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Diabetes & Metabolism|November 6, 2001
Can fructosamine be a surrogate for HbA(1c) in evaluating the achievement of therapeutic goals in diabetes?H Narbonne, E Renacco, V Pradel, et al.
Annales De L'Institut Pasteur. Virology|April 1, 1988
Evaluation of herpes simplex virus susceptibility to acyclovir using an enzyme-linked immunosorbent assayP M André, C H Narbonne, P Y Donnio, et al.
Diabetes & Metabolism|March 19, 2004
Gastrointestinal tract symptoms in Maternally Inherited Diabetes and Deafness (MIDD)H Narbonne, V Paquis-Fluckinger, R Valero, et al.
Biochemical and Biophysical Research Communications|November 4, 2000
Mitochondrial DNA variations in patients with maternally inherited diabetes and deafness syndromeD Perucca-Lostanlen, H Narbonne, J B Hernandez, et al.
Cell Death and Differentiation|July 7, 2007
Human lipodystrophies linked to mutations in A-type lamins and to HIV protease inhibitor therapy are both associated with prelamin A accumulation, oxidative stress and premature cellular senescenceM Caron, M Auclair, B Donadille, et al.
Diabetes|March 29, 2001
Acute hyperinsulinism modulates plasma apolipoprotein B-48 triglyceride-rich lipoproteins in healthy subjects during the postprandial periodA Harbis, C Defoort, H Narbonne, et al.
Biochimica Et Biophysica Acta|October 24, 2002
Molecular and functional effects of the T14709C point mutation in the mitochondrial DNA of a patient with maternally inherited diabetes and deafnessD Perucca-Lostanlen, R W Taylor, H Narbonne, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|June 10, 2011
Could thyroid dysfunction influence outcome in sunitinib-treated metastatic renal cell carcinoma?R Sabatier, J C Eymard, J Walz, et al.
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.
Diabetologia|June 27, 2008
Retinal and renal complications in patients with a mutation of mitochondrial DNA at position 3,243 (maternally inherited diabetes and deafness). A case-control studyP Massin, D Dubois-Laforgue, T Meas, et al.
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