Neudle.com: "pons hypoplasia"

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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 0 to 50 of 88 Next >>

A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
Neurol 104:e210290, Voloshyna-Farber, E.Y.,et al, 2025

Characteristic Head Jerks in Congenital Oculomotor Apraxia due to Joubert Syndrome
Neurol 93:e1125-e1126, Borngraber, F.,et al, 2019

A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
Neurol 89:e220-e223, Xiao, F. & Wang, X.F., 2017

Computed Tomographic Findings in Microcephaly Associated with Zika Virus
NEJM 374:2193-2195, Hazin, A.,et al, 2016

Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency
NEJM 375:1879-1890, Case 34-2016, 2016

Clinicopathologic Conference, Severe Methylenetetrahydrofolate Reductase Deficiency
NEJM 371:847-858, Case 27-2014, 2014

Degenerative Diseases of the Nervous System, Multiple System Atrophy
Adams & Victors Principles of Neurology, Chp 39, pg 1095, Ropper, A.H.,et al, 2014

Degenerative Diseases of the Nervous System, Olivopontocerebellar Atrophy
Adams & Victors Principles of Neurology, Chp 39, pg 1106, Ropper, A.H.,et al, 2014

Neuroimaging in Cockayne Syndrome
AJNR 31:1623-1630, Koob,M.,et al, 2010

Vertebral Artery Hypoplasia: A Predisposing Factor for Posterior Circulation Stroke?
Neurol 68:65-67, Perren,F.,et al, 2007

Clinicopath Conf., Paraneoplastic Cerebellar Degeneration Due to Anti-Yo Antibodies From Breast Cancer
NEJM 356:612-620, Case 4-2007, 2007

Hypoplastic Vertebral Artery: Frequency and Associations With Ischaemic Stroke Territory
JNNP 78:954-958, Park-J.-H.,et al, 2007

Congenital Lymphocytic Choriomeningitis Virus Infection: Spectrum of Disease
Ann Neurol 62:347-355, Bonthius,D.J.,et al, 2007

Oligophrenin 1 Mutations Frequently Cause X-Linked Mental Retardation with Cerebellar Hypoplasia
Neurol 65:1364-1369,1346, Zanni,G.,et al, 2005

Neurologic Features of Horizontal Gaze Palsy and Progressive Scoliosis with Mutations in ROBO3
Neurol 64:1196-1203, Bosley, T.M.,et al, 2005

MR Imaging of Brain-Stem Hypoplasia in Horizontal Gaze Palsy with Progressive Scoliosis
AJNR 25:1046-1048, Rossi, A.,et al, 2004

Evolution of Sporadic Olivopontocerebellar Atrophy Into Multiple System Atrophy
Neurol 55:527-532, Gilman,S. et al, 2000

MRI Findings in Mobius Syndrome: Correlation with Clinical Features
Neurol 55:1058-1060, Pedraza,S.,et al, 2000

Percutaneous Electrical Nerve Stimulation for Low Back Pain,A Randomized Crossover Study
JAMA 281:818-823, Ghoname,E.A.,et al, 1999

Progressive Atrophy of Cerebellum & Brainstem, Age & Size of Expanded CAG Repeats in the MJDI Gene in Machado-Joseph Dis
Ann Neurol 43:288-296, Onokera,O.,et al, 1998

Neuroradiologic Findings in Marinesco-Sjogren Syndrome
AJNR 19:281-283, Georgy,B.A.,et al, 1998

Clinical Usefulness of Magnetic Resonance Imaging in Multiple System Atrophy
JNNP 65:65-71, Schrag,A.,et al, 1998

CAG Repeat Number Correlates with the Rate of Brainstem and Cerebellar Atrophy in Machado-Joseph Disease
Neurol 51:882-884, Abe,Y.,et al, 1998

Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
Neurol 51:1666-1671, Moseley,M.L.,et al, 1998

Bilat Periventricular Nodular Heterotopia with Mental Retard & Syndactyly in Boys:New X-Linked MR Synd
Neurol 49:1042-1047, Dobyns,W.B.,et al, 1997

Atrophy of Cerebellum & Brainstem in Dentatorubral Pallidoluysian Atrophy, CAG Repeat Size on MRI Findings
Neurol 49:1605-1612, Koide,R.,et al, 1997

Machado-Joseph Disease in 4 Chinese Pedigrees:Molecular Analysis of 15 Pts
Neurol 48:482-485, Zhou,Y.X.,et al, 1997

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

Clinicopathological Study of 35 Cases of Multiple System Atrophy
JNNP 58:160-166, Wenning,G.K.,et al, 1995

The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
Neurol 45:311-317, Barth,P.G.,et al, 1995

Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
Neurol 45:24-30, Genis,D.,et al, 1995

Autosomal Dominant Cerebellar Phenotypes:The Genotype has Settled the Issue
Neurol 45:1-5, Rosenberg,R.N., 1995

Double-Blind Study with Levorotatory form of Hydroxytryptophan in Pts with Degen Cerebellar Dis
Arch Neurol 52:451-455, 4401995., Wessel,K.,et al, 1995

PET Studies on the Dopaminergic Sys & Striatal Opioid Binding in the OPCA Variant of Multiple System Atrophy
Ann Neurol 37:568-573, Rinne,J.O.,et al, 1995

Neurodegeneration and Diabetes:UK Nationwide Study of Wolfram (DIDMOAD) Syndrome
Lancet 1458-1463, Barrett,T.G.,et al, 1995

The Brain in Infantile Autism:Posterior Fossa Structures are Abnormal
Neurol 44:214-223, Courchesne,E.,et al, 1994

Evidence of a Congenital Midline Brain Anomaly in Pituitary Dwarfs:A Magnetic Resonance Imaging Study in 101 Patients
Pediatrics 93:409-416, Triulzi,F.,et al, 1994

Trinucleotide Repeat Expansion in Neurological Disease
Ann Neurol 36:814-822, LaSpada,A.R.,et al, 1994

Magnetic Resonance Imaging in Hereditary and Idiopathic Ataxia
Neurol 43:318-325, Wullner,U.,et al, 1993

Wolfram Syndrome:Evidence of a Diffuse Neurodegenerative Disease by Magnetic Resonance Imaging
Neurol 42:1220-1224, 1992,, Rando,T.A.,et al, 1992

Twinning and Neurologic Morbisity
Am J Dis Child 146:1110-1113, Scheller,J.M.&Nelson,K.B., 1992

MRI Findings in Neuro-Behcet's Disease
Neurol 41:405-408, AlKawi,M.Z.,et al, 1991

Brain and Ocular Abnormalities in Infants with In Utero Exposure to Cocaine and other Street Drugs
Am J Dis Child 145:688-695, Dominguez,R.,et al, 1991

Presynaptic Parkinsonism in Olivopontocerebellar Atrophy:Clinical, pathological, and Neurochemical Evidence
Ann Neurol 30:425-428, Pascual,J.,et al, 1991

Neuroanatomy of Fragile X Syndrome:The Posterior Fossa
Ann Neurol 29:26-32, Reiss,A.L.,et al, 1991

Magnetic Resonance Imaging of the Brain in Congenital Rubella Virus and Cytomegalovirus Infections
Neuroradiology 33:239-242, Sugita,K.,et al, 1991

The Marinesco-Sjogren Syndrome Examined by CT, MR, and 18F-2-Fluoro-2-Deoxy-D-Glucose & PET
Arch Neurol 47:1239-1242, Bromberg,M.B.,et al, 1990

Joubert Syndrome:A Clinico-Radiological Study
Neuroradiology 31:502-506, Kendall,B.,et al, 1990

Olivopontocerebellar Atrophy:MR Diagnosis and Relationahip to Multisystem Atrophy
Radiology 174:693-696, Savoiardo,M.,et al, 1990

Showing articles 0 to 50 of 88 Next >>