Neudle.com: "dysdiadochokinesia"

Differential
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acute ataxia of childhood

acute cerebellar ataxia

adult-onset leukodystrophy, with neuroaxonal spheroids

alcohol intolerance

alternating rapid movement

alternating rapid movement, impaired

ataxia telangiectasia

autoimmune cerebellar ataxia

autoimmune encephalopathy

axonal spheroid

Babinski sign

basal ganglia, lesion of

basal ganglia, lesion, bilateral

cauda equina, enhancement

cerebellar ataxia, autosomal recessive

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar cognitive affective syndrome

cerebellar degeneration

cerebellar lesion

cerebellitis

cerebellitis, autoimmune

cerebellum, disease of

cerebral cortex

cerebral cortical atrophy

cerebrospinal fluid, oligoclonal IgG in

ceruloplasmin, serum

choking

chromosomal abnormality

Claude's syndrome

Clinical Pathologic Conference(C.P.C.)

corpus callosum, lesion of

cough

cranial nerve enhancement

cranial neuropathy

cranial neuropathy, multiple

Creutzfeldt-Jakob disease, genetic

deep gray nuclei

degenerative diseases of CNS

dementia

dementia, familial

dementia, presenile

dementia, rapidly progressive

difficulty climbing stairs

diplopia

disability, neurological

dizziness

DPPX

DPPX, antibodies, encephalitis

encephalitis, autoimmune

encephalomyelitis, postinfectious

enolase

Epstein-Barr virus

esophageal varices

eye movement, disorders of

facial expression abnormality

falling

familial

fatigue

fine motor function, impaired

finger nose finger test

frontal lobe, anatomy and physiology

gait disorder

gammaglobulin therapy, intravenous

gaze palsy, horizontal

gene

gene mutation

genetic neurologic disorders

genetic testing

genu of corpus callosum

granular osmiphilic material

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

iatrogenic neurologic disorders

inclusion bodies, eosinophilic cytoplasmic

incoordination

infectious mononucleosis

infectious mononucleosis, neurologic findings with

inferior olivary nucleus

insomnia

intellectual deficit

intellectual deterioration

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

Kayser-Fleischer ring

lateropulsion

leukodystrophy

leukoencephalopathy

leukoencephalopathy, adult onset, sporadic

leukopenia

liver disease

liver function enzymes

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

masked facies

memory, defect of recent

memory, impairment of

meningeal enhancement

mental status, abnormal

midbrain

midbrain, atrophy

midbrain, infarction of

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, diffusion weighted

MRI, false negative

MRI, negative

MRI, punctate pattern

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

muscle biopsy

myelinolysis, extrapontine

nerve conduction studies

nerve root biopsy

neuroaxonal dystrophy

neuroaxonal leukodystrophy

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic signs

neuron specific enolase

neuronal ceroid-lipofuscinosis

neuronopathy, sensory

numbness, generalized

nystagmus

olivary degeneration, hypertrophic

ophthalmoplegia, progressive external

optic atrophy

osmotic demyelination syndrome

otitis, neurologic complications with

palatal myoclonus

paraneoplastic cerebellar degeneration

paresthesias

paresthesias, hands

Parkinson disease

Parkinsonism syndrome

PAS positive

PAS positive material in the brain

penicillamine

personality change

pleocytosis of cerebrospinal fluid

POLG1 gene

polyneuropathy, chronic inflammatory demyelinating

pons, lesion of

positional head-hanging test

post infectious cerebellar ataxia

postinfectious

postural abnormality

pregnancy, neurologic complications in

prion disease

prognosis

progressive ataxia and palatal tremor

progressive neurologic disorder

protein 14-3-3, cerebrospinal fluid

protein 14-3-3, cerebrospinal fluid, false negative

psychiatric disorder

psychiatric problems in neurologic disorders

psychosis

ptosis

ptosis, bilateral

pursuit eye movements, abnormal

rapidly progressing neurologic illness

reading disorder, acquired

real-time quaking-induced conversion

rehabilitation for neurologic disorders

remote effect of cancer on the nervous system

saccadic eye movements, abnormal

seizure

slit lamp examination

slurred speech

spasticity

speech disorder

speech disorder, non aphasic

spinocerebellar ataxia

spinocerebellar ataxia type 7

splenomegaly

spongy degeneration of brain

spontaneous remission

storage disease of CNS

stuttering

suicide

symmetric brain lesions

thalamus, lesion of-bilateral

third nerve palsy

third nerve palsy, bilateral

thrombocytopenia

titubation

treatment of neurologic disorder

tremor

tremor, cerebellar

tremor, intention

trientine dihydrochloride

trinucleotide repeats

upgaze, paralysis of

vertigo

vestibulopathy

vibratory sensation, abnormal

viral infection

viral infection, CNS

vision, blurred

visual acuity, decreased

vitamin E deficiency

vitiligo

voice, abnormality of

walking frame

walking, difficulty with

weakness

weakness, progressive

Showing articles 0 to 22 of 22

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

More Than a Little Unsteady
NEJM 387:e9, Kraft, A.W.,et al, 2022

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

A 47-year-old Man with Rapidly Progressive Ataxia and Vitiligo
Neurol 94:e1664-e1669, Han, F.,et al, 2020

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

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

Clinical Reasoning: A 49-year-old man with Progressive Numbness, Weakness, and Evidence of Leptomeningeal Enhancement
Neurol 90:e90-e93, Lovett, A.,et al, 2018

A 27-year-old man with Acute-Onset Ataxia
Neurol 88:e207-e211, Risco, J. & Weiss, M., 2017

A 58-year-old man with Progressive Ptosis and Walking Difficulty
Neurol 89:e1-e5, Kuo, P.,et al, 2017

A 40-year old Woman with Difficulty Going Down Stairs in High-Heeled Shoes
Ann Neurol 77:1-7, Scripko, P.,et al, 2015

Progressive Neuropsychiatric Symptoms and Motor Impairment
JAMA Neurol 71:794-798, Ghadiri, M.,et al, 2014

Clinicopathologic Conference, Acute Infectious Mononucleosis due to Epstein-Barr Virus Infection, Complicated by Acute Otitis Media and Postinfectious Cerebellitis
NEJM 369:1253-1261, Case 30-2013, 2013

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

Clinicopathologic Conference, Kufs Disease (Autosomal Dominant) Parry Type Neuronal Ceroid Lypofuscinosis
NEJM 364:1062-1074, Case 8-2011, 2011

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

Clinicopath conf., Human Prion Disease, Sporadic CJD
Neurol 69:1881-1887, Geschwind,M.D., et al, 2007

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

Midbrain Syndromes of Benedikt, Claude, and Nothnagel:Setting the Record Straight
Neurol 42:1820-1822, Liu,G.T.,et al, 1992

Wilson Disease
Medicine 71:139-164, Brewer,G.J.&Yuzbasiyan-Gurkan,V., 1992

Neurological and Neuropsychiatric Spectrum of Wilson's Disease:A Prospective Study of 45 Cases
J Neurol 238:281-287, Oder,W.,et al, 1991

Clinical Assessment of 31 Patients with Wilson's Disease, Correlations with Struct. Changes on MRI
Arch Neurol 44:365-370, Starosta-Rubinstein,S.,et al, 1987

A Simple Test of Cordination in the Fingers
Neurol 10:745, Fisher,C.M., 1960

Showing articles 0 to 22 of 22