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acoustic nerve
adolescent medicine
advances in neurology
alien hand syndrome
alpha-fetoprotein
alternating hemiplegia
alternating hemiplegia of childhood
AMPA receptor antibodies
anosmia
anti GQ1b IgG antibody
anti IgLON5
anticholinergic drugs
anxiety
aphasia
aphasia, progressive, primary
aphonia
applause sign
apraxia
apraxia of eye movements
areflexia
arm swing, reduced
aspiration
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic-dystonia syndromes
athetosis
ATP1A3 gene
attention span
autoantibodies
autoimmune basal ganglia encephalitis
autonomic dysfunction
Babinski sign
basal ganglia, calcification of
basal ganglia, degeneration
basilar impression
behavioral disorder
biologic markers
biopterin deficiency
bladder dysfunction
blepharospasm
bradykinesia
brainstem, atrophy
brainstem, lesion of
bruxism
bulbar palsy
calcitonin
carbamazepine
carcinoembryonic antigen
carcinoma
cardiomyopathy
cataplexy
cataracts
central hypoventilation
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar degeneration
cerebral cortical atrophy
cerebral palsy
cerebral palsy, associated problems with
cerebrovascular accident
cerebrovascular accident, young adult
children
chorea
choreoathetosis
chorioretinitis
chromosomal abnormality
chromosome 11
chromosome 14
chromosome 20
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
cognition
cogwheel rigidty
comorbidities
compression fracture
conjugate gaze, forced
conversion reaction
cortical-basal ganglionic degeneration
cranial neuropathy, multiple
crying, pathologic
cultured skin fibroblasts
degenerative diseases of CNS
delay in diagnosis
dementia
developmental milestones, loss of
developmental retardation
dexterity, impaired
diabetes insipidus
diabetes mellitus
diagnostic criteria
differential diagnosis
diplopia
diurnal variation
dopa responsive dystonia
downward gaze
drooling
dysarthria
dysarthria-clumsy hand syndrome
dyskinesia
dysmetria
dysphagia
dyspraxia
dystonia
dystonia musculorum deformens
dystonia, cervical
dystonia, face
dystonia, focal
dystonia, psychogenic
dystonia, treatment of
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, brainstem
encephalitis, paraneoplastic
encephalopathy
enzyme, defect
equinovarus
exercise
exercise-induced neurologic dysfunction
exome sequencing
exophthalmus
eye movement, disorders of
facial nerve palsy
falling
familial
fine motor function, impaired
foam cells
foot deformity
frontal behavioral spatial syndrome
gait disorder
gait, apraxic
gamma amino butyric acid receptor antibody
gammaglobulin therapy, intravenous
gangliosidosis GM1
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
glabellar sign
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glutamic acid decarboxylase, antibody
grasp reflex
grimacing
growth retardation
Hallervorden Spatz disease
Hallervorden Spatz disease, late onset
hand weakness
hands, fisted
head circumference
headache
hearing loss
heart block
hemidystonia
hemifacial spasm
hemiplegia
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatosplenomegaly
HLA
hoarseness
Hodgkin's disease
hydrocephalus
hyperreflexia
hypometric saccades
hypophonia
hyposmia
hypotonia
ideomotor apraxia
imbalance
imbalance, postural
immunodeficiency
immunosuppression
immunotherapy
inattention
inclusion bodies, intranuclear
incontinence, fecal
incoordination
insomnia
intellectual deficit
intellectual deterioration
intestinal pseudoobstruction
iron, brain
Jakob-Creutzfeldt disease
jaundice
Kayser-Fleischer ring
Kearns-Sayre syndrome
laughing, pathologic
L-dopa
Leber's hereditary optic neuropathy
leg weakness, bilateral
Leigh's disease
leucine rich glioma inactivated 1 antibodies
leukemia
limbic encephalitis
lipid storage disorder of CNS
liver disease
low back pain
lymphoma
macular degeneration
masked facies
MELAS syndrome
memory, defect of recent
memory, impairment of
meningitis
meningitis, carcinomatous
mental retardation
mental status, abnormal
MERRF syndrome
microcephaly
midbrain
midbrain, atrophy
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
molecular genetics
monoclonal antibodies
mortality
motor dysfunction
movement disorder
movement disorder, extrapyramidal
movement disorder, hyperkinetic
movement disorder, psychogenic
movement disorder, treatment of
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, eye of tiger sign
MRI, mouse ears
MRI, negative
MRI, paramagnetic effect
MRI, spine
multiple system atrophy
muscle spasm, face
myelopathy
myelopathy, chronic progressive
myoclonic jerks
myoclonus
myopathy
myopathy, mitochondrial
neurocutaneous disease
neuroendocrinology
neurofibrillary degeneration
neurologic complications of, systemic cancer
neurologic disease
neurologic disease, diagnoses of
neurologic disease, diagnoses of, clinical bedside
neurologic disease, tempo
neurologic evaluation
neurologic examination
neurologic signs
neurologic symptoms
neurologic symptoms, unexplained
neuronal intranuclear inclusion disease
neuroophthalmology
neuropathology
neuropathy
Niemann-Pick disease
NMDA antagonists
numb clumsy hands syndrome
nystagmus
nystagmus, monocular
ocular motility, disorders of
opened mouth
ophelia syndrome
ophthalmoplegia
optic atrophy
optic atrophy, unilateral
optic neuropathy
optokinetic nystagmus, abnormal
Paget's disease
Paget's disease, psychosis in
Paget's disease, spinal cord problem in
pain
palilalia
pancytopenia
PANK2 mutation
paraparesis
parasomnia
Parkinson disease
Parkinson disease, axial symptoms
Parkinson disease, differential diagnosis of
Parkinson disease, dystonia with
Parkinson disease, juvenile
Parkinson disease, L-dopa nonresponsive
Parkinson disease, treatment of
Parkinson disease, tremor, absence of
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
pathology
pediatric autoimmune neuropsychiatric disorders associated with streptococcal infection
penguin silhouette sign
personality change
personality disorder
pigmentary retinopathy
pitfalls
pleocytosis of cerebrospinal fluid
postural abnormality
potassium channel antibodies
practice guidelines
precipitating factors
PRKN gene
procyclidine
progeria
prognosis
progressive neurologic disorder
progressive supranuclear palsy
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychomotor retardation
psychosis
ptosis
pull test
radiation hypersensitivity
radiculopathy
ragged-red fibers
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
recurrent
Red flags
release phenomena
respirations in CNS disease
retinal artery occlusion
retinal hemorrhages
retinopathy
retrocollis
Rett's syndrome
reversible neurologic disorder
review article
rigidity
rigidity, axial
risk factors
rituximab
root lesion, nerve
running
saccadic eye movements, abnormal
salivation, excessive
screening
seizure
sensorineural hearing loss
sensory loss, cortical
sequencing difficulty
serologic testing
serologic testing, false negative
seronegative
short stature
sinemet
single photon emission computed tomography
skin, lesions in neurologic disorders
skull x-ray, abnormal
sleep apnea, obstructive
sleep pathology and physiology
slit lamp examination
speech disorder
spinal cord
spinal cord, compression of
spinal cord, lesion of
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 28
spinocerebellar degeneration
splenomegaly
stare
status epilepticus
steroid
steroid therapy, CNS treatment and complications with
striatal encephalitis
suck reflex
superior orbital fissure syndrome
swallow evaluation
tau protein
tauopathy
telangiectases
tetrahydrobiopterin
toe walking
tonic foot response
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, intention
tremor, jaw
tremor, postural
tremor, psychogenic
trigeminal neuralgia
tripping
upgaze
upgaze, paralysis of
urinary incontinence
vertebral-basilar insufficiency
vision, blurred
visual symptoms
vocal cord paralysis
walking
walking frame
walking, difficulty with
weight loss
wheelchair
wide based gait
Wolfram syndrome
Showing articles 850 to 900 of 8642 << Previous Next >>

MR Imaging Patterns and Prognosis in Powassan Virus Encephalitis
Neurologist doi.10.1097/NRI.0000000000000533, Finelli,P.F., 2023

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

Guidelines in Action: Worse Headache of Life...Yesterday
Stroke 54:e488-e491, Albin,C.S.W., 2023

Movement Disorders in Patients with Genetic Developmental and Epileptic Encephalopathies
Neurol 101:e1884-e1892, van der Veen,S.,et al, 2023

A 26-Year-Old Woman with Recurrent Pain, Weakness, and Atrophy in Bilateral Upper Limbs During Pregnancy and Puerperium
Neurol 100:631-637, Zeng,T.f.,et al, 2023

A 23-Year-Olf Man With Progressibe Asymmetric Weakness and Numbness
Neurol 100:674-682, Kaplan,E.H.,et al, 2023

Cutaneous a-Synuclein Signatures in Patients with MultipleSystem Atrophy and Parkinson Disease
Neurol 100:e1529-e1539, Gibbons,C.,et al, 2023

Clinicopathologic Conference, Hypocalcemic Myopathy Due to Hypoparathyroidism
NEJM 388:1513-1520, Case 12-2023, 2023

A 25-Year-Old Woman With Eye Swelling and HEadache
Neurol 100:879-883, Hehir,A.,et al, 2023

Lead Poisoning
NEJM 388:e63, Dhar,S. & Garg,D., 2023

Neonatal Seizures
NEJM 388:1692-1700, Ropper.A.H., 2023

Pathogenesis and Clinical Manifestations of IgG4-Related Disease
WWW.UptoDate.com, April, Moutsopoulos,H.M.,et al, 2023

Cavernous Sinus Thrombosis
StatPearls PMID:28846357, Plewa,M.C.,et al, 2023

Clinicopathologic Conference, Functional Vitamin B12 Deficiency from Use of Nitrous Oxide
NEJM 388:1893-1900, Case 15-2023, 2023

A 47-Year-Old Man With an Upper Respiratory Infection, Acute Confusion, Dysarthria, and Ataxia
Neurol 100:978-983, Kubicki,K.,et al, 2023

Carotid Computed Tomography Crescent Sign
Stroke 54:e235-e236, Zedde,M.,et al, 2023

Tersons Syndrome
NEJM 388:e79, Sherman,S.V., 2023

Clinicopathologic Conference, Facioscapulohumeral Muscular Dystrophy
NEJM 388:2379-2387, Case 19-2023, 2023

Antiplatelet Therapy or Not for Asymptomatic/Incidental Lacunar Infarction
Stroke 54:1954-1959, Bilski.A.,et al, 2023

Reversible Splenial Lesion Syndrome in a 43-Year-Old Man with Intraceebral Hemorrhage
Neurol 101:e101-e102, Yang,T.,et al, 2023

A 40-Year-Old Woman Presenting with Encepatholopathy and Paraparesis
Neurol 101:e94-e98, AlSabah,A.,et al, 2023

Paroxysmal Exercise-Induced Dyskinesias Due to Pyruvate Dehydrogenase Deficiency
Neurol 101:46-49, deGusmao,C.M.,et al, 2023

Risk of Parkinson Disease Among Service Members at Marine Corps Base Camp Lejeune
JAMA Neurol 80:673-681, Goldman,S.M.,et al, 2023

A Young Adult Man with Cognitive Changes, Gait Difficulty, and Renal Insufficiency
Neurol 100:206-212, Stamm,B.,et al, 2023

A Young Man With Subacute Onset of Spastic Paraparesis
Neurol 100:199-205, Rossi,S.,et al, 2023

Cashew Nut Sign:A Concave Parenchymal Hemorrhage Caused by Cerebral Venous Thrombosis
Stroke 54:e38-e39, Schlechter,M.,et al, 2023

Phase 2 Trial of Difelikefalin in Notalgia Paresthetica
NEJM 388:511-517, Kin,B.S.,et al, 2023

Rapidly Progressive Dementia in a Man With HIV Infection and Undetectable Plasma Viral Load
Neurol 100:344-348, Chishimba,L.C.,et al, 2023

Progressive Camptocormia with Head Drop and Dysphagia
JAMA Neurol 80:209-210, El-Wahsh,S., et al, 2023

Transient Global Amnesia
NEJM 388:635-640, Ropper,A.H., 2023

Clinicopathologic Conference, Paraneoplastic Vasculitis of the Central Nervous System
NEJM 388:747-757, Case 6-2023, 2023

Neuroimaging Features of Biotinidase Deficiency
AJNR 44:328-333, Biswas,A.,et al, 2023

A 60-Year Old Man with Asymmetric Weakness and Persistent Fever
Neurol 100:530-536, Zheng,Y.,et al, 2023

Severe Cervicodynia in a Patient With Pustules on the Palms
JAMA Neurol 80:323-324, Zia,C. & Lv,Y., 2023

Focusing on the Eye Signs of Alport Syndrome in a 40-Year-Old Man Who Previously Had a Kidney Transplant and Hearing Loss
Lancet 401:e2, Kovalchuk,B. & Khoramnia,R., 2023

Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023

Cauda Equina Syndrome in the Third Trimester
BMJ 395:e078711, Ugas,M.A. & Ashkan,K., 2023

Neurosyphilis Presenting as Syndrome of Limbic Encephalitis Mimicking Herpes Simplex Virus Neuro-Infection Diagnosed Using CXCL13 Point-of-Care Assay-Case Report
Brain Sci 13:503, Maresova,E.,et al, 2023

Overlapping Anti-NMDAR Encephalitis and Multiple Sclerosis: A Case Report and Literature Review
Front Immunol doi:10.3389/Fimmun.2023.1088801, Liu,P.,et al, 2023

Mild Encephalitis/Encephalopathy with a Reversible Splenial Lesion Associated with Systemic Mycoplasma Pneumoniae Infection in North America: A Case Report
J Med Case Reports doi:10.1186/s13256-022-03299-6, Talukder,N.T.,et al, 2022

Postpartum Posterior Reversible Encephalopathy Syndrome Secondary to Preeclampsia and Cerebrospinal Fluid Leakage:A Case Report and Literature Review
World J Clin Cases 10:10332-10338, Wang,Y. & Zhang, Q., 2022

Imaging Findings in Children Presenting with CNS Nelarabine Toxicity
AJNR 43:1802-1809, Serrallach,B.L.,et al, 2022

Amyotrophic Lateral Sclerosis
Lancet 400:1363-1380, Feldman, E.L.,et al, 2022

An 80-Year-Old Woman with a Homonymous Hemianopsia
Neurol 99:713-717, Tajfirouz, D.,et al, 2022

Major Neurological Deficit Following Neck Hyperextension During Dental Treatment
Neurologist 6:361-363, El-Hajj, V.G.,et al, 2022

Bilateral Hypertrophic Olivary Degeneration as a Paraneoplastic Syndrome of a Poorly Differentiated Carcinoma of the Upper Gastrointestinal Tract
Neurologist 6:357-360, Daneshmand, A.,et al, 2022

Clinicopathologic Conference, Cotards Syndrome, Catatonia, Depression and Coronavirus Disease 2019
NEJM 387:1795-1802, , 2022

Extracranial Etiology of Acute Onset Ataxia and Weakness
Neurol 99:898-899, Nordli,D.,et al, 2022

New Onset Focal Tremor in Patient with Human Immunodeficienccy Virus
Clin Infect Dis 75:1861-1863, Finelli,P.F., 2022

Spinal Muscular Atrophy
UpToDate, Oct, Bodamer,O.A., 2022



Showing articles 850 to 900 of 8642 << Previous Next >>