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abdominal distention
abdominal x-ray
adverse drug reaction
affect, flat
agitation
akathisia
alcohol intolerance
alien hand syndrome
altered states of consciousness
alternating rapid movement
aluminum
AMPA receptor antibodies
anemia
angiokeratoma
anorexia
anti IgLON5
anti Ri antibody
antibiotics
antibiotics, neurologic complications with
antibodies to measles
anticonvulsants
anticonvulsants, effectiveness
anticonvulsants, selection of
antidepressant
antioxidant
antithyroid antibodies
aphasia
apnea
apraxia
arm swing, reduced
arm weakness
arthralgia
arthritis
Asia
asterixis
asymptomatic
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, truncal
ataxia, truncal, associated with ocular oscillations
ataxic gait
athetosis
autoantibodies
autoimmune disease
autonomic dysfunction
axonal spheroid
Babinski sign
bacterial infection
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
bismuth
blindness
boomerang sign
bovine spongiform encephalopathy
bradykinesia
brain atrophy
brain biopsy
brainstem, atrophy
brainstem, lesion of
bruxism
bulbar palsy
CAG repeats
carbon monoxide poisoning
carcinoma
carcinoma of breast
carcinoma of lung
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataracts
celiac disease, adult
central nervous system, infection of
cephalosporins
cerebellar ataxia, children
cerebellar atrophy, primary
cerebellar degeneration
cerebellar lesion
cerebellum
cerebellum, disease of
cerebral cortex
cerebral cortical atrophy
cerebral glucose metabolism
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
cerebrovascular accident, young adult
cherry red spot
cherry red spot-myoclonus syndrome
chewing movements
children
choking
chorea
chorea, familial
choreoathetosis
chorioretinitis
chromosomal abnormality
chromosome 12
chromosome 2
chromosome 21
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
clonazepam
clonus
coenzyme Q10 deficiency
cognition
cogwheel rigidty
cold intolerance
color vision, impaired
coma
coma, episodic
complications
confabulation
confusion
congenital infection, CNS
congenital paresis
conjugate gaze, forced
contactin associated protein like 2 antibodies
cortical-basal ganglionic degeneration
cranial nerve palsies
Creutzfeldt-Jakob disease, genetic
crying
deafness
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
delirium
dementia
dementia, differential diagnosis of
dementia, rapidly progressive
dementia, reversible
dementia, transmissible
dementia, treatment of
demyelinating disease
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
depression
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes insipidus
diabetes mellitus
dialysis
dialysis dementia
diarrhea
diet
differential diagnosis
diplopia
disability, neurological
dizziness
doll's head maneuver
downward gaze, paralysis of
Dravet syndrome
drooling
drug induced neurologic disorders
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dysphasia
dyspraxia
dyssynergia cerebellaris myoclonica
dystonia
dystonia, focal
Ekbom's Syndrome
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
electroencephalogram, triphasic delta waves
electromyogram
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, diagnosis of
encephalitis, etiology
encephalitis, paraneoplastic
encephalitis, viral
encephalitis, viral-causes of
encephalomyelitis
encephalomyelitis, postinfectious
encephalopathy
encephalopathy, delayed
encephalopathy, Hashimoto's
encephalopathy, parainfectious
enterovirus
enterovirus infection of CNS
enzyme, defect
epidemic
epidemiology of neurology
episodic disorders
episodic neurologic deficits
episodic unconsciousness
eye movement, disorders of
facial movement disorder
faciobrachial dystonic seizure
falling
familial
fasciculation
fatal familial insomnia
fatigue
fever
fine motor function, impaired
finger nose finger test
fingerprint bodies
flaccid paralysis
gait disorder
gait, apraxic
gammaglobulin therapy, intravenous
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
gene therapy
genetic counselling
genetic neurologic disorders
genetic testing
gliadin antibodies
globus pallidus, lesion of
GluD2
glutamic acid decarboxylase, antibody
gram positive rod
granular osmiphilic material
grasp reflex
gray matter
gyrus, abnormal
Hallervorden Spatz disease
hallucination
hand-foot-mouth disease
handwriting
head lag
headache
hearing loss
heart block
heavy metal intoxication
heel-knee-shin test
hemimyoclonic jerks
hemiparesis
hemiplegia
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hepatosplenomegaly
heralding manifestation
hoarseness
human immunodeficiency virus type 1
hydrocephalus
hyperhidrosis
hyperpigmentation of skin
hyperreflexia
hypersomnia
hypertension
hyperthermia
hyperthyroidism
hyponatremia
hypophonia
hypothalamus, disturbance of
hypothyroidism
hypotonia
hypotonia, infants
iatrogenic neurologic disorders
idiopathic
imbalance
imbalance, postural
immunohistochemistry
immunosuppressive agents
immunotherapy
impotence
inattention
inborn errors of metabolism
incidence
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, eosinophilic intranuclear
incontinence, fecal
incoordination
infection
influenza
insight, loss
insomnia
intellectual deficit
intellectual deterioration
intestinal biopsy
intestinal pseudoobstruction
intrauterine infection
intrauterine infection, viral of CNS
introverted
irritability
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, variant
Jakob-Creutzfeldt disease, young adult
juvenile paresis
Kearns-Sayre syndrome
kuru plaques
lactic acidemia
Lafora's disease
lateropulsion
Leber's hereditary optic neuropathy
Leigh's disease
Leigh's disease, adult variety
leucine rich glioma inactivated 1 antibodies
leukocyte enzyme abnormality
leukocytosis
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
leukoencephalopathy, hereditary diffuse
level of consciousness, decreased
limbic encephalitis
linear lesion
lipid storage disorder of CNS
lithium
liver function enzymes
lymphadenopathy
macular degeneration
maculopathy
malabsorption
malabsorption syndrome
malaise
masked facies
MELAS syndrome
memory, defect of recent
memory, impairment of
meningitis
meningitis, aseptic
meningoencephalitis
mental retardation
mental status, abnormal
MERRF syndrome
metronidazole
micrographia
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
monoparesis
mortality
motor cortex
motor neuron disease
motor neuron disease, misdiagnosis
movement disorder
movement disorder, drug induced
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, false negative
MRI, FLAIR
MRI, high signal intensity of basal ganglia
MRI, negative
MRI, pelvis
MRI, spinal cord
MRI, susceptibility weighted
mutism
myelitis
myelitis, longitudinal
myelitis, transverse
myelopathy
myoclonic ataxia
myoclonic jerks
myoclonus
myoclonus, cortical
myoclonus, epilepsy
myoclonus, orthostatic
myoclonus, segmental
myoclonus, stimulus sensitive
myoclonus, treatment of
myopathy
myopathy, mitochondrial
myorhythmia
N-acetylcysteine
nausea and vomiting
negative
neuraminidase deficiency
neuroaxonal dystrophy
neuroaxonal dystrophy, infantile
neuroaxonal dystrophy, juvenile
neuroaxonal leukodystrophy
neuroblastoma
neurologic complications of, systemic cancer
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic disease, diagnoses of, clinical bedside
neurologic signs
neurologic symptoms
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, ataxia, retinitis pigmentosa
neurosyphilis
neurotoxic
neurotoxin
next-generation sequencing
night sweats
nystagmus
nystagmus, rotary
nystagmus, vertical
ocular flutter
ocular motility, disorders of
oculomasticatory myorhythmia
old age, neurology of
olivary degeneration, hypertrophic
ophthalmoplegia
ophthalmoplegia, progressive external
opsoclonus
opsoclonus, differential diagnosis of
opsoclonus-myoclonus syndrome
optic atrophy
optic atrophy, hereditary
optic neuropathy
oral ulcerations
orthostatic hypotension
pain, abdominal
palatal myoclonus
pancytopenia
papilledema
paralysis, acute
paralysis, acute areflexic
paraparesis, spastic
parasomnia
Parkinson disease
Parkinsonism syndrome
paroxysmal neurologic deficits
PAS positive
PAS positive material in the brain
pathologic reflex
penicillin
pericarditis
personality change
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
pleurisy
pneumonia
polymerase chain reaction
polyneuropathy
pons, lesion of
pontocerebellar atrophy
potassium channel antibodies
pregnancy, neurologic complications in
prevention of neurologic disorders
prion disease
prognosis
progressive infantile poliodystrophy
progressive myoclonic epilepsy
progressive neurologic disorder
progressive pallidum atrophy
protein 14-3-3, cerebrospinal fluid
protein 14-3-3, cerebrospinal fluid, false negative
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
psychosis, acute
ptosis
pulmonary edema
Purkinje cell
Purkinje cell surface antibody
pursuit eye movements, abnormal
pyramidal tract dysfunction
pyruvate metabolism, abnormality of
quadriparesis
ragged-red fibers
Ramsay Hunt syndrome
rapidly progressing neurologic illness
rash
rash, hand
real-time quaking-induced conversion
release phenomena
REM sleep behavior disorder
remote effect of cancer on the nervous system
renal failure
respiratory failure
respiratory tract infection
retinal degeneration
retinopathy
Rett's syndrome
review article
rigidity
risk factors
Romberg's sign
rooting reflex
rubella encephalitis
rubella encephalitis, progressive
rubella syndrome
rubella virus
rubeola virus
saccadic eye movements, abnormal
salivation, excessive
SCN1A gene
sedimentation rate, elevated
seizure
seizure, children
seizure, familial
seizure, febrile
seizure, intractable
seizure, neonatal
seizure, paradoxical
seizure, photosensitive
seizure, tonic-clonic
seizure, treatment of
senile plaques
sensorineural hearing loss
sensory loss, cortical
seroconversion
serologic testing
serologic testing of cerebrospinal fluid
short stature
sleep apnea, obstructive
sleep pathology and physiology
slow virus infection of CNS
slurred speech
snout reflex
sodium channel dysfunction
sodium valproate
somnolence
spasticity
speech disorder
speech, loss of
spinal cord
spinal cord, lesion of
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 16
spinocerebellar ataxia type 7
splenium of corpus callosum
spongy degeneration of brain
square wave jerks
standing difficulty
startle myoclonus
startle reaction
status epilepticus
steatorrhea
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
storage disease of CNS
striatonigral degeneration
striatonigral degeneration, infantile
stuporous
stuttering
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
suck, poor
suicide
symmetric brain lesions
syphilis, diagnosis and treatment
syphilis, neurologic complications with
systemic illness
tachycardia
tandem gait, ataxic
tau protein
temporal lobe, lesion, bilateral
teratoma, ovarian
term infant
thalamus, lesion of
thalamus, lesion of-bilateral
thyroiditis
thyrotropin
titubation
tonic spasms
topiramate
toxins, nervous system
transplacental virus infections
treatment of neurologic disorder
tremor
tremor, intention
tremor, postural
triangle of Guillain and Mollaret
trinucleotide repeats
ultrasonography
unconsciousness
unconsciousness, episodic
unconsciousness, transient
Unverricht-Lundborg disease
upgaze
upgaze, paralysis of
urinary incontinence
uveitis
vaccine
vasculitides
vertigo
viral infection
viral infection, CNS
viral isolation
virus, slow
vision, blurred
visual acuity, decreased
visual impairment
visual loss
visuospatial disturbance
vitreous opacities
vocalizations
walking, difficulty with
weakness, acute
weakness, focal
weight loss
wheelchair
Whipple's disease
white matter disease
wide based gait
Wolfram syndrome
writing
Showing articles 0 to 50 of 1424 Next >>

Clinicopathologic Conference, Anti-IgLON5 IgG-Associated Neurologic Disorder
NEJM 386:173-180, Case 1-2022, 2022

Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
NEJM 386;674-687, Case 5-2022, 2022

A 77-Year-Old Man with Involuntary Movements, Sleep Changes, Falls, Bulbar Symptoms, and Cognitive Complaints
Neurol 99:26-30, Cao, T.Q.,et al, 2022

A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
Neurol 94:e1213-e1218, Lima, J.E.E.,et al, 2020

An Adolescent Girl Presenting with Worsening Vertigo, Headache, and Ataxia
Neurol 95:e1760-e1763, Brigham, E.,et al, 2020

Palatal Myoclonus, Abnormal Eye Movements, and Olivary Hypertrophy in GAD65-Related Disorder
Neurol 94:273-275, Macaron, G.,et al, 2020

Rapid Progression of Prion Disease Associated with Transverse Myelitis
Neurol 94:e1670-e1672, Hussein, O.,et al, 2020

Clinicopathologic Conference, Creutzfeldt-Jakob Disease
NEJM 381:1569-1578, Case 32-2019, 2019

Glutamate Receptor D2 Serum Antibodies in Pediatric Opsoclonus Myoclonus Ataxia Syndrome
Neurol 91:e714-e723, Berridge, G.,et al, 2018

Progressive cognitive decline, cerebellar ataxia, recurrent myoclonus, and epilepsy
Neurol 90:e1827-e1831, Xiao, F.,et al, 2018

IgLON5-mediated neurodegeneration is a differential diagnosis of CNS Whipple disease
Neurol 90:1113-1115, Morales-Briceno, H.,et al, 2018

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

A 54-year-old woman with Dementia, Myoclonus, and Ataxia
Neurol 89:e7-e12, Ali, F.,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 Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
Neurol 89:e220-e223, Xiao, F. & Wang, X.F., 2017

Choreoathetosis, Dystonia, and Myoclonus in 3 Siblings with Autosomal Recessive Spinocerebellar Ataxia Type 16
JAMA Neurol 73:888-890, Kawarai, T.,et al, 2016

Antibiotic-Associated Encephalopathy
Neurol 86:963-971, Bhattacharyya, S.,et al, 2016

Orthostatic Myoclonus Associated with CASPR2 Antibodies
Neurol 86:1353-1355, Govert, F.,et al, 2016

Leukodystrophy and Progressive Myoclonic Epilepsy Disclosing DRPLA
Neurol 86:e58-e59, Sgobbi de Souza, P.V.,et al, 2016

A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
Ann Neurol 77:1-7, Scripko, P.,et al, 2015

Enterovirus Vaccines for an Emerging Cause of Brain-Stem Encephalitis
NEJM 370:792-794, McMinn, P.C., 2014

A 72-year-old Man with Rapid Cognitive Decline and Unilateral Muscle Jerks
Neurol 82:e194-e197, Duncan, M.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Neuronal Ceroid Lipofuscinosis (Batten Disease)
Adams & Victors Principles of Neurology, Chp 37, pg 973, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Subacute Necrotizing Encephalopathy (Leigh Disease)
Adams & Victors Principles of Neurology, Chp 37, pg 996, Ropper, A.H.,et al, 2014

Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Whipple Disease
Adams & Victors Principles of Neurology, Chp 32, pg 710, Ropper, A.H.,et al, 2014

The Acquired Metabolic Disorders of the Nervous System, Hashimoto Encephalopathy (Steroid Responsive Encephalopathy Syndrome)
Adams & Victors Principles of Neurology Chp 40, pg 1155, Ropper, A.H.,et al, 2014

Disorders of the Nervous System Caused by Drugs, Toxins, and Chemical Agents, Lithium
Adams & Victors Principles of Neurology Chp 43, pg 1212, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Acute Encephalitis
Adams & Victors Principles of Neurology, Chp 33, pg 748, Ropper, A.H.,et al, 2014

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

Clinical Reasoning: A Woman with Rapidly Progressive Apraxia
Neurol 80:e162-e165, Pressman, P.,et al, 2013

Subacute Sclerosing Panencephalitis
www.MedLink.com, February, Auwaeter,P.G.&Johnson,R.T., 2013

Progressive Gait Deterioration in Adolescents with Dravet Syndrome
Arch Neurol 69:873-878, Rodda, J.M.,et al, 2012

Adult-Onset Opsoclonus-Myoclonus Syndrome
Arch Neurol 69:1598-1607, Klaas, J.,et al, 2012

Acquired Neurosyphilis Presenting as Movement Disorders
Mov Disord 27:690-695, Shah, B.B. & Lang, A.E., 2012

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

Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
NEJM 364:1062-1074, Case 8-2011, 2011

Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
JNNP 80:943-953, Rahman,S. &Hanna,M.G., 2009

Opsoclonus-Myoclonus-Ataxia Syndrome with Autoantibodies to Glutamic Acid Decarboxylase
Clin Neurol Neurosurg 110:619-621, Markakis,I.,et al, 2008

Orthostatic Myoclonus: A Contributor to Gait Decline in Selected Elderly
Neurol 68:1826-1830, Glass,G.A.,et al, 2007

Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006

Epilepsy Syndromes in Infancy
Pediatr Neurol 34:253-263, Korff,C.M. &Nordii,D.R.,Jr., 2006

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

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

Glutamic Acid Decarboxylase Autoantibodies and Neurological Disorders
Neurol Sci 23:145-151, Vianello,M.,et al, 2002

Hashimoto's Encephalitis as a Differential Diagnosis of Creutzfeldt-Jakob Disease
JNNP 66:172-176, Seipelt,M.,et al, 1999

N-Acetylcysteine Therapy for Unverricht-Lundborg Disease
Neurol 52:426-427, Selwa,L.M., 1999

Dancing Eyes-Dancing Feet
Lancet 354:390, Imtiaz,K.E.&Vora,J.P., 1999

Clinicopath Conf, Creutzfeldt-Jakob Disease,Case 28-1999
NEJM 341:901-908, , 1999

Neurologic Complications in Children with Enterovirus 71 Infection
NEJM 341:936-942, Huang,C-C.,et al, 1999



Showing articles 0 to 50 of 1424 Next >>