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alpha-fetoprotein
alternating hemiplegia
alternating hemiplegia of childhood
alternating rapid movement
aminoacidurias
anti MAG antibodies
anti Yo antibody
aphasia
aphasia, children
apraxia, speech
aspiration
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic gait
ataxic hemiparesis
attention deficit disorder with hyperactivity
attention span
autism
autoantibodies
Babinski sign
basal ganglia, degeneration
basilar artery stenosis
behavioral disorder
Benedict's solution test
bifid uvula
bradykinesia
brainstem, atrophy
brainstem, lesion of
calcification, intracranial
carcinoma
carcinoma of breast
carcinoma of ovary
CAT scan, emission, abnormal
catalepsy
cataplexy
cerebellar ataxia, children
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar lesion
cerebral cortex
cerebral cortical atrophy
cerebral palsy
cerebral palsy, associated problems with
cerebral palsy, pure ataxic
cerebrospinal fluid, abnormal
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
chairbound
chemotherapy, CNS treatment and complications with
children
chorea
choreoathetosis
cleft palate
Clinical Pathologic Conference(C.P.C.)
cognition
complications
confusion
consanguinity
cortical-basal ganglionic degeneration
cranial nerve palsies
cranial nerve palsies, bilateral
cranial neuropathy, multiple
crying, pathologic
cryptococcal antigen
cryptococcal meningitis
cultured skin fibroblasts
deep gray nuclei
degenerative diseases of CNS
dementia
dementia, presenile
demyelinating disease
developmental milestones, loss of
diagnostic criteria
dinitrophenylhydrazine(D.N.P.H.)reaction
diplegia, atonic
diplegia, spastic cerebral
diplopia
disability, neurological
disease modifying agents
dizziness
drooling
drowsiness
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dysphonia
dysplasia of C.N.S.
dyspraxia
dystonia
electroencephalogram
electromyogram
emotional lability
encephalitis
encephalitis, autoimmune
encephalopathy
encephalopathy, acute
epileptic encephalopathy
exome sequencing
eye movement, disorders of
facial nerve palsy
failure to thrive
falling
familial
FARS2 deficiency
ferric chloride test
fine motor function, impaired
foam cells
fungal infection
fungal infection, CNS
gait disorder
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
glabellar sign
grasp reflex
head nodding
headache
headache, intractable
hearing loss
hearing problems in children
heel-knee-shin test
hemiplegia
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatosplenomegaly
hyperreflexia
hypoglycorrhachia
hypotonia
iatrogenic neurologic disorders
imbalance
immunocompetent
immunodeficiency
immunomodulation
immunotherapy
inattention
incontinence, fecal
incoordination
infection
intellectual deficit
intellectual deficit, treatable causes of
intellectual deterioration
intelligence quotient
jaundice
karyotyping
Kayser-Fleischer ring
klippel feil syndrome
language disorders in children
laughing, pathologic
lethargy
leukemia
lipid storage disorder of CNS
liver disease
locked-in syndrome
lysosomal storage disease
maple syrup urine disease
masked facies
memory, impairment of
meningeal enhancement
meningeal enhancement, nodular
meningitis
meningitis, CSF cell count-normal
meningitis, fungal
meningitis, neutrophilic
meningitis, neutrophilic, persistent
mental retardation
mental status, abnormal
methotrexate
microcephaly
midbrain
midbrain, infarction of
midline defect in children
mimics
misdiagnosis
mitochondrial disease
monoclonal antibodies
monoparesis
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, angiography
MRI, contrast enhanced
MRI, disappearing lesion on
MRI, negative
MRI, nodular enhancement
multiple system atrophy
mutism
myelodysplasia
nasal speech
nausea and vomiting
negative
neurofibrillary degeneration
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neurologic symptoms
neuropathology
neuropathy
neurotoxic
neurotoxicity, acute
Niemann-Pick disease
ocular motility, disorders of
palatopharyngeal incompetence
paraneoplastic cerebellar degeneration
paraparesis, familial spastic
paraparesis, spastic
Parkinson disease
Parkinsonism syndrome
personality change
phenylketonuria
pleocytosis of cerebrospinal fluid
pleocytosis of cerebrospinal fluid, neutrophilic
pneumonia
primary lateral sclerosis
prognosis
progressive neurologic disorder
progressive supranuclear palsy
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, neurologic problems
psychosis
psychosis, childhood
psychosocial aspects
ptosis
ptosis, unilateral
pulmonary infection
pure motor hemiplegia
pursuit eye movements, abnormal
pyramidal tract
pyramidal tract dysfunction
quadriparesis
quadriplegia
recurrent
release phenomena
remote effect of cancer on the nervous system
review article
rigidity
saccadic eye movements, abnormal
salivation, excessive
seizure
seizure, advice to parents and teachers regarding
seizure, children
seizure, psychosocial aspects of
seizure, treatment of
single photon emission computed tomography
skin, lesions in neurologic disorders
slit lamp examination
spastic diplegia
spasticity
speech disorder
speech disorder, childhood
speech, loss of
spina bifida
splenomegaly
stare
stuttering
suck reflex
telangiectases
third nerve palsy
third nerve palsy, bilateral
third nerve palsy, partial
toe walking
tongue, impaired movements of
transient neurologic deficit
treatment of neurologic disorder
tremor
upgaze
upgaze, paralysis of
urinary incontinence
urine test for metabolic disorders
vertigo
walking, difficulty with
weight loss
wheelchair
wide based gait
Showing articles 50 to 100 of 15263 << Previous Next >>

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

A 58-year-old man with Progressive Ptosis and Walking Difficulty
Neurol 89:e1-e5, Kuo, P.,et al, 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

Wernekink Commissure Syndrome Secondary to Bilateral Caudal Paramedian Midbrain Infarction Presenting with a Unique "Heart or V" Appearance Sign:Case Report and Review of the Literature
Front Neurol soi.10.3389/fneur.2017.00376,Aug, Zhou,C.,et al, 2017

Adult-Onset Niemann-Pick Disease Type C: Rapid Treatment Initiation Advised but Early Diagnosis Remains Difficult
Front Neurol doi.10.3398/jneur.2017.00108, Piroth,T.,et al, 2017

Complete Lingual Palsy from Bilateral Dejerine Syndrome (Bilateral Medial Medullary Stroke)
Neurol 87:550, Tsetsou, S.,et al, 2016

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

Ocular Motor Abnormalities in Bilateral Paramedian Thalamic Stroke
Neurol 84:e155-e158, Gooneratne, I.K.,et al, 2015

Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Legionella
Adams & Victors Principles of Neurology, Chp 32, pg 709, Ropper, A.H.,et al, 2014

Infections of the Nervous System, (Bacterial, Fungal, Spirochetal, Parasitic) and Sarcoidosis, Whipple Disease
Adams & Victors Principles of Neurology, Chp 32, pg 710, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Hepatolenticular Degeneration (Wilson Disease)
Adams & Victors Principles of Neurology, Chp 37, pg 982, Ropper, A.H.,et al, 2014

Inherited Metabolic Diseases of the Nervous System, Adrenoleukodystrophy
Adams & Victors Principles of Neurology, Chp 37, pg 988, Ropper, A.H.,et al, 2014

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

Progressive Cerebellar Ataxia and New-Onset Diabetes
Lancet 383:186, Kong, M.,et al, 2014

Psychosis in an Adolescent Girl: A Common Manifestation in Niemann-Pick Type C Disease
Child Adolesc Pych Ment Health 8:20, Wouters,S.,et al, 2014

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

Extensive Striatal, Cortical, and White Matter Brain MRI Abnormalities in Wilson Disease
Neurol 81:1557, Trocello, J.M.,et al, 2013

Central Nervous System Involvement in Whipple Disease
Medicine 92:324-330, Compain, C.,et al, 2013

Clinicopathologic Conference, Acute Ischemic Stroke due to Basilar Artery Embolism. Patent Foramen Ovale
NEJM 367:1450-1460, Case 31-2012, 2012

The Autosomal Recessive Cerebellar Ataxias
NEJM 366:636-646, Anheim,M.,et al, 2012

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

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

A 23-Year-Old Man With Seizures and Visual Deficit
Neurol 70:73-78, Boustany,R.-M.,et al, 2008

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

Pontine Warning Syndrome
Arch Neurol 65:1375-1377, Saposnik, G.,et al, 2008

Clinicopath Conf,Lyme Disease of the Nervous System
NEJM 356:1561-1570, Case Record 11-2007, 2007

Clinicopath Conf., Severe Microangiopathy of Diabetic Vasculopathy with Multiple Cerebral Infarcts
NEJM 357:164-173, Case Study 21-2007, 2007

Congenital Lymphocytic Choriomeningitis Virus Infection: Spectrum of Disease
Ann Neurol 62:347-355, Bonthius,D.J.,et al, 2007

"Salt and Pepper" in the Eye and Face: A Prelude to Brainstem Ischemia
Am J Ophthalmol 144:322-325, Conforto, A.B.,et al, 2007

Cerebellar Infarction int he Territory of the Medial Branch of the Superior Cerebellar Artery
Neurol 66:115-117, Sohn,S.-I.,et al, 2006

Early Clinical Signs and Imaging Findings in Gerstmann-Straussler-Scheinker Syndrome (Pro102Leu)
Neurol 66:1672-1678, Arata,H.,et al, 2006

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

Clinicopath Conf., Giant-Cell Arteritis
NEJM 349:170-180, Case 21-2003, 2003

Neurological Presentation of Fabry's Disease in a 52 Year Old Man
JNNP 73:340-342, Mohanraj,R.,et al, 2002

Cerebellar Ataxia With Anti-Glutamic Acid Decarboxylase Antibodies
Arch Neurol 58:225-230, Honorat,J.,et al, 2001

Brainstem Gliomas in Adults: Prognostic Factors and Classification
Brain 124:2528-2539, Guillamo,J.-S.,et al, 2001

Niemann-Pick Disease Type C: Two Cases and an Update
Movement Disorders 15:1199-1203, Uc,E.Y.,et al, 2000

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

Clinicopath Conf
Wegener's Granulomatosis Involving Sinuses, Skull, and Cranial Nerves, Case 28-1998, NEJM 339:755-76, , 199, 1998

The Phenotypic Spectrum of CADASIL:Clinical Findings in 102 Cases,
Ann Neurol 44:731-739,715, Dichgans,M.,et al, 1998

Posterior Cerebral Artery Syndromes
, Caplan,L.R. &Bogousslavsky,J., 1998

Cerebral Manifestation of Erdheim-Chester Disease:Clinical and Radiologic Findings
Neurol 49:1702-1705, Bohlega,S.,et al, 1997

Paraneoplastic Cerebellar Degeneration
Arch Int Med 157:1258-1262, Bolla,L.&Palmer,R.M., 1997

Spinocerebellar Ataxia Type 6, Molecular & Clin Features of 35 Japanese Pts (1 Homozygous for CAG Repeat Expan)
Neurol 49:1238-1243, 11961997., Matsumura,R.,et al, 1997

Pure or Predominant Sensory Stroke Due to Brain Stem Lesion
Stroke 28:1761-1764, Kim,J.S.&Bae,Y.H., 1997

Cytomegalovirus Encephalitis
Ann Int Med 125:577-578, Arribas,J.R.,et al, 1996

Diagnostic Guidelines in Central Nervous System Whipple's Disease
Ann Neurol 40:561-568, Louis,E.D.,et al, 1996

Chronic Lymphocytic Leukemia and the Central Nervous System:A clinical and Pathological Study
Neurol 46:19-25, Cramer,S.C.,et al, 1996

Restricted Nonacral Sensory Syndrome
Stroke 27:988-990, Kim,J.S., 1996

Neurologic Aspects of Inflammatory Bowel Disease
Neurol 45:416-421, Lossos,A.,et al, 1995



Showing articles 50 to 100 of 15263 << Previous Next >>