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Differential
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abducens nerve paralysis
abscess, intracerebral
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome dementia complex
agitation
agnosia
agnosia, visual
agraphia
alexia
alien hand syndrome
aluminum
Alzheimer's disease
Alzheimer's disease, early onset
Alzheimer's disease, familial
Alzheimer's disease, visual variant
amyloid angiopathy, cerebral
amyloid beta-related angiitis
ANA
anomic aphasia
anterior cerebral artery, occlusion of
antibiotics
antiviral agents
aphasia
aphasia, classification of
aphasia, logopenic, progressive
aphasia, progressive
aphasia, progressive, non-fluent
aphasia, progressive, primary
aphasia, transcortical
aphasia, transcortical-sensory
aphonia
apolipoprotein E
apraxia
apraxia, constructional
arteritides
arthralgia
arthritis
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
autoimmune disease
automobile accidents
basal cell carcinoma
behavior, combative
behavioral disorder
biologic markers
Borrelia miyamotoi infection
bradykinesia
brain atrophy
brain biopsy
brainstem, dysfunction
Broca's aphasia
cachexia
carotid angiogram
carotid artery stenosis
carphology
CAT scan
CAT scan, abnormal
CAT scan, contrast enhanced
CAT scan, disappearing lesion on
CAT scan, emission
CAT scan, emission, abnormal
central nervous system, infection of
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar plaques, amyloid
cerebral cortical atrophy
cerebral dominance
cerebral infarction
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, mimics
chromosomal abnormality
chromosome 17
Clinical Pathologic Conference(C.P.C.)
cognition
coinfection
collagen vascular disease
comorbidities
complications
compulsivity
confusion
cortical-basal ganglionic degeneration
cough
COVID-19
crying, pathologic
cryptococcal meningitis
cryptococcal meningoencephalitis
deafness
deafness, bilateral progressive vs.unilateral acute
deafness, unilateral
degenerative diseases of CNS
delusion
dementia
dementia, age at onset
dementia, differential diagnosis of
dementia, familial
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
diagnostic criteria
dialysis
dialysis dementia
differential diagnosis
dysarthria
dysphagia
dysphasia
dyspnea
dystonia
ecchymoses
electroencephalogram, abnormalities of
electroencephalogram, focal delta activity
encephalitis
encephalitis, focal
encephalitis, human immunodeficiency virus type 1
encephalitis, Rasmussen's
encephalopathy
encephalopathy, metabolic
encephalopathy, progressive
executive dysfunction
exercise intolerance
eye movement, disorders of
eye movement, painful
eye, pain in
facial nerve palsy
facial nerve palsy, bilateral
false negative
familial
fatigue
fever
floaters
fluency
foot drop
foreign accent syndrome
frontal behavioral spatial syndrome
frontotemporal dementia, behavioral variant
frozen section
fungal infection
fungal infection, CNS
gadolinium
gait disorder
gammaglobulin therapy, intravenous
gene
gene mutation
genetic neurologic disorders
genetic testing
gram positive rod
granulomatosis with polyangiitis
granulomatous disease
hallucination
headache
hearing loss
hemianopia
hemianopia, homonymous
hemianopia, transient
hemifacial atrophy
hemiparesis
hemiplegia
hemosiderosis of CNS, superficial
heralding manifestation
highly active antiretroviral therapy
homosexual
human immunodeficiency virus type 1
hyperreflexia
hypertension
hypoglycorrhachia
iatrogenic neurologic disorders
imbalance
imbalance, postural
immunosuppression
immunosuppressive agents
impulsivity
in situ hybridization
inappropriate behavior
inattention
inclusion bodies
inclusion bodies, intracytopasmic
infection
inflexibility, mental
Jakob-Creutzfeldt disease
Kaposi's sarcoma
Korsakoff's psychosis
lactate
lactic acidemia
laminar necrosis, cortical
language disorder in adults
leukemia
leukemia, neurologic findings assoc.with
leukocytosis
leukopenia
listeria monocytogenes
listeriosis, CNS
lobar atrophy
logopenia
lymphadenopathy
lymphoma
lymphoma involving CNS
lymphomatoid granulomatosis
MELAS syndrome
memory, defect of recent
memory, impairment of
memory, recent
meningeal enhancement
meningitis
meningitis, neutrophilic
meningitis, treatment of
meningoencephalitis
mental status, abnormal
microabscesses, cerebral
microaneurysm, retinal
microhemorrhage, intracerebral
middle cerebral artery, occlusion of
migraine
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
mortality
motor neuron disease
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, disappearing lesion on
MRI, false negative
MRI, linear enhancement
MRI, mass effect on
MRI, ring sign
MRI, serial
MRI, sulcal hyperintensity
MRI, T1 weighted high signal foci
MRS
muscle biopsy
muscle weakness, proximal
mutism
myasthenia gravis
mycophenolate
myelopathy
myelopathy, chronic progressive
myoclonic jerks
myoclonus
myopathy
myopathy, mitochondrial
neck stiffness
neoplastic angioendotheliosis
neurocutaneous disease
neurocutaneous melanosis
neurofilament light chain protein
neurologic complications
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic disease, multiple
neurologic disease, tempo
neurologic examination, focal
neuropathology
neuropathology, brain
neuropathy, peripheral
neurotoxin
neutropenia
New England
nystagmus
nystagmus, dissociated
nystagmus, vertical
ophthalmoplegia
ophthalmoplegia, progressive external
opportunistic infection, CNS
pain, increased response
pancytopenia
papilledema
paraparesis
paraparesis, spastic
paraphasias
paratonia
Parkinson disease
Parkinson disease, L-dopa nonresponsive
Parkinsonism syndrome
parotid gland swelling
personality change
phonophobia
Pick bodies
Pick's disease
Pittsburgh Compound B
PLEDs
PLEDs, bilateral independent
PLEDs, etiology of
pleocytosis of cerebrospinal fluid
pneumonia
polymerase chain reaction
polyneuropathy
posterior cortical atrophy
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
progressive supranuclear palsy
proteinuria
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
ptosis
pulmonary infiltrates
rapidly progressing neurologic illness
rash
recurrent
Red flags
release phenomena
renal failure
retro-orbital pain
review article
rigidity
scleroderma
scleroderma, neurologic involvement with
screening
seizure
seizure, focal
seizure, intractable
semantic dementia
sensorineural hearing loss
short stature
simultanagnosia
single photon emission computed tomography
Sjogren's syndrome
Sjogren's syndrome, neurologic manifestations of
skin, biopsy
skin, lesions in neurologic disorders
somnolence
sonophobia
speech arrest
speech disorder
speech, loss of
spirochete infection
splenomegaly
spongy degeneration of brain
stare
staring spells
stereotyped behavior
steroid therapy, CNS treatment and complications with
strokelike episodes
stuttering
systemic lupus erythematosus
tachycardia
tau protein
tauopathy
temporal lobe
temporal lobe, atrophy
temporal lobe, lesion
temporalis muscle wasting
thrombocytopenia
tinnitus
transient neurologic deficit
treatment of neurologic disorder
tremor
upgaze, paralysis of
uremia
valium
vertigo
vision, blurred, monocular
visual field defect
visual fields
visual loss
visuospatial disturbance
walking, difficulty with
weakness
weakness, generalized
weight loss
Wernicke's aphasia
white matter disease
word-finding difficulty
Showing articles 750 to 800 of 2320 << Previous Next >>

Neurologic Manifestations of von Hippel-Lindau Disease
JAMA 300:1334-1342, Butman,J.A.,et al, 2008

Curable Cause of Paraplegia: Spinal Dural Arteriovenous Fistulae
Stroke 39:2756-2759, Aghakhani,N.,et al, 2008

Neurologic Manifestations of Localized Scleroderma: A Case Report and Literature Review
Neurol 71:1538-1545, Kister,I.,et al, 2008

Combining Beta Interferon and Atorvastatin May Increase Disease Activity in Multiple Sclerosis
Neurol 71:1390-1395,1386, Birnbaum,G.,et al, 2008

Anteroir Cerebral Artery Infarction: Stroke Mechanism and Clinical-Imaging Study in 100 Patients
Neurol 70:2386-2393, Kang,S.Y. &Kim,J.S., 2008

Electrocardiographic Abnormalities and Sudden Death in Myotonic Dystrophy Type 1
NEJM 358:2688-2697, Groh,W.J.,et al, 2008

Spinal Muscular Atrophy
Lancet 371:2120-2133, Lunn,M.R. &Wang,C.H., 2008

Reduction of Disease Activity and Disability With High-Dose Cyclophosphamide in Patients With Aggressive Multiple Sclerosis
Arch Neurol 65:1044-1051, Krishnan,C.,et al., 2008

Guillain-Barre Syndrome
BMJ 337:227-231, Winer,J.B., 2008

Rapidly Progressive Dementia
Ann Neurol 64:97-108, Geschwind,M.D.,et al., 2008

Diagnosis and Etiology of Congenital Muscular Dystrophy
Neurol 71:312-321,308, Peat,R.A.,et al., 2008

Assessment: The Use of Natalizumab (Tysabri) for the Treatment of Multiple Sclerosis (An Evidence-Based Review): Report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology
Neurol 71:766-773, Goodin,D.S.,et al., 2008

Idiopathic Sudden Sensorineural Hearing Loss
NEJM 359:833-840, Rauch,S.D., 2008

Isolated Cortical Signal Increase on MR Imaging as a Frequent Lesion Pattern in Sporadic Creutzfeldt-Jakob Disease
AJNR 29:1519-1524, Meissner,B.,et al., 2008

Cardiac Involvement in Patients With Limb-Girdle Muscular Dystrophy Type 2 and Becker Muscular Dystrophy
Arch Neurol 65:1196-1201, Sveen,M.-L.,et al., 2008

Monoclonal Antibody Therapies and Neurologic Disorders
Arch Neurol 65:1162-1165, Novack,J.C.,et al., 2008

Voltage-Gated Potassium Channel Autoimmunity Mimicking Creutzfeldt-Jakob Disease
Arch Neurol 65:1341-1346, Geschwind,M.D.,et al, 2008

Genetics of Familial Amyotrophic Lateral Sclerosis
Neurol 70:144-152, Valdmanis,P.N. &Rouleau,G.A., 2008

A 23-Year-Old Man With Seizures and Visual Deficit
Neurol 70:73-78, Boustany,R.-M.,et al, 2008

Primary Lateral Sclerosis With HIV-1 Infection
Neurol 70:575-577, Verma,A. &Berger,J.R., 2008

Diagnosis and Management of Motor Neurone Disease
BMJ 336:658-662, McDermott,C.J. &Shaw,P.J., 2008

Complete Ophthalmoplegia: An Unusual Sign of Bilateral Paramedian Midbrain-Thalamic Infarction
Stroke 39:1355-1357, Thurtell,M.J. &Halmagyi,M., 2008

Progressive Supranuclear Palsy: A Current Review
The Neurologist 14:79-88, Lubarsky,M. &Juncos,J.L., 2008

Woke Up Paralysed--Without Injury or Stroke
Lancet 371:870, Bawaskar,H.S. &Bawaskar,P.H., 2008

A Parkinsonian Syndrome in Methcathinone Users and the Role of Manganese
NEJM 358:1009-1017, Stepens,A.,et al, 2008

Acute Intermittent Porphyria Presenting as Acute Pancreatitis and Posterior Reversible Encephalopathy Syndrome
Acta Neurol Taiwan 17:177-183, Shen, F.,et al, 2008

Primary Central Nervous System Vasculitis with Prominent Leptomeningeal Enhancement
Arthritis Rheum:58:595-603, Salvarani, C.,et al, 2008

Clinical and Radiological Characteristics of Methotrexate-Induced Acute Encephalopathy in Pediatric Patients with Cancer
Ann Oncol 19:178-184, Inaba, H.,et al, 2008

Spectrum of Neurological Syndromes Associated with Glutamic Acid Decarboxylase Antibodes: Diagnostic Clues for this Association
Brain 131:2553-2563, Saiz,A., et al, 2008

Isolated Lymphoma of the Anterior Visual Pathway Diagnosed by Optic Nerve Biopsy
J Neuro-Ophthalmol 28:36-40, Zelefsky, J.R.,et al, 2008

Pontine Warning Syndrome
Arch Neurol 65:1375-1377, Saposnik, G.,et al, 2008

Paraneoplastic Vasculitis of Central Nervous System Presenting as Recurrent Cryptogenic Stroke
Int J Clin Oncol 12:155-159, Taccone,F.S.,et al, 2007

Misdiagnosis of stroke
Expert Rev Neurother 7:989-1001, Nor, A.M.,et al, 2007

Leukoencephalopathy during administration of etanercept for refractory rheumatoid arthritis
Mod Rheumatol 17-72-74, Yamamoto, M.,et al, 2007

Age and High-Dose Methotrexate are Associated to Clinical Acute Encephalopathy in FRALLE 93 Trial for Acute Lymphoblastic Leukemia in Children
Leukemia 21:238-247, Dufourg, M.N.,et al, 2007

Rapidly Fatal Acanthamoeba Encephalitis and Treatment of Cryoglobulinemia
Emerg Infect Dis 13:469-471, Meersseman, W.,et al, 2007

Progressive Multifocal Leukoencephalopathy After Rituximab in a Case of Non-Hodgkin Lymphoma
Neurol 69:704-706, Kranick,S.M.,et al, 2007

Gene Therapy for Duchenne Muscular Dystrophy: Expectations and Challenges
Arch Neurol 64:1236-1241, Rodino-Klapac,L.R.,et al, 2007

Cerebral Cortical and White Matter Lesions in Amyotrophic Lateral Sclerosis With Dementia; Correlation With MR and Pathologic Examinations
AJNR 28:1505-1510, Matsusue,E.,et al, 2007

Lead Poisoning From the Beauty Case: Neurologic Manifestations in an Elderly Woman
Neurol 69:929-930, Fluri,F.,et al, 2007

Clinicopath conf., Human Prion Disease, Sporadic CJD
Neurol 69:1881-1887, Geschwind,M.D., et al, 2007

Acute Fulminant Demyelinating Disease: A Descriptive Study of 60 Patients
Arch Neurol 64:1426-1432, de Seze,J.,et al, 2007

How Effective Are Disease-Modifying Drugs in Delaying Progression in Relapsing-Onset MS?
Neurol 69:1498-1507, Brown,M.G.,et al, 2007

Primary Central Nervous System Vasculitis: Analysis of 101 Patients
Ann Neurol 62:442-451,430, Salvarani,C.,et al, 2007

Central Nervous System Infections in Heart Transplant Recipients
Arch Neurol 64:1715-1720, van de Beek,D.,et al, 2007

Reactivation of JC Virus and Development of PML in Patients With Multiple Sclerosis
Neurol 68:985-990, Khalili,K.,et al, 2007

Congenital Muscular Dystrophy
eMedicine (Jan), Lopate,G., 2007

A 34-Year-Old Man With Progressive Behavioral and Language Disturbance
Neurol 68:68-74, Miller,B.L.,et al, 2007

Fulminant Idiopathic Intracranial Hypertension
Neurol 68:229-232, Thambisetty,M.,et al, 2007

Bilateral Ocular Paralysis: Analysis of 31 Inpatients
Arch Neurol 64:178-180, Keane,J.R., 2007



Showing articles 750 to 800 of 2320 << Previous Next >>