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Goldstein, Norman

A5112250528 | I1330342723

Mayo Clinic

Mayo Clinic

Citations 14

Dysarthria in Multiple Sclerosis

Journal of Speech and Hearing Research | July 29, 2014 | Volume: 15 | Issue: 2 | Pages: 229-245

10.1044/jshr.1502.229 | PMID 5047862

Less than half of a series of 168 patients with multiple sclerosis presented significant speech deviations. The most frequent speech deviations observed were impaired loudness control and harshness; less frequently occurring deviations were defective articulation, restricted use of vocal variations for emphasis, poor pitch control, hypernasality, inappropriate pitch level, and breathiness. “Scanning speech” was not a prominent characteristic. Speech deviations were not solely attributable to cerebellar involvement. Their incidence was positively related to severity of neurologic involvement, becoming more prominent as additional motor systems were implicated.
Dysarthria in Wilson’s Disease

Journal of Speech and Hearing Research | July 29, 2014 | Volume: 17 | Issue: 2 | Pages: 169-183

10.1044/jshr.1702.169 | PMID 4836038

Three judges rated a number of speech characteristics of 20 patients with Wilson’s disease, an inherited metabolic disease. The perceptual data suggest the presence of a mixed dysarthria with prominent ataxic, spastic, and hypokinetic features which were predictable from neurologic data on the patients. Perceptual data on 10 patients, recorded at two specific points in a treatment program, indicate that speech can be used as an effective monitor of progress in the treatment of this disease.
Some where's and why's of neuritis

Neurology | May 13, 2012 | Volume: 8 | Issue: 3 | Pages: 187-187

10.1212/wnl.8.3.187 | PMID 13517484

Experimental Allergic Encephalomyelitis Following Administration of Homologous Brain Lipid Fractions

Neurology | May 13, 2012 | Volume: 5 | Issue: 8 | Pages: 550-550

10.1212/wnl.5.8.550 | PMID 13244769

Relationship of Homologous Brain Proteolipid to Allergic Encephalomyelitis in Guinea Pigs

Neurology | May 13, 2012 | Volume: 3 | Issue: 8 | Pages: 609-609

10.1212/wnl.3.8.609 | PMID 13087581

A hereditary disorder with dementia, spastic dysarthria, vertical eye movement paresis, gait disturbance, splenomegaly, and abnormal copper metabolism

Neurology | May 13, 2012 | Volume: 23 | Issue: 10 | Pages: 1039-1039

10.1212/wnl.23.10.1039 | PMID 4795418

Myxedema and ataxia

Neurology | May 13, 2012 | Volume: 19 | Issue: 1 | Pages: 37-37

10.1212/wnl.19.1.37 | PMID 4304453

Experimental cerebral edema

Neurology | May 13, 2012 | Volume: 17 | Issue: 7 | Pages: 669-669

10.1212/wnl.17.7.669 | PMID 4165505

Foreign body reaction of the brain

Neurology | May 13, 2012 | Volume: 17 | Issue: 4 | Pages: 337-337

10.1212/wnl.17.4.337 | PMID 4164418

Gilles de la Tourette's syndrome

Neurology | May 13, 2012 | Volume: 16 | Issue: 5 | Pages: 453-453

10.1212/wnl.16.5.453 | PMID 5219863