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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 650 to 700 of 2320 << Previous Next >>

Rhombencephalitis A Series of 97 Patients
Medicine 90:256-261, Moragas, M.,et al, 2011

A Dramatic Case of Intraventricular Cysticercosis
Arch Neurol 6:828-829, Cardenas, G.,et al, 2011

Rituximab-Associated Progressive Multifocal Leukoencephalopathy in Rheumatoid Arthritis
Arch Neurol 68:1156-1164, Clifford, D.B.,et al, 2011

Immune Reconstitution Inflammatory Syndrome in Natalizumab-Associated PML
Neurol 77:1061-1067,1033, Tan, I.L.,et al, 2011

Rapidly Progressive Alzheimer Disease
Arch Neurol 68:1124-1130, Schmidt, C.,et al, 2011

Treatable Neurological Disorders Misdiagnosed as Creutzfeldt-Jakob Disease
Ann Neurol 70:437-444, Chitravas, N.,et al, 2011

Clinical Reasoning: A 34-year-old man with recurrent limb weakness
Neurol 77:e68-e72, Karam, C.,et al, 2011

A Rare Cause of Gait Ataxia
Lancet 378:1274, Rous, C.,et al, 2011

Treatment of Severe Neurological Deficits with IgG Depletion through Immunoadsorption in Patients with Escherichia coli O104:H4-Associated Haemolytic Uraemic Syndrome: A Prospective Trial
Lancet 378:1166-1173,1120, Greinacher, A.,et al, 2011

Clinicopathologic Conference, Limbic Encephaitis with Antibodies to Leucine - Rich Glioma - inactivated 1 (LGI 1).
NEJM 365:1825-1833, Case 34-2011, 2011

The Evaluation of Rapidly Progressive Dementia
The Neurologist 17:67-74, Rosenbloom,M.H. &Atri,A., 2011

Muscle Histology vs MRI in Duchenne Muscular Dystrophy
Neurol 76:346-353, Kinali,M.,et al, 2011

Evidence-Based Guideline Update: Plasmapheresis in Neurologic Disorders: Report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology
Neurol 76:294-300, Cortese,I.,et al, 2011

Clinical outcomes of natalizumab-associated progressive multifocal leukoencephalopathy
Neurol 76:1697-1704, Vermersch,P.,et al, 2011

Diffusion-weighted MRI hyperintensity patterns differentiate CJD from other rapid dementias
Neurol 76:1711-1719, Vitali, P.,et al, 2011

Myoglobinuria and Muscle Pain are Common in Patients With Limb-Girdle Muscular Dystrophy 21
Neurol 76:194-195, Mathews,K.D.,et al, 2011

LMNA Cardiomyopathy:Cell Biology and Genetics Meet Clinical Medicine
Disease Models & Mechanisms 4:562-568, Lu,J.T., et al, 2011

Clinicopathologic Conference, Cystoisospora Belli Enteritis and HIV Infection
NEJM 365:2306-2316, Case 38-2011, 2011

Functional Weakness: Clues to Mechanism from the Nature of Onset
JNNP 83:67-69, Stone, J.,et al, 2011

Frontal Headache
JAMA 306:317-318, Chang,H.J.,et al, 2011

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

Progressive Multifocal Leukoencephalopathy: Prognosis and treatment
UpToDate, June, Koralnik, I.J.,et al, 2011

Spinal Muscular Atrophy A Timely Review
Arch Neurol 68:979-984, Kolb, S.J.,et al, 2011

Progressive Encephalomyelitis with Rigidity and Myoclonus Gycine and NMDA Receptor Antibodies
Neurol 77:439-443,414, Turner, M.R.,et al, 2011

Progressive Multifocal Leukoencephalopathy in a Patient without Immunodeficiency
Neurol 77:297-299, Tan, I.L.,et al, 2011

Management and Outcome of CSF-JC Virus PCR-negative PML in a Natalizumab-treated Patient with MS
Neurol 77:2010-2016, Kuhle, J.,et al, 2011

Cancer Risk Among Patients with Myotonic Muscular Dystrophy
JAMA 306:2480-2486, Gadalla, S.M.,et al, 2011

Demographic and Clinical Characteristics of Malignant Multiple Sclerosis
Neurol 76:1996-2001, Gholipour, T.,et al, 2011

Autoimmune Encephalopathy
Semin Neurol 31:144-157, Flanagan, E.,et al, 2011

Cortical Restricted Diffusion as the Predominant MRI Finding in Sporadic Creutzfeldt-Jakob Disease
Acta Radiologica 52:336-339, Talbott,S.D.,et al, 2011

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

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

Compressive Myelopathy Mimicking Transverse Myelitis
Neurologist 16:120-122, Kelley, B.,et al, 2010

Tumefactive Multiple Sclerosis
www.medlink.com, JUne, Bunyan, R.F. and Lucchinetti, C.F., 2010

Successful Management of Natalizumab-Associated Progressive Multifocal Leukoencephalopathy and Immune Reconstitution Syndrome in a Patient With Multiple Sclerosis
Arch Neurol 67:1391-1394, Schr�der,A.,et al, 2010

Huntingtons Disease
BMJ 341:34-40, Novak,M.J. &Tabrizi,S.J., 2010

Clinicopath Conf., Progressive Multifocal Leukoencephalopathy
NEJM 362:1431-1437, Case 11-2010, 2010

Sudden Sensorineural Hearing Loss
The Lancet 375:1203-1211, Schreiber,B.E., et al, 2010

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

Natalizumab and Progressive Multifocal Leukoencephalopathy: What are the Causal Factors and Can It be Avoided?
Arch Neurol 67:923-930, Warnke,C., et al, 2010

Redefining Dysferlinopathy Phenotypes Based on Clinical Findings and Muscle Imaging Studies
Neurol 75:316-323,298, Paradas,C., 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

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

Clinicopath Conf, Infantile Krabbe Disease
NEJM 362:346-356, Case 3-2010, 2010

MRI in Methylmalonic Acidemia
Neurol 74:e14, Bindu, P.S.,et al, 2010

Diffusely Abnormal White Matter in Progressive Multiple Sclerosis: In Vivo Quantitative MR Imaging Characterization and Comparison between Disease Types
AJNR 31:541-548, 390, Vrenken,H.,et al, 2010

Clinicopath Conf, The POEMS Syndrome, with Demyelinating Neuropathy and Solitary Pharmacytoma of Bone
NEJM 362:929-940, Case 7-2010, 2010

Assessment: Symptomatic Treatment for Muscle Cramps (an Evidence-Based Review): Report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology
Neurol 74:691-696, Katzberg,H.D.,et al, 2010

Increased Tissue Damage and Lesion Volumes in African Americans with Multiple Sclerosis
Neurol 74:538-544,532, Weinstock-Guttman,B.,et al, 2010

The Spectrum of Mutations in Progranulin: A Collaborative Study Screening 545 Cases of Neurodegeneration
Arch Neurol 67:161-170,145, Yu,C.-E.,et al, 2010



Showing articles 650 to 700 of 2320 << Previous Next >>