H. Narbonne

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 senescence

C. Bodemer, B. Donadille, C. Vigouroux, 2007, Cell Death and Differentiation.

Mitochondrial Diabetes: Clinical Specificity and Diagnosis

B. Vialettes, H. Narbonne, 2002 .

Can fructosamine be a surrogate for HbA(1c) in evaluating the achievement of therapeutic goals in diabetes?

H. Portugal, B. Vialettes, H. Narbonne, 2001, Diabetes & metabolism.

Gastrointestinal tract symptoms in Maternally Inherited Diabetes and Deafness (MIDD).

B. Vialettes, H. Narbonne, R. Valéro, 2004, Diabetes & metabolism.

Searching for A3243G mitochondrial DNA mutation in buccal mucosa in order to improve the screening of patients with mitochondrial diabetes.

C. Desnuelle, B. Vialettes, H. Narbonne, 2001, European journal of endocrinology.

Hypothyroidism and survival during sunitinib therapy in metastatic renal cell carcinoma (mRCC): A prospective observational analysis.

F. Bladou, N. Salem, J. Walz, 2010 .

Hydroxychloroquine and azithromycin tolerance in haemodialysis patients during COVID-19 infection

C. Solas, J. Bergounioux, R. Guilhaumou, 2020, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

New metabolic phenotypes in laminopathies: LMNA mutations in patients with severe metabolic syndrome.

B. Donadille, C. Vigouroux, C. Lebbé, 2007, The Journal of clinical endocrinology and metabolism.

Could thyroid dysfunction influence outcome in sunitinib-treated metastatic renal cell carcinoma?

F. Bladou, N. Salem, P. Viens, 2012, Annals of oncology : official journal of the European Society for Medical Oncology.

Retinal and renal complications in patients with a mutation of mitochondrial DNA at position 3,243 (maternally inherited diabetes and deafness). A case–control study

H. Gin, G. Charpentier, P. Massin, 2008, Diabetologia.

Acute hyperinsulinism modulates plasma apolipoprotein B-48 triglyceride-rich lipoproteins in healthy subjects during the postprandial period.

D. Lairon, H. Portugal, C. Defoort, 2001, Diabetes.

Phenotypic Expression of Diabetes Secondary to a T14709C Mutation of Mitochondrial DNA: Comparison with MIDD syndrome (A3243G mutation): a case report

P. Cozzone, J. Pouget, C. Desnuelle, 1997, Diabetes Care.

Could thyroid dysfunction influence outcome in sunitinib-treated metastatic renal cell carcinoma?

F. Bladou, N. Salem, P. Viens, 2012 .

Mitochondrial DNA variations in patients with maternally inherited diabetes and deafness syndrome.

C. Desnuelle, B. Vialettes, P. Staccini, 2000, Biochemical and biophysical research communications.