Citations 329

Insights into the dynamics of hereditary diffuse leukoencephalopathy with axonal spheroids

Neurology | September 15, 2008 | Volume: 71 | Issue: 12 | Pages: 925-929

10.1212/01.wnl.0000325916.30701.21 | PMID 18794495

Susceptibility genes for restless legs syndrome are not associated with Parkinson disease

Neurology | July 14, 2008 | Volume: 71 | Issue: 3 | Pages: 222-223

10.1212/01.wnl.0000317101.67684.e3 | PMID 18625969

Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease

Neurology | March 13, 2008 | Volume: 70 | Issue: 16_part_2 | Pages: 1456-1460

10.1212/01.wnl.0000304044.22253.03 | PMID 18337586

Study of a Swiss dopa-responsive dystonia family with a deletion in GCH1

Neurology | September 6, 2007 | Volume: 70 | Issue: 16_part_2 | Pages: 1377-1383

10.1212/01.wnl.0000275527.35752.c5 | PMID 17804835

Speech Characteristics of Patients With Pallido-Ponto-Nigral Degeneration and Their Application to Presymptomatic Detection in At-Risk Relatives

American Journal of Speech-Language Pathology | May 3, 2007 | Volume: 15 | Issue: 3 | Pages: 226-235

10.1044/1058-0360(2006/021) | PMID 16896172

Purpose This report describes the speech characteristics of individuals with a neurodegenerative syndrome called pallido-ponto-nigral degeneration (PPND) and examines the speech samples of at-risk, but asymptomatic, relatives for possible preclinical detection. Method Speech samples of 9 members of a PPND kindred were subjected to perceptual characterization. Speech deterioration patterns were reported for 2 participants followed longitudinally at 6-month intervals. Cross-sectional findings were reported for 3 participants at various stages of disease. Longitudinal and cross-sectional findings were used to guide the examination of 4 at-risk, but asymptomatic, participants. Results Results revealed a progressive mixed dysarthria with hypokinetic, spastic, and flaccid features. It was characterized primarily by vocal tremor and high-frequency vocal flutter, speaking rate abnormalities most often in the direction of slowing, and a tendency toward monopitch. Dysarthria progression was marked by exacerbation and increasing severity of early features, progressive decrease in spontaneous speech output, verbal perseverations, and eventual mutism. Results for at-risk participants revealed preclinical speech abnormalities that preceded other motor signs. Speech results were examined in light of available autopsy findings for site of lesion associations. Conclusion The dysarthria of PPND is an early harbinger of disease onset. It has a mixed presentation, with hypokinetic, spastic, and flaccid features.
Distinctive MRI findings in pallidopontonigral degeneration (PPND)

Neurology | February 19, 2007 | Volume: 68 | Issue: 8 | Pages: 620-621

10.1212/01.wnl.0000254614.39759.3d | PMID 17310038

Parkinson disease

Neurology | July 12, 2006 | Volume: 64 | Issue: 11 | Pages: 1925-1930

10.1212/01.wnl.0000163993.82388.c8 | PMID 15955945

Brain acetylcholinesterase activity in FTDP-17 studied by PET

Neurology | April 24, 2006 | Volume: 66 | Issue: 8 | Pages: 1276-1277

10.1212/01.wnl.0000208515.50924.94 | PMID 16636254

Accurate Determination of Ataxin-2 Polyglutamine Expansion in Patients with Intermediate-Range Repeats

Genetic Testing | January 6, 2003 | Volume: 6 | Issue: 3 | Pages: 217-220

10.1089/109065702761403397 | PMID 12490063