Paquis-Flucklinger V - Search Results

1

Clinical phenotype of mitochondrial diabetes due to rare mitochondrial DNA mutations.

Decoux-Poullot AG, Bannwarth S, Procaccio V, Lebre AS, Jardel C, Vialettes B, Paquis-Flucklinger V, Chevalier N. Decoux-Poullot AG, et al. Ann Endocrinol (Paris). 2020 Jun;81(2-3):68-77. doi: 10.1016/j.ando.2020.04.007. Epub 2020 Apr 28. Ann Endocrinol (Paris). 2020. PMID: 32409007

2

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.

3

[Clinical manifestation of diabetes from mitochondrial cytopathy].

Vialettes B, Narbonne H, Silvestre-Aillaud P, Bendahan D, Paquis-Flucklinger V. Vialettes B, et al. Journ Annu Diabetol Hotel Dieu. 1997:17-23. Journ Annu Diabetol Hotel Dieu. 1997. PMID: 9296972 Review. French. No abstract available.

4

[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.

5

Phenotypic expression of diabetes secondary to a T14709C mutation of mitochondrial DNA. Comparison with MIDD syndrome (A3243G mutation): a case report.

Vialettes BH, Paquis-Flucklinger V, Pelissier JF, Bendahan D, Narbonne H, Silvestre-Aillaud P, Montfort MF, Righini-Chossegros M, Pouget J, Cozzone PJ, Desnuelle C. Vialettes BH, et al. Diabetes Care. 1997 Nov;20(11):1731-7. doi: 10.2337/diacare.20.11.1731. Diabetes Care. 1997. PMID: 9353617

6

Importance of searching for mtDNA defects in patients with diabetes and hearing deficit.

Paquis-Flucklinger V, Vialettes B, Vague P, Canivet B, Hieronimus S, Oliver C, Pellissier JF, Saunières A, Desnuelle C. Paquis-Flucklinger V, et al. Diabetologia. 1998 Jun;41(6):740-1. doi: 10.1007/s001250050978. Diabetologia. 1998. PMID: 9662060 No abstract available.

7

Importance of searching for associated mitochondrial DNA alterations in patients with multiple deletions.

Paul R, Desnuelle C, Pouget J, Pellissier JF, Richelme C, Monfort MF, Butori C, Saunieres A, Paquis-Flucklinger V. Paul R, et al. Eur J Hum Genet. 2000 May;8(5):331-8. doi: 10.1038/sj.ejhg.5200463. Eur J Hum Genet. 2000. PMID: 10854092

8

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

Perucca-Lostanlen D, Narbonne H, Hernandez JB, Staccini P, Saunieres A, Paquis-Flucklinger V, Vialettes B, Desnuelle C. Perucca-Lostanlen D, et al. Biochem Biophys Res Commun. 2000 Nov 2;277(3):771-5. doi: 10.1006/bbrc.2000.3751. Biochem Biophys Res Commun. 2000. PMID: 11062027

9

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

10

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

Narbonne H, Perucca-Lostanlen D, Desnuelle C, Vialettes B, Saunières A, Paquis-Flucklinger V. Narbonne H, et al. Eur J Endocrinol. 2001 Oct;145(4):541-2. doi: 10.1530/eje.0.1450541. Eur J Endocrinol. 2001. PMID: 11581015 No abstract available.

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