Results 81 to 90 of about 21,237 (225)

QT Interval Evaluation in Right Ventricular Pacing: Validation of a Novel Formula

open access: yesPacing and Clinical Electrophysiology, EarlyView.
Abstract Background QT interval measurement in the presence of right ventricular pacing (RVP) represents a clinical challenge. We therefore aimed to derive and validate a formula for QT estimation during RVP in a large cohort of pacemaker patients. Methods and Results We prospectively enrolled 100 patients in a derivation cohort and 487 in a validation
Amr Abdin   +9 more
wiley   +1 more source

Werner syndrome: quantitative assessment of skin aging

open access: yes, 2018
Vittorio Mazzarello, Marco Ferrari, Pasquale Ena Skinlab, Department of Biomedical Sciences, University of Sassari, Sassari, Italy Background: Werner syndrome (WS) is a rare autosomal recessive disorder characterized by premature aging in adults ...
Ena P, Mazzarello V, Ferrari M
core  

Transient overexpression of Werner protein rescues starvation induced autophagy in Werner syndrome cells

open access: yes, 2014
Reduced autophagy may be associated with normal and pathological aging. Here we report a link between autophagy and Werner protein (WRNp), mutated in Werner syndrome, the human premature aging Werner syndrome (WS).
Bohr, Vilhelm A.   +4 more
core   +1 more source

Werner Irnich: Pioneer in the Development of the Dual‐Chamber Pacemaker—An Obituary

open access: yesPacing and Clinical Electrophysiology, EarlyView.
ABSTRACT Fifty years ago, Werner Irnich presented the concept of an optimal pacemaker capable of responding appropriately to various cardiac arrhythmias and perceptual disturbances, and intended to be used in 85% of patients. With this concept, Irnich was far ahead of his time. His proposed circuitry for AV block and atrial fibrillation, as well as his
Bernd Lemke
wiley   +1 more source

Atypical meningioma in Werner syndrome: a case report

open access: yes, 2006
INTRODUCTION: Werner Syndrome, or adult progeria, is a rare autosomal recessive disorder caused by a mutation in the Werner Syndrome Gene belonging to the family of RecQ helicase.
BUSATO S   +3 more
core   +1 more source

Emotions in Meaning‐Making: Toward a Sociological Theory of Cathexis

open access: yesSociological Forum, EarlyView.
ABSTRACT The role of emotion in meaning‐making remains undertheorized in cultural sociology. This article argues that emotions and affect are intrinsic to meaning‐making and proposes cathexis—the attachment of emotions generated in social interaction to objects, symbols, and ideas—as the fundamental mechanism by which emotions co‐constitute cultural ...
Dmitry Kurakin
wiley   +1 more source

Lateral Tarsorrhaphy and Fixation on the Orbital Ligament to Correct Macroblepharon in Dogs: 77 Palpebral Fissures

open access: yesVeterinary Ophthalmology, Volume 28, Issue 2, Page 448-456, March 2025.
ABSTRACT Purpose To describe a surgical method for correcting lower lid entropion, lateral canthal entropion, and macroblepharon. Methods Lid margins were incised at a 45° angle, and lateral lid margins and a rhomboid shaped piece of skin were resected based on the degree of macroblepharon.
Maximilian Werner‐Tutschku   +1 more
wiley   +1 more source

Herlyn-Werner-Wunderlich syndrome presenting with dysmenorrhea: a case report

open access: yesJournal of Medical Case Reports, 2019
Background Herlyn-Werner-Wunderlich syndrome is a rare congenital anomaly characterized by uterus didelphys, obstructed hemivagina, and ipsilateral renal agenesis. The most common presentation is abdominal pain, dysmenorrhea, and abdominal mass secondary
Dilruba Sharmen Nishu   +5 more
doaj   +1 more source

Potential health benefits of cold‐water immersion: the central role of PGC‐1α

open access: yesThe Journal of Physiology, EarlyView.
Abstract figure legend Cold‐water immersion (CWI) elicits autonomic, somato‐motoric (shivering thermogenesis), endocrine and metabolic, sensory transduction, and local biophysical effects that may converge on the transcriptional co‐activator PGC‐1α (centre).
Erich Hohenauer   +2 more
wiley   +1 more source

WRN Protein and Werner Syndrome

open access: yes, 2010
Werner syndrome is an autosomal recessive disorder associated with premature aging and cancer predisposition. Cells from Werner syndrome patients show increased genomic instability and are hypersensitive to DNA damage agents. Werner syndrome is caused by
Luo, PhD, Jianyuan
core  

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