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Differential
(Click to cross reference)
akinetic mute
apraxia of eyelid opening
athetosis
basal ganglia, lesion of
behavioral disorder
bilirubin encephalopathy
biologic markers
blinking, reduced
bradykinesia
bradyphrenia
breast feeding
cerebral cortical atrophy
Clinical Pathologic Conference(C.P.C.)
compulsivity
cortical-basal ganglionic degeneration
cry, abnormal
cry, high-pitched
degenerative diseases of CNS
dementia, frontotemporal
diagnostic criteria
differential diagnosis
disability, neurological
dizziness
dysphagia
encephalopathy
eye movement, disorders of
falling
fever
fracture, long bone
frontal lobe, pathologic signs of
gait disorder
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
head injury
hearing loss
heralding manifestation
hummingbird sign
hyperbilirubinemia
hyperbilirubinemia, CNS abnormality after
imbalance
imbalance, postural
intellectual deficit
jaundice
kernicterus
life expectancy
masked facies
memory, impairment of
mental retardation
midbrain
midbrain, atrophy
misdiagnosis
moro reflex
mortality
movement disorder
MRI
MRI, abnormal
MRI, high signal foci on
MRI, high signal intensity of basal ganglia
multiple system atrophy
neurologic disease, diagnoses of
neurologic signs
neuroophthalmology
neuropathology
neuropathology, brain
nystagmus
obsessive-compulsive disorder
oculogyric crisis
ophthalmoplegia
ophthalmoplegia, neonatal
ophthalmoplegia, total
opisthotonus
Parkinson disease, atypical
Parkinson disease, L-dopa nonresponsive
Parkinsonism syndrome
personality change
preclinical
premature infant
prognosis
progressive supranuclear palsy
progressive supranuclear palsy, natural history
rapidly progressing neurologic illness
reading disorder, acquired
reading problem, causes of
release phenomena
review article
rigidity, axial
saccadic eye movements
saccadic eye movements, abnormal
seizure
sensorineural hearing loss
setting sun phenomena
speech disorder
suck, poor
synucleinopathy
tau protein
tauopathy
treatment of neurologic disorder
upgaze, paralysis of
vertical gaze
walking, difficulty with
Showing articles 0 to 50 of 8969 Next >>

Atypical Parkinsonian Syndromes: A General Neurologists Perspective
Eur J Neurol 25:41-58, Deutschlander, A.B.,et al, 2018

Advances in Progressive Supranuclear Palsy: New Diagnostic Criteria, Biomarkers, and Therapeutic Approaches
Lancet Neurol 16:552-563, Boxer, A.L.,et al, 2017

Functional Impairment in Progressive Supranuclear Palsy
Neurol 80:380-384, Duff, K.,et al, 2013

Clinical Features and Natural Histry of Progressive Supranuclear Palsy, A Clinical Cohort Study
Neurol 60:910-916, Nath,W.,et al, 2003

Progressive Supranuclear Palsy, A Survey of the Disease Course
Neurol 50:1637-1647, Santacruz,P.,et al, 1998

Bilirubin Metabolism and Kernicterus
Adv Pediatr 44:173-229, Gourley,G.R., 1997

Natural History of Progressive Supranuclear Palsy & Clin Predictors of Survival:A Clinicopath Study
JNNP 61:615-620, Litvan,I.,et al, 1996

Prevalence and Natural History of Progressive Supranuclear Palsy
Neurol 38:1031-1034, Golbe,L.I.,et al, 1988

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

Expanding Clinical Spectrum an Anti-GQ1b Antibody Syndrome, A Review
JAMA Neurol 81:762-770, Lee,S-U.,et al, 2024

Spinal Muscular Atrophy
UpToDate, Oct, Bodamer,O.A., 2022

The Phenotypic Continuum of ATP1A3-Related Disorders
Neurol 99:e1511-e1526, Vezyroglou,A., et al, 2022

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

Progressive Ataxia and Palatal Tremor
Neurol 94:e1445-e1447, Pradeep, S.,et al, 2020

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

A Man with Rapidly Progressive Weakness and Respiratory Failure
Neurol 91:e686-e691, Xu,D.,et al, 2018

A 35-year-old Woman with Diplopia, Ataxia, and Altered Mental Status
Neurol 91:e1942-e1946, Bauer, Z.,et al, 2018

Mystery Case: A 48-year-old Woman with Bizarre Behavior, Neurologic Symptoms, and Progressive Decline
Neurol 90:242-247, Kesari, N.K.,et al, 2018

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

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

Intracranial Dural Arteriovenous Fistulae
Stroke 48:1424-1431, Reynolds, M.R.,et al, 2017

Rapidly Progressive Quadriplegia and Encephalopathy
JAMA Neurol 73:1363-1366, Wynn, D.,et al, 2016

Myasthenia Gravis
NEJM 375:2570-2581, Gilhus, N.E.,et al, 2016

A Young Man with Progressive Language Difficulty and Early-Onset Dementia
JAMA Neurol 73:595-599, Botha, H.,et al, 2016

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

Rapid Multifocal Neurologic Decline in an Immunocompromised Patient
JAMA Neurol 73:226-231, Kromm, J.A.,et al, 2016

Paraneoplastic Cerebellar Degeneration with Anti-Yo Antibodies - A Review
Ann Clin Trans Neurol 3:655-663, Venkatraman,A. & Opal,P., 2016

Degenerative Diseases of the Nervous System, Amyotrophic Lateral Sclerosis
Adams & Victors Principles of Neurology, Chp 39, pg 1109, Ropper, A.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Acute Anterior Poliomyelitis
Adams & Victors Principles of Neurology, Chp 33, pg 763, Ropper, A.H.,et al, 2014

Bilirubin-Induced Neurologic Damage - Mechanisms and Management Approaches
NEJM 369:2021-2030, Watchko, J.F.,et al, 2013

Aspergillus Meningitis: A Rare Clinical Manifestation of Central Nervous System Aspergillosis
J Infect 66:218-238, Antinori, S.,et al, 2013

Risk Factors for Spinal Cord Lesions in Dystonic Cerebral Palsy and Generalised Dystonia
JNNP 83:159-163, Guettard,E.,et al, 2012

Cogan Syndrome An Analysis of Reported Neurological Manifestations
The Neurologist 18:55-63, Antonios,N. and Silliman,S., 2012

Transition to Adult Care for Children with Chronic Neurological Disorders
Ann Neurol 69:437-444, Camfiled, P. & Camfield, C., 2011

Rhombencephalitis A Series of 97 Patients
Medicine 90:256-261, Moragas, M.,et al, 2011

Clinical and Genetic Spectrum of Mitochondrial Neurogastrointestinal Encephalomyopathy
Brain 134:3326-3332, Garone, C.,et al, 2011

Diagnosis and Management of Motor Neurone Disease
BMJ 336:658-662, McDermott,C.J. &Shaw,P.J., 2008

Amyotrophic Lateral Sclerosis
Lancet 369:2031-2041, Mitchell,J.D. & Borasio,G.D., 2007

Ruptured Cavernous Sinus Aneurysms Causing Carotid Cavernous Fistula: Incidence, Clinical Presentation, Treatment, and Outcome
AJNR 27:185-189, van Rooij, W.J.,et al, 2006

West Nile Virus Infection in the United States
Arch Neurol 61:1190-1195, Tyler,K.L., 2004

Neurologic Manifestations in Primary Sjogren Syndrome: A Study of 82 Patients
Medicine 83:280-291, Delalande,S.,et al, 2004

Vascular Syndromes of the Thalamus
Stroke 34:2264-2278, Schumahmann,J.D., 2003

Neuropathological Findings in West Nile Virus Encephalitis: A Case Report
Ann Neurol 54:547-551, Agamanolis,D.P.,et al, 2003

Practice Parameter:The Care of the Patient with Amyotrophic Lateral Sclerosis (An Evidence-Based Review), Report of the Quality Standards Subcommittee of the AAN
Neurol 52:1311-1323, Miller,R.G.,et al, 1999

Neurologic Complications in Children with Enterovirus 71 Infection
NEJM 341:936-942, Huang,C-C.,et al, 1999

Adult Botulism
Muscle & Nerve, 20:100-10297., Shapiro,B.E.,et al, 1997

Complete Ophthalmoplegia After Zoster Ophthalmicus
J Neuro-Ophthalmol 17:262-265, Chang-Godinich,A.,et al, 1997

Clinical Variability in Adult-Onset Acid Maltase Deficiency:Report of Affected Sibs and Review of Literature
Medicine 74:131-135, Felice,K.J.,et al, 1995

Myotonic Dystrophy
In Myology, Engel & Franzini-Armstrong, McGraw-Hill, Inc, New York V2, Ch 43, P1192, Harper,P.S.&Rudel,R., 1994



Showing articles 0 to 50 of 8969 Next >>