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Differential
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accommodation
accomodation, abnormal
acetylcholine receptor antibody
acquired immunodeficiency syndrome
acrocyanosis
acute disseminated encephalomyelitis
advances in neurology
afebrile
affect, flat
affect, inappropriate
aggression
agitation
agnosia
agnosia, visual
Aicardi-Goutieres syndrome
akinesia
akinesia of eyelid function
alcohol
alternating rapid movement
aluminum
alveolar hypoventilation
Alzheimer's disease
aminoacidurias
amnesia
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, atypical
amyotrophic lateral sclerosis, complications with
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, treatment of
Angelman syndrome
ankle edema
ankle, swelling of
anomic aphasia
anterior cerebral artery, occlusion of
anterior cerebral artery, occlusion, language disorder with
anticholinesterase
antiviral agents
anxiety
aphasia
aphasia, cerebellar
aphasia, children
aphasia, global
aphasia, progressive
aphasia, progressive, primary
aphasia, transcortical
aphasia, transcortical-motor
aphonia
apraxia
apraxia, speech
areflexia
arm drift
arylsulfatase A
ascites
aspiration
astrocytoma
ataxia
ataxia, cerebellar
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
attention deficit disorder with hyperactivity
attention span
atypical
audiologic test to localize site of pathology
audiology
auditory processing, impaired
autism
autoantibodies
autoimmune disease
autoimmune encephalopathy
automatism, postictal
autonomic dysfunction
B cell lymphoma
Babinski sign
bacterial infection
basal ganglia
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavior
behavior, combative
behavioral disorder
behavioral disorder, acute
Benedict's solution test
benign essential tremor
bifid uvula
bilingual
blepharospasm
blinking
blinking, reduced
botulinum toxin
brachial plexus neuropathy, children
brachycephaly
bradykinesia
brain atrophy
brain biopsy
brainstem, lesion of
Broca's aphasia
bruit
bulbar palsy
bulbar palsy, progressive
cafe au lait spots
calcification, intracranial
calculations
calf hypertrophy
carbon monoxide poisoning
carcinoma
carotid artery occlusion, bilateral
carotid artery occlusion, intracranial
carotid artery occlusion, neck
carotid siphon
carotid-siphon occlusion
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
catatonia
CD19-directed chimeric antigen receptor T-cell therapy
celiac disease, adult
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar disease, eye movement disorder in
cerebellar hypoplasia
cerebellar infarction
cerebellar lesion
cerebellar mutism
cerebellitis, autoimmune
cerebellum, disease of
cerebellum, neoplasms of
cerebral cortical atrophy
cerebral dominance
cerebral infarction
cerebral palsy
cerebral palsy, associated problems with
cerebral palsy, pure ataxic
cerebrospinal fluid, abnormal
cerebrovascular accident
cerebrovascular accident, acute management of
cerebrovascular accident, clinical diagnosis
cerebrovascular accident, mimics
cerebrovascular accident, thrombolytic agents in treatment
cerebrovascular disease
chemotherapy, CNS treatment and complications with
chewing, impaired
chilbran skin lesions
children
choking
chorea
chorea, Sydenham's
choreoathetosis
chromosomal abnormality
chromosome 12
chromosome 15
chromosome 17
chromosome 7
cleft palate
Clinical Pathologic Conference(C.P.C.)
clonazepam
cochlear implant
cognition
cogwheel rigidty
comorbidities
complications
comprehension, impaired
confusion
confusional state, acute
congenital bilateral perisylvian syndrome
consanguinity
constipation
contractures, joint
convergence
convergence, impaired
conversion reaction
copper metabolism, abnormal
cornea, abnormal
cortical-basal ganglionic degeneration
cough
cranial nerve palsies
cranial neuropathy, multiple
C-reactive protein, elevated
creatine phosphokinase(CPK)elevated
crying, pathologic
cyclosporine
cytokine release syndrome
cytoreductive surgery
deafness
deafness, congenital
degenerative diseases of CNS
delay in diagnosis
delirium
dementia
dementia, differential diagnosis of
dementia, familial
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
demyelinating disease
dentate nuclei, lesion of
depression
developmental disability
developmental milestones
developmental milestones, loss of
developmental retardation
diagnostic criteria
dialysis
dialysis dementia
diarrhea
diaschisis
dichotic hearing
differential diagnosis
difficulty climbing stairs
dinitrophenylhydrazine(D.N.P.H.)reaction
diplegia, atonic
diplegia, spastic cerebral
diplopia
disability, neurological
disorientation
dopa responsive dystonia
down-beat nystagmus
down-beat nystagmus, primary position of gaze
DPPX
DPPX, antibodies, encephalitis
drooling
drug interactions
dying
dysarthria
dysdiadochokinesia
dyskinesia
dyskinesia, buccal lingual facial
dysmorphic
dysnomia
dysphagia
dysphasia
dysphonia
dysplasia of C.N.S.
dyspraxia
dystonia
dystonia musculorum deformens
dystonia, children
dystonia, face
dystonia, focal
dystonia, laryngeal
dystrophin
echolalia
EDTA(ehtylenediamine tetraacetic acid)
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, depth electrode
electroencephalogram, sleep
electromyogram
ELISA
emergencies, neurologic
emergency medical technicians
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, etiology
encephalitis, viral
encephalopathy
encephalopathy, acute
encephalopathy, delayed
encephalopathy, metabolic
encephalopathy, post anoxic
encephalopathy, progressive
enuresis
enzyme, defect
epidemiology of neurology
episodic disorders
episodic neurologic deficits
epsilon sarcoglycan gene
esophageal manometry
euthanasia
executive dysfunction
external laryngeal nerve paralysis
eye movement, disorders of
eyedness
face arm speech test
face, inexpressive
facial appearance, abnormal
facial expression abnormality
facial weakness
facial weakness, bilateral
falling
false negative
familial
fasciculation
fatigable chewing
fatigue
feeding disorder
ferric chloride test
fetal alcohol syndrome
fetus
fever
fine motor function, impaired
fish
Fisher C.M.
fluorescene in situ hybridization
food-borne infection
foreign accent syndrome
frontal lobe, atrophy
gait disorder
gait, festinating
galactorrhea
gangliosidosis GM1
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
give-way weakness
glabellar sign
glioblastoma multiforme(astrocytoma Gr.III)
glioma
globus pallidus
globus pallidus, lesion of
Gowers maneuver
grimacing
growth retardation
Hallervorden Spatz disease
hallucination
hallucination, auditory
hand weakness
handedness
hands, fisted
handwriting
head circumference
head injury
head lag
headache
hearing loss
hearing problems in children
heel-knee-shin test
hemianopia
hemianopia, homonymous
hemichorea
hemidystonia
hemiparesis
hemiplegia
hepatolenticular degeneration(Wilson's disease)
heralding manifestation
hiccoughs
hiccoughs, intractable
hip abductor sign
hippocampal atrophy
hippocampus
hippocampus, hyperintense
hoarseness
Hoover's sign
human herpesvirus 6
human immunodeficiency virus type 1
Huntington's chorea
hydrocephalus
hyperactivity
hyperesthesia
hyperlipoproteinemia
hyperpyrexia, CNS disorder causing
hyperreflexia
hypertension
hypertonia
hypoglycemia
hypophonia
hypopigmentation of skin
hyporeflexia
hypothyroidism
hypotonia
hypotonia, infants
imbalance
imbalance, postural
immune effector cell-associated neurotoxicity syndrome
immune-related adverse events
immunosuppression
immunosuppressive agents
immunotherapy
inattention
inclusion bodies
inclusion bodies, intracytopasmic
incoordination
infection
insomnia
insular cortex
insulinoma
intellectual deficit
intellectual deficit, treatable causes of
intellectual deterioration
intelligence quotient
interferon alpha
intestinal biopsy
intrauterine
inverted writing
iris, abnormal
iron, brain
irritability
jaundice
jaw jerk, abnormal
karyotyping
Kayser-Fleischer ring
kinesia paradoxica
klippel feil syndrome
Kluver-Bucy syndrome
Landau-Kleffner syndrome
language
language development, neurologic basis of
language disorder in adults
language disorders in children
language mapping
laughing, pathologic
L-dopa
learning disability
learning disability, in children
left-right orientation
leg dragging
leg weakness, unilateral
lenticular nucleus, lesion of, bilateral
leukocyte alkaline phosphotase
leukocytosis
leukodystrophy
leukoencephalopathy
leukopenia
level of consciousness, decreased
lid
lid abnormalities
lid closure, weakness of
limbic encephalitis
limbic system
Lisch nodules
listeria monocytogenes
listeriosis, CNS
liver biopsy
liver disease
liver function enzymes
liver transplantation
lobar atrophy
locked-in syndrome
logopenia
long bone lesion
lymphoma
lymphoma, systemic
lysosomes, abnoral
macrocephaly
macrognathia
malabsorption syndrome
manganese intoxication
maple syrup urine disease
marche a petits pas
masked facies
medulla oblongata, lesion of
medulloblastoma
megalencephaly
megalencephaly, idiopathic
memory, defect of recent
memory, impairment of
meningitis-encephalitis PCR panel
mental retardation
mental status, abnormal
metachromatic leukodystrophy
metachromatic leukodystrophy, juvenile
microcephaly
micrographia
midbrain, atrophy
midbrain, infarction of
midline defect in children
migraine
migraine, equivalents
mimics
mirror speech
mirror writing
misdiagnosis
molecular genetics
monoclonal antibodies
mood change
mortality
motor dysfunction
motor neuron disease
movement disorder
movement disorder, extrapyramidal
movement disorder, psychogenic
moyamoya
MRI
MRI, abdomen
MRI, abnormal
MRI, contrast enhanced
MRI, disappearing lesion on
MRI, functional
MRI, negative
MRI, paramagnetic effect
MRI, pelvis
MRI, ring sign
MRI, serial
MRI, T1 weighted high signal foci
multiple sclerosis
multiple sclerosis, differential diagnosis of
muscle atrophy, progressive
muscle stiffness
muscle weakness
muscular dystrophy
muscular dystrophy, central nervous system abnormality
muscular dystrophy, Duchenne
mutism
myasthenia gravis
myasthenia gravis, diagnosis
myasthenia gravis, misdiagnosis of
myasthenia gravis, seronegative
myasthenia gravis, thymectomy in
myasthenia gravis, treatment of
myasthenic sneer
myelodysplasia
myoclonic dystonia
myoclonus
myoclonus, action
myoclonus, epilepsy
myoclonus, stimulus sensitive
myoglobinuria
nasal regurgitation
nasal speech
neck pain
neoplasm, posterior fossa
neoplasm, primary intracerebral
neoplasm, primary intracerebral, resection
neoplasm, primary of CNS
neoplasm, primary of CNS-children
neoplasm, primary of CNS-surgical treatment of
neoplasm, primary of CNS-treatment of
nerve biopsy
nerve conduction studies
neuroendocrinology
neurofibroma
neurofibromatosis 1
neuroglycopenia
neurologic complications
neurologic complications of, surgery
neurologic disease, diagnoses of
neurologic disease, diagnoses of, clinical bedside
neurologic examination
neurologic history
neurologic signs
neurologic symptoms
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, sensory
neurotoxin
NMDA antagonists
nonverbal
nystagmus
nystagmus, vertical
ocular motility, disorders of
opened mouth
operculum syndrome
operculum syndrome, bilateral
opisthotonus
optic atrophy
organ transplantation
oropharyngeal weakness
palatal myoclonus
palatopharyngeal incompetence
palilalia
palliative care
palmomental response
PANK2 mutation
paramimia
paranoia
paraparesis
paraparesis, spastic
paraphasias
paraplegia, in flexion
paresthesias
Parkinson disease
Parkinson disease, diagnosis
Parkinson disease, freezing phenomena in
Parkinson disease, L-dopa nonresponsive
Parkinsonism syndrome
pathologic reflex
patient information and support
perseveration
personality change
phenylketonuria
pheochromocytoma
Pick bodies
Pick's disease
pigeon English
pleocytosis of cerebrospinal fluid
pneumoencephalogram(PEG)
pneumonia
polycythemia, primary
polymerase chain reaction
polyneuropathy
positional head-hanging test
postictal neurologic deficits
postpartum
postural abnormality
precipitating factors
pregnancy, neurologic complications in
prenatal
prevention of neurologic disorders
primary lateral sclerosis
prognathism
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
progressive supranuclear palsy
prolactin, elevated
pruritus
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychological testing, neurologic problems
psychomotor retardation
psychosis
psychosis, childhood
psychosocial aspects
psychosomatic disease
ptosis
pull test
pure akinesia
pure word deafness
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quadriplegia
quality of life
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
reading disorder, acquired
release phenomena
remote effect of cancer on the nervous system
repetition, impaired
repetitive nerve stimulation
respirator
respiratory failure
retinitis pigmentosa
retropulsion
reversible neurologic disorder
review article
rhabdomyolysis
rheumatic brain disease
rheumatic fever
rheumatic heart disease
rigidity
risk factors
rituximab
roaming behavior
saccadic eye movements, abnormal
salivation, excessive
scoliosis
sea-blue histiocytes
sedimentation rate, elevated
seizure
seizure, advice to parents and teachers regarding
seizure, children
seizure, differential diagnosis of
seizure, focus
seizure, hysterical
seizure, psychomotor-temporal lobe
seizure, psychosocial aspects of
seizure, recurrent
seizure, treatment of
semantic dementia
sensory loss
seronegative
sexual behavior, disorder of
sign language
single photon emission computed tomography
single-fiber electromyography
skin, lesions in neurologic disorders
sleep pathology and physiology
slit lamp examination
smiling
spastic dysphonia
spasticity
speech disorder
speech disorder, childhood
speech disorder, non aphasic
speech lateralization
speech therapy
speech, delayed development of
speech, loss of
speech, pressured
speech, slowed
spina bifida
spongy degeneration of brain
stammering
stare
startle reaction
stooped posture
stuttering
stuttering following CVA
substantia nigra
suck reflex
swallow evaluation
sweating
symmetric brain lesions
synkinesis
systemic illness
tachycardia
tandem gait, ataxic
tauopathy
teeth, wide-spaced
temporal lobe
temporal lobe, atrophy
temporal lobe, lesion
temporal lobe, lesion, bilateral
teratoma
teratoma, ovarian
thalamus, infarction of
thrombocytopenia
thrombocytosis
thrombosis, cerebral
thymectomy
thyroidectomy
thyroiditis
tissue plasminogen activator, intravenous
titubation
tongue, atrophy
tongue, fasciculations of
tongue, impaired movements of
tongue, protrusion of
toothache
torticollis
transient ischemic attack
transient neurologic deficit
transient neurologic deficit, benign syndrome in young adults
transverse smile
treatment of neurologic disorder
tremor
tremor, intention
tremor, resting
tripping
tyrosine hydroxylase deficiency
upgaze
upgaze, paralysis of
urinary incontinence
urine test for metabolic disorders
urine, dark
vertical writing
vestibulopathy
vibratory sensation, abnormal
visual allesthesia
visual evoked response
visual impairment
visual loss
vocal cord paralysis
voice, abnormality of
walking frame
walking, difficulty with
weakness
weakness, fatiguable
weakness, functional
weakness, generalized
weakness, progressive
weight loss
welder
Wernicke's aphasia
wheelchair
white matter disease
wide based gait
word-finding difficulty
workup
writing
Showing articles 0 to 50 of 17315 Next >>

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024

Manganese Accumulation in the Brain
NEJM 389:1320, Sherman,S.V., 2023

Multidisciplinary End-of-Life Care for a Patient with Amyotrophic Lateral Sclerosis Requesting Euthanasia
Lancet 402:484, Kruithof,W.J.,et al, 2023

Confused About Confusion
NEJM 386:80-87, Spanjaart, A.M.,et al, 2022

A 37-Year-Old Man with Involuntary Movements, Gait Disturbance, and Hyperasthesia
Neurol 98:851-853, Meng, D.,et al, 2022

Functional Neurological Disorders
Neurologist 27:276-289, Mishra, A. & Pandey, S., 2022

A 29-Year-Old Man with Fevers and Rapidly Progressive Cranial Neuropathies
Neurol 97:95-98, Dessy, A.,et al, 2021

Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
NEJM 385:165-175, Case 20-2021, 2021

Duchenne Muscular Dystrophy
BMJ 368:L7012, Fox, H.,et al, 2020

Functional Neurological Disorder
Stroke 51:1629-1635, Popkirov, S., et al, 2020

Clinicopathological Conference, Insulinoma
NEJM 379:376-384, Case 23-2018, 2018

Pantothenate Kinase - Associated Neurodegeneration (PKAN)
Emedicine.Medscape Sept, Hanna, P.A. & Benbadis, S.R., 2018

Wilson Disease
NIDDK Oct2018, , 2018

Clinicopathologic Conference, Primary Progressive Aphasia, Semantic Variant, due to TAR DNA Binding Protein 43 associated Frontotemporal Lobar Degen
NEJM 376:158-167, Case 1-2017, 2017

Clinical Manifestations of Myasthenia Gravis
UptoDate Aug 2016, Bird, S.J., 2016

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

An 11-year-old Boy with Language Disorder and Epilepsy
Neurol 86:e48-e53, Dong, L. & Zhou, X., 2016

Identifying and Managing Common Childhood Language and Speech Impairments
BMJ 350:h2318, Reilly, S.,et al, 2015

The Acquired Metabolic Disorders of the Nervous System, Dialysis Encephalopathy (Dialysis Dementia)
Adams & Victors Principles of Neurology Chp 40, pg 1146, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Progressive Bulbar Palsy
Adams & Victors Principles of Neurology, Chp 39, pg 1111, 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

A Welsh-Sparing Dysphasia
Lancet 382: 1608, Rice, S.P.,et al, 2013

Myasthenia Gravis
BMJ 345:e8497, Spillane, J.,et al, 2012

Clinical Reasoning: A 13-year-old Boy Presenting with Dystonia,Myoclonus,and Anxiety
Neurol 78:e72-e76, Blackburn,J.S. and Cirillo,M.L., 2012

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

Genetic Susceptibility to Stuttering
NEJM 362:750-752, Fisher,S.E. &Phil,D., 2010

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

Profound Deafness in Childhood
NEJM 363:1438-1450, Kral,A.,et al, 2010

Anti-N-Methyl-D-Aspartate Receptor (NHMDAR) Encephalitis in Children and Adolescents
Ann Neurol 66:11-18,1, Florance,N.R.,et al, 2009

Aicardi-Gouti�res Syndrome
Br Med Bull 89:183-201, Orcesi, S.,et al, 2009

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

Functional Outcome After Language Mapping for Glioma Resection
NEJM 358:18-27, Sanai,N.,et al, 2008

Is This Patient Having a Stroke?
JAMA 293:2391-2402, Goldstein,L.B. &Simel,D.L., 2005

Dysphagia as the Sole Manisfestation of Myasthenia Gravis
JNNP 76:1297-1300, Llabrs,M.,et al, 2005

Clinical Features and Natural Histry of Progressive Supranuclear Palsy, A Clinical Cohort Study
Neurol 60:910-916, Nath,W.,et al, 2003

Emergency Calls in Acute Stroke
Stroke 34:1005-1009, Handschu,R.,et al, 2003

Language Function and Dysfunction in Corticobasal Degeneration
Neurol 61:493-499, Graham,N.L.,et al, 2003

Postictal Language Dysfunction in Complex Partial Seizures: Effect of Contralateral Ictal Spread
Neurol 56:1590-1592, Ficker,D.M.,et al, 2001

Language Disturbances in Corticobasal Degeneration
Neurol 54:990-992, Frattali,C.M.,et al, 2000

Effects of Resective Surgery for Left-Sided Intracranial Tumors on Language Function:A Prospective Study
Lancet 351:1014-1018, Whittle,I.R.,et al, 1998

Clinical Characteristics of a Chromosome 17-Linked Rapidly Progressive Familial Frontotemporal Dementia
Arch Neurol 54:539-544, Basun,H.,et al, 1997

Neurodevelopmental Dysfunction Among Nonreferred Children with Idiopathic Megalencephaly
J Pediatr 131:320-324, Sandler,A.D.,et al, 1997

Identification of Brain Region for Coordianting Speech Articulation
Lancet 394:221-222, Donnan,G.A.,et al, 1997

Unusual Clinical Presentations of Cortical-Basal Ganglionic Degeneration
Ann Neurol 40:893-900, Bergeron,C.,et al, 1996

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

Functional Dysphonia
BMJ 311:1039-1040, Wilson,J.A.,et al, 1995

The Landau-Kleffner Syndrome
Arch Dis Child 72:386-387, Appleton,R.E., 1995



Showing articles 0 to 50 of 17315 Next >>