Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
abulia
acute disseminated encephalomyelitis
adverse drug reaction
affect, flat
affect, inappropriate
aggression
agitation
agnosia
akinetic mute
alternating hemiplegia
alternating hemiplegia of childhood
Alzheimer's disease
Alzheimer's disease, familial
amimia
aminoacidurias
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, differential diagnosis
ANA
anemia
anemia, hemolytic
aneurysm, intracranial
aneurysm, intracranial, acute deterioration
aneurysm, intracranial, delayed cerebral ischemia with
aneurysm, intracranial, natural history
anomic aphasia
anterior cerebral artery
anterior cerebral artery territory infarction
anterior cerebral artery, emboli to
anterior cerebral artery, occlusion of
anterior cerebral artery, occlusion, language disorder with
anterior choroidal artery
aphasia
aphasia, cerebellar
aphasia, conduction
aphasia, global
aphasia, global-without hemiparesis
aphasia, metabolic disorder causing
aphasia, progressive
aphasia, progressive, primary
aphasia, transcortical
aphemia
aphonia
apraxia
apraxia of eyelid closure
arthralgia
arthritis
astrocytoma
ataxia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic gait
ATP1A3 gene
autism
Babinski sign
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavior, combative
behavioral disorder
benzodiazepine
blepharospasm
brain atrophy
brain biopsy
brainstem, lesion of
Broca's aphasia
Broca's aphasia, without hemiparesis
calculations
carbon monoxide poisoning
carotid artery disease
carotid artery occlusion, bilateral
carotid artery occlusion, neck
carphology
CAT scan
CAT scan, abnormal
CAT scan, cerebrovascular disease
CAT scan, emission
CAT scan, emission, abnormal
catatonia
caudate nucleus
caudate nucleus, infarction
caudate nucleus, lesion of, bilateral
celiac disease, adult
central nervous system, infection of
cerebellar atrophy, secondary
cerebellar edema
cerebellar infarction
cerebellar lesion
cerebellar mutism
cerebellitis
cerebellum, disease of
cerebellum, neoplasms of
cerebral cortex
cerebral cortical atrophy
cerebral dominance
cerebral embolism
cerebral infarction
cerebral palsy
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, bilateral
cerebrovascular accident, etiology
chemotherapy, CNS treatment and complications with
children
choreoathetosis
chromosomal abnormality
chromosome 17
cirrhosis
cirrhosis, causes of childhood
climate change
Clinical Pathologic Conference(C.P.C.)
complications
comprehension, impaired
confusion
confusional state, acute
controversies in neurology
coronavirus
corpus callosum, lesion of
cortical-basal ganglionic degeneration
COVID-19
crying, pathologic
cyanosis
cyclosporine
deafmute
deafness
degenerative diseases of CNS
dementia
dementia, familial
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, transmissible
demyelinating disease
depression
developmental milestones
developmental milestones, loss of
developmental retardation
dialysis
dialysis dementia
diarrhea
diaschisis
differential diagnosis
disability, neurological
disorientation
drooling
drug induced neurologic disorders
dysarthria
dyskinesia
dysmorphic
dysnomia
dysphagia
dysphonia
dystonia
dystonia, face
dystonia, focal
dystonia, treatment of
ecchymoses
echolalia
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
emotional lability
encephalitis
encephalitis, acute
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, paraneoplastic
encephalitis, Powassan
encephalitis, viral
encephalopathy
encephalopathy, delayed
encephalopathy, parainfectious
encephalopathy, post anoxic
encephalopathy, progressive
executive dysfunction
exome sequencing
extralimbic encephalitis
eye closure
eye movement, disorders of
facial rigidity
facial weakness
facial weakness, bilateral
falling
familial
fasciculation
fatigue
fever
flavivirus
fourth ventricle, compression
frontal lobe, atrophy
frontal lobe, pathologic signs of
gag reflex, depressed
gait disorder
gastroenteritis
gaze palsy
gaze palsy, horizontal
gaze palsy, vertical
gene mutation
genetic neurologic disorders
genetic testing
globus pallidus
globus pallidus, lesion of
grasp reflex
hallucination
haloperidol
hand weakness
hands, fisted
handwriting
head injury
headache
hearing loss
hemidystonia
hemiparesis
hemiparesis, transient
hemorrhage, thalamic
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
herpes simplex encephalitis
hoarseness
hydrocephalus
hypercalcemia
hyperparathyroidism
hyperreflexia
hypersomnia
hypertension
hypothyroidism
hypothyroidism, congenital
imbalance, postural
immunosuppression
immunosuppressive agents
in situ hybridization
inborn errors of metabolism
incontinence, fecal
insect sting
insomnia
intellectual deterioration
internal capsule
intestinal biopsy
intestinal pseudoobstruction
intracerebral hemorrhage
intrathecal chemotherapy
intrauterine
intraventricular hemorrhage
iodine deficiency
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
jaw jerk, abnormal
Kayser-Fleischer ring
Kluver-Bucy syndrome
lactic acidemia
language disorder in adults
laughing, pathologic
Leigh's disease
lenticular nucleus, lesion of, bilateral
leukemia
leukemia, neurologic findings assoc.with
level of consciousness, decreased
limbic encephalitis
liver transplantation
lobar atrophy
locked-in syndrome
logopenia
lorazepam
magnetic stimulation
magnetic stimulation, brain
malabsorption syndrome
marche a petits pas
masked facies
medulloblastoma
memory, impairment of
meningeal enhancement
meningismus
meningoencephalitis
mental retardation
mental status, abnormal
MERS
methotrexate
microaneurysm, retinal
microcephaly
micrographia
middle cerebellar peduncle, lesion
middle cerebral artery territory infarction
middle cerebral artery territory infarction, without hemiparesis
migraine
migraine, hemiplegic
miosis
misdiagnosis
monoclonal antibodies
motor cortex
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, negative
MRI, serial
multiple sclerosis
multiple sclerosis, differential diagnosis of
muscle atrophy, progressive
muscle biopsy
muscle weakness
muscle weakness, proximal
mutism
myasthenia gravis
myasthenia gravis, paraneoplastic
myelopathy, chronic progressive
myoclonic jerks
myoclonus
myoclonus, epilepsy
myoclonus, stimulus sensitive
myxedema, neurologic manifestations of
nausea and vomiting
neck stiffness
neoplasm, posterior fossa
neoplasm, primary of CNS
neoplasm, primary of CNS-children
neuroendocrinology
neuroleptic
neuroleptic induced catatonia
neuroleptic malignant syndrome
neurologic complications
neurologic complications of, surgery
neurologic disease, diagnoses of
neuropathology
neuropathology, brain
neurotoxic
New England
NMDA antagonists
non-dominant hemisphere
nonverbal
nystagmus
nystagmus, rotary
ocular motility, disorders of
operculum syndrome
operculum syndrome, bilateral
opisthotonus
optic atrophy
organ transplantation
osteomalacia
palatal myoclonus
palate, paralysis
palilalia
pancytopenia
paranoia
paraparesis
paraparesis, spastic
paraphasias
paraplegia, in flexion
parathyroid adenoma
Parkinson disease
Parkinson disease, freezing phenomena in
Parkinson disease, L-dopa nonresponsive
Parkinsonism syndrome
paroxysmal neurologic deficits
pathologic reflex
penicillamine
perseveration
personality change
Pick bodies
Pick's disease
pleocytosis of cerebrospinal fluid
pneumonia
polymerase chain reaction
pons, lesion of
postural abnormality
precipitating factors
pretectal syndrome
prevention of neurologic disorders
primary lateral sclerosis
prion disease
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
protein 14-3-3, cerebrospinal fluid
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
psychosis, childhood
pull test
pupil, abnormality in neurologic disorders
pupil, light reflex, abnormal
pyramidal tract
pyramidal tract dysfunction
pyruvate metabolism, abnormality of
quadriparesis
quadriplegia
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
rash
rash, malar
release phenomena
remote effect of cancer on the nervous system
renal stones
repetition, impaired
reversible splenial lesion syndrome
review article
rigidity
risk factors
rituximab
rodents
rotavirus
saccadic eye movements, abnormal
salivation, excessive
schizophrenia
season
seizure
seizure, children
seizure, focal
semantic dementia
serologic testing
single photon emission computed tomography
slit lamp examination
somnolence
spasticity
speech arrest
speech disorder
speech disorder, childhood
speech disorder, non aphasic
speech, loss of
splenium of corpus callosum
splenomegaly
spongy degeneration of brain
stare
startle myoclonus
startle reaction
status epilepticus
stereotyped behavior
steroid therapy, CNS treatment and complications with
striatonigral degeneration
striatonigral degeneration, infantile
subarachnoid hemorrhage
subdural hematoma
substantia nigra
suicide
swallow evaluation
systemic lupus erythematosus
systemic lupus erythematosus, neurologic complications with
tachycardia
tandem gait, ataxic
tauopathy
temporal lobe, atrophy
temporal lobe, lesion
temporal lobe, status
thrombocytopenia
thymoma
thyrotoxicosis
tick bite
tick-borne encephalitis
titubation
tongue, enlarged
tongue, fasciculations of
tongue, impaired movements of
tongue, weakness
toothache
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, intention
tremulousness
upgaze, paralysis of
uric acid, low
urinary incontinence
vaccination, neurologic complications with
vaccine
valium
viral infection
viral infection, CNS
visual impairment
walking, difficulty with
weakness
weakness, generalized
weight loss
Wernicke's aphasia
wheelchair
white matter disease
wide based gait
word-finding difficulty
writing
Showing articles 0 to 50 of 822 Next >>

COVID-19-Booster Vaccine-Induced Encephalitis
Acta Neurol Belg 122:579-581, Sluyts,Y.,et al, 2022

Pediatric Parainfectious Encephalitis Associated with COVID-19
Neurol 96:541-544, Gaughan, M.,et al, 2021

A 71-Year-Old Man with Horizontal Gaze Palsy, Anarthria, and Quadriparesis
Neurol 96:1146-1150, Cheema, I.,et al, 2021

Clinicopathologic Conference, Powassan Virus Encephalitis
NEJM 380:380-387, Case 3-2019, 2019

An unusual neuropsychiatric manifestation of systemic lupus erythematosus
Neurol 90:e1929-e1932, Dongkyung, D.,et al, 2018

Cerebellar Ataxia and Hearing Impairment
JAMA Neurol 74:243-244, Lin, C.Y. & Kuo, S.H., 2017

Precipitous Deterioration of Motor Function, Cognition, and Behavior
JAMA Neurol 74:591-596, Fernandez-Fournier, M.,et al, 2017

A 55-year-old Man with Rapidly Progressive Dementia and Parkinsonism
Neurol 89:e182-e187, Tabuas-Pereira, M.,et al, 2017

A Young Man with Progressive Language Difficulty and Early-Onset Dementia
JAMA Neurol 73:595-599, Botha, H.,et al, 2016

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Creutzfeldt-Jakob Disease (Subacute Spongiform Encephalopathy)
Adams & Victors Principles of Neurology, Chp 33, pg 769, Ropper, A.H.,et al, 2014

The Acquired Metabolic Disorders of the Nervous System, Cretinism and Neonatal Myxedema
Adams & Victors Principles of Neurology Chp 40, pg 1156, Ropper, A.H.,et al, 2014

Gait Freezing and Speech Disturbance in Parkinsons Disease
Neurol Sci 35:357-363, Park,H.K.,et al, 2014

Heterozygous de-Novo Mutations in ATP1A3 in Patients with Alternating Hemiplegia of Childhood:A Whole-Exome Sequencing Gene-Identification Study
Lancet Neurol 11:764-773, Rosewich,H.,et al, 2012

Late onset autism and anti-NMDA-receptor encephalitis
Lancet 378:98;378, Creten, C.,et al, 2011

Clinicopath Conf, Rapid-Onset-Dystonia-Parkinsonism Due to a Mutation in the ATP1A3 Gene
NEJM 362:2213-2219, Case 17-2010, 2010

Clinical and Radiological Features of Rotavirus Cerebellitis
AJNR 31:1591-1595, Takanashi,J.,et al, 2010

Multifocal Paraneoplastic Cortical Encephalitis Associated With Myasthenia Gravis and Thymoma
Arch Neurol 66:1407-1409, Hammoud,K.,et al, 2009

The Logopenic/Phonological Variant of Primary Progressive Aphasia
Neurol 71:1227-1234, Gorno-Tempini,M.L.,et al, 2008

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

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

Bilteral Caudate Infarct--A Case Report
Ann Acad Med Singapore 28:569-571, Lim,J.K.H., 1999

Hereditary Frontotemporal Dementia is Linked to Chromosome 17q21-q22:Genetic & Clinicopath Study of 3 Dutch Families
Ann Neurol 41:150-159, Heutnik,P.,et al, 1997

Anterior Opercular Syndrome, Caused by Herpes Simplex Encephalitis
Neurol 49:494-497, McGrath,M.N.,et al, 1997

Frontotemporal Dementia, Pick Disease, and Corticobasal Degeneration
Arch Neurol 54:1427-1429, Kertesz,A., 1997

Cyclosporine-Associated Mutism in Liver Transplant Patients
Neurol 46:252-254, Valldeoriola,F.,et al, 1996

Clinical, Neuroimaging, and Pathologic Features of Progressive Nonfluent Aphasia
Ann Neurol 39:166-173, Turner,R.S.,et al, 1996

Clinicopath Conf
Demyelinating Disease, Case 8-1996, NEJM 334:715-720996., , 1996

Cerebellar Induced Aphasia: Case Report of Cerebellar Induced Prefrontal Aphasic Language Phenomena Supported by SPECT Findings
J Neurol Sciences 144:34-43, Mari�n,P.,et al, 1996

Clinicopath Conf
Progressive Multifocal Leukoencephalopathy & Systemic Lupus Erythematosus, Case 20-1995, NEJM 332:17, 3-17995., 1995

The Syndrome of'Cerebellar'Mutism and Subsequent Dysarthria
Neurol 44:2040-2046, vanDongen,H.R.,et al, 1994

Acute Pseudobulbar Mutism with Good Functional Recovery
Neurol 44:176-177, Chesser,M.Z.,et al, 1994

The Cerebellum Contributes to Linguistic Production: A Case of Agrammatic Speech Following a Right Cerebellar Lesion
Neurol 44:2047-2050, Silveri,M.C.,et al, 1994

Rapidly Progressive Aphasic Dementia and Motor Neuron Disease
Ann Neurol 33:200-207, Caselli,R.J.,et al, 1993

Magnetic Resonance Imaging of Brain and the Neuromotor Disorder in Endemic Cretinism
Ann Neurol 34:91-94, Ma,T.,et al, 1993

Neuroleptic-Induced Catatonia as a Stage in the Progression Toward NMS
J Am Acad Child Adolesc Psychiatry 31:1161-1164, Woodbury,M.M.&Woodbury,M.A., 1992

Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992

Primary Lateral Sclerosis, Clin Features, Neuropath & Dx Criteria
Brain 115:495-520, Pringle,C.E.,et al, 1992

Progressive Language Disorder Due to Lobar Atrophy
Ann Neurol 31:174-183, Snowden,J.S.,et al, 1992

Induction of Speech Arrest and Counting Errors with Rapid-Rate Transcranial Magnetic Stimulation
Neurol 41:697-702, Pascual-Leone,A.,et al, 1991

Dysphagia, Speech Disorders and Centrotemporal Spikes-Waves
Arch Francaises De Pediatrie 47:115-117, Boulloche,J.,et al, 1990

Anterior Cerebral Artery Territory Infarction in the Lausanne Stroke Registry
Arch Neurol 47:144-150, Bogousslavsky,J.&Regli,F., 1990

Multiple Forms of Epileptic Attacks Secondary to a Small Chronic Subdural Haematoma
BMJ 299:439-441, Jones,S.C.,et al, 1989

Anterior Operculum Syndrome
Neurol 39:1169-1172, Mao,C.C.,et al, 1989

Primary Lateral Sclerosis, A Clinical Diagnosis Reemerges
Arch Neurol 45:1304-1307, Younger,D.S.,et al, 1988

Familial Alzheimer's Disease with Myoclonus and'Spongy Change'
Arch Neurol 45:1097-1100, Duffy,P.,et al, 1988

Chronic Progressive Spinobulbar Spasticity, A Rare Form of Primary Lateral Sclerosis
Arch Neurol 45:509-513, Gastaut,J.L.,et al, 1988

Clinicopath. Conference
Pick's Disease of Brain, with Frontal Lobar Atrophy, Degen of Basal Ganglia, Case 16-1986, NEJM 314:, 101-,1986., 1986

Delayed Cerebral Ischemia after Aneurysmal Subarachnoid Hemorrhage:Clinicoanatomic Correlations
Neurol 36:329-333, Hijdra,A.,et al, 1986

Muteness of Cerebellar Origin
Arch Neurol 42:697-698, Rekate,H.L.,et al, 1985



Showing articles 0 to 50 of 822 Next >>