Results 61 to 70 of about 1,723,261 (194)

Improvement of Primary Writing Tremor in Parkinson's Disease with Carbidopa/Levodopa [PDF]

open access: yes, 2015
Background: Primary writing tremor is a task-specific phenomenon that has been described as variants of essential tremor or dystonia. Phenomenology Shown: We describe the case of a 63-year-old female who initially had primary writing tremor, later ...
Paule E. Greene   +3 more
core   +1 more source

Exploring the Chemical Complexity and Toxicological Behaviour of Semi‐permanent Make‐Up Pigments: A Systematic Review

open access: yesJournal of Applied Toxicology, EarlyView.
ABSTRACT Semi‐permanent make‐up (SPMU), or micropigmentation, involves implanting pigments into the dermal layer of the skin for cosmetic enhancement. Unlike topical cosmetics, which are rapidly cleared from the body, SPMU pigments persist in living tissues, raising unique toxicological considerations.
T. A. N. Kaye   +3 more
wiley   +1 more source

Transoral Robotic Surgery in Head and Neck Oncology: A Scoping Review of Evidence, Technological Advancements, and Future Trajectories

open access: yesJournal of Surgical Oncology, EarlyView.
ABSTRACT Robotic surgery has transformed head and neck cancer (HNC) treatment. This scoping review synthesizes evidence on transoral robotic surgery (TORS), focusing on applications, limitations, and future directions. Following PRISMA‐ScR guidelines, this review used the PCC framework (Population: HNC patients; Concept: technological advancements ...
Anna Luíza Damaceno Araújo   +6 more
wiley   +1 more source

Tremor: Clinical Phenomenology and Assessment Techniques [PDF]

open access: yes, 2012
Tremors are among the most common movement disorders. As there can be considerable variability in the manner in which clinicians assess tremor, objective quantitative tools such as electromyography, accelerometry, and computerized, spiral analysis can be
Seth L. Pullman   +3 more
core   +1 more source

SLC7A6OS Founder Mutation: A Rare Cause of Progressive Myoclonus Epilepsy Dated to 1100 Years Ago

open access: yesMovement Disorders, EarlyView.
Abstract Background SLC7A6OS c.191A>G is a rare, autosomal recessive cause of progressive myoclonus epilepsy (PME). The c.191A>G variant, first discovered in two families from Türkiye and Portugal, was recently identified in three additional probands from the USA, all of Puerto Rican ancestry.
Bronwyn E. Grinton   +17 more
wiley   +1 more source

Enhanced deep learning approach for detecting and locating tectonic tremors in the Nankai subduction zone

open access: yesEarth, Planets and Space
Tectonic tremors are key indicators of slow-slip phenomena, and detecting them accurately is a challenging task. Conventional techniques often fail to detect tremors during periods of intense tremor activity.
Yuya Jinde   +2 more
doaj   +1 more source

ATXN8OS Intermediate Expansion Acts as a Genetic Modifier in Spinocerebellar Ataxia Type 48 (SCA48/STUB1)

open access: yesMovement Disorders, EarlyView.
Abstract Background Association between monoallelic STUB1 variant and expanded ATXN8OS alleles was recently reported, suggesting a pathogenic interaction that may influence spinocerebellar ataxia type 48 (SCA48) phenotype. Objectives We investigated the frequency and clinical impact of ATXN8OS in a large cohort of STUB1 carriers compared to individuals
Charlotte Mouraux   +11 more
wiley   +1 more source

Characterizing Orthostatic Tremor Using a Smartphone Application [PDF]

open access: yes, 2017
Background: Orthostatic tremor is one of the few tremor conditions requiring an electromyogram for definitive diagnosis since leg tremor might not be visible to the naked eye.Phenomenology Shown: An iOS application (iSeismometer, ObjectGraph ...
Fasano, Alfonso   +3 more
core   +1 more source

Mortality in People with Action Tremor: Findings from Three Population‐Based Cohort Studies

open access: yesMovement Disorders, EarlyView.
Abstract Background Action tremor is common in adults and increases with age. Although essential tremor (ET) is a major subgroup, action tremor comprises heterogeneous phenotypes, and its prognostic implications remain uncertain. Objectives Our aim was to examine the association between action tremor and all‐cause mortality using complementary ...
Katrine Lawaetz Kristensen   +5 more
wiley   +1 more source

Consensus Guidelines for Diagnosis and Management of Pyruvate Dehydrogenase Complex Deficiency. [PDF]

open access: yesJ Inherit Metab Dis
ABSTRACT Primary pyruvate dehydrogenase complex deficiency (PDCD) comprises a group of monogenic disorders caused by pathogenic variants in genes encoding subunits of, or regulatory components affecting, the pyruvate dehydrogenase complex. The clinical phenotype spans a broad continuum, ranging from early onset congenital lactic acidosis to infantile ...
Keshavan N   +23 more
europepmc   +2 more sources

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