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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 0 to 50 of 3961 Next >>

Clinicopathologic Conference, Infant Botulism, Case 3-2024
NEJM 390:358-366, Case 3-2024, 2024

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

An 11-year-old Boy with Language Disorder and Epilepsy
Neurol 86:e48-e53, Dong, L. & Zhou, X., 2016

The Acquired Metabolic Disorders of the Nervous System, Central Pontine Myelinolysis and other Patterns of Osmotic Demyelination
Adams & Victors Principles of Neurology Chp 40, pg 1149, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Adrenoleukodystrophy
Adams & Victors Principles of Neurology, Chp 37, pg 988, Ropper, A.H.,et al, 2014

Human Botulism Immune Globulin for the Treatment of Infant Botulism
NEJM 354:462-471, Arnon,S.S.,et al, 2006

The Phenotypic Spectrum of CADASIL:Clinical Findings in 102 Cases,
Ann Neurol 44:731-739,715, Dichgans,M.,et al, 1998

Familial Hemiplegic Migraine and Autosomal Dominant Arteriopathy with Leukoencephalopathy (CADASIL)
Ann Neurol 38:817-824, Hutchinson,M.,et al, 1995

Clinical Spectrum of CADASIL:A Study of 7 Families
Lancet 346:934-939, Chabriat,H.,et al, 1995

Symmetrical Thalamic Degeneration with Calcifications of Infancy
Am J Dis Child 143:1056-1060, DiMario,F.J.&Clancy,R., 1989

Vitamin E Deficiency Associated with Vision Loss & Bulbar Weakness
Ann Neurol 18:725-727, Larsen,P.D.,et al, 1985

Progressive Pontobulbar Palsy With Deafness
Arch Neurol 38:186-190, Brucher,J.M.,et al, 1981

Clinical Syndromes of Myasthenia in Infancy & Childhood
Arch Neurol 35:97, Fenichel,G.M., 1978

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

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

Pharmaceutical Interventions for Emotionalism After Stroke
Stroke 54:e213-e214, Hackett,M.L.,et al, 2023

Disabling Jaw Clonus in a Patient with Bulbar-Onset Amyotrophic Lateral Sclerosis Successfully Treated with Botulinum Toxin
Neurol 99:671, Santos, M.O.,et al, 2022

Clinicopathologic Conference, Anti-IgLON5 IgG-Associated Neurologic Disorder
NEJM 386:173-180, Case 1-2022, 2022

Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
NEJM 385:165-175, Case 20-2021, 2021

An Adolescent Girl Presenting with Worsening Vertigo, Headache, and Ataxia
Neurol 95:e1760-e1763, Brigham, E.,et al, 2020

Rapidly Progressive Gait Disorder and Cranial Nerves Involvement in a 9-year-old boy
Neurol 94:e330-e334, Lipp, A.,et al, 2020

A 16-year-old Girl with Ataxia, Oscillopsia, and Behavioral Changes
Neurol 94:713-717, Silverman, A.,et al, 2020

Ears of the Lynx Magnetic Resonance Imaging Sign
Ann Neurol 88:16-17, Baghbanian, S.M.,et al, 2020

A 14-Year-Old Boy with Acute Weakness, Parethesias, and Headache
Neurol 95:e1285-e1289, Seese, R.R.,et al, 2020

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

A 15-year-old Boy with Bilateral Wrist Pain in the Setting of Weight Loss
Neurol 92:486-492, Lau, K.H.V.,et al, 2019

Clinicopathologic Conference, Amyotrophic Lateral Sclerosis
NEJM 380:1566-1574, Case 12-2019, 2019

Limbic-Predominant Age-Related TDP-43 Encephalopathy (LATE): Consensus Working Group Report
Brain DOI: 10.1093/brain/awz099, Nelson, P.T.,et al, 2019

Proptosis and Double Vision in a Child
JAMA Neurol 75:1142-1143, Lu, A.J.,et al, 2018

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

Clinical Presentation and Cranial MRI Findings of Listeria Monocytogenes Encephalitis
Neurologist 23:198-203, Arslan, F.,et al, 2018

Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
Neurol 90:e625-e631, Set, K.K.,et al, 2018

Clinical Reasoning: A Teenager with Left Arm Weakness
Neurol 90:e907-e910, Al-Ghamdi, F.,et al, 2018

Clnicopathologic Conference Anti-N-Methyl-D-Aspartate (NMDA) Receptor Encephalitis
NEJM 379:870-878, CASE 27-2018, 2018

A Child with Arthrogryposis
Neurol 91:e995-e998, Irumudomom, O. & Ghosh, P.S., 2018

Brachial Plexus Ultrasound and MRI in Children with Brachial Plexus Birth Injury
AJNR 39:1745-1750, Gunes, A.,et al, 2018

Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect
Front Neurol doi:10.3389/fneur.2018.0069, Gagliardi, D.,et al, 2018

FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018

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

Incomplete Miller-Fisher Syndrome with Advanced Stage Burkitt Lymphoma
Indian Pediat 54:413-415, Ozdemir,Z.C.,et al, 2017

A Child with Delayed Motor Milestones and Ptosis
Neurol 88:e158-e163, Ghosh, P.S., 2017

Clinical Manifestations of the anti-IgLON5 Disease
Neurol 88:1736-1743,1688, Gaig, C.,et al, 2017

A 54-year-old woman with Dementia, Myoclonus, and Ataxia
Neurol 89:e7-e12, Ali, F.,et al, 2017

Amyotrophic Lateral Sclerosis
NEJM 377:162-172, Brown, R.H.,et al, 2017

My Weeping Patient
Neurol 89:e202, Peters, J.,et al, 2017

Clinicopathologic Conference, Primary Progressive Aphasia, Semantic Variant, due to TAR DNA Binding Protein 43 associated Frontotemporal Lobar Degen
NEJM 376:158-167, Case 1-2017, 2017

Performance of Bedside Stroke Recognition Tools in Discrimination Childhood Stroke from Mimics
Neurol 86:2154-2161, Mackay, M.T.,et al, 2016

Acute Flaccid Myelitis; A Clinical Review of US Cases 2012-2015
Ann Neurol 80:326-338, Messacar, K.,et al, 2016



Showing articles 0 to 50 of 3961 Next >>