Results 131 to 140 of about 582,403 (259)

Bulletin mensuel de la Maison du peuple du VIe arrondissement

open access: yes, 1904
Variante(s) de titre : Bulletin mensuel de la Maison du peuple du sixième arrondissementVariante(s) de titre : Bulletin de la Maison du peuple du sixième arrondissementVariante(s) de titre : Bulletin de la Maison du peuple du VIe ...
Maison du peuple du VIe arrondissement (Paris). Auteur du texte
core   +1 more source

Five‐Year Outcomes of Laparoscopic Sphincter‐Preserving Surgery for Rectal Cancer: A Prospective Study in Elderly Vietnamese Patients

open access: yesAging and Cancer, EarlyView.
This prospective study demonstrates that laparoscopic sphincter‐preserving surgery is feasible for elderly patients. While overall survival reaches 70% at 5 years, advanced T‐stage and the omission of neoadjuvant therapy significantly drive recurrence, highlighting the need for personalized geriatric protocols despite logistical challenges.
Huu Duc Ho   +4 more
wiley   +1 more source

Chronobiology of Cancer: How Aging Fuels Oncogenesis at the Molecular Level

open access: yesAging and Cancer, EarlyView.
This graphical abstract illustrates the key biological pathways linking aging with cancer development and progression. In the upper left, cumulative exposure to ultraviolet radiation, toxins, and reactive oxygen species (ROS) causes DNA damage and genomic instability, whereas age‐related decline in repair mechanisms, such as ATM/ATR, BER, and NER ...
Anu Singh, Aroonima Misra, Sufian Zaheer
wiley   +1 more source

Ce que la science fait à la vie

open access: yes, 2016
Cet ouvrage se situe à la croisée de deux problèmes bien identifiés dans le domaine des science studies : celui de la création scientifique d’une part, et d’autre part celui du rapport entre la vie et l’œuvre des savants.
Nicolas Adell
core  

Clinical Impact of NOTCH3 Variant Location After First Stroke in CADASIL

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Despite its monogenic origin, Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy exhibits marked variability in clinical expression and severity. Variants in the NOTCH3 gene, within epidermal growth factor‐like repeat domains 1–6 or 7–34, are known to influence disease onset, but their impact ...
Léa Aguilhon   +5 more
wiley   +1 more source

Préoccupation des clients pour le respect de la vie privée et réponse à une sollicitation portant sur des données personnelles [PDF]

open access: yes
Cette recherche s'intéresse aux perceptions et aux comportements des clients lorsqu'un site marchand leur propose de remplir un formulaire en ligne. Il s'agit à la fois d'analyser la cohérence de la réponse avec le niveau de préoccupation du client pour ...
Caroline Miltgen, Pierre Volle
core  

Deep Learning Pose Estimation for Phenotyping of Co‐Occurring Hyperkinetic Movement Disorders

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To explore whether routine outpatient video combined with deep learning‐based pose estimation and clinically interpretable kinematic features can support multi‐label phenotyping of co‐occurring hyperkinetic movement disorders (HMDs).
Laura Cif   +17 more
wiley   +1 more source

L'intrusion des images dans la vie quotidienne. Eléments d'histoire récente

open access: yes, 2010
La vie sociale des images - chapitre 10 Historiquement, l’essor de l’image au quotidien est lié pour l’essentiel au développement des villes et même en priorité à celui des grandes villes.
Sylvain Maresca
core  

Natural Frequencies of Levodopa‐Induced Dyskinesia in Parkinson's Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objectives Abnormal involuntary movements, known as dyskinesias, are common complications of levodopa treatment in patients with Parkinson's disease and can significantly impair quality of life. The underlying pathophysiology remains unclear, and current therapeutic options are limited.
Ioannis U. Isaias   +3 more
wiley   +1 more source

Augmenting and Assaying Nav1.1 Protein Quantity for Dravet Syndrome Therapy

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Dravet Syndrome (DS) is a developmental and epileptic encephalopathy predominantly caused by heterozygous loss‐of‐function variants in SCN1A, which encodes Nav1.1. Conserved upstream open reading frames (uORFs) in SCN1A were validated to regulate translation in reporter assays, demonstrating the therapeutic viability of increasing Nav1.1 from ...
Aiswarya Saravanan   +7 more
wiley   +1 more source

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