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Clinics and Research in Hepatology and Gastroenterology|April 8, 2024
Phenotype and molecular characterization of Wilson's disease in MoroccoNadia Abbassi, Aicha Bourrahouat, Eduardo Couchonnal Bedoya, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|June 21, 2022
Variability of Primary Sjögren's Syndrome Is Driven by Interferon-α and Interferon-α Blood Levels Are Associated With the Class II HLA-DQ LocusDiana Trutschel, Pierre Bost, Xavier Mariette, et al.
Orphanet Journal of Rare Diseases|February 5, 2010
Retrospective French nationwide survey of childhood aggressive vascular anomalies of bone, 1988-2009Sébastien Héritier, Martine Le Merrer, Francis Jaubert, et al.
The Journal of Pediatrics|June 28, 2021
Multisystem Inflammatory Syndrome of Children: Subphenotypes, Risk Factors, Biomarkers, Cytokine Profiles, and Viral SequencingRoberta L DeBiasi, Ashraf S Harahsheh, Hemalatha Srinivasalu, et al.
Global Change Biology|October 24, 2022
Potential for redistribution of post-moult habitat for Eudyptes penguins in the Southern Ocean under future climate conditionsCara-Paige Green, David B Green, Norman Ratcliffe, et al.
Theranostics|March 21, 2020
Identification of a new aggressive axis driven by ciliogenesis and absence of VDAC1-ΔC in clear cell Renal Cell Carcinoma patientsLucilla Fabbri, Maeva Dufies, Sandra Lacas-Gervais, et al.
Joint Bone Spine|December 13, 2002
Validation of the French version of the Childhood Health Assessment Questionnaire (CHAQ) in juvenile idiopathic arthritisJacques Pouchot, Jean-Paul Larbre, Irène Lemelle, et al.
Cell Host & Microbe|May 11, 2022
Persisting uropathogenic Escherichia coli lineages show signatures of niche-specific within-host adaptation mediated by mobile genetic elementsRobert Thänert, JooHee Choi, Kimberly A Reske, et al.
Clinical and Experimental Rheumatology|August 21, 2001
The French version of the Childhood Health Assessment Questionnaire (CHAQ) and the Child Health Questionnaire (CHQ)J Pouchot, N Ruperto, I Lemelle, et al.
Clinical and Experimental Immunology|September 21, 2020
Clinical, functional and genetic characterization of 16 patients suffering from chronic granulomatous disease variants - identification of 11 novel mutations in CYBBM Mollin, S Beaumel, B Vigne, et al.
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