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Differential
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abortion, spontaneous
acetylcholine receptor
acetylcholine receptor antibody
advances in neurology
adverse drug reaction
agenesis of corpus callosum
Aicardi's syndrome
alpha-fetoprotein
Alzheimer's disease
amniocentesis
amyotrophic lateral sclerosis
amyotrophic lateral sclerosis, epidemiology of
amyotrophic lateral sclerosis, familial
amyotrophic lateral sclerosis, guamian type of
ANA
anesthesia, general
anesthesia, local
anti basal ganglia antibodies
anti MAG antibodies
antimetabolite
antistreptolysin titer
antithyroid antibodies
aphasia
areflexia
arthrogryposis multiplex
asymptomatic
ataxia
ataxia, truncal
atidarsagene autotemcel
autism
autoantibodies
autoimmune disease
axonal spheroid
azathioprine
Babinski sign
basal ganglia
basal ganglia, lesion of
basal ganglia, lesion, bilateral
bilateral periventricular nodular heterotopia
brain atrophy
brain biopsy
breast feeding
burst suppression pattern, electroencephalogram
CAT scan, abnormal
catatonia
central core disease
cerebellar degeneration
cerebral cortex
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, lactic acid concentration
cesarean section
Charcot-Marie-Tooth
cherry red spot
cherry red spot-myoclonus syndrome
children
chorioretinitis
chromosomal abnormality
chromosome 5
Clinical Pathologic Conference(C.P.C.)
coloboma
complications
confusion
confusional state, acute
congenital malformation
congenital malformation, non CNS
congenital myasthenic syndromes
corpus callosum
cortical dysplasia, focal
cyst, porencephalic
deep gray nuclei
degenerative diseases of CNS
dentate nuclei
dentate nuclei, lesion of
developmental milestones
developmental milestones, loss of
developmental retardation
differential diagnosis
drooling
dropped head syndrome
drug induced neurologic disorders
dyskinesia
dysphagia
dystonia
efficacy
electroencephalogram
electroencephalogram, abnormalities of
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, focal
encephalitis, Rasmussen's
encephalomyelitis, postinfectious
encephalopathy
encephalopathy, Hashimoto's
enzyme, defect
epidemiology of neurology
epilepsia partialis continua
eye movement, disorders of
Fabry's disease
facial asymmetry
falling
familial
Fazio-Londe's disease
fever
FLAMES
floppy infant
Friedreich's ataxia
gammaglobulin therapy, intravenous
gangliosidosis GM2
gaze palsy
gaze palsy, supranuclear
gene
gene therapy
genetic neurologic disorders
genetic screening
hallucination
headache
heavy metal intoxication
hemihypertrophy, congenital
hemiparesis
hemispherectomy
hepatomegaly
heterotopia
hexosaminidase-A
hexosaminidase-A and B
histopathology
Huntington's chorea
hyperreflexia
hypomelanosis of Ito
hypomyelination
hypopigmentation of skin
hypotonia
hypotonia, infants
immunologic disease
immunosuppressive agents
inborn errors of metabolism
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
infantile bilateral striatal necrosis
infantile neuronal degeneration
infantile spasm
insomnia
intellectual deficit
intellectual deterioration
iron, brain
Jewish
Kugelberg-Welander syndrome
labor, complicated
lactic acidemia
Leigh's disease
lethargy
leukodystrophy
level of consciousness, decreased
lipid storage disorder of CNS
lysosomal storage disease
macrocephaly
magnesium sulfate
malabsorption
malformation, CNS, congenital
Mary Walker phenomenon
megalencephaly
meningeal enhancement
mental retardation
mental status, abnormal
mesial temporal sclerosis
metachromatic leukodystrophy
metachromatic leukodystrophy, juvenile
metachromatic leukodystrophy, late-infantile
microcephaly
micropthalmia
misdiagnosis
molecular genetics
monoclonal antibodies
mortality
motor neuron disease
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, cortical enhancement
MRI, diffusion weighted
MRI, eye of tiger sign
MRI, gradient-echo
MRI, hypointense signal foci on
MRI, negative
MRI, paramagnetic effect
muscle biopsy
muscle spasm
muscle wasting, diffuse
muscular dystrophy, Duchenne
mutism
myasthenia gravis
myasthenia gravis, classification
myasthenia gravis, congenital
myasthenia gravis, infantile and juvenile
myasthenia gravis, neonatal
myasthenia gravis, neuromuscular junction in
myasthenia gravis, passive transfer of
myasthenia gravis, receptor site in
myasthenia gravis, seronegative
myasthenia gravis, thymectomy in
myasthenia gravis, treatment of
myasthenic crisis
myoclonus
myoclonus, epilepsy
myopathy
myopathy, metabolic
myotonia dystrophica
neoplasm, peripheral nerve
neoplasm, primary of CNS
neoplasm, primary of CNS-children
nerve conduction studies
nerve conduction studies, motor
neuroaxonal dystrophy
neuroaxonal dystrophy, infantile
neurocutaneous disease
neurofibrillary degeneration
neurologic disease, diagnoses of
neurologic examination, focal
neuronal cell death
neuronal ceroid-lipofuscinosis
neuronal degeneration
neuronal migration disorder
neuroophthalmology
neuropathology
neuropathology, brain
neuropathy
night sweats
NMDA antagonists
nystagmus
nystagmus, rotary
opisthotonus
optic atrophy
optic nerve
optic nerve, lesion of
optic neuritis
PANK2 mutation
paraparesis, familial spastic
Parkinson disease
paroxysmal neurologic disorder
patient information and support
pediatric neurology
perineural invasion
personality change
plasmapheresis
pleocytosis of cerebrospinal fluid
pleocytosis of cerebrospinal fluid, neutrophilic
poison, mercury
poison, neurologic problems with
Pompe's disease of glycogen storage
Pompe's disease, infantile
postural abnormality
pregnancy, neurologic complications in
prenatal diagnosis by amniocentesis
prognosis
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis, childhood
pyramidal tract dysfunction
pyruvate metabolism, abnormality of
quadriparesis
recurrent
respiratory depression
respiratory failure
respiratory tract infection
retinal degeneration
retropulsion
review article
rigidity
rituximab
safety
Sandhoff's disease
segmental demyelination
seizure
seizure, adult onset
seizure, children
seizure, focal
seizure, intractable
seizure, intractable, treatment of
seizure, neonatal
seizure, prognosis in childhood
seizure, psychomotor-temporal lobe
seizure, surgical treatment of
seizure, treatment of
serologic testing
serologic testing, false negative
seronegative
skin, biopsy
skin, lesions in neurologic disorders
SMN1 gene
sore throat
spasticity
speech disorder
speech disorder, childhood
speech, loss of
spinal cord
spinal cord degeneration
spinal muscular atrophy
spinal muscular atrophy, adult onset
spinal muscular atrophy, classification
spinal muscular atrophy, intermediate form
spinocerebellar ataxia
startle reaction
status epilepticus
steroid
steroid therapy, CNS treatment and complications with
stillbirth
storage disease of CNS
streptococcal infection
striatal encephalitis
striatonigral degeneration
striatonigral degeneration, infantile
striatum, lesion of
Sturge-Weber syndrome
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
survival motor neuron gene
symmetric brain lesions
systemic lupus erythematosus
systemic lupus erythematosus, neonatal
systemic lupus erythematosus, neurologic complications with
Tay-Sachs disease
temporal lobe, status
thalamus, lesion of
thalamus, lesion of-bilateral
thymectomy
thymus and neuromuscular function
thyroiditis
titubation
tone, muscle, increased
treatment of neurologic disorder
tremor
tremor, intention
tricresylphosphate
trinucleotide repeats
tuberous sclerosis
ventricular enlargement
visual acuity, decreased
visual fields, constricted
visual loss
weakness
weakness, generalized
Werdnig-Hoffman disease
West disease
white matter disease
wide based gait
Showing articles 550 to 600 of 1511 << Previous Next >>

Paraneoplastic Anti-N-methyl-D-aspartate Receptor Encephalitis Associated With Ovarian Teratoma
Ann Neurol 61:25-36,3, Dalmau,J.,et al, 2007

Prognosis of Children With Partial Epilepsy: MRI and Serial 18FDG-Pet
Neurol 68:665-659, Gaillard,W.D.,et al, 2007

Narcolepsy With Cataplexy
Lancet 369:499-511, Dauvilliers,Y.,et al, 2007

Febrile Seizures
BMJ 334:307-11, Sadleir,L.G. &Scheffer,I.E., 2007

NMO-IgG in the Diagnosis of Neuromyelitis Optica
Neurol 68:1076-1077, Jarius,S.,et al, 2007

Autoimmune Limbic Encephalitis in 39 Patients: Immunophenotypes and Outcomes
JNNP 78:381-385,332, Bataller,L.,et al, 2007

Individual Dopaminergic Neurons Show Raised Iron Levels in Parkinson Disease
Neurol 68:1820-1825, Oakley,A.E.,et al, 2007

Thrombolysis for Ischemic Stroke in Children. Data From the Natioinwide Inpatient Sample
Stroke 38:1850-1854,1722, Janjua,N.,et al, 2007

Neuroimaging Findings in Human Prion Disease
JNNP 78:664-670, Macfarlane,R.G.,et al, 2007

Amyotrophic Lateral Sclerosis
Lancet 369:2031-2041, Mitchell,J.D. & Borasio,G.D., 2007

Safety and Tolerability of Gene Therapy With an Adeno-Associated Virus (AAV) Borne GAD gene for Parkinsons Disease: An Open Label, Phase I Trial
Lancet 369:2097-2105,2056, Kaplitt,M.G.,et al, 2007

Palliative Care for Patients With Amyotrophic Lateral Sclerosis
JAMA 298:207-216,248, Mitsumoto,H. &Rabkin,J.G., 2007

Classification of Myasthenia Gravis Based on Autoantibody Status
Arch Neurol 64:1121-1124, Suzuki,S.,et al, 2007

Neonatal Seizures
Ann Neurol 62:112-120, Silverstein,F.S. &Jensen,F.E., 2007

Limbic Encephalitis and Variants: Classification, Diagnosis and Treatment
Neurologist 13:261-271, Tuzun,E. &Dalmau,J., 2007

Mysterious Falls and a Nasal Voice
Lancet 370:712, Bhandari,A. &Adenwalla,F., 2007

Recurrent Hemorrhagic Stroke in Children: A Population-Based Cohort Study
Stroke 38:2658-2662, Fullerton,H.J.,et al, 2007

Long-Term Prognosis in Children With Neonatal Seizures: A Population-Based Study
Neurol 69:1816-1822, Ronen,G.M.,et al, 2007

Reassessment: Neuroimaging in the Emergency Patient Presenting With Seizure (an Evidence-Based Review): Report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology
Neurol 69:1772-1780, Harden,C.L.,et al, 2007

Patterns of Guillain-Barre Syndrome in Children: Results From a Mexican Population
Neurol 69:1665-1671,1647, Nachamkin,I.,et al, 2007

Limbic Encephalitis: Under-Recognition of Voltage-Gated Potassium Channel Antibodies
Eur Neurol 58:184, Irani,S.R., et al, 2007

Continuous Spectrum of Pharyngeal-Cervical-Brachial Variant of Guillain-Barr� Syndrome
Arch Neurol 64:1519-1523, Nagashima,T.,et al, 2007

Differential Diagnosis of Bilateral Thalamic Lesions
Clin Neuroradiol 17:3-22, Linn,J.,et al, 2007

Asymmetric Cerebellar Ataxia and Limbic Encephalitis as a Presenting Feature of Primary Sjogrens Syndrome
J Neurol 254:1609-1611, Collison,K. and Rees,J., 2007

Age and High-Dose Methotrexate are Associated to Clinical Acute Encephalopathy in FRALLE 93 Trial for Acute Lymphoblastic Leukemia in Children
Leukemia 21:238-247, Dufourg, M.N.,et al, 2007

Autoimmune Encephalopathies
The Neurologist 13:140-147, Vernino, S.,et al, 2007

Non-Herpetic Acute Limbic Encephalitis-like Manifestation in a Case of Hashimotos Encephalopathy with Positive Autoantibodies against Ionotropic Glutamate Receptor Epsilon
Rinsho Shinkeigaku 47:629-634, Shindo, A.,et al, 2007

Isolated Abducens Nerve Palsy as a Regional Variant of Guillain-Barre Syndrome
JNS 243:35-38, Tatsumoto, M.,et al, 2006

Phenotypic Spectrum Associated with Mutations of the Mitochondrial Polymerase y Gene
Brain 129:1674-1684, Horvath, R.,et al, 2006

Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006

Epilepsy Syndromes in Infancy
Pediatr Neurol 34:253-263, Korff,C.M. &Nordii,D.R.,Jr., 2006

Glycogen-Storage Disease Type II
eMedicine, May 2, Ibrahim,J. &McGovern,M., 2006

Voltage-Gated Potassium Channel Antibodies Associated Limbic Encephalitis in a Patient with Invasive Thymoma
J Neurol Sci 250:167-169, Ohshita,T., et al, 2006

Voltage-Gated Potassium Channel Antibody-Associated Encephalitis with Basal Ganglia Lesions
Neurol 66:1780-1781, Hiraga,A., et al, 2006

A Case of Voltage-Gated Potassium Channel Antibody-Related Limbic Encephalitis
Nat Clin Pract Neurol 2:339-343, Harrower,T., et al, 2006

Psychiatric Presentation of Voltage-Gated Potassium Channel Antibody-Associated Encephalopathy
Br J Psychiatry 189:182-183, Parathasarathi,U.D., et al, 2006

Voltage-gated Potassium Channel Antibody-Associated Encephalitis with Basal Ganglia Lesions
Neurol 66:1780-1781, Hiraga,A.,et al, 2006

Incidence, Cause, and Short-Term Outcome of Convulsive Status Epilepticus in Childhood: Prospective Population-Based Study
Lancet 368:222-229, Chin,R.F.M.,et al, 2006

Evolution of Cerebral Arteriopathies in Childhood Arterial Ischemic Stroke
Ann Neurol 59:620-626, Danchaivijitr,N.,et al, 2006

First Seizure Presentation:Do Multiple Seizures Within 24 Hours Predict Recurrence?
Neurol 67:1047-1049,927, Kho,L.K.,et al, 2006

The Tuberous Sclerosis Complex
NEJM 355:1345-1356, Crino,P.B.,et al, 2006

Practice Parameter: Diagnostic Assessment of the Child with Status Epilepticus (An Evidence-Based Review): Report of the Quality Standards Subcommittee of the American Academy of Neurology and the practice Committee of the Child Neurology Society
Neurol 67:1542-1550, Riviello,J.J. Jr.,et al, 2006

Neuromyelitis Optica IgG Status in Acute Partial Transverse Myelitis
Arch Neurol 63:1398-1400, Scott,T.F.,et al, 2006

Developmental Neurotoxivity of Industrial Chemicals
Lancet 368:2167-2178, Grandjean,P. &Landrigan,P.J., 2006

Time Is Brain--Quantified
Stroke 37:263-266,10, Saver,J.L., 2006

Urgent Clinical Challenges in Children With Ischemic Stroke
Stroke 37:116-122,3, Kuhle,S.,et al, 2006

A 24-Week Open-Label Extension Study of Memantine in Moderate to Severe Alzheimer Disease
Arch Neurol 63:49-54, Reisberg,B.,et al, 2006

Alternating Hemiplegia of Childhood Successfully Treated with Topiramate: 18 Months of Follow-up
Neurol 66:146, Di Rosa,G.,et al, 2006

Prevalence of Fabry Disease in Patients with Cryptogenic Stroke: A Prospective Study
Lancet 366:1794-1796,1754, Rolfs,A.,et al, 2006

Migraine with Aura Is a Risk Factor for Unprovoked Seizures in Children
Ann Neurol 59:210-213, Ludvigsson,P.,et al, 2006



Showing articles 550 to 600 of 1511 << Previous Next >>