Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
abducens nerve paralysis
acetazolamide
adenosine deaminase deficiency
adverse drug reaction
Africa
agenesis of corpus callosum
albinism
alcohol
alcohol, neurologic complications with
alpha-fetoprotein
alternating hemiplegia
alternating hemiplegia of childhood
anemia
anosmia
anterior spinal artery
aphasia
apnea
apnea, primary central
apraxia of eye movements
areflexia
Arnold Chiari malformation
arthralgia
ascites
aspartocyclase
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, hereditary
ataxia, paroxysmal
ataxia, progressive
ataxia, truncal
ataxic gait
athetosis
atlanto-axial subluxation
ATP1A3 gene
autonomic dysfunction
autosomal rcessive spastic ataxia of Charlevoix-Saguenay
Babinski sign
bacterial infection
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
benign essential tremor
blindness
bone marrow biopsy
brain biopsy
brainstem, atrophy
brainstem, dysfunction
brainstem, hypoplasia
brainstem, lesion of
brainstem, malformation
brainstem, neoplasms of
Brown-Vialetto-Van Laere syndrome
CAG repeats
Canavan's disease
carcinoma
cardiomyopathy
carotid angiogram
case studies
cassava
CAT scan
CAT scan, abnormal
cerebellar ataxia, children
cerebellar ataxia, hereditary
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar ataxia, primary
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar degeneration
cerebellar hypoplasia
cerebellar peduncle
cerebellar vermis
cerebellum, disease of
cerebellum, neoplasms of
cerebral edema
cerebrospinal fluid
cerebrospinal fluid, lactic acid concentration
cerebrovascular accident
cerebrovascular accident, multiple
cerebrovascular accident, young adult
channelopathy
Chediak-Higashi syndrome
cherry red spot
children
chorea
choreoathetosis
chromosomal abnormality
chromosome 11
chromosome 19
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
Collier's sign
coma
coma, episodic
complicated migraine
congenital malformation
congenital ocular motor apraxia
consanguinity
contractures, joint
conus medullaris, lesion of
corneal dystrophy
cough
cranial nerve palsies
cranial nerves
cranial neuropathy
cranial neuropathy, multiple
cranio-cervical junction
cultured skin fibroblasts
cyanide poison
deafness
deafness, bilateral progressive vs.unilateral acute
deafness, unilateral
degenerative diseases of CNS
dementia
dementia, familial
dementia, frontotemporal
dementia, presenile
demyelinating disease
developmental abnormality of brain
developmental milestones
developmental milestones, loss of
developmental retardation
diabetes insipidus
diabetes mellitus
diabetes mellitus, chemical
diabetes mellitus, neurologic manifestations of
diabetes mellitus, ocular complications in
diabetic cranialneuropathies
diagnostic criteria
differential diagnosis
diplopia
disconnection syndrome
down-beat nystagmus
down-beat nystagmus, primary position of gaze
drought
dysarthria
dysdiadochokinesia
dysmetria
dysphagia
dyspnea
dyspraxia
dystonia
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
electronystagmography
electroretinograph
encephalopathy
enzyme, defect
epidemiology of neurology
episodic disorders
episodic neurologic deficits
evoked potentials
exercise
eye movement, disorders of
Fabry's disease
face, numbness of
facial nerve palsy
facial nerve palsy, bilateral
failure to thrive
falling
familial
familial hemiplegic migraine
familial periodic ataxia
fasciculation
feeding disorder
fever
finger nose finger test
flunarizine
foam cells
foot drop
foot numbness
fourth ventricle, enlargement of
Friedreich's ataxia
frontotemporal dementia, behavioral variant
fundus, abnormality of
gadolinium
gait disorder
gait, spastic
gaze palsy
gaze palsy, congenital horizontal
gaze palsy, horizontal
gaze palsy, horizontal-bilateral
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
Gerstmann-Straussler-Scheinker disease
granulomatosis with polyangiitis
granulomatous disease
hammertoes
hand deformity
head circumference
head lag
head nodding
headache
hearing loss
hemangioblastoma
hemianopia
hemiparesis
hemiplegia
hemophagocytic lymphohistiocytosis, cerebromeningeal
hemophagocytosis
hepatomegaly
hepatosplenomegaly
HGPPS
Horner's syndrome
hyperreflexia
hypertension
hyperthyroidism
hypertriglyceridemia
hypofibrinogenemia
hypomyelination
hyporeflexia
hypotonia
imbalance
immunologic disease
immunosuppression
impulsivity
inborn errors of metabolism
inclusion bodies, intracytopasmic
incoordination
infantile bilateral striatal necrosis
infection, recurrent
intellectual deficit
internuclear ophthalmoplegia
internuclear ophthalmoplegia, bilateral
intracranial pressure, increased
iritis
irritability
Jakob-Creutzfeldt disease
jaundice
Jewish
Joubert syndrome
karyotyping
konzo
kyphoscoliosis, neurologic causes of
kyphosis
lactic acidemia
Leber's congenital amaurosis
Leigh's disease
leukocyte peroxidase
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
leukopenia
light-near dissociation, causes of
lipid storage disorder of CNS
livedo reticularis
lymphadenopathy
lymphoma involving CNS
lymphomatoid granulomatosis
macrocephaly
malformation, CNS, congenital
medulla oblongata
medulla oblongata, lesion of
medulla oblongata, malformation
memory, impairment of
meningismus
meningitis, carcinomatous
microcephaly
middle cerebellar peduncle, lesion
middle cerebellar peduncle, lesion, bilateral
migraine
migraine, hemiplegic
misdiagnosis
mitochondrial disease
molecular genetics
movement disorder
movement disorder, extrapyramidal
movement disorder, hyperkinetic
MRI
MRI, abnormal
MRI, contrast enhanced
MRI, spinal cord
multiple sclerosis, differential diagnosis of
multiple system atrophy
myasthenia gravis
myasthenia gravis, familial incidence of
myasthenia gravis, nystagmus in
myasthenia gravis, ocular
myasthenia gravis, sensory loss with
myelopathy
myoclonic jerks
myoclonus
myoclonus, epilepsy
myokymia
nausea and vomiting
neoplasm, primary of CNS
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic signs
neuromyotonia
neuronopathy
neuronopathy, sensory
neuroophthalmology
neuropathology
neuropathy
neuropathy, demyelinating
neuropathy, peripheral
neurotoxin
neutropenia
next-generation sequencing
Niemann-Pick disease
nystagmus
nystagmus, dissociated
nystagmus, gaze-evoked
nystagmus, gaze-paretic
nystagmus, hereditary
nystagmus, monocular
nystagmus, pendular
nystagmus, periodic
nystagmus, primary position of gaze
nystagmus, rotary
nystagmus, upbeating-in primary position of gaze
nystagmus, vertical
ocular motility, disorders of
ophthalmic artery occlusion
ophthalmoplegia
opisthotonus
optic ataxia
optic atrophy
optic disc cup
optical coherence tomography
optokinetic nystagmus, abnormal
oscillopsia
palatal myoclonus
pancytopenia
papilledema
paranoia
paraparesis
paraparesis, spastic
paraplegia
Parkinson disease
Parkinson disease, dystonia with
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
Pelizaeus Merzbacher
personality change
pes cavus
photophobia
pleocytosis of cerebrospinal fluid
POLG1 gene
pons, hypoplasia
precipitating factors
pregnancy, neurologic complications in
pretectal syndrome
primary episodic ataxia
prion disease
prognosis
progressive neurologic disorder
pseudointernuclear ophthalmoplegia
psychiatric problems in neurologic disorders
psychological testing, neurologic problems
psychomotor retardation
psychosis
ptosis
pulmonary infiltrates
pupil, abnormality in neurologic disorders
pupil, light reflex, abnormal
Purkinje cell
pursuit eye movements, abnormal
pyramidal tract dysfunction
pyramidal tract, uncrossed
pyruvate metabolism, abnormality of
quadriparesis
quadriplegia
rapid onset dystonia parkinsonism
rapidly progressing neurologic illness
rash
recurrent
release phenomena
renal tubular acidosis
respiratory failure
retinal degeneration
review article
RFC1 gene
rheumatoid arthritis
rheumatoid arthritis, neurologic complications of
riboflavin transporter deficiency
rigidity
Romberg's sign
scoliosis
scoliosis, neurologic association with
seizure
seizure, children
sensorineural hearing loss
sensory loss
sensory loss, leg
skin, lesions in neurologic disorders
slurred speech
Sneddon's syndrome
spastic ataxia
spastic diplegia
spasticity
speech, loss of
spinal cord, ischemic lesion of
spinal cord, neoplasm
spinocerebellar ataxia
spinocerebellar ataxia type 1
spinocerebellar ataxia type 3/Machado Joseph disease
spinocerebellar ataxia type 6
spinocerebellar degeneration
spinopontine atrophy, dominant
splenomegaly
spongy degeneration of brain
status epilepticus
steroid therapy, CNS treatment and complications with
stress, emotional
striatonigral degeneration
striatonigral degeneration, infantile
striatum, lesion of
striatum, lesion of, bilateral
subcortical U fibers
syphilis, neurologic complications with
tandem gait, ataxic
telangiectases
tensilon test
thalamus, lesion of
thalamus, lesion of-bilateral
thrombocytopenia
thyrotoxicosis
tinnitus
titubation
transient neurologic deficit
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
trinucleotide repeats
uremia
urinary incontinence
uveitis
vertigo
vertigo, episodic
vertigo, treatment of
vestibular areflexia
vestibulopathy
vision, failure of in childhood
visual acuity, decreased
visual evoked response
Von Hippel Lindau
walking, difficulty with
walking, difficulty with in dark
weakness
weakness, generalized
weakness, progressive
weight loss
wheelchair
white matter disease
wide based gait
Wolfram syndrome
wrist drop
Showing articles 700 to 750 of 2207 << Previous Next >>

Spinocerebellar Ataxia Type 8
Neurol 55:649-657, Day,J.W. et al, 2000

Multiple Sclerosis
NEJM 343:938-952, Noseworthy,J.H. et al, 2000

Recommendations for the Management of Patients with Unruptured Intracranial Aneurysms
Stroke 31:2742-2750, Bederson,J.B.,et al, 2000

Pulmonary Arteriovenous Malformations
Neurol 55:959-964, Moussouttas,M.,et al, 2000

Linkage of Familial Amyotrophic Lateral Sclerosis with Frontotemporal Dementia to Chromosome 9q21-q22
JAMA 284:1664-1669, Hosler,B.A.,et al, 2000

Familial Occipital Calcifications, hemorrhagic Strokes, Leukoencephalopathy, Dementia, and External Carotid Dysplasia
Neurol 55:1661-1667, Iglesias,S.,et al, 2000

Conjugal Multiple Sclerosis: Population-Based Prevalence and Recurrence Risks in Offspring
Ann Neurol 48:927-931, Evers,G.C.,et al, 2000

MR Imaging of the Cauda Equina in Hereditary Motor Sensory Neuropathies: Correlations with Sural Nerve Biopsy
AJNR 21:1793-1798,1779, Cellerini,M.,et al, 2000

Distribution of Cranial MRI Abnormalities in Patients with Symptomatic and Subclinical CADASIL
BJR 73:256-265, Coulthard, A.,et al, 2000

Tectal Gliomas: Natural History of an Indolent Lesion in Pediatric Patients
Pediatr Neurosurg 32:24-29, Bowers,D.C.,et al, 2000

Familial Neuromyelitis Optica (Devics Syndrome) with Late Onset in Japan
Neurol 55:318-320, Yamakawa,K.,et al, 2000

Bicuspid Aortic Valve - A Silent Danger: Analysis of 50 Cases of Infective Endocarditis
Clin Inf Dis 30:336-341, Lamas, C.C. & Eykyn, S.J., 2000

Treatment of Attention-Deficit-Hyperactivity Disorder
NEJM 340:780-788, Elia,J.,et al, 1999

Primary and Transitional Progressive MS,A Clinical and MRI Cross-Sectional Study
Neurol 52:839-845, Stevenson,V.L.,et al, 1999

N-Acetylcysteine Therapy for Unverricht-Lundborg Disease
Neurol 52:426-427, Selwa,L.M., 1999

What Level of Care for the Neurofibromatoses?
Lancet 353:1114-1116, Huson,S.M., 1999

Familial Subarachnoid Hemorrhage, Outcome Study
Stroke 30:1099-1102, Ronkainen,A.,et al, 1999

Oculogyric Crisis as an Initial Manifestation of Wilson's Disease
Neurol 52:714-715, Lee,M.S.,et al, 1999

A Randomized Placebo-Controlled Comparative Trial of Gabapentin and Propranolol in Essential Tremor
Arch Neurol 56:475-480, Gironell,A.,et al, 1999

MR Imaging of Dejerine-Sottas Disease
AJNR 20:378-380, Make,D.D.,et al, 1999

Sjogren-Larsson Syndrome, Clinical and MRI/MRS Findings in FALDH-Deficient Patients
Neurol 52:1345-1352,1307, Van Domburg,P.H.M.F.,et al, 1999

Hyperintense Basal Ganglia on T1-Weighted MR Imaging
AJR 172:1109-1115, Lai,P.H.,et al, 1999

Familial Paroxysmal Dystonic Choreoathetosis,Clinical Findings in a Large Japanese Family and Genetic Linkage to 2q
Arch Neurol 56:721-726, Matsuo,H.,et al, 1999

Serial Magnetic Resonance Imaging of Cerebral Atrophy in Preclinical Alzheimer's Disease
Lancet 353:2125, Fox,N.C.,et al, 1999

Molecular Basis of the Neurodegenerative Disorders
NEJM 340:1970-1980, Martin,J.B., 1999

Stereotactic Radiosurgical Pallidotomy and Thalamotomy with the Gamma Knife:MR Imaging Findings with Clinical Correlation-Preliminary Experience
Radiology 212:143-150, Friedman,D.P.,et al, 1999

Prethrombotic Disorders in Children with Arterial Ischemic Stroke and Sinovenous Thrombosis
Arch Neurol 56:967-971, Bonduel,M.,et al, 1999

Cerebroretinal Vasculopathy Mimicking a Brain Tumor:A Case of a Rare Hereditary Syndrome
Neurol 53:629-631, Weil,S.,et al, 1999

Dancing Eyes-Dancing Feet
Lancet 354:390, Imtiaz,K.E.&Vora,J.P., 1999

Rapid-Onset Dystonia-Parkinsonism:Linkage to Chromosome 19q13
Ann Neurol 46:176-182, Kramer,P.L.,et al, 1999

Aneurysms in Relatives of Patients with Subarachnoid Hemorrhage,Frequency and Risk Factors
Neurol 53:982-988, Raaymakers,T.W.M.&the MARS Study Group, 1999

Clinical and MRI Findings in Spinocerebellar Ataxia Type 5
Neurol 53:1355-1357, Stevanin,G.,et al, 1999

Risks and Benefits of Screening for Intracranial Aneurysms in First-Degree Relatives of Patients with Sporadic Subarachnoid Hemorrhage
NEJM 341:1344-1350, The Magnetic Resonance Angiography in Relatives of, 1999

New Developments in the Neurobiology of the Tuberous Sclerosis Complex
Neurol 53:1384-1390, Crino,P.B.&Henske,E.P., 1999

Bilateral Thalamic Stimulation for the Treatment of Essential Tremor
Neurol 53:1447-1450, Pahwa,R.,et al, 1999

Neuropsychological and Quality of Life Outcome after Thalamic Stimulation for Essential Tremor
Neurol 53:1774-1780, Troster,A.I.,et al, 1999

Altered Brain Activation in Cognitively Intact Individuals at High Risk for Alzheimer's Disease
Neurol 53:1391-1396, Smith,C.D.,et al, 1999

Benign paroxysmal Positional Vertigo
NEJM 341:1590-1596, Furman,J.M .&Cass,S.P., 1999

Autosomal Dominant Myofibrillar Myopathy with Arrhythmogenic Right Ventricular Cardiomyopathy Linked to Chromosome 10q
Ann Neurol 46:684-692,681, Melberg,A.,et al, 1999

The Roussy-Levy Family:From the Original Description to the Gene
Ann Neurol 46:770-773, Plante-Bordeneuve,V.,et al, 1999

Recurrent Orbital Myositis,Report of a Familial Incidence
Arch Neurol 56:1407-1409, Maurer,I.&Zierz,S., 1999

Hypertrophy of Multiple Cranial Nerves and Spinal Roots in Chronic Inflammatory Demyelinating Neuropathy
JNNP 67:685-687, Duarte,J.,et al, 1999

Brainstem Tuberculoma Mimicking Glioma:The Role of Antituberculous Drugs as a Diagnostic Tool
Neurol 52:210-211, DelBrutto,O.H.&Mosquera,A., 1999

Should We Screen for Familial Intracranial Aneurysm?
Stroke 30:312-316, Crawley,F.,et al, 1999

Multicentre European Study of Thalamic Stimulation in Paarkinsonisn and Essential Tremor
JNNP 66:289-296, Limousin,P.,et al, 1999

Cerebral Injury After Cardiac Surgery,Identification of a Group of Extraordinary Risk
Stroke 30:514-522, Wolman,R.L.,et al, 1999

Compression of Spinal Cord and Cauda Equina in Charcot-Marie-Tooth Disease Type 1A
Neurol 52:890-891, Butefisch,C.,et al, 1999

Neuro-Ophthalmologic Manifestations of a paraneoplastic Syndrome and Testicular Carcinoma
Neurol 52:864-867, Bennett,J.L.,et al, 1999

Parkinson Disease in Twins,An Etiologic Study
JAMA 281:341-346,376, Tanner,C.M.,et al, 1999

Adult-Onset MELAS Presenting as Herpes Encephalitis
Arch Neurol 56:241-243, Sharfstein,S.R.,et al, 1999



Showing articles 700 to 750 of 2207 << Previous Next >>