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Differential
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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 0 to 50 of 17689 Next >>

A Young Woman With Hypertonia, Severe Scoliosis, and Encephalopathy
JAMA Neurol 81:83-84, Hua,L.,et al, 2024

Duchenne Muscular Dystrophy
BMJ 368:L7012, Fox, H.,et al, 2020

Wilson Disease
NIDDK Oct2018, , 2018

Pantothenate Kinase - Associated Neurodegeneration (PKAN)
Emedicine.Medscape Sept, Hanna, P.A. & Benbadis, S.R., 2018

An 11-year-old Boy with Language Disorder and Epilepsy
Neurol 86:e48-e53, Dong, L. & Zhou, X., 2016

Identifying and Managing Common Childhood Language and Speech Impairments
BMJ 350:h2318, Reilly, S.,et al, 2015

Clinical Reasoning: A 13-year-old Boy Presenting with Dystonia,Myoclonus,and Anxiety
Neurol 78:e72-e76, Blackburn,J.S. and Cirillo,M.L., 2012

Folic Acid Supplements in Pregnancy and Severe Language Delay in Children
JAMA 36:1566-1573, Roth, C.,et al, 2011

Late onset autism and anti-NMDA-receptor encephalitis
Lancet 378:98;378, Creten, C.,et al, 2011

Profound Deafness in Childhood
NEJM 363:1438-1450, Kral,A.,et al, 2010

Anti-N-Methyl-D-Aspartate Receptor (NHMDAR) Encephalitis in Children and Adolescents
Ann Neurol 66:11-18,1, Florance,N.R.,et al, 2009

Autism
Lancet 374:1627-1638, Levy,S.,et al, 2009

Aicardi-Gouti�res Syndrome
Br Med Bull 89:183-201, Orcesi, S.,et al, 2009

Magnetoencephalography (MEG) and Magnetic Source Imaging (MSI)
The Neurologist 10:138-153, Wheless,J.W.,et al, 2004

Neurodevelopmental Dysfunction Among Nonreferred Children with Idiopathic Megalencephaly
J Pediatr 131:320-324, Sandler,A.D.,et al, 1997

The Landau-Kleffner Syndrome
Arch Dis Child 72:386-387, Appleton,R.E., 1995

Postictal Behavior:A Clinical and Subdural Electroencephalographic Study
Arch Neurol 51:254-259, Devinsky,O.,et al, 1994

The Syndrome of'Cerebellar'Mutism and Subsequent Dysarthria
Neurol 44:2040-2046, vanDongen,H.R.,et al, 1994

Mental Development of 2-Year-Old Children Exposed to Alcohol in Utero
J Pediatr 120:740-746, Autti-Ramo,I.,et al, 1992

The Landau-Kleffner Syndrome or Acquired Aphasia with Convulsive Disorder
Arch Neurol 49:354-359, 3531992., Paquier,P.F.,et al, 1992

Angelman Syndrome: Clinical Profile
J Child Neurol 7:270-280, Zori,R.T.,et al, 1992

Hallervorden-Spatz Syndrome and Brain Iron Metabolism
Arch Neurol 48:1285-1293, Swaiman,K.F., 1991

Dyslexia
Editorial, Lancet 2:719-7201989., , 1989

Delayed Speech in Children
BMJ 297:1281-1282, Hall,D., 1988

Diagnostic Criteria for Rett Syndrome
The Rett Syndrome Diagnostic Criteria Work Group, Ann Neurol 23:425-4281988., , 1988

Unclear Speech:Recognition & Significance of Unintelligible Speech in Preschool Children
Pediatrics 82:447-452, Coplan,J.&Gleason,J.R., 1988

The Child Who is Slow to Talk
BMJ 285:671-672, Robinson,R.J., 1982

Acquired Aphasia with Convulsive Disorder:Course & Prognosis
Neurol 30:524-529, Mantovani,J.F.,et al, 1980

Human Cerebellar Hypoplasia, A Syndrome of Diverse Causes
Arch Neurol 37:300-305, Sarnatt,H.B.,et al, 1980

Juvenile Metachromatic Leukodystrophy
Arch Neurol 37:42-46, Haltia,T.,et al, 1980

Sydenham Chorea:An Update
Neurol 30:331-334, Nausieda,P.A.,et al, 1980

Children's Language Disorders:Recent Research Advances
Ann Neurol 7:497-507, Ludlow,C.L., 1980

Speech Defects in Children Aged 7 yrs, A National Study
BMJ 253, 1973 Feb., Butler,N.,et al, 1973

Pediatric Neurology
Psych Annals 2:1, , 1972

Children with Develpmental Language Diorders
Neurol 2:421, Wilson,J.,et al, 1972

Learning & Language Disorders in Children
Part II:The School-age Child, Curr Prob Pediatr 1:, 1971 Sept., Gofman,H.,et al, 1971

Learning & Language Disorders in Children
Part I:The School-age Child, Current Problems in Pediatrics 1:1971 Aug., Gofman,H.,et al, 1971

Three Pediatric Problems That Worry Parents
Consultant, MayJun, p. 1270., Bakwin,H.,et al, 1970

Huntington's Chorea
Bruyn, G. W. In Vinken & Bruyn, Handbk of Clin Neurol, North-Holland Publ Co, Amsterdam, 6:298, , 1968

Clinicopathologic Conference, Infant Botulism, Case 3-2024
NEJM 390:358-366, Case 3-2024, 2024

Study Finds ChatGPT Provides Inaccurate Responses to Drug Questions-Press Release
Am Soc Health Sys Pharm, Dec 5, Grossman,S., 2023

A Teenager With Right-Sides Headache and Periorbital Changes
Neurol 100:144-150, Lax,D.M.,et al, 2023

Brain Calcification in a Young Woman With Seizures, Explore the Rare Differentials
Neurol 100:397-398, Menon,B.,et al, 2023

Neuroimaging Features of Biotinidase Deficiency
AJNR 44:328-333, Biswas,A.,et al, 2023

Artificial Intelligence and Machine Learning in Clinical Medicine, 2023
NEjM 388:1201-1208,1220, Haug,C.H. & Drazen,J.M., 2023

Benefits, Limits, and Risks of GPT-4 as an AI Chatbot for Medicine
NEJM 388:1233-1239, Lee,P., et al, 2023

Changing Trends in Demographics, Risk Factors, and Clinical Features of Patients with Infective Endocarditis-Related Stroke, 2005-2015
Neurol 100:e1555-e1564, Ridha,M.,et al, 2023

Salt and Pepper Sign, PLNTY for Drug-Resistant Epilepsy
Neurol 100:791-795, Paredes-Aragon,E.M.,et al, 2023

Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD): Clinical Features and Diagnosis
UptoDate.com, March, Flanagan,E.P. & Tillema,J-M, 2023



Showing articles 0 to 50 of 17689 Next >>