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Differential
(Click to cross reference)
abdominal distention
abdominal reflex, absent
abducens nerve paralysis
abscess, intracerebral
abulia
aceruloplasminemia
acquired immunodeficiency syndrome
acquired immunodeficiency syndrome dementia complex
acquired immunodeficiency syndrome, infants and children
acute disseminated encephalomyelitis
acute disseminated encephalomyelitis, multiphasic
acute respiratory distress syndrome
addiction, heroin
adult polyglucosan body disease
adverse drug reaction
aggression
agitation
alcohol intolerance
algorithm
altered states of consciousness
alternating rapid movement
Alzheimer's disease
amenorrhea
amniocentesis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, differential diagnosis
amyotrophic lateral sclerosis, epidemiology of
ANA
anemia
anemia, megaloblastic
ankle clonous
ankle reflex, absent
anomic aphasia
anorexia
antecedent illness
anterior tibial muscle weakness
anti GQ1b IgG antibody
anticholinergic drugs
anticoagulant, complications of
anticoagulant, treatment
antiviral agents
aphasia
arachnodactyly
areflexia
Argyll Robertson pupil
arm swing, reduced
Arnold Chiari malformation
aspiration
asymptomatic
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, truncal
ataxic gait
attention deficit disorder with hyperactivity
attention span
atypical
autism
autoantibodies
autoimmune disease
autonomic dysfunction
autosomal rcessive spastic ataxia of Charlevoix-Saguenay
azidodeoxythymidine
B 12 deficiency
Babinski sign
Babinski sign in new born
bacterial infection
bacterial infection, CNS
basal ganglia
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
bedridden
behavior modification
behavioral disorder
Bell's phenomenon
Bickerstaff's brainstem encephalitis
bladder dysfunction
blepharospasm
blinking
bradykinesia
brain atrophy
brain biopsy
brain biopsy, false negative
brainstem
brainstem, infarction of
brainstem, lesion of
Brudzinski's sign
bruxism
bulbar palsy
bulbar palsy, progressive
burning feet
burning paresthesia
CAG repeats
calculations
cane
carbamazepine
carcinoma
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, emission, abnormal
CAT scan, metrizamide
CAT scan, myelogram with
central nervous system, infection of
cerebellar atrophy, primary
cerebellar lesion
cerebral cortical atrophy
cerebral venous thrombosis
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, pressure increased
cerebrospinal fluid, proteincytologic dissociation
cerebrospinal fluid, red cells in
cerebrovascular accident
ceruloplasmin, serum
Chaddock's sign
Charcot-Marie-Tooth
cherry red spot
cherry red spot-myoclonus syndrome
children
choking
choreoathetosis
chromosomal abnormality
chromosome 9
chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids
claudication, intermittent of cauda equina
Clinical Pathologic Conference(C.P.C.)
clivus
clonus
clubfoot as related to neurologic disease
cobalamin C deficiency
cognition
Collier's sign
coma
complications
comprehension, impaired
compression fracture
concentration, impaired
confusion
congenital bilateral perisylvian syndrome
congenital malformation
consanguinity
constipation
convergence, impaired
conversion reaction
copper
copper deficiency
corneomandibular reflex
coronavirus
corpus callosum, lesion of
corpus callosum, thinning
cortical-basal ganglionic degeneration
COVID-19
cranial neuropathy
C-reactive protein, elevated
critical care unit
cry, abnormal
crying, pathologic
D-dimer
decompressive spinal cord surgery
deep gray nuclei
deep tendon reflexes
degenerative diseases of CNS
Dejerine's sign
Dejerine-Sottas syndrome
delay in diagnosis
dementia
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, subcortical
demyelinating disease
dental procedure, neurologic complications with
dentate nuclei
dentate nuclei, lesion of
denture cream
depression
developmental abnormality of brain
developmental disability
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes mellitus
diagnostic criteria
diaphragmatic paralysis
diaphragmatic paralysis, causes of
diarrhea
diet
differential diagnosis
difficulty climbing stairs
difficulty going down stairs
diplopia
disability, neurological
disorientation
distal muscle atrophy
distal muscle weakness
dizziness
dopa responsive dystonia
drooling
dropped head syndrome
drowsiness
drug abuse
drug abuse, inhalation
drug abuse, neurologic complications of
dysarthria
dyskinesia, buccal lingual facial
dysmetria
dysmorphic
dysphagia
dysphonia
dyspraxia
dystonia
dystonia musculorum deformens
dystonia, focal
dystonia, treatment of
ear, abnormal
ears of the Lynx MR sign
electrical sensation
electroencephalogram, abnormalities of
electroencephalogram, triphasic delta waves
electromyogram
emergencies, neurologic
emergencies, neurosurgical
emotional lability
Emperor's clothes syndrome
empyema, epidural-spinal
encephalitis
encephalitis, brainstem
encephalopathy
encephalopathy, acute
encephalopathy, Hashimoto's
encephalopathy, progressive
enzyme, defect
enzyme, muscle disease
eosinophilia
ependymal
epidemiology of neurology
episodic disorders
episodic neurologic deficits
evoked potentials
executive dysfunction
exome sequencing
eye movement, disorders of
face, numbness of
facial weakness
facial weakness, bilateral
falling
familial
fasciculation
fatigue
feeding disorder
ferritin, elevated
ferritinemia
fever
fine motor function, impaired
finger nose finger test
fingers, abnormal
Fisher's syndrome
flaccid paralysis
foot deformity
fragile-X syndrome
frataxin
Friedreich's ataxia
Friedreich's ataxia, late onset
frontal lobe, atrophy
frontal lobe, behavior with disease of
frontal lobe, pathologic signs of
frontotemporal dementia, behavioral variant
gadolinium
gag reflex, depressed
gait disorder
gait, apraxic
gait, spastic
gammaglobulin therapy, intravenous
gangliosidosis GM2
gastric partitioning
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic screening
genetic testing
giant axonal neuropathy
glabellar sign
glioma
gliomatosis cerebri
globoid cells
globus pallidus
globus pallidus, lesion of
glutamate dehydrogenase deficiency
glutamic acid decarboxylase, antibody
Google
granular osmiphilic material
grasp reflex
grasping
Guillain Barre syndrome
Guillain Barre syndrome, axonal form
Guillain Barre syndrome, variant forms of
Hallervorden Spatz disease
hammertoes
hands, fisted
handwriting
head lag
headache
headache, positional
headache, recurrent
headache, severe
hearing loss
heel-knee-shin test
hematoma, epidural-spinal
hemiparesis
hemiplegia
hemiplegia, progressive
hepatomegaly
hexosaminidase-A
high arched feet
hip flexor weakness
Hispanics
history of neurology
Hoffmann's sign
homocysteine, serum
homocystinuria
horse bite
human immunodeficiency virus type 1
hypercalcemia
hypercapnia
hypereosinophilic syndrome(HES)
hyperhomocysteinemia
hyperparathyroidism
hyperpigmentation of skin
hyperreflexia
hypersegmented polys
hypertension
hyperthyroidism
hypertonia
hypomyelination
hypophonia
hyporeflexia
hypothalamus
hypothalamus, disturbance of
imbalance
imbalance, postural
immunosuppression
inattention
inborn errors of metabolism
inclusion bodies
incontinence, fecal
incoordination
initiative, lack of
insomnia
intellectual deficit
intellectual deterioration
internet
internuclear ophthalmoplegia
interobserver agreement
intrinsic hand muscles, wasting of
introverted
intubation
iron, brain
iron, serum, low
irritability
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
jaw jerk, abnormal
Jewish
karyotyping
Kernig's sign
Krabbe's disease
lactic acidemia
laminectomy, cervical
laminectomy, lumbar
language disorder in adults
Lasegues sign
laughing, pathologic
L-dopa
left-right orientation
leg spasms, painful
leg weakness, bilateral
Leigh's disease
lenticular nucleus, lesion of, bilateral
lethargy
leukemia
leukemia, neurologic findings assoc.with
leukocyte enzyme abnormality
leukodystrophy
leukoencephalopathy
level of consciousness, decreased
Lhermitte's sign
lipid storage disorder of CNS
lobar atrophy
locked-in syndrome
logopenia
loss of sympathy
low back pain
lymphadenopathy
lymphadenopathy, hilar
lymphoma
lymphoma involving CNS
lysosomal storage disease
malformation, CNS, congenital
manganese intoxication
meconium staining
mediastinum, lymph-node biopsy
mediastinum, mass of
memory, defect of recent
memory, impairment of
meningeal enhancement
meningitis
meningitis, bacterial
meningitis, neutrophilic
meningitis, pneumococcal
mental retardation
mental retardation, familial
mental status, abnormal
methylmalonic acid, serum
methylmalonic acidemia
midbrain, lesion of
middle cerebellar peduncle, lesion
mimics
miosis
misdiagnosis
molecular genetics
Montreal cognitive assessment
mortality
motor dysfunction
motor neuron disease
movement disorder
movement disorder, extrapyramidal
movement disorder, psychogenic
movement disorder, treatment of
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, contrast enhanced, high dose
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, emergent
MRI, FLAIR
MRI, gradient-echo
MRI, high signal intensity of basal ganglia
MRI, hypointense signal foci on
MRI, linear enhancement
MRI, negative
MRI, nodular enhancement
MRI, paramagnetic effect
MRI, ring sign
MRI, spinal cord
MRI, spinal cord, increased intramedullary cord signal
MRI, spine
MRI, susceptibility weighted
MRS
multinucleated giant cell
multiple sclerosis
multiple sclerosis, differential diagnosis of
muscle atrophy, progressive
muscle biopsy
muscle spasm
muscle weakness
mutism
mycoplasma
mycoplasma pneumoniae
myelitis
myelitis, longitudinal
myelitis, post infectious
myelitis, transverse
myelogram
myelogram, cervical
myelomalacia
myeloneuropathy
myelopathy
myelopathy, chronic progressive
myelopathy, vacuolar
myeloradiculopathy
myoclonus
myoclonus, epilepsy
nausea and vomiting
neck pain
neck stiffness
neglect
neoplasm, primary of CNS
nerve biopsy
nerve conduction studies
nerve root hypertrophy
neuroendocrinology
neurofibrillary degeneration
neurogenic bladder
neurologic complications of, surgery
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic examination
neurologic signs
neurologic symptoms
neuromuscular disease, electrodiagnosis of
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, demyelinating
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, sensory
neuropsychiatry
neurotoxin
next-generation sequencing
night sweats
nitrous oxide
nonverbal
nutritional deficiency
nystagmus
nystagmus, gaze-evoked
nystagmus, rotary
nystagmus, upbeating on upgaze
nystagmus, vertical
ocular motility, disorders of
old age, neurology of
operculum syndrome, bilateral
ophthalmoplegia
ophthalmoplegia, total
opisthotonus
optic atrophy
optic chiasm, enlarged
optic nerve
optic nerve, enlarged
optic nerve, lesion of
optic neuropathy
oral contraceptives
orthostatic hypotension
oscillopsia
osteomyelitis
osteomyelitis, spinal
pain
pain, back
pain, foot
pain, interscapular
pain, severe
palmomental response
palpebromandibular synkinesia
pancytopenia
papilledema
paralysis
paranoia
paraparesis
paraparesis, familial spastic
paraparesis, familial spastic, classification
paraparesis, familial spastic, variants
paraparesis, flaccid
paraparesis, spastic
paraplegia
paraplegia, in flexion
paraplegia, progressive
parathormone
parathyroid adenoma
paresthesias
paresthesias, feet
paresthesias, hands
Parkinson disease
Parkinson disease, hemiparesis in
Parkinson disease, unilateral
Parkinson disease, young onset
Parkinsonism syndrome
paroxysmal neurologic disorder
PAS positive
PAS positive material in the brain
past pointing
pathologic reflex
patient information and support
pediatric neurology
perivascular enhancement
pernicious anemia
perseveration
Persistent postural-perceptual dizziness
personality change
pes cavus
pharyngeal sensation
photic sneeze reflex
Pick bodies
Pick's disease
pituitary stalk
pituitary stalk, lesion of
plantar reflex
pleocytosis of cerebrospinal fluid
polyglucosan body
polyglucosan body disease
polymicrogyria
polyneuropathy, familial
pons, infarction of
pons, lesion of
position sensation, abnormal
posterior column disease
posterior leukoencephalopathy syndrome
postictal neurologic deficits
precipitating factors
precocious puberty
prenatal diagnosis by amniocentesis
primary lateral sclerosis
prion disease
prognosis
progressive encephalomyelitis with rigidity syndrome
progressive myoclonic epilepsy
progressive neurologic disorder
proprioception, abnormal
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
pupil
pupil, light reflex, abnormal
pyramidal tract
pyramidal tract dysfunction
pyruvate metabolism, abnormality of
quadriparesis
quadriparesis, progressive
quadriplegia
radiculopathy
rash
recurrent
reflex, cutaneous
release phenomena
renal failure
renal stones
repetition, impaired
respirator
respiratory failure
respiratory tract infection
retinal degeneration
retinal exudates
retinitis pigmentosa
retinopathy
retropulsion
reversible neurologic disorder
review article
rigidity
risk factors
Romberg's sign
rooting reflex
saccadic eye movements, abnormal
saddle anesthesia
sarcoidosis
sarcoidosis, CNS
schizophrenia
scoliosis
screening
sea-blue histiocytes
seizure
seizure, children
seizure, familial
seizure, hysterical
selective serotonin reuptake inhibitors
senile plaques
sensory level
sensory loss
sensory loss, cutaneous
serologic testing
serotonin norepinephrine reuptake inhibitors
severe acute respiratory syndrome
skin, lesions in neurologic disorders
sleep pathology and physiology
slow virus infection of CNS
slurred speech
sneeze
snout reflex
somnolence
spastic ataxia
spastic paraplegia, type 11
spasticity
speech disorder
speech disorder, childhood
speech, loss of
spinal cord
spinal cord, compression of
spinal cord, lesion of
spinal cord, pathologic exam of
spinal stenosis
spinal stenosis, familial
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar ataxia type 7
spongy degeneration of brain
spontaneous remission
startle myoclonus
startle reaction
status epilepticus
steroid therapy, CNS treatment and complications with
stiff legs
stooped posture
striatonigral degeneration
striatonigral degeneration, infantile
subarachnoid hemorrhage
substantia nigra
suck reflex
superior sagittal sinus thrombosis
swallowing
symmetric brain lesions
syncope
syringomyelia
systemic illness
systemic lupus erythematosus
systemic lupus erythematosus, neurologic complications with
tachycardia
tandem gait, ataxic
tangential
tau protein
tauopathy
Tay-Sachs disease
temporal lobe, lesion
temporal lobe, lesion, bilateral
testicular enlargement
thalamus, lesion of
thalamus, lesion of-bilateral
tinnitus
titubation
toe walking
tone, muscle, increased
tongue, fasciculations of
tongue, impaired movements of
tonic foot response
transient neurologic deficit
trauma
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
trinucleotide repeats
tripping
unconsciousness
upgaze
upgaze, paralysis of
urinary frequency
urinary incontinence
urinary retention
urinary urgency
vaccination, neurologic complications with
valsalva maneuver
vegetarianism
ventricular enlargement
vertigo
vertigo, episodic
vibratory sensation, abnormal
viral infection
viral infection, CNS
visual acuity, decreased
visual evoked response
visual fields, constricted
visual loss
vitamin deficiency
vitamin E
vitamin E deficiency
walking frame
walking, delayed
walking, difficulty with
watershed infarcts
weakness
weakness, generalized
weakness, progressive
weaning from respirator, failure to
weight loss
wheelchair
white matter disease
wide based gait
workup
x-linked mental retardation
x-ray, spine
x-ray, thoracic spine
zinc
zoonoses
Showing articles 0 to 50 of 726 Next >>

A 26-Year-Old Woman with Chronic Progressive Gait Dysfunction
Neurol 103:e2098-e2030, Jones,F.J.S. & Orthmann-Murphy,J., 2024

A 48-Year-Old Man With Spasticity and Progressive Ataxia
Neurol 101:e1747-e1752, Vizcarra,J.A.,et al, 2023

A 13-Year-Old Boy with Subacute-Onset Spastic Gait
JAMA Neurol 78:e1-e2, Xie, N.,et al, 2021

Clinicopathologic Conference,Aceruloplasminemia, Hereditary
NEJM 383:1974-1983, Case 35-2020, 2020

Clinicopathologic conference, Frontotemporal Lobar Degeneration with tau-positive inclusions consistent with Picks disease
NEJM 383:2666-2675, Case 41-2020, 2020

A Young Health Woman with Difficult-to-Wean Acute Ventilator Dependence
Neurol 94:e1340-e1343, Chandrashekhar, S.,et al, 2020

Neurologic Features in Severe SARS-CoV-2 Infection
NEJM 382:2268-2270, e110, , 2020

Spasms and Myoclonus in a Young Woman with Hashimoto Thyroiditis
JAMA Neurol 77:650-651, Shen, D.,et al, 2020

Ears of the Lynx Magnetic Resonance Imaging Sign
Ann Neurol 88:16-17, Baghbanian, S.M.,et al, 2020

Complex Ataxia
Neurol 95:136-141, Abkur, T.,et al, 2020

A 14-Year-Old Girl with Headache, Seizures, and Confusion
Neurol 92:e161-e167, Xiao, L.,et al, 2019

Pes Cavus and Neuropathy
Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019

Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches
Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019

A young woman with symmetric weakness and behavioral disturbance
Neurol 90:e1442-e1447, Rosenberg, J.,et al, 2018

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

A 35-year-old Woman with Diplopia, Ataxia, and Altered Mental Status
Neurol 91:e1942-e1946, Bauer, Z.,et al, 2018

Persistent Postural-Perceptual Dizziness (PPPD): A Common, Characteristic and Treatable Cause of Chronic Dizziness
Pract Neurol 18:5-13, Popkirov, S.,et al, 2018

Progressive Weakness and Memory Impairment in a Middle-aged Man
JAMA 320:197-198, DeFilippis, E.M.,et al, 2018

Man with Recurrent Paralysis and Cerebral White Matter Lesions
JAMA Neurol 74:599-600, Xiao, F., 2017

A 27-year-old man with unsteady gait
Neurol 89:e120-e123, Fernandez, D.,et al, 2017

A 34-Year-Old Man with Headache, Diploplia, and Hemiparesis
Neurol 86:e28, Lincoln, M.R.,et al, 2016

A Young Man with Acute Encephalopathy Loss of Vision, and Upper Motor Neuron Signs
Neurol 86:e173-e176, Elkhider, H.,et al, 2016

Idiopathic Thoracic Spontaneous Spinal Epidural Hematoma
Case Reports Surg doi:10.1155/2016/5430708, Aycan, A.,et al, 2016

A 73-year-old Man with Diplopia and Ataxia
Neurol 85:e96-e100, Gupta, H.V.,et al, 2015

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

Degenerative Diseases of the Nervous System, Hereditary Spastic Paraplagia
Adams & Victors Principles of Neurology, Chp 39, pg 1119, Ropper, A.H.,et al, 2014

Clinical Case Conference: A 41-Year-Old Woman with Progressive Weakness and Sensory Loss
Ann Neurol 75:9-19, Stephen, C.D.,et al, 2014

Clinicopathologic Conference, Tay-Sacks Disease (GM2, Gangliosidosis)
NEJM 370:1830-1841, Case 14-2014, 2014

A Young Woman with Rapid Mental Deterioration and Leukoencephalopathy
Neurol 83:e182-e186, Biotti, D.,et al, 2014

Degenerative Diseases of the Nervous System, Machado-Joseph-Azorean Disease
Adams & Victors Principles of Neurology, Chp 39, pg 1107, Ropper, A.H.,et al, 2014

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

A Horse Bite to Remember
Lancet 376:1194, Brouwer,M.C.,et al, 2010

Clinicopath Conf, Neurosarcoidosis
NEJM 360:802-809, Case 6-2009, 2009

A 63-Year-Old Woman with Urinary Incontinence and Progressive Gait Disorder
Neurol 72:1607-1613, Lossos,A.,et al, 2009

Clinicopath Conf., Gliomatosis Cerebri
Neurol 69:600-606, Fleming,J.O.,et al, 2007

Glabellar and Palmomental Reflexes in Parkinsonian Disorders
Neurol 63:1096-1098, Brodsky,H.,et al, 2004

Bickerstaff's Brainstem Encephalitis: Clinical Features of 62 Cases and a Subgroup Associated with Guillain-Barre Syndrome
Brain 126:2279-2290, Odaka,M.,et al, 2003

CMT with Pyramidal Features
Neurol 60:696-699, Vucic,S.,et al, 2003

Clinicopath Conf, Neuronal Ceroid Lipofuscinosis, Late-Onset Infantile Subtype
NEJM 347:672-680, Case 27-2002, 2002

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

The Babinski Sign:100 Years On
BMJ 313:1029-1030, Ditunno,J.F.&Bell,R., 1996

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

Pharyngeal Sensation and Gag Reflex in Healthy Subjects
Lancet 345:487-488, Davies,A.E.,et al, 1995

Clinicopath Conf
Mycoplasma Pneumoniae Infection, Case 42-1994, NEJM 331:1437-1444994., , 1994

Spontaneous Palpebromandibular Synkinesia:A Localizing Clinical Sign
Ann Neurol 35:222-228, Pullicino,P.M.,et al, 1994

Plantar Responses after Epileptic Seizures
Neurol 44:2191-2193, Walczak,T.S.&Rubinsky,M., 1994

Congenital Bilateral Perisylvian Syndrome:Study of 31 Patients
Lancet 341:608-612, Kuzniecky,R.,et al, 1993

Extrapyramidal Signs and Other Neurologic Findings in Clinically Diagnosed Alzheimer's Dis, A Community-Based Study
Arch Neurol 50:51-56, Funkenstein,H.H.,et al, 1993

The Photic Sneeze Reflex:Literature Review and Discussion
Neurol 43:868-871, Whitman,B.W.&Packer,R.J., 1993



Showing articles 0 to 50 of 726 Next >>