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Differential
(Click to cross reference)
alien hand syndrome
alpha-fetoprotein
anti IgLON5
anticholinergic drugs
aphasia
aphasia, progressive, primary
aphonia
applause sign
apraxia
apraxia of eye movements
arm swing, reduced
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic-dystonia syndromes
athetosis
autoantibodies
Babinski sign
basal ganglia, degeneration
biologic markers
biopterin deficiency
blepharospasm
bradykinesia
bruxism
bulbar palsy
carbamazepine
carcinoembryonic antigen
carcinoma
central hypoventilation
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar degeneration
cerebral cortical atrophy
cerebral palsy
cerebral palsy, associated problems with
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 14
chromosome 20
Clinical Pathologic Conference(C.P.C.)
cognition
cogwheel rigidty
comorbidities
conjugate gaze, forced
conversion reaction
cortical-basal ganglionic degeneration
crying, pathologic
degenerative diseases of CNS
delay in diagnosis
dementia
dexterity, impaired
diabetes mellitus
diagnostic criteria
differential diagnosis
diplopia
diurnal variation
dopa responsive dystonia
downward gaze
drooling
dysarthria
dysarthria-clumsy hand syndrome
dysmetria
dysphagia
dyspraxia
dystonia
dystonia musculorum deformens
dystonia, cervical
dystonia, face
dystonia, focal
dystonia, treatment of
emotional lability
enzyme, defect
equinovarus
exercise
exercise-induced neurologic dysfunction
exome sequencing
eye movement, disorders of
falling
familial
fine motor function, impaired
foot deformity
frontal behavioral spatial syndrome
gait disorder
gait, apraxic
gangliosidosis GM1
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic testing
glabellar sign
globus pallidus, lesion of
globus pallidus, lesion of, bilateral
grasp reflex
grimacing
growth retardation
Hallervorden Spatz disease
Hallervorden Spatz disease, late onset
hand weakness
hands, fisted
hemidystonia
hemifacial spasm
hepatolenticular degeneration(Wilson's disease)
HLA
hoarseness
hyperreflexia
hypometric saccades
hypophonia
hypotonia
ideomotor apraxia
imbalance
imbalance, postural
immunodeficiency
immunosuppression
inattention
incontinence, fecal
insomnia
intellectual deficit
intellectual deterioration
iron, brain
Jakob-Creutzfeldt disease
Kayser-Fleischer ring
laughing, pathologic
L-dopa
leg weakness, bilateral
leukemia
liver disease
lymphoma
masked facies
memory, defect of recent
memory, impairment of
meningitis
mental retardation
midbrain
midbrain, atrophy
misdiagnosis
molecular genetics
mortality
movement disorder
movement disorder, extrapyramidal
movement disorder, psychogenic
movement disorder, treatment of
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, eye of tiger sign
MRI, mouse ears
MRI, negative
MRI, paramagnetic effect
MRI, spine
multiple system atrophy
muscle spasm, face
myelopathy
myelopathy, chronic progressive
myoclonic jerks
myoclonus
neurocutaneous disease
neuroendocrinology
neurologic disease, diagnoses of
neurologic disease, diagnoses of, clinical bedside
neurologic disease, tempo
neurologic evaluation
neurologic examination
neurologic signs
neurologic symptoms
neuroophthalmology
neuropathology
neuropathy
numb clumsy hands syndrome
nystagmus
ocular motility, disorders of
opened mouth
palilalia
PANK2 mutation
paraparesis
parasomnia
parkin gene
Parkinson disease
Parkinson disease, axial symptoms
Parkinson disease, differential diagnosis of
Parkinson disease, juvenile
Parkinson disease, L-dopa nonresponsive
Parkinson disease, treatment of
Parkinson disease, tremor, absence of
Parkinsonism syndrome
pathology
penguin silhouette sign
personality change
pigmentary retinopathy
pitfalls
postural abnormality
procyclidine
progeria
prognosis
progressive neurologic disorder
progressive supranuclear palsy
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
pull test
radiation hypersensitivity
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
Red flags
release phenomena
respirations in CNS disease
retinopathy
retrocollis
Rett's syndrome
reversible neurologic disorder
review article
rigidity
rigidity, axial
risk factors
running
saccadic eye movements, abnormal
salivation, excessive
sensory loss, cortical
sequencing difficulty
short stature
sinemet
single photon emission computed tomography
skin, lesions in neurologic disorders
sleep apnea, obstructive
sleep pathology and physiology
slit lamp examination
speech disorder
spinal cord
spinal cord, lesion of
spinal muscular atrophy
spinocerebellar ataxia
spinocerebellar ataxia type 28
spinocerebellar degeneration
stare
suck reflex
swallow evaluation
tau protein
tauopathy
telangiectases
tetrahydrobiopterin
toe walking
tonic foot response
treatment of neurologic disorder
tremor
tremor, intention
tremor, jaw
tremor, postural
tripping
upgaze
upgaze, paralysis of
urinary incontinence
vision, blurred
visual symptoms
vocal cord paralysis
walking
walking frame
walking, difficulty with
wheelchair
wide based gait
Showing articles 0 to 50 of 8277 Next >>

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

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

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

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

A Demure Teenager and Her Dystonic Foot
Neurol 89:e71-e75, Cullinane, P.W.,et al, 2017

Degenerative Diseases of the Nervous System, Progressive Supranuclear Palsy
Adams & Victors Principles of Neurology, Chp 39, pg 1096, Ropper, A.H.,et al, 2014

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

Rapidly Progressive Corticobasal Degeneration Syndrome
Case Rep Neurol 3:185-190, Herrero Valverde, A.,et al, 2011

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

A 75-Year-Old Woman with Progressive Right-Hand Tremor and Inability to Use Her Right Side
Neurol 73:1399-1405, Kertesz,A.,et al, 2009

Clinical Spectrum of Ataxia-Telangiectasia in Adulthood
Neurol 73:430-437, Verhagen,M.M.M.,et al, 2009

Progressive Supranuclear Palsy: A Current Review
The Neurologist 14:79-88, Lubarsky,M. &Juncos,J.L., 2008

Dopamine-Responsive Dystonia
eMedicine (Apr), Nikhar,N.K., 2006

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

Clinical Presentation and Pharmacological Therapy in Corticobasal Degeneration
Arch Neurol 55:957-961, Kompoliti,K.,et al, 1998

Dopa-Responsive Dystonia, Some Pieces of the Puzzle are Still Missing
Neurol 50:853-855, Nygaard,T.G.&Wooten,G.F., 1998

Accuracy of the Clinical Diagnosis of Corticobasal Degeneration:A clinicopathologic Study
Neurol 48:119-125, Litvan,I.,et al, 1997

Clinicopath Conf
progressive Supranuclear Palsy, Case 46-1993, NEJM 329:1560-1567993., , 1993

GM1 Gangliosidosis in Adults:Clinical and Molecular Analysis of 16 Japanese Patients
Ann Neurol 31:328-332, Yoshida,K.,et al, 1992

Wilson's Disease:The Problem of Delayed Diagnosis
JNNP 55:692-696, Walshe,J.M.&Yealland,M., 1992

Dopa-Responsive Dystonia:Long-Term Treatment Response and Prognosis
Neurol 41:174-181, Nygaard,T.G.,et al, 1991

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

Extrapyramidal Involvement in Rett's Syndrome
Neurol 40:293-295, FitzGerald,P.M.,et al, 1990

Dopa Responsive Dystonia:A Treatable Condition Misdiagnosed as Cerebral Palsy
BMJ 298:1019-1020, Boyd,K.&Patterson,V., 1989

Hereditary Dystonia-Parkinsonism Syndrome of Juvenile Onset
Neurol 36:1424-1428, Nygaard,T.C.&Duvoisin,R.C., 1986

Corticodentatonigral Degeneration with Neuronal Achromasia
Arch Neurol 18:20-33, Rebeiz,J.J.,et al, 1968

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

Posttransplant Anti-GABAA Receptor Antibody-Associated Autoimmune Encephalitis
Neurol 102:e209245, Togni,C.L.,et al, 2024

A 35-Year-Old Woman with Personality Change and Gait Impairment
Neurol 104:e210252, Bernardes,C.,et al, 2024

Clinical Manifestations and Diagnostic Challenges in a 16-Year-Old With Early-Onset Ataxia
Neurol 104:e210253, Chadha,D.,et al, 2024

A 26-Year-Old Woman with Chronic Progressive Gait Dysfunction
Neurol 103:e2098-e2030, Jones,F.J.S. & Orthmann-Murphy,J., 2024

A 24-Year-Old Man with Gait Impairment, Hearing Loss, and Recurrent Fever
Neurol 102:e209358, Barbosa,A.R.,et al, 2024

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

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

An 82-Year-Old Woman with Subacute Ophthalmoparesis and Ataxia
Neurol 101:e570-e575, Rodrigo-Gisbert,M.,et al, 2023

Wernekinck Commissure Syndrome
Radiopaedia doi.org/10.53347/rlD-85274, Aug, Deng,F.,et al, 2023

Occult Breast Cancer with Anti-Ri Antibody Positivity and Pontine Hot Cross Bun Sign
JAMA Neurol 80:207-208, Liu,Y.,et al, 2023

Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
Neurol 100:766-783, Manini,A.,&Pantoni,L., 2023

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

Fragile X-Associated Tremor or Ataxia Syndrome in a Patient with Difficulty Walking, Falls, a Tremor, and Erectile Dysfunction
Lancet 400:1144, Sabino de Oliveira, D.,et al, 2022

Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
NEJM 386;674-687, Case 5-2022, 2022

Clinicopathologic Conference, Diffuse Large B-Cell Lymphoma
NEJM 386:977-986, Case 7-2022, 2022

A 57-Year-Old Man with Stepwise Progressive Paraparesis, Sensory Loss, Urinary Retention, and Constipation
Neurol 98:e555-e560, Alkabie, S.,et al, 2022

A 67-Year-Old Woman with Progressive Diplopia, Vertigo, and Ataxia
Neurol 98:e669-e674, Sakoda, M.,et al, 2022

A 48-Year-Old Woman Presenting with Vertigo, Ptosis, and Red Eyes
Neurol 98:678-683, Kim, K.T.,et al, 2022

A Dizzy Architect
Neurol 98:543-549, Scutelnic, A.,et al, 2022



Showing articles 0 to 50 of 8277 Next >>