Neudle.com: genetic diagnosis prenatal

Differential
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abscess, intracerebral

acetazolamide

acetylcholinesterase

acid maltase deficiency

acid maltase deficiency, adult

acoustic neurinoma

acoustic neurinoma, bilateral

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

advances in neurology

agenesis of corpus callosum

Aicardi-Goutieres syndrome

algorithm

alpha glucosidase

alpha-fetoprotein

alveolar hypoventilation

anterior horn cell disease

anticonvulsants

anticonvulsants, absorption

anticonvulsants, bioavailability

anticonvulsants, blood level determination of

anticonvulsants, compliance

anticonvulsants, subtherapeutic

anticonvulsants, teratogenicity of

anticonvulsants, untoward effects of

arteriovenous malformation

arteriovenous malformation, pulmonary

arthralgia

arylsulfatase B

ascites

aspartate aminotransferase

attention deficit disorder with hyperactivity

atypical

audiogram

auditory evoked brainstem potentials

autism

Babinski sign

baldness

basal ganglia, calcification of

bone marrow transplantation

brachial neuritis

brachial neuritis, acute

brachial neuritis, bilateral

brachial plexus neuropathy

brachial plexus neuropathy, bilateral

brachial plexus neuropathy, familial

brachial plexus neuropathy, recurrent

calcification, intracranial

cardiac surgery, hypothermia and circulatory arrest for

cardiac surgery, neurologic complications with

CAT scan, indications for

cataracts

cataracts, congenital

Central America

central nervous system, infection of

cerebellar ataxia, children

cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral cortical atrophy

cerebral embolism

cerebral infarction

cerebral palsy

cerebral palsy, risk factors

cerebral palsy, work up

cerebro hepato renal syndrome

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, protein of

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, infancy and childhood

cerebrovascular accident, intrauterine

cerebrovascular accident, multiple

cerebrovascular accident, neonatal

cerebrovascular accident, recurrent

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

chronic graft versus host disease

cleft lip

Clinical Pathologic Conference(C.P.C.)

congenital birth defects

congenital heart disease

congenital infection, viral

congenital malformation

congenital malformation, dilantin therapy causing

congenital malformation, non CNS

congestive heart failure

consanguinity

constipation

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

cyanosis

cyst, porencephalic

deafness

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

dissociated sensory loss

distal muscle weakness

dysarthria-clumsy hand syndrome

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electroencephalogram, monitoring, continuous

electromyogram

electron microscopy

embolism, paradoxical

employment

encephalocele

encephalopathy

encephalopathy, neonatal

epidemiology of neurology

epileptic encephalopathy

extracorporeal membrane oxygenation

Fabry's disease

facial appearance, abnormal

facial expression abnormality

facial weakness

facial weakness, bilateral

failure to thrive

familial

fasciculation

fatty acid, elevated plasma content

fistula, arterio-venous

fistula, arterio-venous, dural

fistula, arterio-venous, dural, spinal

flavivirus

flow study, carotid artery

folic acid

fragile-X syndrome

fragile-X syndrome, carrier

gastrointestinal bleeding

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

glucocerebrosidase

glycogen storage disease

glycoprotein

granular osmiphilic material

gray matter

grimacing

growth hormone deficiency

growth retardation

Guillain Barre syndrome

hemiplegia, congenital

hemorrhage, intracranial, newborn

hemorrhage, periventricular

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatomegaly

hepatosplenomegaly

hereditary hemorrhagic telangiectasia(HHT)

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

hypopigmentation of skin

hypothyroidism, congenital

hypoxic-ischemic leukoencephalopathy

imbalance

immunohistochemistry

in situ hybridization

inborn errors of metabolism

inborn errors of metabolism, screening

infant, evaluation of

infection

infection, recurrent

intellectual deficit

intellectual deterioration

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

Kayser-Fleischer ring

klippel feil syndrome

Krabbe's disease

kyphoscoliosis, neurologic causes of

lamotrigine

learning disability

learning disability, in children

leg weakness, bilateral

lipid storage disorder of CNS

Lisch nodules

lissencephaly

liver disease

liver function enzymes

lysosomal storage disease

lysosomes, abnoral

macrocephaly

malformation, CNS, congenital

malformation, vascular, cerebral

medical-legal aspects of neurology

meningocele

mental retardation

mental retardation, familial

metabolic disorder, primary

metachromatic leukodystrophy

microcephaly

micrognathia

migraine

Miller-Dieker syndrome

misdiagnosis

mitral valve prolapse

molecular genetics

molybdenum cofactor deficiency

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, fetal

MRI, indications for

MRI, intrauterine

mucopolysaccharidoses

multiple sclerosis, misdiagnosis

muscle atrophy, focal

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

myelomeningocele

myelopathy

myelopathy, chronic progressive

myotonia dystrophica, classification

myotonia dystrophica, type 2

nasal bridge, wide

nausea and vomiting

neonatal epilepsy syndromes

neonatal epileptic encephalopathy

neoplasm, primary of CNS

nerve conduction studies

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination

neurologic practice

neurologic signs

neuronal ceroid-lipofuscinosis

neuronal migration disorder

neuropathology

neuropathy

neuropathy, hereditary peripheral

neuropathy, peripheral

neurosis

newborn, evaluation of

nystagmus, hereditary

nystagmus, periodic

obesity

obstetric neurologic injuries

oculopharyngeal muscular dystrophy

ornithine transcarbamylase deficiency

parasitic infection, CNS

paresthesias

Parkinsonism syndrome

paroxysmal neurologic deficits

partruition

pathology

patient information and support

penicillamine

percussion induced muscle contraction

periventricular leukomalacia

pleocytosis of cerebrospinal fluid

polymerase chain reaction

polyneuropathy, chronic inflammatory demyelinating

Pompe's disease of glycogen storage

post hemorrhagic hydrocephalus

postoperative neurologic complications

Prader-Labhart-Willi syndrome

pramipexole

precipitating factors

pregnancy, anticonvulsants during

pregnancy, neurologic complications in

premature infant

premature infant, problems in

prenatal

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

prognosis

progressive neurologic disorder

proteinuria

proximal muscle atrophy

proximal myotonic myopathy

pruritus

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

psychosis

ptosis

puerperium

pyramidal tract dysfunction

restless leg syndrome

retinal degeneration

retinal hamartoma

reversible neurologic disorder

scoliosis, neurologic association with

screaming

screening

seizure

seizure, complications following

seizure, diagnosis of

seizure, treatment of

seizure, treatment of, monotherapy

skin, lesions in neurologic disorders

slit lamp examination

SMN1 gene

South America

Southern immunoblot test

speech disorder

speech disorder, childhood

sphingolipodoses

spina bifida

spinal cord

spinal cord, compression of

spinal cord, lesion of

spinal cord, vascular malformation of

spinal muscular atrophy

spinal muscular atrophy, classification

splenomegaly

spongy degeneration of brain

startle reaction

stem cell transplantation

strabismus

subarachnoid fluid collection, benign

subarachnoid hemorrhage

subdural hematoma

subdural hematoma, neonates and infants

subependymal nodules

suck, poor

sudden infant death syndrome

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

testicular enlargement

thrombocytopenia

thyroxine

tissue plasminogen activator, intravenous

titinopathy

tongue, enlarged

tongue, fasciculations of

tongue, protrusion of

tongue, weakness

toxoplasmosis, CNS

toxoplasmosis, congenital

trauma

treatment of neurologic disorder

tremor

tremulousness

trichopoliodystrophy

trientine dihydrochloride

trinucleotide repeats

tuberous sclerosis, screening for

twins

ultrasonography

ultrasonography, head

ultrasonography, head, fetus-neonate

umbilical-cord blood transplantation

undiagnosed

urea-cycle enzymopathies

uric acid, low

urine test for metabolic disorders

vertigo, episodic

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

Zika virus infection

zinc

Showing articles 1100 to 1150 of 2198 << Previous Next >>

Wolfram Syndrome:Hereditary Diabetes Mellitus with Brainstem and Optic Atrophy
Ann Neurol 39:352-360, Scolding,N.J.,et al, 1996

Stroke in Williams Syndrome
Stroke 27:143-146, Wollack,J.B.,et al, 1996

Familial Hemiplegic Migraine, Nystagmus and Cerebellar Atrophy
Ann Neurol 39:100-106, Elliott,M.A.,et al, 1996

Brief Report:Deficiency of a Dystrophin-Assoc Glycoprotein (Adhalin) in Pt with Muscular Dystrophy & Cardiomyopathy
NEJM 334:362-366, Fadic,R.,et al, 1996

Bent Spine Syndrome
JNNP 60:51-54, Serratrice,G.,et al, 1996

Clinical, Neuroimaging, and Pathologic Features of Progressive Nonfluent Aphasia
Ann Neurol 39:166-173, Turner,R.S.,et al, 1996

Trinucleotide Repeat Length and Clinical Progression in Huntington's Disease
Neurol 46:527-531, Brandt,J.,et al, 1996

Progressive Familial Leukodystrophy of Late Onset
Neurol 46:429-434, Knopman,D.,et al, 1996

Familial Migraine with Vertigo and Essential Tremor
Neurol 46:458-460, Baloh,R.W.,et al, 1996

Diagnosis of Merosin (Laminin-2) Deficient Congenital Muscular Dystrophy by Skin Biopsy
Lancet 347:582-584, Sewry,C.A.,et al, 1996

From Enigmatic to Problematic:The New Molecular Genetics of Childhood Spinal Muscular Atrophy
Neurol 46:335-340, Crawford,T.O., 1996

Uncertain Value of Electronic Fetal Monitoring in Predicting Cerebral Palsy
NEJM 334:613-618, 6591996., Nelson,K.B.,et al, 1996

Pregnancy and the Risk of Stroke
NEJM 335:768-774, Kittner,S.J.,et al, 1996

Recurrent Spontaneous Arterial Dissections-Risk in Familial Vs Nonfamilial Disease
Stroke 27:662-624, Schievink,W.,et al, 1996

Bromocriptine and Postpartum Cerebral Angiopathy:A Causal Relationship
Neurol 46:1754-1756, Comabella,M.,et al, 1996

Cerebral Venous Sinus Thrombosis Associated with Factor V Gene Mutation
JNNP 61:204-205, Kimber,T.,et al, 1996

Psychiatric Symptoms Do Not Correlate with Cognitive Decline, Motor Sympt or CAG Repeat Length in Huntington's
Arch Neurol 53:493-497, Zappacosta,B.,et al, 1996

Motor Changes in Presymptomatic Huntington Disease Gene Carriers
Arch Neurol 53:487-492, Siemers,E.,et al, 1996

Misdiagnosis Revealed by Genetic Linkage Analysis in a Family with Wilson Disease
Neurol 46:1485-1486, Vidaud,D.,et al, 1996

Evidence for Genetic Basis of Multiple Sclerosis
Lancet 347:1728-1730, Sadovnick,A.D.,et al, 1996

Clinical and Subclinical Neurological Involvement in Children of Conjugal Multiple Sclerosis Patients
Multiple Sclerosis 1:170-172, Constantinescu,C.S.,et al, 1996

Apolipoprotein E Genotyping in Alzheimer's Disease
Lancet 347:1091-1095, Tanzi,R.,et al, 1996

Presynaptic Dopaminergic Deficits in Lesch-Nyhan Disease
NEJM 334:1568-1572, 16021996., Ernst,M.,et al, 1996

Fatal Insomnia in a Case of Familial Creutzfeldt-Jakob Disease with the Codon 200Lys Mutation
Neurol 46:758-761, Chapman,J.,et al, 1996

The Challenge of the Dementias
Lancet 347:1301-1307, Eastwood,R.,et al, 1996

Risk Factors for Creutzfeldt-Jakob Disease:A Reanalysis of Case-Control Studies
Neurol 46:1287-1291, Wientjens,D.P.W.M.,et al, 1996

Creutzfeldt-Jakob Disease in a Young Woman
Lancet 347:945-948, Tabrizi,S.J.,et al, 1996

A Simplified Six-Item Checklist for Screening for Fragile X Syndrome in the Pediatric Population
J Pediatr 129:611-614, Giangreco,C.A.,et al, 1996

The Inherited Ataxias and the New Genetics
JNNP 61:327-332, Hammans,S.R., 1996

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
Medicine 75:233-250, Murakami,T.,et al, 1996

Confirmation of Linkage of Oculopharyngeal Muscular Dystrophy to Chromosome 14q11. 2-q13
Ann Neurol 40:801-804, Stajich,J.M.,et al, 1996

A Gene for Parkinson's Disease
BMJ 313:1278, Hawkes,C., 1996

Clinical Genetic Analysis of Parkinson's Disease in the Contursi Kindred
Ann Neurol 40:767-775, Golbe,L.I.,et al, 1996

Postpartum Neuralgic Amyotrophy
Neurol 47:1213-1219, Lederman,R.J.&Wilbourn,A.J., 1996

Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
Neurol 47:1269-1277, Baser,M.E., 1996

Diagnostic Test for the Prader-Willi Syndrome by SNRPN Expression in Blood
Lancet 348:1068-1069, Wevrick,R.&Francke,U., 1996

Routine Indomethacin Prophylaxis:Has the Time Come
Pediatrics 98:784-785, Bada,H.S., 1996

Long-term Prognosis in Cerebral Venous Thrombosis:Follow-up of 77 Patients
Stroke 27:243-246, Preter,M.,et al, 1996

Relationship Between Trinucleotide Repeats and Neuropathological Changes in Huntington's Disease
Ann Neurol 39:132-136, Furtado,S.,et al, 1996

Management of Patients Receiving Interferon Beta-1b for MS:Report of a Consensus Conf
Neurol 46:12-18, Lublin,F.D.,et al, 1996

Dopa-Responsive parkinsonism Phenotype of Machado-Jospeh Disease:Confirmation of 14q CAG Expansion
Ann Neurol 48:684-687, Tuite,P.J.,et al, 1995

Apolipoprotein E Allele E4, Dementia, and Cognitive Decline in a Population Sample
Lancet 346:1387-1390, Henderson,A.S.,et al, 1995

Statement of Use of Apolipoprotein E Testing for Alzheimer Disease
JAMA 274:1627-1629, Farrer,L.A.,et al, 1995

Apoliprprotein E E4 Allele & the Lifetime Risk of Alzheimer's Disease:What Physicians Know, & What They Should Know
Arch Neurol 52:1074-1079, Seshadri,S.,et al, 1995

Apolipoprotein E Genotype in Patients with Alzheimer's Disease:Implications for Risk of Dementia Among Relatives
Ann Neurol 38:797-808, Farrer,L.A.,et al, 1995

Hereditary Hemorrhagic Telangiectasia
NEJM 333:918-924, Guttmacher,A.E.,et al, 1995

Screening Family Members of Patients with Hereditary Hemorrhagic Telangiectasia
Am J Med 99:519-524, Haitjema,T.,et al, 1995

Adult-Onset Spinocerebellar Dysfunction Caused by a Mutation in the Gene for the a-Tocopherol-Transfer Protein
NEJM 333:1313-1318, 13511995., Gotoda,T.,et al, 1995

Cerebrovascular Complications in Ehlers-Danlos Syndrome Type IV
Ann Neurol 38:960-964, North,K.N.,et al, 1995

Showing articles 1100 to 1150 of 2198 << Previous Next >>