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European Journal of Medical Genetics|December 30, 2018
Oro-dental and cranio-facial characteristics of osteogenesis imperfecta type VJean-Marc Retrouvey, Doaa Taqi, Faleh Tamimi, et al.
Biochemical and Biophysical Research Communications|December 16, 2019
Uremic toxins promote accumulation of oxidized protein and increased sensitivity to hydrogen peroxide in endothelial cells by impairing the autophagic fluxSilvia D Rodrigues, Sabrina S Santos, Tassiana Meireles, et al.
The Journal of Chemical Physics|February 20, 2008
Temperature dependence of the electrical conductivity of imidazolium ionic liquidsJan Leys, Michael Wübbenhorst, Chirukandath Preethy Menon, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 12, 2011
Comparison of removal capacity of two consecutive generations of high-flux dialysers during different treatment modalitiesNatalie Meert, Sunny Eloot, Eva Schepers, et al.
Cancer|November 1, 1986
Metastatic interstitial pneumonitis after autologous bone marrow transplantation. A consequence of reinjection of malignant cells?P Glorieux, E Bouffet, I Philip, et al.
American Journal of Human Genetics|February 17, 2015
Cole-Carpenter syndrome is caused by a heterozygous missense mutation in P4HBFrank Rauch, Somayyeh Fahiminiya, Jacek Majewski, et al.
Acta Biomaterialia|January 6, 2026
Osteoarthritic chondrocytes exert higher contractile forces and exhibit enhanced protrusive activity when cultured in 3D degradable hydrogelsMaxim Vovchenko, Nele Vaes, Jorge Barrasa-Fano, et al.
Pediatric Critical Care Medicine : a Journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies|August 13, 2016
Translating Neurodevelopmental Care Policies Into Practice: The Experience of Neonatal ICUs in France-The EPIPAGE-2 Cohort StudyVeronique Pierrat, Anaëlle Coquelin, Marina Cuttini, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 1, 1992
Two hereditary defects related to vitamin D metabolism map to the same region of human chromosome 12q13-14M Labuda, T M Fujiwara, M V Ross, et al.
Journal of Medical Genetics|December 15, 2012
Osteogenesis imperfecta type V: marked phenotypic variability despite the presence of the IFITM5 c.-14C>T mutation in all patientsFrank Rauch, Pierre Moffatt, Moira Cheung, et al.
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