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Differential
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aciduria
adolescent medicine
adverse drug reaction
algorithm
alien hand syndrome
alternating hemiplegia
alternating hemiplegia of childhood
anticholinergic drugs
aphasia
aphasia, progressive, primary
aphonia
apraxia
areflexia
ataxia
ataxia, cerebellar
ATP1A3 gene
autoantibodies
autoimmune basal ganglia encephalitis
autoimmune disease
Babinski sign
biopterin deficiency
blepharospasm
botulinum toxin
bradykinesia
brain atrophy
camptocormia
carbamazepine
CAT scan, emission
CAT scan, emission, abnormal
central nervous system, infection of
cerebral palsy
children
chorea
chromosomal abnormality
chromosome 14
chromosome 19
Clinical Pathologic Conference(C.P.C.)
cognition
cogwheel rigidty
contractures, joint
cortical-basal ganglionic degeneration
degenerative diseases of CNS
delay in diagnosis
dementia
depression
developmental milestones, loss of
developmental retardation
diagnostic criteria
differential diagnosis
diurnal variation
dopa responsive dystonia
dopamine
drug induced neurologic disorders
dysarthria
dyskinesia
dysphagia
dystonia
dystonia musculorum deformens
dystonia, axial
dystonia, cervical
dystonia, children
dystonia, classification
dystonia, etiology of
dystonia, evaluation of
dystonia, face
dystonia, focal
dystonia, painful
dystonia, treatment of
DYT1 mutation
encephalitis, autoimmune
encephalitis, brainstem
encephalopathy
encephalopathy, progressive
enzyme, defect
equinovarus
eye movement, disorders of
falling
familial
foot deformity
frontal behavioral spatial syndrome
gait disorder
galactorrhea
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
gests antagoniste
GLUT1 deficiency syndrome
hand weakness
hands, fisted
head nodding
hearing loss
hemidystonia
hepatolenticular degeneration(Wilson's disease)
hyperreflexia
hypertonia
hyporeflexia
hypotonia
imbalance
imbalance, postural
inborn errors of metabolism
inclusion bodies, intranuclear
intellectual deficit
L-dopa
leg spasms
leg spasms, painful
Lewy body disease, diffuse
masked facies
meningitis
meningitis, carcinomatous
microcephaly
mimics
misdiagnosis
molecular genetics
movement disorder
movement disorder, drug induced
movement disorder, extrapyramidal
movement disorder, hyperkinetic
movement disorder, treatment of
MRI
MRI, negative
myoclonus
neurochemistry
neurologic disease, diagnoses of
neurologic disease, tempo
neurologic signs
neuronal intranuclear inclusion disease
neuropathology
neurotomy
next-generation sequencing
nystagmus
nystagmus, monocular
obsessive-compulsive disorder
optic atrophy
pain
Parkinson disease
Parkinson disease, differential diagnosis of
Parkinson disease, dystonia with
Parkinson disease, juvenile
Parkinson disease, L-dopa nonresponsive
Parkinson disease, rapid onset
Parkinson disease, tremor, absence of
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
personality change
postural abnormality
precipitating factors
PRKN gene
prognosis
progressive neurologic disorder
progressive supranuclear palsy
prolactin, elevated
psychiatric problems in neurologic disorders
pull test
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
recurrent
Red flags
reversible neurologic disorder
review article
rigidity
scoliosis
seizure
sensorineural hearing loss
sensory tricks
short stature
sinemet
speech disorder
speech disorder, childhood
status epilepticus
stimulation, deep brain
striatal encephalitis
substantia nigra
swallow evaluation
tardive dystonia
tau protein
tauopathy
tetrahydrobiopterin
toe walking
tonic foot response
torticollis
treatment of neurologic disorder
tremor
tremor, postural
tripping
tyrosine hydroxylase deficiency
walking
walking frame
walking, difficulty with
wheelchair
wide based gait
workup
Showing articles 50 to 100 of 779 << Previous Next >>

Stereotactic Ventrolateralis Thalamotomy for Refractory Tremor in Post-Levodopa Era Parkinson's Dis
J Neurosurg 75:723-730, Fox,M.W.,et al, 1991

Young-Onset Parkinson's Disease:A Clinical Review
Neurol 41:168-173, Golbe,L.I., 1991

Early Development of Levodopa-Induced Dyskinesias and Response Fluctuations in Young-Onset Parkinson's Disease
Neurol 41:202-205, Kostic,V., 1991

Levodopa-Induced Dyskinesia:Review, Observations, and Speculations
Neurol 40:340-345, Nutt,J.G., 1990

Stereotaxic Thalamotomy-Experiences from the Levodopa Era
JNNP 53:427-430, Wester,K.&Hauglie-Hanssen,E., 1990

The Dystonias
BMJ 300:139-144, Marsden,C.D.&Quinn,N.P., 1990

Diffuse Lewy Body Disease:Clinical Features in 15 Cases
JNNP 52:709-717, Byrne,E.J., 1989

Continuous Levodopa Infusions to Treat Complex Dystonia in Parkinson's Disease
Neurol 39:888-891, Sage,J.I.,et al, 1989

Dystonia in Parkinson's Disease:Clinical & Pharmacological Features
Ann Neurol 23:73-78, Poewe,W.H.,et al, 1988

Forms of Dystonia in Patients with Parkinson's Disease
Neurol 37:1009-1011, Kidron,D.&Melamed,E., 1987

Painful Parkinson's Disease
Lancet 1:1366-1369, Quinn,N.P.,et al, 1986

Dystonia-Parkinson Syndrome:Differential Effects of Levodopa and Dopamine Agonists
Clin Neuropharmacol 9:298-302, Klawans,H.L.&Paleologos,N., 1986

Dystonia Musculorum Deformans, Implications of Therapeutic Response to Levodopa & Carbamazepine
Arch Neurol 39:376-377, Garg,B.P., 1982

L-Dopa in Children with Progressive Neurological Disorders
Ann Neurol 7:93, Bugiani,O.,et al, 1980

Early-Morning Dystonia-A Late Side Effect of Long-Term Levodopa Therapy
Arch Neurol 36:308-310, Melamed,E., 1979

Onset & End-of-dose Levodopa-induced Dyskinesias
Arch Neurol 35:261, Lhermitte,F.,et al, 1978

Progressive Supranuclear Palsy-Case Study
NEJM 293:346, Richardson,E.P., 1975

Catecholamines & Neurologic Diseases
NEJM 293:274, Moskowitz,M.A.,et al, 1975

Drug-Induced Movement Disorders
Postgrad Med 180, 1971, Sept., North,R., 1971

An 81-Year-Old Man with Imbalance and Memory Impairment
, Golbe,L.I.,et al,

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

Efficacy and Safety of Sodium Oxybate in Isolated Focal Laryngeal Dystonia:A Phase IIb Double-Blind Placebo-Controlled Cross-Over Randomized Clinical Trial
Ann Neurol 97:329-343, Simonyan,K.,et al, 2025

A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
Neurol 103:e210046, Panigrahi,B.,et al, 2024

Parkinsons Disease
NEJM 391:442-452, Tanner,C.M. & Ostrem,J.L., 2024

Supratentorial Lymphocytic Inflammation with Parenchymal Perivascular Enhancement Responsive to Steroids:A Potentially Overlooked Diagnosis
Ann Neurol 95:407-409, Tsibonakis,A.,et al, 2024

Bilateral Hemifacial Spasm and Left Glossopharyngeal Neuralgia Caused by Bilateral Vertebral Artery Displacement
Neurol 102:e209422, Han,Z.,et al, 2024

Immunosuppressive Therapy Reversing Obstructive Hydrocephalus in CLIPPERS
Neurol 102:e209396, Yang,Y.,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

Paroxysmal Exercise-Induced Dyskinesias Due to Pyruvate Dehydrogenase Deficiency
Neurol 101:46-49, deGusmao,C.M.,et al, 2023

Current and Emerging Issues in Wilsons Disease
NEJM 389:922-938, Roberts,E.A. & Schilsky, M.L., 2023

Manganese Accumulation in the Brain
NEJM 389:1320, Sherman,S.V., 2023

Clinicopathologic Conference,Limb-Shaking Transient Ischemia Attacks
NEJM 389:1416-1423, Case 31-2023, 2023

Movement Disorders in Patients with Genetic Developmental and Epileptic Encephalopathies
Neurol 101:e1884-e1892, van der Veen,S.,et al, 2023

Case 302:Supratentorial Lymphocytic Inflammation with Parenchymal Perivascular Enhancement Responsive to Steroids
Radiology 303:726-730, Vattoth,S.,et al, 2022

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

Clinical and Structural Findings in Patients with Lesion-Induced Dystonia
Neurol 99:e1957-e1967, Corp, D.T.,et al, 2022

A 23-Year-Old Woman Presenting with Cognitive Impairment and Gait Disturbance
Neurol 99:997-1003, Chaity,D.K.,et al, 2022

Adults with Cerebral Palsy Require Ongoing Neurologic Care
Ann Neurol 89:860-871, Smith, S.E.,et al, 2021

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

Choreoathetosis and Focal Dystonia in Vitamin B12 Deficiency
Neurol 97:e1545, Ng, C.F.,et al, 2021

Hashimoto Encephalopathy in the 21st Century
Neurol 94:e217-e224, Mattozzi, S.,et al, 2020

Clinical and Radiologic Features of Pedicatric Opioid Use-Associated Neurotoxicity with Cerebellar Edema (POUNCE) Syndrome
Neurol 94:710-712, Kim, D.D. & Prasad, A.N., 2020

Diagnosis and Treatment of Parkinson Disease
JAMA 323:548-560, Armstrong, M.J. & Okun, M.S., 2020

Spasms and Myoclonus in a Young Woman with Hashimoto Thyroiditis
JAMA Neurol 77:650-651, Shen, D.,et al, 2020

Clinicopathologic Conference, LGI1 autoimmune encephalitis
NEJM 382:1943-1950, Case 15-2020, 2020

Functional Gait Disorders
Neurol 94:1093-1099, Nonnekes, J.,et al, 2020

Vitamin B6 Deficiency Presenting with New-Onset Epilepsy and Status Epilepticus in a Patient with Parkinson Disease
Neurol 94:e2605-e2607, Modica, J.S.,et al, 2020

Psychogenic Paroxysmal Hemifacial Spasm
Ann Neurol 88:14-15, Park, J.E., 2020

Steroid-Responsive Encephalitis in Coronavirus Disease 2019
Ann Neurol 88:423-427, Pilotto, A.,et al, 2020

A Young Generalized Dystonia Patient with Globus-Pallidus-Specific Lesion
Ann Neurol 88:637-638, Wu, H.,et al, 2020



Showing articles 50 to 100 of 779 << Previous Next >>