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acetylcholinesterase
acid maltase deficiency
acid maltase deficiency, adult
acrocyanosis
acromicria
Addison's disease
adducted thumb
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
advances in neurology
agenesis of corpus callosum
Aicardi-Goutieres syndrome
algorithm
alpha glucosidase
alpha-fetoprotein
alveolar hypoventilation
aminoacidurias
amniocentesis
anencephaly
anesthesia, general
aneurysm
Angelman syndrome
angiography, spinal
angiokeratoma
anterior horn cell disease
anticonvulsants
anticonvulsants, blood level determination of
anticonvulsants, compliance
anticonvulsants, teratogenicity of
anticonvulsants, untoward effects of
anxiety
arbovirus
arrhythmia, cardiac
arthralgia
aspartate aminotransferase
aspartocyclase
aspiration
asymptomatic
ataxia
attention deficit disorder with hyperactivity
atypical
autism
Babinski sign
baldness
basal ganglia, calcification of
behavior, combative
behavioral disorder
birth injury
bone marrow transplantation
brain atrophy
Brazil
breast feeding
cachexia
CAG repeats
calcification, intracranial
calf hypertrophy
Canavan's disease
cardiac surgery, hypothermia and circulatory arrest for
cardiac surgery, neurologic complications with
cardiomegaly
cardiomyopathy
caribbean
CAT scan
CAT scan, abnormal
CAT scan, indications for
cataracts
Central America
cerebral cortical atrophy
cerebral palsy
cerebral palsy, risk factors
cerebral palsy, work up
cerebro hepato renal syndrome
cerebrospinal fluid, abnormal
cerebrotendinous xanthomatosis
cerebrovascular accident
cerebrovascular accident, infancy and childhood
cerebrovascular accident, intrauterine
cerebrovascular accident, neonatal
cerebrovascular disease
ceruloplasmin, serum
cesarean section
Charcot-Marie-Tooth
chilbran skin lesions
children
chorea
choroid plexus
choroid plexus, abnormality of
choroid plexus, cyst
chromosomal abnormality
chromosome 15
chromosome 19
chromosome 3
chronic graft versus host disease
cleft lip
cocaine
Cockayne's syndrome
cognition
complications
confidentiality
congenital birth defects
congenital heart disease
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, weak
cultured skin fibroblasts
cyst, porencephalic
degenerative diseases of CNS
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
diet
differential diagnosis
digits, abnormal
dilantin
dilantin, toxicity
disability, neurological
distal muscle weakness
DNA probes
drooling
drug abuse
drug interactions
dying
dysarthria
dysarthria-clumsy hand syndrome
dysmorphic
dysostosis multiplex
dysphagia
dysphasia
dystonia
dystonia, children
dystrophin
ear, abnormal
eating disorder
echocardiogram
electrocardiogram, abnormal
electroencephalogram, abnormalities of
electromyogram
electron microscopy
employment
encephalocele
encephalopathy
encephalopathy, neonatal
endovascular therapy
enzyme treatment
enzyme, defect
enzyme, induction
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
familial
fatty acid, elevated plasma content
feeding disorder
fetus
fever
fistula, arterio-venous
fistula, arterio-venous, dural
fistula, arterio-venous, dural, spinal
flavivirus
folic acid
fragile-X syndrome
fragile-X syndrome, carrier
fucosidosis
gait disorder
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
hand flapping
head lag
headache
health insurance
hearing loss
heart block
hemiplegia, congenital
hemorrhage, intracranial, newborn
hemorrhage, periventricular
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
hepatomegaly
hepatosplenomegaly
hexosaminidase-A
high arched palate
hormone replacement
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
hyperactivity
hypercapnia
hyperphagia
hyperpyrexia, CNS disorder causing
hyperreflexia
hypertonia
hypogonadism
hypopigmentation of skin
hypothermia
hypothyroidism
hypothyroidism, congenital
hypothyroxinemia
hypotonia
hypotonia, infants
imbalance
immunohistochemistry
in situ hybridization
infection
infection, recurrent
intellectual deficit
intelligence quotient
intelligence testing in children
interferon alpha
internet
intracranial hemorrhage
intrauterine
intrauterine growth retardation
intrauterine infection
intrauterine infection, viral
intrauterine infection, viral of CNS
intraventricular hemorrhage
irritability
karyotyping
klippel feil syndrome
Krabbe's disease
kyphoscoliosis, neurologic causes of
learning disability
learning disability, in children
leg weakness, bilateral
lens, dislocation of
leukodystrophy
leukoencephalopathy
levonorgestrel
lipid storage disorder of CNS
lissencephaly
Lorenzo's oil
low birth weight
lysosomal storage disease
lysosomes, abnoral
macrocephaly
malformation, CNS, congenital
medical-legal aspects of neurology
meningocele
mental retardation
mental retardation, familial
metabolic disorder, primary
metachromatic leukodystrophy
microcephaly
Miller-Dieker syndrome
misdiagnosis
mitral valve prolapse
molecular genetics
molybdenum cofactor deficiency
mongolism
mortality
mosquito
motor dysfunction
motor neuron disease
movement disorder
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, fetal
MRI, indications for
MRI, intrauterine
mucopolysaccharidoses
multiple sclerosis, misdiagnosis
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
myelomeningocele
myelopathy
myelopathy, chronic progressive
myopathy
myopathy, distal
myopathy, metabolic
myopathy, vacuolar
myotonia
myotonia dystrophica
myotonia dystrophica, classification
myotonia dystrophica, type 2
neural tube defect
neuroendocrinology
neurofibromatosis 1
neurologic disease
neurologic disease, diagnoses of
neurologic evaluation
neurologic practice
neurologic signs
neuronal ceroid-lipofuscinosis
neuronal migration disorder
neuropathology
neuropathy
neuropathy, peripheral
neurosis
newborn, evaluation of
Niemann-Pick disease
nose, abnormal
obesity
obstetric neurologic injuries
oculopharyngeal muscular dystrophy
omphalocele
optic atrophy
oral contraceptives
orthopnea
pain
paraparesis
paraparesis, spastic
parasitic infection, CNS
Parkinsonism syndrome
partruition
patient information and support
percussion induced muscle contraction
periventricular leukomalacia
peroxisomal disease
peroxisomes
personality change
pleocytosis of cerebrospinal fluid
polymerase chain reaction
polyneuropathy, chronic inflammatory demyelinating
Pompe's disease of glycogen storage
post hemorrhagic hydrocephalus
postoperative neurologic complications
practice guidelines
Prader-Labhart-Willi syndrome
pregnancy, anticonvulsants during
pregnancy, neurologic complications in
premature infant
premature infant, problems in
prenatal
prenatal diagnosis by amniocentesis
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
Rankin score
rash
recombinant DNA
Refsum's disease
respiratory failure
retinal degeneration
reversible neurologic disorder
review article
RFLPs
rigidity
risk factors
scoliosis, neurologic association with
screaming
seizure
seizure, familial
seizure, intractable
seizure, neonatal
seizure, pregnancy
seizure, treatment of
seizure, treatment of, monotherapy
seizure, women
short stature
skin, biopsy
skin, darkening of
skin, lesions in neurologic disorders
slit lamp examination
South America
Southern immunoblot test
speech disorder
speech disorder, childhood
sphingolipodoses
spina bifida
spinal cord
spinal cord, lesion of
spinal cord, vascular malformation of
spinal muscular atrophy
splenomegaly
spongy degeneration of brain
startle reaction
stem cell transplantation
strabismus
subarachnoid fluid collection, benign
subarachnoid hemorrhage
subdural hematoma
subdural hematoma, neonates and infants
suck, poor
sudden infant death syndrome
suicide
Tay-Sachs disease
temper tantrums
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
toxoplasmosis, CNS
toxoplasmosis, congenital
treatment of neurologic disorder
tremulousness
trichopoliodystrophy
trinucleotide repeats
trisomes
trisomy 18
ultrasonography
ultrasonography, head
ultrasonography, head, fetus-neonate
uric acid, low
urine test for metabolic disorders
very long chain fatty acids
viral infection
viral infection, CNS
vital capacity
vitamin K
vitamin supplementation
walking, difficulty with
weakness
weakness, progressive
weakness, proximal
weight loss
Werdnig-Hoffman disease
Western immunoblot test
wheelchair
white matter disease
wide based gait
x-linked hydrocephalus
x-linked mental retardation
Zika virus infection
Showing articles 0 to 50 of 607 Next >>

Use of MRI in the Diagnosis of Fetal Brain Abnormalities in Utero (MERIDIAN): A Multicentre, Prospective Cohort Study
Lancet: 389:538-546,483, Griffiths, P.D.,et al, 2017

Zika Virus Associated with Microcephaly
NEJM 374: DOI:10.1056/NEJMoa1600651, Mlakar, J.,et al, 2016

Molybdenum Cofactor Deficiency
Neurol 85:e175-e178, Nagappa, M.,et al, 2015

Huntingtons Disease
BMJ 341:34-40, Novak,M.J. &Tabrizi,S.J., 2010

Aicardi-Gouti�res Syndrome
Br Med Bull 89:183-201, Orcesi, S.,et al, 2009

Prevalence and Evolution of Intracranial Hemorrhage in Asymptomatic Term Infants
AJNR 29:1082-1089, Rooks,V.J.,et l, 2008

Curable Cause of Paraplegia: Spinal Dural Arteriovenous Fistulae
Stroke 39:2756-2759, Aghakhani,N.,et al, 2008

Glycogen-Storage Disease Type II
eMedicine, May 2, Ibrahim,J. &McGovern,M., 2006

Neonatal MRI to Predict Neurodevelopmental Outcomes in Preterm Infants
NEJM 355:685-694,727, Woodward,L.J.,et al, 2006

Adrenoleukodystrophy
JAMA 294:3131-3134, Moser,H.W.,et al, 2005

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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



Showing articles 0 to 50 of 607 Next >>