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Differential
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abiotrophy
acetylcholinesterase
acetylcholinesterase deficiency
Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
affect, inappropriate
alcohol, neurologic complications with
alcoholism
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, bulbar
amyotrophic lateral sclerosis, juvenile
antibiotics
antibiotics, neurologic complications with
antitoxin
arteriopathy
autoimmune disease
autonomic dysfunction
basal ganglia, infarction
basal ganglia, lesion of
blindness
bone marrow transplantation
botulinum toxin
botulism
botulism antitoxin
botulism immune globulin
botulism, infant
brainstem, dysfunction
brainstem, lesion of
bulbar palsy
bulbar palsy, acute
bulbar palsy, childhood
bulbar palsy, progressive
calcification, intracranial
CAT scan
CAT scan, abnormal
central pontine myelinolysis
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebral cortical atrophy
cerebral infarction, subcortical
cerebrovascular accident
cerebrovascular accident, familial occurrence
cerebrovascular accident, multiple
cerebrovascular accident, neonatal
cerebrovascular accident, recurrent
cerebrovascular accident, young adult
cerebrovascular disease
children
chromosomal abnormality
chromosome 19
Clinical Pathologic Conference(C.P.C.)
collagen vascular disease
confusion
congenital bilateral perisylvian syndrome
congenital myasthenic syndromes
cortical blindness
cry, abnormal
cry, weak
crying
crying, pathologic
cultured skin fibroblasts
deafness
decerebrate posture
degenerative diseases of CNS
dementia
dementia, cerebrovascular disease causing
dementia, subcortical
demyelinating disease
depression
drooling
dysarthria
dysphagia
dyspnea
efficacy
electroencephalogram, pediatric patients
electromyogram
face, inexpressive
facial weakness, bilateral
familial
familial hemiplegic migraine
fasciculation
feeding disorder
fibrillations
floppy infant
food poisoning
food-borne infection
gait disorder
gammaglobulin therapy, intravenous
gender
gene
genetic neurologic disorders
genetic screening
head bobbing
headache
hearing loss
hoarseness
honey
hyperpigmentation of skin
hyperreflexia
hypertension
hyponatremia
hyporeflexia
hypotonia
hypotonia, infants
hypoxia, intrauterine
hypoxia, newborn
infant, evaluation of
insular cortex
intellectual deficit
intellectual deterioration
irritability
irritable baby
lacunar infarction
language disorders in children
lethargy
leukodystrophy
leukoencephalopathy
liver disease
locked-in syndrome
mania
manic-depressive
mental retardation
microangiopathy, brain
migraine
migraine, hemiplegic
misdiagnosis
motor neuron disease
MRI
MRI, abnormal
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
muscle atrophy, progressive
muscle twitching
muscle wasting, diffuse
muscle weakness
myasthenia gravis
myasthenia gravis, congenital
myasthenia gravis, distal weakness
myasthenia gravis, familial incidence of
myasthenia gravis, infantile and juvenile
myasthenia gravis, limb-girdle
myasthenia gravis, neonatal
myasthenia gravis, treatment of
myasthenic syndrome
nasal speech
neck weakness
neurologic complications of, burns
neurologic disease, diagnoses of
neuromuscular junction, abnormality of
neuropathology
neurotoxin
nonverbal
opened mouth
operculum syndrome
operculum syndrome, bilateral
ophthalmoplegia
optic atrophy
osmotic demyelination syndrome
paraparesis, spastic
peroxisomal disease
personality change
polymerase chain reaction
pons, lesion of
premature infant
premature infant, problems in
prognosis
pseudobulbar palsy
pseudocoma
psychiatric disorder
psychiatric problems in neurologic disorders
ptosis
ptosis, bilateral
quadriparesis
quadriplegia
respiratory failure
review article
rheumatoid arthritis
rheumatoid arthritis, neurologic complications of
seizure
seizure, recurrent
spasticity
speech disorder
spinal cord, infarction of
suck, poor
symmetric brain lesions
systemic lupus erythematosus
systemic lupus erythematosus, neurologic complications with
tachycardia
temporal lobe, lesion
temporal lobe, lesion, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
tongue, atrophy
tongue, fasciculations of
tongue, impaired movements of
tongue, weakness
transient ischemic attack
transient ischemic attack, recurrent
treatment of neurologic disorder
urinary incontinence
vasculopathy
very long chain fatty acids
vestibular function, tests of
visual acuity, decreased
visual loss
vitamin E
vitamin E deficiency
weakness
weakness, generalized
weakness, infant
weight loss
white matter disease
Showing articles 400 to 450 of 4074 << Previous Next >>

Clinicopathologic Conference, Granulomatosis with Polyangiitis
NEJM 387:1022-1032, Case 28-2022, 2022

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

A 65-Year-Old Woman with Cancer History and Wrist Drop
Neurol 99:570-576, Merrill, R.,et al, 2022

Torticollis in a Child with Otalgia
BMJ 378:e070608, Sarathi, C.I.P.,et al, 2022

Cerebrovascular Ischemic Events in Patients with Takayasu Arteritis
Stroke 53:1550-1557, Mirouse, A.,et al, 2022

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

A 37-Year-Old Man with Involuntary Movements, Gait Disturbance, and Hyperasthesia
Neurol 98:851-853, Meng, D.,et al, 2022

Rituximab Therapy in the Treatment of Juvenile Myasthenia Gravis
Neurol 98:e2368-e2376, Molimard, A.,et al, 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

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

A 48-Year-Old Woman with 6 Months of Vivid Visual Hallucinations
Neurol 99:166-171, Kizza, J.,et al, 2022

An 8-Year-Old with Acute Onset Ataxia
Neurol 99:305-310, McLaren, J.R.,et al, 2022

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

A Comprehensive Review of Cluneal Neuralgia as a Cause of Lower Back Pain
Orthopedic Reviews doi:10.52965/001c-35505, Anderson,D.,et al, 2022

Neurobrucellosis:The Great Mimicker
Rev Soc Bras Med Trop 55:e0567-e2012, Soares,C.N.,et al, 2022

Carbon Monoxide Poisoning During Major U.S. Power Outages
NEJM 386:191, Worsham, C.M., et al, 2022

Spectrum of Neuroradiologic Findings Associated with Monogenic Interferonopathies
AJNR 43:2-10, Benjamin, P.,et al, 2022

Multiple Cranial Nerve Gadolinium Enhancement in Norrie Disease
Ann Neurol 91:158-159, Jokela, M.,et al, 2022

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

Leptomeningeal Enhancement Associated with Cerebral Venous Thrombosis
JAMA Neurol 79:195-196, Lozano-Chinga, M.,et al, 2022

A 6-Year-Old Girl with Progressive Toe Walking
Neurol 98:e769-e773, Libdeh, A.A. & Ibrahim, A., 2022

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

Efficacy and Safety of Selumetinib in Pediatric Patients with Neurofibromatosis Type 1
Neurol 98:e938-e946, Hwang, J.,et al, 2022

Contemporary Trends in the Nationwide Incidence of Primary Intracerebral Hemorrhage
Stroke 53:e70-e74, Bako, A.T.,et al, 2022

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

Recent Advances in the Diagnosis and Management of Cluster Headache
BMJ 376:e059577, Schindler, E. & Burish, M.J., 2022

A 48-Year-Old Woman Presenting with Vertigo, Ptosis, and Red Eyes
Neurol 98:678-683, Kim, K.T.,et al, 2022

Clinicopathological Conference, Systemic Lupus Erythematosus with Antiphospholipid Syndrome
NEJM 386:1560-1570, Case 12-2022, 2022

A 73-Year-Old Woman with Episodic Dysarthria and Horizontal Binocular Diplopia
Neurol 98:767-772, Bower, A.S.,et al, 2022

Cerebrovascular Ischemic Events in Patients with Takayasu Arteritis
Stroke 53:1550-1557, Mirouse, A.,et al, 2022

Molecular and Neurological Features of MELAS Syndrome in Paediatric Patients: A Case Series and Review of the Literature
Mal Genet Genomic Med 10:e1955, Seed,L.M.,et al, 2022

Autoimmune Nodopathies, An Emerging Dignostic Category
Curr Opin Neurol 35:579-585, Martin-Agullar, L.,et al, 2022

Anti-NMDAR Encephalitis Presenting as Stroke-Like Episodes in Children: A Case Series from a Tertiary Care Referral Centre from Southern India
J Pediatr Neurosci 16:194-198, Gowda,V.K.,et al, 2021

Focal Cerebral Arteriopathy of Childhood, Clinical and Imaging Correlates
Stroke 52:2258-2265, Oesch,G.,et al, 2021

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

A 40-Year-Old Woman With Scapular Winging and Dysphonia
Neurol 97:503-507, Aladawi, M.,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

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

A 47-Year-Old With Headache, Vertigo, and Double Vision
Neurol 97:e535-e539, Frey, J.,et al, 2021

A 59-Year-Old Woman Presenting with Diplopia, Dysarthria, Right-sided Weakness, and Encephalopathy
Neurol 97:e859-e864, Manzano, G.S.,et al, 2021

A 42-Year-Old Woman with Mysterious Monocytic Meningitis
Neurol 97:449-454, Nothem, M.E., et al, 2021

Chronic Meningitis
NEJM 385:930-936, Aksamit, A.J., 2021

Garcin Syndrome in a Patient with Neurolymphomatosis
Neurol 97:600-601, Nishida, K.,et al, 2021

Clinicopathologic Conference, Systemic Juvenile Idiopathic Arthritis
NEJM 385:1220-1229, Case 29-2021, 2021

Clinicopathologic Conference, Vascular Ehlers-Danlos Syndrome
NEJM 385:1317-1325, Case 30-2021, 2021

Frequency and Characterization of Movement Disorders in Anti-IgLON5 Disease
Neurol 97:e1367-e1381, Gaig, C.,et al, 2021

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

Facial Numbness, Dysarthria, Muscle Atrophy, and Weakness in a Young Patient
JAMA Neurol 78:1273-1274, Liu, Y.,et al, 2021



Showing articles 400 to 450 of 4074 << Previous Next >>