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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
ammonia
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 cortex
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
cingulate gyrus
Clinical Pathologic Conference(C.P.C.)
cognition
coinfection
collagen vascular disease
coma
coma, sudden onset
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, acute
encephalopathy, metabolic
encephalopathy, progressive
executive dysfunction
exercise intolerance
exome sequencing
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
HHH syndrome
highly active antiretroviral therapy
homosexual
human immunodeficiency virus type 1
hyperammonemic encephalopathy
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
insular cortex
insular cortex, lesion
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, diffusion weighted
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
ornithine transcarbamylase deficiency
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
temporal lobe, lesion, bilateral
temporalis muscle wasting
thrombocytopenia
tinnitus
transient neurologic deficit
treatment of neurologic disorder
tremor
upgaze, paralysis of
urea-cycle enzymopathies
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 1650 to 1700 of 2439 << Previous Next >>

Prevalence and Incidence of Becker Muscular Dystrophy
Lancet 337:1022-1024, Bushby,K.M.D.,et al, 1991

The Frequency of Patients with Dystrophic Abnormalities in a Limb-Girdle Patient Population
Neurol 41:1491-1496, Arikawa,E.,et al, 1991

Autosomal Recessive Distal Dystrophy
Neurol 41:1365-1370, Barohn,R.J.,et al, 1991

Pyomyositis Presenting as Rapidly Progressive Generalized Weakness
Neurol 41:944-945, Felice,K.,et al, 1991

Parental Sex Effect in Familial Amyotrophic Lateral Sclerosis
Neurol 41:1292-1294, Leone,M., 1991

Linkage of a Gene Causing Familial ALS to Chromosome 21 & Evidence of Genetic-Locus Heterogeneity
NEJM 324:1381-1384, 1430-14321991., Siddique,T.,et al, 1991

Dysphagia in Patients with the Post-Polio Syndrome
NEJM 324:1162-1167, 1206-12071991., Sonies,B.C.&Dalakas,M.C., 1991

Clinical and Electrodignostic Features of X-Linked Recessive Bulbospinal Neuronopathy
Neurol 41:823-828, Olney,R.K.,et al, 1991

Hyperintensity in the Globus Pallidus on T1-Weighted & Inversion-Recovery MRI:A Possible Marker of Advanced Liver Dise
Neurol 41:1526-1527, Pujol,A.,et al, 1991

Portal-Systemic Encephalopathy:Presence of Basal Galglia Lesions with High Signal Intensity on MR Images
Radiology 179:551-555, Inoue,E.,et al, 1991

Myotonic Heart Disease:A Clinical Follow-Up
Neurol 41:259-262, Hawley,R.J.,et al, 1991

The Effect of Spine Fusion on Respiratory Function in Duchenne Muscular Dystrophy
Neurol 41:38-40, Miller,R.G.,et al, 1991

Proximal Posterior Cerebral Artery Occlusion Simulating Middle Cerebral Artery Occlusion
Neurol 41:385-390, Chambers,B.R.,et al, 1991

Plasma Exchange in Chronic Progressive Multiple Sclerosis:A Long-Term Study
Neurol 41:409-414, Khatri,B.O.,et al, 1991

Scleroderma and Central Nervous System Vasculitis
Stroke 22:410-413, Pathak,R.&Gabor,A.J., 1991

Is JC Virus Latent in Brain?
Ann Neurol 29:433-434, Lipton,H.L., 1991

Radiation Injury of the Brain
AJNR 12:45-62, Valk,P.E. & Dillon,W.P., 1991

Kearns-Sayre Syndrome Presenting as Renal Tubular Acidosis
Neurol 40:1761-1763, Eviatar,L.,et al, 1990

Graves Orbitopathy:Correlation of CT and Clinical Findings
Radiology 177:675-682, Nugent,R.A.,et al, 1990

Antemortem Diagnosis of Diffuse Lewy Body Disease
Neurol 40:1523-1528, Crystal,H.A.,et al, 1990

Progressive Myoclonic Ataxia (The Ramsay Hunt Syndrome)
Arch Neurol 47:1121-1125, Marsden,C.D.,et al, 1990

Direct Diagnosis of Carriers of Duchenne & Becker Muscular Dystrophy by Amplification of Lymphocyte RNA
Roberts. R. G. , et al, Lancet 336:1523-1526., , 1990

Clinical Features and Associations of 560 Cases of Motor Neuron Disease
JNNP 53:1043-1045, Li,T.,et al, 1990

Selective Involvement of the Pyramidal Tract on Magnetic Resonance Imaging in Primary Lateral Sclerosis
Neurol 40:1799-1800, Marti-Fabregas,J.&Pujol,J., 1990

X-Linked Spinal Muscular Atrophy (Kennedy's Syndrome) A Kindred with Hypobetalipoproteinemia
Arch Neurol 47:1117-1120, Warner,C.L.,et al, 1990

Phenotypic Heterogeneity of Spinal Muscular Atrophy Mapping to Chromosome 5q11. 2-12. 3 (SMA5q)
Neurol 40:1831-1836, Munsat,T.L.,et al, 1990

What Causes Motoneuron Disease?
Editorial, Lancet 336:1033-10351990., , 1990

Misdiagnosis in Patients with Amyotrophic Lateral Sclerosis
Arch Int Med 150:2301-2305, Belsh,J.M.&Schiffman,P.L., 1990

Clinicopath Conf
Hodgkin's Disease and Guillain Barre Syndrome, Case Record 39-1990, NEJM 323:895-908990., , 1990

Neurological Sequelae of Cerebral Malaria in Children
Lancet 336:1039-1043, Brewster,D.R.,et al, 1990

Quadriceps Myopathy:Forme Fruste of Becker Muscular Dystrophy
Ann Neurol 28:634-639, Sunohara,N.,et al, 1990

Dystrophin Analysis in Duchenne & Becker Muscular Dystrophy Carriers:Correl with Intracellular Calcium & Albumin
Ann Neurol 28:674-679, Morandi,L.,et al, 1990

Anti-GM1 IgM Antibodies in Motor Neuron Disease and Neuropathy
Neurol 40:1747-1750, Nobile-Orazio,E.,et al, 1990

Non Alzheimer's Disease Forms of Cerebral Atrophy
Editorial, JNNP 53:929-9311990., Neary,D., 1990

Incomplete Unilateral Ophthalmoplegia as the Presenting Manifestation of Waldenstrom's Macroglobulinemia
Neurol 40:1801-1802, Lossos,A.,et al, 1990

Clinicopath Conf
Acute Multiple Sclerosis, Case Record 42-1990, NEJM 323:1123-1135990., , 1990

Fulminant Monophasic Multiple Sclerosis, Marburg's Type
JNNP 53:918-921, Johnson,M.D.,et al, 1990

Hemiplegia in Posterior Cerebral Artery Occlusion
Neurol 40:1496-1499, Hommel,M.,et al, 1990

The Large Striatocapsular Infarct, A Clinical and Pathophysiological Entity
Arch Neurol 47:1085-1091, Weiller,C.,et al, 1990

Perineural Spread of Cutaneous Head and Neck Cancer
Arch Neurol 47:73-77, Clouston,P.D.,et al, 1990

Follow-up MR STudies in Hallervorden-Spatz Disease
J Comput Assist Tomogr 14:118-120, Gallucci,M.,et al, 1990

Patterns of Disease Activity in Multiple Sclerosis:Clinical and Magnetic Resonance Imaging Study
BMJ 300:631-634, Thompson,A.J.,et al, 1990

Scleroderma, fasciitis, and Eosinophilia Associated with the Ingestion of Tryptophan
NEJM 322:874-881, 9261990., Silver,R.M.,et al, 1990

Mitochondrial Myopathy with a Defect of Mitochondrial-Protein Transport
NEJM 323:37-42, Schapira,A.H.V.,et al, 1990

Location of Facioscapulohumeral Muscular Dystrophy Gene on Chromosome 4
Lancet 336:651-653, Wijmenga,C.,et al, 1990

Mapping of Acute (Type 1) Spinal Muscular Atrophy to Chromosome 5q12-q14
Lancet 336:271-273, Melki,J.,et al, 1990

Spinal Muscular Atrophies
Editorial, Lancet 336:280-2811990., , 1990

Paraneoplastic Motor Neuron Disease and Renal Cell Carcinoma:Improvement after Nephrectomy
Neurol 40:960-962, Evans,B.K.,et al, 1990

Lower Motor Neuron Disease in a Patient with Autoantibodies Against Gangliosides GM1 and GD1b:Improvement with Immunotherapy
Neurol 40:842-844, Shy,M.E.,et al, 1990

Polyclonal IgM Anti-GM1 Ganglioside Antibody in Patients with Motor Neuron Disease and Variants
Ann Neurol 27:558-563, Salazar-Grueso,E.F.,et al, 1990



Showing articles 1650 to 1700 of 2439 << Previous Next >>