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Differential
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abducens nerve paralysis
acetylcholine receptor antibody
acetylcholinesterase
acetylcholinesterase deficiency
adverse drug reaction
airway obstruction
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
aneurysm
aneurysm, cavernous sinus
aneurysm, cavernous sinus-bilateral
aneurysm, intracranial
anterior tibial muscle weakness
antibiotics
antibiotics, neurologic complications with
antibodies to voltage-gated calcium channels
areflexia
arthrogryposis multiplex
ataxia, paroxysmal
autoimmune disease
benign congenital hypotonia
botulism
brainstem, lesion of
bulbar palsy
bulbar palsy, acute
calcium channel dysfunction
cardiomyopathy
case studies
CAT scan
CAT scan, abnormal
cavernous sinus, meningioma
cavernous sinus, syndrome
central core disease
Charcot-Marie-Tooth
children
chronic polyneuritis, children
chronic progressive external ophthalmoplegia
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
collagen vascular disease
congenital malformation
congenital myasthenic syndromes
congenital myopathy
congestive heart failure
consanguinity
contractures, joint
cranial neuropathy
cranial neuropathy, multiple
creatine phosphokinase(CPK)elevated
degenerative diseases of CNS
delay in diagnosis
delivery, complicated
developmental retardation
diabetes mellitus
diplopia
diplopia, transient
diplopia, vertical
distal muscle weakness
electromyogram
electromyogram, decremental response
ephedrine
epidemiology of neurology
exome sequencing
eye closure
eye, pain in
face, numbness of
facial nerve palsy
facial nerve palsy, bilateral
facial nerve, lesion of
facial weakness
facioscapulohumeral syndrome
familial
familial hemiplegic migraine
fatigue
Fazio-Londe's disease
fluctuate
foot drop
gene mutation
genetic neurologic disorders
genetic testing
headache
headache, frontal
headache, sudden onset of
headache, unilateral
heavy metal intoxication
high arched palate
HLA
hyperthyroidism
hyperthyroidism, familial incidence of
hypokalemic periodic paralysis
hyporeflexia
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
internuclear ophthalmoplegia
Kearns-Sayre syndrome
Kugelberg-Welander syndrome
lid closure, weakness of
lordosis
malignant hyperpyrexia
medical-legal aspects of neurology
Melkersson's syndrome
meningioma
meningioma, sphenoid wing
mental retardation
mestinon
migraine, hemiplegic
mimics
misdiagnosis
motor neuron disease
MRI
MRI, abnormal
muscle atrophy, progressive
muscle biopsy
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, cardiovascular changes with
muscular dystrophy, congenital
muscular dystrophy, differential diagnosis of
muscular dystrophy, facioscapulohumeral
muscular dystrophy, limb-girdle
myasthenia gravis
myasthenia gravis, congenital
myasthenia gravis, diagnosis
myasthenia gravis, distal weakness
myasthenia gravis, etiology of
myasthenia gravis, familial incidence of
myasthenia gravis, infantile and juvenile
myasthenia gravis, limb-girdle
myasthenia gravis, misdiagnosis of
myasthenia gravis, neonatal
myasthenia gravis, neuromuscular junction in
myasthenia gravis, nystagmus in
myasthenia gravis, ocular
myasthenia gravis, sensory loss with
myasthenia gravis, seronegative
myasthenia gravis, treatment of
myasthenic syndrome
mycophenolate
myopathy
myopathy, centronuclear
myopathy, mitochondrial
myotonia dystrophica
nasal speech
neck weakness
nemaline rod myopathy
nerve conduction studies
neurofibrillary degeneration
neurologic disease
neurologic disease, diagnoses of
neuromuscular disease, electrodiagnosis of
neuromuscular junction
newborn, evaluation of
next-generation sequencing
nystagmus
nystagmus, dissociated
nystagmus, monocular
ocular myopathy
old age, neurology of
opened mouth
ophthalmoplegia
ophthalmoplegia, total
Oppenheim muscular dystrophy
optic neuropathy
orbicularis oculi muscle
pain, periorbital
poison, mercury
poison, neurologic problems with
polymyositis
postpartum
practice guidelines
pregnancy, neurologic complications in
progressive muscular dystrophy
pseudointernuclear ophthalmoplegia
pseudomyasthenia
ptosis
ptosis, bilateral
ptosis, unilateral
repetitive nerve stimulation
respiratory failure
retro-orbital pain
review article
rheumatoid arthritis
rheumatoid arthritis, neurologic complications of
risk factors
safety
serologic testing
serologic testing, false negative
seronegative
spinal muscular atrophy
spinocerebellar ataxia
stridor
systemic lupus erythematosus
systemic lupus erythematosus, neurologic complications with
tensilon test
tensilon test, false negative
tensilon test, false positive
third nerve palsy
third nerve palsy, partial
third nerve palsy, pupil sparing in
thyrotoxicosis
treatment of neurologic disorder
tricresylphosphate
trigeminal neuropathy
twins
type 1 muscle fiber
visual acuity, decreased
vocal cord paralysis
weakness
weakness, fatiguable
weakness, proximal
Werdnig-Hoffman disease
whistle, inability to
winging of scapula
xerostomia
Showing articles 450 to 500 of 1505 << Previous Next >>

Congenital Zika Syndrome
NEJM 394:e2, Bacin,F. & Montenegro,M.A., 2026

Clinical Insights Into CASPR1 and CASPR1/Contactin1 Com-lex Autoimmune Nodopathies
Neurol 106:e214403, Paramasivan,N.K.,et al, 2026

Iatrogenic Cerebral Amyloid Angiopathy after Cardiac Surgery, Two Case Reports
Neurol 106:e214819, Brunet de Courssou,J-B.,et al, 2026

A 52-Year Old Man with Acute-Onset Blindness
Neurol 106:e214827, Brown,A.M.,et al, 2026

Case Fatality of Subarachnoid hemorrhge by Aneurysm Location
Neurol 106:e214918, Asikinen,.,et al, 2026

Spontaneous Calcified Cerebral Emboli from Bicuspid Aortic Valve in Young Patients: Case Series and Review
Stroke:Vasc Inter Neurol doi.org/10.1161/svi 270000.138, Sardana,S.,et al, 2025

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

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

Infantile Epileptic Spasms Syndrome (West Syndrome)
Stat Pearls PMID:30725936, Smith,M.S.,et al, 2025

Unruptured Intracranial Aneurysms
NEJM 392:2357-2366, Ogilvy,C.S., 2025

Congenital Titinopathy:Comprehensive Characterization of the Most Severe End of the Disease Spectrum
Ann Neurol 97:611-628, Coppens,S.,et al, 2025

Functional Outcome in Patients with Carotid Artery Dissection Undergoing Thrombectomy or Standard Medical Treatment
Neurol 104:e213465, Sykora,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

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

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

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

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

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

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

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

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

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

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

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

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

Spina Bifida
NEJM 387:444-450, Iskandar, B.J. & Finnell, R.H., 2022

Bilateral Hearing Loss and Constricted Visual Fields
BMJ 378:e070672, Sachdeva, G. & Shafquat, S., 2022

Spontaneous Subarachnoid Haemorrhage
Lancet 400:846-862, Claassen, J. & Park, S., 2022

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

CLOVES Syndrome
Neurol 96:e1487-e1488, Collins, M.,et al, 2021

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

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

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

Vessel Wall MR Imaging for the Detection of Intracranial Inflammatory Vasculopathies
Cardiovasc Diagn Ther 10:1108-1119, Edjlali,M.,et al, 2020

Ondine Curse Syndrome Cause by Dorsolateral Medullary Stroke
Neurol 94:e1557-e1558, Fiedler, E. & Gill, R., 2020

Delayed Leukoencephalopathy: A Rare Complication after Coiling of Cerebral Aneurysms
AJNR 41:286-292, Ikemura, A.,et al, 2020

Acute Ischemic Stroke in Adolescents
Neurol 94:e158-e169, Rambaud, R.,et al, 2020

Feasibility, Safety, and Outcome of Endovascular Recanalization in Childhood Stroke
JAMA Neurol 77:25-34, Sporns, P.B.,et al, 2020

Management of Stroke in Neonates and Children
Stroke 50:e51-e96, Ferriero, D.M.,et al, 2019

Fibromuscular Dysplasia and Its Neurologic Manifestations
JAMA Neurol 76:217-226, Touze, E.,et al, 2019

Muscular Dystrophies
Lancet 394:2025-2038, Mercuri, E.,et al, 2019

Bilateral Alopecia as Clue to Diagnosis of Gomez-Lopez-Hernandez Syndrome in a 38-Year-Old Man
Neurol 93:408-410, Kronlage,C.&Healy,D.G., 2019

Declining Malformation Rates with Changed Antiepileptic Drug Prescribing, An Observational Study
Neurol 93:e831-e840, Tomson,T.,et al, 2019

Characteristic Head Jerks in Congenital Oculomotor Apraxia due to Joubert Syndrome
Neurol 93:e1125-e1126, Borngraber, F.,et al, 2019



Showing articles 450 to 500 of 1505 << Previous Next >>