Neudle.com: "dysarthria-clumsy hand syndrome"

Differential
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acetazolamide

Addison's disease

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adrenoleukodystrophy, carrier

akinetic mute

alternating rapid movement

alternating rapid movement, impaired

amyotrophic lateral sclerosis

ataxia telangiectasia

attention deficit disorder with hyperactivity

attention span

Babinski sign

basal ganglia, degeneration

basal ganglia, lesion of

basal ganglia, lesion, bilateral

biologic markers

bone marrow transplantation

bradykinesia

brain atrophy

brainstem, infarction of

brainstem, lesion of

brainstem, neoplasms of

cerebellar ataxia, autosomal recessive

cerebellar ataxia, hereditary

cerebellar ataxia, neuropathy and vestibular areflexia syndrome

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar hemorrhage

cerebellar infarction

cerebellum, disease of

cerebral cortex

cerebral cortical atrophy

cerebral embolism

cerebral embolism, cardiac origin

cerebral palsy

cerebral palsy, associated problems with

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, gammaglobulin of

cerebrovascular accident

Charcot-Marie-Tooth

children

chorea

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

cognition

congestive heart failure

consanguinity

corona radiata

cortical-basal ganglionic degeneration

cough

cranial neuropathy

cultured skin fibroblasts

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, rapidly progressive

depression

developmental milestones, loss of

down-beat nystagmus, primary position of gaze

drooling

dying

dysarthria

dysarthria-clumsy hand syndrome

dystonia musculorum deformens

dystonia, cervical

electroencephalogram, abnormalities of

electromyogram

electrophoretic pattern, CSF

embolism

encephalitis

encephalopathy

epileptic encephalopathy

exome sequencing

eye movement, disorders of

failure to thrive

falling

familial

familial periodic ataxia

FARS2 deficiency

fatigue

fine motor function, impaired

finger nose finger test

Friedreich's ataxia, late onset

gait disorder

gaze palsy

gaze palsy, supranuclear

genetic diagnosis, prenatal

genetic neurologic disorders

genetic screening

genetic testing

Gerstmann-Straussler-Scheinker disease

glabellar sign

granular osmiphilic material

hepatolenticular degeneration(Wilson's disease)

hepatosplenomegaly

heralding manifestation

hypogonadism, hypogonadotropic

hypometric saccades

hypotonia

iatrogenic neurologic disorders

inferior olivary nucleus

insomnia

intellectual deficit

intellectual deterioration

intelligence quotient

internal capsule

introverted

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, variant

jaundice

Kayser-Fleischer ring

lacunar infarction

lacunar infarction, differential diagnosis of

lateropulsion

leg weakness, bilateral

leukodystrophy

leukoencephalopathy

lipid storage disorder of CNS

liver disease

Lorenzo's oil

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

medulla oblongata, neoplasm of

memory, defect of recent

memory, impairment of

meningitis, CSF cell count-normal

microcephaly

midbrain, atrophy

misdiagnosis

mitochondrial disease

molecular genetics

motor neuron disease

movement disorder

movement disorder, extrapyramidal

MRI

MRI, abnormal

MRI, contrast enhanced

MRI, diffusion weighted

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

myelomalacia

myelopathy

myelopathy, chronic progressive

myoclonic jerks

myoclonus

nausea and vomiting

neoplasm, primary of CNS

neoplasm, primary of CNS-children

nerve conduction studies

neurofibrillary degeneration

neurofibromatosis 1

neurologic disease, diagnoses of

neurologic signs

neurologic symptoms

neuronal ceroid-lipofuscinosis

neuropathology

neuropathy

neuropathy, demyelinating

neuropathy, hereditary peripheral

neuropathy, sensory

next-generation sequencing

Niemann-Pick disease

numb clumsy hands syndrome

nystagmus

ocular motility, disorders of

olivary degeneration, hypertrophic

paraparesis, familial spastic

paraparesis, spastic

Parkinson disease

Parkinsonism syndrome

positional head-hanging test

prevention of neurologic disorders

prion disease

prion protein gene

prognosis

progressive ataxia and palatal tremor

progressive myoclonic epilepsy

progressive neurologic disorder

proprioception, abnormal

protein 14-3-3, cerebrospinal fluid

psychiatric disorder

psychiatric problems in neurologic disorders

psychological testing

psychological testing, neurologic problems

psychosis

pure dysarthria

pure motor hemiplegia

pursuit eye movements, abnormal

pyramidal tract dysfunction

rapidly progressing neurologic illness

reading disorder, acquired

real-time quaking-induced conversion

rubella encephalitis, progressive

rubella virus

saccadic eye movements, abnormal

sensorineural hearing loss

sensory loss

serologic testing

serologic testing of cerebrospinal fluid

slit lamp examination

speech disorder, non aphasic

spinal cord

spinal cord, lesion of

spinocerebellar ataxia

splenomegaly

spontaneous remission

superior cerebellar artery infarction

superior cerebellar artery syndrome

symmetric brain lesions

tandem gait, ataxic

tau protein

tauopathy

thalamus, lesion of-bilateral

titubation

toe walking

transient neurologic deficit

treatment of neurologic disorder

tremor

tremor, cerebellar

tremor, intention

trinucleotide repeats

upgaze, paralysis of

vertigo

vertigo, episodic

very long chain fatty acids

vestibulopathy

vibratory sensation, abnormal

viral infection, CNS

vision, blurred

vitamin E deficiency

voice, abnormality of

walking frame

walking, difficulty with

weakness

weakness, progressive

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Syndromes of Pontine Base Infarction:A Clinical-Radiological Correlation Study
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Clinical Anatomic Study of Pure Dysarthria
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Infarction in the Anterior Rostral Cerebellum (the Territory of the Lateral Branch of the Superior Cerebellar Artery)
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Dysarthria-Clumsy Hand Syndrome & Cerebellar Hemorrhage
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Clinical Assessment of 31 Patients with Wilson's Disease, Correlations with Struct. Changes on MRI
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