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Integrated care for diabetes.
Chedin P, Cahen-Varsaux J. Chedin P, et al. Among authors: cahen varsaux j. BMJ. 1994 Jul 23;309(6949):275. doi: 10.1136/bmj.309.6949.275. BMJ. 1994. PMID: 8069165 Free PMC article. No abstract available.
The clinical variability of maternally inherited diabetes and deafness is associated with the degree of heteroplasmy in blood leukocytes.
Laloi-Michelin M, Meas T, Ambonville C, Bellanné-Chantelot C, Beaufils S, Massin P, Vialettes B, Gin H, Timsit J, Bauduceau B, Bernard L, Bertin E, Blickle JF, Cahen-Varsaux J, Cailleba A, Casanova S, Cathebras P, Charpentier G, Chedin P, Crea T, Delemer B, Dubois-Laforgue D, Duchemin F, Ducluzeau PH, Bouhanick B, Dusselier L, Gabreau T, Grimaldi A, Guerci B, Jacquin V, Kaloustian E, Larger E, Lecleire-Collet A, Lorenzini F, Louis J, Mausset J, Murat A, Nadler-Fluteau S, Olivier F, Paquis-Flucklinger V, Paris-Bockel D, Raynaud I, Reznik Y, Riveline JP, Schneebeli S, Sonnet E, Sola-Gazagnes A, Thomas JL, Trabulsi B, Virally M, Guillausseau PJ; Mitochondrial Diabetes French Study Group. Laloi-Michelin M, et al. Among authors: cahen varsaux j. J Clin Endocrinol Metab. 2009 Aug;94(8):3025-30. doi: 10.1210/jc.2008-2680. Epub 2009 May 26. J Clin Endocrinol Metab. 2009. PMID: 19470619
Focal segmental glomerulosclerosis associated with mitochondrial cytopathy.
Doleris LM, Hill GS, Chedin P, Nochy D, Bellanne-Chantelot C, Hanslik T, Bedrossian J, Caillat-Zucman S, Cahen-Varsaux J, Bariety J. Doleris LM, et al. Among authors: cahen varsaux j. Kidney Int. 2000 Nov;58(5):1851-8. doi: 10.1111/j.1523-1755.2000.00356.x. Kidney Int. 2000. PMID: 11044204 Free article.
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.
Massin P, Dubois-Laforgue D, Meas T, Laloi-Michelin M, Gin H, Bauduceau B, Bellanné-Chantelot C, Bertin E, Blickle JF, Bouhanick B, Cahen-Varsaux J, Casanova S, Charpentier G, Chedin P, Dupuy O, Grimaldi A, Guerci B, Kaloustian E, Lecleire-Collet A, Lorenzini F, Murat A, Narbonne H, Olivier F, Paquis-Flucklinger V, Virally M, Vincenot M, Vialettes B, Timsit J, Guillausseau PJ; GEDIAM (Mitochondrial Diabetes French Study Group). Massin P, et al. Among authors: cahen varsaux j. Diabetologia. 2008 Sep;51(9):1664-70. doi: 10.1007/s00125-008-1073-1. Epub 2008 Jun 26. Diabetologia. 2008. PMID: 18581092
Heterogeneity of diabetes phenotype in patients with 3243 bp mutation of mitochondrial DNA (Maternally Inherited Diabetes and Deafness or MIDD).
Guillausseau PJ, Dubois-Laforgue D, Massin P, Laloi-Michelin M, Bellanné-Chantelot C, Gin H, Bertin E, Blickle JF, Bauduceau B, Bouhanick B, Cahen-Varsaux J, Casanova S, Charpentier G, Chedin P, Derrien C, Grimaldi A, Guerci B, Kaloustian E, Lorenzini F, Murat A, Olivier F, Paques M, Paquis-Flucklinger V, Tielmans A, Vincenot M, Vialettes B, Timsit J; GEDIAM, Mitochondrial Diabetes French Study Group. Guillausseau PJ, et al. Among authors: cahen varsaux j. Diabetes Metab. 2004 Apr;30(2):181-6. doi: 10.1016/s1262-3636(07)70105-2. Diabetes Metab. 2004. PMID: 15223991