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European Journal of Nuclear Medicine and Molecular Imaging|January 27, 2021
18F-FDG brain PET hypometabolism in patients with long COVIDE Guedj, J Y Campion, P Dudouet, et al.Arthritis and Rheumatism|January 2, 2009
Transfer of the shared epitope through microchimerism in women with rheumatoid arthritisJ M Rak, L Maestroni, N Balandraud, et al.Arthritis and Rheumatism|January 5, 2002
Phenotypic diversity is not determined by independent genetic factors in familial spondylarthropathyR Said-Nahal, C Miceli-Richard, M A D'Agostino, et al.Journal of Medical Genetics|August 10, 2010
The severity of phenotype linked to SUCLG1 mutations could be correlated with residual amount of SUCLG1 proteinC Rouzier, S Le Guédard-Méreuze, K Fragaki, et al.Arthritis and Rheumatism|June 17, 2000
The familial form of spondylarthropathy: a clinical study of 115 multiplex families. Groupe Français d'Etude Génétique des SpondylarthropathiesR Said-Nahal, C Miceli-Richard, J M Berthelot, et al.Mitochondrion|December 15, 2007
Rapid identification of mitochondrial DNA (mtDNA) mutations in neuromuscular disorders by using surveyor strategyS Bannwarth, V Procaccio, C Rouzier, et al.Pageof 27