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acquired immunodeficiency syndrome
acquired immunodeficiency syndrome dementia complex
acquired immunodeficiency syndrome, congenital
acquired immunodeficiency syndrome, infants and children
acromicria
advances in neurology
Aicardi-Goutieres syndrome
Alexanders disease
anemia
aneurysm
aneurysm, asymptomatic
aneurysm, intracranial
anorexia
apraxia of eye movements
aqueduct of Sylvius, stenosis
arm swing, reduced
arthritis
aspartocyclase
aspiration
aspirin
ataxia
ataxia, truncal
ataxic gait
attention span
autoimmune epilepsy
B 12 deficiency
B 12 deficiency, infants
Babinski sign
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
biologic markers
blindness
blood transfusion
bone marrow biopsy
bradykinesia
brain atrophy
brain biopsy
breast feeding
Brown-Vialetto-Van Laere syndrome
cachexia
calcification, gyral
calcification, intracranial
Canavan's disease
CAT scan
CAT scan, abnormal
cataplexy
cerebellar lesion
cerebral cortical atrophy
cerebral palsy
cerebral vasculature
cerebral venous infarction
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, proteincytologic dissociation
cerebrovascular accident
cerebrovascular disease
cherry red spot
cherry red spot-myoclonus syndrome
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 3
Clinical Pathologic Conference(C.P.C.)
cold hands sign
complications
consanguinity
contractures, joint
controversies in neurology
corpus callosum, atrophy of
corpus callosum, thinning
cough
cranial nerve enhancement
cranial nerve enlargement
cranial neuropathy
cranial neuropathy, multiple
crawl regression
cry, abnormal
crying
cultured skin fibroblasts
cyst
cyst, parenchymal
D-dimer
decision analysis
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, childhood
demyelinating disease
dentate nuclei
dentate nuclei, lesion of
developmental milestones
developmental milestones, loss of
developmental retardation
diagnostic criteria
differential diagnosis
difficulty climbing stairs
diplopia
dopa responsive dystonia
drooling
dropped head syndrome
dysarthria
dysmetria
dysphagia
dysphonia
dystonia
dystonia, children
electroencephalogram, abnormalities of
encephalitis
encephalitis, autoimmune
encephalopathy
encephalopathy, neonatal
encephalopathy, progressive
endoscopic surgery
endoscopy
enzyme, defect
epileptic encephalopathy
episodic disorders
evoked potentials
eye movement, disorders of
facial weakness
facial weakness, bilateral
failure to thrive
falling
familial
FARS2 deficiency
feeding disorder
fever
fine motor function, impaired
finger tapping
foam cells
fontanel, bulging
frontal bossing
fundus, abnormality of
gait disorder
galactorrhea
gangliosidosis GM2
Gaucher's disease
gaze palsy
gaze palsy, supranuclear
gender
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
glaucoma
globoid cells
glucocerebrosidase
glutamic acid decarboxylase, antibody
granular osmiphilic material
growth retardation
Hallervorden Spatz disease
hand deformity
hands, fisted
head circumference
head lag
headache
hearing loss
hepatic failure
hepatitis
hepatomegaly
hepatosplenomegaly
hexosaminidase-A
human immunodeficiency virus type 1
human immunodeficiency virus type 1, infants and children
hydrocephalus
hydrocephalus, complications with
hydrocephalus, etiology
hydrocephalus, fetal
hydrocephalus, non-communicating(obstructive)
hydrocephalus, treatment of
hyperhomocysteinemia
hyperpigmentation of skin
hyperreflexia
hypertonia
hypomyelination
hyporeflexia
hypothermia
hypotonia
hypotonia, infants
immunomodulation
inattention
inborn errors of metabolism
incoordination
infant, evaluation of
infantile tremor syndrome
intellectual deficit
intellectual deterioration
interferon alpha
intracranial pressure, increased
introverted
iron, brain
irritability
jaundice
Jewish
Krabbe's disease
lactic acidemia
L-dopa
Leigh's disease
lethargy
leukocyte enzyme abnormality
leukocytosis
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
life expectancy
lipid storage disorder of CNS
liver disease
liver function enzymes
lymphadenopathy
lymphadenopathy, axillary
lymphadenopathy, paraaortic
lysosomal storage disease
macrocephaly
malformation, vascular
masked facies
meconium staining
memory, impairment of
meningeal enhancement
meningitis, CSF cell count-normal
mental retardation
metabolic disorder, primary
metabolic disorder, primary-screening tests
metachromatic leukodystrophy
metachromatic leukodystrophy, late-infantile
microcephaly
midbrain, lesion of
misdiagnosis
mitochondrial disease
monoclonal antibodies
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, angiography
MRI, contrast enhanced
MRI, diffusion weighted
MRI, hypointense signal foci on
MRI, paramagnetic effect
MRS
mucopolysaccharidoses
muscle biopsy
muscle spasm
myasthenia gravis
myasthenia gravis, infantile and juvenile
myelination of nervous system
myoclonus
myoclonus, epilepsy
nasal speech
nausea and vomiting
neck trauma
nerve conduction studies
neuroaxonal dystrophy
neurocutaneous disease
neurofibrillary degeneration
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic disease, tempo
neurologic examination
neurologic signs
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
Niemann-Pick disease
nystagmus
nystagmus, rotary
ophthalmoplegia
opisthotonus
opportunistic infection
opportunistic infection, CNS
optic atrophy
optic chiasm, enlarged
optic nerve
optic nerve, enlarged
pain
PANK2 mutation
papilledema
paraparesis, familial spastic
paraparesis, spastic
PAS positive material in the brain
pediatric neurology
pleocytosis of cerebrospinal fluid
port wine nevus
postural abnormality
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
prolactin, elevated
psychological testing
psychomotor retardation
psychosis
ptosis
pulmonary infiltrates
pyramidal tract
pyramidal tract dysfunction
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
quadriparesis
quadriplegia
rash
rectal biopsy
renal tubular acidosis
retinal degeneration
retinitis pigmentosa
retropulsion
Rett's syndrome
reversible neurologic disorder
review article
riboflavin transporter deficiency
rigidity
rituximab
Rosenthal fibers
running
scoliosis
scoliosis, neurologic association with
screening
sedimentation rate, elevated
seizure
seizure, children
seizure, drug resistance
seizure, intractable
serositis
short stature
shunt procedure, ventricular
shunt procedure, ventricular-complications of
skin, lesions in neurologic disorders
slurred speech
somnolence
spastic diplegia
spasticity
speech disorder
speech disorder, childhood
speech, loss of
splenomegaly
spongy degeneration of brain
spontaneous remission
startle reaction
status epilepticus
stereotyped behavior
stiff joints
strabismus
striatonigral degeneration
striatonigral degeneration, infantile
strokelike episodes
Sturge-Weber syndrome
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
substantia nigra
suck, poor
symmetric brain lesions
systemic illness
systemic juvenile idiopathic arthritis
Tay-Sachs disease
thalamus, lesion of
thalamus, lesion of-bilateral
thrombocytosis
titubation
toe walking
tone, muscle, increased
toxoplasmosis, CNS
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, intention
trichopoliodystrophy
tuberous sclerosis
tumor necrosis factor
tyrosine hydroxylase deficiency
vasculopathy
vegetarianism
ventricular enlargement
ventriculostomy
ventriculostomy, endoscopic
visual acuity, decreased
visual evoked response
visual field defect
visual fields, constricted
visual impairment
visual loss
vitamin deficiency
vomiting, episodic
vomiting, recurrent
walking, difficulty with
weakness
weakness, generalized
weakness, progressive
Werdnig-Hoffman disease
West disease
wheelchair
white hair
white matter disease
wide based gait
workup
wrist drop
x-linked hydrocephalus
Showing articles 200 to 250 of 2279 << Previous Next >>

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

A 46-year-old man with Persistent Hiccups, Cognitive Dysfunction, and Imbalance
Neurol 89:e193-e196, Lamb, C.J.,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

Maternal Use of antiepileptic Agents During Pregnancy and Major Congenital Malformations in Children
JAMA 318:1700-1701, Bromley, R.L.,et al, 2017

Paraneoplastic and Autoimmune Encephalitis
UptoDate July, Dalmau, J.,et al, 2017

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

Use of MRI in the Diagnosis of Fetal Brain Abnormalities in Utero (MERIDIAN): A Multicentre, Prospective Cohort Study
Lancet: 389:538-546,483, Griffiths, P.D.,et al, 2017

Diagnosis and Management of Dementia with Lewy Bodies
Neurol 89:88-100, McKeith, I.G.,et al, 2017

Clinicopathologic Conference, Advanced AIDS Complicated by HSV-1 Encephalopathy. Basal-Cell Carcinoma. Kaposis Sarcoma.
NEJM 376:2580-2589, Case 20-2017, 2017

An Older Man with Memory Impairment and Convulsions
BMJ 358:J2824, Zhao, X.,et al, 2017

A 54-year-old woman with Dementia, Myoclonus, and Ataxia
Neurol 89:e7-e12, Ali, F.,et al, 2017

A New Potential Biomarker for Dementia with Lewy Bodies
Neurol 89:318-326, Donadio, V.,et al, 2017

Amyotrophic Lateral Sclerosis
NEJM 377:162-172, Brown, R.H.,et al, 2017

MRI of the Swallow Tail Sign: A Useful Marker in the Diagnosis of Lewy Body Dementia?
AJNR 38:1737-1741, Shams, S.,et al, 2017

Sarcoidosis Limbic Encephalitis
Iran J Neurol 16:156-158, Toudou-Daouda, M.,et al, 2017

Clinical Presentation and Prognosis in MOG-antibody Disease: A UK Study
BRAIN 140:3128-3138, Jurynczyk, M.,et al, 2017

Clinical and Neuroimaging Features in Gorlin-Goltz Syndrome
Neurol 88:e52-e54, da paz Oliveira, G.,et al, 2017

Spontaneous Subarachnoid Haemorrhage
Lancet 389:655-666, Macdonald, R.L. & Schweizer, T.A., 2017

Characteristics in Limbic Encephalitis with Anti-Adenylate Kinase 5 Autoantibodies
Neurol 88:514-524,508, Do, L. & Chanson, E., 2017

Professional Football may be Linked to Brain Injuries Usually Seen in Boxing
BMJ 356:j811, Hawkes, N., 2017

Personality Changes, Executive Dysfunction, and Motor and Memory Impairment
JAMA Neurol 74:245-246, Lopez Chiriboga, A.S.,et al, 2017

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

A 13-year-old boy with Chronic Ataxia and Developmental Delay
Neurol 88:e116-e121, Libdeh, A.A.,et al, 2017

Sugar- and Artificially Sweetened Beverages and the Risks of Incident Stroke and Dementia
Stroke 48:1139-1146, Pase, M.P.,et al, 2017

Primary Angiitis of the Central Nervous System
Stroke 48:1248-1255, Boulouis, G.,et al, 2017

A Child with Delayed Motor Milestones and Ptosis
Neurol 88:e158-e163, Ghosh, P.S., 2017

Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
NEJM 376:1668-1678, CASE 13-2017, 2017

Clinical Manifestations of the anti-IgLON5 Disease
Neurol 88:1736-1743,1688, Gaig, C.,et al, 2017

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

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

Action Tremor, Impaired Balance, and Executive Dysfunction in Midlife
JAMA Neurol 74:603-604, Birch, R.C. & Trollor, J.N., 2017

Autoimmune Encephalitis: Pathophysiology and Imaging Review of an Overlooked Diagnosis
AJNR 38:1070-1078, Kelley, B.P.,et al, 2017

Intractable Epilepsy and Progressive Cognitive Decline in a Young Man
JAMA Neurol 74:737-740, Cohen, A.L.,et al, 2017

A 71-year-old Man with Rapidly Progressive Dementia
Neurol 86:e89-e92, Niemann, N.,et al, 2016

Pseudotumoral Presentation of Cerebral Amyloid Angiopathy-Related Inflammation
Neurol 86:912-919, Ronsin, S.,et al, 2016

Reversible Cognitive Decline Diagnosed on Ear Examination
BMJ 352:e1215, Ellis, R.J.B.,et al, 2016

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

Validation of Clinicoradiological Criteria for the Diagnosis of Cerebral Amyloid Angiopathy-Related Inflammation
JAMA Neurol 73:197-202, Auriel, E.,et al, 2016

Diagnostic Value of Prenatal MR Imaging in the Detection of Brain Malformations in Fetuses before the 26th Week of Gestational Age
AJNR 37:946-951, Conte, G.,et al, 2016

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

Patients with Rosacea have Increased Risk of Dementia
Ann Neurol 79:921-928, Egeberg, A.,et al, 2016

Atypical Presentations of Intracranial Hypotension: Comparison with Classic Spontaneous Intracranial Hypotension
AJNR 37:1256-1261, Capizzano, A.A.,et al, 2016

The Syndrome of Cutaneous Photosensitivity, Growth Failure, and Basal Ganglia Calcification
Neurol 87:e56-e57, Saini, A.G.,et al, 2016

Association of Cerebral Microbleeds with Cognitive Decline and Dementia
JAMA Neurol 73:934-943, Akoudad, S.,et al, 2016

Zika Virus as an Emerging Global Pathogen
JAMA Neurol 73:875-879, Beckham, J.D.,et al, 2016

Long-Term Outcome of Allogeneic Hematopoietic Stem Cell Transplantation in Patients with Juvenile Metachromatic Leukodystrophy Compared with Nontransplanted Control Patients
JAMA Neurol 73:1133-1140, Groeschel, S.,et al, 2016

Cortical Superficial Siderosis
Neurol 87:1110-1117, Shams, S.,et al, 2016

Neurovascular Manifestations of Hereditary Hemorrhagic Telangiectasia: A Consecutive Series of 376 Patients during 15 Years
AJNR 37:1479-1486, Brinjikji, W.,et al, 2016

A Case of Subacute Cognitive Decline in a 76-year-old Man
Neurol 87:e124-e128, MacLellan, A.,et al, 2016

Aphasic Variant of Alzheimer Disease
Neurol 87:1337-1343, Rogalski, E.,et al, 2016



Showing articles 200 to 250 of 2279 << Previous Next >>