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abducens nerve paralysis

abducens nerve paralysis, bilateral

acetazolamide

achilles tendon, enlarged

acoustic nerve

Adies pupil

adverse drug reaction

aggression

alcohol

alcohol, neurologic complications with

Alexanders disease

Alexanders disease, adult onset

alpha-fetoprotein

alternating hemiplegia

alternating hemiplegia of childhood

alternating rapid movement

alternating rapid movement, impaired

AMPA receptor antibodies

anti GQ1b IgG antibody

apraxia of eye movements

areflexia

Arnold Chiari malformation

arterial dissection

arterial dissection, vertebral

ataxia telangiectasia

ataxic-dystonia syndromes

autoimmune encephalopathy

autonomic dysfunction

autonomic neuropathy

basal ganglia

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery stenosis

behavioral disorder, acute

benign positional vertigo

brainstem, dysfunction

brainstem, dysfunction, eye movement disorders with

brainstem, glioma

brainstem, hemorrhage, primary

brainstem, hypoplasia

brainstem, infarction of

brainstem, lesion of

brainstem, malformation

brainstem, neoplasms of

carcinoembryonic antigen

CAT scan, emission, abnormal

CAT scan, pelvis

cataracts

celiac disease, adult

central hypoventilation

central nervous system, infection of

cerebellar ataxia, autosomal recessive

cerebellar ataxia, children

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar ataxia, primary

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar disease, eye movement disorder in

cerebellar hemorrhage

cerebellar hypoplasia

cerebellar infarction

cerebellitis, autoimmune

cerebellum

cerebellum, disease of

cerebral edema

cerebral infarction

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrospinal fluid, oligoclonal IgG in

cerebrotendinous xanthomatosis

cerebrovascular accident

cerebrovascular accident, mimics

chenodeoxycholic acid

chest x-ray, abnormal

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

cognition

cogwheel pursuit movements

collagen vascular disease

congenital malformation

conjugate gaze, forced

conjunctivitis

consanguinity

cough

cranial nerve palsies

cranial neuropathy

cranial neuropathy, multiple

cranio-cervical junction

creatine phosphokinase(CPK)elevated

cystic fibrosis, neurologic complications with

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, familial

dementia, rapidly progressive

dentate nuclei, lesion of

depression

developmental abnormality of brain

developmental milestones, loss of

developmental retardation

differential diagnosis

diplopia

dizziness

down-beat nystagmus

down-beat nystagmus, primary position of gaze

downward gaze, paralysis of

DPPX

DPPX, antibodies, encephalitis

drooling

drug induced neurologic disorders

ejection fraction, abnormal

electrocardiogram, abnormal

electromyogram

electroretinograph

encephalitis

encephalitis, autoimmune

encephalitis, brainstem

encephalitis, focal

encephalitis, paraneoplastic

encephalitis, viral

encephalomyelitis

encephalomyelitis, postinfectious

encephalopathy

encephalopathy, parainfectious

encephalopathy, progressive

enzyme, defect

epidemiology of neurology

episodic neurologic deficits

erythema migrans

exercise intolerance

exome sequencing

eye movement, disorders of

eye, pain in

face, numbness of

facial nerve palsy

facial nerve palsy, bilateral

facial weakness, bilateral

familial hemiplegic migraine

fasciculation

fatigue

fever

fine motor function, impaired

finger nose finger test

finger numbness

Fisher's syndrome

flu-like illness

fourth ventricle, enlargement of

Friedreich's ataxia

fundus, abnormality of

gaze palsy, congenital horizontal

gaze palsy, horizontal

gaze palsy, horizontal-bilateral

gaze palsy, supranuclear

genetic neurologic disorders

genetic testing

Gerstmann-Straussler-Scheinker disease

GFAP gene

GluD2

glutamic acid decarboxylase, antibody

granulomatous disease

gray hair

growth retardation

Guillain Barre syndrome

Guillain Barre syndrome, ophthalmoplegia in

Guillain Barre syndrome, variant forms of

hypoparathyroidism, idiopathic

hyposmia

hypothalamus, disturbance of

iatrogenic neurologic disorders

inferior olivary nucleus

insomnia

intellectual deficit

intellectual deterioration

internuclear ophthalmoplegia

internuclear ophthalmoplegia, bilateral

intestinal biopsy

intracranial pressure, increased

iridoplegia

irritability

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

Joubert syndrome

Kearns-Sayre syndrome

kelch-like protein 11 antibodies

labyrinthitis

labyrinthitis, acute

lactic acidemia

lateral medullary syndrome

lateropulsion

lateropulsion, ocular

level of consciousness, decreased

light-near dissociation, causes of

liver disease

Lyme disease

lymphadenopathy

lymphadenopathy, hilar

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

macrocephaly

malabsorption syndrome

malformation, CNS, congenital

malignancy, occult

mammillary bodies

medulla oblongata

medulla oblongata, infarction of

medulla oblongata, lesion of

medulla oblongata, malformation

medulla oblongata, neoplasm of

MELAS syndrome

memory, defect of recent

memory, impairment of

meningismus

meningitis

meningitis, aseptic

meningitis, carcinomatous

meningitis, chronic

meningitis, meningococcal

meningitis, prevention

meningitis, prophylaxis against

meningoencephalitis

mental retardation

mental status, abnormal

metabolic disorder, primary

metabolic disorder, primary-screening tests

microcephaly

midbrain

midbrain, atrophy

midbrain, infarction of

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

mononeuritis multiplex

mortality

movement disorder

movement disorder, extrapyramidal

movement disorder, hyperkinetic

MRI

MRI, abnormal

MRI, angiography

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

multiple system atrophy

muscle weakness, proximal

myopathy, mitochondrial

nerve conduction studies

neuritis

neuroblastoma

neurocutaneous disease

neuroendocrinology

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic examination, focal

neuropathy, peripheral

nystagmus, cerebellar

nystagmus, direction changing

nystagmus, dissociated

nystagmus, gaze-paretic

nystagmus, monocular

nystagmus, pendular

nystagmus, periodic alternating

nystagmus, positional

nystagmus, primary position of gaze

nystagmus, retractorius

nystagmus, rotary

nystagmus, upbeating on upgaze

nystagmus, upbeating-in primary position of gaze

ocular motility, disorders of

oculogyric crisis

olivary degeneration, hypertrophic

one and a half syndrome

ophthalmoplegia

ophthalmoplegia, acute

ophthalmoplegia, bilateral, acute

ophthalmoplegia, progressive external

ophthalmoplegia, total

opsoclonus

opsoclonus, differential diagnosis of

opsoclonus-myoclonus syndrome

optic atrophy

optic neuropathy

optical coherence tomography

paraneoplastic cerebellar degeneration

Parkinson disease, dystonia with

Parkinsonism syndrome

paroxysmal hemiplegia

paroxysmal neurologic deficits

PAS positive

pathology

pelvic mass

periaqueductal lesion

pericarditis

periodic alternating gaze

peripheral nerve, lesion of

pleocytosis of cerebrospinal fluid

pleurisy

pneumoencephalogram(PEG)

pneumonia

polymyositis

polyradiculoneuropathy

pons, hypoplasia

pons, lesion of

pontine glioma

Poretti-Boltshauser syndrome

positional head-hanging test

posterior inferior cerebellar artery syndrome

precipitating factors

progressive ataxia and palatal tremor

progressive multifocal leucoencephalopathy

progressive neurologic disorder

proteinuria

pseudoabducens palsy

pseudointernuclear ophthalmoplegia

psychiatric problems in neurologic disorders

psychomotor retardation

pulmonary infiltrates

pupil, abnormality in neurologic disorders

pupil, dilated and fixed, bilateral

pupil, dilated, bilateral

pupil, ectopic-acquired

pupil, light reflex, abnormal

pupil, tonic

pure motor hemiplegia

Purkinje cell

Purkinje cell surface antibody

purpura

pursuit eye movements, abnormal

pyramidal tract dysfunction

pyramidal tract, uncrossed

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

radiation hypersensitivity

ragged-red fibers

rapid onset dystonia parkinsonism

rapidly progressing neurologic illness

reading disorder, acquired

real-time quaking-induced conversion

recurrent

reflex, brainstem

remote effect of cancer on the nervous system

renal failure

renal stones

respirations in CNS disease

respiratory tract infection

saccadic eye movements, abnormal

salivation, excessive

scoliosis, neurologic association with

sedimentation rate, elevated

seizure

seizure, children

seminoma

sensorineural hearing loss

Sjogren's syndrome, neurologic manifestations of

skew deviation

skew deviation, alternating

skin, lesions in neurologic disorders

skull x-ray

skull x-ray, abnormal

sleep apnea, obstructive

sleep pathology and physiology

slurred speech

speech disorder

speech disorder, childhood

speech disorder, non aphasic

speech, delayed development of

spinal cord, lesion of

spinal muscular atrophy

spinocerebellar ataxia

spinocerebellar ataxia type 1

spinocerebellar ataxia type 2

spinocerebellar ataxia type 28

spinocerebellar ataxia type 6

spinocerebellar ataxia type 7

spinocerebellar degeneration

spontaneous remission

sports medicine, neurology of

square wave jerks

staggering

status epilepticus

steroid therapy, CNS treatment and complications with

strabismus

strokelike episodes

sweating

sweating, abnormality of

swimming

symmetric brain lesions

syphilis, neurologic complications with

temporal lobe, lesion

teratoma

teratoma, ovarian

thalamus, lesion of

thalamus, lesion of-bilateral

thiamine

thiamine deficiency

third nerve

third nerve lesions, nuclear

third nerve palsy

third nerve palsy, partial

third ventricle, wall

thyrotropin-releasing hormone

tonsillar herniation of cerebellum

transient ischemic attack

treatment of neurologic disorder

triangle of Guillain and Mollaret

trigeminal neuralgia

trigeminal neuropathy

trigeminal neuropathy, sensory

trinucleotide repeats

vertigo, treatment of

vestibular function, tests of

vestibular neuritis

vestibulopathy

vibratory sensation, abnormal

viral infection

vision, blurred

visual loss

visual loss, progressive

voice, abnormality of

walking frame

walking, difficulty with

weakness

weight loss

Wernekinck commissure syndrome

Wernicke's encephalopathy

Showing articles 0 to 50 of 18280 Next >>

Unmasking Cerebrotendinous Xanthomatosis, Clinical Recognition of a Treatable Cause of Progressive Ataxia
Neurol 105:e214099, Mizutani,H.,et al, 2025

Expanding Clinical Spectrum an Anti-GQ1b Antibody Syndrome, A Review
JAMA Neurol 81:762-770, Lee,S-U.,et al, 2024

A 50-Year-Old Man with Ataxia, Dystonia, and Abnormal Ocular Movements
Neurol 103:e210046, Panigrahi,B.,et al, 2024

A Dizzy Architect
Neurol 98:543-549, Scutelnic, A.,et al, 2022

A 48-Year-Old Woman Presenting with Vertigo, Ptosis, and Red Eyes
Neurol 98:678-683, Kim, K.T.,et al, 2022

A 37-Year-Old Man with Involuntary Movements, Gait Disturbance, and Hyperasthesia
Neurol 98:851-853, Meng, D.,et al, 2022

The Phenotypic Continuum of ATP1A3-Related Disorders
Neurol 99:e1511-e1526, Vezyroglou,A., et al, 2022

Clinicopathologic Conference, Cerebellar Ataxia, Neuropathy and Vestibular Areflexia Syndrome
NEJM 385:165-175, Case 20-2021, 2021

A 28-Year-Old Woman with Vision Loss and an Unusual Gait
Neurol 97:e1860-e1865, Dohlman, J.C.,et al, 2021

An Adolescent Girl Presenting with Worsening Vertigo, Headache, and Ataxia
Neurol 95:e1760-e1763, Brigham, E.,et al, 2020

Palatal Myoclonus, Abnormal Eye Movements, and Olivary Hypertrophy in GAD65-Related Disorder
Neurol 94:273-275, Macaron, G.,et al, 2020

Progressive Ataxia and Palatal Tremor
Neurol 94:e1445-e1447, Pradeep, S.,et al, 2020

A 16-year-old Girl with Ataxia, Oscillopsia, and Behavioral Changes
Neurol 94:713-717, Silverman, A.,et al, 2020

Clinicopathologic Conference, Creutzfeldt-Jakob Disease
NEJM 381:1569-1578, Case 32-2019, 2019

Pyruvate Dehydrogenase Deficiency (PDCD)
eMedicine.medscape,com, Aug, Frye,R.E.,et al, 2018

Glutamate Receptor D2 Serum Antibodies in Pediatric Opsoclonus Myoclonus Ataxia Syndrome
Neurol 91:e714-e723, Berridge, G.,et al, 2018

Early-Onset Head Titubation in a Child with Poretti-Boltshauser Syndrome
Neurol 88:1478-1479, Masson, R.,et al, 2017

Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
NEJM 376:1668-1678, CASE 13-2017, 2017

Clinical Manifestations of the anti-IgLON5 Disease
Neurol 88:1736-1743,1688, Gaig, C.,et al, 2017

Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches
Front Neurol doi:10.3389/fneur.2017.00472, Velazquez-Perez, L.C.,et al, 2017

Wernekink Commissure Syndrome Secondary to Bilateral Caudal Paramedian Midbrain Infarction Presenting with a Unique "Heart or V" Appearance Sign:Case Report and Review of the Literature
Front Neurol soi.10.3389/fneur.2017.00376,Aug, Zhou,C.,et al, 2017

Clinicopathologic Conference, Dissection of the left vertebral artery and cerebellar infarction
NEJM 369:1736-1748, Case 34-2013, 2013

Miller Fisher Syndrome with Positivity of Anti-GAD Antibodies
Clin Neurol Neurosurg 115:1479-1481, Pietrini, V.,et al, 2013

The Autosomal Recessive Cerebellar Ataxias
NEJM 366:636-646, Anheim,M.,et al, 2012

GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
Neurol 77:1287-1294, Prust, M.,et al, 2011

Sjogren Syndrome: Neurologic Complications
www.Medlink.com,Jan, Roman,G.C., 2010

MR Imaging Findings in 56 Patients with Wernicke Encephalopathy: Nonalcoholics May Differ from Alcoholics
AJNR 30:171-176, Zuccoli,Z.,et al, 2009

HINTS to Diagnose Stroke in the Acute Vestibular Syndrome: Three-Step Bedside Oculomotor Examination More Sensitive Than Early MRI Diffusion-Weighted Imaging
Stroke 40:3504-3510, Kattah,J.,et al, 2009

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

West Nile Virus Presenting as Opsoclonus-myoclonus Cerebellar Ataxia
Neurol 64: 1095-1096, Khosla,J.S., 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

Clinicopath Conf., Meningencephalitis and Sepsis Due to Neisseria Meningitidis Infection
NEJM 349:2341-2349, Case 38-2003, 2003

Positional Down Beating Nystagmus in 50 Patients: Cerebellar Disorders and Possible Anterior Semicircular Canalithiasis
JNNP 72:366-372, Bertholon,P.,et al, 2002

Clinicopath Conf, Primary Lymphoma of CNS
NEJM 346:1009-1015, Case 10-2002, 2002

Recessive Ataxia With Ocular Apraxia
Arch Neurol 58:201-205,173, Barbot,C.,et al, 2001

Opsoclonus as a Dominant Sign in Primary Sjogrens Syndrome
Neuro-Opthlhal 22:135-138, Lubec,D.,et al, 1999

Spinocerebellar Ataxia Type 6, Frequency of the Mutation & Genotype-Phenotype Correl
NEurol 49:1247-1251, Geschwind,D.H.,et al, 1997

Familial Hemiplegic Migraine, Nystagmus and Cerebellar Atrophy
Ann Neurol 39:100-106, Elliott,M.A.,et al, 1996

Opsoclonus
Semin Neurol 16:21-26, Averbuch-Heller,L.&Remler,B., 1996

Clinicopath Conf
Ganglioneuroblastoma of Adrenal Gland, Opsoclonus-Myoclonus-Ataxia Syndrome, Paraneoplastic, Case 27, 199EJM 333:579-586,1995., 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

Anti-Ri Antibodies Associated with Opsoclonus and Progressive Encephalomyelitis with Rigidity
Neurol 44:1521-1522, Casado,J.L.,et al, 1994

Pure Midbrain Infarction:Clinical Syndromes, MRI, and Etiologic Patterns
Neurol 44:2032-2040, Bogousslavsky,J.,et al, 1994

Abnormal Eye Movements in Creutzfeldt-Jakob Disease
Ann Neurol 34:192-197, Grant,M.P.,et al, 1993

Periodic Alternating Gaze Deviation in Infancy
Neurol 42:1740-1743, Legge,R.H.,et al, 1992

Anti-Ri:An Antibody Associated with Paraneoplastic Opsoclonus and Breast Cancer
Ann Neurol 29:241-251, Luque,F.A.,et al, 1991

Acetazolamide-Responsive Vestibulocerebellar Syndrome:Clinical & Oculographic Features
Neurol 41:429-433, Baloh,R.W.&Winder,A., 1991

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

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

Showing articles 0 to 50 of 18280 Next >>