Results 161 to 170 of about 155,071 (257)

Differentiating Persistent and Recurrent Dysphagia in Zenker Diverticulum: A POuCH Study

open access: yesThe Laryngoscope, EarlyView.
In longitudinal follow up of 160 patients who underwent surgery for Zenker's diverticulum, 29 patients did not respond (< 50% improvement in EAT‐10 and final EAT‐10 greater than 3). Two cohorts of patients emerged: the majority (23/29), who had persistent symptoms after surgery and never improved to a new baseline, and a smaller cohort (6/29) who had ...
Ari D. Schuman   +32 more
wiley   +1 more source

Modular Polymers With Tuneable Charge and Amphiphilicity for Effective Antimicrobial Photodynamic Therapy

open access: yesMacromolecular Rapid Communications, EarlyView.
A modular dual‐strategy platform combining free radical copolymerisation and post‐polymerisation modification yields a library of ruthenium‐functionalised polymers for antimicrobial photodynamic therapy. Tuneable composition and net charge govern activity against multidrug‐resistant Pseudomonas aeruginosa biofilms and Staphylococcus aureus under ...
Ali Balasini   +8 more
wiley   +1 more source

An Approach to Antibody-Mediated Rejection in Pediatric Liver Transplantation. [PDF]

open access: yesPediatr Transplant
Jaramillo C   +8 more
europepmc   +1 more source

Cognitive, Motor and Oculomotor Contributions to the Trail Making Test in Progressive Supranuclear Palsy

open access: yesMovement Disorders Clinical Practice, EarlyView.
Abstract Background Progressive supranuclear palsy (PSP) is a neurodegenerative disorder characterized by motor, oculomotor and cognitive impairments. Yet disentangling cognitive deficits from motor and oculomotor dysfunction remains a diagnostic and methodological challenge.
Indira Garcia‐Cordero   +12 more
wiley   +1 more source

DNAJC13 Variants Show No Robust Association With Parkinson's Disease in a Multiancestry Cohort

open access: yesMovement Disorders, EarlyView.
Abstract Background DNAJC13 was initially linked to autosomal dominant (AD) Parkinson's disease (PD) in a European Mennonite family carrying the p.N855S variant. However, imperfect segregation and conflicting reports of pathogenicity raised uncertainty of the role of DNAJC13 in the disease.
César Luis Ávila   +11 more
wiley   +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

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