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Differential
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abdominal x-ray
adverse drug reaction
affect, flat
agitation
akathisia
akinetic mute
aluminum
Alzheimer's disease
Alzheimer's disease, early onset
Alzheimer's disease, familial
ammonia
amyloid angiopathy, cerebral
angiitis
angiitis, granulomatous of CNS
angiitis, isolated of CNS
anorexia
anti IgLON5
antibiotics
antibodies to measles
anticonvulsants
anticonvulsants, selection of
antithyroid antibodies
aphasia
aphasia, progressive
apnea
apraxia
arm swing, reduced
arm weakness
asterixis
asymptomatic
ataxia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic gait
atypical
autoantibodies
autoimmune disease
autonomic dysfunction
Babinski sign
basal ganglia, calcification of
basal ganglia, degeneration
basal ganglia, lesion, bilateral
behavioral disorder
biologic markers
bismuth
Borrelia miyamotoi infection
bradykinesia
brain atrophy
brain biopsy
brain biopsy, false negative
brainstem, atrophy
brainstem, lesion of
bulbar palsy
cachexia
CAG repeats
calcification, intracranial
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, chest
CAT scan, emission
CAT scan, emission, abnormal
CAT scan, false negative
cataracts
central nervous system, infection of
cerebellar atrophy, primary
cerebellar degeneration
cerebellar plaques, amyloid
cerebral cortex
cerebral cortical atrophy
cerebral glucose metabolism
cerebral vasculature
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, lactic acid concentration
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, young adult
cherry red spot-myoclonus syndrome
chewing movements
children
chorea
chorea, familial
choreoathetosis
chromosomal abnormality
chronic progressive external ophthalmoplegia
cigarette smoking
Clinical Pathologic Conference(C.P.C.)
coenzyme Q10 deficiency
cognition
color vision, impaired
coma
coma, episodic
coma, sudden onset
confabulation
confusion
congenital infection, CNS
congenital paresis
cortical blindness
cranial nerve palsies
Creutzfeldt-Jakob disease, genetic
crying, pathologic
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
delirium
delusion
dementia
dementia, differential diagnosis of
dementia, familial
dementia, presenile
dementia, rapidly progressive
dementia, transmissible
dementia, treatment of
dentate nuclei, lesion of
dentatorubral-pallidoluysian atrophy
developmental milestones, loss of
diabetes mellitus
diagnostic criteria
dialysis
dialysis dementia
differential diagnosis
diplopia
doll's head maneuver
downward deviation of eyes
Dravet syndrome
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dysphasia
dyssynergia cerebellaris myoclonica
dystonia
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
electroencephalogram, triphasic delta waves
electroencephalogram, video monitoring with
electromyogram
electron microscopy
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, paraneoplastic
encephalitis, viral
encephalomyelitis
encephalomyelitis, autoimmune
encephalopathy
encephalopathy, Hashimoto's
encephalopathy, metabolic
encephalopathy, progressive
enterovirus
enterovirus infection of CNS
epidemic
episodic disorders
episodic neurologic deficits
episodic unconsciousness
extralimbic encephalitis
eye movement, disorders of
eye movement, painful
eye, pain in
faciobrachial dystonic seizure
failure to thrive
falling
familial
fasciculation
fatal familial insomnia
fatigue
fever
fine motor function, impaired
finger nose finger test
flaccid paralysis
floaters
gait disorder
gamma amino butyric acid receptor antibody
gaze palsy, vertical
gene
gene mutation
gene therapy
genetic counselling
genetic neurologic disorders
genetic testing
globus pallidus, lesion of
glutamic acid decarboxylase, antibody
glycine receptor antibodies
granular osmiphilic material
gray matter
growth retardation
hallucination
hallucination, visual
hand-foot-mouth disease
handwriting
headache
hearing loss
heart block
hemimyoclonic jerks
hemiparesis
hepatosplenomegaly
heralding manifestation
hoarseness
hyperammonemic encephalopathy
hyperreflexia
hypersomnia
hyperthyroidism
hypoglycorrhachia
hyponatremia
hypophonia
hypothermia
hypothyroidism
hypotonia
imbalance
imbalance, postural
immunohistochemistry
immunosuppression
immunotherapy
inattention
inborn errors of metabolism
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, eosinophilic intranuclear
inclusion bodies, intracytopasmic
incoordination
infection
insight, loss
insomnia
intellectual deficit
intellectual deterioration
intestinal pseudoobstruction
intracranial pressure, increased
intrauterine infection
intrauterine infection, viral of CNS
introverted
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, variant
juvenile paresis
Kearns-Sayre syndrome
lactic acidemia
Lafora body
Lafora's disease
lateropulsion
Leber's hereditary optic neuropathy
Leigh's disease
Leigh's disease, adult variety
lethargy
leucine rich glioma inactivated 1 antibodies
leukocyte enzyme abnormality
leukocytosis
leukodystrophy
leukoencephalopathy
life expectancy
limbic encephalitis
linear lesion
maculopathy
mediastinum, mass of
MELAS syndrome
memory, defect of recent
memory, impairment of
meningitis
meningitis, aseptic
meningitis, neutrophilic
meningitis, treatment of
meningoencephalitis
mental retardation
mental status, abnormal
MERRF syndrome
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
MNGIE syndrome
molecular genetics
monoparesis
mortality
motor cortex
motor neuron disease
motor neuron disease, misdiagnosis
movement disorder
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion weighted
MRI, false negative
MRI, negative
MRI, pelvis
MRI, spinal cord
MRI, sulcal hyperintensity
MRI, susceptibility weighted
multinucleated giant cell
muscle biopsy
muscle weakness
muscle weakness, proximal
mutism
myasthenia gravis, differential diagnosis
myasthenia gravis, misdiagnosis of
myelination of nervous system
myelitis
myelitis, longitudinal
myelitis, transverse
myelopathy
myoclonic jerks
myoclonus
myoclonus, cortical
myoclonus, epilepsy
myoclonus, segmental
myoclonus, stimulus sensitive
myopathy
myopathy, mitochondrial
nausea and vomiting
neck stiffness
negative
neuroendocrinology
neurologic complications
neurologic complications of, systemic cancer
neurologic disease
neurologic disease, diagnoses of
neurologic disease, multifocal
neurologic symptoms
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, ataxia, retinitis pigmentosa
neurotoxic
neurotoxin
neutropenia
New England
next-generation sequencing
nicotine
NMDA antagonists
normal
ophthalmoplegia
ophthalmoplegia, progressive external
opsoclonus
opsoclonus-myoclonus syndrome
optic atrophy
optic atrophy, hereditary
optic neuropathy
oral ulcerations
ornithine transcarbamylase deficiency
ovarian tumor
palatal myoclonus
pancytopenia
papilledema
paralysis, acute
paralysis, acute areflexic
paraparesis, spastic
parasomnia
paratonia
Parkinsonism syndrome
paroxysmal neurologic deficits
PAS positive
PAS positive material in the brain
persistent vegetative state
personality change
phonophobia
pigmentary retinopathy
pleocytosis of cerebrospinal fluid
polymerase chain reaction
polyneuropathy
pontocerebellar atrophy
potassium channel antibodies
prion disease
prognosis
progressive encephalomyelitis with rigidity syndrome
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 problems in neurologic disorders
psychomotor retardation
psychosis
psychosis, acute
ptosis
pursuit eye movements, abnormal
pyruvate metabolism, abnormality of
quadriparesis
ragged-red fibers
Ramsay Hunt syndrome
rapidly progressing neurologic illness
real-time quaking-induced conversion
REM sleep behavior disorder
remote effect of cancer on the nervous system
renal failure
respiratory failure
retinopathy
retro-orbital pain
reversible neurologic disorder
review article
rigidity
Romberg's sign
rubella encephalitis
rubella encephalitis, progressive
rubella syndrome
rubella virus
rubeola virus
saccadic eye movements, abnormal
seizure
seizure, children
seizure, drug resistance
seizure, focal
seizure, intractable
seizure, paradoxical
seizure, teenager
seizure, treatment of
sensorineural hearing loss
serologic testing
serologic testing of cerebrospinal fluid
short stature
skin, biopsy
sleep pathology and physiology
slow virus infection of CNS
slurred speech
somnolence
sonophobia
speech disorder
spinal cord
spinal cord, lesion of
spinocerebellar ataxia
spirochete infection
spongy degeneration of brain
square wave jerks
stare
staring spells
startle myoclonus
startle reaction
status epilepticus
status epilepticus, intractable
steroid
steroid therapy, CNS treatment and complications with
stiff man syndrome
strokelike episodes
stuporous
stuttering
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
sudden death
symmetric brain lesions
systemic illness
tandem gait, ataxic
tau protein
temporal lobe, lesion, bilateral
temporalis muscle wasting
teratoma, ovarian
thalamus, lesion of-bilateral
thymoma
thyroiditis
toxins, nervous system
transient neurologic deficit
transplacental virus infections
treatment of neurologic disorder
tremor
tremor, postural
tremulousness
trichopoliodystrophy
uncal herniation
unconsciousness
unconsciousness, episodic
unconsciousness, transient
Unverricht-Lundborg disease
upgaze, paralysis of
urea-cycle enzymopathies
vertigo
viral infection
viral infection, CNS
viral isolation
virus, slow
vision, blurred
vision, blurred, monocular
visual loss
visuospatial disturbance
vocalizations
walking, difficulty with
weakness
weakness, acute
weakness, focal
weakness, generalized
weight loss
wheelchair
white matter disease
white matter disease, subcortical
wide based gait
word-finding difficulty
Showing articles 750 to 800 of 5415 << Previous Next >>

Acute Maternal Confusion and Neonatal Seizure Postpartum
BMJ 364:k5399, Jakes, A.D.,et al, 2019

Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
Neurol 92:101-103, Kang, M.J.,et al, 2019

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

"Ears of the Lynx" MRI Sign is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia
AJNR 40:199-203, Pascual, B.,et al, 2019

The Dangers of PRES
Neurol 92:e282-e285, Chaterine, C.,et al, 2019

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

Paraoxysmal Tonic Upgaze in Children, Three Case Reports and a Review of the Literature
Pediatr Emer Care 35:e67-e69, Kartal,A., 2019

Neurodegeneration with Brain Iron Accumulation
AIAN 22:267-276, Batla, A. & Gaddipati, C., 2019

Human Parechovirus Meningoencephalitis: Neuroimaging in the Era of Polymerase Chain Reaction-Based Testing
AJNR 40:1418-1421, Sarma, A.,et al, 2019

Clinicopathologic Conference, Lymphocytic Choriomeningitis Virus Infection
NEJM 381:2553-2560, Case Record 40-2019, 2019

GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy
Ann Neurol 86:962-968,809, Okubo, M.,et al, 2019

Randomized Trial of Three Anticonvulsant Medications for Status Epilepticus
NEJM 381:2103-2113,2171, Kapur, J.,et al, 2019

Muscular Dystrophies
Lancet 394:2025-2038, Mercuri, E.,et al, 2019

Clinical Manifestations and Diagnosis of Nocardiosis
UptoDate May, Spelman, D., 2019

Nivolumab-Induced Autoimmune Encephalitis in Two Patients with Lung Adenocarcinoma
Case Rep Neurol Med 2018;doi:10.1155/2018/2548528, Shah, S.,et al, 2018

Human Parechovirus: An Increasingly Recognized Cause of Sepsis-Like Illness in Young Infants
Clin Microbiol Reviews 31:1-17, Olijve, L.,et al, 2018

Ophthalmic Manifestations of Giant Cell Arteritis
Rheumatology 57:ii63-1172, Vodopivec, I. & Rizzo, J.F. III, 2018

Pyruvate Dehydrogenase Deficiency (PDCD)
eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018

Progressive Multifocal Leukoencephalopathy after Treatment with Nivolumab
Emerg Inf Dis 24:1594-1596, Martinot, M.,et al, 2018

Heart Transplantation in a Patient with Myotonic Dystrophy Type 1 and End-Stage Dilated Cardiomyopathy: A Short Term Follow-up
Acta Myologica 37:267-271, Papa, A.A.,et al, 2018

Neuromyelitis Optica Spectrum Disorder (NMOSD) in a Male with Hiccups and Quadriparesis
IJCMR 5:K28-K30, Tuteja,H.S.,et al, 2018

Endoscopic Management of a Fourth Ventricular Cyst
Asian J Neurosurg 13:503-506, Jafarpour,S., et al, 2018

Tocilizumab Treatment for New Onset Refractory Status Epilepticus
Ann Neurol 84:940-945, Jun, J.,et al, 2018

Switching the Manufacturer of Antiepileptic Drugs is Associated with Higher Risk of Seizures: A Nationwide Study of Prescription Data in Germany
Ann Neurol 84:918-925, Lang, J.D.,et al, 2018

Rapid Progression of Reversible Cognitive Impairment in an 80-year-old Man
Neurol 91:1109-1113, Bouthour, W.,et al, 2018

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

Mystery Myelitis in Children
JAMA 320:2069, Kuehn, B., 2018

Progressive Gait Difficulty and Incontinence in a 40-year-old Man with HIV
Neurol 91:1065-1070, Silverman, A.,et al, 2018

An Unusual Fundus Finding in a Teenage Girl
JAMA Neurol 75:1566-1567, Filho, F.M.R.,et al, 2018

Distinctive Imaging in a Paucisymptomatic Child with Leukodystrophy
Neruol 91:e1368-e1369, Sharawat, I.K.,et al, 2018

Antiepileptic Drug Treatment After An Unprovoked First Seizure
Neurol 91:e1429-e1439,684, Bao, E.L.,et al, 2018

Selenium Toxicity Associated with Reversible Leukoencephalopathy and Cortical Blindness
JAMA Neurol 75:1282-1283, Rae, W.,et al, 2018

Subacute Progressive Ptosis, Ophthalmoplegia, Gait Instability, and Cognitive Changes
JAMA Neurol 75:1284-1285, Lin, J.,et al, 2018

Coagulation Test Interpretation in a Patient Taking Direct Oral Anticoagulant Therapy
JAMA 320:1485-1486, Sholzberg, M. & Xu, Y., 2018

Characteristics of Motor Vehicle Crashes Associated with Seizure
Neurol 91:e1102-e1111,543, Neal, A.,et al, 2018

A 58-year-old Woman with Systemic Scleroderma and Progressive Cervical Cord Compression
Neurol 91:e1262-e1264, Karschnia, P.,et al, 2018

Childhood Seizures After Phototherapy
Pediatrics 142:e20180648, Newman, T.B.,et al, 2018

Facial Myokymia and Myorhythmia in Anti-IgLON5 Disease
Neurol 91:e1659, Vetter, E.,et al, 2018

Atypical Presentation and Aggresive Evolution of Primary CNS Lymphoma (PCNSL)
Cancer Res Front 4:131-143, Topiwala, K.,et al, 2018

A 12-year-old girl with headache and change in mental status
Neurol 90:524-529, Patel, P.,et al, 2018

Young Adult with Dysphagia and Severe Weight Loss
Neurol 91:e1083-e1086, Irumudomon, O. & Ghosh, P.S., 2018

A Curable Myopathy Manifesting as Exercixe Intolerance and Respirtory Failure
Neurol 91:187-190, Silva,A.M.S.,et al, 2018

Noninvasive Vagus Nerve Stimulation as Acute Therapy for Migraine
Neurol 91:e364-e373, Tassorelli,C., et al, 2018

Andexxa-An Antidote for Apixaban and Rivaroxaban
JAMA 320:399-400, , 2018

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

Cost-Effectiveness of Left Atrial Appendage Closure With the WATCHMAN Device Compared with Warfarin or Non-Vitamin K Antagonist Oral Anticoagulants for Secondary Prevention in Nonvalvular Atrial Fibrillation
Stroke 49:1464-1470, Reddy, V.Y.,et al, 2018

Encephalitis with mGluR5 antibodies
Neurol 90:e1964-e1972, Spatola, M.,et al, 2018

An 18-year-old man with progressive headache and visual loss
Neurol 90:1076-1081, Jiang, N.,et al, 2018

Persistent Respiratory Failure Following Cardiac Arrest
Neurol 90:e2174-e2178, Fullam, T. & Sladky, J.H., 2018

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



Showing articles 750 to 800 of 5415 << Previous Next >>