Neudle.com: "neonatal epilepsy syndromes"

Differential
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abstinence syndrome

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, infants and children

ACTH

addiction, heroin

addiction, heroin-neurologic complications with

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

adverse drug reaction

agenesis of corpus callosum

alcohol, heart involvement with

alcohol, neurologic complications with

alcoholic blackout

alcoholic coma

alcoholic dementia

alcoholic polyneuropathy

alcoholic withdrawal states, DT's, convulsions, etc.

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, treatment of

antibiotics, neurologic complications with

anticonvulsants

anticonvulsants, bioavailability

anticonvulsants, blood level determination of

anticonvulsants, cognitive function with

anticonvulsants, discontinuation

anticonvulsants, discontinuation in seizure-free epileptics

anticonvulsants, effectiveness

anticonvulsants, mechanism of action of

anticonvulsants, pharmacokinetics

anticonvulsants, selection of

anticonvulsants, subtherapeutic

anticonvulsants, teratogenicity of

anticonvulsants, untoward effects of

antiphospholipid antibodies

attention deficit disorder with hyperactivity

autism

autoimmune disease

automatisms

autonomic dysfunction

Babinski sign

baclofen

bacterial infection

bacterial infection, CNS

barbiturate

barbiturate anesthesia

bartonella henselae

basal ganglia, calcification of

basal ganglia, hemorrhage

basal ganglia, lesion of

basal ganglia, lesion, bilateral

behavioral disorder

benign epilepsy of childhood

benzodiazepine

bilateral periventricular nodular heterotopia

blindness, sudden

blood transfusion

body odor

bone marrow transplantation

burst suppression pattern, electroencephalogram

calcification, gyral

calcification, intracranial

CAT scan, false negative

CAT scan, indications for

CAT scan, isodense lesion with acute hemorrhage

cat-scratch disease

central nervous system, infection of

central pontine myelinolysis

cerebellar ataxia, children

cerebellar degeneration

cerebellar hemorrhage

cerebellitis

cerebral arteries

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortex

cerebral cortical atrophy

cerebral edema

cerebral embolism

cerebral embolism, cardiac origin

cerebral infarction

cerebral infarction, subcortical

cerebral palsy

cerebral vasculature

cerebral vasculature, calcification

cerebral venous infarction

cerebral venous thrombosis

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, lactic acid concentration

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, location of

cerebrovascular accident, mimics

cerebrovascular accident, neonatal

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, prevention of

cerebrovascular accident, recurrent

cerebrovascular accident, work up for

cerebrovascular accident, young adult

cerebrovascular disease

cherry red spot

cherry red spot-myoclonus syndrome

children

chlorpromazine

chorioretinitis

chromosomal abnormality

chromosome 1

chromosome 2

cleft lip

Clinical Pathologic Conference(C.P.C.)

coma, medically induced

confusional state, acute

congenital heart disease

congenital heart disease, CNS complications with

congenital infection, CNS

congenital infection, viral

congenital malformation

congenital malformation, non CNS

conjugate gaze, forced

consanguinity

controversies in neurology

conversion reaction

corpus callosum

corpus callosum, lesion of

cortical blindness

cortical blindness, transient

cortical dysplasia, focal

cranial nerve palsies

Creutzfeldt-Jakob disease, genetic

cultured skin fibroblasts

cyst, porencephalic

cytomegalovirus infection

cytomegalovirus infection, congenital

deafness

degenerative diseases of CNS

dehydration

delay in diagnosis

delirium

delivery, complicated

dementia

dementia, childhood

dementia, frontal lobe type

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

demyelinating disease

dentatorubral-pallidoluysian atrophy

depression

detoxification

developmental disability

developmental milestones

developmental milestones, loss of

developmental retardation

diagnosis of exclusion

diarrhea

diencephalon

diet

differential diagnosis

dilantin

disability, neurological

drug abuse, neonatal abstinence syndrome with

drug abuse, neurologic complications of

drug abuse, toxic screen In

drug addiction

drug induced neurologic disorders

drug interactions

drug withdrawal

dural sinus thrombosis

Eisenmenger's syndrome

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, monitoring, continuous

electroencephalogram, sleep

electroencephalogram, spike activity

electroencephalogram, video monitoring with

electrolyte imbalance

electron microscopy

embolism

embolism, paradoxical

embolism, septic

emergency room

encephalitis

encephalitis, autoimmune

encephalitis, focal

encephalitis, Rasmussen's

encephalitis, unknown etiology

encephalocele

encephalopathy

encephalopathy, metabolic

encephalopathy, neonatal

encephalopathy, post traumatic

encephalopathy, progressive

enzyme, induction

epicanthal folds

epidemiology of neurology

epilepsia partialis continua

epilepsy

epilepsy referral centers

epileptic encephalopathy

episodic disorders

episodic neurologic deficits

Epstein-Barr virus

ethics in neurology

evidence-based research

executive dysfunction

exercise intolerance

eye movement, disorders of

Fabry's disease

facial anomalies

facial appearance, abnormal

fatty acid, elevated plasma content

febrile infection-related epilepsy syndrome

feeding disorder

felbamate

fetal alcohol syndrome

fever

fibrinolytic agents

fibroma, ungual

fine motor function, impaired

frontotemporal dementia, behavioral variant

fundus, abnormality of

gabapentin

gadolinium

gait disorder

gammaglobulin therapy, intravenous

gaze palsy

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic neurologic disorders

GLUT1 deficiency syndrome

gram negative rod

grasp reflex

growth retardation

Guillain Barre syndrome

head circumference and brain development

headache

hearing loss

hearing loss, bilateral

hemangioma, facial

hemangioma, leptomeningeal

hemorrhage, intracranial, newborn

hemorrhagic diathesis

hemorrhagic shock encephalopathy syndrome

hepatic encephalopathy

hepatic failure

hepatomegaly

hepatosplenomegaly

heralding manifestation

herniation syndromes, intracranial

herpes simplex virus

herpes simplex virus infection, newborn

herpes virus

heterotopia

hippocampus, hyperintense

hormone replacement

human immunodeficiency virus type 1

hydrocephalus

hyperactivity

hyperperfusion syndrome

hyperreflexia

hypertelorism

hypertension

hypertensive encephalopathy

hyperthermia

hypertonia

hypertrophic cardiomyopathy

hyperviscosity

hypocalcemia

hypoglycorrhachia

hypoglycorrhachia, causes of

hypopigmentation of skin

hypoxic-ischemic leukoencephalopathy

inappropriate antidiuretic(A.D.H.)hormone

inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with

inattention

inborn errors of metabolism

inborn errors of metabolism, screening

inclusion bodies

infantile spasm

infection

infectious mononucleosis, neurologic findings with

injection neuropathy

intellectual deficit

intellectual deterioration

intelligence quotient

intracerebral hemorrhage

intracerebral hemorrhage, causes of

intracerebral hemorrhage, clot evacuation

intracerebral hemorrhage, incidence of

intracerebral hemorrhage, lobar

intracerebral hemorrhage, location of

intracerebral hemorrhage, pathophysiology

intracerebral hemorrhage, progression of

intracerebral hemorrhage, recurrent

intracerebral hemorrhage, treatment of

intracranial hemorrhage

intracranial pressure, increased

intrauterine

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intraventricular hemorrhage

intubation

irritability

islet cell tumor

Jakob-Creutzfeldt disease

joint hypermobility

ketogenic diet

klippel feil syndrome

Landau-Kleffner syndrome

Leigh's disease

Lennox-Gastaut syndrome

leukodystrophy

leukoencephalopathy

level of consciousness, decreased

lymphomatoid granulomatosis

lysosomal storage disease

macrocephaly

malabsorption

malformation, CNS, congenital

malformation, vascular

malformation, vascular, cerebral

Marchiafava-Bignami disease

medication withdrawal

megalencephaly

MELAS syndrome

meningeal enhancement

meningitis

meningitis, CSF cell count-normal

meningocele

meningoencephalitis

mental retardation

mental status, abnormal

MERRF syndrome

mesial temporal sclerosis

metabolic disorder, primary

methadone

microcephaly

microdontia

microhemorrhage, intracerebral

micropthalmia

middle cerebellar peduncle

middle cerebellar peduncle, lesion, bilateral

middle cerebral artery territory infarction

middle cerebral artery, occlusion of

migraine

migraine, prophylaxis

migraine, seizures in

migraine, treatment of

mimics

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

MRI, abnormal, seizure causing

MRI, angiography

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, cortical enhancement

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, negative

MRI, serial

MRI, susceptibility weighted

MRI, venography

multiple subpial transection

muscle biopsy

muscle weakness, proximal

myasthenia gravis

myasthenia gravis, treatment of

myoclonus, stimulus sensitive

myoglobinuria

myopathy

myopathy, alcoholic

myopathy, mitochondrial

neonatal abstinence syndrome

neonatal epilepsy syndromes

neonatal epileptic encephalopathy

neoplasm, primary of CNS

neural tube defect

neurocutaneous disease

neuroendocrinology

neurologic complications

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination

neurologic examination, focal

neurologic signs

neurological intensive care

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, peripheral, treatment

neurosyphilis

newborn, evaluation of

next-generation sequencing

Noonan Syndrome

nutritional deficiency

nystagmus

nystagmus, rotary

obsessive-compulsive disorder

obstetric neurologic injuries

occipital lobe, lesion of

oculodentodigital dysplasia

old age, neurology of

ophthalmoplegia

ophthalmoplegia, progressive external

opiate

opisthotonus

opportunistic infection

opportunistic infection, CNS

optic atrophy

optic nerve

optic nerve, lesion of

optic neuritis

optic neuropathy

optic neuropathy, nutritional

oral contraceptives

organ transplantation

paraparesis, familial spastic

paraparesis, spastic

parasitic infection, CNS

Parkinsonism syndrome

paroxysmal neurologic disorder

patent ductus arteriosus

patient information and support

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

poison, neurologic problems with

polycythemia, secondary

polyhydramnios

polymerase chain reaction

polymyositis

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

porphyria

port wine nevus

post hemorrhagic hydrocephalus

postoperative neurologic complications

posttransplant lymphoproliferation disorder

practice guidelines

precipitating factors

pregnancy, anticonvulsants during

pregnancy, neurologic complications in

premature infant

prenatal diagnosis by amniocentesis

prethrombotic state

prevention of neurologic disorders

primary familial brain calcification

prion disease

prognosis

progressive myoclonic epilepsy

progressive neurologic disorder

pseudohypoparathyroidism

pseudoxanthoma elasticum

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

psychosis

psychosocial aspects

pulmonary infiltrates

pulmonary stenosis

pure word deafness

pyramidal tract dysfunction

pyruvate metabolism, abnormality of

quadrantanopsia, superior

rapidly progressing neurologic illness

real-time quaking-induced conversion

respiratory tract infection

rhabdomyosarcoma of heart

risk factors

risk-benefit assessment

seizure, age of onset

seizure, cardiac arrhythmia causing

seizure, children

seizure, classification of

seizure, complications following

seizure, diagnosis of

seizure, diencephalic

seizure, driving with

seizure, drug resistance

seizure, drug-induced

seizure, injury following

seizure, intractable

seizure, intractable, treatment of

seizure, minor motor

seizure, neonatal

seizure, neonatal abstenence syndrome

seizure, paradoxical

seizure, petit mal

seizure, photosensitive

seizure, precipitating factors

seizure, pregnancy

seizure, prevention of

seizure, prognosis in adults

seizure, prognosis in childhood

seizure, psychomotor-frontal lobe

seizure, psychomotor-temporal lobe

seizure, psychosocial aspects of

seizure, recurrent

seizure, remission

seizure, restrictions following

seizure, risk factors for

seizure, stimulus sensitive

seizure, surgical treatment of

seizure, systemic disease causing

seizure, tonic-clonic

seizure, treatment of

seizure, treatment of, first

seizure, treatment, adjunctive therapy

seizure, withdrawal

seizure, women

seizure, workup of

sensorineural hearing loss

skin, lesions in neurologic disorders

small vessel disease

small vessel disease, cerebral

sodium channel dysfunction

speech disorder, childhood

speech, loss of

spina bifida

spontaneous remission

status epilepticus

status epilepticus, autonomic

status epilepticus, intractable

status epilepticus, nonconvulsive

steroid

steroid therapy, CNS treatment and complications with

straight sinus

striatonigral degeneration

striatonigral degeneration, infantile

striopallidodentate calcifications, familial idiopathic

strokelike episodes

Sturge-Weber syndrome

subarachnoid hemorrhage

subdural hematoma

subependymal nodules

sudden infant death syndrome

suicide

superior sagittal sinus thrombosis

symmetric brain lesions

syncope

syndactyly

syphilis, congenital

syphilis, diagnosis and treatment

syphilis, neurologic complications with

temporal lobe, atrophy

temporal lobe, lesion

temporal lobe, status

temporal lobectomy

temporal lobectomy, complications

thalamus, lesion of-bilateral

toxoplasmosis, congenital

transient neurologic deficit

transplacental virus infections

transposition of the great vessels

treatment of neurologic disorder

tuberous sclerosis, screening for

ultrasonography

ultrasonography, head, fetus-neonate

unconsciousness

Unverricht-Lundborg disease

upgaze, paralysis of

urinary incontinence

vagus nerve stimulation

valium

valvulopathy

vascular malformation, children, intracranial

vasculopathy

ventricular enlargement

vigabatrin

viral infection

viral infection, CNS

visual acuity, decreased

visual field defect

visual fields, constricted

visual impairment

visual loss

vitamin K

vomiting, intractable

vomiting, recurrent

Wada test

walking, difficulty with

Wernicke's encephalopathy

wheelchair

white matter disease

white matter disease, subcortical

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Genetic Causes of Cerebral Small Vessel Diseases, A Parctical Guide for Neurologists
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Neonatal Seizures
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Unpacking the CNS Manifestations of Epstein-Barr Virus:An Imaging Perspective
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Updates on Sturge-Weber Syndrome
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Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
NEJM 386;674-687, Case 5-2022, 2022

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

Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
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Basa Ganglia Calcifications (Fahrs Syndrome): Related Conditions and Clinical Features
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FARS2 dificiency; new cases, review of clinical, biochemical, and molecular spectra, and variants interpretation based on structural, functional, and evolutionary significance
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Neonatal Abstinence Syndrome
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Neonatal Abstinence Syndrome
NEJM 375:2468-2479, McQueen, K. & Murphy-Oikonen, J., 2016

A 62-Year-Old Woman with Bizarre Behavior and Recurrent Episodes of Behavioral Arrest
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Clinicopathologic Conference, Frontotemporal Lobar Degeneration with Tau-positive Inclusions (Picks Disease Subtype) Due to a Gly389Arg MAPT Mutation, Resulting in the Behavioral Variant of Frontotemporal Dementia with Parkinsonism
NEJM 372:1151-1162, Miller, B.L.,et al, 2015

Clinicopathologic Conference, CAT Scratch Disease (Encephalopathy Associated with Bartonella Henselae)
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Sturge-Weber Syndrome
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Recognition and Management of Withdrawal Delirium
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Drug Treatment of Epilepsy in Adults
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Stroke and NonStroke Brain Attacks in Children
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Alcohol and Alcoholism
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Sturge-Weber Syndrome
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Evidence-Based Guideline Update: Vagus Nerve Stimulation for the Treatment of Epilepsy
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Febrile Infection-Related Epilepsy Syndrome: A Study of 12 Patients
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Progressive Gait Deterioration in Adolescents with Dravet Syndrome
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Clinical Reasoning: Encephalopathy in a 10-year-old boy
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Presentation, Diagnosis, Pathophysiology, and Treatment of the Neurological Features of Sturge-Weber Syndrome
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Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
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Clinical Reasoning: Seizures in a Child With Sensorineural Deafness and Agitation
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Frequency and Prognosis of Convulsive Status Epilepticus of Different Causes: A Systematic Review
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The Expanding Phenotype of GLUT1-Deficiency Syndrome
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Response of Infantile Spasms to Levetiracetam
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Generalized Tonic-Clonic Seizures After Acute Oxcarbazepine Withdrawal
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Death in Children With Febrile Seizures: A Population-Based Cohort Study
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Overview of Phenylketonuria
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Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies
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Epilepsy Syndromes in Infancy
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The First Seizure and Its Management in Adults and Children
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The Tuberous Sclerosis Complex
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Four-Year Outcome after Early Withdrawal of Antiepileptic Drugs in Childhood Epilepsy
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Ictal Cardiorespiratory Arrest in Panayiotopoulos Syndrome
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Progressive Myoclonic Epilepsies: A Review of Genetic and Therapeutic Aspects
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Clinical Correlations of Mutations in the SCN1A Gene: From Febrile Seizures to Severe Myoclonic Epilepsy in Infancy
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Neonatal Brain Injury
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The United Kingdom Infantile Spasms Study Comparing Vigabatrin with Prednisolone or Tetracosactide at 14 Days: A Multicentre, Randomised Controlled Trial
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Management of Drug and Alcohol Withdrawal
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Spontaneous Intracerebral Hemorrhage
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Cerebral Sinovenous Thrombosis in Children
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Showing articles 0 to 50 of 10727 Next >>