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Differential
(Click to cross reference)
acalculia
acquired immunodeficiency syndrome
Africa
agitation
alcohol intolerance
alopecia
alternating rapid movement
alternating rapid movement, impaired
ankle reflex, absent
anorexia
antiviral agents
apraxia, constructional
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxia, progressive
ataxia, truncal
ataxic gait
atypical
automobile accidents
autosomal rcessive spastic ataxia of Charlevoix-Saguenay
Babinski sign
Balint's syndrome
basal ganglia, lesion, bilateral
behavioral disorder
bone age
cachexia
CAG repeats
caloric testing
CAT scan, abnormal
CAT scan, chest
CD4 counts
cerebellar atrophy, primary
cerebellar degeneration
cerebellar lesion
cerebellum, disease of
children
choking
chromosomal abnormality
cleft palate
Clinical Pathologic Conference(C.P.C.)
clinodactyly
clonus
cognition, slowed
coinfection
congenital malformation
consanguinity
Cornelia de Lange syndrome
corpus callosum, thinning
Creutzfeldt-Jakob disease, genetic
cry, abnormal
deep gray nuclei
dementia
dementia, familial
dementia, frontotemporal
dementia, rapidly progressive
difficulty climbing stairs
digits, abnormal
diplopia
dizziness
dysarthria
dysdiadochokinesia
dysmetria
dysmorphic
dysphagia
eye movement, disorders of
eyebrows, abnormal
failure to thrive
falling
familial
fatigue
fever
finger nose finger test
foot deformity
frontotemporal dementia, behavioral variant
gait disorder
gene mutation
genetic neurologic disorders
genetic testing
growth retardation
hammertoes
handwriting
headache
headache, progressive
heel-knee-shin test
hirsutism
human immunodeficiency virus type 1
human immunodeficiency virus type 1, false positive
human immunodeficiency virus type 2
hyperreflexia
imbalance
immune reconstitution inflammatory syndrome
immunohistochemistry
immunosuppression
incoordination
insomnia
irritability
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, variant
labyrinth, disorder of
labyrinthitis
labyrinthitis, acute
leg weakness, bilateral
leptospirosis
lethargy
Lewy body disease, diffuse
low birth weight
lymphopenia
memory, defect of recent
memory, impairment of
meningeal enhancement
meningismus
meningitis
meningitis, aseptic
meningitis, leptospira
mental retardation
metamyelocytes
micrognathia
micromelia
middle cerebellar peduncle, lesion
mortality
MRI, abnormal
MRI, contrast enhanced
MRI, diffusion weighted
MRI, false negative
MRI, punctate pattern
MRI, ring sign
myoclonic jerks
myoclonus
nausea and vomiting
neurologic disease, diagnoses of
neuropathology
neuropathy
nystagmus
nystagmus, direction fixed
nystagmus, rotary
nystagmus, spontaneous
oligodactyly
opportunistic infection
opportunistic infection, CNS
optic atrophy
paranoia
past pointing
phocomelia
polymerase chain reaction
polymerase chain reaction, false negative
pons, lesion of
posterior cortical atrophy
prion disease
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
psychiatric problems in neurologic disorders
psychomotor retardation
pupil, ectopic-congenital
pursuit eye movements, abnormal
rapidly progressing neurologic illness
real-time quaking-induced conversion
Romberg's sign
saccadic eye movements, abnormal
saddle nose
serologic testing
simian crease
simultanagnosia
single photon emission computed tomography
snout reflex
spasticity
spinocerebellar ataxia
spinocerebellar ataxia type 7
spirochete infection
square wave jerks
startle myoclonus
subconjunctival hemorrhage
subcortical U fibers
symmetric brain lesions
syndactyly
synophrys
tandem gait, ataxic
tau protein
thalamus, lesion of-bilateral
thrush
toxoplasmosis, CNS
treatment of neurologic disorder
tremor
tremor, intention
trinucleotide repeats
upgaze, paralysis of
vertigo
vision, blurred
visual acuity, decreased
visuospatial disturbance
walking frame
walking, difficulty with
weight loss
wheelchair
wide based gait
workup
WORLD spelling test
Showing articles 0 to 50 of 209 Next >>

More Than a Little Unsteady
NEJM 387:e9, Kraft, A.W.,et al, 2022

Complex Ataxia
Neurol 95:136-141, Abkur, T.,et al, 2020

Clinicopathologic Conference, HIV Type 2 Infection & Cerebral Toxoplasmosis
NEJM 383:859-866, Case 27-2020, 2020

A 72-year-old Man with a Progressive Cognitive and Cerebellar Syndrome
Neurol 95:e2707-e2710, Lad, M. & Griffiths, T.D., 2020

Clinicopathologic Conference, Creutzfeldt-Jakob Disease
NEJM 381:1569-1578, Case 32-2019, 2019

A 52-year-old woman with a 3 weeks of progressive gait ataxia and dysarthria
Neurol 90:e985-e989, Ly, C.,et al, 2018

A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
Ann Neurol 77:1-7, Scripko, P.,et al, 2015

A 75-year-old man with 3 years of Visual Difficulties
Neurol 83:e160-e165, Berkowitz, A.L.,et al, 2014

Slurred Speech and Spirochaetes
Lancet 373:978, Thukral,A.,et al, 2009

Vertigo and Dizziness
In Diseases of the Nervous System, Asbury, A. K. , et al, W B Saunders, p. 561, Brandt,T., 1986

The Cornelia de Lange Syndrome
J Pediatr 63:1000-1020, Ptacek,L.J., 1963

A 19-Year-Old Woman with Progressive Weakness and Numbness in Her Arms and Legs
Neurol 104:e213495, Alsabah,A-A.,et al, 2025

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

A 55-Year -Old Woman with Painless Hand Weakness and Atrophy
Neurol 103:e209561, Ticku,H. & Katirji,B.,, 2024

Clinicopathologic Conference, Hypocalcemic Myopathy Due to Hypoparathyroidism
NEJM 388:1513-1520, Case 12-2023, 2023

Skin Lesions, Foot Drop, and Hand Contractures
JAMA doi:10.1001/JAMA.2023.9915, Filley,A.R.,et al, 2023

Multidisciplinary End-of-Life Care for a Patient with Amyotrophic Lateral Sclerosis Requesting Euthanasia
Lancet 402:484, Kruithof,W.J.,et al, 2023

Polymyalgia Rheumatica
Lancet 402:1459-1472, Espigol-Frigole,G.,et al, 2023

Severe Vitamin B12 Deficiency Presenting as Pancytpenia, Hemolytic Anemia, and Parasthesia:Could Your B12 Be Any Lower?
Cureus doi:10.7759/cureus 29225, Pelling,M.M., et al, 2022

Epidemiology, Survival, and Clinical Characteristics of Inclusion Body Myositis
Ann Neurol 92:201-212, Lindgren, U.,et al, 2022

A 65-Year-Old Woman with Cancer History and Wrist Drop
Neurol 99:570-576, Merrill, R.,et al, 2022

A 31-year-Old Man with Bilateral Limited Mobility of Joints
JAMA Neurol 79:1083-1084, Wang, Z.,et al, 2022

A 6-Year-Old Girl with Progressive Toe Walking
Neurol 98:e769-e773, Libdeh, A.A. & Ibrahim, A., 2022

Clinicopathologic Conference, Systemic Juvenile Idiopathic Arthritis
NEJM 385:1220-1229, Case 29-2021, 2021

A Middle-aged Woman with Severe Scoliosis and Encephalopathy
JAMA Neurol 78:251-252, Mohan, G.,et al, 2021

Pyogenic Brain Abscesses in a Patient with Digital Clubbing
JAMA Neurol 77:129-130, Paliwal, V.K.,et al, 2020

A 22-Year-Old Man with Progressive Bilateral Visual Loss
Neurol 94:625-630, Yang, S.L.,et al, 2020

"Cortical" Wrist Drop due to a Cerebral Peduncle Infarct
Case Rep Neurol 12:207-211, Venketasubramanian, N.,et al, 2020

A 17-year-old Baseball Player with Right Hand Weakness
Neurol 92:e76-e80, Vachon, C. & Libdeh, A.A., 2019

A 14-Year-Old Girl with Headache, Seizures, and Confusion
Neurol 92:e161-e167, Xiao, L.,et al, 2019

A 40-Year-Old Woman Presenting with Distal Leg Weakness
Neurol 92:242-247, Fam, D.,et al, 2019

Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
AJNR 40:903-907, Hartin, I.,et al, 2019

Pes Cavus and Neuropathy
Neurol 93:e823-e826, Alderson,J.,& Ghosh,P.S., 2019

A 26-Year Old Man with Right Hand and Arm Weakness
Neurol 93:e927-e933, Elliott,E.J.&Smith,J.D., 2019

Disability in adults with arthrogryposis is severe, partly invisible, and varies by genotype
Neurol 90:e1596-e1604, Dai, S.,et al, 2018

A 58-year-old Woman with Systemic Scleroderma and Progressive Cervical Cord Compression
Neurol 91:e1262-e1264, Karschnia, P.,et al, 2018

Clinical Reasoning: Cardioembolic Stroke in a 23-year-old Man with Elbow Contracture
Neurol 90:e172-e176, Roy, B. & Raynor, E., 2018

A 60-year-old man with arm weakness and numbness
Neurol 90:190-196, Foster, L.A.,et al, 2018

Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
Neurol 90:e625-e631, Set, K.K.,et al, 2018

Clinicopathologic Conference, Homocystinuria due to genetic mutations of the gene encoding cystathionine B-synthase (CBS)
NEJM 378:941-948, Case 7-2018, 2018

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

Making Sense of the Clinical Spectrum of Limb Girdle Muscular Dystrophies
Pract Neurol 18:201-210, Khadilkar,S.V.,et al, 2018

Pseudoradial Nerve Palsy Caused by Acute Ischemic Stroke
J Invest Med Case Report doi:10.1177/2324709616658310, Tahir, H.,et al, 2016

Wilson Disease
Yamada Textbook of Gastroenterology Chp 102, Metabolic Diseases of Liver, 6th Ed, Sunderam, S.S., & Sokol, R.J., 2016

Differential Diagnosis
Thoracic Key, Southerland,A.W.,et al, 2016

Finger Clonus
Neurol 86:e118-e119, Moccia,M.,et al, 2016

Clinicopathologic Conference, IgG4-Related Hypophysitis
NEJM 375:1469-1480, Case 31-2016, 2016

Neonatal Abstinence Syndrome
NEJM 375:2468-2479, McQueen, K. & Murphy-Oikonen, J., 2016

Short Stature, Imperforate Anus, and Polydactyly
Neurol 84:e117, Dumitrascu, O.,et al, 2015



Showing articles 0 to 50 of 209 Next >>