acute Cerebellar Ataxia
Neurol 65:1114-1116, Uchibori,A.,et al, 2005

Late-Onset Friedreich Ataxia
Arch Neurol 62:1865-1869, Bhidayasiri,R.,et al, 2005

MRI T2 Hypointensity of the Dentate Nucleus is Related to Ambulatory Impairment in Multiple Sclerosis
J Neurol Sci 234:17-24, Tjoa,C.W.,et al, 2005

Update on Primary Central Nervous System Lymphoma
Curr Opin Neurol 18:645-653, Plotkin,S.R., 2005

Intermittent Headaches as the Presenting Sign of Subacute Angle-Closure Glaucoma
Neurol 65:757-758, Shindler,K.S.,et al, 2005

Underappreciated Statin-Induced Myopathic Weakness Causes Disability
Neurorehabil Neural Repair 19:259-263, Dobkin,B.H., 2005

Central Nervous System Manifestations of Mycoplasma Pneumoniae Infections
J Infection 51:343-354, Tsiodras, S.,et al, 2005

Left Atrial Myxoma Presenting as Migraine with Aura: A VIP-induced Syndrome
Headache 45:251-254, Kern, R. & Asa, S., 2005

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

Potassium Channel Antibody-Associated Encephalopathy: A Potentially Immunotherapy-Responsive Form of Limbic Encepahlitis
Brain 127:701-712, Vincent,A.,et al, 2004

A Case of Reversible Postpartum Cytotoxic Edema in Preeclampsia
JNeuroSci 221:83-87, Na,S.-J.,et al, 2004

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

Treatment-Induced Leukoencephalopathy in Primary CNS Lymphoma,A Clinical and Autopsy Study
Neurol 62:451-456, Lai,R.,et al, 2004

Penetrance of the Fragile X-Associated Tremor/Ataxia Syndrome in a Premutation Carrier Population
JAMA 291:460-469, Jacquemont,S.,et al, 2004

Late-Onset Cerebellar Ataxia with Hypogonadism and Muscle Coenzyme Q10 Deficiency
Neurol 62:818-820, Gironi,M.,et al, 2004

Riversible Diffusion MRI Abnormalities and Transient Mutism after Liver Trnasplantation
Neurol 62:981-983, Bianco,F.,et al, 2004

B- and T-cell Markers in Opsoclonus-Myoclonus Syndrome
Neurol 62:1526-1532,1466, Pranzatelli,M.R.,et al, 2004

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

Acute Cerebellar Ataxia Due to Sjogren Syndrome
Neurol 62:2332-2333, Wong,S.,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

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

Five New Cases of a Recently Described Leukoencephalopathy with High Brain Lactate
Neurol 63:688-692, Linnankivi,T.,et al, 2004

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

Clinicopath Conf, Pernicious Anema with Autoimmune Gastritis and B12 Deficiency
NEJM 351:1333-1341, Case 30-2004, 2004

Reversible Corpus Callosum Lesion in Legionnaires Disease
JNNP 75:651-654, Morgan, J.C.,et al, 2004

Bickerstaff's Brainstem Encephalitis: Clinical Features of 62 Cases and a Subgroup Associated with Guillain-Barre Syndrome
Brain 126:2279-2290, Odaka,M.,et al, 2003

The Accuracy of the Diagnosis of Paroxysmal Events in Children
Neurol 60:979-982, Stroink,H.,et al, 2003

Amnesia, Cerebral Atrophy, and Autoimmunity
Lancet 361:1266, Schott,J.M., et al, 2003

Cerebellar Ataxia and Coenzyme Q10 Deficiency
Neurol 60:1206-1208, Lamperti,C.,et al, 2003

Prevalence of Antigliadin Antibodies in Ataxia Patients
Neurol 60:1674-1675,1566, Abele,M.,et al, 2003

Neurologic Manifestations of Vitamin B12 Deficiency
NEJM 348:2208, Scherer,K., 2003



Showing articles 550 to 600 of 1608 << Previous Next >>