Neudle.com: microcephaly

Differential
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abortion, spontaneous

abstinence syndrome

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, congenital

acquired immunodeficiency syndrome, infants and children

acquired immunodeficiency syndrome-related complex

acrocyanosis

acromicria

acute disseminated encephalomyelitis

acute necrotizing encephalitis

addiction, heroin

adverse drug reaction

agenesis of aqueduct of Sylvius

agenesis of corpus callosum

aggression

Aicardi-Goutieres syndrome

Aicardi's syndrome

alcohol

alcohol, neurologic complications with

algorithm

alpha-fetoprotein

altered states of consciousness

alternating hemiplegia

alternating hemiplegia of childhood

Angelman syndrome

angiotensin-converting enzyme, inhibitors

anticoagulant, complications of

anticoagulant, treatment

anticonvulsants, teratogenicity of

anticonvulsants, untoward effects of

antiviral agents

aphasia, conduction

apnea

aqueduct of Sylvius, stenosis

arthrogryposis multiplex

attention deficit disorder with hyperactivity

attention span

atypical

autism

Babinski sign in new born

banana sign

basal ganglia, calcification of

Brown-Vialetto-Van Laere syndrome

bruising

burst suppression pattern, electroencephalogram

cachexia

calcification, intracranial

calcification, intraventricular

calcification, periventricular

cataracts, congenital

Central America

central nervous system, infection of

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hypoplasia

cerebellar lesion

cerebellar vermis

cerebral cortical atrophy

cerebral palsy

cerebral venous thrombosis

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cytology

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, protein of

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, intrauterine

cerebrovascular accident, neonatal

cerebrovascular disease, infant and childhood

chilbran skin lesions

chromosomal abnormality

chromosome 1

chromosome 15

chromosome 3

cisterna magna, enlarged

cisternogram, radionuclide

cleft lip

cleft palate

Clinical Pathologic Conference(C.P.C.)

cocaine

cocaine, intrauterine exposure

Cockayne's syndrome

Coffin-Siris syndrome

congenital birth defects

congenital heart disease

congenital heart disease, CNS complications with

congenital infection, CNS

congenital infection, viral

congenital malformation

congenital malformation, non CNS

congenital myopathy

congenital myopathy, inflammatory

corpus callosum, atrophy of

corpus callosum, thinning

cortical blindness

coumarin

cranial neuropathy

cranial neuropathy, multiple

creatine phosphokinase(CPK)elevated

cytomegalic inclusion disease

cytomegalovirus infection

cytomegalovirus infection, congenital

cytosine arabinoside

Dandy Walker malformation

dentate nuclei, lesion of

depression

depression, psychotic

dermatitis

dermatoglyphics

developmental abnormality of brain

developmental disability

developmental evaluation

developmental milestones

developmental milestones, loss of

developmental retardation

differential diagnosis

digits, abnormal

dilantin

dilantin, toxicity

disability, neurological

dislocated hip, congenital

drooling

drug abuse

drug abuse, toxic screen In

drug withdrawal

dural sinus thrombosis

electroencephalogram, abnormalities of

encephalitis, brainstem

encephalitis, viral

encephalopathy

encephalopathy, metabolic

epidemiology of neurology

epileptic encephalopathy

ethylmalonic aciduria

ethylmalonic encephalopathy

evoked potentials

eye movement, disorders of

facial anomalies

facial appearance, abnormal

facial asymmetry

facial expression abnormality

fetal alcohol syndrome

fetus

fever

fine motor function, impaired

finger tapping

fingernails, abnormal

fingernails, hypoplastic

fish

flavivirus

floppy infant

fluorescene in situ hybridization

genetic diagnosis, prenatal

genetic neurologic disorders

genetic testing

geographic location

glioblastoma multiforme(astrocytoma Gr.III)

GLUT1

GLUT1 deficiency syndrome

growth retardation

Guillain Barre syndrome

hand deformity

head bobbing

head circumference

head circumference and brain development

head lag

headache

hearing loss

hearing problems in children

hemophagocytic lymphohistiocytosis

hemophagocytic lymphohistiocytosis, cerebromeningeal

hemorrhage, intracranial, newborn

heparin

hepatosplenomegaly

heralding manifestation

herpes labialis

herpes simplex encephalitis

herpes simplex encephalitis, differential diagnosis of

herpes simplex encephalitis, infancy and childhood

herpes simplex encephalitis, prognosis of

herpes simplex encephalitis, recurrent

herpes simplex encephalitis, treatment of

herpes simplex myelitis

herpes simplex virus

herpes simplex virus infection, immunosuppressed patient

herpes simplex virus infection, newborn

herpes simplex virus, human nervous system and

herpes simplex virus, localization of

herpes simplex virus, malignancy with

herpes simplex virus, pathogenesis of

herpes simplex virus, pathology of

herpes simplex, neurocutaneous lesions in

human immunodeficiency virus type 1

hydranencephally

hydrocephalus

hydrocephalus, communicating

hydrocephalus, congenital

hydrocephalus, exvacuo

hydrocephalus, normal pressure

hydrocephalus, normal pressure in children

hyperpigmentation of skin

hyperpyrexia, CNS disorder causing

hypopigmentation of skin

hypoplastic left heart syndrome

hyporeflexia

hypotelorism

hypothyroidism

hypothyroidism, congenital

immunofluorescent exam of CSF cells

immunosuppression

in situ hybridization

inborn errors of metabolism

inclusion bodies, intranuclear

infant, evaluation of

infantile spasm

infection

infectious mononucleosis

influenza A virus

insect repellent

intellectual deficit

intellectual deterioration

intelligence quotient

interferon

interferon alpha

interferon inducer

intracranial pressure, increased

intrauterine

intrauterine growth retardation

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

level of consciousness, decreased

liver function enzymes

low birth weight

lumbar puncture

lymphadenopathy

lymphocytic choriomeningitis

macrognathia

malformation, CNS, congenital

meningitis

meningitis, aseptic

meningitis, carcinomatous

meningitis, CSF cell count-normal

meningoencephalitis

mental retardation

mental status, abnormal

mestinon

metabolic disorder, primary

methadone

methylene tetrahydrofolate reductase

methylenetetrahydrofolate reductase deficiency

midline defect in children

migraine, seizures in

Miller-Dieker syndrome

misdiagnosis

mitochondrial disease

molecular genetics

molybdenum cofactor deficiency

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI

MRI, abnormal

MRI, CAT scan compared to

multiple system atrophy

myxedema, neurologic manifestations of

nasal bridge, wide

nasal stuffiness

neonatal abstinence syndrome

neonatal infection, viral

neoplasm, primary intracerebral

nerve root enhancement

neural tube defect

neurocutaneous disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination

neuronal ceroid-lipofuscinosis

neuronal migration disorder

neuropathology

neuropathology, brain

neuropathy

neuropathy, peripheral

neuroradiology

neurosyphilis

newborn, evaluation of

nose, abnormal

nutritional deficiency

opportunistic infection

optic atrophy

optic nerve

optic nerve, hypoplasia of

optic nerve, lesion of

optic neuropathy

oxycodone

pachygyria

palpebral fissure, short

paraparesis, familial spastic

paraparesis, spastic

parasitic infection, CNS

Parkinson disease, dystonia with

Parkinsonism syndrome

parotitis

paroxysmal hemiplegia

paroxysmal neurologic deficits

parvovirus

pediatric neurology

periventricular leukomalacia

personality change

petechiae

phenobarbital

philtrum, hypoplastic

photosensitivity, skin

pigmentary retinopathy

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

polyinosinic cytidic acid(poly IC)

polymerase chain reaction

pons, atrophy

postural abnormality

practice guidelines

precipitating factors

pregnancy, anticonvulsants during

pregnancy, neurologic complications in

premature infant

prenatal

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

progeria

prognathism

prognosis

progressive neurologic disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychological testing, neurologic problems

psychomotor retardation

psychosis

pupil, abnormality in neurologic disorders

pyramidal tract dysfunction

quadriparesis

radiation therapy, CNS treatment and complications with

radiation, ionizing

radiation, ionizing, intrauterine

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

rash

recurrent

remote effect of cancer on the nervous system

renal tubular acidosis

riboflavin transporter deficiency

scoliosis, neurologic association with

seizure, psychomotor-temporal lobe

seizure, withdrawal

sensorineural hearing loss

septo-optic dysplasia

serologic testing

serum alanine aminotransferase

sexual intercourse

sexually transmitted disease

short neck

short stature

simian crease

skin, lesions in neurologic disorders

skull x-ray, bony defect on

small for dates infant, problems in

speech disorder, childhood

speech, delayed development of

spina bifida

startle reaction

status epilepticus

stem cell transplantation

stereotyped behavior

steroid therapy, CNS treatment and complications with

stillbirth

strabismus

subacute myelo-opticoneuropathy(S.M.O.N.)complex

subdural effusion

subdural hematoma

subdural hematoma, neonates and infants

subtemporal decompression

suck, poor

sudden infant death syndrome

sulfite oxidase deficiency

superior sagittal sinus thrombosis

symmetric brain lesions

syphilis, congenital

syphilis, diagnosis and treatment

syphilis, neurologic complications with

tongue, protrusion of

TORCH infections

toxoplasmosis, CNS

toxoplasmosis, congenital

transilumination of skull

transplacental virus infections

travel, foreign

treatment of neurologic disorder

tremor

trigeminal neuralgia

trinucleotide repeats

trisomes

trisomy 9p

ultrasonography

ultrasonography, head

ultrasonography, head, fetus-neonate

uric acid, low

vaccinia

varicella zoster virus

viral infection, transmission

weakness, generalized

weakness, progressive

wheelchair

white matter disease

white matter disease, periventricular

white matter disease, subcortical

Showing articles 50 to 85 of 85 << Previous

Congenital Inflammatory Myopathy
Neurol 40:1111-1114, Shevell,M.,et al, 1990

Congenital Brain Anomalies Associated with the Hypoplastic Left Heart Syndrome
Pediatrics 85:984-990, Glauser,T.A.,et al, 1990

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

Sulfite Oxidase Deficiency:Clinical, Neuroradiologic, and Biochemical Features in Two New Patients
Neurol 39:252-257, Brown,G.K.,et al, 1989

Pediatric Acquired Immunodefieiency Syndrome
Am J Dis Child 142:29-35, Belman,A.L.,et al, 1988

Difference Between Herpes Simplex Virus Type I & Type 2 Neonatal Encephalitis in Neurological Outcome
Lancet 1:1-4, Corey,L.,et al, 1988

Computed Tomographic Findings of Brain & Skull in Myotonic Dystrophy
JNNP 50:435-438, Avrahami,E.,et al, 1987

Neurological Manifestations in Xeroderma Pigmentosum
Ann Neurol 20:70-75, Mimaki,T.,et al, 1986

Ultrasound Screening for Spina Bifida:Cranial & Cerebellar Signs
Lancet 2:72-74, Nicolaides,K.H.,et al, 1986

Natural History of the Fetal Alcohol Syndrome:A 10-Year Follow-Up of Eleven Patients
Lancet 2:85-91, Streissguth,A.P.,et al, 1985

Coffin-Siris Syndrome, Neuropathologic Findings
Arch Neurol 42:350-353, DeBassio,W.A.,et al, 1985

Neurological Complications in Infants & Children with Acquired Immune Deficiency Syndrome
Ann Neurol 18:560-566, Belman,A.L.,et al, 1985

Human Cytomegalovirus Infection & Disorders of the Nervous System
Jr. , Arch Neurol 41:310-320984., Bale,J.F., 1984

Schizencephaly:A Clinical & CT Study
Neurol 34:997-1001, Miller,G.M.,et al, 1984

A Progressive Syndrome of Autism, Dementia, Ataxia, & Loss of Purposeful Hand Use in Girls:Rett's Syndrome
Ann Neurol 14:471-491, Hagberg,B., 1983

Familial Porencephaly
Arch Neurol 40:567-569, Berg,R.A.,et al, 1983

Santavuori Disease:Diagnosis by Leukocyte Ultrastructure
Neurol 32:1277-1281, Baumann,R.J.,et al, 1982

Cockayne Syndrome
J Comput Assist Tomogr 6:1172-1174, Levinson,E.D.,et al, 1982

Maternal Seizure Disorder, Outcome of Pregnancy, & Neurologic Abnormalities in the Children
Neurol 32:1247-1254, Nelson,K.B.,et al, 1982

Septo-optic Dysplasia in an Infant of a Diabetic Mother
Arch Neurol 38:590-591, Donat,J.F.G., 1981

Maternal & Fetal Sequelae of Anticoagulation During Pregnancy
Am J Med 68:122-140, Hall,J.G.,et al, 1980

The Aicardi Syndrome:Report of 4 Cases & Review of the Literature
Ann Neurol 5:475-482, Bertoni,J.M.,et al, 1979

Cockayne Syndrome:Unusual Neuropathological Findings & Review of the Literature
Ann Neurol 6:340-348, 1979, Soffer,D.,et al, 1979

Normal Pressure Hydrocephalus, Recog & Relation to Neuro Abnormalities in Cockayne's Sydrome
Arch Neurol 35:337, Brumback,R.A.,et al, 1978

The Lissencephaly, (Agyria) Syndrome in Siblings
Arch Neurol 35:608-611, Garcia,C.A.,et al, 1978

Adverse Effects on Offspring of Maternal Alcohol Abuse During Pregnancy
NEJM 297:528, Ouellette,E.M.,et al, 1977

EEG Recognition of Aicardi's Syndrome
Arch Neurol 34:563, Fariello,R.G.,et al, 1977

School Failure & Deafness After"Silent"Congenital Cytomegalovirus Infection
NEJM 295:468, Hanshaw,J.B.,et al, 1976

Herpes Simplex & the Human Nervous System
Milit Med 140:765, Finelli,P.F., 1975

Maternal Epilepsy & Abnormalities of the Fetus & Newborn
Lancet 839, Oct1972., Speidel,B.,et al, 1972

Effects of Viral Infection on the Developing Nervous System
Seminars in Medicine of the Beth Israel Hosp, Boston NEJM 287:5991972., Johnson,R., 1972

Fetal & Newborn Virus Infections
J Pediatr 77:315, Overall,J.,et al, 1970

Microcephaly & Mental Retardation
Am J Dis Child 119:128, Martin,H.P., 1970

Diagnostic Significance of Median Facial Anomalies for Holoprosencephaly
Pediatr 256, 1964 Aug., DeMeyer,W.,et al, 1964

Neuro CPC of MGH
Congenital Toxoplasmosis Involving CNS, NEJM 269:369-3741963., , 1963

Microcephaly
Arch Dis Child 37:623-627, Davies,H.,et al, 1962

Showing articles 50 to 85 of 85 << Previous