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Differential
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abscess, intracerebral

acetylcholinesterase

acid maltase deficiency

acid maltase deficiency, adult

acoustic neurinoma

acoustic neurinoma, bilateral

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

adrenomyeloneuropathy

advances in neurology

agenesis of corpus callosum

Aicardi-Goutieres syndrome

alpha glucosidase

alpha-fetoprotein

alveolar hypoventilation

anesthesia, general

Angelman syndrome

angiofibroma, facial

angiography, spinal

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

arrhythmia, cardiac

arteriovenous malformation

arteriovenous malformation, pulmonary

arylsulfatase B

aspartate aminotransferase

ataxia, hereditary

ataxia, paroxysmal

attention deficit disorder with hyperactivity

auditory evoked brainstem potentials

basal ganglia, calcification of

behavior, combative

behavioral disorder

bleeding disorder

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

cafe au lait spots

calcification, intracranial

calf hypertrophy

Canavan's disease

cardiac surgery, hypothermia and circulatory arrest for

cardiac surgery, neurologic complications with

CAT scan, abnormal

CAT scan, chest

CAT scan, indications for

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, 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

choroid plexus, abnormality of

choroid plexus, cyst

chromosomal abnormality

chronic graft versus host disease

Clinical Pathologic Conference(C.P.C.)

clubbing of fingers

Cockayne's syndrome

cold temperature

confidentiality

congenital birth defects

congenital heart disease

congenital infection, viral

congenital malformation

congenital malformation, dilantin therapy causing

congenital malformation, non CNS

congestive heart failure

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

creatine phosphokinase(CPK)elevated

cultured skin fibroblasts

cyst, porencephalic

degenerative diseases of CNS

dementia, childhood

demyelinating disease

dentate nuclei, lesion of

developmental abnormality of brain

developmental disability

developmental evaluation

developmental milestones

developmental retardation

diagnostic criteria

diaphragmatic paralysis

differential diagnosis

digits, abnormal

dilantin, toxicity

disability, neurological

dissociated sensory loss

distal muscle weakness

diurnal variation

dopamine agonist

drug interactions

dysarthria-clumsy hand syndrome

dysdiadochokinesia

dysostosis multiplex

dystonia, children

eating disorder

electrocardiogram, abnormal

electroencephalogram, abnormalities of

electroencephalogram, monitoring, continuous

electron microscopy

embolism, paradoxical

encephalopathy, neonatal

endovascular therapy

enzyme treatment

enzyme, induction

epidemiology of neurology

epileptic encephalopathy

epistaxis, recurrent

epoxide hydrolase

esophageal varices

ethics in neurology

extracorporeal membrane oxygenation

Fabry's disease

facial appearance, abnormal

facial expression abnormality

facial weakness

facial weakness, bilateral

failure to thrive

fatty acid, elevated plasma content

feeding disorder

fibroma, ungual

fistula, arterio-venous

fistula, arterio-venous, dural

fistula, arterio-venous, dural, spinal

flow study, carotid artery

fragile-X syndrome

fragile-X syndrome, carrier

galactocerebrosidase

gangliosidosis GM1

gangliosidosis GM2

gastrointestinal bleeding

Gaucher's disease

genetic counselling

genetic diagnosis

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

glucocerebrosidase

glycogen storage disease

granular osmiphilic material

growth hormone deficiency

growth retardation

Guillain Barre syndrome

health insurance

hemiplegia, congenital

hemorrhage, intracranial, newborn

hemorrhage, periventricular

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

hepatosplenomegaly

hereditary hemorrhagic telangiectasia(HHT)

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, congenital

hydrocephalus, fetal

hydrocephalus, intrauterine

hyperpyrexia, CNS disorder causing

hypoalbuminemia

hypopigmentation of skin

hypothyroidism, congenital

hypothyroxinemia

hypotonia, infants

hypoxic-ischemic leukoencephalopathy

immunohistochemistry

in situ hybridization

inborn errors of metabolism

inborn errors of metabolism, screening

infant, evaluation of

infection, recurrent

intellectual deficit

intellectual deterioration

intelligence quotient

intelligence testing in children

interferon alpha

intracranial hemorrhage

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

learning disability

learning disability, in children

leg weakness, bilateral

lens, dislocation of

leukoencephalopathy

lipid storage disorder of CNS

liver function enzymes

long bone lesion

low birth weight

lymphangiomyomatosis

lysosomal storage disease

lysosomes, abnoral

malformation, CNS, congenital

malformation, vascular, cerebral

medical-legal aspects of neurology

mental retardation

mental retardation, familial

metabolic disorder, primary

metachromatic leukodystrophy

Miller-Dieker syndrome

mitral valve prolapse

molecular genetics

molybdenum cofactor deficiency

motor dysfunction

motor neuron disease

movement disorder

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, indications for

MRI, intrauterine

mucopolysaccharidoses

multiple sclerosis, misdiagnosis

muscle atrophy, focal

muscle atrophy, progressive

muscle diseases, characteristics of

muscle hypertrophy

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, chronic progressive

myopathy, distal

myopathy, metabolic

myopathy, vacuolar

myotonia dystrophica

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

nerve growth factor

neural tube defect

neuroendocrinology

neurofibromatosis 1

neurofibromatosis 2

neurologic disease

neurologic disease, diagnoses of

neurologic evaluation

neurologic examination

neurologic practice

neurologic signs

neuronal ceroid-lipofuscinosis

neuronal migration disorder

neuropathy, hereditary peripheral

neuropathy, peripheral

newborn, evaluation of

Niemann-Pick disease

nystagmus, hereditary

nystagmus, periodic

obstetric neurologic injuries

oculopharyngeal muscular dystrophy

oral contraceptives

ornithine transcarbamylase deficiency

paraparesis, spastic

parasitic infection, CNS

Parkinsonism syndrome

paroxysmal neurologic deficits

patient information and support

percussion induced muscle contraction

periventricular leukomalacia

peroxisomal disease

personality change

phenylketonuria

pheochromocytoma

pleocytosis of cerebrospinal fluid

polymerase chain reaction

polyneuropathy, chronic inflammatory demyelinating

Pompe's disease of glycogen storage

post hemorrhagic hydrocephalus

postoperative neurologic complications

postpartum coma

postural abnormality

practice guidelines

Prader-Labhart-Willi syndrome

precipitating factors

pregnancy, anticonvulsants during

pregnancy, neurologic complications in

premature infant

premature infant, problems in

prenatal diagnosis by amniocentesis

prevention of neurologic disorders

progressive neurologic disorder

proximal muscle atrophy

proximal myotonic myopathy

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

pyramidal tract dysfunction

recombinant DNA

Refsum's disease

respiratory failure

restless leg syndrome

retinal degeneration

retinal hamartoma

reversible neurologic disorder

rhabdomyoma, cardiac

rubella syndrome

scoliosis, neurologic association with

seizure, complications following

seizure, diagnosis of

seizure, etiology of

seizure, familial

seizure, intractable

seizure, neonatal

seizure, pregnancy

seizure, treatment of

seizure, treatment of, monotherapy

seizure, workup of

self-mutilation

skin, darkening of

skin, lesions in neurologic disorders

slit lamp examination

Southern immunoblot test

speech disorder

speech disorder, childhood

sphingolipodoses

spinal cord, compression of

spinal cord, lesion of

spinal cord, vascular malformation of

spinal muscular atrophy

spinal muscular atrophy, classification

spongy degeneration of brain

startle reaction

stem cell transplantation

subarachnoid fluid collection, benign

subarachnoid hemorrhage

subdural hematoma

subdural hematoma, neonates and infants

subependymal nodules

sudden infant death syndrome

Tay-Sachs disease

temper tantrums

temporalis muscle wasting

temporalis muscle weakness

temporomandibular joint, dislocation

teratogenic drugs

testicular atrophy

testicular enlargement

thrombocytopenia

tissue plasminogen activator, intravenous

tongue, enlarged

tongue, fasciculations of

tongue, protrusion of

tongue, weakness

toxoplasmosis, CNS

toxoplasmosis, congenital

treatment of neurologic disorder

trichopoliodystrophy

trientine dihydrochloride

trinucleotide repeats

tuber, cortical

tuberous sclerosis

tuberous sclerosis, screening for

ultrasonography

ultrasonography, head

ultrasonography, head, fetus-neonate

umbilical-cord blood transplantation

urea-cycle enzymopathies

urine test for metabolic disorders

vertigo, episodic

very long chain fatty acids

viral infection

viral infection, CNS

vitamin supplementation

walking, difficulty with

weakness, congenital

weakness, progressive

weakness, proximal

Werdnig-Hoffman disease

Western immunoblot test

white matter disease

wide based gait

x-linked hydrocephalus

x-linked mental retardation

Zika virus infection

Showing articles 700 to 750 of 2198 << Previous Next >>

Heritability of Carotid Artery Atherosclerotic Lesions
Stroke 36:5-8, Moskau,S.,et al, 2005

Clinicopath Conf, Neurofibromatosis Type 1, with Multiple Spinal Neurofibromas
NEJM 352:1800-1808, Case 13-2005, 2005

The Genetic Causes of Basal Ganglia Calcification, Dementia, and Bone Cysts
Neurol 64:1502-1507, Klunemann,H.H.,et al, 2005

Pallidal Stimulation Improves Pantothenate Kinase-Associated Neurodegeneration
Ann Neurol 57:738-741,613, Castelnau,P.,et al, 2005

Malignant Hyperthermia, Update on Susceptibility Testing
JAMA 293:2918-2924,2958, Litman,R.S.&Rosenberg,H., 2005

Prothrombin 20210A and Oral Contraceptive Use as Risk Factors for Cerebral Venous Thrombosis
Cerebrovasc Dis 19:49-52, Gadelha,T.,et al, 2005

Cerebral Venous Thrombosis: Influence of Risk Factors and Imaging Findings on Prognosis
Clin Neurol Neurosurg 107:371-378, Appenzeller,S.,et al, 2005

Brain Magnetic Resonance Imaging in Patients with Cowden Syndrome
Medicine 84:129-136, Lok,C.,et al, 2005

Psychosocial Impact of Screening for Intracranial Aneurysms in Relatives with Familial Subarachnoid Hemorrhage
Stroke 36:836-840, Wermer,M.J.H.,et al, 2005

Maternal and Infant Characteristics Associated with Perinatal Arterial Stroke in the Infant
JAMA 293:723-729, Lee,J.,et al, 2005

The Clinical and Genetic Spectrum of Spinocerebellar Ataxia 14
Neurol 64:1258-1260, Chen,D-H.,et al, 2005

Value of Gradient-Echo Magnetic REsonance Imaging in the Diagnosis of Familial Cerebral Cavernous Malformation
Arch Neurol 62:653-658, Lehnhardt,F-G.,et al, 2005

Neurologic Symptoms are Common During Gestation and Puerperium in CADASIL
Neurol 64:1441-1443, Roine,S.,et al, 2005

Autonomic Peripheral Neuropathy
Lancet 365:1259-1270, Freeman,R., 2005

Cerebral MR Imaging in Uninfected Children Born to HIV-Seropositive Mothers and Perinatally Exposed to Zidovudine
AJNR 26:695-701,687, Tardieu,M.,et al, 2005

Thrombosis of the Cerebral VEins and Sinuses
NEJM 352:1791-1798, Stam,J., 2005

Magnetic Resonance Imaging of Pituitary Adenomas
Eur Radiol 15:543-548, Bonneville,J.-F.,et al, 2005

Phaeochromocytoma
Lancet 366:665-675, Lenders,J.W.M.,et al, 2005

In Utero Magnetic Resonance Imaging for Brain and Spinal Abnormalities in Fetuses
BMJ 331:562-565, Griffiths,P.D.,et al, 2005

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

Hereditary Motor and Sensory Neuropathies
Peripheral Neuropathy, Dyck,P.J. & Thomas,P.K. (Ed). Elsevier Publ, Vol 2, Ch 69: 1623-1635, Shy,M.E., et al, 2005

Late-Onset Friedreich Ataxia
Arch Neurol 62:1865-1869, Bhidayasiri,R.,et al, 2005

Neuroblastoma -- from Genetic Profiles to Clinical Challenge
NEJM 353:2215-2217, Kushner,B.H. &Cheung,N.-K.V., 2005

Pregnancy, Delivery, and Birth Outcome in Women with Multiple Sclerosis
Neurol 65:1961-1963, Dahl,J.,et al, 2005

Migraine and Cerebral White Matter Lesions
The Neurologist 11:19-29, Gladstone,J.P. &Dodick,D.W., 2005

A Variant in the HS1-BP3 Gene is Associated with Familial Essential Tremor
Neurol 64:417-421, Higgins, J.J., et al, 2005

Genetic Screening for a Single Common LRRK2 Mutation in Familial Parkinson's Disease
Lancet 365:410-412, Nichols, W.C., et al, 2005

Genetic Factors in Alzheimer's Disease
NEJM 352: 862-863, 884, Bird, T., 2005

Fatal Avian Influenza A (H5N1) in a Child Presenting with Diarrhea Followed by Coma
NEJM 352:686-691, de Jong,M.D., et al, 2005

Unusual Variants of Alexander's Disease
Ann Neurol 57:327-338, van der Knaap,M.S., et al, 2005

Sensorineural Hearing Loss in Children
Lancet 365:879-890, Smith, R.J.H.,et al, 2005

Increased Rate of Major Malformations in Offspring Exposed to Valproate Durng Pregnancy
Neurol 64:961-965, 938, Wyszynski,D.F., et al, 2005

Lamotrigine and the Risk of Malformations in Pregnancy
Neurol 64:955-960, 938, Cunnington, M. , et al, 2005

Neuropsychological Effects of Exposure to Anticonvulsant Medication in Utero
Neurol 64:949-954, 938, Vinten,J., et al, 2005

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

Clinical and Molecular Findings in Patients with Giant Axonal Neuropathy (GAN)
Neurol 62:13-16, Bruno,C.,et al, 2004

Infantile Bilateral Striatal Necrosis Maps to Chromosome 19q
Neurol 62:87-90, Basel-Vanagaite,L.,et al, 2004

The Parkinsonian Phenotype of Spinocerebellar Ataxia Type 2
Arch Neurol 61:35-38, Lu,C.,et al, 2004

Penetrance of the Fragile X-Associated Tremor/Ataxia Syndrome in a Premutation Carrier Population
JAMA 291:460-469, Jacquemont,S.,et al, 2004

Charcot-Marie-Tooth Disease:Extensive Cranial Nerve Involvement on CT and MR Imaging
AJNR 25:494-497, Aho,T.R.,et al, 2004

Postpartum Angiopathy with Reversible Posterior Leukoencephalopathy
Arch Neurol 61:411-416, Singhal,A.B., 2004

Practice Parameter:Diagnostic Assessment of the Child with Cerebral Palsy
Neurol 62:851-863, Ashwal,S.,et al, 2004

The AED (Antiepileptic Drug) Pregnancy Registry
Arch Neurol 61:673-678, Holmes,L.B.,et al, 2004

Developmental Dyslexia
Lancet 363:1451-60, Demonet,J-F.,et al, 2004

Aromatic L-Amino Acid Decarboxylase Deficiency
Neurol 62:1058-1065, Pons,R.,et al, 2004

Parkinson's Disease
Lancet 363:1783-1793, Samii,A.,et al, 2004

Functional Brain Changes in Presymptomatic Hunington's Disease
Ann Neurol 55:879-883, Reading,S.A.,et al, 2004

Recurrent Acroparaesthesia During Febrile Infections
Lancet 363:1698, Bodamer,O.A.,et al, 2004

Familial Multiple Sclerosis and Other Inherited Disorders of the White Matter
The Neurologist 10:201-215, Kalman,B. &Leist,T.P., 2004

Showing articles 700 to 750 of 2198 << Previous Next >>