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Page 1
Clinical aspects of mitochondrial diabetes.
Vialettes B, Paquis-Flucklinger V, Bendahan D. Vialettes B, et al. Diabetes Metab. 1997 Mar;23 Suppl 2:52-6. Diabetes Metab. 1997. PMID: 9105784 Review.
[Detection and prevalence of mitochondrial genome mutations in diabetes].
Paquis-Flucklinger V, Vialettes B, Canivet B, Freychet P, Hieronimus S, Vague P, Saunières A, Desnuelle C. Paquis-Flucklinger V, et al. Journ Annu Diabetol Hotel Dieu. 1997:25-31. Journ Annu Diabetol Hotel Dieu. 1997. PMID: 9296981 Review. French. No abstract available.
Maternally inherited diabetes and deafness: a multicenter study.
Guillausseau PJ, Massin P, Dubois-LaForgue D, Timsit J, Virally M, Gin H, Bertin E, Blickle JF, Bouhanick B, Cahen J, Caillat-Zucman S, Charpentier G, Chedin P, Derrien C, Ducluzeau PH, Grimaldi A, Guerci B, Kaloustian E, Murat A, Olivier F, Paques M, Paquis-Flucklinger V, Porokhov B, Samuel-Lajeunesse J, Vialettes B. Guillausseau PJ, et al. Ann Intern Med. 2001 May 1;134(9 Pt 1):721-8. doi: 10.7326/0003-4819-134-9_part_1-200105010-00008. Ann Intern Med. 2001. PMID: 11329229
Molecular and functional effects of the T14709C point mutation in the mitochondrial DNA of a patient with maternally inherited diabetes and deafness.
Perucca-Lostanlen D, Taylor RW, Narbonne H, Mousson de Camaret B, Hayes CM, Saunieres A, Paquis-Flucklinger V, Turnbull DM, Vialettes B, Desnuelle C. Perucca-Lostanlen D, et al. Biochim Biophys Acta. 2002 Dec 12;1588(3):210-6. doi: 10.1016/s0925-4439(02)00167-9. Biochim Biophys Acta. 2002. PMID: 12393175 Free article.
126 results