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Differential
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abdominal distention

abducens nerve paralysis

acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, congenital

acquired immunodeficiency syndrome, infants and children

adrenal crisis, acute

adverse drug reaction

agenesis of corpus callosum

alcohol, neurologic complications with

Alexanders disease

Alexanders disease, adult onset

alpha-fetoprotein

alveolar hypoventilation

Alzheimer's disease

aminoacidopathies

amyotrophic lateral sclerosis

Angelman syndrome

anorexia nervosa

anticonvulsants

apraxia of eye movements

aqueduct of Sylvius, stenosis

aqueductal stenosis

arteriovenous malformation

arteriovenous malformation, cerebral

arylsulfatase B

ascending paralysis

ataxia telangiectasia

ataxia, cerebellar

ataxia, progressive

ataxia, truncal

atlanto-axial subluxation

atrial enlargement

attention deficit disorder with hyperactivity

autoimmune disease

autonomic dysfunction

axonal degeneration

basal ganglia, calcification of

basilar impression

battered child syndrome

behavior modification

behavior, combative

behavioral disorder

biologic markers

bitemporal visual field defect

blepharophimosis

blind spot, enlarged

blindness, sudden

bone marrow transplantation

brachial plexus neuropathy

brachial plexus neuropathy, familial

brainstem, atrophy

breech delivery

Brown-Vialetto-Van Laere syndrome

calcification, intracranial

carbonic anhydrase II deficiency

carcinoembryonic antigen

CAT scan, abnormal

CAT scan, false negative

cauda equina, enhancement

cavernous sinus

cavernous sinus, metastasis to

celiac disease, adult

celiac disease, childhood

central hypoventilation, congenital

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hemorrhage

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral vasculature

cerebral venous thrombosis

cerebrospinal fluid, biochemical markers of CNS tumors

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, pressure increased

cerebrospinal fluid, proteincytologic dissociation

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, familial occurrence

cerebrovascular accident, infancy and childhood

cerebrovascular accident, mimics

cerebrovascular accident, multiple

cerebrovascular accident, recurrent

cerebrovascular accident, young adult

chemotherapy, CNS treatment and complications with

choreoathetosis

chorionic gonadotropin

chorioretinitis

chromophobe adenoma

chromosomal abnormality

chronic graft versus host disease

chronic progressive external ophthalmoplegia

cisterna magna, enlarged

Clinical Pathologic Conference(C.P.C.)

Cockayne's syndrome

codfish vertebrae

cold hands sign

collagen vascular disease

compression fracture

congenital heart disease

congenital heart disease, CNS complications with

congenital infection, CNS

congenital infection, viral

congenital malformation

congenital malformation, non CNS

congestive heart failure

contractures, joint

cornea, abnormal

cornea, opacity of

Cornelia de Lange syndrome

corpus callosum, atrophy of

corpus callosum, hypoplastic

corpus callosum, thinning

cortical blindness

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

craniopharyngioma

creatine phosphokinase(CPK)elevated

cryopyrin-associated periodic syndrome

cultured skin fibroblasts

cytochrome c oxidase

cytochrome c oxidase, deficiency

degenerative diseases of CNS

dementia, childhood

dementia, rapidly progressive

dermatitis herpetiformis

developmental disability

developmental evaluation

developmental milestones

developmental milestones, loss of

developmental retardation

diabetes insipidus

diabetes mellitus

diagnostic criteria

differential diagnosis

difficulty climbing stairs

digits, abnormal

dislocated hip, congenital

dissociated sensory loss

distal muscle atrophy

distal muscle weakness

dopa responsive dystonia

dural sinus thrombosis

dysostosis multiplex

eating disorder

echocardiogram, transesophageal

ectopic pinealoma

ejection fraction

ejection fraction, abnormal

electroencephalogram

electroencephalogram, abnormalities of

electron microscopy

emergencies, neurologic

encephalopathy, progressive

endovascular therapy

enzyme treatment

enzyme, muscle disease

epicanthal folds

epidemiology of neurology

epileptic encephalopathy

episodic disorders

evoked potentials

exercise intolerance

exome sequencing

eye movement, disorders of

eyebrows, abnormal

facial anomalies

facial appearance, abnormal

facial hypoplasia

facial nerve palsy

facial weakness, bilateral

failed medical management

failure to thrive

FARS2 deficiency

feeding disorder

fetal alcohol syndrome

fever, recurrent

fine motor function, impaired

follicle stimulating hormone

fontanel, bulging

foot drop, bilateral

fracture, pathologic

frontal bossing

gangliosidosis GM1

gangliosidosis GM2

gastrointestinal disease, neurologic complications

gastrointestinal motility

genetic counselling

genetic diagnosis

genetic diagnosis, prenatal

genetic linkage

genetic neurologic disorders

genetic screening

genetic testing

genital hypoplasia

glucose tolerance test, abnormal

gluten sensitivity

gluten-free diet

glycogen debranching enzyme deficiency

glycogen storage disease

Gowers maneuver

growth hormone deficiency

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, infantile and childhood form

hair, darkening of

head circumference

head injury, hypothalamic and pituitary damage

head injury, pediatric

headache, recurrent

hemoglobin abnormality, neurologic complications of

hemorrhage, intracranial, newborn

hemorrhagic diathesis

hepatosplenomegaly

heralding manifestation

hereditary multiple exostoses

herpes simplex virus

herpes simplex virus infection, newborn

herpes simplex virus, human nervous system and

high arched palate

Hirschprung's disease

human immunodeficiency virus type 1

Hunter's syndrome

hydrocephalus, communicating

hydrocephalus, congenital

hydrocephalus, etiology

hydrocephalus, fetal

hydrocephalus, infants and children

hydrocephalus, intrauterine

hydrocephalus, treatment of

hyperhomocysteinemia

hyperpigmentation of skin

hypertrophic cardiomyopathy

hypertrophic intracranial pachymeningitis

hypomyelination

hypoparathyroidism

hypopigmentation of skin

hypopituitarism

hypothalamus, disturbance of

hypothalamus, lesion of

hypothalamus, neoplasm of

hypothermia, causes of

hypotonia, infants

iatrogenic neurologic disorders

immunodeficiency

immunosuppression

imperforate anus

inability to stand on tiptoes

inclusion bodies, intranuclear

infection, recurrent

insulin resistance

intellectual deficit

intellectual deterioration

intelligence quotient

intestinal biopsy

intestinal pseudoobstruction

intracerebral hemorrhage

intracranial hemorrhage

intracranial hypertension, benign

intracranial hypertension, benign, differential diagnosis

intracranial hypertension, benign, pathogenesis of

intracranial pressure, increased

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intraventricular hemorrhage

joint hypermobility

Kearns-Sayre syndrome

Klinefelter's syndrome

Krabbe's disease

kyphoscoliosis, neurologic causes of

lactic acidemia

laminar necrosis, cortical

language disorders in children

learning disability

learning disability, in children

Leber's hereditary optic neuropathy

leg weakness, bilateral

Leigh's disease

lens, dislocation of

leukodystrophy, 4H

leukoencephalopathy

level of consciousness, decreased

libido, decreased

lid abnormalities

life expectancy

lipid storage disorder of CNS

livedo reticularis

low birth weight

Lowe's syndrome

lumbar puncture

luteinizing hormone

lymphadenopathy

lysosomal storage disease

malabsorption syndrome

malformation, vascular

malformation, vascular, cerebral

malformation, Vein of Galen

meconium staining

melanomatosis, primary malignant

meningitis, aseptic

meningitis, CSF cell count-normal

mental retardation

mental status, abnormal

metabolic acidosis

metabolic disorder, primary

metachromatic leukodystrophy

methylene tetrahydrofolate reductase

methylenetetrahydrofolate reductase deficiency

microspherophakia

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

molybdenum cofactor deficiency

monoclonal gammopathy

Morquio syndrome

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI, angiography

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, false negative

mucopolysaccharidoses

multiple sclerosis

multiple system atrophy

muscle stiffness

muscle weakness

muscle weakness, proximal

myasthenia gravis, differential diagnosis

myasthenia gravis, misdiagnosis of

myelination of nervous system

myelomeningocele

myoclonus, epilepsy

myoclonus, stimulus sensitive

myopathy, distal

myopathy, distal, vacuolar

myopathy, inclusion body

myopathy, inclusion body, hereditary

myopathy, mitochondrial

myopathy, vacuolar

nasal bridge, wide

nausea and vomiting

neoplasm, intracranial with metastasis extracranially

neoplasm, intracranial, congenital

neoplasm, intracranial, infants

neoplasm, pituitary

neoplasm, primary intracranial

neoplasm, primary intracranial-treatment of

neoplasm, primary of CNS

neoplasm, primary of CNS-children

neoplasm, primary of CNS-incidence of

neoplasm, primary of CNS-survival

neoplasm, primary of CNS-treatment of

nerve growth factor

nerve growth stimulating activity

nerve root enhancement

neurocutaneous disease

neuroendocrinology

neurofibromatosis 1

neurologic complications of, systemic cancer

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic examination, focal

neurologic signs

neuroophthalmology

neuropathy, hereditary peripheral

neuropathy, peripheral

neuropathy, sensory, hereditary

neuroprotective agents

Niemann-Pick disease

Noonan Syndrome

numbness, ascending

numbness, extremity

nutritional deficiency

nystagmus, see-saw

ocular motility, disorders of

ophthalmoplegia

ophthalmoplegia, progressive external

opportunistic infection

optic atrophy, bilateral

optic foramina, abnormal

optic nerve sheath fenestration

optic nerve, decompression of

optic nerve, hypoplasia of

optic neuropathy

oral ulcerations

orthostatic hypotension, idiopathic

osteogenesis imperfecta

palatal myoclonus

Pallister-Hall syndrome

palpebral fissure, short

paraparesis, familial spastic

paraparesis, spastic

Parkinson disease

Parkinson disease, differential diagnosis of

Parkinsonism syndrome

paroxysmal neurologic deficits

patent ductus arteriosus

pectus carinatum

pectus excavatum

pediatric neurology

perceptual-motor dysfunction

personality change

pheochromocytoma

philtrum, hypoplastic

philtrum, tented

photosensitivity, skin

pigmentary retinopathy

pituitary, adenoma

pituitary, dysfunction

pituitary, enlargement

pituitary, hormones of

pituitary, lesion of

PLEDs, bilateral independent

PLEDs, etiology of

pleocytosis of cerebrospinal fluid

polyps, gastrointestinal tract

postural abnormality

Prader-Labhart-Willi syndrome

precocious puberty

pregnancy, neurologic complications in

premature infant

prenatal diagnosis by amniocentesis

pretectal syndrome

prevention of neurologic disorders

primitive neuroectodermal tumors

progressive neurologic disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, children

psychomotor retardation

psychosocial aspects

puberty, delayed

pulmonary stenosis

pupil, ectopic-congenital

pyramidal tract dysfunction

radiation hypersensitivity

radiation therapy, CNS treatment and complications with

ragged-red fibers

rapidly progressing neurologic illness

reading problem, causes of

renal tubular acidosis

respirations in CNS disease

respiratory failure

respiratory tract infection

retinal degeneration

retinitis pigmentosa

Rett's syndrome

riboflavin transporter deficiency

Riley-Day syndrome

root lesion, nerve

Rosenthal fibers

Sanfilippo syndrome

Schwartz-Jampel syndrome

scoliosis, neurologic association with

seizure, children

seizure, drug resistance

seizure, injury following

seizure, intractable

seizure, neonatal

sella turcica, enlargement of

sensorineural hearing loss

sensory ganglia

sensory ganglia, abnormal

serologic testing

shunt procedure, lumboperitoneal

shunt procedure, ventricular

shunt procedure, ventricular-complications of

Shy-Drager syndrome

sickle cell trait

skin, darkening of

skin, lesions in neurologic disorders

skull bone, thickening

skull x-ray, abnormal

sleep pathology and physiology

small vessel disease

somatosensory evoked potentials

spastic diplegia

speech disorder

speech disorder, childhood

speech, absence of

speech, delayed development of

spinal cord, compression of

spinal cord, lesion of

spinal muscular atrophy

spongy degeneration of brain

standing difficulty

stem cell transplantation

stent, venous sinus

stereotyped behavior

stimulant drugs

stooped posture

strokelike episodes

subarachnoid hemorrhage

subdural hematoma

subdural hematoma, neonates and infants

subgaleal fluid collection

superior sagittal sinus thrombosis

suprasellar lesion

systemic illness

teeth, abnormal

temper tantrums

temporal lobe, lesion

third ventricle, mass of

thrombophlebitis

thyroid function tests

tongue, enlarged

tongue, protrusion of

transplacental virus infections

treatment of neurologic disorder

tremor, postural

trichopoliodystrophy

upgaze, paralysis of

urea-cycle enzymopathies

urinary 17 hydroxycorticosteroids

urinary 17 ketosteroids

vascular endothelial growth factor

ventriculostomy, endoscopic

viral infection, CNS

visual acuity, decreased

visual field defect

visual field testing

visual impairment

visual tracking

vomiting, recurrent

walking, difficulty with

weakness, generalized

weakness, progressive

Werner's syndrome

white matter disease

whole genome sequencing

wide based gait

xeroderma pigmentosa

x-linked mental retardation

x-ray, cervical spine

Showing articles 1400 to 1450 of 1868 << Previous Next >>

Homing in on Wilson's Disease
Editorial, Lancet 1:822-8231989., , 1989

Randomised Double Blind Controlled Trial of Cyclosporin in Multiple Sclerosis
JNNP 52:559-565, Rudge,P.,et al, 1989

Tetrahydroaminoacridine (THA) in Alzheimer's Disease, Not Ready for Routine Use
BMJ 298:845-846, Graham,T.R.&Lewis,C.T., 1989

Autonomic Nervous System Involvement in Patients with Human Immunodeficiency Virus Infection
Neurol 39:1111-1112, Cohen,J.A.&Laudenslager,M., 1989

Clinicopath Conf
HTLV-I Infection, with Adult T-Cell Lymphoma and Tropical Spastic Paraparesis, Case 36-2989, NEJM 32, :6675,1989., 1989

Cerebrospinal Fluid Shunt Infections
Editorial, Lancet 1:1304-13051989., , 1989

Occluded Fourth Ventricle After Multiple Shunt Revisions for Hydrocephalus
Pediatrics 83:981-985, Coker,S.B.&Anderson,C.L., 1989

Management Problems in Acute Hydrocephalus after Subarachnoid Hemorrhage
Stroke 20:747-753, Hasan,D.,et al, 1989

Duchenne Muscular Dystrophy:Patterns of Clinical Progression and Effects of Supportive Therapy
Neurol 39:475-481, Brooke,M.H.,et al, 1989

Peripheral Neuropathy in Primary Sjogren's Syndrome
Neurol 39:390-394, Mellgren,S.I.,et al, 1989

Cholesterol Embolism:Experience with 22 Histologically Proven Cases
Surgery 105:737-746, Dahlberg,P.J.,et al, 1989

Respiratory Complications and Their Management in Motor Neuron Disease
Brain 112:1155-1170, Howard,R.S.,et al, 1989

Left Ventricular Thrombus and Systemic Emboli Complicating the Cardiomyopathy of Duchenne's Muscular Dystrophy
Arch Neurol 46:1249-1252, Gaffney,J.F.,et al, 1989

3, 4-Diaminopyridine in the Treatment of Lambert-Eaton Myasthenic Syndrome
NEJM 321:1567-1571, 1607-16081989., McEvoy,K.M.,et al, 1989

The Rational Management of Idiopathic Intracranial Hypertension
Arch Neurol 46:1049-1051, Corbett,J.J.&Thompson,H.S., 1989

Symptomatic Congenital Hydrocephalus in the Elderly Simulating Normal Pressure Hydrocephalus
Neurol 39:1596-1600, Graff-Radford,N.R.&Godersky,J.C., 1989

The Remote Effects of Cancer on the Nervous System
in Neurol Manif of Systemic Dis, W. B. Saunders, Co, Phila, Neurologic Clinics 7:579-603, Dropcho,E.J., 1989

Cancer-Associated Retinopathy (Car Syndrome) with Antibodies Reacting with Retinal, Optic-Nerve, and Cancer Cells
NEJM 321:1589-1594, 1607-16081989., Thirkill,C.E.,et al, 1989

Surgery for Intractable Epilepsy:Issues and Outcome
Pediatrics 84:886-894, Duchowny,M.S., 1989

Convulsions in Children Undergoing Renal Transplantation
J Pediatr 115:532-536, McEnery,P.T.,et al, 1989

Rigid Spine Syndrome and Rigid Spine Sign in Myopathies
J Child Neurol 4:273-282, Merlini,L.,et al, 1989

Follow-up and Diagnostic Reappraisal of 75 Patients with Leber's Congenital Amaurosis
Am J Ophthalmol 107:624-631, Lambert,S.R.,et al, 1989

Human Leptospirosis-A Review of 50 Cases
Infection 17:10-14, Lecour,H.,et al, 1989

The Lambert-Eaton Myasthenic Syndrome, A Review of 50 Cases
Brain 111, 577-5961988., O'Neill,J.H.,et al, 1988

Cerebrovascular Disorders of Infancy
In Handbk of Clin Neurol, Elsevier Sci Publ, NY, 2:3188., Salam-Adams,M.&Adams,R.D., 1988

Ventriculo-pleural Shunting for Adult Hydrocephalus
Br J Neurosurg 2:503-505, Megison,D.P.&Benzel,E.C., 1988

Transient Paroxysmal Dystonia in Infancy
Neuropediatr 19:171-174, Angelini,L.,et al, 1988

Paraneoplastic Syndromes Involving the Eyes
In Walsh & Hoyt's Clin Neuro-ophthal, 4th ed, Williams & Wilkins, Vol 3, p 1735-1746, Miller,N.R., 1988

Terson's Syndrome
Neuroophthalmol 9:223-233, Huber,A.,et al, 1988

Acquired Hepatocerebral Degeneration:MR Similarity with Wilson Disease
J Comput Assist Tomogr 12:1076-1077, Hanner,J.S.,et al, 1988

Improvement of Hepatic Encephalopathy Treated with Flumazenil
Lancet 2:1392-1394, Grimm,G.,et al, 1988

Radiological Case of the Month:3rd Ventricle Arachnoid Cyst
Am J Dis Child 142:1081-1082, Wells,R.G.,et al, 1988

Unilateral Hyperhidrosis after Cerebral Infarction
Neurol 38:1679-1682, Labar,D.R.,et al, 1988

Pulmonary Function and Dysfunction in Multiple Sclerosis
Arch Neurol 45:1245-1249, Smeltzer,S.C.,et al, 1988

Medullary Lesion Revealed by MRI in a Case of MS with Respiratory Arrest
Neuroradiology 30:574-576, Mochizuki,A.,et al, 1988

Isolated Central Respiratory Failure Due to Syringomyelia and Arnold-Chiari Malformation
BMJ 297:1448-1449, Bullock,R.,et al, 1988

Risk Factors for Falls Among Elderly Persons Living in the Community
NEJM 319:1701-1707, Tinetti,M.E.,et al, 1988

Portosystemic Encephalopathy in Hereditary Hemorrhagic Telangiectasia
Am J Med 85:858-860, Fagel,W.J.,et al, 1988

Rett Syndrome:Natural History and Management
Pediatrics 82:1-10, Moeschler,J.B.,et al, 1988

Right-Sided Brain Lesions in Infants Following Extracorporeal Membrane Oxygenation
Pediatrics 82:155-161, Schumacher,R.E.,et al, 1988

Neurologic and Cognitive Deficits in Children with Cystinosis
J Pediatr 112:912-914, Trauner,D.A.,et al, 1988

Stroke Rehabilitation Outcome:Impact of Coronary Artery Disease
Stroke 19:42-47, Roth,E.J.,et al, 1988

Autonomic Nervous Function in Huntington's Disease
Arch Neurol 45:309-312, DenHeijer,J.C.,et al, 1988

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

Human Growth Hormone Therapy & Creutzfeldt-Jakob Disease:A Drama in Three Acts
Pediatrics 81:85-92, Brown,P., 1988

Cardiovascular Autonomic Dysfunction in Guillain-Barre Syndrome, Therapeutic Implications of Swan-Ganz Monitoring
Arch Neurol 45:115-117, Dalos,N.P.,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

Ocular Findings in Infants Treated with Extracorporeal Membrane Oxygenator Support
Pediatrics 82:560-564, Patrias,M.C.,et al, 1988

An Adolescent with Intermittent Headache, Transient Hemiparesis, and Urinary Abnormalities
J Pediatr 113:769-776, Gruskin,A.B.&Chang,C., 1988

MR Imaging of a Group I Case of Hallervorden-Spatz Disease
J Comput Assist Tomogr 12:851-853, Mutoh,K.,et al, 1988

Showing articles 1400 to 1450 of 1868 << Previous Next >>