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Differential
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abdominal cramps
acid maltase deficiency
acid maltase deficiency, adult
acral sensory symptoms
adrenoleukodystrophy
adrenomyeloneuropathy
adult polyglucosan body disease
adverse drug reaction
agalsidase alfa
agitation
alpha glucosidase
alternating rapid movement
aminoacidopathies
aminoacidurias
amniocentesis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, guamian type of
angina pectoris
angiokeratoma
anhidrosis
anterior horn cell disease
anterior tibial muscle weakness
anti GQ1b IgG antibody
anticonvulsants
anticonvulsants, selection of
antiviral agents
apraxia
areflexia
arm swing, reduced
Arnold Chiari malformation
arthropathy
arthropathy, neuropathic
arylsulfatase A
aspartate aminotransferase
aspiration
asymptomatic
ataxia
ataxia telangiectasia
ataxia, cerebellar
ataxia, progressive
ataxia, sensory
athetosis
atidarsagene autotemcel
attention
attention deficit disorder with hyperactivity
attention span
atypical
autoantibodies
autonomic dysfunction
axonal degeneration
axonal spheroid
Babinski sign
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basilar impression
Bassen-Kornzweig syndrome
behavioral disorder
bladder dysfunction
blindness
blood dyscrasias, neurologic findings with
bone marrow biopsy
bone marrow transplantation
bradykinesia
brain atrophy
brain biopsy
brain biopsy, complications of
brain biopsy, false negative
brain biopsy, indication
brainstem, infarction of
bulbar palsy
burning feet
burning feet, differential diagnosis of
burning hands
burning paresthesia
cardiomyopathy
CAT scan
CAT scan, abnormal
CAT scan, false negative
catalepsy
cataplexy
cataracts
cerebellar ataxia, children
cerebellar ataxia, children, differential diagnosis of
cerebellar atrophy, primary
cerebellar degeneration
cerebellar infarction
cerebral cortical atrophy
cerebral ischemia
cerebro hepato renal syndrome
cerebrospinal fluid, gammaglobulin of
cerebrotendinous xanthomatosis
cerebrovascular accident
cerebrovascular accident, cryptogenic
cerebrovascular accident, familial occurrence
cerebrovascular accident, non atherosclerotic cause of
cerebrovascular accident, young adult
cerebrovascular disease
cerebrovascular disease, cardiovascular disease with
cherry red spot
cherry red spot-myoclonus syndrome
children
chorea
choreoathetosis
chromosomal abnormality
chronic graft versus host disease
Clinical Pathologic Conference(C.P.C.)
coagulopathy
Cockayne's syndrome
cognition
cogwheel rigidty
complications
compression fracture
congestive heart failure
conjunctival biopsy
consanguinity
contractures, joint
cornea, abnormal
cornea, opacification in infancy-causes of
cornea, opacity of
corneal dystrophy
corpus callosum
corpus callosum, hypoplastic
corpus callosum, lesion of
creatine phosphokinase(CPK)elevated
creatinine, elevated
cry, abnormal
cultured skin fibroblasts
cystinosis
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, childhood
dementia, diagnostic evaluation of
dementia, presenile
dentatorubral-pallidoluysian atrophy
depression
developmental disability
developmental milestones, loss of
developmental retardation
diagnostic criteria
diarrhea
differential diagnosis
difficulty going down stairs
diplopia
disease modifying agents
distal muscle weakness
DNA probes
drooling
dropped head syndrome
drug induced neurologic disorders
dysarthria
dysmetria
dysmorphic
dysostosis multiplex
dysphagia
dystonia
dystonia, face
dystonia, focal
dystonic lipidosis
echocardiogram
efficacy
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
electron microscopy
electronystagmography
electroretinograph
encephalitis, brainstem
encephalopathy
enzyme treatment
enzyme, defect
episodic disorders
episodic neurologic deficits
executive dysfunction
exercise intolerance
exome sequencing
eye movement, disorders of
Fabry's disease
facial appearance, abnormal
falling
familial
Farber's disease
fever
fine motor function, impaired
fingerprint bodies
Fisher's syndrome
foam cells
fracture, pathologic
Friedreich's ataxia
fucosidosis
fundus, abnormality of
gait disorder
gait, spastic
galactosidase
gangliosides
gangliosidosis GM1
gangliosidosis GM2
gangliosidosis, generalized
gargoylism
Gaucher's disease
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
glucocerebrosidase
glycogen storage disease
glycoprotein
GM1 ganglioside
GM1 ganglioside antibodies
granular osmiphilic material
growth retardation
Guillain Barre syndrome, ophthalmoplegia in
Hallervorden Spatz disease
hallucination
hallucination, visual
hand pain
handwriting
head injury
hearing loss
heat intolerance
hemorrhagic diathesis
hepatic failure
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatomegaly
hepatosplenomegaly
heralding manifestation
herpes virus infection
hexosaminidase-A
hexosaminidase-A and B
high arched feet
Hurler's syndrome
hydrocephalus
hyperreflexia
hypertonia
hypohidrosis
hypomyelination
hypotension, systemic
hypotonia
hypotonia, infants
imbalance
immunofluorescence
immunosuppression
inattention
inborn errors of metabolism
inborn errors of metabolism, screening
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, intracytopasmic
incoordination
infection, recurrent
intellectual deficit
intellectual deterioration
intelligence quotient
internuclear ophthalmoplegia
internuclear ophthalmoplegia, bilateral
intrathecal medication
intrinsic hand muscles, wasting of
introverted
iridoplegia
Jakob-Creutzfeldt disease
jaundice
Jewish
Kearns-Sayre syndrome
klippel feil syndrome
Krabbe's disease
kyphoscoliosis, neurologic causes of
lactic acidemia
Lafora's disease
laughing
laughing, pathologic
Laurence-Moon-Bardet-Biedl syndrome
lead poisoning
learning disability, in children
Leigh's disease
leukocyte enzyme abnormality
leukocyte peroxidase
leukodystrophy
leukoencephalopathy
leukoencephalopathy, hereditary diffuse
Lewy body disease, diffuse
life expectancy
limb-girdle weakness
lipid storage disorder of CNS
liver disease
lymphadenopathy
lymphocyte fingerprint profiles
lysosomal storage disease
lysosomes, abnoral
macrocephaly
macular degeneration
marche a petits pas
Marinesco-Sjogren syndrome
megalencephaly
memory, defect of recent
memory, impairment of
meningitis, chronic
mental retardation
MERRF syndrome
metabolic disorder, primary
metabolic disorder, primary-screening tests
metachromatic leukodystrophy
metachromatic leukodystrophy, adult onset
metachromatic leukodystrophy, juvenile
metachromatic leukodystrophy, late-infantile
microcephaly
miglustat
mimics
Mini Mental Status Examination
misdiagnosis
mitral valve prolapse
molecular genetics
mongolism
monoclonal antibodies
mortality
motor neuron disease
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, hypointense signal foci on
MRI, negative
MRI, serial
MRS
mucopolysaccharidoses
multiple sclerosis
multiple sclerosis, differential diagnosis of
muscle biopsy
muscle spasm
muscle wasting, diffuse
muscle weakness
muscle weakness, proximal
muscular dystrophy, Duchenne
myelomalacia
myeloneuropathy
myelopathy
myocardial infarction
myoclonic jerks
myoclonus
myoclonus, epilepsy
myopathy
myopathy, metabolic
myopathy, mitochondrial
myopathy, vacuolar
myopia
N-acetyl-L-aspartic acid
N-acetyl-L-leucine
negative
neonatal screening, genetic neurologic disorders
neoplasm, primary of CNS
neuraminidase deficiency
neuroaxonal dystrophy
neuroaxonal dystrophy, infantile
neuroaxonal leukodystrophy
neurofibrillary degeneration
neurogenic bladder
neuroichthyosis
neurolipidosis IV
neurologic complications of, systemic disease
neurologic disease
neurologic disease, diagnoses of
neurologic testing
neuronal ceroid-lipofuscinosis
neuroophthalmology
neuropathic pain scale
neuropathology
neuropathy
neuropathy, ataxic
neuropathy, demyelinating
neuropathy, hereditary peripheral
neuropathy, painful
neuropathy, small-fiber
neuropathy, small-fiber, painful sensory
neurosis
next-generation sequencing
Niemann-Pick disease
night blindness
nystagmus
nystagmus, dissociated
one and a half syndrome
ophthalmoplegia
ophthalmoplegia, acute
ophthalmoplegia, bilateral, acute
ophthalmoplegia, plus syndrome
ophthalmoplegia, progressive external
ophthalmoplegia, total
optic atrophy
optic nerve
optic neuropathy
optokinetic nystagmus, abnormal
osteopetrosis
overlap syndrome
pain
pain, neuropathic
papillitis
paranoia
paraparesis, familial spastic
Parkinson disease, postencephalitic
Parkinsonism syndrome
paroxysmal neurologic deficits
PAS positive
PAS positive material in the brain
patient in waiting
pediatric neurology
peroxisomal disease
pes cavus
photophobia
pigmentary retinopathy
polyglucosan body
polyglucosan body disease
polymerase chain reaction
polyneuropathy
Pompe's disease of glycogen storage
Pompe's disease, infantile
precipitating factors
preclinical
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
prognosis
progressive myoclonic epilepsy
progressive neurologic disorder
proteinuria
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychomotor retardation
psychosis
pupil, abnormality in neurologic disorders
putamen, lesion of
putamen, lesion of, bilateral
pyramidal tract
quadriparesis
quadriplegia
radiculopathy
rectal biopsy
refractive errors
Refsum's disease
remote effect of cancer on the nervous system
renal failure
respiratory failure
respiratory tract infection
retina, abnormal
retinal degeneration
retinal lesion
retinitis pigmentosa
retinopathy
retropulsion
review article
rigidity
safety
salivation, excessive
Salla disease
Sandhoff's disease
schizophrenia
scoliosis, neurologic association with
screening
sea-blue histiocytes
seizure
seizure, children
seizure, laughing as manifestation
seizure, paradoxical
seizure, treatment of
sensorineural hearing loss
serologic testing
short stature
sick sinus syndrome
skin, biopsy
skin, lesions in neurologic disorders
skull x-ray, abnormal
slit lamp examination
slurred speech
small vessel disease
spasticity
speech, delayed development of
sphingomyelin
spinal cord, compression of
spinocerebellar degeneration
splenomegaly
startle reaction
stem cell transplantation
storage disease of CNS
strabismus
stuttering
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subdural hematoma
systemic illness
tandem gait, ataxic
tapetoretinal degeneration
Tay-Sachs disease
thalamus, lesion of
thalamus, lesion of-bilateral
thrombocytopenia
toe walking
tone, muscle, increased
tongue, enlarged
treatment of neurologic disorder
tremor
tremor, intention
tripping
tuberous sclerosis
Unverricht-Lundborg disease
urea-cycle enzymopathies
urinary incontinence
urinary sulfatidase excretion
urine test for metabolic disorders
Usher's syndrome
vasculopathy
ventricular enlargement
vertebral-basilar insufficiency
vertigo
vestibulopathy
viral infection, CNS
vision, failure of in childhood
visual acuity, decreased
visual field defect
visual fields, constricted
visual loss
visual loss, progressive
visual loss, slow
visual loss, transient
visuospatial disturbance
Von Hippel Lindau
walking, delayed
walking, difficulty with
weakness
weakness, progressive
weakness, proximal
Werdnig-Hoffman disease
West disease
wheelchair
white matter disease
whole genome sequencing
wide based gait
writing
Showing articles 550 to 600 of 895 << Previous Next >>

Spontaneous "Second Wind" and Glucose-Induced Second "Second Wind" in McArdle Disease
Arch Neurol 59:1395-1402, Haller,R.G.&Vissing,J., 2002

Spinocerebellar Ataxia Type 10 is Rare in Populations Other Than Mexicans
Neurol 58:983-984, Matsuura,T.,et al, 2002

Paraneoplastic Chorea Associated with CRMP-5 Neuronal Antibody and Lung Carcinoma
Ann Neurol 51:625-630, Vernino,S.,et al, 2002

Cholinergic Vesicular Transporters in Progressive Supranuclesar Palsy
Neurol 58:1013-1018,997, Suzuki,M.,et al, 2002

Dopamine Transporter Brain Imaging to Assess the Effects of Pramipexole vs Levodopa on Parkinson Disease Progression
JAMA 287:1653-1661, Parkinson Study Group, 2002

Glutamic Acid Decarboxylase Autoantibodies and Neurological Disorders
Neurol Sci 23:145-151, Vianello,M.,et al, 2002

Genetic Testing in Spinocerebellar Ataxias
Arch Neurol 58:191-195, Tan,E. &Ashizawa,T., 2001

Encephalitis Associated with Glutamic Acid Decarboxylase Autoantibodies
Neurol 56:814, Marchiori,G.C.,et al, 2001

Neurodegenerative Diseases and Prions
NEJM 344:1516-1526,1548, Prusiner,S.B., 2001

CSF Detection of the 14-3-3 Protein in Unselected Patients with Dementia
Neurol 56:1528-1533, Burkhard,P.R.,et al, 2001

Stem-Cell Research: Drawing the Line
Lancet 358:163,217, Greenberg,D.S., 2001

Acute Compartment Syndrome After Forearm Ischemic Work Test in a Patient with McArdle's Disease
Neurol 56:1779-1780, Lindner,A.,et al, 2001

Positron Emission Tomography in Evaluation of Dementia
JAMA 286:2120-2127,2194, Silverman,D.H.S.,et al, 2001

Clinicopath Conf, Lymphocytic Meningitis and Lymphocytic Encephalomyelitis, Sensory Neuronopathy, Gangliositis, Small-Cell Carcinoma of Lung
NEJM 345:1758-1765, Case 38-2001, 2001

High-dose Intravenous Immune Globulin for Stiff-person Syndrome
NEJM 345:1870-1876, Dalakas,M.B.,et al, 2001

Recessive Ataxia With Ocular Apraxia
Arch Neurol 58:201-205,173, Barbot,C.,et al, 2001

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

SCA-12: Tremor with Cerebellar and Cortical Atrophy is Associated with a CAG Repeat Expansion
Neruol 56:299-303,287, O'Hearn,E.,et al, 2001

Headache and CNS White Matter Abnormalities Associated with Gluten Sensitivity
Neurol 56:385-388, Hadjivassiliou,M.,et al, 2001

Bilateral Abducens Nerve Paresis Associated with Anti-GQ1b IgG Antibody
Am J Ophthalmol 131:816-818, Sato, K. and Yoshikawa, H., 2001

Morvans Syndrome: Peripheral and Central Nervous System and Cardiac Involvement With Antibodies to Voltage-Gated Potassium Channels
Brain 124:2417-2426, Liguori,R., et al, 2001

Morvans Syndrome Associated With Voltage-Gated K+ Channel Antibodies
Neurol 54:771-772, Barber,P.A., et al, 2000

Immune Cytopenias as the Presenting Finding in Primary Sjogrens Syndrome
QJM 93:825-829, Schattner,A.,et al, 2000

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

Antiphospholipid and Antinuclear Antibodies in Patients with Epilepsy or New-onset Seizure Disorders
Am J Med 109:712-717, Peltola,J.T.,et al, 2000

Autoantibodies to Ganglionic Acetylcholine Receptors in Autoimmune Autonomic Neuropathies
NEJM 343:847-855, Verning,S. et al, 2000

Chorea Resulting From Paraneoplastic Striatal Encephalitis
JNNP 69:512-515, Tani,T.,et al, 2000

The Clinical Spectrum of Anti-GAD Antibody-Positive Patients with Stiff-Person Syndrome
Neurol 55:1531-1535, Dalakas,M.C.,et al, 2000

Gray Matter Heterotopia
Neurol 55:1603-1608, Barkovich,A.J. & Kuzniecky,R.I., 2000

Paraneoplastic Cerebellar Ataxia Due to Autoantibodies Against a Glutamate Receptor
NEJM 342:21-27, Smitt,P.S.,et al, 2000

Autosomal Dominant Diffuse Leukoencephalopathy with Neuroaxonal Spheroids
Neurol 54:463-468, van der Knaap,M.S.,et al, 2000

Clinicopath Conf,Guillain-Barre Syndrome, Campylobacter Jejuni Enteritis,Case 39-1999
NEJM 341:1996-2003, , 1999

Ion Channel Diseases:Episodic Disorders of the Nervous System
Semin Neurol 19:363-369, Ptacek,L.J., 1999

Late-Onset Myasthenia Graivs,A Changing Scene
Arch Neurol 56:25-27, Aarli,J.A., 1999

Epilepsia Partialis Continua:A New Manifestation of Anti-Hu-Associated Paraneoplastic Encephalomyelitis
Ann Neurol 45:255-258, Shavit,Y.B.,et al, 1999

Antiamphiphysin Antibodies Are Associated with Various Paraneoplastic Neurological Syndromes and Tumors
Arch Neurol 56:172-177,151, Antoine,J.C.,et al, 1999

Paraneoplastic Syndromes
Arch Neurol 56:405-408, Dalmau,J.O.&Posner,J.B., 1999

Infantile Neuroaxonal Dystrophy,Clinical Spectrum and Diagnostic Criteria
Neurol 52:1472-1478, Nardocci,N.,et al, 1999

Clinicopath Conf:Lymphoplasmocytic Lymphoma with Motor Neuronopathy,Waldenstrom's Macroglobulinemia
NEJM 340:1661-1669, , 1999

A Serologic Marker of Paraneoplastic Limbic and Brain-Stem Encephalitis in Patients with Testicular Cancer
NEJM 340:1788-1795,1831, Voltz,R.,et al, 1999

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

Carcinoma Associated Paraneoplastic Peripheral Neuropathies in Patients with and without Anti-Onconeural Antibodies
JNNP 67:7-14,4, Antoine,J.,et al, 1999

Paraneoplastic Painful Ulnar Neuropathy
Muscle & Nerve 22:952-955, Sharief,M.K.,et al, 1999

Pathologic Heterogeneity in Clinically Diagnosed Corticobasal Degeneration
Neurol 53:795-800, Boeve,B.F.,et al, 1999

Ion Channels and Neurological Disease:DNA Based Diagnosis is Now Possible,and Ion Channels May be Important in Common Paroxysmal Disorders
JNNP 65:427-431, Hanna,M.G.,et al, 1998

Stiff-Leg Syndrome:A Focal Form of Stiff-Man Syndrome
Ann Neurol 43:400-403, Saiz,A.,et al, 1998

Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
Pediatrics 102:98-100, Cabana,M.D.,et al, 1998

Neurological Channelopathies, Dysfunctional Ion Channels May Cause Many Neurological Diseases
BMJ 316:1104-1105, Rose,M.R., 1998

Utility of Anti-Hu Antibodies in the Diagnosis of Paraneoplastic Sensory Neuropathy
Ann Neurol 44:976-980, Molinuevo,J.L.,et al, 1998

Axonal Transection in the Lesions of Multiple Sclerosis
NEJM 338:278-285, 3231998., Trapp,B.D.,et al, 1998



Showing articles 550 to 600 of 895 << Previous Next >>