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acrocyanosis
advances in neurology
affect, flat
aggression
agitation
Aicardi-Goutieres syndrome
alcohol
alternative medicine
alveolar hypoventilation
aminoacidurias
Angelman syndrome
ankle, swelling of
anxiety
aphasia
aphasia, children
apraxia, speech
arylsulfatase A
ascites
Asperger's syndrome
ataxia
ataxia, cerebellar
ataxia, truncal
ataxic gait
attention deficit disorder with hyperactivity
attention span
atypical
audiologic test to localize site of pathology
audiology
auditory processing, impaired
autism
autism, screening for
autoantibodies
autoimmune disease
automatism, postictal
autonomic dysfunction
Babinski sign
basal ganglia
basal ganglia, calcification of
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavior
behavior, combative
behavioral disorder
Benedict's solution test
bifid uvula
brachial plexus neuropathy, children
brachycephaly
bradykinesia
brain atrophy
bruxism
calcification, intracranial
calf hypertrophy
carcinoma
CAT scan, abnormal
catatonia
cerebellar atrophy, primary
cerebellar disease, eye movement disorder in
cerebellar hypoplasia
cerebellar mutism
cerebellum, neoplasms of
cerebral cortical atrophy
cerebral palsy
cerebral palsy, associated problems with
cerebral palsy, pure ataxic
cerebrospinal fluid, abnormal
chilbran skin lesions
children
chorea
chorea, Sydenham's
choreoathetosis
chromosomal abnormality
chromosome 15
chromosome 7
cleft palate
cochlear implant
cognition
comorbidities
complications
comprehension, impaired
compulsivity
confusion
congenital bilateral perisylvian syndrome
consanguinity
contractures, joint
creatine phosphokinase(CPK)elevated
deafness
deafness, congenital
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, childhood
dentate nuclei, lesion of
depression
developmental disability
developmental evaluation
developmental milestones
developmental milestones, loss of
developmental retardation
diagnostic criteria
dichotic hearing
differential diagnosis
difficulty climbing stairs
dinitrophenylhydrazine(D.N.P.H.)reaction
diplegia, atonic
diplegia, spastic cerebral
disorientation
dopa responsive dystonia
drooling
dysarthria
dyskinesia
dyskinesia, buccal lingual facial
dyslexia
dysmorphic
dysphagia
dysplasia of C.N.S.
dyspraxia
dystonia
dystonia, children
dystrophin
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, depth electrode
electroencephalogram, sleep
electromyogram
ELISA
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, etiology
encephalitis, viral
encephalopathy
encephalopathy, progressive
enuresis
enzyme, defect
epidemiology of neurology
epsilon sarcoglycan gene
face, inexpressive
facial appearance, abnormal
facial expression abnormality
facial weakness, bilateral
falling
familial
fatigue
feeding disorder
ferric chloride test
fetal alcohol syndrome
fetus
fever
fine motor function, impaired
fish
fluorescene in situ hybridization
folic acid
gait disorder
gait, apraxic
galactorrhea
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
globus pallidus
globus pallidus, lesion of
Gowers maneuver
grimacing
growth retardation
Hallervorden Spatz disease
head circumference
head lag
hearing loss
hearing problems in children
hemichorea
hepatolenticular degeneration(Wilson's disease)
hippocampus
Huntington's chorea
hyperactivity
hyperpyrexia, CNS disorder causing
hyperreflexia
hypertension
hypertonia
hypopigmentation of skin
hyporeflexia
hypotonia
hypotonia, infants
immunosuppression
immunosuppressive agents
inattention
insomnia
insular cortex
intellectual deficit
intellectual deficit, treatable causes of
intellectual deterioration
intelligence quotient
interferon alpha
intrauterine
iron, brain
irritability
jaundice
karyotyping
klippel feil syndrome
Landau-Kleffner syndrome
language
language delay
language development, neurologic basis of
language disorder in adults
language disorders in children
laughing, pathologic
L-dopa
learning disability
learning disability, in children
lenticular nucleus, lesion of, bilateral
leukodystrophy
leukoencephalopathy
liver function enzymes
macrocephaly
macrognathia
magnetic source image
magnetoencephalography
maple syrup urine disease
medulloblastoma
megalencephaly
megalencephaly, idiopathic
memory, defect of recent
memory, impairment of
mental retardation
metachromatic leukodystrophy
metachromatic leukodystrophy, juvenile
microcephaly
midline defect in children
misdiagnosis
monoclonal antibodies
mood change
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abdomen
MRI, abnormal
MRI, diffusion tensor
MRI, disappearing lesion on
MRI, functional
MRI, negative
MRI, paramagnetic effect
MRI, pelvis
muscle stiffness
muscular dystrophy
muscular dystrophy, central nervous system abnormality
muscular dystrophy, Duchenne
mutism
myelodysplasia
myoclonic dystonia
myoclonus
myoclonus, action
myoglobinuria
nasal speech
neoplasm, posterior fossa
neoplasm, primary of CNS-children
nerve biopsy
neurologic complications of, surgery
neurologic disease, diagnoses of
neurologic evaluation
neurologic testing
neuropathology
neuropathology, brain
NMDA antagonists
nonverbal
nystagmus
opened mouth
operculum syndrome
operculum syndrome, bilateral
opisthotonus
optic atrophy
palatopharyngeal incompetence
PANK2 mutation
paraphasias
personality change
phenylketonuria
pleocytosis of cerebrospinal fluid
pneumoencephalogram(PEG)
postictal neurologic deficits
postural abnormality
pregnancy, neurologic complications in
prenatal
prevention of neurologic disorders
prognathism
prognosis
progressive neurologic disorder
prolactin, elevated
pruritus
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychological testing
psychological testing, children
psychological testing, neurologic problems
psychomotor retardation
psychosis
psychosis, childhood
psychosocial aspects
pure word deafness
pyramidal tract
pyramidal tract dysfunction
release phenomena
remote effect of cancer on the nervous system
respirations in CNS disease
respirator
retinitis pigmentosa
Rett's syndrome
review article
rhabdomyolysis
rheumatic brain disease
rheumatic fever
rheumatic heart disease
rigidity
risk factors
rituximab
rocking
scoliosis
screening
sea-blue histiocytes
seizure
seizure, advice to parents and teachers regarding
seizure, children
seizure, focus
seizure, psychomotor-temporal lobe
seizure, psychosocial aspects of
seizure, recurrent
seizure, surgical treatment of
seizure, treatment of
seizure, workup of
sexual behavior, disorder of
sign language
skin, lesions in neurologic disorders
sleep pathology and physiology
smiling
socialisation
spastic dysphonia
spasticity
speech disorder
speech disorder, childhood
speech disorder, non aphasic
speech lateralization
speech therapy
speech, delayed development of
speech, slowed
spina bifida
stammering
startle reaction
stereotyped behavior, drug induced
stuttering
substantia nigra
symmetric brain lesions
systemic illness
teeth, wide-spaced
temporal lobe, lesion
temporal lobe, lesion, bilateral
teratoma
teratoma, ovarian
titubation
tongue, impaired movements of
tongue, protrusion of
treatment of neurologic disorder
tremor
tremor, intention
tripping
tyrosine hydroxylase deficiency
urine test for metabolic disorders
urine, dark
visual evoked response
visual impairment
vitamin supplementation
weakness, progressive
weight loss
wheelchair
white matter disease
workup
Showing articles 500 to 550 of 18280 << Previous Next >>

Ethosuximide, Valproic Acid, and Lamotrigine in Childhood Absence Epilepsy
NEJM 362:790-799, Glauser,T.A.,et al, 2010

Prospective Study of New-Onset Seizures Presenting as Status Epilepticus in Childhood
Neurol 74:636-642, 624, Singh,R.K.,et al, 2010

Randomized Trial of Adjunctive Topiramate Therapy in Infants with Refractory Partial Seizures
Neurol 74:714-720, Novotny,E.,et al, 2010

Genetic Susceptibility to Stuttering
NEJM 362:750-752, Fisher,S.E. &Phil,D., 2010

Practice Parameter: Pharmacologic Treatment of Spasticity in Children and Adolescents with Cerebral Palsy (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 74:336-343, Delgado,M.R.,et al, 2010

Clinicopath Conf, Infantile Krabbe Disease
NEJM 362:346-356, Case 3-2010, 2010

MRI in Methylmalonic Acidemia
Neurol 74:e14, Bindu, P.S.,et al, 2010

Recent Advances in Neuroblastoma
NEJM 362:2202-2011, Maris,J.M., et al, 2010

Clinical and Radiological Features of Rotavirus Cerebellitis
AJNR 31:1591-1595, Takanashi,J.,et al, 2010

Acute Necrotizing Encephalopathy During Novel Influenza A (H1N1) Virus Infection
Ann Neurol 68:111-114, Mariotti,P., et al, 2010

Neonatal Cerebral Sinovenous Thrombosis From Symptom to Outcome
Stroke 41:1382-1388, Berfelo,F.J., et al, 2010

Pediatric Moyamoya Disease: An Analysis of 410 Consecutive Cases
Ann Neurol 68:92-101, Kim,S.-K., et al, 2010

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

Clinical Reasoning: A 9-year-old Girl With Seizures and Encephalopathy
Neurol 74:e97-e100, Nguyen,T.P. &El-Hakam,L.M., 2010

Huntingtons Disease
BMJ 341:34-40, Novak,M.J. &Tabrizi,S.J., 2010

Response to Immunotherapy in a 20-Month-Old Boy With Anti-NMDA Receptor Encephalitis
Neurol 74:1550-1551, Wong-Kisiel,L.C., et al, 2010

Clinical Reasoning: Seizures in a Child With Sensorineural Deafness and Agitation
Neurol 74:e61-e63, Auvin,S., et al, 2010

Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
Brain 133:655-670, Leen,W.G., et al, 2010

Diagnosis and Management of the Antiphospholipid Syndrome
BMJ 340:1125-1132, Cohen,D., et al, 2010

Recent Insights into Cerebral Cavernous Malformations: The Molecular Genetics of CCM
FEBS J 277:1070-1075, Riant, F.,et al, 2010

Treating Childhood Acute Lymphoblastic Leukemia Without Cranial Irradiation
NEJM 360:2730-2741, Pui,C.-H.,et al, 2009

Cyclophosphamide Therapy in Pediatric Multiple Sclerosis
Neurol 72:2076-2082,2064, Makhani,N.,et al, 2009

Lyme Neuroborreliosis: Manifestations of a Rapidly Emerging Zoonosis
AJNR 30:1079-1087, Hildenbrand,P.,et al, 2009

Clinicopath Conf., Atypical Hemolytic-Uremic Syndrome
NEJM 361:389-400, Case 23-2009, 2009

Intracranial Aneurysms in Childhood: 27-Year Single-Institution Experience
AJNR 30:1315-1324, Hetts,S.W.,et al, 2009

Clinicopath Conf. Rickets Due to Vitamin D Deficiency
NEJM 360:398-407, Case 3-2009, 2009

Association Between Recent Sports Activity, Sports Activity in Young Adulthood, and Stroke
Stroke 40:425-431, Grau,A.J.,et al, 2009

Thrombolysis in Childhood Stroke: Report of 2 Cases and Review of the Literature
Stroke 40:801-807, Arnold,M.,et al, 2009

Can a Subset of Intracerebral Hemorrhage Patients Benefit from Hemostatic Therapy with Recombinant Activated Factor VII?
Stroke 40:833-840, Mayer,S.A.,et al, 2009

Unexplained Seizures in an Infant
Lancet 373:94, Astuto,M.,et al, 2009

Hepatitis B Vaccine and the Risk of CNS Inflammatory Demyelination in Childhood
Neurol 72:873-880,870, Mikaeloff,Y.,et al, 2009

Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease
NEJM 360:1729-1739, Hara,K.,et al, 2009

Spinal Dural Arteriovenous Fistulas
AJNR 30:639-648, Krings,T. &Geibprasert,S., 2009

A Systematic Review of Antiepilpetic Drug Initiation and Withdrawal
The Neurologist 15:122-131, Shih,J.J &Ochoa,J.G., 2009

Antivenom for Critically Ill Children with Neurotoxicity from Scorpion Stings
NEJM 360:2090-2098, Boyer,L.V.,et al, 2009

Lateral Sinus Thrombosis: Complication of Minor Head Injury
Int J Pediatr Otorhinolaryngol 73:629-635, Nehme, J.,et al, 2009

The Floppy Infant: Evaluation of Hypotonia
Pediatrics in Review 30:e66-e76, Peredo, D. & Hannibal M., 2009

Spontaneous Primary Intraventricular Hemorrhage in Adults: Clinical Data, Etiology and Outcome
Turkish Neurosurgery 19:338-344, Giray, S.,et al, 2009

The Expanding Phenotype of GLUT1-Deficiency Syndrome
Brain & Dev 31:545-552, Brockmann,K., 2009

Generic Anticonvulsant Use in Children: Do We Have Evidence to Recommend Brand Formulations?
Arch Neurol 66:1417-1418, Hamiwka,L., 2009

Leukodystrophies: Classification, Diagnosis, and Treatment
Neurologist 15:319-328, Costello,D.,et al, 2009

Motor Development in Very Preterm and Very Low-Birth-Weight Children From Birth to Adolescence: A Meta-Analysis
JAMA 302:2235-2242, 2257, De Kieviet,J.,et al, 2009

Clinical and Mutational Spectrum of Neurofibromatosis Type 1-Like Syndrome
JAMA 302:2111-2118, 2150, 2170, Messian,L.,et al, 2009

Practice Parameter: Evaluation of the Child with Microcephaly (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 73:887-897, Ashwal,S.,et al, 2009

Epilepsy in Children with Infantile Thiamine Deficiency
Neurol 73:828-833, Fattal-Valevski,A.,et al, 2009

Obesity Is a Common Comorbidity for Pediatric Patients with Untreated, Newly Diagnosed Epilepsy
Neurol 73:658-664, 654, Daniels, Z.S.,et al, 2009

N-Methyl-D-Aspartate Receptor Antibodies in Pediatric Dyskinetic Encephalitis Lethargica
Ann Neurol 66:704-709, Dale,R.,et al, 2009

Long-Term Outcomes Among Adult Survivors of Childhood Central Nervous System Malignancies in the Childhood Cancer Survivor Study
J Natl Cancer Inst 101:946-958, Armstrong,G.T.,et al, 2009

Clinicopath Conf., Leighs syndrome, Intraventricular Hemorrhage and Periventricular Leukomalacia
NEJM 359:1156-1166, Case 28-2008, 2008

Clinicopath Conf., Allergic Fungal Sinusitis
NEJM 359:2825-2833, Case 40-2008, 2008



Showing articles 500 to 550 of 18280 << Previous Next >>