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Differential
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abdominal protrusion
abortion, spontaneous
acanthocytosis
agenesis of aqueduct of Sylvius
alpha-fetoprotein
aneurysm
aneurysm, asymptomatic
aneurysm, intracranial
angiography, cerebral
aniridia
anterior tibial muscle weakness
antibodies to voltage-gated calcium channels
apraxia of eye movements
aqueduct of Sylvius, stenosis
aqueductal stenosis
areflexia
arenavirus
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, congenital
ataxia, paroxysmal
ataxia, sensory
ataxia, truncal
ataxic gait
bacterial endocarditis, neurologic manifestations of
Balint's syndrome
Bassen-Kornzweig syndrome
blindness
blindness, sudden
blood cultures
blue tongue virus
brain biopsy
brainstem, atrophy
brainstem, lesion of
bulbar palsy
bulbar palsy, progressive
calcification, intracranial
calcification, periventricular
calcium channel dysfunction
carcinoembryonic antigen
carcinoma
CAT scan
CAT scan, abnormal
CAT scan, emission
CAT scan, emission, abnormal
cataracts
cataracts, congenital
central core disease
central nervous system, infection of
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar hypoplasia
cerebellar infarction
cerebellar lesion
cerebellar vermis
cerebral cortical atrophy
cerebral embolism
cerebral infarction
cerebral infarction, hemorrhagic
cerebral ischemia
cerebral palsy
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, red cells in
cerebrovascular accident
cerebrovascular accident, bilateral
children
chloride channel dysfunction
chorea
choreoathetosis
chorioretinitis
chromosomal abnormality
chromosome 11
Clinical Pathologic Conference(C.P.C.)
Coats syndrome
Cockayne's syndrome
coma
congenital infection, CNS
congenital infection, viral
congenital malformation
congenital myopathy
congenital paresis
consanguinity
contactin associated protein like 1 antibodies
contactin associated protein like 1 auto antibodies.(CNTN1)
cornea, abnormal
cyst
cyst, parenchymal
cyst, porencephalic
cyst, subcortical
Dandy Walker malformation
Dandy Walker malformation, adult
deafmute
deafness
degenerative diseases of CNS
dementia
dental procedure, neurologic complications with
diabetes mellitus
difficulty climbing stairs
distal muscle weakness
drooling
dwarfism
dysarthria
dysphagia
dyspnea
dystonia
electroencephalogram, abnormalities of
electromyogram
electron microscopy
embolism
embolism, septic
embolism, systemic
embryogenesis
encephalitis
encephalitis, viral
encephalopathy
endocarditis
endocarditis, neurologic manifestations with
endocarditis, subacute bacterial
endovascular therapy
eye movement, disorders of
facial weakness
facial weakness, bilateral
facioscapulohumeral syndrome
familial
familial hemiplegic migraine
fever
fibrillations
foot deformity
foot drop
Friedreich's ataxia
gait disorder
gait, spastic
gammaglobulin therapy, intravenous, refractory
gargoylism
gene
gene mutation
genetic linkage
genetic neurologic disorders
Gillespie syndrome
glaucoma
growth retardation
Hallgren's syndrome
hand flapping
head circumference
headache
hearing loss
heart block
hematoma, intracerebral
hepatosplenomegaly
herpes simplex virus
histochemistry of muscle
Hurler's syndrome
hydranencephally
hydrocephalus
hydrocephalus, congenital
hydrocephalus, non-communicating(obstructive)
hydrocephalus, treatment of
hypokalemic periodic paralysis
hypotonia
immunodeficiency
immunohistochemistry
immunosuppression
incoordination
influenza A virus
intellectual deterioration
intracerebral hemorrhage
intrauterine
intrauterine infection
intrauterine infection, viral
intrauterine infection, viral of CNS
iris, abnormal
jittery baby
juvenile paresis
Kearns-Sayre syndrome
keratoconus
Laurence-Moon-Bardet-Biedl syndrome
leukemia
lid closure, weakness of
lymphocytic choriomeningitis
lymphoma
maculopathy
malformation, CNS, congenital
malignant hyperpyrexia
Marinesco-Sjogren syndrome
mental retardation
microcephaly
migraine
migraine, hemiplegic
mimics
misdiagnosis
mitral valve lesion
mitral valve prolapse
mitral valve regurgitation
monoclonal gammopathy
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
mucopolysaccharidoses
multiple system atrophy
mumps virus
muscle biopsy
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, differential diagnosis of
muscular dystrophy, facioscapulohumeral
myasthenic syndrome
mycotic aneurysm
myelomalacia
myeloschisis
myoclonic jerks
myoclonus, epilepsy
myopathy
myopia
myotonia congenita
nausea and vomiting
neck pain
nemaline rod myopathy
nemaline rod myopathy, adult onset
neonatal infection, viral
neuritis
neurocutaneous disease
neuroendocrinology
neurologic disease
neurologic disease, diagnoses of
neurologic signs
neuropathology
neuropathology, brain
neuropathy
neuropathy, autoimmune
nodopathy, autoimmune
nystagmus
obesity
occipital lobe, infarction
occipital lobe, infarction, bilateral
ocular motility, disorders of
ocular myopathy
old age, neurology of
optic ataxia
pachygyria
pain, neuropathic
papilledema
paramyotonia congenita
paraspinal muscle
paraspinal muscle weakness
parietal lobe, infarction
paroxysmal neurologic deficits
parvovirus
pathology
periodic paralysis
personality change
pleocytosis of cerebrospinal fluid
polydactyly
Poretti-Boltshauser syndrome
posterior cerebral artery occlusion
posterior fossa, lesion of
potassium channel antibodies
potassium channel dysfunction
progeria
prognosis
progressive neurologic disorder
pseudoaneurysm
pseudoretinitis pigmentosa
psychiatric disorder
psychomotor retardation
radiation hypersensitivity
rapidly progressing neurologic illness
respiratory failure
retinal degeneration
retinitis pigmentosa
retinopathy
review article
rituximab
rubella encephalitis
rubella encephalitis, progressive
rubella syndrome
rubella virus
rubeola virus
schizophrenia
seizure
serologic testing
serologic testing of cerebrospinal fluid
shunt procedure, ventricular
shunt procedure, ventriculo-peritoneal
simultanagnosia
skin, lesions in neurologic disorders
sloped shoulders
slow virus infection of CNS
sodium channel dysfunction
spasticity
Spielmeyer Vogt syndrome
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 6
standing difficulty
stem cell transplantation
stooped posture
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subarachnoid hemorrhage
superior cerebellar artery infarction
sweating
telangiectases
teratogenesis
teratogenesis, viral
thrombectomy
thyroiditis
titubation
transplacental virus infections
transverse smile
treatment of neurologic disorder
unconsciousness
urinary incontinence
Usher's syndrome
vasculitides
vertigo
viral infection
viral infection, CNS
viral isolation
virus, slow
visual field defect
visual fields, constricted
visual loss
walking, difficulty with
weakness
weakness, progressive
weakness, proximal
weight loss
wheelchair
white matter disease
wide based gait
winging of scapula
Showing articles 50 to 100 of 2289 << Previous Next >>

Unmasking Cerebrotendinous Xanthomatosis, Clinical Recognition of a Treatable Cause of Progressive Ataxia
Neurol 105:e214099, Mizutani,H.,et al, 2025

Clinicopathologic Features, Pathogenesis, and Treatment of Monoclonal Gammopathy-Associated Myopathies
Neurol 105:213101, Soontrapa,P.,et al, 2025

A 58-Year-Old Man With Resting tremor, Bradykinesia, and Distal Numbness
Neurol 105:e214183, Costa,R., et al, 2025

A 59-Year-Old Female Patient with Urinary Dysfunction and Lightheadedness
Neurol 105:e214233, Bu,S.,et al, 2025

A 38-Year-Old Man With Involuntary Jerk-Like Movements and Ataxia
Neurol 105:e214381, Gomez,A.C.et al, 2025

Multivessel Cerebral Occlusion in Noonan Syndrome
Stroke 56:e359-362, deLima, M.M.,et al, 2025

A 19-Month Old Girl with Infantile-Onset Myopathy and White Matter Changes
Neurol 102:e209258, Lail,G.,et al, 2024

Posttransplant Anti-GABAA Receptor Antibody-Associated Autoimmune Encephalitis
Neurol 102:e209245, Togni,C.L.,et al, 2024

Anti-NMDA Receptor Encephalitis Presenting with Cerebellitis in a Pediatric Patient
Neurol 102:e209259, Moehlman,M. & Kornbluh,A.B., 2024

Diffusely Enhancing Lesions on MRI in DPPX Antibody-Associated Encephalitis
JAMA Neurol 8:418-419, Liu,M.,et al, 2024

A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
Neurol 102:e209358, Barbosa,A.R.,et al, 2024

Clinicopatholigic Conference, Rheumatoid Arthritis with Vasculitis Causing A Confluent Mononeuritis Multiplex
NEJM 390:1312-1322, Case 11-2024, 2024

Clinicopathological Conference, Glutamic Acid Decarborylase 65 Autoantibody-Associated Stiff-Person Syndrome
NEJM 390:1712-1719, Case 14-2024, 2024

A 24-Year-Old Man with Spastic Ataxia and Hypodontia
JAMA Neurol 81:658-659, Marien,L.,et al, 2024

Congenital and Acquired Chiari Syndrome
NEJM 390:2191-2198, Friedlander,R.M., 2024

Vitamin B12 Deficiency:NICE Guideline Summary
BMJ 385:q1019, q1262, Sands,T.,et al, 2024

Expanding Clinical Spectrum an Anti-GQ1b Antibody Syndrome, A Review
JAMA Neurol 81:762-770, Lee,S-U.,et al, 2024

Infective Endocarditis
Lancet 404:377-392, Li,M.,et al, 2024

Ptosis as Partial Oculomotor Nerve Palsy Due to Compression by Infundibular Dilatation of Posterior Communicating Artery, Visualized with Three-Dimensional Computer Graphics:Case Report
Neurol Med Chir (Tokyo) 54:214-218, Fukushima,Y.,et al, 2024

Recurrent Rhombencephalitis Associatedwith Anti-GAD65 Antibody
Neurol 102:e208040, Alferes,A.R.,et al, 2024

Supratentorial Lymphocytic Inflammation with Parenchymal Perivascular Enhancement Responsive to Steroids:A Potentially Overlooked Diagnosis
Ann Neurol 95:407-409, Tsibonakis,A.,et al, 2024

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

Clinical Neurologic Features and Evaluation of PTEN Hamartoma Tumor Syndrome, A Systematic Review
Neurol 103:e209844, Dhawan,A.,et al, 2024

A 22-Year-Old Woman with Episodic Weakness and Jaundice
Neurol 103:e210018, Rathinasbapathi,M.,et al, 2024

Powassan Virus Encephalitis: A Tertiary Center Experience
Clin Inf Dis 78:80-89, Mendoza,M.A.,et al, 2024

A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
Neurol 103:e210046, Panigrahi,B.,et al, 2024

A 35-Year-Old Woman with Personality Change and Gait Impairment
Neurol 104:e210252, Bernardes,C.,et al, 2024

Clinical Manifestations and Diagnostic Challenges in a 16-Year-Old With Early-Onset Ataxia
Neurol 104:e210253, Chadha,D.,et al, 2024

Cerebral and Retinal Infarction in Bicuspid Aortic Valve
J Am Heart Assoc 12:e028789, Huntley,G.D.,et al, 2023

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

An 82-Year-Old Woman with Subacute Ophthalmoparesis and Ataxia
Neurol 101:e570-e575, Rodrigo-Gisbert,M.,et al, 2023

A 67-YEar-Old Man with Multiple Intracranial Lesions
Neurol 101:e845-e851, Ngo,A.,et al, 2023

Wernekinck Commissure Syndrome
Radiopaedia doi.org/10.53347/rlD-85274, Aug, Deng,F.,et al, 2023

Neurologic Complications of Babesiosis, United States, 2011-2021
Emerg Inf Dis 29:1127-1135, Locke,S.,et al, 2023

A 17-Year-Old Girl with Progressive Cognitive Impairment
Neurol 101:e1466-e1472, Zhao,B.,et al, 2023

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

Shrimp Sign in Ataxic Cerebellar Progressive Multifocal Leukoencephalopathy
Neurol 101:918-919, Varela,F.J.,et al, 2023

Pachymeningitis and Aortitis as the Initial Presentation of Granulomatosis with Polyangiitis
Neurol 101:979-980, Li,X.,et al, 2023

Subarachnoid Hemmorhage During Pregnancy and Puerperium:A Population-Based Study
Stroke 54:198-207, Korhonen,A., et al, 2023

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

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

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

Occult Breast Cancer with Anti-Ri Antibody Positivity and Pontine Hot Cross Bun Sign
JAMA Neurol 80:207-208, Liu,Y.,et al, 2023

Brain Calcification in a Young Woman With Seizures, Explore the Rare Differentials
Neurol 100:397-398, Menon,B.,et al, 2023

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

Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
Neurol 100:766-783, Manini,A.,&Pantoni,L., 2023

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

Miller Fisher Syndrome and Acute Motor and Sensory Axonal Neuropathy (AMSAN) Variant Guillain-Barre Overlap Syndrome (MFS/AMSAN-GBS) After Upper Respiratory Tract Infection (URTI)
Acta Sci Clin Case Reports 3:19-24, Chau,T.C. & Muhamad,N.A.N., 2022



Showing articles 50 to 100 of 2289 << Previous Next >>