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Diabetes Care|November 14, 1997
Phenotypic expression of diabetes secondary to a T14709C mutation of mitochondrial DNA. Comparison with MIDD syndrome (A3243G mutation): a case reportB H Vialettes, V Paquis-Flucklinger, J F Pelissier, et al.British Journal of Clinical Pharmacology|February 12, 1998
Trimetazidine does not modify blood levels and immunosuppressant effects of cyclosporine A in renal allograft recipientsN Simon, P Brunet, D Roumenov, et al.Neurogenetics|March 25, 2000
Mutations in the X-linked form of Charcot-Marie-Tooth disease in the French populationP Latour, N Lévy, M Paret, et al.Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|August 24, 1999
Karyological and dental identification of Microtus limnophilus in a large focus of alveolar echinococcosis (Gansu, China)F Courant, P Brunet-Lecomte, V Volobouev, et al.Journal of Investigative Medicine : the Official Publication of the American Federation for Clinical Research|February 24, 2001
Adenosine and hemodialysis in humansR Guieu, P Brunet, J Sampol, et al.Biochemical and Biophysical Research Communications|July 3, 2021
Spleen route accelerates engraftment of human hematopoietic stem cellsA Bedel, J Boutin, S Amintas, et al.Revue Neurologique|September 7, 2013
The French Pompe registry. Baseline characteristics of a cohort of 126 patients with adult Pompe diseaseP Laforêt, K Laloui, B Granger, et al.Revue Neurologique|April 4, 2016
Multiple acyl-CoA dehydrogenase deficiency (MADD) as a cause of late-onset treatable metabolic diseaseA Béhin, C Acquaviva-Bourdain, S Souvannanorath, et al.The International Journal of Artificial Organs|January 31, 2002
Uremic toxicity: present state of the artR Vanholder, A Argilés, U Baurmeister, et al.Neuropathology and Applied Neurobiology|April 29, 2020
Novel CAPN3 variant associated with an autosomal dominant calpainopathyM Cerino, E Campana-Salort, A Salvi, et al.Pageof 36