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Differential
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abdominal distention

acetylcholine receptor antibody

acid maltase deficiency

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, congenital

acquired immunodeficiency syndrome, infants and children

adverse drug reaction

agenesis of corpus callosum

Aicardi-Goutieres syndrome

airway obstruction

alternating hemiplegia

alternating hemiplegia of childhood

anemia, megaloblastic

Angelman syndrome

anterior horn cell disease

antiviral agents

arrhythmia, cardiac

arthrogryposis multiplex

ataxia, cerebellar

ataxia, truncal

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, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavior, combative

behavioral disorder

biopterin deficiency

bone density, increased

bone marrow transplantation

botulinum toxin

botulism antitoxin

botulism immune globulin

botulism, infant

brainstem, atrophy

breech delivery

Brown-Vialetto-Van Laere syndrome

bulbar palsy, childhood

calcification, intracranial

Canavan's disease

cardiac surgery, hypothermia and circulatory arrest for

cardiac surgery, neurologic complications with

CAT scan, abnormal

celiac disease, childhood

central core disease

central nervous system, infection of

cerebellar atrophy, primary

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar hypoplasia

cerebellar vermis

cerebral cortical atrophy

cerebral embolism

cerebral gigantism

cerebral infarction

cerebral palsy, associated problems with

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, protein of

cerebrospinal fluid, proteincytologic dissociation

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

cherry red spot

chilbran skin lesions

choreoathetosis

chorioamnionitis

chorioretinitis

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

clubfoot as related to neurologic disease

cobalamin C deficiency

cognitive delay

congenital heart disease

congenital heart disease, CNS complications with

congenital infection, CNS

congenital infection, viral

congenital myopathy

congenital myopathy, inflammatory

contractures, joint

cornea, opacity of

corpus callosum

corpus callosum, thinning

cortical blindness

cranial neuropathy

cranial neuropathy, multiple

Craniosynostosis

creatine phosphokinase(CPK)elevated

crying, pathologic

cultured skin fibroblasts

cytomegalic inclusion disease

cytomegalovirus infection

cytomegalovirus infection, congenital

deep gray nuclei

delay in diagnosis

delayed dentition

delivery, complicated

dementia, childhood

dentate nuclei, lesion of

descending paralysis

developmental abnormality of brain

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diagnostic criteria

differential diagnosis

diphtheria-tetanus-pertussis immunization

dislocated hip, congenital

dural sinus thrombosis

dysostosis multiplex

dystonia, children

eating disorder

electroencephalogram, abnormalities of

electron microscopy

embolism, paradoxical

encephalomyelitis

encephalopathy, anoxic

encephalopathy, neonatal

epidemiology of neurology

epileptic encephalopathy

evoked potentials

exome sequencing

eye movement, disorders of

facial anomalies

facial appearance, abnormal

facial expression abnormality

facial weakness

facial weakness, bilateral

failure to thrive

FARS2 deficiency

feeding disorder

fetal movements, reduced

fine motor function, impaired

fontanel, bulging

food-borne infection

forceps delivery

fundus, abnormality of

gag reflex, depressed

gammaglobulin therapy, intravenous

gangliosidosis GM2

genetic counselling

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

genital hypoplasia

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

GLUT1 deficiency syndrome

gluten-free diet

glycogen storage disease

Gowers maneuver

growth hormone deficiency

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, infantile and childhood form

head circumference

hemorrhage, intracranial, newborn

hemorrhage, periventricular

hemorrhagic diathesis

hepatosplenomegaly

hexosaminidase-A

high arched feet

high arched palate

histochemistry of muscle

Horner's syndrome

Horner's syndrome, bilateral

Horner's syndrome, congenital

Hunter's syndrome

hydrocephalus, communicating

hydrocephalus, congenital

hydrocephalus, exvacuo

hydroxyglutaric aciduria

hyperbilirubinemia

hyperbilirubinemia, CNS abnormality after

hyperhomocysteinemia

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hypertrophic cardiomyopathy

hypogammaglobulinemia

hypoglycorrhachia

hypomyelination

hypopigmentation of skin

hypotonia, causes of

hypotonia, infants

hypoxic encephalopathy

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

interferon alpha

intestinal biopsy

intracranial hemorrhage

intracranial pressure, increased

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

islet cell tumor

joint hypermobility

kyphoscoliosis, neurologic causes of

lactic acidemia

leg weakness, bilateral

Leigh's disease

leukoencephalopathy

lid closure, weakness of

listeria monocytogenes

liver function enzymes

lumbar puncture

lysosomal storage disease

malformation, CNS, congenital

malformation, vascular

malignant hyperpyrexia

McArdle's disease

meningitis, carcinomatous

meningitis, CSF cell count-normal

mental retardation

metabolic acidosis

metabolic disorder, primary

metabolic disorder, primary-screening tests

methylene tetrahydrofolate reductase

methylenetetrahydrofolate reductase deficiency

methylmalonic acidemia

middle cerebellar peduncle

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

migraine, seizures in

mitochondrial disease

mitral valve prolapse

molecular genetics

motor neuron disease

movement disorder

movement disorder, hyperkinetic

MRI, diffusion weighted

MRI, high signal foci on

MRI, spinal cord

mucopolysaccharidoses

mucopolysacchariduria

muscle atrophy, progressive

muscle atrophy, static

muscle diseases, characteristics of

muscle phosphorylase deficiency

muscle weakness

muscle weakness, proximal

muscle weakness, sudden onset of

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

myoclonic jerks

myopathy, centronuclear

myotonia congenita

myotonia dystrophica

nasal bridge, wide

nausea and vomiting

nemaline rod myopathy

neonatal infection, viral

neonatal intensive care unit

neonatal screening, genetic neurologic disorders

nerve conduction studies

nerve conduction studies, motor

neuroaxonal dystrophy

neuroaxonal dystrophy, infantile

neurologic disease, diagnoses of

neurologic evaluation

neurologic signs

neuromuscular blockade

neuromuscular disease, electrodiagnosis of

neuromuscular junction, abnormality of

neuronal ceroid-lipofuscinosis

neuronal migration disorder

neuropathology, brain

neurophysiology

newborn, evaluation of

Noonan Syndrome

nystagmus, monocular

obstetric neurologic injuries

ophthalmoplegia

ophthalmoplegia, neonatal

ophthalmoplegia, total

optic atrophy, infants

optic nerve, hypoplasia of

paraparesis, familial spastic

paraparesis, spastic

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

patient information and support

pectus excavatum

pediatric neurology

periventricular leukomalacia

pertussis immunization

phenylketonuria, variant form of

placenta, infection of

placenta, thrombosis of

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

poison, neurologic problems with

poliomyelitis vaccine

polymerase chain reaction

polymyositis, infantile

pons, lesion of

postoperative neurologic complications

Prader-Labhart-Willi syndrome

precipitating factors

precocious puberty

pregnancy, neurologic complications in

premature infant

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

progressive neurologic disorder

psychiatric problems in neurologic disorders

psychomotor retardation

psychosis, childhood

ptosis, bilateral

pulmonary stenosis

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

quadriparesis, acute

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

reflex, stretch

reflex, tonic stretch

renal tubular acidosis

repetitive nerve stimulation

respiratory arrest

respiratory depression

respiratory distress syndrome, neurologic status with

respiratory failure

respiratory tract infection

Rett's syndrome

riboflavin transporter deficiency

rigid spine syndrome

rubella vaccine

scoliosis, neurologic association with

segmental demyelination

seizure, children

seizure, injury following

seizure, neonatal

self-mutilation

semialdehyde dehydrogenase deficiency

sensorineural hearing loss

serum alanine aminotransferase

shunt procedure, ventricular

skin, lesions in neurologic disorders

skull x-ray, abnormal

small for dates infant, problems in

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

spongy degeneration of brain

standing difficulty

startle reaction

status epilepticus

stereotyped behavior

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

subdural effusion

subdural hematoma, neonates and infants

subgaleal hematoma

superior sagittal sinus thrombosis

symmetric brain lesions

systemic lupus erythematosus

systemic lupus erythematosus, neonatal

systemic lupus erythematosus, neurologic complications with

Tay-Sachs disease

teeth, abnormal

teeth, number of in infants

temper tantrums

temporalis muscle wasting

tetrahydrobiopterin

thiamine deficiency

thrombocytopenia

tongue, fasciculations of

tongue, protrusion of

tongue, weakness

toxins, nervous system

toxoplasmosis, CNS

transilumination of skull

treatment of neurologic disorder

tremor, intention

trinucleotide repeats

type 1 muscle fiber

ultrasonography

ultrasonography, head

ultrasonography, head, fetus-neonate

urine test for metabolic disorders

vaccination, neurologic complications with

vacuum delivery

vision, failure of in childhood

visual evoked response

visual impairment

visual tracking

vitamin deficiency

vomiting, recurrent

walking, difficulty with

weakness, acute

weakness, congenital

weakness, generalized

weakness, infant

weakness, progressive

Werdnig-Hoffman disease

white matter disease

wide based gait

Showing articles 150 to 200 of 1556 << Previous Next >>

Review of Vitamin B12 Deficiency in Pregnancy:A Diagnosis Not to Miss as Veganism and Vegetarianism Become More Prevalent
Eur J Haematol 106:450-455, Rashid,S.,et al, 2021

Efficacy and Safety of Adjunctive Lacosamide in the Treatment of Primary Generalised Tonic-Clonic Seizures: A Double-Blind, Randomised, Placebo-Controlled Trial
JNNP 91:1067-1075, Vossler, D.G.,et al, 2020

Cyclic Vomiting Syndrome in Children
AJGH 2:doi:10.33552/AJGH.2020, Al-Ansari, N., 2020

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

A 16-year-old Girl with Ataxia, Oscillopsia, and Behavioral Changes
Neurol 94:713-717, Silverman, A.,et al, 2020

Association of Pediatric Acute-Onset Neuropsychiatric Syndrome with Microstructural Differences in Brain Regions Detected via Diffusion-Weighted Magnetic Resonance Imaging
JAMA Network Open 3:doi:10.1001/JAMANETWORKOPEN.2020.4063, Zheng, J.,et al, 2020

An Infant with Developmental Delay, Epileptic Spasms, and Acrocyanosis
Neurol 94:939-942, Madaan, P.,et al, 2020

CASPR2 Autoimmunity in Children Expanding to Mild Encephalopathy with Hypertension
Neurol 94:e2290-e2301,953, Syrbe, S.,et al, 2020

Complex Ataxia
Neurol 95:136-141, Abkur, T.,et al, 2020

Childhood Multisystem Inflammatory Syndrome
NEJM 383:393-395, Levin, M., 2020

A 10-Year-Old Girl with Muscle Stiffness
Neurol 95:e773-e778, Prior, D.E. & Ghosh, P.S., 2020

Determination of Brain Death/Death by Neurologic Criteria
JAMA doi:10.1001/JAMA.2020.11586, Greer, D.M.,et al, 2020

Pediatric Leigh Syndrome
Ann Neurol 88:218-232, Alves, C.A.P.F.,et al, 2020

A 14-Year-Old Boy with Acute Weakness, Parethesias, and Headache
Neurol 95:e1285-e1289, Seese, R.R.,et al, 2020

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

Acute Ischemic Stroke in Adolescents
Neurol 94:e158-e169, Rambaud, R.,et al, 2020

Feasibility, Safety, and Outcome of Endovascular Recanalization in Childhood Stroke
JAMA Neurol 77:25-34, Sporns, P.B.,et al, 2020

Rapidly Progressive Gait Disorder and Cranial Nerves Involvement in a 9-year-old boy
Neurol 94:e330-e334, Lipp, A.,et al, 2020

Clinicopathologic Conference, Intraparenchymal & Intracranial Hemorrhage due to Birth Trauma
NEJM 382:656-664, Case 5-2020, 2020

Hopkins Syndrome
Neurol 94:e996-e997, Sgobbi de Souza, P. V.,et al, 2020

Clinical and Radiologic Features of Pedicatric Opioid Use-Associated Neurotoxicity with Cerebellar Edema (POUNCE) Syndrome
Neurol 94:710-712, Kim, D.D. & Prasad, A.N., 2020

A 22-Year-Old Man with Progressive Bilateral Visual Loss
Neurol 94:625-630, Yang, S.L.,et al, 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

Sydenham Chorea
www.UptoDate.com, Oct, Gilbert, D.L., 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

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

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

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

Showing articles 150 to 200 of 1556 << Previous Next >>