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acetazolamide
alcohol
Alexanders disease
Alexanders disease, adult onset
alternating hemiplegia
alternating hemiplegia of childhood
aminoacidopathies
aminoacidurias
antibodies to voltage-gated calcium channels
areflexia
arrhythmia, cardiac
arthralgia
astrogliopathy
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
ataxia, truncal
ataxic gait
ATP1A3 gene
autonomic dysfunction
Babinski sign
bulbar palsy
calcium channel dysfunction
cardiomyopathy
CAT scan
CAT scan, abnormal
cataracts
central core disease
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar atrophy, primary
cerebellar degeneration
cerebellar lesion
cerebellar vermis
cerebrospinal fluid, proteincytologic dissociation
cerebrovascular accident
channelopathy
Charcot-Marie-Tooth
children
chloride channel dysfunction
chorea
chromosomal abnormality
chromosome 19
ciguatera poisoning
clubfoot as related to neurologic disease
coma
coma, episodic
congestive heart failure
conjunctivitis
cryopyrin-associated periodic syndrome
deafness
deep gray nuclei
degenerative diseases of CNS
dementia
dentate nuclei, lesion of
developmental retardation
dexterity, impaired
diabetes mellitus
diagnostic criteria
differential diagnosis
diplopia
down-beat nystagmus
down-beat nystagmus, primary position of gaze
dysarthria
dystonia
electrocardiogram, abnormal
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
encephalopathy
episodic disorders
episodic neurologic deficits
exercise
exercise intolerance
exome sequencing
eye movement, disorders of
failure to thrive
familial
familial hemiplegic migraine
familial periodic ataxia
fatal familial insomnia
fever
fever, recurrent
foot deformity
Friedreich's ataxia
frontal bossing
gait disorder
gait, spastic
gene
gene mutation
genetic neurologic disorders
genetic testing
GFAP gene
globus pallidus, lesion of, bilateral
Guillain Barre syndrome
hammertoes
head circumference
headache
hearing loss
heart block
hyperhidrosis
hyperreflexia
hypertension
hyperthermia
hyperthyroidism
hypertrophic intracranial pachymeningitis
hypokalemic periodic paralysis
hypotonia
imbalance
inborn errors of metabolism
incoordination
insomnia
intellectual deficit
kyphoscoliosis, neurologic causes of
lactic acidemia
leukodystrophy
leukoencephalopathy
lysosomal storage disease
macrocephaly
malignant hyperpyrexia
maple syrup urine disease
meningitis, aseptic
meningitis, carcinomatous
metabolic acidosis
metabolic disorder, primary
microcephaly
middle cerebellar peduncle
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
migraine, hemiplegic
molecular genetics
mortality
motor neuron disease
movement disorder
movement disorder, hyperkinetic
MRI
MRI, abnormal
MRI, diffusion weighted
muscle atrophy, progressive
muscle weakness
muscular dystrophy
muscular dystrophy, Becker
muscular dystrophy, cardiovascular changes with
muscular dystrophy, Duchenne
myasthenic syndrome
myoclonus
myokymia
myopathy
myotonia
myotonia congenita
myotonia dystrophica
nausea and vomiting
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic signs
neurologic testing
neuromyotonia
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
neuropathy, amyloid
neuropathy, ataxic
neuropathy, hereditary peripheral
neuropathy, hypertrophic
neuropathy, onion bulb
night blindness
nystagmus
nystagmus, gaze-paretic
nystagmus, hereditary
nystagmus, monocular
nystagmus, periodic
nystagmus, vertical
optic atrophy
optic atrophy, bilateral
oscillopsia
palatal myoclonus
paralysis
paramyotonia congenita
paraparesis
paraparesis, spastic
Parkinson disease, dystonia with
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
periodic paralysis
peroxisomal disease
pes cavus
phytanic acid
pleocytosis of cerebrospinal fluid
polyneuropathy
pons, lesion of
potassium channel antibodies
potassium channel dysfunction
precipitating factors
pregnancy, neurologic complications in
primary episodic ataxia
prion disease
prognosis
progressive neurologic disorder
psychiatric problems in neurologic disorders
pyramidal tract
pyramidal tract dysfunction
pyruvate dehydrogenase deficiency
pyruvate metabolism, abnormality of
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
rash
recurrent
red eye
Refsum's disease
respiratory tract infection
retinitis pigmentosa
review article
Romberg's sign
scoliosis
seizure
sensorineural hearing loss
sensory loss
short stature
skin, lesions in neurologic disorders
skull bone, thickening
sleep pathology and physiology
slurred speech
sodium channel dysfunction
spinocerebellar ataxia
spinocerebellar ataxia type 6
spinocerebellar degeneration
status epilepticus
stress, emotional
strokelike episodes
sudden death
symmetric brain lesions
tachycardia
thalamus, lesion of
tinnitus
transient neurologic deficit
treatment of neurologic disorder
trinucleotide repeats
urea-cycle enzymopathies
vertigo
vertigo, episodic
vertigo, treatment of
visual fields, constricted
vitamin E deficiency
weakness
weight loss
white matter disease
Showing articles 400 to 450 of 3728 << Previous Next >>

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

A 67 YEar-Old Woman with Progressive Headache, Visual Hallucinations, and Seizures
Neurol 104:e213496, Gheihman,G.,et al, 2025

Left Atrial Appendage Closure After Ablation for Atrial Fibrillation
NEJM 392:1277-1287, Wazni,O.M.,et al, 2025

Abnormal and Persistent Mineralization of Globi Pallidi in GAMT Deficiency
Neurol 104:e213636, Chanda,G.,et al, 2025

A 59-Year-Old Man with Progressive Dysarthria and Gait Instability
Neurol 104:e213729, Shen,D.,et al, 2025

Upadacitinib - An Up-and-Comer for Treatment of Giant-Cell Arteritis
NEJM 392:2062-2064, Koster,M.J. & Warrington,K.J., 2025

Stroke-Like Migraine Attacks After Radiation Therapy Syndrome
Neurol 104:e210203, Lubotzky,A.,t al, 2025

A 68-YEar-Old Man with Progressive Numbness, Vertigo, and Cognitive Decline
Neurol 104:e213437, Regan,S.M. & Davalos,L.F., 2025

Clinical Presentation, Investigation Findings, and Outcomes of IgG4-Related Pachymeningitis,A Systematic Review
JAMA Neurol 82:193-199, Terrim,S.,et al, 2025

Methamphetamine-Induced Basal Ganglia Toxicity Presenting as Parkinsonism
Neurol 104:e213365, Yi,M.Y.,et al, 2025

RNF213 Polymorphisms in Intracranial Artery Dissection
Genes doi.org/10.3390/genesis 15060725, Zedde,M.,et al, 2024

Middle Meningeal Artery Embolisation for Nonacute Subdural Hematoma
NEJM 391:1901-1912, Ni,J.L.W.,et al, 2024

Adjunctive Middle Meningeal Artery Embolization for Subdural Hematoma
NEJM 391:1890-1900, Davies,J.M.,et al, 2024

Left Atrial Appendage Occlusion vs Standard of Care After Ischemic Stroke Despite Anticoagulation
JAMA Neurol 81:1150-1158, Maarse,M.,et al, 2024

A 65-Year-Old Woman with Isolated Macroglossia as the Initial Presentation of a Rare Disease
Neurol 103:e210070, Lara,C.,et al, 2024

Safety and Efficacy of Staged, Bilateral Focused Ultrasound Thalamotomy in Essential Tremor, An Open-Label Clinical Trial
JAMA Neurol 81:939-946, Kaplitt,M.G.,et al, 2024

Genome Sequencing in the NICU and PICU is Here to Stay
Neurol 104:e210267, Hoffman,E.P. and Kesari,A., 2024

Clinicopathologic Conference, Myasthenia Gravis
NEJM 391:1441-1450, Case 32-2024, 2024

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

Optimal Timing of Anticoagulation after Acute Ischaemic Stroke with Atrial Fibrillation (OPTIMAS): A Multicentre, Blinded-Endpoint, Phase 4, Randomised Controlled Trial
Lancet 404:1731-1741, Werring,D.J.,et al, 2024

Rationale for Screening Children with Hereditary Hemorrhagic Telangiectasis for Brain Vascular Malformations
AJNR 45:1177-1184, Beslow,L.A.,et al, 2024

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

Primary Central Nervous System Vasculitis
NEJM 391:1028-1037, Salvarani,C.,et al, 2024

Pomalidomide for Epistaxis in Hereditary Hemorrhagic Telangiectasia
NEJM 391:1015-1027, Al-Samkari,H.,et al, 2024

A 50-YEar-Old Man with Intracerebral Hemorrhage and Tortuous Retinal Arterioles
Neurol 103:e209796, Bouchart,J.,et al, 2024

Neuroleptic Malignant Syndrome
NEJM 391:1130-1138, Wijdicks,E.F.M. & Ropper,A.H., 2024

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

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

Roving Eye and Head in a Patient with Genetic Creutzfeldt-Jakob Disease
Neurol 102:e209385, Nishida,K.,, 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

Incidence and Types of Cardiac Arrhythmias in the Pei-Ictal Period in Patients Having a Generalized Convulsive Seizure
Neurol 103; e209501, Vilella,L.,et al, 2024

Recurrent Ischemic Stroke in Patients with Atrial Fibrillation Whle Receiving Oral Anticoagulants
JAMA Neurol 81:805-813, Hindsholm,M.F.,et al, 2024

Hyperventilation-Induced Alternating Hemiplegia with Concomitant Hemispheric EEG Slowing in a 7-Year-Old Girl with Headache
Neurol 103:e209759, Proietti,J.,et al, 2024

Vestibular Drop Attacks Diagnosed with Valuable Insights from CCTV
Lancet 404:787-788, Joffily,L.,et al, 2024

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

Treatment Modalities and Outcomes in Brainstem Cavernous Malformations: A Large Multicenter Observational Cohort Study
Stroke 55:1151-1160, Lu,J.,et al, 2024

Vascular Malformations of the Central Nervous System
www.UptoDate.Com, March, Singer,R.J.,et al, 2024

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

HaNDL Syndrome The Innocent Lymphocytic Pleocytosis
Neurologist 29:163-165, Keskin,K.G.,et al, 2024

Intracranial Hypertension Associated with Poly-Cranio-Radicular-Neuropathies A Case Report and Review of the Literature
Neurologist 29:166-169, Eaton,J.E.,et al, 2024

Treatment and Outcomes of Cervical Artery Dissection in Adults:A Scientific Statement From the American Heart Association
Stroke 55:e91-e106, YaghikS.,et al, 2024

Cavernous Maliformations of the Central Nervous System
NEJM 390:1022-1028, Smith,E.R., 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

A 51-Year-Old Woman with Abnormal Corups Callosum Signal
JAMA Neurol 81:192-193, Xie,N. & Sun, Q, 2024

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024

Reversible Cortical and Basal Ganglia Lesions in Late-Onset Methylmalonic Aciduria
JAMA Neurol 81:1-82, Chu,X.C.,et al, 2024

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

Distinguishing Transient Cerebral Ischemia From Other Brief Neurologic Events
Neurol 102:e208024, Warach,S. & Schellinger, P.D., 2024



Showing articles 400 to 450 of 3728 << Previous Next >>