Difference between revisions of "Template talk:BioblastAlert2023"
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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 | | '''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 – Sep 18-24
World Mitochondrial Disease Week raises awareness of mitochondrial disease through educational, fundraising and advocacy activities.
»See what is happening near you«
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«
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«
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