Publications by authors named "Eduardo Benarroch"

Article Synopsis
  • The study aimed to identify predicting factors and the frequency of phenoconversion from sporadic adult-onset ataxia (SAOA) to multiple system atrophy (MSA) by reviewing Mayo Clinic patient data from 1998 to 2018.
  • Out of 169 ataxia patients, 60 (35.5%) transitioned to MSA, with notable clinical features like early autonomic symptoms, stridor, and dream enactment behavior observed in these patients.
  • Imaging and autonomic testing revealed significant differences, such as pontine atrophy and abnormal blood pressure responses, indicating that specific clinical and testing features can help identify individuals likely to phenoconvert to MSA.
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Levodopa is the most widely used medication for the symptomatic treatment of Parkinson's disease and, despite being an "old" drug, is still considered the gold standard for offering symptomatic relief. The pharmacokinetic and pharmacodynamics of levodopa have been studied extensively. Our review explores the molecular mechanisms that affect the absorption of this drug, focusing on the large intra- and interindividual variability of absorption that is commonly encountered in daily clinical practice, and on the interaction with other medications.

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Purpose: Prior studies reported evidence of autonomic involvement in motor neuron disease and suggested more severe dysfunction in upper motor neuron predominant syndromes. Hence, we sought to characterize autonomic impairment in primary lateral sclerosis.

Methods: Neurological evaluations, thermoregulatory sweat tests, and autonomic reflex screens were analyzed retrospectively in 34 primary lateral sclerosis patients (28 definite and 6 probable).

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Objective: To explore the clinical progression of the brain-/body-first categories within Lewy body disease (LBD): Parkinson's disease (PD), dementia with Lewy bodies (DLB), and PD dementia.

Methods: We used of the Rochester Epidemiology Project to establish a population-based cohort of clinically diagnosed LBD. We used two definitions for differentiating between brain- and body-first LBD: a previously hypothesized body-first presentation in patients with rapid eye movement sleep behavior onset before motor symptoms onset; and an expanded definition of body-first LBD when a patient had at least 2 premotor symptoms between constipation, erectile dysfunction, rapid eye movement sleep behavior, anosmia, or neurogenic bladder.

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Objective: To evaluate the associations between prescription opioid exposures in community-dwelling older adults and gray and white matter structure by magnetic resonance imaging.

Methods: Secondary analysis was conducted of a prospective, longitudinal population-based cohort study employing cross-sectional imaging of older adult (≥65 years) enrollees between November 1, 2004, and December 31, 2017. Gray matter outcomes included cortical thickness in 41 structures and subcortical volumes in 6 structures.

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Background: Young-onset multiple system atrophy (YOMSA) is defined as the onset of multiple system atrophy (MSA) before the age of 40 years old. YOMSA is rare and there is much uncertainty of the phenotype and natural history in patients with YOMSA.

Objective: The objective is to evaluate the characteristics and disease course of patients with YOMSA.

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We describe a 66-year-old woman with Parkinson's disease, carrying a known pathogenic missense variant in the Valosin-containing-protein () gene. She responded excellently to L-dopa, had no cognitive or motoneuronal dysfunction. Laboratory analyses and MRI were unremarkable.

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Pain-sensitive structures in the head and neck, including the scalp, periosteum, meninges, and blood vessels, are innervated predominantly by the trigeminal and upper cervical nerves. The trigeminal nerve supplies most of the sensation to the head and face, with the ophthalmic division (V1) providing innervation to much of the supratentorial dura mater and vessels. This creates referral patterns for pain that may be misleading to clinicians and patients, as described by studies involving awake craniotomies and stimulation with electrical and mechanical stimuli.

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Article Synopsis
  • Restless legs syndrome (RLS) significantly disrupts sleep and daily life for many individuals, and while standard medications help some, not all patients experience relief or can tolerate these treatments.
  • This review focuses on spinal cord stimulation (SCS) as a potential new treatment for RLS, considering its similarities with pain syndromes in terms of underlying mechanisms and treatment strategies.
  • Although current evidence from cases is limited and doesn't confirm SCS's effectiveness for RLS, its ability to modulate brain activity shows promise, highlighting the need for more comprehensive research in this area.
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Objective: Advanced Parkinson's Disease (PD) is associated with Parkinson's Disease gait impairment (PDg), which increases the risk for falls and is often treatment-refractory. Subthalamic nucleus (STN) and globus pallidus pars interna (GPi) deep brain stimulation (DBS) often fails to improve axial symptoms like PDg. Spinal cord stimulation (SCS) has been suggested to improve PDg.

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