Neudle.com: pontocerebellar degeneration

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acetylcholine

advances in neurology

aneurysm, thoracic aortic

angiography, cerebral

anomic aphasia

anticholinesterase

anticonvulsants

anticonvulsants, selection of

antineutrophil cytoplasmic autoantibodies

aortic wall, thickened

aortitis

aphasia

aphasia, progressive, primary

aphasia, transcortical

aphasia, transcortical-motor

apolipoprotein E

apraxia

apraxia of eye movements

apraxia, constructional

apraxia, speech

areflexia

arterial dissection

arterial dissection, aorta

arterial dissection, carotid

arterial dissection, wall thickness

arteriovenous malformation

arteritic anterior ischemic optic neuropathy

auditory evoked brainstem potentials

autonomic dysfunction

basal ganglia, degeneration

basal ganglia, lesion, bilateral

calcification, lymph node

carcinoma

carcinoma of breast

cardiomyopathy

carotid artery disease

carotid artery stenosis

carotid artery stenosis, tandem

carpal tunnel syndrome

CAT scan

CAT scan, abnormal

CAT scan, angiography

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, orbits

cavernous sinus

cavernous sinus, lesion of

cavernous sinus, syndrome

central bright spot sign

central retinal artery occlusion

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar degeneration

cerebellar lesion

cerebellar vermis

cerebellum

cerebral cortical atrophy

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, prevention of

chemosis

cherry red spot

cherry red spot-myoclonus syndrome

chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids

cigarette smoking

Clinical Pathologic Conference(C.P.C.)

cobalt toxicity

cognition

color vision, impaired

complications

congestive heart failure

conjunctival engorgement

conjunctival injection

controversies in neurology

corpus callosum

corpus callosum, atrophy of

cortical-basal ganglionic degeneration

cough

cranial nerve enhancement

cranial nerve enlargement

cranial nerve palsies

cranial nerve palsies, unilateral

cranial nerve palsy, alternating

cranial neuropathy

cranial neuropathy, multiple

C-reactive protein, elevated

degenerative diseases of CNS

dementia

dementia, frontotemporal

dentate nuclei, lesion of

dentatorubral-pallidoluysian atrophy

differential diagnosis

diplopia

donut sign

down-beat nystagmus, primary position of gaze

drug abuse

drug abuse, neurologic complications of

dysarthria

dyskinesia, buccal lingual facial

dysphagia

dyspnea

dyspraxia

dysthyroid ocularmyopathy

ejection fraction, abnormal

emergencies, neurologic

eosinophilic granulomatosis with polyangiitis

extraocular muscle enlargement

extraocular muscle lesion

extraocular muscle, metastasis to

eye movement, disorders of

eye movement, painful

fistula, arterio-venous

fistula, arterio-venous, carotid-cavernous

fragile-X syndrome

Friedreich's ataxia

frontal behavioral spatial syndrome

fundus, abnormality of

gaze palsy, supranuclear

genetic neurologic disorders

globe, flattened posteriorly

globus pallidus, lesion of

glutamate dehydrogenase deficiency

glutamic acid

granulomatosis with polyangiitis

Graves ophthalmopathy

halo sign

headache

headache, bitemporal

headache, retro-orbital

headache, unilateral

hearing loss

heralding manifestation

herpes zoster

herpes zoster, ophthalmicus

hydroxytryptophan L-5(L-5 HTP)

hypothalamus, lesion of

internal carotid artery

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

intracranial hypertension, benign

intracranial hypertension, benign, differential diagnosis

intracranial hypertension, benign, pathogenesis of

intracranial pressure, increased

Jakob-Creutzfeldt disease

jaw claudication

jaw pain

jocularity

lacrimal gland enlargement

Lafora's disease

language disorder in adults

liver function enzymes

lobar atrophy

lymph node biopsy

lymphadenopathy

lymphadenopathy, hilar

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

macroglobulinemia

macular degeneration

malformation, vascular

malignant optic glioma of adulthood

memory, defect of recent

memory, impairment of

meningeal enhancement

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, angiography

MRI, contrast enhanced

MRI, cranial nerves

MRI, diffusion weighted

MRI, extraocular muscle enhancement

MRI, FLAIR

MRI, nodular enhancement

MRI, vessel wall enhancement

mucormycosis

multimodal neuroimaging

multiple system atrophy

muscle biopsy, extraocular

myoclonus, stimulus sensitive

myopathy, necrotizing

myopathy, steroid responsive

myositis

myositis, ocular

myotonia dystrophica

necrotizing vasculitis

neoplasm, metastatic

neoplasm, metastatic to CNS

neoplasm, metastatic to eye

neoplasm, metastatic to muscle

neoplasm, metastatic to orbit

neuroaxonal degeneration

neurofibromatosis 1

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, diagnoses of, clinical bedside

neurologic disease, tempo

neurologic signs

neurologic symptoms

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology

neuropathology, brain

ocular motility, disorders of

ophthalmic artery

ophthalmoplegia

ophthalmoplegia, painful

ophthalmoplegia, total

ophthalmoplegia, unilateral

optic atrophy

optic canal

optic canal, enlargement of

optic chiasm, enhancement

optic chiasm, enlarged

optic chiasm, lesion of

optic nerve sheath enhancement

optic nerve, biopsy

optic nerve, enhancement

optic nerve, enlarged

optic nerve, lesion of

optic nerve, neoplasm of

optic nerve, tortuosity

optic neuritis

optic neuropathy

optic neuropathy, bilateral

optic neuropathy, ischemic

optic neuropathy, ischemic, anterior

optic neuropathy, ischemic, posterior

orbit, inflammation in

orbit, lesions of

orbit, mass

orbit, neoplasms of

orbit, pseudotumor of

orbital apex

orbital apex syndrome

orbital compartment syndrome

orthostatic hypotension

Parkinson disease, atypical

Parkinson disease, dementia with

Parkinson disease, differential diagnosis of

Parkinson disease, L-dopa nonresponsive

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

pathology

perineuritis

perineuritis, optic

perivascular enhancement

personality change

photophobia

photosensitivity, skin

physostigmine

Pick's disease

pleocytosis of cerebrospinal fluid

polymerase chain reaction

pons, atrophy

pons, lesion of

pontocerebellar atrophy

postoperative neurologic complications

postoperative visual loss

postpartum

pregnancy, neurologic complications in

prognosis

progressive myoclonic epilepsy

progressive neurologic disorder

progressive supranuclear palsy

proptosis

proptosis, unilateral

proteinopathy

pseudobulbar palsy

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

ptosis

ptosis, unilateral

puerperium

pupil, abnormality in neurologic disorders

pupil, dilated, unilateral

pupil, midposition and fixed, unilateral

Purkinje cell

purpura

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract dysfunction

radiation therapy, CNS treatment and complications with

rapidly progressing neurologic illness

retinopathy, ischemic

saccadic eye movements

saccadic eye movements, abnormal

salivary gland enlargement

Saturday night retinopathy

scalp tenderness

scotoma

sedimentation rate

sedimentation rate, elevated

seizure

seizure, paradoxical

seizure, treatment of

sella turcica, enlargement of

sensorineural hearing loss

sensory loss

sensory loss, cortical

serum alanine aminotransferase

skin, lesions in neurologic disorders

sleep apnea

sleep pathology and physiology

speech disorder

sphenoid sinus

sphenoid sinus biopsy

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

Spot sign

steroid

steroid therapy, CNS treatment and complications with

striatonigral degeneration

subthalamic nucleus

suck reflex

superior ophthalmic vein, dilated

temporal artery, biopsy

temporalis muscle enhancement

temporalis muscle swelling

tissue plasminogen activator, intravenous

tongue, enlarged

tram-track sign

transient neurologic deficit

trazodone

treatment of neurologic disorder

tremor

tremor, intention

trigeminal neuropathy

trigeminal neuropathy, sensory

trinucleotide repeats

Unverricht-Lundborg disease

upgaze, paralysis of

uveitis

vasculitides

vasculitis, large vessel

vertebral artery wall thickness

vision, blurred

vision, blurred, monocular

visual acuity, decreased

visual acuity, decreased, monocular

visual field defect

visual field defect, altitudinal

visual loss

visual loss, alternating

visual loss, permanent

visual loss, progressive

visual loss, sudden

visual loss, sudden-unilateral

visual loss, transient

visual symptoms

visuospatial disturbance

vitiligo

Vogt-Koyanagi-Harada syndrome

Waldenstrom's macroglobulinemia

weight loss

Wernicke's aphasia

white matter disease

X-linked bulbospinal neuronopathy

Showing articles 50 to 100 of 115 << Previous Next >>

Imaging-Pathologic Correlation in Corticobasal Degeneration
AJNR 30:1884-1892, Tokumaru,A.,et al, 2009

Progressive Myoclonic Epilepsies: A Review of Genetic and Therapeutic Aspects
Lancet Neurol 4:239-248, Shahwan, A., et al, 2005

Recent Developments in Thyroid Eye Disease
BMJ 329:385-390, Cawood,T.,et al, 2004

Correlation Between Antemortem Magnetic Resonance Imaging Findings and Pathologically Confirmed Corticobasal Degeneration
Arch Neurol 61:1881-1884, Josephs,K.A.,et al, 2004

Central Retinal Artery Occlusion and Ophthalmoplegia Following Spinal Surgery
BR J Ophthalmol;88-1350-1352, Halfon, M.J.,et al, 2004

Language Function and Dysfunction in Corticobasal Degeneration
Neurol 61:493-499, Graham,N.L.,et al, 2003

Genetic Testing in Spinocerebellar Ataxias
Arch Neurol 58:191-195, Tan,E. &Ashizawa,T., 2001

Language Disturbances in Corticobasal Degeneration
Neurol 54:990-992, Frattali,C.M.,et al, 2000

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

Pathologic Heterogeneity in Clinically Diagnosed Corticobasal Degeneration
Neurol 53:795-800, Boeve,B.F.,et al, 1999

Dementia as the Most Common Presentation of Cortical-Basal Ganglionic Degeneration
Neurol 53:1969-1974, Grimes,D.A.,et al, 1999

Natural History & Survival of 14 Pts with Corticobasal Degeneration Confirmed as Postmortem Exam
JNNP 64:184-189, Wenning,G.K.,et al, 1998

Atrophy of the Corpus Callosum, Cortical Hypometabolism, and Cognitive Impairment in Corticobasal Degeneration
Arch Neurol 55:609-614, Yamauchi,H.,et al, 1998

Clinical Presentation and Pharmacological Therapy in Corticobasal Degeneration
Arch Neurol 55:957-961, Kompoliti,K.,et al, 1998

Fluid Attenuation Inversion Recovery (FLAIR) Images of Dentatorubropalliodoluysian Atrophy:Case Report
JNNP 65:396-399, Yoshii,F.,et al, 1998

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

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

Frontotemporal Degeneration, Pick Disease, and Corticobasal Degeneration
Arch Neurol 54:1425-1427, 14291997., Neary,D., 1997

Frontotemporal Dementia, Pick Disease, and Corticobasal Degeneration
Arch Neurol 54:1427-1429, Kertesz,A., 1997

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

Accuracy of the Clinical Diagnosis of Corticobasal Degeneration:A clinicopathologic Study
Neurol 48:119-125, Litvan,I.,et al, 1997

Corticobasal Degeneration:Neuropathologic and Clinical Heterogeneity
Neurol 48:959-969, Schneider,J.A.,et al, 1997

Unusual Clinical Presentations of Cortical-Basal Ganglionic Degeneration
Ann Neurol 40:893-900, Bergeron,C.,et al, 1996

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

Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
Ann Neurol 37:769-775, Ikeuchi,T.,et al, 1995

Apolipoprotein E Genotype in Diverse Neurodegenerative Disorders
Ann Neurol 38:131-135, Schneider,J.A.,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

Eye Movements in Parkinsonian Syndromes:Vidailhet
M. , et al, Neurol 35:420-42694., , 1994

Trinucleotide Repeat Length and Rate of Progression of Huntington's Disease
Ann Neurol 36:630-635, Illarioshkin,S.N.,et al, 1994

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

Gliomas of the Anterior Visual Pathway
Surv Ophthalmol 38:427-452, Dutton, J., 1994

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

Stimulus-Sensitive Myoclonus in Akinetic-Rigid Syndromes
Brain 115:1875-1888, Chen,R.,et al, 1992

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

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

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

Cortical-Basal Ganglionic Degeneration
Neurol 40:1203-1212, Riley,D.E.,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

Hereditary Dentatorubral-Pallidoluysian Atrophy:Clinical and Pathologic Variants in a Family
Neurol 38:1065-1070, Takahashi,H.,et al, 1988

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

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

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

Showing articles 50 to 100 of 115 << Previous Next >>