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Differential
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aminoacidopathies
aminoacidurias
aneurysm
aneurysm, intracranial
anosognosia
aphasia
aphasia, global
aphasia, transcortical
areflexia
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
ataxic-dystonia syndromes
athetosis
Babinski sign
basal ganglia, calcification of
basal ganglia, lesion of
bilirubin encephalopathy
blindness, sudden
brain atrophy
brain damage
brainstem, lesion of
breast feeding
bulbar palsy
CAG repeats
CAT scan
CAT scan, abnormal
cerebellar ataxia, hereditary
cerebellar lesion
cerebrospinal fluid, glycine
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, infancy and childhood
cerebrovascular accident, mimics
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
cherry red spot
cherry red spot-myoclonus syndrome
children
choreoathetosis
chromosomal abnormality
chromosome 6
Clinical Pathologic Conference(C.P.C.)
congenital myasthenic syndromes
conjugate gaze, forced
cortical blindness
cranial nerve palsies
cranial neuropathy
cranial neuropathy, multiple
cry, abnormal
cry, high-pitched
degenerative diseases of CNS
dementia
dementia, rapidly progressive
developmental milestones, loss of
developmental retardation
dinitrophenylhydrazine(D.N.P.H.)reaction
downward gaze, paralysis of
dysarthria
dyspnea
dystonia
electroencephalogram, abnormalities of
electromyogram
encephalopathy
encephalopathy, neonatal
encephalopathy, progressive
epidemiology of neurology
exercise intolerance
exome sequencing
eye movement, disorders of
facial weakness
facial weakness, bilateral
falling
false negative
familial
fever
floppy infant
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic neurologic disorders
genetic testing
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
glycine
Guillain Barre syndrome, infantile and childhood form
head injury
headache
hearing loss
hemiparesis
hemorrhage, thalamic
hoarseness
hydrocephalus
hyperbilirubinemia
hyperbilirubinemia, CNS abnormality after
hypophonia
hyporeflexia
imbalance
impulsivity
intellectual deficit
intellectual deterioration
internuclear ophthalmoplegia, bilateral
intracerebral hemorrhage
intracerebral hemorrhage, location of
intracerebral hemorrhage, volume
intraventricular hemorrhage
jaundice
kernicterus
lactic acidemia
leucine
lid closure, weakness of
lysosomal storage disease
maple syrup urine disease
MELAS syndrome
meningitis
meningitis, aseptic
mental retardation
metabolic disorder, primary
migraine
miosis
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
moro reflex
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, disappearing lesion on
MRI, high signal foci on
MRI, high signal intensity of basal ganglia
muscle atrophy, progressive
muscle biopsy
muscle weakness
muscle weakness, proximal
myasthenia gravis
myasthenia gravis, congenital
myasthenia gravis, familial incidence of
myopathy
myopathy, mitochondrial
nasal speech
nausea and vomiting
neglect
neoplasm, primary of CNS
nerve conduction studies
neurologic examination, focal
neuromuscular junction
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathology
neurotoxic
neurotoxin
nystagmus
ocular motility, disorders of
oculogyric crisis
ophthalmoplegia
ophthalmoplegia, head injury causing
ophthalmoplegia, neonatal
ophthalmoplegia, progressive external
ophthalmoplegia, total
ophthalmoplegic migraine
opisthotonus
personality change
premature infant
prevention of neurologic disorders
prognosis
progressive neurologic disorder
proteinuria
psychosis
ptosis
ptosis, bilateral
pupil, abnormality in neurologic disorders
pyramidal tract dysfunction
ragged-red fibers
rapidly progressing neurologic illness
renal failure
retinal degeneration
retropulsion
review article
seizure
seizure, children
sensorimotor stroke
sensorineural hearing loss
setting sun phenomena
short stature
skew deviation
spinal cord, lesion of
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 28
spinocerebellar degeneration
strokelike episodes
subthalamic nucleus
suck, poor
temporal lobe, lesion
term infant
thalamic aphasia
third nerve palsy
third nerve palsy, childhood
third nerve palsy, congenital
third nerve palsy, cyclic
transverse smile
treatment of neurologic disorder
tremor
trinucleotide repeats
upgaze, paralysis of
ventricular enlargement
vertical gaze
viral infection
viral infection, CNS
visual acuity, decreased
visual fields, constricted
visual loss
walking, difficulty with
weakness
weakness, fatiguable
weakness, progressive
weakness, proximal
weakness, rapidly progressive
weight loss
wheelchair
wide based gait
Showing articles 50 to 100 of 1755 << Previous Next >>

Unpacking the CNS Manifestations of Epstein-Barr Virus:An Imaging Perspective
AJNR 44:1002-1008, Soni,N.,et al, 2023

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

Progressive Cranial Neuropathy
JAMA Neurol 80:1375-1376, Buchberger,D.S.,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

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

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

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

Salt and Pepper Sign, PLNTY for Drug-Resistant Epilepsy
Neurol 100:791-795, Paredes-Aragon,E.M.,et al, 2023

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

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

Diplopia and Ptosis in an Older Woman
JAMA Neurol 79:947-948, Stallworth, J.Y.,et al, 2022

A 51-Year-Old Woman with Diplopia and Headache
Neurol 99:524-530, Kathuria, G.,et al, 2022

Fragile X-Associated Tremor or Ataxia Syndrome in a Patient with Difficulty Walking, Falls, a Tremor, and Erectile Dysfunction
Lancet 400:1144, Sabino de Oliveira, D.,et al, 2022

Clinical Manifestations and Diagnosis of Listeria Monocytogenes Infection
UptoDate Aug, Gelfand, M.S.,et al, 2022

Spontaneous Intracerebral Hemorrhage
NEJM 387:1589-1596, Sheth, K.N., 2022

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

Updates on Sturge-Weber Syndrome
Stroke 53:3769-3779, Yeom,S.E.&Comi,A.M., 2022

Infantile and Childhood Hydrocephalus
NEJM 387:2067-2073, Whitehead,W.E.&Weiner,J.L., 2022

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

The Phenotypic Continuum of ATP1A3-Related Disorders
Neurol 99:e1511-e1526, Vezyroglou,A., et al, 2022

A 67-Year-Old Woman with Progressive Diplopia, Vertigo, and Ataxia
Neurol 98:e669-e674, Sakoda, M.,et al, 2022

Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
NEJM 386;674-687, Case 5-2022, 2022

Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
UptoDate 2022 Jan, Darras, B.T., 2022

A Dizzy Architect
Neurol 98:543-549, Scutelnic, A.,et al, 2022

Multicenter Consensus Approach to Evaluation of Neonatal Hypotonia in the Genomic Era
JAMA Neurol 79:405-413, Morton, S.U.,et al, 2022

Brain Tumors in Children
NEJM 386:1922-1931, Cohen, A.R., 2022

Thalamus L-Sign: A Potential Biomarker of Neonatal Partial, Prolonged Hypoxic-Ischemic Brain Injury or Hypoglycemic Encephalopathy
AJNR 43:919-925, Misser, S.K.,et al, 2022

Unilateral Leukoencephalopathy Revealing Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
Ann Neurol 91:889-890, Gollion, C.,et al, 2022

Case Report of Lambl Excrescences in a Pediatric Patient with Multifocal Strokes
Neurol 99:73-76, Robertson, D.M.,et al, 2022

Bilateral Complete Ophthalmoplegia in a 50-Year-Old Man
JAMA Neurol 79:724-725, Arora, N.,et al, 2022

A 67-Year-Old Woman with Abdominal Pain, Constipation, and Urinary Retention
Neurol 99:117-122, Hanna, S.S.,et al, 2022

Neuroimaging Findings in Parechovirus Encephalitis: A Case Series of Pediatric Patients
Pediatr Neurol 130:41-45, Tierradentro-Garcia, L.O.,et al, 2022

A Rare Treatable and Under Recognized Cause of Recurrent Convexity Subarachnoid Hemorrhage:Lupus anticoagulant Hypoprothombinemia Syndrome
Ann Indian Acad Neurol 24:986-989, Jain, S.,et al, 2021

When Should a Brain MRI Be Performed in Children with New-Onset Seizures? Results of a Large Prospectice Trial
AJNR 42:1645-1701, Hourani, R.,et al, 2021

Molecular Diagnostic Yield of Exome Sequencing in Patients with Cerebral Palsy
JAMA 325:467-475, Moreno-De-Luca, A.,et al, 2021

A Middle-aged Woman with Severe Scoliosis and Encephalopathy
JAMA Neurol 78:251-252, Mohan, G.,et al, 2021

A 48-Year-Old Man Presenting With Diplopia
Neurol 96:399-405, Pehere,N.K.,& Gofer,K., 2021

A 7-Year-Old Boy with Acute-Onset Altered Mental Status
Neurol 96:e2774-e2778, Wong, G.J.,et al, 2021

Vagus Nerve Stimulation and Seizure Outcomes in Pediatric Refractory Epilepsy
Neurol 96:1041-1051, Jain, P. & Arya, R., 2021

A 71-Year-Old Man with Horizontal Gaze Palsy, Anarthria, and Quadriparesis
Neurol 96:1146-1150, Cheema, I.,et al, 2021

Imaging Patterns Characterizing Mitochondrial Leukodystrophies
AJNR 42:1334-1340, Roosendaal, S.D.,et al, 2021

Nonalcoholic Wernicke Encephalopathy
Neurol 97:e1541-e1542, Hansen, G.,et al, 2021

Hypotonia and Delayed Teeth Eruption in a 2-Year-Old Girl
Neurol 97:875-878, Dinov, D.,et al, 2021

A 28-Year-Old Woman with Vision Loss and an Unusual Gait
Neurol 97:e1860-e1865, Dohlman, J.C.,et al, 2021

"Disappearing Infarct" Is Late-Onset MELAS
Ann Neurol 90:1001-1002, Landis,T.M.,et al, 2021

Congenital Cytomegalovirus Infection
BMJ 373:m1212, Pesch, M.H.,et al, 2021

The Tolosa-Hunt Syndrome
NJJP 71:577-582, Kline,L.B. & Hoyt,W.F., 2021

Review of Vitamin B12 Deficiency in Pregnancy:A Diagnosis Not to Miss as Veganism and Vegetarianism Become More Prevalent
Eur J Haematol 106:450-455, Rashid,S.,et al, 2021



Showing articles 50 to 100 of 1755 << Previous Next >>