Neudle.com: inutero

Differential
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abortion, spontaneous

abstinence syndrome

acetylcholinesterase

acid maltase deficiency

acid maltase deficiency, adult

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome, congenital

acquired immunodeficiency syndrome, infants and children

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

advances in neurology

adverse drug reaction

agenesis of corpus callosum

Aicardi-Goutieres syndrome

alcohol

alcohol, neurologic complications with

algorithm

alpha glucosidase

alpha-fetoprotein

alveolar hypoventilation

aminoacidurias

amniocentesis

amniotic fluid, infection

aneurysm, intracranial

aneurysm, intracranial, treatment of

Angelman syndrome

angiofibroma, facial

angiography, cerebral

angiography, spinal

angiokeratoma

anterior horn cell disease

anticonvulsants

anticonvulsants, blood level determination of

anticonvulsants, cognitive function with

anticonvulsants, compliance

anticonvulsants, dosage

anticonvulsants, selection of

anticonvulsants, teratogenicity of

anticonvulsants, untoward effects of

arterial dissection, childhood

arteritides

arthralgia

arthrogryposis multiplex

aspartate aminotransferase

attention deficit disorder with hyperactivity

basal ganglia, calcification of

basal ganglia, lesion of

bone marrow transplantation

calcification, intracranial

calcification, periventricular

cardiac surgery, hypothermia and circulatory arrest for

cardiac surgery, neurologic complications with

CAT scan, indications for

cataracts

cavernous hemangioma

Central America

central nervous system, infection of

cerebellar hypoplasia

cerebral cortical atrophy

cerebral edema, vasogenic

cerebral embolism

cerebral embolism, cardiac origin

cerebral hemisphere left-right asymmetry

cerebral infarction

cerebral ischemia

cerebral palsy

cerebral palsy, etiology

cerebral palsy, risk factors

cerebral palsy, work up

cerebral venous thrombosis

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, culture of

cerebrospinal fluid, culture of, viral

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, protein of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, cardiac disease causing

cerebrovascular accident, etiology

cerebrovascular accident, infancy and childhood

cerebrovascular accident, intrauterine

cerebrovascular accident, neonatal

cerebrovascular accident, postpartum

cerebrovascular accident, prevention of

cerebrovascular accident, recurrent

cerebrovascular accident, work up for

cerebrovascular disease

ceruloplasmin, serum

cesarean section

Charcot-Marie-Tooth

chilbran skin lesions

choroid plexus, abnormality of

choroid plexus, cyst

chromosomal abnormality

chromosome 15

chromosome 19

chromosome 3

chronic graft versus host disease

cleft lip

Clinical Pathologic Conference(C.P.C.)

cocaine

cocaine, intrauterine exposure

congenital birth defects

congenital heart disease

congenital infection, CNS

congenital infection, viral

congenital malformation

congenital malformation, dilantin therapy causing

congenital malformation, non CNS

congestive heart failure

consanguinity

contractures, joint

controversies in neurology

copper metabolism, abnormal

cornea, abnormal

cornea, opacification in infancy-causes of

cornea, opacity of

corneal dystrophy

corpus callosum, atrophy of

counselling

creatine phosphokinase(CPK)elevated

cry, abnormal

cry, high-pitched

cry, weak

cultured skin fibroblasts

cyanosis

cyst

cyst, porencephalic

cytomegalovirus infection

cytomegalovirus infection, congenital

degenerative diseases of CNS

delivery, complicated

dementia

dementia, childhood

demyelinating disease

dentate nuclei, lesion of

depression

developmental abnormality of brain

developmental disability

developmental evaluation

developmental milestones

developmental retardation

diagnostic criteria

diaphragmatic paralysis

diarrhea

diet

differential diagnosis

digits, abnormal

dilantin

dilantin, toxicity

disability, neurological

disease modifying agents

distal muscle weakness

DNA probes

drooling

drug abuse

drug abuse, neurologic complications of

drug abuse, toxic screen In

drug induced neurologic disorders

drug induced neurologic disorders in children

drug interactions

drug withdrawal

dying

Dyke-Davidoff-Masson syndrome

dysarthria

dysarthria-clumsy hand syndrome

electrocardiogram, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electromyogram

electron microscopy

embolism, paradoxical

employment

encephalocele

encephalopathy

encephalopathy, anoxic

encephalopathy, neonatal

epidemiology of neurology

epoxide hydrolase

ethics in neurology

extracorporeal membrane oxygenation

Fabry's disease

facial appearance, abnormal

facial weakness

facial weakness, bilateral

failure to thrive

false negative

familial

fatty acid, elevated plasma content

feeding disorder

fetal alcohol syndrome

fetal death

fetal surgery

fetal valproate syndrome

fetus

fever

fibroma, ungual

fine motor function, impaired

fish

fish poisoning

fistula, arterio-venous

fistula, arterio-venous, dural

fistula, arterio-venous, dural, spinal

flavivirus

flow study, carotid artery

folic acid

folic acid deficiency

fourth ventricle, floor

fragile-X syndrome

fragile-X syndrome, carrier

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

glucocerebrosidase

glycogen storage disease

glycoprotein

gray matter

grimacing

growth hormone deficiency

growth retardation

Guillain Barre syndrome

head circumference and brain development

heavy metal intoxication

hemiatrophy

hemiatrophy, cerebral

hemiatrophy, congenital

hemiparesis

hemiplegia

hemiplegia, congenital

hemorrhage, intracranial, newborn

hemorrhage, periventricular

heparin, low-molecular-weight

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatomegaly

hepatosplenomegaly

herniation syndromes, intracranial

herpes simplex virus

herpes simplex virus infection, newborn

herpes simplex virus, human nervous system and

herpes virus

herpes virus infection

hexosaminidase-A

high arched palate

hormone replacement

human immunodeficiency virus type 1

human T-lymphotropic virus type I(HTLV-I)

Huntington's chorea

Huntington's chorea, genetic counselling

Huntington's chorea, presymptomatic detection of

hydrocephalus

hydrocephalus, congenital

hydrocephalus, fetal

hydrocephalus, intrauterine

hydrocephalus, treatment of

hyperactivity

hypercapnia

hyperphagia

hyperpyrexia, CNS disorder causing

hyperreflexia

hypertonia

hypertonia, congential

hypogonadism

hypokinesia

hypopigmentation of skin

hypospadias

hypothermia

hypothyroidism

hypothyroidism, congenital

hypoxic encephalopathy

iatrogenic neurologic disorders

imbalance

immunohistochemistry

in situ hybridization

infant, evaluation of

infection

infection, recurrent

intellectual deficit

intelligence quotient

intelligence testing in children

intracerebral hemorrhage

intracerebral hemorrhage, work up

intracranial hemorrhage

intrauterine

intrauterine growth retardation

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intraventricular hemorrhage

klippel feil syndrome

Krabbe's disease

kyphoscoliosis, neurologic causes of

lamotrigine

language

language delay

language disorders in children

learning disability

learning disability, in children

leg weakness, bilateral

lipid storage disorder of CNS

lissencephaly

listeria monocytogenes

lymphocytic choriomeningitis

lysosomal storage disease

lysosomes, abnoral

macrocephaly

malformation, CNS, congenital

malpractice

meconium staining

medical-legal aspects of neurology

mental retardation, familial

metabolic disorder, primary

metachromatic leukodystrophy

methadone

microcephaly

middle cerebral artery territory infarction

Miller-Dieker syndrome

misdiagnosis

mitochondrial disease

mitral valve prolapse

molecular genetics

molybdenum cofactor deficiency

mongolism

monoclonal antibodies

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, early changes in CVA

mucopolysaccharidoses

multiple sclerosis

multiple sclerosis, misdiagnosis

multiple sclerosis, relapsing

multiple sclerosis, treatment of

muscle atrophy, progressive

muscle biopsy

muscle diseases, characteristics of

muscle hypertrophy

muscle pain

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

muscular dystrophy

muscular dystrophy, Becker

muscular dystrophy, cardiovascular changes with

muscular dystrophy, classification

muscular dystrophy, congenital

muscular dystrophy, Duchenne

muscular dystrophy, Duchenne, carrier

muscular dystrophy, Duchenne, neonatal screening

muscular dystrophy, facioscapulohumeral

muscular dystrophy, limb-girdle

mutism

myelomeningocele

myelopathy

myelopathy, chronic progressive

myotonia dystrophica, classification

myotonia dystrophica, type 2

myxedema, neurologic manifestations of

nasal stuffiness

natalizumab

neonatal abstinence syndrome

neonatal infection, viral

nerve conduction studies

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination

neurologic practice

neurologic signs

neuronal ceroid-lipofuscinosis

neuronal migration disorder

neuropathology

neuropathy

neuropathy, peripheral

newborn, evaluation of

Niemann-Pick disease

nose, abnormal

nutritional deficiency

obesity

obstetric neurologic injuries

oculopharyngeal muscular dystrophy

omphalocele

opiate

opportunistic infection

optic atrophy

optic nerve, hypoplasia of

parasitic infection, CNS

Parkinsonism syndrome

parotitis

partruition

patent ductus arteriosus

patent foramen ovale

pathology

patient information and support

percussion induced muscle contraction

periventricular leukomalacia

placenta, infection of

placenta, thrombosis of

pleocytosis of cerebrospinal fluid

poison, mercury

poison, neurologic problems with

polychlorinated biphenyls

polymerase chain reaction

polyneuropathy, chronic inflammatory demyelinating

polypharmacy

Pompe's disease of glycogen storage

pons, lesion of

pontine tegmental cap dysplasia

post hemorrhagic hydrocephalus

postoperative neurologic complications

postpartum

practice guidelines

Prader-Labhart-Willi syndrome

pre-eclampsia

pregnancy, anticonvulsants during

pregnancy, neurologic complications in

premature infant

premature infant, problems in

prenatal

prenatal cephalocentesis

prenatal diagnosis by amniocentesis

prethrombic state, screening for

prevention of neurologic disorders

prognosis

proteinuria

proximal myotonic myopathy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

psychosis

ptosis

pyramidal tract dysfunction

quadriplegia

radiation therapy, CNS treatment and complications with

radiation, ionizing

radiation, ionizing, intrauterine

reversible neurologic disorder

risk-benefit assessment

rubella syndrome

rubeola virus

safety

scoliosis, neurologic association with

seizure, treatment of

seizure, treatment of, monotherapy

seizure, treatment of, polytherapy

seizure, withdrawal

seizure, women

sexual intercourse

sexually transmitted disease

shagreen patch

short stature

shunt procedure, lumboperitoneal

shunt procedure, ventricular

sickle cell disease

single photon emission computed tomography

sinus, enlargement

skin, biopsy

skin, darkening of

skin, lesions in neurologic disorders

skull bone, thickening

slit lamp examination

sodium valproate

sodium valproate, toxicity

South America

Southern immunoblot test

spasticity

speech disorder

speech disorder, childhood

sphingolipodoses

spina bifida

spinal cord

spinal cord, lesion of

spinal cord, vascular malformation of

spinal muscular atrophy

spirochete infection

splenomegaly

spongy degeneration of brain

startle reaction

stem cell transplantation

stillbirth

strabismus

subarachnoid fluid collection, benign

subarachnoid hemorrhage

subdural hematoma

subdural hematoma, neonates and infants

subependymal nodules

suck, poor

sudden infant death syndrome

suicide

superior sagittal sinus thrombosis

syphilis, congenital

syphilis, diagnosis and treatment

syphilis, neurologic complications with

Tay-Sachs disease

temper tantrums

temporal lobe, infarction

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

testicular enlargement

thyroxine

titinopathy

tongue, enlarged

tongue, protrusion of

tongue, weakness

tonsillar herniation of cerebellum

topiramate

TORCH infections

toxins, nervous system

toxoplasmosis, CNS

toxoplasmosis, congenital

transplacental virus infections

travel, foreign

treatment of neurologic disorder

tremor

tremulousness

trichopoliodystrophy

trinucleotide repeats

tuberous sclerosis, screening for

twins

ultrasonography

ultrasonography, carotid artery

ultrasonography, head

ultrasonography, head, fetus-neonate

umbilical-cord blood transplantation

umbilical-cord phlebitis

uric acid, low

urine test for metabolic disorders

urine test in toxic screen

vasculitides

vasculopathy

vasospasm, cerebral

very long chain fatty acids

vitamin supplementation

walking, difficulty with

weakness

weakness, congenital

weakness, progressive

weakness, proximal

weight loss

Werdnig-Hoffman disease

Western immunoblot test

x-linked hydrocephalus

x-linked mental retardation

yawning movements

Zika virus infection

Showing articles 100 to 150 of 177 << Previous Next >>

Tay-Sachs Disease-Carrier Screening, Prenatal Diagnosis, and the Molecular Era
JAMA 270:2307-2315, Kaback,M.,et al, 1993

Miller-Dieker Syndrome:Detection of a Cryptic Chromosome Translocation Using in Situ Hybridization in a Family
Am J Dis Child 147:1291-1294, Alvarado,M.,et al, 1993

Prenatal Alcohol Exposure and Long-Term Developmental Consequences
Lancet 341:907-910, Spohr,H.,et al, 1993

Analysis of Dystrophin Expression after Activation of Myogenesis in Amniocytes, Chorionic-Villus Cells, and Fibroblasts
NEJM 329:915-920, Sancho,S.,et al, 1993

TORCH Infections in the Newborn
Semin Neurol 13:106-115, Donley,D.K., 1993

Epilepsy and Pregnancy
BMJ 307:492-495, O'Brien,M.D.&Gilmour-White,S., 1993

Reversed Cerebral Asymmetry in Women with Breast Cancer
Lancet 339:523-524, Sandson,T.A.,et al, 1992

Familial Neurofibromatosis Type 1:Clinical Experience with DNA Testing
J Pediatr 120:394-398, Hofman,K.J.&Boehm,C.D., 1992

Detection of Full Fragile X Mutation
Lancet 339:271-272, Pergolizzi,R.G.,et al, 1992

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

Meningoencephalitis in a Neonate Congenitally Infected with Human Immunodeficiency Virus Type 1
J Pediatr 120:93-95, Srugo,I.,et al, 1992

Lethal Cytomegalovirus Infection in Preterm Infants:Clinical, Radiological, and Neuropathological Findings
Ann Neurol 31:64-68, Perlman,J.M.&Argyle,C., 1992

GM1 Gangliosidosis in Adults:Clinical and Molecular Analysis of 16 Japanese Patients
Ann Neurol 31:328-332, Yoshida,K.,et al, 1992

Effect of Cocaine Use On the Fetus
NEJM 327:399-407, Volpe,J.J., 1992

CNS Complications of Cocaine Abuse:Prevalence, Pathophysiology, and Neuroradiology
AJR 159:137-147, Brown,E.,et al, 1992

Prenatal Diagnosis of Wilson's Disease by Analysis of DNA Polymorphism
NEJM 327:57, Cossu,P.,et al, 1992

Clinical and NEuroradiol Findings of Congen Hydroceph in Infant Born to Mother with HTLV-I-Assoc Myelopathy
Neurol 42:1406-1408, Tohyama,J.,et al, 1992

Diagnosis of Duchenne & Becker Muscular Dystrophies by Polymerase Chain Reaction
Multicenter Study Group, JAMA 267:2609-26151992., , 1992

Duplication of Part of Chromosome 17 is Commonly Associated with HMSN Type I (Charcot-Marie-Tooth Disease Type 1)
Ann Neurol 31:570-572, Hallam,P.J.,et al, 1992

Genetic Diagnosis of Gaucher's Disease
Lancet 339:889-892, Mistry,P.K.,et al, 1992

Value of Cranial Untrasound and MRI in Predicting Neurodevelopmental Outcome in Preterm Infants
Pediatrics 90:196-199, vandeBor,M.,et al, 1992

Population Screening for Fragile X
Lancet 339:1210-1213, Turner,G.,et al, 1992

Cognitive Development of Yu-Cheng ('Oil Disease') Children Prenatally Exposed to Heat-Degraded PCBs
JAMA 268:3213-3218, Chen,Y.J.,et al, 1992

Outlook for the Child with a Cephalocele
Pediatrics 90:914-919, Brown,M.S.,et al, 1992

Destructive Brain Lesions of Presumed Fetal Onset:Antepartum Causes of Cerebral Palsy
Pediatrics 88:898-906, 10591991., Scher,M.S.,et al, 1991

Prenatal Origin of Hemiparetic Cerebral Palsy:How Often and Why?
Pediatrics 88:1059-1062, Nelson,K.B., 1991

Cesarean Section Before Onset of Labor & Motor Function in Infants with Meningomyelocele Diag Antenatally
NEJM 324:662-666, 6901991., Luthy,D.S.,et al, 1991

Sensitivity of Ultrasound in Detecting Spina Bifida
Letter, NEJM 324:769-7721991., , 1991

Brain and Ocular Abnormalities in Infants with In Utero Exposure to Cocaine and other Street Drugs
Am J Dis Child 145:688-695, Dominguez,R.,et al, 1991

Predictive Testing for Wilson's Disease Using Tightly Linked and Flanking DNA Markers
Neurol 41:992-999, Farrer,L.A.,et al, 1991

Neonatal Opiate Abstinence Syndrome in Term and Preterm Infants
J Pediatr 118:933-937, Doberczak,T.M.,et al, 1991

Direct Diagnosis by DNA Analysis of the Fragile X Syndrome of Mental Retardation
NEJM 325:1673-1681, Rousseau,F.,et al, 1991

Prenatal Diagnosis of Fragile X Syndrome by Direct Detection of the Unstable DNA Sequence
NEJM 325:1720-1738, Sutherland,G.R.,et al, 1991

Maternal Cocaine Abuse:The Spectrum of Radiologic Abnormalities in the Neonatal CNS
AJR 157:1105-1110, Heier,L.A.,et al, 1991

Fucosidosis Revisited:A Review of 77 Patients
Am J Med Genet 38:111-131, Willems,P.J.,et al, 1991

Perinatal Loss and Neurological Abnormalities Among Children of the Atomic Bomb
JAMA 264:605-609, 6221990., Yamazaki,J.N.&Schull,W.J., 1990

Molecular Genetics of Duchenne and Becker Muscular Dystrophy
J Pediatr 117:1-15, Darras,B.T., 1990

Presymptomatic and Prenatal Diagnosis in Myotonic Dystrophy by Genetic Linkage Studies
Neurol 40:671-676, Speer,M.C.,et al, 1990

Mapping of Acute (Type 1) Spinal Muscular Atrophy to Chromosome 5q12-q14
Lancet 336:271-273, Melki,J.,et al, 1990

Periventricular-Intraventricular Hemorrhage Sonographic Localization in Low Birth Weight Infants
Pediatrics 85:1027-1032, Krishamoorthy,K.,et al, 1990

Prenatal Prediction of Risk of the Fetal Hydantoin Syndrome
NEJM 322:1567-1572, Buehler,B.A.,et al, 1990

Congenital AIDS:Review of Neurological Problems
Child's Nerv Syst 5:9-11, Curles,R.G., 1989

Predictive Testing for Huntington's Disease with Linked DNA Markers
Lancet 2:463-466, Brock,D.J.H.,et al, 1989

Uptake of Presymptomatic Predictive Testing for Huntington's Disease
Lancet 2:603-605, Craufurd,D.,et al, 1989

Molecular Biology of Duchenne and Becker's Muscular Dystrophy:Clinical Applications
Ann Neurol 26:189-194, Gutmann,D.H.&Fischbeck,K.H., 1989

Origins of Cerebral Palsy
Am J Dis Child 143:1154-1160, Naeye,R.L.,et al, 1989

Perinatal Asphyxia and Cerebral Palsy
Am J Dis Child 143:1139-1140, Bedrick,A.D., 1989

Cerebral Palsy
Intrapartum Care, and a Shot in the Foot, Editorial, Lancet 2:1251-125289., , 1989

Predictive Testing for Huntington's Disease with Use of a Linked DNA Marker
NEJM 318:535-542, Meissen,G.J.,et al, 1988

Prenatal Testing for Duchenne & Becker Muscular Dystrophy
Lancet 1:262-266, Cole,C.G.,et al, 1988

Showing articles 100 to 150 of 177 << Previous Next >>