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Difference between revisions of "Template talk:BioblastAlert2023"

From Bioblast
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:{|
| width="100" align="center" | [[File:VASCage logo.png|130px|link=https://wiki.oroboros.at/index.php/Functional_Mitochondrial_Diagnostics]]
| width="100" align="center" | [[File:VASCage logo.png|130px|link=https://wiki.oroboros.at/index.php/Functional_Mitochondrial_Diagnostics]]
| '''Research into mitochondrial medicine offers hope that treatments and cures for mitochondrial diseases will be found.'''<br>
| '''Research in the field of mitochondrial medicine offers hope that treatments and cures for mitochondrial diseases will be found.'''<br>
* [[2nd Workshop on Mitochondrial Functional Diagnostics Innsbruck AT]]
* [[2nd Workshop on Mitochondrial Functional Diagnostics Innsbruck AT]]
:::- as part of the joint project between Oroboros and VASCage
:::- as part of the joint project between Oroboros and VASCage
:::- October 16, 2023
:::- October 16, 2023
:::- Join in person: inform us until Oct 1 by email to [email protected], limited spaces available
:::- Location: MiPArt, Schoepfstrasse 18, 6020 Innsbruck, AT
|}
|}
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Revision as of 17:25, 18 September 2023

Bioblast alert 2023(06) - World Mitochondrial Disease Week: 2023-09-18

World Mitochondrial Disease Week logo.jpg World Mitochondrial Disease Week – Sep 18-24

World Mitochondrial Disease Week raises awareness of mitochondrial disease through educational, fundraising and advocacy activities.
»See what is happening near you«

O2k-Publications in the MiPMap In 1962, the first report of a patient with a mitochondrial disease was published.
  • Luft R, Ikkos D, Palmieri G, Ernster L, Afzelius B (1962). A case of severe hypermetabolism of nonthyroid origin with a defect in the maintenance of mitochondrial respiratory control: a correlated clinical, biochemical, and morphological study. »Bioblast link«


O2k-Network.png The first mitochondrial DNA mutations associated with disease were described in 1988.

These discoveries were a game changer in the field of mitochondrial diseases. 

  • Holt IJ, Harding A E, Morgan-Hughes JA (1988) Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies. »Bioblast link«
  • Wallace DC, Singh G, Lott MT, Hodge JA, Schurr TG, Lezza AM, Elsas LJ 2nd, Nikoskelainen EK (1988) Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy. »Bioblast link«
  • Zeviani M, Moraes CT, DiMauro S, Nakase H, Bonilla E, Schon EA, Rowland LP (1988) Deletions of mitochondrial DNA in Kearns-Sayre syndrome. »Bioblast link«


VASCage logo.png Research in the field of mitochondrial medicine offers hope that treatments and cures for mitochondrial diseases will be found.
- as part of the joint project between Oroboros and VASCage
- October 16, 2023
- Join in person: inform us until Oct 1 by email to [email protected], limited spaces available
- Location: MiPArt, Schoepfstrasse 18, 6020 Innsbruck, AT