Brain anomalies in maternally inherited diabetes and deafness syndrome-Reference-Cited by-同舟云学术

Brain anomalies in maternally inherited diabetes and deafness syndrome

Published:2009-06-18 Issue:10 Volume:256 Page:1696-1704
ISSN:0340-5354
Container-title:Journal of Neurology
language:en
Short-container-title:J Neurol

Author:

Fromont I.,Nicoli F.,Valéro R.,Felician O.,Lebail B.,Lefur Y.,Mancini J.,Paquis-Flucklinger V.,Cozzone P. J.,Vialettes Bernard

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),Neurology

Link

http://link.springer.com/content/pdf/10.1007/s00415-009-5185-4.pdf

Reference39 articles.

1. Maassen JA (2002) Mitochondrial diabetes: pathophysiology, clinical presentation, and genetic analysis. Am J Med Genet 115:66–70

2. Matsumoto J, Saver JL, Brennan KC, Ringman JM (2005) Mitochondrial encephalomyopathy with lactic acidosis and stroke (MELAS). Rev Neurol Dis 2:30–34

3. Kadowaki T, Kadowaki H, Mori Y, Tobe K, Sakuta R, Suzuki Y, Tanabe Y, Sakura H, Awata T, Goto Y et al (1994) A subtype of diabetes mellitus associated with a mutation of mitochondrial DNA. N Engl J Med 330:962–968

4. 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 (2001) Maternally inherited diabetes and deafness: a multicenter study. Ann Intern Med 134:721–728

5. Narbonne H, Perucca-Lostanlen D, Desnuelle C, Vialettes B, Saunieres A, Paquis-Flucklinger V (2001) Searching for A3243G mitochondrial DNA mutation in buccal mucosa in order to improve the screening of patients with mitochondrial diabetes. Eur J Endocrinol 145:541–542

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