Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
alcohol, neurologic complications with
alcoholism
alien hand syndrome
ANA
anticardiolipin antibodies
antiphospholipid antibody syndrome
aphasia
aphasia, progressive, primary
apraxia
ataxia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic gait
autoantibodies
autoimmune encephalopathy
autonomic dysfunction
Babinski sign
basal ganglia
basal ganglia, lesion of
basal ganglia, lesion, bilateral
bradykinesia
brain atrophy
cachexia
cerebellar degeneration
cerebellitis, autoimmune
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, three territory involvement
children
chorea
choreoathetosis
cirrhosis
Clinical Pathologic Conference(C.P.C.)
cognition
cogwheel rigidty
confusion
consanguinity
contractures, joint
corpus callosum, thinning
cortical-basal ganglionic degeneration
degenerative diseases of CNS
dementia
developmental milestones, loss of
diagnostic criteria
differential diagnosis
diplopia
disorientation
dopa responsive dystonia
DPPX
DPPX, antibodies, encephalitis
dysarthria
dysdiadochokinesia
dyskinesia, buccal lingual facial
dysphagia
dystonia
dystonia, children
encephalitis, autoimmune
encephalopathy
encephalopathy, progressive
enzyme, defect
extrapyramidal movement disorder, progressive
eye movement, disorders of
falling
familial
frontal behavioral spatial syndrome
gait disorder
galactorrhea
gene mutation
genetic neurologic disorders
genetic testing
globus pallidus
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
Hallervorden Spatz disease
hemiparesis
hepatic failure
hepatolenticular degeneration, non-Wilsonian
hyperammonemic encephalopathy
hyperesthesia
hyperreflexia
hypertonia
hypocomplementemia
hypophonia
hyporeflexia
imbalance
imbalance, postural
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
intellectual deficit
intellectual deterioration
iron, brain
L-dopa
lenticular nucleus, lesion of, bilateral
liver disease
manganese intoxication
marche a petits pas
memory, impairment of
meningitis
mental status, abnormal
Mini Mental Status Examination
misdiagnosis
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, high signal intensity of basal ganglia
MRI, paramagnetic effect
MRI, T1 weighted high signal foci
multiple system atrophy
myelopathy
myelopathy, hepatic
neurologic disease, diagnoses of
neurologic disease, tempo
neuropathology
neuropathology, brain
optic atrophy
orthostatic hypotension
PANK2 mutation
paraparesis, spastic
Parkinson disease, L-dopa nonresponsive
Parkinsonism multiple-system atrophy
Parkinsonism syndrome
personality change
portal caval shunt
postural abnormality
progressive neurologic disorder
progressive supranuclear palsy
prolactin, elevated
pyramidal tract
pyramidal tract dysfunction
retinitis pigmentosa
review article
rigidity
Romberg's sign
scoliosis
sea-blue histiocytes
seizure
spasticity
speech disorder
speech disorder, childhood
stare
substantia nigra
synucleinopathy
tandem gait, ataxic
tau protein
tauopathy
Three territory sign
thrombophlebitis
titubation
treatment of neurologic disorder
tremor
tyrosine hydroxylase deficiency
visual evoked response
visual impairment
walking frame
walking, difficulty with
weight loss
wheelchair
wide based gait
workup
Showing articles 0 to 50 of 18108 Next >>

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

Clinicopathologic Conference, Antiphospholipid Syndrome due to SLE with Hypocomplimentemia
NEJM 389: 2277-2285, Case 38-2023, 2023

A 37-Year-Old Man with Involuntary Movements, Gait Disturbance, and Hyperasthesia
Neurol 98:851-853, Meng, D.,et al, 2022

A Middle-Aged Man with Progressive Gait Abnormalities
Neurol 97:e2423-e2428, Lin, J.,et al, 2021

Pantothenate Kinase - Associated Neurodegeneration (PKAN)
Emedicine.Medscape Sept, Hanna, P.A. & Benbadis, S.R., 2018

Acquired Hepatocerebral Degeneration
Neurol 87:e144, Bateman, J.R. & Roque, D.A., 2016

Criteria for the Diagnosis of Corticobasal Degeneration
Neurol 80:496-503, Armstrong, M.J.,et al, 2013

Clinicopath Conf, Multiple-System Atrophy
NEJM 351:912-921, Case 27-2004, 2004

Hallervorden-Spatz Syndrome and Brain Iron Metabolism
Arch Neurol 48:1285-1293, Swaiman,K.F., 1991

Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023

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

A 77-Year-Old Man with Involuntary Movements, Sleep Changes, Falls, Bulbar Symptoms, and Cognitive Complaints
Neurol 99:26-30, Cao, T.Q.,et al, 2022

Functional Neurological Disorders
Neurologist 27:276-289, Mishra, A. & Pandey, S., 2022

Vitamin B12 Deficiency in a 29-Year-Old Woman
Neurol 97:e643-e646, Huddar, A.,et al, 2021

A 65-Year-Old Woman with Tremor
Neurol 97:e1257-e1261, Ye, J.,et al, 2021

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

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

Telemedicine in Neurology
Neurol 94:30-38,16, Hatcher-Martin, J.M.,et al, 2020

A Rare Presentation of Whipple Disease
Neurol 94:e758-e761, Koek, A.T.,et al, 2020

A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
Neurol 94:e1213-e1218, Lima, J.E.E.,et al, 2020

GGC Repeat Expansion of NOTCH2NLC in Adult Patients with Leukoencephalopathy
Ann Neurol 86:962-968,809, Okubo, M.,et al, 2019

Chronic Dengue Virus Panencephalitis in a Patient with Progressive Dementia with Extrapyramidal Features
Ann Neurol 86:695-703, Johnson, T.P.,et al, 2019

A Middle-Aged Man with New Onset Seizures and Myoclonic Jerks
Neurol 92:e274-e281, Chen, Z. & Neo, S., 2019

Neurodegeneration with Brain Iron Accumulation
AIAN 22:267-276, Batla, A. & Gaddipati, C., 2019

Wilson Disease
NIDDK Oct2018, , 2018

Cerebral Atrophy and Leukoencephalopathy in a Young Man Presenting with Encephalitic Episodes
JAMA Neurol 75:1563-1564, Xiao, F.,et al, 2018

Clinicopathological Conference, Insulinoma
NEJM 379:376-384, Case 23-2018, 2018

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

Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017

Action Tremor, Impaired Balance, and Executive Dysfunction in Midlife
JAMA Neurol 74:603-604, Birch, R.C. & Trollor, J.N., 2017

An 82-year-old man with Worsening Gait
Neurol 89:e246-e252, Chew, S.,et al, 2017

Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
NEJM 377:2376-2385, Case 38-2017, 2017

Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
Front Neurol doi:10.3389/fneur.2017.00472, Velazquez-Perez, L.C.,et al, 2017

Degenerative Diseases of the Nervous System, Progressive Bulbar Palsy
Adams & Victors Principles of Neurology, Chp 39, pg 1111, Ropper, A.H.,et al, 2014

Facial Bradykinesia
JNNP 84:681-685, Bologna, M.,et al, 2013

Incidence and Pathology of Synucleinopathies and Tauopathies Related to Parkinsonism
JAMA Neurol 70:859-866, Savica, R.,et al, 2013

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

Clinical Reasoning: A 13-year-old Boy Presenting with Dystonia,Myoclonus,and Anxiety
Neurol 78:e72-e76, Blackburn,J.S. and Cirillo,M.L., 2012

Clinicopath Conf, Rapid-Onset-Dystonia-Parkinsonism Due to a Mutation in the ATP1A3 Gene
NEJM 362:2213-2219, Case 17-2010, 2010

Anti-N-Methyl-D-Aspartate Receptor (NHMDAR) Encephalitis in Children and Adolescents
Ann Neurol 66:11-18,1, Florance,N.R.,et al, 2009

Aicardi-Gouti�res Syndrome
Br Med Bull 89:183-201, Orcesi, S.,et al, 2009

A Parkinsonian Syndrome in Methcathinone Users and the Role of Manganese
NEJM 358:1009-1017, Stepens,A.,et al, 2008

Tau Forms in CSF as a Reliable Biomarker for Progressive Supranuclear Palsy
Neurol 71:1796-1803, Borroni,B.,et al, 2008

Clinicopath conf., Human Prion Disease, Sporadic CJD
Neurol 69:1881-1887, Geschwind,M.D., et al, 2007

Mitochondrial DNA Polymerase-y and Human Disease
Hum Mol Genet 15:R244-R252, Hudson, G.,et al, 2006

Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome
NEJM 348:33-40, Hayflick,S.J.,et al, 2003

Progressive Multifocal Leukoencephalopathy Presenting with an Isolated Focal Movement Disorder
Movement Disorder 15:1006-1009, Stockhammer,G.,et al, 2000

Review of 23 Patients Affected by the Stiff Man Syndrome:Clinical Subdivision into Stiff Trunk (man) Syndrome,Stiff Limb Syndrome,and Progressive Encephalopmyelitis with Rigidity
JNNP 65:633-640, Barker,R.A.et al, 1998

Bent Spine Syndrome
JNNP 60:51-54, Serratrice,G.,et al, 1996



Showing articles 0 to 50 of 18108 Next >>