Neudle.com: pons hypoplasia

Differential
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acetylcholine

acromicria

adult polyglucosan body disease

advances in neurology

agenesis of corpus callosum

alternating rapid movement

apnea, primary central

apraxia of eye movements

aqueduct of Sylvius, stenosis

auditory evoked brainstem potentials

autism

autoantibodies

autonomic dysfunction

Babinski sign

baclofen

basal ganglia, calcification of

basal ganglia, lesion, bilateral

brainstem, hypoplasia

brainstem, infarction of

brainstem, malformation

calcification, intracranial

calcification, intraventricular

calcification, periventricular

CAT scan, emission, abnormal

cataracts

cataracts, congenital

central nervous system, infection of

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar hypoplasia

cerebellar infarction

cerebral cortical atrophy

cerebral palsy

cerebral vasculature

cerebral venous thrombosis

cerebro hepato renal syndrome

cerebrospinal fluid, leak

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, intrauterine

cerebrovascular accident, neonatal

cerebrovascular accident, young adult

cerebrovascular disease, infant and childhood

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

clinodactyly

cocaine

cocaine, intrauterine exposure

Cockayne's syndrome

codfish vertebrae

colpocephaly

congenital birth defects

congenital infection, CNS

congenital infection, viral

congenital malformation

congenital ocular motor apraxia

contractures, joint

controversies in neurology

cornea, opacity of

corpus callosotomy

corpus callosum, hypoplastic

cortical blindness

craniofacial dysostosis

cytomegalic inclusion disease

cytomegalovirus infection

cytomegalovirus infection, congenital

deafness

degenerative diseases of CNS

dementia

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

depression

developmental abnormality of brain

developmental retardation

diabetes insipidus

diabetes mellitus

diabetes mellitus, neurologic manifestations of

digits, abnormal

disability, neurological

distal muscle atrophy

dizziness

down-beat nystagmus, primary position of gaze

drug abuse

dural sinus thrombosis

exophthalmus, unilateral

eye movement, disorders of

facial anomalies

facial appearance, abnormal

facial hypoplasia

facial nerve palsy, bilateral

facial nerve palsy, congenital

facial weakness, bilateral

failure to thrive

falling

familial

fibrous dysplasia of orbit

flavivirus

foot deformity

fourth ventricle, enlargement of

fourth ventricle, floor

gaze palsy, congenital horizontal

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, supranuclear

gene mutation

genetic neurologic disorders

glutamate dehydrogenase deficiency

glutamic acid

growth hormone deficiency

hemianopia, congenital

hemianopia, homonymous

hemiatrophy, cerebral

hemiatrophy, congenital

hemiplegia, congenital

heralding manifestation

hydrocephalus, congenital

hydroxytryptophan L-5(L-5 HTP)

inclusion bodies, intracytopasmic

insulin resistance

intellectual deficit

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

intrauterine

intrauterine infection

intrauterine infection, viral

intrauterine infection, viral of CNS

intrinsic hand muscles, wasting of

kyphoscoliosis, neurologic causes of

L-dopa

Leber's congenital amaurosis

leg weakness, bilateral

lymphocytic choriomeningitis

macular degeneration

malformation, CNS, congenital

Marinesco-Sjogren syndrome

medulla oblongata

medulla oblongata, lesion of

medulla oblongata, malformation

melanomatosis, primary malignant

memory, impairment of

mental retardation

metabolic disorder, primary

methylene tetrahydrofolate reductase

methylenetetrahydrofolate reductase deficiency

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, CAT scan compared to

MRS

multiple system atrophy

neurologic disease, diagnoses of

neuronal migration disorder

ocular motility, disorders of

old age, neurology of

optic nerve, hypoplasia of

orbit

orbit, fractures, neurologic complications of

orbit, hypoplasia of

orbit, neoplasms of

orbit, pseudotumor of

orbit, trauma to

orbit, venography of

orthostatic hypotension

pain, management of chronic

palatal myoclonus

paraneoplastic cerebellar degeneration

Parkinson disease

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

paroxysmal nonkinesigenic dyskinesia

pectus excavatum

pediatric neurology

Percutaneous electrical nerve stimulation

periventricular leukomalacia

photosensitivity, skin

physostigmine

pigmentary retinopathy

pituitary

pituitary stalk

pituitary, hyppoplasia

pleocytosis of cerebrospinal fluid

pneumoencephalogram(PEG)

polycystic kidneys

polyglucosan body disease

pons, atrophy

pons, hypoplasia

pontocerebellar atrophy

posterior cerebral artery territory infarction

posterior pituitary ectopia

Prader-Labhart-Willi syndrome

pregnancy, neurologic complications in

progressive neurologic disorder

progressive supranuclear palsy

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychomotor retardation

psychosis

Purkinje cell

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract dysfunction

pyramidal tract, uncrossed

quadrigeminal plate

red free light

red free light, fundus exam with

remote effect of cancer on the nervous system

saccadic eye movements, abnormal

scissors gait

scoliosis

scoliosis, neurologic association with

screening

seizure

seizure, neonatal

sella turcica, hypoplasia of

sensorineural hearing loss

septo-optic dysplasia

short stature

Shy-Drager syndrome

sleep apnea

sleep pathology and physiology

spasticity

speech disorder, childhood

speech, delayed development of

spinal cord, lesion of

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 2

spinocerebellar ataxia type 3/Machado Joseph disease

spinocerebellar ataxia type 6

spinocerebellar ataxia type 7

spinocerebellar degeneration

spinopontine atrophy, dominant

startle myoclonus

strabismus

striatonigral degeneration

substantia nigra

superior cerebellar peduncle

superior colliculus

superior sagittal sinus thrombosis

treatment of neurologic disorder

tremor

tremor, intention

trinucleotide repeats

twins

ultrasonography, orbit

urinary incontinence

vein of Galen

vertebral artery

vertebral artery hypoplasia

vertebral-basilar insufficiency

vertigo

viral infection

viral infection, CNS

vision, failure of in childhood

visual acuity, decreased

visual field defect

visual field defect, altitudinal

visual loss

visual tracking

Walker-Warburg syndrome

walking, difficulty with

weakness

wheelchair

white matter disease

white matter disease, periventricular

white matter disease, subcortical

Wolfram syndrome

X-linked bulbospinal neuronopathy

x-linked mental retardation

Zika virus infection

Showing articles 50 to 88 of 88 << Previous

Idiopathic Cerebellar Ataxia of Late Onset:Natural History and MRI Morphology
JNNP 53:297-305, Klockgether,T.,et al, 1990

Neuropsychological Changes in Olivopontocerebellar Atrophy
Arch Neurol 47:997-1001, Berent,S.,et al, 1990

Cerebral Cortex and Brainstem Involvement in Marinesco-Sjogren Syndrome
Ann Neurol 27:448-449, Katafuchi,Y.,et al, 1990

A Quantitative Evaluation of Pontine Volume by Computed Tomography in Patients with Cerebral Degeneration
Neurol 40:1241-1245, Chida,K.,et al, 1990

Physical Features of Prader-Willi Syndrome in Neonates
Am J Dis Child 144:1251-1254, Aughton,D.J.&Cassidy,S.B., 1990

MR Imaging in Progressive Suupranuclear Palsy and Shy-Drager Syndrome
J Comput Assist Tomogr 13:555-560, Savoiardo,M.,et al, 1989

Magnetic Resonance Imaging in Parkinson's Syndromes
Neurol 39:1524-1526, Stern,M.B.,et al, 1989

Cerebellar & Brainstem Hypometabolism in Olivo-pontocerebellar Atrophy Detected with Positron Emission Tomography
Ann Neurol 23:223-230, Gilman,S.,et al, 1988

Spinocerebellar Degeneration:Qualitative & Quantitative MR Analysis of Atrophy
J Comput Assist Tomogr 12:298-303, Nabatame,H.,et al, 1988

Sleep Apnea in Olivopontocerebellar Degeneration:Treatment with Trazodone
Ann Neurol 23:399-401, Salazar-Grueso,E.F.,et al, 1988

Hypoplasia of Cerebellar Vermal Lobules VI and VII in Autism
NEJM 318:1349-1354, 13901988., Courchesne,E.,et al, 1988

Optic Nerve Hypoplasia & Maternal Diabetes Mellitus
Arch Neurol 43:20-25, Nelson,M.,et al, 1986

The Role of Glutamate in Neurotransmission & in Neurologic Disease
Arch Neurol 43:1058-1063, Greenamyre,J.T., 1986

Olivopontocerebellar Atrophy with Dementia, Blindness, & Chorea, Response to Baclofen
Arch Neurol 42:757-758, Trauner,D.A., 1985

Colpocephaly:Clinical, Radiologic, & Pathogenetic Aspects
Neurol 35:1594-1598, Herskowitz,J.,et al, 1985

Neurological Disorders Associated with Deficiency of Glutamate Dehydrogenase
Ann Neurol 15:144-153, Plaitakis,A.,et al, 1984

Leber's Congenital Amaurosis
Arch Neurol 41:204-206, Weinstein,J.M.,et al, 1984

Autonomic Dysfunction & Sleep Apnea in Olivoponto Cerebellar Degeneration
Arch Neurol 41:926-931, Chokroverty,S.,et al, 1984

Congenital Hydrocephalus & Eye Abnormalities with Severe Developmental Brain Defects:Warburg's Syndrome
Ann Neurol 16:60-65, Bordarier,C.,et al, 1984

Dominant Spinopontine Atrophy
Arch Neurol 40:259-260, Pogacar,S.,et al, 1983

Evoked Potentials in Olivopontocerebellar Atrophy
Arch Neurol 40:366-369, Hammond,E.J.,et al, 1983

Unilateral Cerebellar Hypoplasia
J Comput Assist Tomogr 7:1077-1078, Mendelsohn,D.B.,et al, 1983

Glutamate Dehydrogenase Deficiency in Patients with Olivopontocerebellar Atrophy
Neurol 33:1322-1326, Duvoisin,R.C.,et al, 1983

Ataxia with Aniridia of Gillespie:A Case Report
Neurol 31:95-97, Lechtenberg,R.,et al, 1981

Olivopontocerebellar Atrophy in Children:A Report of Seven Cases in Two Families
Ann Neurol 10:355-363, Colan,R.V.,et al, 1981

Septo-optic Dysplasia in an Infant of a Diabetic Mother
Arch Neurol 38:590-591, Donat,J.F.G., 1981

Human Cerebellar Hypoplasia, A Syndrome of Diverse Causes
Arch Neurol 37:300-305, Sarnatt,H.B.,et al, 1980

A Family with Hereditary Ataxia:HLA Typing
Neurol 30:12-20, Nino,H.E.,et al, 1980

Clin. Path. Conference
Olivopontocerebellar atrophy, sporadic form. Case Record 39-1980, NEJM 303:803-80980., , 1980

Cranial Computerized Tomography & Marie's Ataxia
Arch Neurol 35:55, Aita,J.F., 1978

Dominant Spinopontine Atrophy
Arch Neurol 35:156, Pogacar,S.,et al, 1978

Computerized Tomography & Auditory-evoked Potentials:Use in the Diagnosis of Olivopontocerebellar Degeneration
Arch Neurol 35:143, Gilroy,J.,et al, 1978

Physostigmine in Familial Ataxias
Neurol 27:70, Kark,R.A.,et al, 1977

Spinocerebellar Ataxia & HLA Linkage:Risk Prediction by HLA Typing
NEJM 296:1138, Jackson,J.F.,et al, 1977

Globoid cells, Glial nodules, & Peculiar Fibrillary Changes in the cerebro-hepato-renal Syndrome of Zellweger
Ann Neurol 2:473, deLeon,G.A.,et al, 1977

The Orbit
Arch Ophthalmol 89:152, Trokel,S., 1973

Homonymous Hemioptic Hypoplasia
Br J Ophthalmol 56:537, Hoyt,W.F.,et al, 1972

Olivopontocerebellar Atrophies:A Review
Medicine 49:227, Konigsmark,B., 1970

A Case of Cerebellar Ataxia, with a Discussion of Classification
Arch Neurol 3:71, Locke,S.,et al, 1960

Showing articles 50 to 88 of 88 << Previous