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Differential
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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 200 to 250 of 1507 << Previous Next >>

An Interdisciplinary Response to Contemporary Concerns About Brain Death Determination
Neurol 90:423-426, Lewis, A.,et al, 2018

Antibody-Mediated Encephalitis
NEJM 378:840-851, Dalmau, J.,et al, 2018

Abdominal Migraine
BMJ 360;k179, Angus-Leppan, H.,et al, 2018

Clinical Reasoning: A Teenager with Left Arm Weakness
Neurol 90:e907-e910, Al-Ghamdi, F.,et al, 2018

A 12-year-old girl with headache and change in mental status
Neurol 90:524-529, Patel, P.,et al, 2018

Long-Term Risk of Hemorrhagic Stroke In Young Patients with Congenital Heart Disease
Stroke 49:1155-1162, Giang, K.W.,et al, 2018

Incidence of Sudden Unexpected Death in Epilepsy in Children is Similar to Adults
Neurol 91:e107-e111, Keller, A.E.,et al, 2018

Neurologic Outcomes in Pediatric Cardiac Arrest Survivors Enrolled in the THAPCA trials
Neurol 91:e123-e131, Ichord, R.,et al, 2018

Treatable Bilateral Striatal Lesions Related to Anti-Dopamine 2 Receptor
Neurol 91:98-101, Marques-Matos, C.,et al, 2018

An Infant with Episodic Facial Flushing
Neurol 91:278-281, Kang,J.H.,et al, 2018

Glutamate Receptor D2 Serum Antibodies in Pediatric Opsoclonus Myoclonus Ataxia Syndrome
Neurol 91:e714-e723, Berridge, G.,et al, 2018

Clnicopathologic Conference Anti-N-Methyl-D-Aspartate (NMDA) Receptor Encephalitis
NEJM 379:870-878, CASE 27-2018, 2018

Brachial Plexus Ultrasound and MRI in Children with Brachial Plexus Birth Injury
AJNR 39:1745-1750, Gunes, A.,et al, 2018

Pseudo-Leptomeningeal Contrast Enhancement at 3T in Pediatric Patients Sedated by Propofol
AJNR 39:1739-1744, McKinney, A.M.,et al, 2018

Proptosis and Double Vision in a Child
JAMA Neurol 75:1142-1143, Lu, A.J.,et al, 2018

Pediatric HIV Infection: Classification, Clinical Manifestations, and Outcome
www.UptoDate.com, June, Gillespie, S.L., 2018

Making Sense of the Clinical Spectrum of Limb Girdle Muscular Dystrophies
Pract Neurol 18:201-210, Khadilkar,S.V.,et al, 2018

Congenital Asymmetric Crying Facies Syndrome, A Case Report
Medicine 97:31(e11403), Liang,X. & He,B., 2018

Teaching NeuroImages: Acute Necrotizing Encephalopathy of Childhood
Neurol 90:e177-e178, Biswas, A.,et al, 2018

A 10-year-old boy with Bilateral Vision Loss
Neurol 88:e221-e224, Bulwa, Z.,et al, 2017

Endovascular Therapies for Acute Ischemic Stroke in Children
Stroke 48:2026-2030, Huang, M.I.,et al, 2017

Outcomes of Colorado Children with Acute Flaccid Myelitis at 1 Year
Neurol 89:129-137, Martin, J.A.,et al, 2017

BMI Increase through Puberty and Adolescence is Associated with Risk of Adult
Neurol 89:363-369, Ohlsson, C.,et al, 2017

A Demure Teenager and Her Dystonic Foot
Neurol 89:e71-e75, Cullinane, P.W.,et al, 2017

A 15-month-old boy with Progressive Lethargy and Spasticity
Neurol 89:e135-e139, Zhang, R.,et al, 2017

Neuroimaging Changes in Menkes Disease, Part 1
AJNR 38:1850-1857, Manara, R.,et al, 2017

Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery
NEJM 377:1648-1656, Blumcke, I.,et al, 2017

Surgery for Drug-Resistant Epilepsy in Children
NEJM 377:1639-1647, Dwivedi, R.,et al, 2017

Single-Dose Gene-Replacement Therapy for Spinal Muscular Atrophy
NEJM 377:1713-1722,1786, Mendell, J.R.,et al, 2017

Nusinersen Versus Sham Control in Infantile-Onset Spinal Muscular Atrophy
NEJM 377:1723-1732,1786, Finkel, R.S.,et al, 2017

Maternal Use of antiepileptic Agents During Pregnancy and Major Congenital Malformations in Children
JAMA 318:1700-1701, Bromley, R.L.,et al, 2017

Population-based Study of Ischemic Stroke Risk after Trauma in Children and Young Adults
Neurol 89:2310-2316, Fox, C.K.,et al, 2017

Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
NEJM 377:2376-2385, Case 38-2017, 2017

Autoimmune Encephalitides: A Broadening Field of Treatable Conditions
Neurologist 22:1-13, Kalman, B., 2017

"Phacing" a New Cause of Carotid Artery Dissection
Neurologist 22:54-56, Kulyk, C.,et al, 2017

Prehospital Emergency Care in Childhood Arterial Ischemic Stroke
Stroke 48:1095-1097, Stojanovski, B.,et al, 2017

A 13-year-old boy with Chronic Ataxia and Developmental Delay
Neurol 88:e116-e121, Libdeh, A.A.,et al, 2017

The Tadpole Pupil
JAMA Neurol 74:481, Aggarwal, K. & Hildebrand, G.D., 2017

Early-Onset Head Titubation in a Child with Poretti-Boltshauser Syndrome
Neurol 88:1478-1479, Masson, R.,et al, 2017

Patient with Severe Moyamoya Disease Who Presents with Acute Cortical Blindness
Stroke 48:e126-e129, Sajja, A.,et al, 2017

A Child with Delayed Motor Milestones and Ptosis
Neurol 88:e158-e163, Ghosh, P.S., 2017

Incomplete Miller-Fisher Syndrome with Advanced Stage Burkitt Lymphoma
Indian Pediat 54:413-415, Ozdemir,Z.C.,et al, 2017

Guillain-Barre Syndrome following tuberculosis: A rare association
J Neurosci Rural Pract 8:296-299, Lakhotia, A.N.,et al, 2017

Menkes Disease Mimicking Child Abuse
Pediat Dermatol 34:e132-e134, Droms, R.J.,et al, 2017

Mouse Infestation Likely Source of Lymphocytic Choriomeningitis in Teen
MMWR 65:248-249, Rostad, C.A. & Pickering, L.K., 2016

Wilson Disease
Yamada Textbook of Gastroenterology Chp 102, Metabolic Diseases of Liver, 6th Ed, Sunderam, S.S., & Sokol, R.J., 2016

Small Fiber Neuropathy in Fabry Disease:A Review of Pathophysiology and Treatment
JIEMS 4:1-5, Politeri,J.M.,et al, 2016

Listeria infections in Neonates
Neoreviews 17:e515-e520, McKinney, J.S., 2016

Clinicopathologic Conference, Aqueductal Stenosis with Hydrocephalus
NEJM 375:2583-2593, Case 40-2016, 2016

Neonatal Abstinence Syndrome
NEJM 375:2468-2479, McQueen, K. & Murphy-Oikonen, J., 2016



Showing articles 200 to 250 of 1507 << Previous Next >>