Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
abdominal distention
acetylcholine receptor antibody
acid maltase deficiency
acromicria
adverse drug reaction
airway obstruction
aminoacidurias
amitriptyline
amniocentesis
anemia
anemia, megaloblastic
Angelman syndrome
angiokeratoma
anorexia
anterior horn cell disease
antitoxin
antiviral agents
apnea
areflexia
arrhythmia, cardiac
arthrogryposis multiplex
aspartocyclase
ataxia
ataxia, cerebellar
ataxia, truncal
athetosis
athetosis, infant
attention deficit disorder with hyperactivity
autonomic dysfunction
B 12 deficiency
B 12 deficiency, infants
Babinski sign in new born
bacterial infection
basal ganglia, lesion, bilateral
behavior, combative
behavioral disorder
biopterin deficiency
birth injury
bone marrow transplantation
botulinum toxin
botulism
botulism antitoxin
botulism immune globulin
botulism, infant
brain biopsy
breast feeding
breech delivery
bulbar palsy
bulbar palsy, childhood
calcification, intracranial
Canavan's disease
cardiomyopathy
CAT scan
CAT scan, abnormal
celiac disease, childhood
central core disease
central nervous system, infection of
cerebellar disease, eye movement disorder in
cerebellar hypoplasia
cerebral cortical atrophy
cerebral embolism
cerebral gigantism
cerebral infarction
cerebral palsy
cerebral palsy, associated problems with
cerebral venous thrombosis
cerebrospinal fluid
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, protein of
cerebrospinal fluid, red cells in
cerebrospinal fluid, xanthochromia of
cerebrovascular accident
cerebrovascular accident, infancy and childhood
cerebrovascular accident, intrauterine
cerebrovascular accident, neonatal
cerebrovascular accident, postpartum
cervical spine injury
child abuse
children
choreoathetosis
chorioamnionitis
chorioretinitis
chromosomal abnormality
chromosome 1
chromosome 15
chromosome 5
Clinical Pathologic Conference(C.P.C.)
clubfoot as related to neurologic disease
coma
congenital heart disease
congenital infection, CNS
congenital infection, viral
congenital myopathy
congenital myopathy, inflammatory
consanguinity
constipation
contractures, joint
cornea, opacity of
corpus callosum
corpus callosum, thinning
Craniosynostosis
creatine phosphokinase(CPK)elevated
cry, abnormal
cry, weak
crying
crying, pathologic
cryptorchidism
cultured skin fibroblasts
cytomegalic inclusion disease
cytomegalovirus infection
cytomegalovirus infection, congenital
delivery, complicated
dementia
developmental abnormality of brain
developmental disability
developmental milestones
developmental milestones, loss of
developmental retardation
diet
differential diagnosis
diphtheria-tetanus-pertussis immunization
dislocated hip, congenital
DNA sequencing
drooling
drug overdose
dysarthria
dysmorphic
dysostosis multiplex
dysphagia
dystonia
ear, abnormal
eating disorder
ecchymoses
efficacy
electroencephalogram, abnormalities of
electromyogram
electron microscopy
embolism, paradoxical
encephalitis
encephalomyelitis
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
enzyme, defect
epidemiology of neurology
exome sequencing
facial appearance, abnormal
facial expression abnormality
facial weakness
facial weakness, bilateral
failure to thrive
familial
fasciculation
feeding disorder
fetal movements, reduced
fetus
fever
fibrillations
floppy infant
fontanel, bulging
food poisoning
food-borne infection
forceps delivery
fucosidosis
gait disorder
gait, apraxic
gammaglobulin therapy, intravenous
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
genital hypoplasia
gluten-free diet
glycogen storage disease
glycoprotein
Gowers maneuver
growth hormone deficiency
growth retardation
Guillain Barre syndrome
Guillain Barre syndrome, infantile and childhood form
hand clapping
hand flapping
hand wringing
head bobbing
head circumference
head lag
hearing loss
hemorrhage, intracranial, newborn
hemorrhage, periventricular
hepatomegaly
hepatosplenomegaly
high arched feet
high arched palate
histochemistry
histochemistry of muscle
hoarseness
homocystinuria
honey
Horner's syndrome
Horner's syndrome, bilateral
Horner's syndrome, congenital
human genome
Hunter's syndrome
hydrocephalus
hydrocephalus, communicating
hydrocephalus, congenital
hydrocephalus, exvacuo
hyperbilirubinemia
hyperbilirubinemia, CNS abnormality after
hyperphagia
hyperpigmentation of skin
hyperreflexia
hypertelorism
hypertension
hypertonia
hypogammaglobulinemia
hypogonadism
hypokinesia
hypopigmentation of skin
hyporeflexia
hypothermia
hypotonia
hypotonia, causes of
hypotonia, infants
hypoxic encephalopathy
imbalance
immunization, neurologic complications with
inappropriate antidiuretic(A.D.H.)hormone
inborn errors of metabolism
infant, evaluation of
infantile neuronal degeneration
infantile spasm
infection, recurrent
intellectual deficit
intellectual deterioration
intestinal biopsy
intracranial hemorrhage
intracranial pressure, increased
intrauterine
intrauterine infection
intrauterine infection, viral
intrauterine infection, viral of CNS
intubation
irritability
irritable baby
jaundice
karyotyping
kyphoscoliosis, neurologic causes of
Leigh's disease
lethargy
leukodystrophy
leukotrienes
lissencephaly
listeria monocytogenes
liver function enzymes
lysosomal storage disease
macrocephaly
malabsorption
malformation, CNS, congenital
malformation, vascular
malignant hyperpyrexia
McArdle's disease
mental retardation
merosin
metabolic disorder, primary
microcephaly
micrognathia
micropthalmia
migraine, seizures in
misdiagnosis
mitochondrial disease
mitral valve prolapse
molecular genetics
mortality
motor neuron disease
MRI
MRI, abnormal
MRI, fetal
MRI, muscle
MRI, spinal cord
MRI, spine
mucopolysaccharidoses
mucopolysacchariduria
muscle atrophy, progressive
muscle atrophy, static
muscle biopsy
muscle diseases, characteristics of
muscle phosphorylase deficiency
muscle weakness
muscle weakness, proximal
muscle-eye-brain disease
muscular dystrophy
muscular dystrophy, central nervous system abnormality
muscular dystrophy, congenital
muscular dystrophy, congenital, Fukuyama type
muscular dystrophy, LAMA2
myasthenia gravis, neonatal
myelomalacia
myoclonic jerks
myopathy
myopathy, centronuclear
myopia
myositis
myotonia congenita
myotonia dystrophica
nasal bridge, wide
neck weakness
nemaline rod myopathy
neonatal infection, viral
neonatal intensive care unit
neonatal screening, genetic neurologic disorders
nerve conduction studies
nerve conduction studies, motor
neurologic disease, diagnoses of
neurologic evaluation
neurologic signs
neuromuscular blockade
neuromuscular disease, electrodiagnosis of
neuromuscular junction, abnormality of
neuronal migration disorder
neuropathology
neuropathology, brain
neurotoxin
newborn, evaluation of
nusinersen
nystagmus
obesity
obstetric neurologic injuries
opened mouth
ophthalmoplegia
ophthalmoplegia, neonatal
ophthalmoplegia, total
optic atrophy
pachygyria
pathology
patient information and support
periventricular leukomalacia
pertussis immunization
petechiae
phenylketonuria, variant form of
PICU
placenta
placenta, infection of
placenta, thrombosis of
pleocytosis of cerebrospinal fluid
pneumoencephalogram(PEG)
poison, neurologic problems with
poliomyelitis
poliomyelitis vaccine
polymerase chain reaction
polymicrogyria
polymyositis
polymyositis, infantile
postpartum
Prader-Labhart-Willi syndrome
precocious puberty
pregnancy, neurologic complications in
premature infant
prenatal
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
prognosis
progressive neurologic disorder
psychomotor retardation
psychosis
psychosis, childhood
ptosis
ptosis, bilateral
quadriparesis
rash
reflex, stretch
reflex, tonic stretch
respirator
respiratory arrest
respiratory depression
respiratory distress syndrome, neurologic status with
respiratory failure
Rett's syndrome
review article
RFLPs
rigid spine syndrome
rubella vaccine
scoliosis
scoliosis, neurologic association with
screaming
screening
segmental demyelination
seizure
seizure, children
seizure, focal
seizure, neonatal
sensorineural hearing loss
serum alanine aminotransferase
short stature
shunt procedure, ventricular
skin, biopsy
skin, lesions in neurologic disorders
small for dates infant, problems in
SMN1 gene
spastic diplegia
speech disorder, childhood
speech, delayed development of
spinal cord, enlargement
spinal cord, injury of
spinal cord, injury, New Born
spinal cord, intramedullary cyst of
spinal cord, transection
spinal muscular atrophy
spinal muscular atrophy, classification
splenomegaly
spongy degeneration of brain
stereotyped behavior
stereotypy
stillbirth
strabismus
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
subdural effusion
subdural hematoma, neonates and infants
subgaleal hematoma
suck, poor
systemic lupus erythematosus
systemic lupus erythematosus, neonatal
systemic lupus erythematosus, neurologic complications with
tachycardia
temper tantrums
temporalis muscle wasting
term infant
tetrahydrobiopterin
thrombocytopenia
titinopathy
titubation
tone, muscle
tongue, fasciculations of
tongue, protrusion of
tonic spasms
toxins, nervous system
toxoplasmosis, CNS
tracheostomy
transilumination of skull
treatment of neurologic disorder
tremor
tremor, intention
tremulousness
trinucleotide repeats
type 1 muscle fiber
ultrasonography, head
urine test for metabolic disorders
vaccination, neurologic complications with
vaccine
vacuum delivery
vasculopathy
vegetarianism
visual impairment
visual loss
vitamin deficiency
walking, difficulty with
weakness
weakness, congenital
weakness, generalized
weakness, infant
weakness, progressive
Werdnig-Hoffman disease
white matter disease
wide based gait
workup
Showing articles 150 to 200 of 1507 << Previous Next >>

Radiologically Isolated Syndrome: A Review for Neuroradiologists
AJNR 41:1542-1549, Hosseiny, M.,et al, 2020

A Young Generalized Dystonia Patient with Globus-Pallidus-Specific Lesion
Ann Neurol 88:637-638, Wu, H.,et al, 2020

An Adolescent Girl Presenting with Worsening Vertigo, Headache, and Ataxia
Neurol 95:e1760-e1763, Brigham, E.,et al, 2020

Migraine
NEJM 383:1866-1876, Ashina, M., 2020

An 11-year-old girl with focal seizures, fevers, and unilateral, enhancing cortical lesions
Neurol 95:e3153-e3159, Russ, J.B.,et al, 2020

Analysis of 70 patients with hydrocephalus due to cobalamin C deficiency
Neurol 95:e3129-e3137, He, R.,et al, 2020

Clinicopathologic conference, Vitamin D deficiency
NEJM 383:2462-2470, Case 39-2020, 2020

Treatment Approaches for MOG-Ab-Associated Demyelination in Children
Curr Treat Options Neurol 21:2, Hacohen, Y. & Banweil, B., 2019

Acute Treatment of Migraine in Children and Adolescents
Neurol 93:487-499, Oskoui, M.,et al, 2019

Pharmacologic Treatment for Pediatric Migraine Prevention
Neurol 93:500-509, Oskoui, M.,et al, 2019

Characteristic Head Jerks in Congenital Oculomotor Apraxia due to Joubert Syndrome
Neurol 93:e1125-e1126, Borngraber, F.,et al, 2019

Predicting Developmental Outcomes in Preterm Infants
Neurol 93:e1231-e1240, Cayam-Rand, D.,et al, 2019

Reversible Cerebral Vasoconstriciton Syndrome
www.UptoDate.com, June, Singhal, A., 2019

Recurrent Epistaxis in an Adolescent
BMJ 367:I5393, McLaren, O. & Ronan, N., 2019

Acute Rheumatic Fever: Clinical Manifestations and Diagnosis
www.UptoDate.com, Oct, Steer, A. & Gibofsky, A., 2019

Incidental Brain MRI Findings in Children:A Systematic Review and Meta-Analysis
AJNR 40:1818-1823, Dangouloff-Ros,V.,et al, 2019

When MRI is a Clue in Episodic Ataxia
Neurol 93:e2074-e2075, Dhawan, S.R.,et al, 2019

Strokelike Episodes in a Patient with Chronic Gait Abnormalities
JAMA Neurol 76:621-622, Santoro, J.D. & Chitnis, T., 2019

Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
AJNR 40:903-907, Hartin, I.,et al, 2019

Dog Licks Baby. Baby gets Pasteurella Multocida Meningitis
Lancet 393:e41, Ryan, J.M. & Feder Jr., H.M., 2019

Delayed Complications of Cranial Irradiation
www.UptoDate.com, May, Dietrich, J.,et al, 2019

Case 27-2019:A 16-Year-Old Girl with Head Trauma During a Sailboat Race
CPC,Concussion,Benign Paroxysmal Positional Vertigo, Case 27-2019, NEJM 381:863-871, Iaccarino,M.A.,et al, 2019

Childhood Primary Angiitis of the Central Nervous System
www.UptoDate.com, Dec, Twilt, M. & Benseler, S., 2019

Acute Paraplegia in a Healthy Child
BMJ 367:L6257, Haque, A.K.M.,et al, 2019

Long-Term Treatment Effect in Cerebrotendinous Xanthomatosis Depends on Age at Treatment Start
Neurol 92:e83-e95, Stelten, B.M.L.,et al, 2019

A 14-Year-Old Girl with Headache, Seizures, and Confusion
Neurol 92:e161-e167, Xiao, L.,et al, 2019

Bobblehead-Doll Syndrome
NEJM 380:e5, Sacks, C.A., 2019

Brain Death, the Determination of Brain Death, and Member Guidance for Brain Death Accommodation Requests
Neurol 92:228-232, Russell, J.A.,et al, 2019

Fibromuscular Dysplasia and Its Neurologic Manifestations
JAMA Neurol 76:217-226, Touze, E.,et al, 2019

A 15-year-old Boy with Bilateral Wrist Pain in the Setting of Weight Loss
Neurol 92:486-492, Lau, K.H.V.,et al, 2019

Management of Stroke in Neonates and Children
Stroke 50:e51-e96, Ferriero, D.M.,et al, 2019

Lyme Myelopathy:Case Report and Literature Review of a Rare But Treatable Disorder
Mult Scler Relat Disord 29:1-6, Kaiser,E.A.,et, 2019

Basa Ganglia Calcifications (Fahrs Syndrome): Related Conditions and Clinical Features
Neurol Sci 40:2251-2263, Donzuso,G.,et al, 2019

Human Parechovirus Meningoencephalitis: Neuroimaging in the Era of Polymerase Chain Reaction-Based Testing
AJNR 40:1418-1421, Sarma, A.,et al, 2019

Paraoxysmal Tonic Upgaze in Children, Three Case Reports and a Review of the Literature
Pediatr Emer Care 35:e67-e69, Kartal,A., 2019

Human Parechovirus: An Increasingly Recognized Cause of Sepsis-Like Illness in Young Infants
Clin Microbiol Reviews 31:1-17, Olijve, L.,et al, 2018

Pyruvate Dehydrogenase Deficiency (PDCD)
eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018

FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
Mol Genet Metab 125:281-291, Almannai, M.,et al, 2018

Wilson Disease
NIDDK Oct2018, , 2018

Transient swelling in the globus pallidus and substantia nigra in childhood suggests SENDA/BPAN
Neurol 90:974-976, Ishiyama, A.,et al, 2018

Trial of Fingolimod Versus Interferon Beta-1a in Pediatric Multiple Sclerosis
NEJM 379:1017-1027, Chitnis, T.,et al, 2018

Distinctive Imaging in a Paucisymptomatic Child with Leukodystrophy
Neruol 91:e1368-e1369, Sharawat, I.K.,et al, 2018

Childhood Seizures After Phototherapy
Pediatrics 142:e20180648, Newman, T.B.,et al, 2018

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

Use of Newer Disease-Modifying Therapies in Pediatric Multiple Sclerosis in the US
Neurol 91:e1778-e1787, Krysko, K.M.,et al, 2018

Pontine Tegmental Cap Dysplasia in a Neonate
Neuol 91:e2100-e2101, Bilgin, N.,et al, 2018

Mystery Myelitis in Children
JAMA 320:2069, Kuehn, B., 2018

An Unusual Fundus Finding in a Teenage Girl
JAMA Neurol 75:1566-1567, Filho, F.M.R.,et al, 2018

Clinical Reasoning: Siblings with Progressive Weakness, Hypotonia, Nystagmus, and Hearing Loss
Neurol 90:e625-e631, Set, K.K.,et al, 2018

Nusinersen Versus Sham Control in Later-Onset Spinal Muscular Atrophy
NEJM 378:625-635, Mercuri, E.,et al, 2018



Showing articles 150 to 200 of 1507 << Previous Next >>