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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
acrocyanosis
acromicria
addiction, heroin
Addison's disease
adducted thumb
adrenoleukodystrophy
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
anatomy of
anencephaly
anesthesia, general
aneurysm
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
antiviral agents
anxiety
Apgar score
apnea
arbovirus
arenavirus
arrhythmia, cardiac
arterial dissection
arterial dissection, childhood
arteritides
arthralgia
arthrogryposis multiplex
aspartate aminotransferase
aspartocyclase
Asperger's syndrome
aspiration
asymptomatic
ataxia
atomic bomb
attention deficit disorder with hyperactivity
atypical
autism
autistic behavior
azidodeoxythymidine
Babinski sign
bacterial infection
baldness
basal ganglia, calcification of
basal ganglia, lesion of
behavior, combative
behavioral disorder
birth injury
blood transfusion
bone marrow transplantation
brain atrophy
brainstem, lesion of
Brazil
breast feeding
cachexia
CAG repeats
calcification, intracranial
calcification, periventricular
calf hypertrophy
Canavan's disease
carbamazepine
carcinoma
carcinoma of breast
cardiac surgery, hypothermia and circulatory arrest for
cardiac surgery, neurologic complications with
cardiomegaly
cardiomyopathy
caribbean
CAT scan
CAT scan, abnormal
CAT scan, chest
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
children
chorea
chorioamnionitis
chorioretinitis
choroid plexus
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
Cockayne's syndrome
cognition
complications
confidentiality
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
dysmorphic
dysostosis multiplex
dysphagia
dysphasia
dystonia
dystonia, children
dystrophin
ear, abnormal
eating disorder
echocardiogram
efficacy
electrocardiogram, abnormal
electroencephalogram
electroencephalogram, abnormalities of
electromyogram
electron microscopy
embolism, paradoxical
employment
encephalocele
encephalopathy
encephalopathy, anoxic
encephalopathy, neonatal
endovascular therapy
enzyme treatment
enzyme, defect
enzyme, induction
epicanthal folds
epidemic
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
fucosidosis
gait disorder
galactocerebrosidase
gangliosidosis GM1
gangliosidosis GM2
Gaucher's disease
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis
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
hamartin
hamartoma
hand flapping
head circumference
head circumference and brain development
head lag
headache
health insurance
hearing loss
heart block
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
hypopigmentation of skin
hypospadias
hypothermia
hypothyroidism
hypothyroidism, congenital
hypothyroxinemia
hypotonia
hypotonia, infants
hypoxia
hypoxia, newborn
hypoxic encephalopathy
iatrogenic neurologic disorders
imbalance
immunohistochemistry
in situ hybridization
infant, evaluation of
infection
infection, recurrent
intellectual deficit
intelligence quotient
intelligence testing in children
interferon alpha
interferon beta 1-a
interferon beta 1-b
internet
intracerebral hemorrhage
intracerebral hemorrhage, work up
intracranial hemorrhage
intrauterine
intrauterine growth retardation
intrauterine infection
intrauterine infection, viral
intrauterine infection, viral of CNS
intraventricular hemorrhage
iodine deficiency
irritability
jittery baby
karyotyping
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
lens, dislocation of
leukodystrophy
leukoencephalopathy
levetiracetam
levonorgestrel
lip, abnormal
lipid storage disorder of CNS
lissencephaly
listeria monocytogenes
Lorenzo's oil
low birth weight
lymphadenopathy
lymphangiomyomatosis
lymphocytic choriomeningitis
lysosomal storage disease
lysosomes, abnoral
macrocephaly
malformation, CNS, congenital
malpractice
meconium staining
medical-legal aspects of neurology
meningocele
meningoencephalitis
meningomyelitis
mental retardation
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
mortality
mosquito
motor dysfunction
motor neuron disease
movement disorder
moyamoya
MRI
MRI, abnormal
MRI, ADC maps
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, early changes in CVA
MRI, fetal
MRI, indications for
MRI, intrauterine
MRI, negative
MRI, spine
MRI, venography
mucopolysaccharidoses
multiple sclerosis
multiple sclerosis, misdiagnosis
multiple sclerosis, relapsing
multiple sclerosis, treatment of
muscle atrophy, progressive
muscle biopsy
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
myopathy
myopathy, distal
myopathy, metabolic
myopathy, vacuolar
myotonia
myotonia dystrophica
myotonia dystrophica, classification
myotonia dystrophica, type 2
myxedema, neurologic manifestations of
nasal stuffiness
natalizumab
neonatal abstinence syndrome
neonatal infection, viral
nerve conduction studies
neural tube defect
neuroendocrinology
neurofibromatosis 1
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neurologic examination
neurologic practice
neurologic signs
neuronal ceroid-lipofuscinosis
neuronal migration disorder
neuropathology
neuropathy
neuropathy, peripheral
neurosis
neurosyphilis
neurotoxic
neurotoxin
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
oral contraceptives
orthopnea
oxycodone
pachygyria
pain
paraparesis
paraparesis, spastic
parasitic infection, CNS
Parkinsonism syndrome
parotitis
partruition
patent ductus arteriosus
patent foramen ovale
patient information and support
percussion induced muscle contraction
periventricular leukomalacia
peroxisomal disease
peroxisomes
personality change
phakomatoses
phenobarbital
placenta
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
Rankin score
rash
recombinant DNA
recurrent
Refsum's disease
renal cyst
respiratory failure
retinal degeneration
retinal hamartoma
retinopathy
reversible neurologic disorder
review article
RFLPs
rhabdomyoma, cardiac
rigidity
risk factors
risk-benefit assessment
rubella syndrome
rubeola virus
safety
scoliosis, neurologic association with
screaming
seizure
seizure, familial
seizure, focal
seizure, intractable
seizure, neonatal
seizure, pregnancy
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
teratogenesis
teratogenic drugs
term infant
testicular atrophy
testicular enlargement
thyroxine
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
trisomes
trisomy 18
tuber, cortical
tuberin
tuberous sclerosis
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
viral infection
viral infection, CNS
viral isolation
visual loss
vital capacity
vitamin deficiency
vitamin K
vitamin supplementation
walking, difficulty with
weakness
weakness, progressive
weakness, proximal
weight loss
Werdnig-Hoffman disease
Western immunoblot test
wheelchair
white freckles
white matter disease
wide based gait
x-linked hydrocephalus
x-linked mental retardation
yawning movements
Zika virus infection
Showing articles 50 to 100 of 176 << Previous Next >>

Pregnancy Outcomes During Treatment with Interferon Beta-1a in Patients with Multiple Sclerosis
Neurol 65:802-806, Sandberg-Wollheim,M.,et al, 2005

The Reproductive Effects of Beta Interferon Therapy in Pregnancy, A longitudinal Cohort
Neurol 65:807-811,788, Boskovic,R.,et al, 2005

Normal Intelligence in Children with Prenatal Exposure to Carbamazepine
Neurol 62:28-32,8, Gaily,E.,et al, 2004

Prenatal Diagnosis Requests for Huntington's Disease when the Father is at Risk, and Does Not Want to Know His Genetic Status: Clinical, Legal, and Ethical Viewpoints
BMJ 326:331-333, Tassicker,R.,et al, 2003

Insights Into the Diagnosis and Treatment of Lysosomal Storage Diseases
Arch Neurol 60:322-328, Wegner,D.A.,et al, 2003

Central Nervous System Infection in Congenital Syphilis
NEJM 346:1792-1798, Michelow,I.C.,et al, 2002

New Strategy for Prenatal Diagnosis of X-Linked Disorders
NEJM 346:1502, Costa,J.,et al, 2002

Practice Paramenter: Neuroimaging of the Neonate
Neurol 58:1726-1738, Ment,L.R.,et al, 2002

Demonstration of Acute Ischemic Lesions in the Fetal Brain by Diffusion Magnetic Resonance Imaging
Ann Neurol 52:243-246, Baldoli,C.,et al, 2002

The Teratogenicity of Anticonvulsant Drugs
NEJM 344:1132-1138, Holmes,L.B.,et al, 2001

New Nomenclature and DNA Testing Guidelines for Myotonic Dystrophy Type 1 (DM1)
Neurol 54:1218-1221, The International Myotonic Dystrophy Consortium (I, 2000

Fetal Alcohol Syndrome and Alcohol-Related Neurodevelopmental Disorders
Pediatrics 106:358-361, Jacobs,E.A. et al, 2000

Fetal Surgery for Myelomeningocele, Promise, Progress, and Problems
JAMA 282:1873-1874,1819,1826, Simpson,J.L., 1999

Brain Structure and Neurocognitive and Behavioural Function in Adolescents Who Were Born Very Preterm
Lancet 353:1653-1657, Stewart,A.L.,et al, 1999

Maternal Thyroid Deficiency During Pregnancy and Subsequent Neuropsychological Development of the Child
NEJM 341:549-555,601, Haddow,J.E.,et al, 1999

Folic Acid for the Prevention of Neural Tube Defects
Pediartrics 104:325-327, Committee on Genetics, 1999

Effects of Prenatal & Postnatal Methylmercury Exposure from Fish Consump on Neurodevelop; Outcomes at 66 Months
JAMA 280:701-707, 7371998., Davidson,P.W.,et al, 1998

Prader-Willi and Angelman Syndromes
Medicine 77:140-151, Cassidy,S.B.&Schwartz,S., 1998

Hematopoietic Stem-Cell Transplantation in Globoid-Cell Leukodystrophy
NEJM 338:1119-1126, Krivit,W.,et al, 1998

Genetic Analysis Enables Definite and Rapid Diagnosis of Cerebrotendinous Xanthomatosis
Neurol 51:865-867, Chen,W.,et al, 1998

The Muscular Dystrophies
BMJ 317:991-995, Emery,A.E.H., 1998

Antepartum Risk Factors for Newborn Encephalopathy:The Western Australian Case-Control Study
BMJ 317:1549-1553,1537, Badawi,N.,et al, 1998

Intrapartum Risk Factors for Newborn Encephalopathy:The Western Australian Case-Control Study
BMJ 317:1554-1558,1537, Badawi,N.,et al, 1998

Analysis of Prenatal and Gestational Care Given to Women with Epilepsy
Neurol 51:1039-1045, Seale,C.G.,et al, 1998

Practice Parameter,Management Issues for Women with Epilepsy (Summary Statement)
Neurol 51:944-948, Rpt of the Quality Stnds Subcmte AAN, 1998

X Linked Adrenoleukodystrophy:Clinical Presentation, Diagnosis, and Therapy
JNNP 63:4-14, vanGeel,B.M.,et al, 1997

Anticedents of Cerebral Palsy in a Multicenter Trial of Indomethacin for Intraventricular Hemorrhage
Arch Pediatr Adolesc Med 151:580-585, Allan,W.C.,et al, 1997

Maternal Infection and Cerebral Palsy in Infants of Normal Birth Weight
JAMA 278:207-211, 2471997., Grether,J.K.&Nelson,K.B., 1997

Clinicopath Conf
Placental Vascular Thrombosis Due to Listeria Infection, Cerebral Embolism and Infarction, Case 15-1, 97EJM 336:1439-1446,1997., 1997

Prenatal Diagnosis of Duchenne Muscular Dystrophy Using a Single Fetal Nucleated Erythrocyte in Maternal Blood
Neurol 46:1350-1353, Sekizawa,A.,et al, 1996

The Relation of Transient Hypothyroxinemia in Preterm Infants to Neurologic Development at Two Years of Age
NEJM 334:821-827, 8571996., Reuss,M.L.,et al, 1996

Intellectual Impairment in Children Exposed to Polychlorinated Biphenyls in Utero
NEJM 335:783-789, Jacobson,J.L.,et al, 1996

Neurologic Status of HIV-1 Infected Infants and Their Controls:A Prospective Study from Birth to 2 Yrs
Pediatrics 98:1109-1118, Belman,A.L.,et al, 1996

Intracranial Abnor in Infants Treated with Extracorporeal Membrane Oxygenation:Update on Sonographic & CT Findings
AJNR 17:287-294, Bulas,D.I.,et al, 1996

Subarachnoid Fluid Collections:A Cause of Macrocrania in Preterm Infants
J Pediatr 128:234-236, AlSaedi,S.A.,et al, 1996

In Utero Exposure to Phenobarbital and Intelligence Deficits in Adult Men
JAMA 274:1518-1525, Reinisch,J.M.,et al, 1995

Canavan Disease:From Spongy Degeneration to Molecular Analysis
J Pediatr 127:511-517, Matalon,R.,et al, 1995

Gene Analysis of L1 Neural Cell Adhesion Molecule in Prenatal Diagnosis of Hydrocephalus
Lancet 345:161-162, Jouet,M.&Kenwrick,S., 1995

Cranial Ultrasound Predict of Disabling & Nondisabling Cerebral Palsy at Age Two in Low Birth Wt Population
Pediatrics 95:249-254, Pinto-Martin,J.A.,et al, 1995

Postoperative Neurologic Complications after Open Heart Surgery on Young Infants
Arch Pediatr Adolesc Med 149:764-768, Miller,G.,et al, 1995

Clinical Significance of Fetal Choroid Plexus Cysts
Lancet 346:724-729, Gupta,J.K.,et al, 1995

Neurological Correlated of Fetal Cocaine Exposure:Transient Hypertonia of Infancy and Early Childhood
Pediatrics 96:1070-1077, Chiriboga,C.A.,et al, 1995

Effects of HIV on Cognitive & Motor Devel in Children Born to HIV-Seropositive Women with no Reported Drug Use:Birth-24 mo
Pediatrics 96:1078-1082, Gay,C.L.,et al, 1995

Myotonic Dystrophy
In Myology, Engel & Franzini-Armstrong, McGraw-Hill, Inc, New York V2, Ch 43, P1192, Harper,P.S.&Rudel,R., 1994

Cerebrotendinous Xanthomatosis:Molecular Diagnosis Enables Presymptomatic Detection of a Treatable Disease
Neurol 44:288-290, Meiner,V.,et al, 1994

Advances in Molecular Analysis of Fragile X Syndrome
552, Warren,W.T.&Nelson,D.L.JAMA 271:536-553, 1994

Neurodevelopment of Children Exposed In Utero to Phenytoin and Carbamazepine Monotherapy
JAMA 271:767-770, Scolnik,D.,et al, 1994

Asking the Courts to Set the Standard of Emergency Care-The Case of Baby K
NEJM 330:1542-1545, Annas,G.J., 1994

Rapid Fragile X Carrier Screening and Prenatal Diagnosis Using a Nonradioactive PCR Test
JAMA 270:1569-1575, Brown,W.,et al, 1993

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



Showing articles 50 to 100 of 176 << Previous Next >>