University of Strasbourg-ko ikertzaileekin lankidetzan egindako argitalpenak (13)

2023

  1. Evaluating the Construct of Damage in Systemic Lupus Erythematosus

    Arthritis Care and Research, Vol. 75, Núm. 5, pp. 998-1006

2021

  1. Impact of glucocorticoids on the incidence of lupus-related major organ damage: A systematic literature review and meta-regression analysis of longitudinal observational studies

    Lupus Science and Medicine, Vol. 8, Núm. 1

  2. Self-Similar Dynamics for the Modified Korteweg-de Vries Equation

    International Mathematics Research Notices, Vol. 2021, Núm. 13, pp. 9958-10013

2020

  1. Asymptotics in Fourier space of self-similar solutions to the modified Korteweg-de Vries equation

    Journal des Mathematiques Pures et Appliquees, Vol. 137, pp. 101-142

2019

  1. Optimal Antiplatelet Therapy in Moderate to Severe Asymptomatic and Symptomatic Carotid Stenosis: A Comprehensive Review of the Literature

    European Journal of Vascular and Endovascular Surgery, Vol. 57, Núm. 2, pp. 199-211

2018

  1. Editor's Choice – Management of Atherosclerotic Carotid and Vertebral Artery Disease: 2017 Clinical Practice Guidelines of the European Society for Vascular Surgery (ESVS)

    European Journal of Vascular and Endovascular Surgery, Vol. 55, Núm. 1, pp. 3-81

2016

  1. Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356

    Autophagy

  2. Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

    Autophagy, Vol. 12, Núm. 1, pp. 1-222

  3. Uncommon nucleotide excision repair phenotypes revealed by targeted high-throughput sequencing

    Orphanet Journal of Rare Diseases, Vol. 11, Núm. 1

2014

  1. Highly sensitive diagnosis of 43 monogenic forms of diabetes or obesity through one-step pcrbased enrichment in combination with next-generation sequencing

    Diabetes Care, Vol. 37, Núm. 2, pp. 460-467

2010

  1. Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome

    Human Mutation, Vol. 31, Núm. 2, pp. 113-126

2005

  1. Trends and geographic inequalities in the prevalence of Down syndrome in Europe, 1980-1999

    Revue d'Epidemiologie et de Sante Publique

2004

  1. Prenatal diagnostic procedures used in pregnancies with congenital malformations in 14 regions of Europe

    Prenatal Diagnosis, Vol. 24, Núm. 11, pp. 908-912