Citations 118

New and Appropriate Goals for Parkinson Disease Physical Therapy

JAMA Neurology | January 19, 2016 | Volume: 73 | Issue: 3 | Pages: 269

10.1001/jamaneurol.2015.4449 | PMID 26785221

Orthostatic tremor

Neurology | January 9, 2016 | Volume: 86 | Issue: 5 | Pages: 458-464

10.1212/wnl.0000000000002328 | PMID 26747880

Expanding Phenotypic Spectrum ofNKX2-1–Related Disorders—Mitochondrial and Immunologic Dysfunction

JAMA Neurology | December 8, 2015 | Volume: 73 | Issue: 2 | Pages: 237

10.1001/jamaneurol.2015.2976 | PMID 26640963

Basal ganglia T1 hyperintensity in LGI1-autoantibody faciobrachial dystonic seizures

Neurology Neuroimmunology & Neuroinflammation | October 2, 2015 | Volume: 2 | Issue: 6 | Pages: No page available

10.1212/nxi.0000000000000161 | PMID 26468474

Responses to and Outcomes of Treatment of Autoimmune Cerebellar Ataxia in Adults

JAMA Neurology | September 28, 2015 | Volume: 72 | Issue: 11 | Pages: 1304

10.1001/jamaneurol.2015.2378 | PMID 26414229

Role for the microtubule-associated protein tau variant p.A152T in risk of α-synucleinopathies

Neurology | September 3, 2015 | Volume: 85 | Issue: 19 | Pages: 1680-1686

10.1212/wnl.0000000000001946 | PMID 26333800

Effectiveness of ECT in Patients With Parkinsonism

The Journal of Neuropsychiatry and Clinical Neurosciences | December 17, 2014 | Volume: 10 | Issue: 2 | Pages: 187-193

10.1176/jnp.10.2.187 | PMID 9608407

Multiple system atrophy: Prognostic indicators of survival

Movement Disorders | June 7, 2014 | Volume: 29 | Issue: 9 | Pages: 1151-1157

10.1002/mds.25927 | PMID 24909319

AbstractNeurological and autonomic presentation in multiple system atrophy (MSA) may predict early mortality. Quantification of early autonomic failure as a mortality predictor is lacking. Early neurological and autonomic clinical features were retrospectively reviewed in 49 MSA cases (median age at onset, 56.1 years; 16 women) confirmed by autopsy at Mayo Clinic. When available, the 10‐point composite autonomic severity score derived from the autonomic reflex screen provided quantification of the degree of autonomic failure and thermoregulatory sweat test quantitated body surface anhidrosis. Symptoms at onset were autonomic in 50%, parkinsonian in 30%, and cerebellar in 20% of cases. Survival (median [95% confidence interval]) was 8.6 [6.7‐10.2] years. Survival was shorter in patients with early laboratory evidence of generalized (composite autonomic severity score ≥ 6) autonomic failure (7.0 [3.9‐9.8] vs. 9.8 [4.6‐13.8] years; P = 0.036), and early requirement of bladder catheterization (7.3 [3.1‐10.2] vs. 13.7 [8.5‐14.9] years; P = 0.003) compared with those without these clinical features. On Cox proportional analysis, prognostic indicators of shorter survival were older age at onset (hazard ratio [95% confidence interval], 1.04 [1.01‐1.08]; P = 0.03), early requirement of bladder catheterization (7.9 [1.88‐38.63]; P = 0.004), and early generalized (composite autonomic severity score ≥ 6) autonomic failure (2.8 [1.01‐9.26]; P = 0.047). Gender, phenotype, and early development of gait instability, aid‐requiring ambulation, orthostatic symptoms, neurogenic bladder, or significant anhidrosis (thermoregulatory sweat test ≥ 40%) were not indicators of shorter survival. Our data suggest that early development of severe generalized autonomic failure more than triples the risk of shorter survival in patients with MSA. © 2014 International Parkinson and Movement Disorder Society
Swiss Cheese Striatum

JAMA Neurology | April 14, 2014 | Volume: 71 | Issue: 6 | Pages: 735

10.1001/jamaneurol.2014.286 | PMID 24733660

Clinical and imaging characterization of progressive spastic dysarthria

European Journal of Neurology | September 21, 2013 | Volume: 21 | Issue: 3 | Pages: 368-376

10.1111/ene.12271 | PMID 24053325

Background and purposeTo describe speech, neurological and imaging characteristics of a series of patients presenting with progressive spastic dysarthria as the first and predominant sign of a presumed neurodegenerative disease.MethodsParticipants were 25 patients with spastic dysarthria as the only or predominant speech disorder. Clinical features, pattern of MRI volume loss on voxel‐based morphometry and pattern of hypometabolism on F18‐fluorodeoxyglucose positron emission tomography (FDG‐PET) scan are described.ResultsAll patients demonstrated speech characteristics consistent with spastic dysarthria, including strained voice quality, slow speaking rate, monopitch and monoloudness, and slow and regular speech alternating motion rates. Eight patients did not have additional neurological findings on examination. Pseudobulbar affect, upper motor neuron pattern limb weakness, spasticity, Hoffman sign and positive Babinski reflexes were noted in some of the remaining patients. Twenty‐three patients had electromyographic assessment and none had diffuse motor neuron disease or met El Escorial criteria for amyotrophic lateral sclerosis. Voxel‐based morphometry revealed striking bilateral white matter volume loss affecting the motor cortex (BA 4), including the frontoparietal operculum (BA 43) with extension into the middle cerebral peduncle. FDG‐PET showed subtle hypometabolism affecting the premotor and motor cortices in some patients, particularly in those who had a disease duration longer than 2 years.ConclusionsA neurodegenerative disorder that begins focally with spastic dysarthria due to involvement of the motor and premotor cortex and descending corticospinal and corticobulbar pathways is characterized. The descriptive label ‘progressive spastic dysarthria’ to best capture the dominant presenting feature of the syndrome is proposed.